Posts belonging to Category 'Symptoms Of Thyroid Problems'

Second Opinion after Diagnosis?

Question:

Even the intial diagnosis may be dependant on the doctor’s attitude. I

have read on this newsgroup and heard from friends of some doctors who have seen someone clearly with diabetes, but have called it a "pre diabetic condition" or "low level diabetes", not giving the patient the required urgency. What we DON’T hear about is people who were told they DID have diabetes when in fact they didn’t! So if you’re told you have it, it’s highly UNlikely that you don’t. bj

Response:

Check with your GP or the lab that performed the Hb1Ac test.  If sub 6% is in the normal range for that lab, you have reason to look for second opinions.  If your lab is one where the normal numbers are lower and 5.2% is high, the previous advice would stick (though note I am not a medical professional). If your lab is one of the common labs where sub 6% is normal, I would recommend a different course.  First, if your BG levels are shooting up toward 200 after any kind of normal food and or you are having hypoglycemic events, there is something wrong with your glucose metabolism – it may be temporary or it may be permanent – but something is wrong.  There are many things that can cause a systemic disruption.  (Thyroid mentioned in this group is certainly one of them. Another thing to check would be Lupus.)  Pregnancy and the aftermath can certainly trigger problems. If you can control your BG levels with diet, you can, in my non-professional opinion, take some time to sort it out. If I were in your shoes, I would get a good BG meter and test several times per day – waking and 1 or 2 postprandial (2 hours after eating).  Your levels should be sub 125 waking (sub 110 would be better) and sub 140 2hour postprandial.  Adjust your diet accordingly.  I believe a low carb diet is best (note: I say low carb diet as the kind of food, not as a way to lose weight – if you are thin you should eat enough calories of protein, fat and carbs to maintain weight).  I recommend you eat 5 or 6 small meals per day to counter your hypoglycemia.  You should take some vitamins – I think LEF has the best in the market, but they are pricey – Twinlab is a more economical alternative. EXERCISE – exercise is a must.  No matter how tired you feel you MUST get out and do some aerobic exercise.  Exercise is part of how your body moves out toxins and keeps itself in tune – your lymph circulation system has no pump – it moves with your body’s exercise (your lymph system is a primary infection fighter).  Exercise also helps your body’s glucose metabolism. One final side note: You asked in a earlier post if saturated fats can cause an increase in insulin resistance.  I have read this was the case and, if you think about, it would make perfect sense.  We tend to think of glucose (sugar) and fat as 2 totally separate substances.  In fact, fat is just a lot of sugar molecules added together with a COOH group.  Fat is our body’s way of storing glucose for later use (long term – glucogen is the short term storage form).  Our glucose metabolism is an interaction of many chemical substances – among them are sugars(glucose), hormones (insulin, glucagon, somatostatin, cortisol, etc), fats, etc.  It would make sense for the body to react to high levels of saturated fat(the kind of fat we store in our fat cells) in the blood as a signal the body needed to pull stored energy out of storage for use – insulin is a hormone to push glucose (energy) into the cells – thus high levels of saturated fat could be a counter chemical signal to insulin.  I do not know if this is what really happens – I am speculating.  But it does make sense and I have read that saturated fats increase insulin resistance. In summary, if you have had 175+ BG readings after a normal meal and or hypoglycemic events there is something wrong with your glucose metabolism.  If you can control your BG levels with diet, you can afford to take some time to sort out a diagnosis.  Test your BG levels regularly. Exercise is a must. If you are one of the lucky ones for whom this problem is transient, keep lurking.  I have read a lot of posts from smart people with a lot of good information. Best wishes!     – Hide quoted text — Show quoted text – What is your Hb1Ac reading?   Most of the time, the diagnosis of diabetes comes 5 to 10 years after the disease has begun to cause damage.  But upon occaision a diagnosis can be wrong (or maybe partially wrong).  Stress, usually due to physical causes such as a chronic infection, can cause temporarily high BG levels.  This may resolve itself after the cause of the stress is removed (note: I am not talking about a busy lifestyle or work hassles – the stressor needs to stimulate the liver to raise BG levels). The truth teller is usually the Hb1Ac level, though even here a chronic long term infection can prompt a misdiagnosis.  If your Hb1Ac level is above 6% (levels vary from lab to lab, but these are lab ‘normals’) you have a problem.  6% to 8% is a twilight zone where errors, though not likely, may be made.  Above 8% would be very unlikely. Taking from your other posts, Hb1Ac is an AGE and, to a limited degree, a measure of your rate of aging.  5% to 6% is normal.  Above 6% you are aging faster than normal.  Diabetes has been characterized as accelerated aging. There is a high probability your Doctor is correct in his diagnosis. Sorry. Is it common for diabetics to go to another Dr. to get a second opinion after a diagnosis of diabetes? If so when you see the second Dr. would you give him all of the information/diagnosis from the first Dr.? I would be affraid of the information influencing the second Dr. Especially if the second Dr. knows the first Dr. and respects and agrees with their diagnoisis. Any comments? What type of infections are we talking about and what type of tests would uncover them? I have been feeling poorly for 8 months now following a stressful pregnancy in which I was on bed rest most of the time, praying that I did not miscarry or go into premature labor. My baby had severe colic (cried excessively day and night) for four months after birth during which time I got about 3-4 hours of sleep per day then the next four months I had insomnia (which I get when I am overly stressed). I was also severly depressed during this time. My blood sugar was being controled all the while by a low carb diet -even though I did not suspect I might have diabetes (still not officially diagnosised). My Hb1ac was checked twice during this time -5.3 and 5.2. My stress has not gone away I am still fighting it everyday, telling myself to calm down and relax. I am still trying to figure out the new mother thing, while also trying to figure out my diet (adjusting it constantly to control skin problems and hypoglycemia), and trying to wind down enough before I go to sleep to avoid insomnia. I worry about the fact that I have not started an exercise routine, because my fatigue these days is overwhelming and I feel like I dont have enough energy to cover it. I have never faired well when it comes to stress, I have just accepted throughout the years that it did not agree with me and have mostly avoided stressful situations. The stress I have experienced during the past year and a half has been unavoidable and at times unbearable.

Response:

If you do indeed have a lump on your thyroid, push for checking it out — maybe an ultrasound to see if it really is there, fine needle aspiration (by an experienced practitioner) to see what it is. For an article on fna, see http://www.thyca.org/fna.htm bj

yesterday I had an appt at my endo’s, I told him I thought my thyroid was acting screwy, … I go monday for all my blood work. btw… he did find a lump so think

that helped in my pushing for further tests as well. – Hide quoted text — Show quoted text –

Response:

Not for an initial diagnosis, but on advice such as bg targets, monitoring for potential complications, diet or dietitian recommendation, medication and excercise recommendations. Even the intial diagnosis may be dependant on the doctor’s attitude. I have read on this newsgroup and heard from friends of some doctors who have seen someone clearly with diabetes, but have called it a "pre diabetic condition" or "low level diabetes", not giving the patient the required urgency. In my own case, after an ankle injury, during my hospital stay I had a routine blood test done which indicated diabetes. Unknown to me a report was sent to my family doctor, who promptly forgot all about it, until I came to him a year later with the "classic" symptoms of thirst and tiredness, with my bg by now *way* higher that it ever was. This was the same doctor who had never bothered to give me a bg test for the past 10 years. And the same doctor who a few months later told me to try "this tablet" (a potent sulphonurea) without bothering to tell me about such insignificant things as hypos. Some years later another doctor told me that a blood pressure of 160/100 was "nothing to worry about". I could go on and on, but I’m already bitching too much. This, in my opinion, is why you should "shop around" for the right doctor. It has been said on this newsgroup that the best diabetic doctor is one who has diabetes or who has a close relative with diabetes. Henry Mydlarz Melbourne, Australia

– Hide quoted text — Show quoted text – I wouldn’t stop at the second opinion. Initially I’d go for a third opinion and maybe a fourth – until I found a doctor who is both caring and knowledgeable on the subject. Do you mean to check out 2,3,4 docs to find one that you can work with in managing the diabetes?  The diagnosis is pretty cut and dry.  I see no reason to go to multiple docs for a diagnosis.  IMHO that only delays the treatment. — Best wishes Louise Type 2, controlling by diet and exercise

Response:

exactly… yesterday I had an appt at my endo’s, I told him I thought my thyroid was acting screwy, he grabbed my file, and was looking at a TSH test i’d had over a year ago! and claimed it was fine.. I told him.. (mind you i’m mouthy anyhow) BULLSHIT! we can just do new tests and I want all them ran NOT just a TSH, he claimed they normally dont run others.. and I said, "I want them!" so… I go monday for all my blood work. btw… he did find a lump so think that helped in my pushing for further tests as well. have to sometimes be demanding… it is our bodies.. not theirs.. — RK [T1 - dx 5/00]-[Lantus/Novolog]-[Experiments in progress...] http://www.alt-support-diabetes.org http://www.faqs.org/faqs/diabetes/faq http://www.alt-support-diabetes.org/files/zl-mirc.exe (chatroom software/verified clean w/Norton) Current Troll List: See ASD site for current list and how to killfile

: *YOU* are *YOUR* best doctor.. learn all about *YOU* then : tell your doctor what *YOU* need. : : Read about a woman doctor who had to go to a specialist out side her field. He : started telling her what they were going to do. She told him differently. He : asked if she was trying to tell him how to run his business. She told him: "No : This is my body and it means more to me that it does to you." Perhaps that is : what we need to remember when dealing with the doctors. Betty.

Response:

*YOU* are *YOUR* best doctor.. learn all about *YOU* then tell your doctor what *YOU* need.

Read about a woman doctor who had to go to a specialist out side her field. He started telling her what they were going to do. She told him differently. He asked if she was trying to tell him how to run his business. She told him: "No This is my body and it means more to me that it does to you." Perhaps that is what we need to remember when dealing with the doctors. Betty.

Response:

If it WAS EVER 126, you are diabetic.

My old doc quit. July 2001 it was 126 fasting. In July 2002 it was 136. Both were fasting.  Nurse told me blood work was OK. Got a new doc in November. He got records. Office called me in for fasting BG. They told me if everything was OK, they would not call. I do not like doing business that way – people forget. I called twice and no one returned my calls. The test was Thursday a week ago. I see him on Dec. 2. Guess I will find out then. And he will find out that I do not like being hung out to dry on a blood test after they were so insistent that I come in for test.  I have gone on 1200 ADA on my own. Need to lose at least 30 pounds. Betty.

Response:

I fully agree with you. Most of my treatments have been initiated by ME. I wouldn’t put my total faith in ANY doctor, even one with diabetes. Henry Mydlarz Melbourne Australia

– Hide quoted text — Show quoted text – heh.. i dont share your assesment that the "best doctor" is one with diabetes or a family member.. the asshole that clearly misdiagnosed me was a T2 himself, told me didn’t need to bother with a dietian, or classes. and kept me on glucophage for 7months while making me run 500+ bg’s constant.. *YOU* are *YOUR* best doctor.. learn all about *YOU* then tell your doctor what *YOU* need. thats my assesment. — RK [T1 - dx 5/00]-[Lantus/Novolog]-[Experiments in progress...] http://www.alt-support-diabetes.org http://www.faqs.org/faqs/diabetes/faq http://www.alt-support-diabetes.org/files/zl-mirc.exe (chatroom software/verified clean w/Norton) Current Troll List: See ASD site for current list and how to killfile : Not for an initial diagnosis, but on advice such as bg targets, monitoring : for potential complications, diet or dietitian recommendation, medication : and excercise recommendations. : : Even the intial diagnosis may be dependant on the doctor’s attitude. I have : read on this newsgroup and heard from friends of some doctors who have seen : someone clearly with diabetes, but have called it a "pre diabetic condition" : or "low level diabetes", not giving the patient the required urgency. : : In my own case, after an ankle injury, during my hospital stay I had a : routine blood test done which indicated diabetes. Unknown to me a report was : sent to my family doctor, who promptly forgot all about it, until I came to : him a year later with the "classic" symptoms of thirst and tiredness, with : my bg by now *way* higher that it ever was. This was the same doctor who had : never bothered to give me a bg test for the past 10 years. And the same : doctor who a few months later told me to try "this tablet" (a potent : sulphonurea) without bothering to tell me about such insignificant things as : hypos. : : Some years later another doctor told me that a blood pressure of 160/100 was : "nothing to worry about". : : I could go on and on, but I’m already bitching too much. : : This, in my opinion, is why you should "shop around" for the right doctor. : : It has been said on this newsgroup that the best diabetic doctor is one who : has diabetes or who has a close relative with diabetes. : : Henry Mydlarz : Melbourne, : Australia : : I wouldn’t stop at the second opinion. Initially I’d go for a third : opinion : and maybe a fourth – until I found a doctor who is both caring and : knowledgeable on the subject. : : Do you mean to check out 2,3,4 docs to find one that you can work with in : managing the diabetes?  The diagnosis is pretty cut and dry.  I see no : reason to go to multiple docs for a diagnosis.  IMHO that only delays the : treatment. : : — : Best wishes : Louise : : Type 2, controlling by diet and exercise : : : : : :

Response:

due to What type of infections are we talking about and what type of tests would uncover them?

I am not so sure I believe this.  This is what my old GP told me.  This was after I had GD and before my diabetes diagnosis.  I was getting these weird skin infections and ear infections.  My BG tested slightly high on one finger stick. Can’t remember now what that number was, but I think it was really close to whatever the cutoff was at that time.  I was told that my elevated BG was from the infections and that I didn’t have diabetes.  I now know that diabetes itself can cause infections.  And I seriously think I did have diabetes at that time.  But I was controlling it with diet and exercise. I have been feeling poorly for 8 months now following a stressful pregnancy in which I was on bed rest most of the time, praying that I did not miscarry or go into premature labor. My baby had severe colic (cried excessively day and night) for four months after birth during which time I got about 3-4 hours of sleep

Mine was the same way.  She slept maybe 5 hours a night if I was lucky. Other than that all she did was eat and cry. per day then the next four months I had insomnia (which I get when I am overly stressed). I was also severly depressed during this time. My blood sugar was being controled all the while by a low carb diet -even though I did not suspect I might have diabetes (still not officially diagnosised). My Hb1ac was checked twice during this time -5.3 and 5.2.

Have you had your thyroid checked?  Mine went wacky during pregnancy, but it is also common to have problems with this after giving birth.  Insomnia and depression are both symptoms of thyroid problems. My stress has not gone away I am still fighting it everyday, telling myself to calm down and relax. I am still trying to figure out the new mother thing, while also trying to figure out my diet (adjusting it constantly to control skin problems and hypoglycemia), and trying to wind down enough before I go to sleep to avoid insomnia. I worry about the fact that I have not started an exercise routine, because my fatigue these days is overwhelming and I feel like I dont have enough energy to cover it. I have never faired well when it comes to stress, I have just accepted throughout the years that it did not agree with me and have mostly avoided stressful situations. The stress I have experienced during the past year and a half has been unavoidable and at times unbearable.

Again, I can relate.  My daughter is 4 now, and there is less stress from her, but more stress due to the fact that we have moved cross country and then all of my medical conditions.  These other things that you’ve mentioned can go along with thyroid problems too.  Skin problems, fatigue and an inability to calm down and relax.  I have been taking meds for my thyroid, but my previous Dr. was allowing me to run high because I wasn’t losing weight as I should.  That in itself was a bad premise since it doesn’t work that way.  I am now on a lower dose and will get another lab done tomorrow to see how it is running now.  I feel much more calm now.  I do not feel the need to nap and I am sleeping soundly at night.  Based on your symptoms, I would give that some thought.  You should probably go to an Endocrinologist to be checked though.  I have heard time and again about GPs not doing thorough enough testing and telling people they are fine when indeed they are not. — Type 2 http://users.bestweb.net/~jbove/ Julie Bove, posting from new account

Response:

heh.. i dont share your assesment that the "best doctor" is one with diabetes or a family member.. the asshole that clearly misdiagnosed me was a T2 himself, told me didn’t need to bother with a dietian, or classes. and kept me on glucophage for 7months while making me run 500+ bg’s constant.. *YOU* are *YOUR* best doctor.. learn all about *YOU* then tell your doctor what *YOU* need. thats my assesment. — RK [T1 - dx 5/00]-[Lantus/Novolog]-[Experiments in progress...] http://www.alt-support-diabetes.org http://www.faqs.org/faqs/diabetes/faq http://www.alt-support-diabetes.org/files/zl-mirc.exe (chatroom software/verified clean w/Norton) Current Troll List: See ASD site for current list and how to killfile

: Not for an initial diagnosis, but on advice such as bg targets, monitoring : for potential complications, diet or dietitian recommendation, medication : and excercise recommendations. : : Even the intial diagnosis may be dependant on the doctor’s attitude. I have : read on this newsgroup and heard from friends of some doctors who have seen : someone clearly with diabetes, but have called it a "pre diabetic condition" : or "low level diabetes", not giving the patient the required urgency. : : In my own case, after an ankle injury, during my hospital stay I had a : routine blood test done which indicated diabetes. Unknown to me a report was : sent to my family doctor, who promptly forgot all about it, until I came to : him a year later with the "classic" symptoms of thirst and tiredness, with : my bg by now *way* higher that it ever was. This was the same doctor who had : never bothered to give me a bg test for the past 10 years. And the same : doctor who a few months later told me to try "this tablet" (a potent : sulphonurea) without bothering to tell me about such insignificant things as : hypos. : : Some years later another doctor told me that a blood pressure of 160/100 was : "nothing to worry about". : : I could go on and on, but I’m already bitching too much. : : This, in my opinion, is why you should "shop around" for the right doctor. : : It has been said on this newsgroup that the best diabetic doctor is one who : has diabetes or who has a close relative with diabetes. : : Henry Mydlarz : Melbourne, : Australia

: : I wouldn’t stop at the second opinion. Initially I’d go for a third : opinion : and maybe a fourth – until I found a doctor who is both caring and : knowledgeable on the subject. : : Do you mean to check out 2,3,4 docs to find one that you can work with in : managing the diabetes?  The diagnosis is pretty cut and dry.  I see no : reason to go to multiple docs for a diagnosis.  IMHO that only delays the : treatment. : : — : Best wishes : Louise : : Type 2, controlling by diet and exercise : : : : : :

Response:

Hmmm.  Is it that you don’t want a diagnosis of Type 1 diabetes?  Or is it that you don’t want *any* diagnosis of diabetes. If it would improve your insurance situation to get diagnosed with Type 2 rather than Type 1, then, yes, it might be worthwhile to get another opinion.  But if you want no diagnosis of diabetes at all, I just don’t think that will work. Why are you unable to exercise, if I might ask?    Because, it would be beneficial if you could get exercise. BL

Response:

What is your Hb1Ac reading?   Most of the time, the diagnosis of diabetes comes 5 to 10 years after the disease has begun to cause damage.  But upon occaision a diagnosis can be wrong (or maybe partially wrong).  Stress, usually due to physical causes such as a chronic infection, can cause temporarily high BG levels.  This may resolve itself after the cause of the stress is removed (note: I am not talking about a busy lifestyle or work hassles – the stressor needs to stimulate the liver to raise BG levels). The truth teller is usually the Hb1Ac level, though even here a chronic long term infection can prompt a misdiagnosis.  If your Hb1Ac level is above 6% (levels vary from lab to lab, but these are lab ‘normals’) you have a problem.  6% to 8% is a twilight zone where errors, though not likely, may be made.  Above 8% would be very unlikely. Taking from your other posts, Hb1Ac is an AGE and, to a limited degree, a measure of your rate of aging.  5% to 6% is normal.  Above 6% you are aging faster than normal.  Diabetes has been characterized as accelerated aging. There is a high probability your Doctor is correct in his diagnosis. Sorry. – Hide quoted text — Show quoted text – Is it common for diabetics to go to another Dr. to get a second opinion after a diagnosis of diabetes? If so when you see the second Dr. would you give him all of the information/diagnosis from the first Dr.? I would be affraid of the information influencing the second Dr. Especially if the second Dr. knows the first Dr. and respects and agrees with their diagnoisis. Any comments?

Response:

- Hide quoted text — Show quoted text – What is your Hb1Ac reading?   Most of the time, the diagnosis of diabetes comes 5 to 10 years after the disease has begun to cause damage.  But upon occaision a diagnosis can be wrong (or maybe partially wrong).  Stress, usually due to physical causes such as a chronic infection, can cause temporarily high BG levels.  This may resolve itself after the cause of the stress is removed (note: I am not talking about a busy lifestyle or work hassles – the stressor needs to stimulate the liver to raise BG levels). The truth teller is usually the Hb1Ac level, though even here a chronic long term infection can prompt a misdiagnosis.  If your Hb1Ac level is above 6% (levels vary from lab to lab, but these are lab ‘normals’) you have a problem.  6% to 8% is a twilight zone where errors, though not likely, may be made.  Above 8% would be very unlikely. Taking from your other posts, Hb1Ac is an AGE and, to a limited degree, a measure of your rate of aging.  5% to 6% is normal.  Above 6% you are aging faster than normal.  Diabetes has been characterized as accelerated aging. There is a high probability your Doctor is correct in his diagnosis. Sorry. Is it common for diabetics to go to another Dr. to get a second opinion after a diagnosis of diabetes? If so when you see the second Dr. would you give him all of the information/diagnosis from the first Dr.? I would be affraid of the information influencing the second Dr. Especially if the second Dr. knows the first Dr. and respects and agrees with their diagnoisis. Any comments?

My Hb1Ac is 5.3 (6 months ago) and 5.2 (3 months ago)

Response:

- Hide quoted text — Show quoted text – What is your Hb1Ac reading?   Most of the time, the diagnosis of diabetes comes 5 to 10 years after the disease has begun to cause damage.  But upon occaision a diagnosis can be wrong (or maybe partially wrong).  Stress, usually due to physical causes such as a chronic infection, can cause temporarily high BG levels.  This may resolve itself after the cause of the stress is removed (note: I am not talking about a busy lifestyle or work hassles – the stressor needs to stimulate the liver to raise BG levels). The truth teller is usually the Hb1Ac level, though even here a chronic long term infection can prompt a misdiagnosis.  If your Hb1Ac level is above 6% (levels vary from lab to lab, but these are lab ‘normals’) you have a problem.  6% to 8% is a twilight zone where errors, though not likely, may be made.  Above 8% would be very unlikely. Taking from your other posts, Hb1Ac is an AGE and, to a limited degree, a measure of your rate of aging.  5% to 6% is normal.  Above 6% you are aging faster than normal.  Diabetes has been characterized as accelerated aging. There is a high probability your Doctor is correct in his diagnosis. Sorry. Is it common for diabetics to go to another Dr. to get a second opinion after a diagnosis of diabetes? If so when you see the second Dr. would you give him all of the information/diagnosis from the first Dr.? I would be affraid of the information influencing the second Dr. Especially if the second Dr. knows the first Dr. and respects and agrees with their diagnoisis. Any comments?

What type of infections are we talking about and what type of tests would uncover them? I have been feeling poorly for 8 months now following a stressful pregnancy in which I was on bed rest most of the time, praying that I did not miscarry or go into premature labor. My baby had severe colic (cried excessively day and night) for four months after birth during which time I got about 3-4 hours of sleep per day then the next four months I had insomnia (which I get when I am overly stressed). I was also severly depressed during this time. My blood sugar was being controled all the while by a low carb diet -even though I did not suspect I might have diabetes (still not officially diagnosised). My Hb1ac was checked twice during this time -5.3 and 5.2. My stress has not gone away I am still fighting it everyday, telling myself to calm down and relax. I am still trying to figure out the new mother thing, while also trying to figure out my diet (adjusting it constantly to control skin problems and hypoglycemia), and trying to wind down enough before I go to sleep to avoid insomnia. I worry about the fact that I have not started an exercise routine, because my fatigue these days is overwhelming and I feel like I dont have enough energy to cover it. I have never faired well when it comes to stress, I have just accepted throughout the years that it did not agree with me and have mostly avoided stressful situations. The stress I have experienced during the past year and a half has been unavoidable and at times unbearable.

Response:

I wouldn’t stop at the second opinion. Initially I’d go for a third opinion and maybe a fourth – until I found a doctor who is both caring and knowledgeable on the subject.

– Hide quoted text — Show quoted text – Is it common for diabetics to go to another Dr. to get a second opinion after a diagnosis of diabetes? If so when you see the second Dr. would you give him all of the information/diagnosis from the first Dr.? I would be affraid of the information influencing the second Dr. Especially if the second Dr. knows the first Dr. and respects and agrees with their diagnoisis. Any comments?

Response:

I wouldn’t stop at the second opinion. Initially I’d go for a third opinion and maybe a fourth – until I found a doctor who is both caring and knowledgeable on the subject.

Do you mean to check out 2,3,4 docs to find one that you can work with in managing the diabetes?  The diagnosis is pretty cut and dry.  I see no reason to go to multiple docs for a diagnosis.  IMHO that only delays the treatment. — Best wishes Louise Type 2, controlling by diet and exercise

Response:

cc’d by email you are in denial YOU ARE DIABETIC no question, and no more testing will change that. "Blame it on MacDonalds" is just pure self-delusional bullcrap.  "RARELY go over 120" more delusional crap.  If it WAS EVER 126, you are diabetic.  If it was always under 126, bust sometimes above 110, you would be "prediabetic" You better stop making lame excuses and start doing something, otherwise you will be back saying "I dinner at Burger King, THAT is why it is over 300" or "I am RARELY over 400, it must be the ice cream I had last month". NOW, T1 or T2 – that is not always so clear, and you may want to see an endo and get a second opinion on which, and on managment options. – Hide quoted text — Show quoted text – In article , Is it common for diabetics to go to another Dr. to get a second opinion after a diagnosis of diabetes? … The criteria are pretty well defined. If a second doctor was to tell you what you wanted to hear, it wouldn’t change anything. Your blood and urine numbers won’t change. If you think the tests themselves were wrong, they weren’t done right, the lab screwed up, or whatever, then have them repeated. But the diagnostic criteria aren’t going to change. And the diagnosis requires a confirmation anyway, so it’s not all riding on one test (unless that one is REALLY ferociously bad, or DKA, or something like that, which makes it pretty obvious). This isn’t like getting a second opinion on whether or not to have your tonsils out or whatever. A second opinion on an actual treatment plan, if you don’t like the first approach &/or the doc is inflexible, is also another matter. bj Well, my Dr. seems to be set on a type 1 diagnosis based 1. I am thin and 2. one high carb meal at McDonalds which registered at 209 BG (2hr) on the blood test (was 190 on one touch glucose monitor). It was a high calorie (over 500kcal), high fat, high carb (over 100g). And it seems to me that all of those factors at up to a higher than high glucose. Yes I know its abnormally high. My other meals rarely go above 120.  My antibodies came back negative and my c-peptide is 2.4. I have no symptoms of diabetes. I have been unable to exercise for two years and was on bed rest during my pregnancy (8mo. ago). I feel like I have impaired glucose tolerance and some insulin resistance. I am on cobra and I could do without this diagnosis.

Response:

Tess I believe there is some good info in the posts above. But heres the thing ,as Ted said – you have diabetes. The way I see things from what you have posted in the past is you are thin and at the same time on a weight losing low carb diet with the possible vain hope you are going to not have diabetes or at the least control it through food alone. This to me rings the alarm bells. If you are already thin you possibly should not lose any more weight by restricting carbs. Unfortunately in your case with carbs also come a lot of vitamins and minerals so you may be missing out on vitals that your body need just in order to control your BSI!  I agree with everyone else that you don’t really need to be diagnosed over again but if your doctor is just a generalist and you are one of those with the weird body responses you need to go and see a doctor from further up the expertise chain. It seems to me you have more than just diabetes as a problem. The food aspect needs to be sorted out as well so your body has some chance to manage other functions adequately in conjunction with medication. A good Endo is where you should be headed with your fistful of questions. If you are already visiting one , By the way stress is not good for diabetes!

– Hide quoted text — Show quoted text – What is your Hb1Ac reading? Most of the time, the diagnosis of diabetes comes 5 to 10 years after the disease has begun to cause damage.  But upon occaision a diagnosis can be wrong (or maybe partially wrong).  Stress, usually due to physical causes such as a chronic infection, can cause temporarily high BG levels.  This may resolve itself after the cause of the stress is removed (note: I am not talking about a busy lifestyle or work hassles – the stressor needs to stimulate the liver to raise BG levels). The truth teller is usually the Hb1Ac level, though even here a chronic long term infection can prompt a misdiagnosis.  If your Hb1Ac level is above 6% (levels vary from lab to lab, but these are lab ‘normals’) you have a problem.  6% to 8% is a twilight zone where errors, though not likely, may be made.  Above 8% would be very unlikely. Taking from your other posts, Hb1Ac is an AGE and, to a limited degree, a measure of your rate of aging.  5% to 6% is normal.  Above 6% you are aging faster than normal.  Diabetes has been characterized as accelerated aging. There is a high probability your Doctor is correct in his diagnosis. Sorry.

– Hide quoted text — Show quoted text – Is it common for diabetics to go to another Dr. to get a second opinion after a diagnosis of diabetes? If so when you see the second Dr. would you give him all of the information/diagnosis from the first Dr.? I would be affraid of the information influencing the second Dr. Especially if the second Dr. knows the first Dr. and respects and agrees with their diagnoisis. Any comments?

Response:

Is it common for diabetics to go to another Dr. to get a second opinion after a diagnosis of diabetes? If so when you see the second Dr. would you give him all of the information/diagnosis from the first Dr.? I would be affraid of the information influencing the second Dr. Especially if the second Dr. knows the first Dr. and respects and agrees with their diagnoisis.

I don’t think so.  Some people don’t believe anything and would ask for a second opinion no matter what!  Now, I can see how a person might be told they didn’t have diabetes.   This happened to me on more than one occasion. Why?  Because at that time I was able to control my BG with diet and exercise.  And I was not given a GTT.  I was only given random or fasting finger sticks and urine tests.  Then low and behold I wound up in the ER only to be diagnosed with diabetes! But if you are told you have diabetes, then why would you need a second opinion?  It is a pretty cut and dried thing.  Denial is common though. Don’t know if it is common with other illnesses, but it seems to be with diabetes. — Type 2 http://users.bestweb.net/~jbove/ Julie Bove, posting from new account

Response:

- Hide quoted text — Show quoted text – Is it common for diabetics to go to another Dr. to get a second opinion  after a diagnosis of diabetes? … The criteria are pretty well defined. If a second doctor was to tell you what you wanted to hear, it wouldn’t change anything. Your blood and urine numbers won’t change. If you think the tests themselves were wrong, they weren’t done right, the lab screwed up, or whatever, then have them repeated. But the diagnostic criteria aren’t going to change. And the diagnosis requires a confirmation anyway, so it’s not all riding on one test (unless that one is REALLY ferociously bad, or DKA, or something like that, which makes it pretty obvious). This isn’t like getting a second opinion on whether or not to have your tonsils out or whatever. A second opinion on an actual treatment plan, if you don’t like the first approach &/or the doc is inflexible, is also another matter. bj

Well, my Dr. seems to be set on a type 1 diagnosis based 1. I am thin and 2. one high carb meal at McDonalds which registered at 209 BG (2hr) on the blood test (was 190 on one touch glucose monitor). It was a high calorie (over 500kcal), high fat, high carb (over 100g). And it seems to me that all of those factors at up to a higher than high glucose. Yes I know its abnormally high. My other meals rarely go above 120.  My antibodies came back negative and my c-peptide is 2.4. I have no symptoms of diabetes. I have been unable to exercise for two years and was on bed rest during my pregnancy (8mo. ago). I feel like I have impaired glucose tolerance and some insulin resistance. I am on cobra and I could do without this diagnosis.

Response:

Is it common for diabetics to go to another Dr. to get a second opinion

after a diagnosis of diabetes? …

The criteria are pretty well defined. If a second doctor was to tell you

what you wanted to hear, it wouldn’t change anything. Your blood and urine numbers won’t change. If you think the tests themselves were wrong, they weren’t done right, the lab screwed up, or whatever, then have them repeated. But the diagnostic criteria aren’t going to change. And the diagnosis requires a confirmation anyway, so it’s not all riding on one test (unless that one is REALLY ferociously bad, or DKA, or something like that, which makes it pretty obvious). This isn’t like getting a second opinion on whether or not to have your tonsils out or whatever. A second opinion on an actual treatment plan, if you don’t like the first approach &/or the doc is inflexible, is also another matter. bj

Response:

– Hide quoted text — Show quoted text – Is it common for diabetics to go to another Dr. to get a second opinion  after a diagnosis of diabetes? … The criteria are pretty well defined. If a second doctor was to tell you what you wanted to hear, it wouldn’t change anything. Your blood and urine numbers won’t change. If you think the tests themselves were wrong, they weren’t done right, the lab screwed up, or whatever, then have them repeated. But the diagnostic criteria aren’t going to change. And the diagnosis requires a confirmation anyway, so it’s not all riding on one test (unless that one is REALLY ferociously bad, or DKA, or something like that, which makes it pretty obvious). This isn’t like getting a second opinion on whether or not to have your tonsils out or whatever. A second opinion on an actual treatment plan, if you don’t like the first approach &/or the doc is inflexible, is also another matter. bj Well, my Dr. seems to be set on a type 1 diagnosis based 1. I am thin and 2. one high carb meal at McDonalds which registered at 209 BG (2hr) on the blood test (was 190 on one touch glucose monitor). It was a high calorie (over 500kcal), high fat, high carb (over 100g). And it seems to me that all of those factors at up to a higher than high glucose. Yes I know its abnormally high. My other meals rarely go above 120.  My antibodies came back negative and my c-peptide is 2.4. I have no symptoms of diabetes. I have been unable to exercise for two years and was on bed rest during my pregnancy (8mo. ago). I feel like I have impaired glucose tolerance and some insulin resistance. I am on cobra and I could do without this diagnosis

We could all do without diabetes, but your comment sounds a bit like denial. That`s quite understandable, it happens with any chronic illness, though not to everybody. Your BGs after that meal should not be that high, so it looks like you *probably* are diabetic :-( ( If you stick around on this NG, alt.support.diabetes, alt.support.diabetes.uk, & alt.food.diabetic you will get lots of love & support. As always, wishing you well.

Response:

<snip (2hr) on the blood test (was 190 on one touch glucose monitor). It was a high calorie (over 500kcal), high fat, high carb (over 100g). And it seems to me that all of those factors at up to a higher than high glucose. Yes I know its abnormally high. My other meals rarely go above 120.  My antibodies came back negative and my c-peptide is 2.4. I have no symptoms of diabetes. I have been unable to exercise for two years and was on bed rest during my pregnancy (8mo. ago). I feel like I have impaired glucose tolerance and some insulin resistance. I am on cobra and I could do without this diagnosis.

Your medical history sounds somewhat like mine.  I took the GTT during pregnancy and failed.  Normally a second, longer test would be given. Diagnostic criteria for GD (at least at that time) was failing two out of three.  My Dr. then told me he was merely going to assume that I had GD and not give me additional tests.  I was rather miffed at not knowing for sure, but relieved that I didn’t have to take the additional tests.  BTW, the highest number that I know of during the pregnancy was 110, fasting.  This was towards the very end of the pregnancy.  My Dr. was not pleased with this number and was going to put me on insulin if I reached this number again.  I did not. I had reactive hypoglycemia for most of my life.  And then oddly for several years prior to getting diabetes, I was able to skip meals and not get sick. Had no symptoms of hypoglycemia at all.  That in itself should have been a clue, but I didn’t know then what I know now. And as I have said before, Drs. kept telling me that I didn’t have diabetes because my numbers were good.  At that time, I was controlling with diet and exercise.  Just didn’t know it.  But I also now suffer from Neuropathy in my feet, lower legs and heart, probably because I WASN’T diagnosed when I should have been.  Nobody wants to have diabetes.  And many Drs. will think they are doing you a favor by not telling you that you really have it.  It sounds to me like you have been escaping high numbers because of your diet. But there is more to diabetes than merely high (or low) BG.  If your Dr. tells you that you have diabetes, take it seriously.  You may not have any symptoms.  I didn’t…aside from the Neuropathy.  And none of my Drs. suspected that.  They all blamed it on something else because I didn’t fit the profile of someone who had it.  Anyway…  Better you should come to terms with it now and take care of the situation.  You might still get complications from it, but at least you’ll know that you did all you could to avoid them. — Type 2 http://users.bestweb.net/~jbove/ Julie Bove, posting from new account

Response:

Is it common for diabetics to go to another Dr. to get a second opinion after a diagnosis of diabetes? If so when you see the second Dr. would you give him all of the information/diagnosis from the first Dr.? I would be affraid of the information influencing the second Dr. Especially if the second Dr. knows the first Dr. and respects and agrees with their diagnoisis. Any comments?

Response:

Is it common for diabetics to go to another Dr. to get a second opinion after a diagnosis of diabetes? If so when you see the second Dr. would you give him all of the information/diagnosis from the first Dr.? I would be affraid of the information influencing the second Dr. Especially if the second Dr. knows the first Dr. and respects and agrees with their diagnoisis. Any comments?

The criteria are pretty well defined. If a second doctor was to tell you what you wanted to hear, it wouldn’t change anything. Your blood and urine numbers won’t change. Ratty — All killer no filler ratty at flyingrat.net Site being rebuilt: www.flyingrat.net

Response:

Cold hands and feet.

Question:

screaming_meemies wrote – Hide quoted text — Show quoted text -

Hi, Meemie, and welcome to a.s.m.! I have not had the cold hands and feet syndrome, but there may be someone else here who can shed light on it for you. re. insomnia.  I sometimes have a week or two each month where the insomnia flares up.  I try to make sure I walk every evening (a brisk walk) — that seems to help me get to sleep.  If many days go by and I start feeling desperate, I take one Tylenol P.M.  A full dose is too much — one tablet is half a dose and seems to take the edge off my insomnia. Catherine G. Sounds like excellent advice…………..I never have any trouble falling to sleep, it’s staying asleep that’s the problem.  I’ll bet the Tylenol will do the trick. Thanks Cathering:-) Meemie

Ooooh, cool morph of my name!  I like that! Yes, the Tylenol is good at getting you through the night, as well as putting you to sleep.  I wake up every night to use the bathroom, but have no trouble slipping back to sleep if it’s a Tylenol night.   The only caution I would give is to use it infrequently — so you don’t get addicted. Cathering

Response:

screaming_meemies wrote:

Do you know what?  I’ve had the physical already and as far as my doctor is concerned I am quite healthy. I’m starting to realize that the best information is from folks who have "been there" and "done that" so to speak. Still, I’ll have to check out some symptoms just to be on the safe side.

That seems wise. After a while, you may find that you become familiar enough with what’s "meno" and what’s not that it becomes much easier to decide when a trip to the doctor is warranted.

My hands, in particular, get cold to the point of numbness when the weather turns chilly (even on a slightly cool summer day). In my case, I think this has less to do with menopause than it does with the sorts of minor circulatory problems that result from 39 years of smoking (I know, I know). Yeah, me too.  Maybe that’s the reason.  I wonder if there has been any research done on menopausal women who smoke and have cold hands and feet :-)

Well, it’s pretty firmly established that men *and* women who smoke for a long time do experience circulatory problems, especiall in the extremities. I suspect it’s a coincidence that it tends to show up around the same time as meno symptoms.

My feet, on the other hand, are often too *hot*, especially in bed; ME TOO!  Would you believe I keep a spray bottle under my bed so I can cool my feet off in the middle of the night!  Especially in the summer when it’s 80 degrees.

*grin* Sibling!

I suffer occasional bouts of night sweats/hot flashes, and have to have my feet sticking out from under the covers, no matter how cold it is at night. So mileage varies considerably from individual to individual. No hot flashes yet.  What are the odds that I’ll escape them (he he).

Pretty good, actually. I can’t recall the numbers, but I’m not sure that even a majority of us have hot flashes. someone else may have the numbers. Even if you get them, they may be pretty minor (mine have been. More "hm, that’s interesting" than anything.) –Pat Kight kig…@peak.org

Response:

Thanks Cathering:-) Meemie Ooooh, cool morph of my name!  I like that!

LMAO – Sorry Catherine.

Response:

screaming_meemies <screaming_meem…@rogers.com

wrote in message

news:2Oeh8.27695$aFN.14695@news1.bloor.is… – Hide quoted text — Show quoted text -> "Cathy Friedmann" <c…@adelphia.net

wrote in message

> news:a63crn$bft6h$1@ID-103542.news.dfncis.de… > > Your symptoms certainly *sound* like perimenopause to me! > > re: your cold hands & feet.  Do they ever turn white or bluish-purple when

they’re cold?  If so, that’s Raynaud’s disease, which is virtually

always

benign.  It popped up on me in early perimeno. WHOA – I just looked at my hands and they are most definately very pale. Something else to look into. I think I’m gonna go take a really long…………….HOT……………relaxing bath. Thanks for the tip Cathy Meemie

You’re welcome.  With Raynaud’s, one’s fingers & toes usually turn white & blue-purple in turn, & actually *hurt* if they get too cold.  Or they may simply look odd, & feel slightly chilly, without huring.  Ever since I was little & would play out in the snow for hours on end, my toes & fingers would get very cold, very easily.  When I got x-country skis in my 20’s, I bought the boots a couple of sizes too large, in order to be able to wear 3 pairs of heavy socks. But not until my early 40’s (perimeno) did my fingers & toes start turning bluish-purple one spring, after a winter where my toes & fingers got *really* cold & hurt, really easily/quickly when out shoveling snow, for example.  Went to the doctor, who took one look & said " Raynaud’s."  I’d never heard of it, but quite a few people – esp. women – have it.  It’s usually benign, although as a ’syndrome’ (Vs. ‘Raynaud’s disease’), can be secondary to an underlying condition.  IIRC, Raynaud’s is classified in w/the various autoimmune disorders. Otoh – as a paradox, since mid-peri, my feet also get too hot easily.  I can’t stand to wear something like leather sneakers, for example – no breathability for my feet, or boots inside stores/ a mall for more than a short time.  Go figure… vasomotor weirdness is my guess. Cathy — "Staccato signals of constant information…" ("The Boy in the Bubble")  Paul Simon – Hide quoted text — Show quoted text –

Response:

Louise Bremner wrote

screaming_meemies <screaming_meem…@rogers.com wrote: Is anyone else experiencing the cold hands and feet problem.  This is the first time I’ve heard of this. I’ve recently noticed that my feet take forever to warm up in bed, if I don’t wear socks. It’s so-o-o-o-o-o unglamorous, but then ice-cold tootsies are too. And it seems like I’m always having to tuck my hands into pockets or up sleeves to warm them up (I don’t like gloves). ________________________________________________________________________                    Louise Bremner (log at gol dot com)    If you want a reply by e-mail, don’t write to my Yahoo address!

I’ve had the cold-feet-in-bed syndrome for many, many years.  My husband thinks I’m soooo romantic to get in bed with — all bundled up in flannel pj’s and knee socks.  My hands don’t get cold, though — just my feet and legs (and they get so cold, they ache).  I chalk it up to poor circulation. Catherineg

Response:

Alterra2 wrote:

  I’ve

been told my hands are the result of carpal tunnel and something called Reynauds syndrome. I know lots of people with carpal, and they all have pink flesh colored fingers ans no numbness!!!

If carpal tunnel syndrome is really bad, you can have numbness. You can also have tingling in your arms, hands and fingers. You can also have pain from your neck and shoulder, down to your finger tips. sue

Response:

Karen Kay wrote:

alter…@aol.com (Alterra2) wrote in news:20020307182512.21308.00000210@mb-cn.aol.com: I know lots of people with carpal, and they all have pink flesh colored fingers ans no numbness!!! Carpal tunnel syndrome is manifested in a variety of ways. Some people only have back pain. But numbness and tingling is a classic symptom. Karen

Not disputing you, just never heard of CTS going to the back. I know of the neck and shoulder, down to the finger tips. sue

Response:

- Hide quoted text — Show quoted text -Karen Kay wrote:

susan and kevin mullen <kjmul…@comcast.net wrote in news:3C880CBE.A5FF2916@comcast.net: Karen Kay wrote: alter…@aol.com (Alterra2) wrote in news:20020307182512.21308.00000210@mb-cn.aol.com: I know lots of people with carpal, and they all have pink flesh colored fingers ans no numbness!!! Carpal tunnel syndrome is manifested in a variety of ways. Some people only have back pain. But numbness and tingling is a classic symptom. Karen Not disputing you, just never heard of CTS going to the back. I know of the neck and shoulder, down to the finger tips. I’ve had friends with this (tough to diagnose), and my sister ended up having her nerves cut because of the back pain. Karen

Interesting, hubby has CTS and has never had back pain from it. That has got to make it difficult to diagnose, if you have pain in the back there are so many other things to look for. sue

Response:

From: Karen Kay Ka…@none.com Date: 3/7/02 4:40 PM Pacific Standard Time CTS is weird; there’s a lot of referred pain. Like I said, I know people who only get back pain from it–wearing wrist braces helps their back pain!

My husband cleared his tendinitis  up with a gadget called Cats Paw…rubber device with holes for fingers that exercise the muscles that aren’t being exercised. IOW,CTS,I believe concerns overdevelopment of some muscles. The way I understand it is that the device strengthens the opposing muscles which either cuts down on inflammation or stops the overdeveloped muscles from pressing on nerves. I am sure someone knows more about it than I do. All I know is that the device helped his problem,and it’s supposed to help CTS also. The operation doesn’t always help. Sharon..who believes in Better Living through Eccentricity

Response:

Karen Kay <Ka…@none.com

wrote in message

news:Xns91CABDFCC1CD8karenwordwritecom@24.28.95.158… – Hide quoted text — Show quoted text -

"Cathy Friedmann" <c…@adelphia.net wrote in news:a69131$ca3p0$1@ID-103542.news.dfncis.de: You’re right, sounds like both.  While having raynaud’s, I experienced what were definitely classic symptoms for CP, w/ no obvious reason, during peri. It showed up out-of-the-blue & disappeared just as mysteriously; right arm from the elbow down to my hand; fingers of right hand were all numb except for my pinky (pinky was not affected at all).  And I’m left-handed, using my righht hand/arm for only throwing a ball, which I hardly ever do.  (Can’t remember the last time I did it.) CTS is weird; there’s a lot of referred pain. Like I said, I know people who only get back pain from it–wearing wrist braces helps their back pain! When I overdo it, my right wrist often hurts–but I mouse with the left one like you do. Karen

Actually – nope, I completely forgot about that – I mouse w/ my right hand, out of (sort of) necessity.  Learned to use a PC at school – where there were only right-handed mice; then my own PC came with an IntelliMouse, which though it *says* is for either hand, they’re nuts – in reality it’s for righties only.  (Yes, you can program it for left use, but it’s shape is for a right hand.)  And I never have bothered to get a lefty or symmetrical mouse.  However, this mousing deal still appears to have had no bearing on the CTS, since I’d been using the same mouse before & after it appeared & disappeared, both spontaneously. Cathy — "Staccato signals of constant information…" ("The Boy in the Bubble")  Paul Simon

Response:

Your symptoms certainly *sound* like perimenopause to me! re: your cold hands & feet.  Do they ever turn white or bluish-purple when they’re cold?  If so, that’s Raynaud’s disease, which is virtually always benign.  It popped up on me in early perimeno. Cathy — "Staccato signals of constant information…" ("The Boy in the Bubble")  Paul Simon screaming_meemies <screaming_meem…@rogers.com

wrote in message

news:3YXg8.3624$YtJ.1820@news2.bloor.is… – Hide quoted text — Show quoted text -

Hello folks, I am 41 years old and as far as I can tell I am perimenopausal.  I’ve been to see my doctor several times because I thought I was losing mymind and

he

gave me anti depressants.  Can you believe that.  I was drunk for 2 weeks until I decided to do some research of my own.  Friends and family were suspecting that it was menopause but I figured that my doctor knew best

and

guess what……………..he didn’t.  After checking this newsgroup and a lot of questions I have discovered that there is nothing else that could

be

"happening" to me. I sometimes feel like there are spiders crawling all

over

my skin,  my periods are, well, all over the place and sometimes

literally -

lol, I get confused for no apparent reason, can’t sleep even though I’m exhausted, I could bawl my eyes out at this very moment if I let myself think about the stupid fight my husband and I had this morning.  I have never EVER been depressed in my entire life and lately I have been having days where everything is going just wonderful but I have this terrible feeling of impending doom.  I guess I could go on and on all night but the one thing that really and truly convinced me is watching the Oprah show today, and I only got a little snippet of the show.  Apparently, according to an expert who appeared on her show today, one of the symptoms are cold hands and feet.  Well, I tell you, it’s winter here in Canada and the only time my hands and feet are warm is when I’m in bed with about 4 blankets.

I

even put my slippers in the microwave once! I’m not a doctor, nor do I have any medical training whatsoever, but one thing’s for sure – just knowing what is wrong with me makes all of the

above

a whole lot easier to cope with.  I don’t think I’m losing my mind which

is

actually quite comforting. Is anyone else experiencing the cold hands and feet problem.  This is the first time I’ve heard of this. Thanks for letting me ramble on – I can’t sleep – AGAIN! Ciao Meemie

Response:

Or benign Raynaud’s, as I mentioned in another post. Cathy — "Staccato signals of constant information…" ("The Boy in the Bubble")  Paul Simon Karen Kay <Ka…@none.com

wrote in message

news:Xns91C88A4725D69karenwordwritecom@24.28.95.158… – Hide quoted text — Show quoted text -

Pat Kight <kig…@ucs.orst.edu wrote in news:3C84F567.8030408@ucs.orst.edu: One thought: Ask your doctor to test your thyroid. I suggest this because you are on the youngish side of normal for peri, and because many of the symptoms of thyroid problems can mimic menopausal symtoms, right down to the irregular periods. The cold hands and feet, in particular, are common to people with certain thyroid disorders. Fortunately, such disorders can usually be controlled pretty well with medication. It’s worth investigating. I second this. Cold hands/feet can also be indicative of circulatory system problems, too. Karen

Response:

Hi, Meemie, and welcome to a.s.m.! I have not had the cold hands and feet syndrome, but there may be someone else here who can shed light on it for you. re. insomnia.  I sometimes have a week or two each month where the insomnia flares up.  I try to make sure I walk every evening (a brisk walk) — that seems to help me get to sleep.  If many days go by and I start feeling desperate, I take one Tylenol P.M.  A full dose is too much — one tablet is half a dose and seems to take the edge off my insomnia. Catherine G.

Sounds like excellent advice…………..I never have any trouble falling to sleep, it’s staying asleep that’s the problem.  I’ll bet the Tylenol will do the trick. Thanks Cathering:-) Meemie

Response:

 I even put my slippers in the microwave once!

*smile* Yep, that all sounds pretty familiar!

Honestly, that’s gotta be THE most annoying thing that’s happened to me so far.

One thought: Ask your doctor to test your thyroid. I suggest this because you are on the youngish side of normal for peri, and because many of the symptoms of thyroid problems can mimic menopausal symtoms, right down to the irregular periods. The cold hands and feet, in particular, are common to people with certain thyroid disorders. Fortunately, such disorders can usually be controlled pretty well with medication. It’s worth investigating.

Yes, I think I will, whenever I get around to calling him again.  He seems to be really big on medication these days.  Every time someone in my family goes to see him they come home with a bottle of pills.  Maybe it’s time to look for another doctor.

In other words: While you may very well be experiencing some of the signs of menopause, it would be a mistake to chalk everything off to the change without getting a good physical. (And some of the things that tend to plague us at middle age can’t really be connected directly with the winding down of ovarian function – the fact that they occur around the same time may fool us into thinking it’s all meno, when some of it may be completely unrelated, other than by the fact that we’re All Getting Older.

Do you know what?  I’ve had the physical already and as far as my doctor is concerned I am quite healthy. I’m starting to realize that the best information is from folks who have "been there" and "done that" so to speak. Still, I’ll have to check out some symptoms just to be on the safe side.

My hands, in particular, get cold to the point of numbness when the weather turns chilly (even on a slightly cool summer day). In my case, I think this has less to do with menopause than it does with the sorts of minor circulatory problems that result from 39 years of smoking (I know, I know).

Yeah, me too.  Maybe that’s the reason.  I wonder if there has been any research done on menopausal women who smoke and have cold hands and feet :-) My feet, on the other hand, are often too *hot*, especially in

bed;

ME TOO!  Would you believe I keep a spray bottle under my bed so I can cool my feet off in the middle of the night!  Especially in the summer when it’s 80 degrees. I suffer occasional bouts of night sweats/hot flashes, and have to

have my feet sticking out from under the covers, no matter how cold it is at night. So mileage varies considerably from individual to individual.

No hot flashes yet.  What are the odds that I’ll escape them (he he).

Ciao

Meemie – Hide quoted text — Show quoted text –

Response:

"Cathy Friedmann" <c…@adelphia.net

wrote in message

news:a63crn$bft6h$1@ID-103542.news.dfncis.de…

Your symptoms certainly *sound* like perimenopause to me! re: your cold hands & feet.  Do they ever turn white or bluish-purple when they’re cold?  If so, that’s Raynaud’s disease, which is virtually always benign.  It popped up on me in early perimeno.

WHOA – I just looked at my hands and they are most definately very pale. Something else to look into. I think I’m gonna go take a really long…………….HOT……………relaxing bath. Thanks for the tip Cathy Meemie

Response:

You’re right, sounds like both.  While having raynaud’s, I experienced what were definitely classic symptoms for CP, w/ no obvious reason, during peri. It showed up out-of-the-blue & disappeared just as mysteriously; right arm from the elbow down to my hand; fingers of right hand were all numb except for my pinky (pinky was not affected at all).  And I’m left-handed, using my righht hand/arm for only throwing a ball, which I hardly ever do.  (Can’t remember the last time I did it.) Cathy — "Staccato signals of constant information…" ("The Boy in the Bubble")  Paul Simon Karen Kay <Ka…@none.com

wrote in message

news:Xns91CAB83047D1Dkarenwordwritecom@24.28.95.158… – Hide quoted text — Show quoted text -> "Cathy Friedmann" <c…@adelphia.net> wrote in > news:a68v2e$cqe9b$1@ID-103542.news.dfncis.de: > > Karen Kay <Ka…@none.com

wrote in message

> > news:Xns91CAB5CD7FC4Dkarenwordwritecom@24.28.95.158… > >> alter…@aol.com (Alterra2) wrote in > >> news:20020307182512.21308.00000210@mb-cn.aol.com: > >> > I know lots of people with carpal, and they all have pink > >> > flesh colored fingers ans no numbness!!! > >> Carpal tunnel syndrome is manifested in a variety of ways. Some > >> people only have back pain. But numbness and tingling is a > >> classic symptom. > >> Karen > > Yeah, true re: numbness & tingling, but white fingers w/ carpal > > tunnel?  And the feet?  Raynauds affects both the fingers & the > > toes. > She said she was diagnosed with CTS *and* Reynauds, I thought? I > wasn’t disputing the diagnosis, just her claim that people with CTS > always don’t have numbness. > Karen

Response:

Karen Kay <Ka…@none.com

wrote in message

news:Xns91CAB5CD7FC4Dkarenwordwritecom@24.28.95.158…

alter…@aol.com (Alterra2) wrote in news:20020307182512.21308.00000210@mb-cn.aol.com: I know lots of people with carpal, and they all have pink flesh colored fingers ans no numbness!!! Carpal tunnel syndrome is manifested in a variety of ways. Some people only have back pain. But numbness and tingling is a classic symptom. Karen

Yeah, true re: numbness & tingling, but white fingers w/ carpal tunnel?  And the feet?  Raynauds affects both the fingers & the toes. Cathy — "Staccato signals of constant information…" ("The Boy in the Bubble")  Paul Simon

Response:

Look back in the thread, to one (or 2) of my replies, re: Raynaud’s.  If your fingers go white, & are super-sensitive to the cold (even a mild winter like we had this winter), see a doctor for a diagnosis. Cathy — "Staccato signals of constant information…" ("The Boy in the Bubble")  Paul Simon Alterra2 <alter…@aol.com

wrote in message

news:20020307182512.21308.00000210@mb-cn.aol.com… – Hide quoted text — Show quoted text -

Ciao Meemie, I thought the Oprah show did not elaborate on the cold hands

and

feet. I am very interested in this, I need info! You wanna talk about

cold? My

fingers go white, drained of blood, and the numbness is getting worse.

Does

this happen to u? Please tell me. U say u are in Canada, that"s cold, I"m

in NY

city and even though we"ve had a pretty mild winter it doesn"t matter I"m

like

this July, Aug, any time. I’m 49 and untill just very recently had a

regular

cycle and no signs of menopause, all of a SUDDEN everything is changing.

I’ve

been told my hands are the result of carpal tunnel and something called Reynauds syndrome. I know lots of people with carpal, and they all have

pink

flesh colored fingers ans no numbness!!! And what about the feet??????

Well,

thanks for listening and let me know.                          Jozee

Response:

Ciao Meemie, I thought the Oprah show did not elaborate on the cold hands and feet. I am very interested in this, I need info! You wanna talk about cold? My fingers go white, drained of blood, and the numbness is getting worse. Does this happen to u? Please tell me. U say u are in Canada, that"s cold, I"m in NY city and even though we"ve had a pretty mild winter it doesn"t matter I"m like this July, Aug, any time. I’m 49 and untill just very recently had a regular cycle and no signs of menopause, all of a SUDDEN everything is changing. I’ve been told my hands are the result of carpal tunnel and something called Reynauds syndrome. I know lots of people with carpal, and they all have pink flesh colored fingers ans no numbness!!! And what about the feet?????? Well, thanks for listening and let me know.                          Jozee

Response:

screaming_meemies <screaming_meem…@rogers.com

wrote: Is anyone else experiencing the cold hands and feet problem.  This is the first time I’ve heard of this.

I’ve recently noticed that my feet take forever to warm up in bed, if I don’t wear socks. It’s so-o-o-o-o-o unglamorous, but then ice-cold tootsies are too. And it seems like I’m always having to tuck my hands into pockets or up sleeves to warm them up (I don’t like gloves). ________________________________________________________________________                    Louise Bremner (log at gol dot com)    If you want a reply by e-mail, don’t write to my Yahoo address!

Response:

fit1 wrote – Hide quoted text — Show quoted text -

"Catherine G." <jord…@comcast.net wrote in message news:MPG.16ee7b954ea80fc89896c7@news.cis.dfn.de… re. insomnia.  I sometimes have a week or two each month where the insomnia flares up.  I try to make sure I walk every evening (a brisk walk) — that seems to help me get to sleep.  If many days go by and I start feeling desperate, I take one Tylenol P.M.  A full dose is too much — one tablet is half a dose and seems to take the edge off my insomnia. Catherine G. I would never recommend that any one stop an exercise program that is working for them but some people, me included, find that vigorous exercise in the evening keeps them awake.  On Monday’s I teach a step class and on Thursday’s a Pilates session, both at 19:30 and I usually can’t get to sleep much before 24:00.  I have heard this complaint from several participants, as well…they would like the classes to be held earlier.

I think the key to what I do might be that it is outside — fresh air somehow helps.  I used to take dance classes in the evening, and I always needed time to wind down before going to bed.  But now I walk — in the early evening, probably around 6:30 or 7:00.  And by 9:30, my eyes are pretty heavy.

Cath (are there enough Cath’s, Cathy’s, Kathy’s, Catherine’s posting to this group?)

LOL!  I normally go by Cath, but have kept it to Catherine G. here.  I like meemie’s morph of my name, though, and I think I’ll make it "Cathering" now. Cathering

Response:

"Catherine G." <jord…@comcast.net

wrote in message

news:MPG.16ee7b954ea80fc89896c7@news.cis.dfn.de…

re. insomnia.  I sometimes have a week or two each month where the insomnia flares up.  I try to make sure I walk every evening (a brisk walk) — that seems to help me get to sleep.  If many days go by and I start feeling desperate, I take one Tylenol P.M.  A full dose is too much — one tablet is half a dose and seems to take the edge off my insomnia. Catherine G.

I would never recommend that any one stop an exercise program that is working for them but some people, me included, find that vigorous exercise in the evening keeps them awake.  On Monday’s I teach a step class and on Thursday’s a Pilates session, both at 19:30 and I usually can’t get to sleep much before 24:00.  I have heard this complaint from several participants, as well…they would like the classes to be held earlier. Cath (are there enough Cath’s, Cathy’s, Kathy’s, Catherine’s posting to this group?)

Response:

screaming_meemies wrote:

Hello folks, I am 41 years old and as far as I can tell I am perimenopausal.  I’ve been to see my doctor several times because I thought I was losing mymind and he gave me anti depressants.  Can you believe that.  I was drunk for 2 weeks until I decided to do some research of my own.  Friends and family were suspecting that it was menopause but I figured that my doctor knew best and guess what……………..he didn’t.

A lot of doctors don’t seem to understand just how common it is for a woman in her early 40s to start experiencing some of the signs of this change. Antidepressents may, indeed, be a good treatment – for depression – but they won’t touch the other things you report. – Hide quoted text — Show quoted text -

 After checking this newsgroup and a lot of questions I have discovered that there is nothing else that could be "happening" to me. I sometimes feel like there are spiders crawling all over my skin,  my periods are, well, all over the place and sometimes literally – lol, I get confused for no apparent reason, can’t sleep even though I’m exhausted, I could bawl my eyes out at this very moment if I let myself think about the stupid fight my husband and I had this morning.  I have never EVER been depressed in my entire life and lately I have been having days where everything is going just wonderful but I have this terrible feeling of impending doom.  I guess I could go on and on all night but the one thing that really and truly convinced me is watching the Oprah show today, and I only got a little snippet of the show.  Apparently, according to an expert who appeared on her show today, one of the symptoms are cold hands and feet.  Well, I tell you, it’s winter here in Canada and the only time my hands and feet are warm is when I’m in bed with about 4 blankets.  I even put my slippers in the microwave once!

*smile* Yep, that all sounds pretty familiar! One thought: Ask your doctor to test your thyroid. I suggest this because you are on the youngish side of normal for peri, and because many of the symptoms of thyroid problems can mimic menopausal symtoms, right down to the irregular periods. The cold hands and feet, in particular, are common to people with certain thyroid disorders. Fortunately, such disorders can usually be controlled pretty well with medication. It’s worth investigating. In other words: While you may very well be experiencing some of the signs of menopause, it would be a mistake to chalk everything off to the change without getting a good physical. (And some of the things that tend to plague us at middle age can’t really be connected directly with the winding down of ovarian function – the fact that they occur around the same time may fool us into thinking it’s all meno, when some of it may be completely unrelated, other than by the fact that we’re All Getting Older.

I’m not a doctor, nor do I have any medical training whatsoever, but one thing’s for sure – just knowing what is wrong with me makes all of the above a whole lot easier to cope with.  I don’t think I’m losing my mind which is actually quite comforting.

I think that sort of reassurance is what this newsgroup provides best. Welcome!

Is anyone else experiencing the cold hands and feet problem.  This is the first time I’ve heard of this.

My hands, in particular, get cold to the point of numbness when the weather turns chilly (even on a slightly cool summer day). In my case, I think this has less to do with menopause than it does with the sorts of minor circulatory problems that result from 39 years of smoking (I know, I know). My feet, on the other hand, are often too *hot*, especially in bed; I suffer occasional bouts of night sweats/hot flashes, and have to have my feet sticking out from under the covers, no matter how cold it is at night. So mileage varies considerably from individual to individual. Best wishes, –Pat Kight kig…@peak.org

Response:

Hello folks, I am 41 years old and as far as I can tell I am perimenopausal.  I’ve been to see my doctor several times because I thought I was losing mymind and he gave me anti depressants.  Can you believe that.  I was drunk for 2 weeks until I decided to do some research of my own.  Friends and family were suspecting that it was menopause but I figured that my doctor knew best and guess what……………..he didn’t.  After checking this newsgroup and a lot of questions I have discovered that there is nothing else that could be "happening" to me. I sometimes feel like there are spiders crawling all over my skin,  my periods are, well, all over the place and sometimes literally – lol, I get confused for no apparent reason, can’t sleep even though I’m exhausted, I could bawl my eyes out at this very moment if I let myself think about the stupid fight my husband and I had this morning.  I have never EVER been depressed in my entire life and lately I have been having days where everything is going just wonderful but I have this terrible feeling of impending doom.  I guess I could go on and on all night but the one thing that really and truly convinced me is watching the Oprah show today, and I only got a little snippet of the show.  Apparently, according to an expert who appeared on her show today, one of the symptoms are cold hands and feet.  Well, I tell you, it’s winter here in Canada and the only time my hands and feet are warm is when I’m in bed with about 4 blankets.  I even put my slippers in the microwave once! I’m not a doctor, nor do I have any medical training whatsoever, but one thing’s for sure – just knowing what is wrong with me makes all of the above a whole lot easier to cope with.  I don’t think I’m losing my mind which is actually quite comforting. Is anyone else experiencing the cold hands and feet problem.  This is the first time I’ve heard of this. Thanks for letting me ramble on – I can’t sleep – AGAIN! Ciao Meemie

Response:

screaming_meemies wrote – Hide quoted text — Show quoted text -

Hello folks, I am 41 years old and as far as I can tell I am perimenopausal.  I’ve been to see my doctor several times because I thought I was losing mymind and he gave me anti depressants.  Can you believe that.  I was drunk for 2 weeks until I decided to do some research of my own.  Friends and family were suspecting that it was menopause but I figured that my doctor knew best and guess what……………..he didn’t.  After checking this newsgroup and a lot of questions I have discovered that there is nothing else that could be "happening" to me. I sometimes feel like there are spiders crawling all over my skin,  my periods are, well, all over the place and sometimes literally – lol, I get confused for no apparent reason, can’t sleep even though I’m exhausted, I could bawl my eyes out at this very moment if I let myself think about the stupid fight my husband and I had this morning.  I have never EVER been depressed in my entire life and lately I have been having days where everything is going just wonderful but I have this terrible feeling of impending doom.  I guess I could go on and on all night but the one thing that really and truly convinced me is watching the Oprah show today, and I only got a little snippet of the show.  Apparently, according to an expert who appeared on her show today, one of the symptoms are cold hands and feet.  Well, I tell you, it’s winter here in Canada and the only time my hands and feet are warm is when I’m in bed with about 4 blankets.  I even put my slippers in the microwave once! I’m not a doctor, nor do I have any medical training whatsoever, but one thing’s for sure – just knowing what is wrong with me makes all of the above a whole lot easier to cope with.  I don’t think I’m losing my mind which is actually quite comforting. Is anyone else experiencing the cold hands and feet problem.  This is the first time I’ve heard of this. Thanks for letting me ramble on – I can’t sleep – AGAIN! Ciao Meemie

Hi, Meemie, and welcome to a.s.m.! I have not had the cold hands and feet syndrome, but there may be someone else here who can shed light on it for you. re. insomnia.  I sometimes have a week or two each month where the insomnia flares up.  I try to make sure I walk every evening (a brisk walk) — that seems to help me get to sleep.  If many days go by and I start feeling desperate, I take one Tylenol P.M.  A full dose is too much — one tablet is half a dose and seems to take the edge off my insomnia. Catherine G.

Response:

Happy is he or she who knows the causes of things

Question:

Is it possible that my carpal tunnel (peripheral neuropathy) is a result of clonazepam withdrawal effect – maybe I should have cut the Xanax but not the Rivotril?  Is it possible that the benzo group does not know everything despite its loveable true believers? Squiggles

Response:

Is it possible that my carpal tunnel (peripheral neuropathy) is a result of clonazepam withdrawal effect – maybe I should have cut the Xanax but not the Rivotril?  Is it possible that the benzo group does not know everything despite its loveable true believers? Squiggles

p.s. Curiouser and curiouser – my mouth does not taste of so much salt now (still a taste of salt and the stripes definitely still there);  Where are you Sherlock? Squiggles

Response:

: Is it possible that my carpal tunnel (peripheral neuropathy) : is a result of clonazepam withdrawal effect – maybe I should : have cut the Xanax but not the Rivotril?  Is it possible : that the benzo group does not know everything despite its : loveable true believers? : : Squiggles I’d be interested to see some research that shows any benzo can contribute to carpal tunnel. Just doesn’t add up. — Sometimes I even jack off(masturbate) after I write an especially warped post. – LostBoyinNC / 2000/07/14

Response:

- Hide quoted text — Show quoted text – : Is it possible that my carpal tunnel (peripheral neuropathy) : is a result of clonazepam withdrawal effect – maybe I should : have cut the Xanax but not the Rivotril?  Is it possible : that the benzo group does not know everything despite its : loveable true believers? : : Squiggles I’d be interested to see some research that shows any benzo can contribute to carpal tunnel. Just doesn’t add up. — Sometimes I even jack off(masturbate) after I write an especially warped post. – LostBoyinNC / 2000/07/14

It’s not the benzos that create it – it is the withdrawal and absence of the usual dose – I will look at some stuff later tonight. Squiggles

Response:

: I’d be interested to see some research that shows any benzo can contribute : to carpal tunnel. Just doesn’t add up. : : It’s not the benzos that create it – it is the withdrawal : and absence of the usual dose – I will look at some stuff : later tonight. : : Squiggles No biggie, no need to do anything special. An interesting theory I haven’t heard before.

Response:

So does Hypothyroidism

– Hide quoted text — Show quoted text – Is it possible that my carpal tunnel (peripheral neuropathy) is a result of clonazepam withdrawal effect – maybe I should have cut the Xanax but not the Rivotril?  Is it possible that the benzo group does not know everything despite its loveable true believers? Squiggles p.s. Curiouser and curiouser – my mouth does not taste of so much salt now (still a taste of salt and the stripes definitely still there);  Where are you Sherlock? Squiggles

Response:

Klonopin withdrawal doesnt cause carpal tunnel. Thats bullshit. Hypothyroidism can cause or exacerbate carpal tunnel however. Thats well known. I had some wrist tendonitis once back in college.  So I started reading medical books and wondered if I had carpal tunnel

so I went to my family doc and told him to order thyroid tests for me as Id read thyroid probs causes carpal tunnel.

Perhaps we see here the root of the sad path which Eric’s life has taken…. – Hide quoted text — Show quoted text – Turned out my thyroid was fine and it was plain old wrist tendonitis, treatable with ice and motrin. Eric "Who Dares, Wins" <motto of ECT patients http://groups.yahoo.com/group/MergePsychiatryIntoNeurology/

Response:

- Hide quoted text — Show quoted text – Klonopin withdrawal doesnt cause carpal tunnel. Thats bullshit. Hypothyroidism can cause or exacerbate carpal tunnel however. Thats well known. I had some wrist tendonitis once back in college.  So I started reading medical books and wondered if I had carpal tunnel so I went to my family doc and told him to order thyroid tests for me as Id read thyroid probs causes carpal tunnel. Turned out my thyroid was fine and it was plain old wrist tendonitis, treatable with ice and motrin. Eric "Who Dares, Wins" <motto of ECT patients http://groups.yahoo.com/group/MergePsychiatryIntoNeurology/

Eric, You just don’t know everything – carpal tunnel is also known as "peripheral neuropathy" and can be cause by so many things – do you want me to send you some sites from medical sources.  Why wouldn’t my doctor fix my thyroid if that was the cause?  It’s possible it’s the thyroid, but it’s possible it’s benzo withdrawal.  I don’t know and you don’t know – are you a doctor?   Squiggles

Response:

<snip sources.  Why wouldn’t my doctor fix my thyroid if that was the cause?  It’s possible it’s the thyroid, but it’s possible it’s benzo withdrawal.  I don’t know and you don’t know – are you a doctor?

Have you heard the results of the thyroid test the hospital did for you the other day? What was it, if you don’t mind sharing? Fiona — If we had no winter, the spring would not be so pleasant: if we did not sometimes taste the adversity, prosperity would not be so welcome.      – Anne Bradstreet, Meditations Divine and Moral, 1664

Response:

Have you heard the results of the thyroid test the hospital did for you the other day? What was it, if you don’t mind sharing?

My turn: P.S. Lithium can cause thyroid problems, usually by reducing or stopping production. This is something that can happen after you’ve been taking it without any trouble for a long time. I took lithium for a year or so before it started effecting my thyroid function. So a thyroid problem may be new, if that’s it. Any other symptoms of thyroid problems? Losing hair? Feeling cold out of proportion to the temperature? Fiona — If we had no winter, the spring would not be so pleasant: if we did not sometimes taste the adversity, prosperity would not be so welcome.      – Anne Bradstreet, Meditations Divine and Moral, 1664

Response:

- Hide quoted text — Show quoted text – <snip sources.  Why wouldn’t my doctor fix my thyroid if that was the cause?  It’s possible it’s the thyroid, but it’s possible it’s benzo withdrawal.  I don’t know and you don’t know – are you a doctor? Have you heard the results of the thyroid test the hospital did for you the other day? What was it, if you don’t mind sharing? Fiona — If we had no winter, the spring would not be so pleasant: if we did not sometimes taste the adversity, prosperity would not be so welcome.      – Anne Bradstreet, Meditations Divine and Moral, 1664

They were not able to have it ready Fiona – swamped ER. But by Monday when I got to my doctor i hope it will be out or he will give me one.  The last one seemed OK – I never know the numbers myself. Squiggles

Response:

- Hide quoted text — Show quoted text – My turn: P.S. Lithium can cause thyroid problems, usually by reducing or stopping production. This is something that can happen after you’ve been taking it without any trouble for a long time. I took lithium for a year or so before it started effecting my thyroid function. So a thyroid problem may be new, if that’s it. Any other symptoms of thyroid problems? Losing hair? Feeling cold out of proportion to the temperature? Fiona — If we had no winter, the spring would not be so pleasant: if we did not sometimes taste the adversity, prosperity would not be so welcome.      – Anne Bradstreet, Meditations Divine and Moral, 1664

I’ve been taking lithium for 20 years.  I became hypothyroidic a few years into and got Synthroid at 0.155 or so.  I think that was too high because I kept getting diarrhea, and could not sleep. I stopped without telling my doc.  I became very hypo. I got a rushed thyroxine dose from an intern, that I think was too high and almsot killed me.  In 6 months my doc. was able to bring it around.  I was very very sick.  Then I was lowered because I complained that my anxiety was thyroxine caused – which they agreed.  I was able to stop my Xanax that way – no more panic attacks.   Last year I complained that maybe the lithium was too high for the thyroid, my symptoms: – skin getting drier – tongue stripes – carpal tunnel (p.n) – enormous weight gain without eating more; – breasts enlarged hugely all of a sudden – very heavy body feeling in the a.m. – heart rate normal – heat waves (maybe withdrawal) – edema in the ankles – exercise intolerance – sinusitis like symptoms – I don’t feel cold at all. I am menopausal but that does not bother me at all, my sex-drive is better than ever. Well, there’s my life story :-) But I don’t know if I am hypo or not – Squiggles

Response:

<snip But I don’t know if I am hypo or not –

Some of these seem similar to when I was hypo-, but some are definately not. I know this is going to sound bizarre, but is it possible you’re hyper-? Is it possible that your menopause is messing with things and making you hyper- or hypo-? I don’t know, I’m just trying to think of every possibility. Feel free to email if you want. I’m very curious to hear what your doctor has to say. Fiona — If we had no winter, the spring would not be so pleasant: if we did not sometimes taste the adversity, prosperity would not be so welcome.      – Anne Bradstreet, Meditations Divine and Moral, 1664

Response:

They were not able to have it ready Fiona – swamped ER. But by Monday when I got to my doctor i hope it will be out or he will give me one.  The last one seemed OK – I never know the numbers myself.

I’m glad to hear this, you really need to be thoroughly checked out. Please keep us up to date, if you don’t mind. Fiona — If we had no winter, the spring would not be so pleasant: if we did not sometimes taste the adversity, prosperity would not be so welcome.      – Anne Bradstreet, Meditations Divine and Moral, 1664

Response:

– Hide quoted text — Show quoted text – Klonopin withdrawal doesnt cause carpal tunnel. Thats bullshit. Hypothyroidism can cause or exacerbate carpal tunnel however. Thats well known. I had some wrist tendonitis once back in college.  So I started reading medical books and wondered if I had carpal tunnel so I went to my family doc and told him to order thyroid tests for me as Id read thyroid probs causes carpal tunnel. Turned out my thyroid was fine and it was plain old wrist tendonitis, treatable with ice and motrin. Eric

Bad Attitude now?  Do you walk the walk and talk the talk.  Ah, nevermind. Well, oddly enough.  I’ve typed for 30+ years, been hypo for 12 and do not have Carpal Tunnel.  I’m R-handed.  In my left hand I have a very painful compressed Ulnar nerve.  I have also lost about 40% strength in this hand. I do believe surgery is going to be a requirement here.  Whether the compressed nerve is in the elbow or wrist is unknown.  In fact, even the neuro is unsure.  I wear a resting brace, which is useless because when I’m not resting I just undo what I fixed! The biggest problem is the 40% reduction in strength.  It makes being productive at times difficult.  My typing speed went from 90+ to a PAINFULL 53 wpm.  And typos are difficult to feel and catch now.  Unlike Carpal, my little finger is numb, my ring finger is nearly numb and my mid finger is numbish.  Outside wrist is totally numb. Without this shit, and depression, I’d probably type into my 90’s. Carrie – Hide quoted text — Show quoted text – "Who Dares, Wins" <motto of ECT patients http://groups.yahoo.com/group/MergePsychiatryIntoNeurology/

Response:

- Hide quoted text — Show quoted text – <snip But I don’t know if I am hypo or not – Some of these seem similar to when I was hypo-, but some are definately not. I know this is going to sound bizarre, but is it possible you’re hyper-? Is it possible that your menopause is messing with things and making you hyper- or hypo-? I don’t know, I’m just trying to think of every possibility. Feel free to email if you want. I’m very curious to hear what your doctor has to say. Fiona — If we had no winter, the spring would not be so pleasant: if we did not sometimes taste the adversity, prosperity would not be so welcome.      – Anne Bradstreet, Meditations Divine and Moral, 1664

I was thinking just the same thing Fiona – is it possible I’m hyper?  Funny.  :-) We’ll see on  Monday I hope – thanks for listening to my primadonna story. Squiggles

Response:

- Hide quoted text — Show quoted text – Klonopin withdrawal doesnt cause carpal tunnel. Thats bullshit. Hypothyroidism can cause or exacerbate carpal tunnel however. Thats well known. I had some wrist tendonitis once back in college.  So I started reading medical books and wondered if I had carpal tunnel so I went to my family doc and told him to order thyroid tests for me as Id read thyroid probs causes carpal tunnel. Turned out my thyroid was fine and it was plain old wrist tendonitis, treatable with ice and motrin. Eric Bad Attitude now?  Do you walk the walk and talk the talk.  Ah, nevermind. Well, oddly enough.  I’ve typed for 30+ years, been hypo for 12 and do not have Carpal Tunnel.  I’m R-handed.  In my left hand I have a very painful compressed Ulnar nerve.  I have also lost about 40% strength in this hand. I do believe surgery is going to be a requirement here.  Whether the compressed nerve is in the elbow or wrist is unknown.  In fact, even the neuro is unsure.  I wear a resting brace, which is useless because when I’m not resting I just undo what I fixed! The biggest problem is the 40% reduction in strength.  It makes being productive at times difficult.  My typing speed went from 90+ to a PAINFULL 53 wpm.  And typos are difficult to feel and catch now.  Unlike Carpal, my little finger is numb, my ring finger is nearly numb and my mid finger is numbish.  Outside wrist is totally numb.

Carrie, How did your carpal tunnel start, when – do you recall any preceding circumstances?  Mine is very even on both hand up to the wrists – one doc thought it was the spine – x-rays show some tear maybe in the cervical area. My carpal tunnel was VERY SUDDEN – I was sitting at the keyboard and my hands went numb literally.  I had to wear braces for a month. Squiggles

Response:

Thyroid/T link?

Question:

I have hypogonadism, and TRT isn’t helping any. I also have a borderline hypothyroid condition, which is not being treated at this time. Is there a possible connection between hypothyroid & low T? Thanks, Dave

Response:

In this business anything is possible. I had what they called subclinical hypothyroidism with multiple cold nodules, most likely hashimoto’s disease. I had my thyroid removed and went on synthroid for hormone replacement. Once I got over the surgery and adjusted to synthroid things were lovely for about a year or so. Then my testosterone level started to drop. My docs basically sat there and watched it drop till it hit the sub basement then I was put on TRT. Maybe the thyroid caused the testosterone problem, mabye both were caused by the same thing since they are both controled by the pituitary, maybe it’s just an unlucky break that both went out. I don’t know. If your TSH is up or your T3 is down, it’s serious. A radio-iodine scan and ultrasound might rule out any serious cause of the problem. You might need to be on a low dosage of synthroid or armour but that’s just a little pill once a day. Get it checked out. The symptoms of thyroid problems and testosterone problems are very similar. Mike – Hide quoted text — Show quoted text – I have hypogonadism, and TRT isn’t helping any. I also have a borderline hypothyroid condition, which is not being treated at this time. Is there a possible connection between hypothyroid & low T? Thanks, Dave

Response:

Spondylitis & cold sensitivity

Question:

Hi folks. This is my first visit to this newsgroup. I have AS, and up until recently I was always warm. My wife liked to call me "the furnace" because whenever she was cold, she could just snuggle up to me & I generated enough heat to keep us both warm. It was nothing for me to walk around the house in shorts and a teeshirt during the middle of winter. That all changed this year, though. I now seem to be freakishly sensitive to the cold. My hands and feet are cold most of the time lately, and on occassion, like when I’m getting dressed after a shower, when cold air touches my skin, I get the shivers like you wouldn’t believe. It’s about 68 degrees in the house now, and I’m wearing a sweatshirt and jeans, thinking about putting on some

<snip I would suggest talking to your doctor about having your circulation checked for any restrictions. I’ve known several people who suddenly started feeling cold all of the time and were then found to have circulation problems. This nay not be the case for you, but it’s better to go to the doctor one time too often than one time too few. — "Television is called a "medium" because it is neither rare nor well done."     Ernie Kovacs Norman Lampert mr-dot-bones-at-att-dot-net

Response:

Hi Jerry-Lots of us have sensitivity to cold.  It seems to go hand in hand with the "arthritides".  In my case it is also sensitivity to heat.  I have a very short comfort window of about10 or 15 degrees.  Get outside that window, in either direction and I am not a happy camper. It wouldnt hurt to have it checked out with your doctor, but I think it is pretty common for us. BTW Welcome to ASA.  I think you will like ikt here. Char "Remember, I’m pulling for ya’.  We’re all in this together."  Red Green

Response:

my husband (an AS victim) says that the cold feels like someone is pouring Ice water into a hole drilled into his  bones. We’ve since moved to AZ! good Luck

Response:

Hi, My father was diagnosed with Spondylitis in his mid forties and has since (past 15 years) improved dramatically with exercise. His only symptom was lack of balance and nausea. According to his doctor this was caused by reduced blood flow to his head. Improved posture and neck exercises has made him near normal. A few years ago, he developed extreme sensitivity to heat and cold in his head. In summer of 1996 he started feeling cold, went under 3 blankets and had an electric heater blow hot air straight at his head but got no relief. Drinking hot liquids made his head sweat and got him some relief. A number of medications were tried and finally Indomethacin, a NSAID, cleared his symptoms within an hour. He has had to take the drug only occaisionally and has been free of his heat & cold symptoms since. I am looking for an explanation for what happened. Was the problem related to Spondylitis? How did an NSAID clear his symptoms? By decreasing neck inflammation and increasing blood flow to his head? Incidentally, his oral tempreture was 3-4 degrees lower than (his) normal when he was feeling cold. Any explanation and suggestions about future course of action would be greatly welcome. Regards, Tripurari Before you buy.

Response:

Thyroid problem? Immune problem (ME/CFS)? Could be a lot of things. Don’t understand how the drug would relate though. – Hide quoted text — Show quoted text – Hi, My father was diagnosed with Spondylitis in his mid forties and has since (past 15 years) improved dramatically with exercise. His only symptom was lack of balance and nausea. According to his doctor this was caused by reduced blood flow to his head. Improved posture and neck exercises has made him near normal. A few years ago, he developed extreme sensitivity to heat and cold in his head. In summer of 1996 he started feeling cold, went under 3 blankets and had an electric heater blow hot air straight at his head but got no relief. Drinking hot liquids made his head sweat and got him some relief. A number of medications were tried and finally Indomethacin, a NSAID, cleared his symptoms within an hour. He has had to take the drug only occaisionally and has been free of his heat & cold symptoms since. I am looking for an explanation for what happened. Was the problem related to Spondylitis? How did an NSAID clear his symptoms? By decreasing neck inflammation and increasing blood flow to his head? Incidentally, his oral tempreture was 3-4 degrees lower than (his) normal when he was feeling cold. Any explanation and suggestions about future course of action would be greatly welcome. Regards, Tripurari Before you buy.

– … My mind wanders, but my body is too tired to follow

Response:

Thyroid problem? Immune problem (ME/CFS)? Could be a lot of things. Don’t understand how the drug would relate though.

What is the mechanism for temperature sensitivity in these illness? Is it a problem of the nervous system/perception or is the body temperature really unstable? – Hide quoted text — Show quoted text – Hi, My father was diagnosed with Spondylitis in his mid forties and has since (past 15 years) improved dramatically with exercise. His only symptom was lack of balance and nausea. According to his doctor this was caused by reduced blood flow to his head. Improved posture and neck exercises has made him near normal. A few years ago, he developed extreme sensitivity to heat and cold in his head. In summer of 1996 he started feeling cold, went under 3 blankets and had an electric heater blow hot air straight at his head but got no relief. Drinking hot liquids made his head sweat and got him some relief. A number of medications were tried and finally Indomethacin, a NSAID, cleared his symptoms within an hour. He has had to take the drug only occaisionally and has been free of his heat & cold symptoms since. I am looking for an explanation for what happened. Was the problem related to Spondylitis? How did an NSAID clear his symptoms? By decreasing neck inflammation and increasing blood flow to his head? Incidentally, his oral tempreture was 3-4 degrees lower than (his) normal when he was feeling cold. Any explanation and suggestions about future course of action would be greatly welcome. Regards, Tripurari Before you buy. — … My mind wanders, but my body is too tired to follow

Before you buy.

Response:

Hi folks. This is my first visit to this newsgroup. I have AS, and up until recently I was always warm. My wife liked to call me "the furnace" because whenever she was cold, she could just snuggle up to me & I generated enough heat to keep us both warm. It was nothing for me to walk around the house in shorts and a teeshirt during the middle of winter. That all changed this year, though. I now seem to be freakishly sensitive to the cold. My hands and feet are cold most of the time lately, and on occassion, like when I’m getting dressed after a shower, when cold air touches my skin, I get the shivers like you wouldn’t believe. It’s about 68 degrees in the house now, and I’m wearing a sweatshirt and jeans, thinking about putting on some longjohns and a sweater over my sweatshirt. I missed the original post, so please forgive me if this has already been asked. Has anyone else noticed such an onset of sensitivity to the cold after a few years of spondylitis symptoms? Or maybe it’s because of several years of the combination of meds my docs have me taking??? Any comments would be greatly appreciated. – Jerry

Response:

Hi, I have spondylitis. Mine started with repeated pain in the right knee, which cleared up so I thought. Then about three yrs later, I was babysitting and was unable to get up from a chair due to incredile pain in my right hip. Now I get pain in my neck, left leg and and two regions in my lower back.  I don’t get nausea but do occasionally have problems with balance due to hip pain. Jo. – Hide quoted text — Show quoted text – Norman, What about poor balance and nausea? Are these symptoms of Spondylitis? From what I’ve read elsewhere, and seen posted here, there are many possible symptoms of spondylitis, and most people only have a few of them. I haven’t had much trouble with balance itself, but I sometimes stumble a bit because of problems with my leg joints. Nausea could be caused by many things, including a reaction to medication, or to Irritable Bowel Syndrome, which many arthritis sufferers have. Whatever problems you are having, try to observe and understand possible connections and causes so that you can discuss them with your RD. My RD says that the patient’s understanding and observations are a very big part of the treatment. Take care and get lots of rest and spoil yourself now and then. — "Television is called a "medium" because it is neither rare nor well done."     Ernie Kovacs Norman Lampert mr-dot-bones-at-att-dot-net

Response:

- Hide quoted text — Show quoted text – Hi, My father was diagnosed with Spondylitis in his mid forties and has since (past 15 years) improved dramatically with exercise. His only symptom was lack of balance and nausea. According to his doctor this was caused by reduced blood flow to his head. Improved posture and neck exercises has made him near normal. A few years ago, he developed extreme sensitivity to heat and cold in his head. In summer of 1996 he started feeling cold, went under 3 blankets and had an electric heater blow hot air straight at his head but got no relief. Drinking hot liquids made his head sweat and got him some relief. A number of medications were tried and finally Indomethacin, a NSAID, cleared his symptoms within an hour. He has had to take the drug only occaisionally and has been free of his heat & cold symptoms since. I am looking for an explanation for what happened. Was the problem related to Spondylitis? How did an NSAID clear his symptoms? By decreasing neck inflammation and increasing blood flow to his head? Incidentally, his oral tempreture was 3-4 degrees lower than (his) normal when he was feeling cold. Any explanation and suggestions about future course of action would be greatly welcome. Regards, Tripurari Before you buy.

I would hazard a wild guess that the AS inflames his capillaries which reduces the blood flow and allows the skin surface to cool.   The NSAID probably clears the inflammation. Ray T.

Response:

 I would suspect that the nsaid may have altered thyroid hormone metabolism. If it was affecting blood flow to head, and to extremities, I doubt it would have changed his core temp as measured by a thermometer, though I could be wrong about that. I have rheumatoid arthritis in my neck, and from my experience,  it affects temperature of my hands more than my head.  It could also be a sign of nerves being pressed on rather than circulation.  Ask the doc if a referral to a neurologist is in order.  Is there any tingling or numbness in his hands/arms present?  If so, I would *demand* a referral.   I would ask the doctor to test his thyroid also in case there is some auto-immune problem going on there.  You might try looking up thyroid in a search engine, to see if there are other symptoms of thyroid problems he should mention to the doctor. Here’s some sites to start you off–have a look at the patient info. http://www.thyroid.com/index.html http://www.thyroid.org/ Poor balance and nausea could be signs of inner ear trouble,  ( I say that from experience with a family member who had those problems ) though there could be other causes as well.  Reposted below my reply here is an article previously posted  to the group about AS and balance.  (Thanks, Kitty!) I wish you and your father well–welcome, and come back often if there is anything the group can help you with!  Liz G Do patients with ankylosing spondylitis have poorer balance than normal subjects? H. C. Murray 1,2, C. Elliott 1,, S. E. Barton 2 and  A. Murray1 1 Regional Medical Physics Department, Freeman Hospital, Newcastle upon Tyne, and 2 Division of Physiotherapy, Bradford University, Bradford, UK Objectives. To investigate whether patients with ankylosing spondylitis have poorer balance than normal subjects, and to study the relationship between balance and posture. Methods. Balance was studied in 30 ankylosing spondylitis subjects using sway magnetometry, making quantitative measurements of movement at the hips with eyes open and eyes closed. The results were compared with data from 58 normal subjects. Balance was also compared with quantitative measurements of posture. Results. The numbers of patients with poor balance, above the 95th percentile for normal, were significantly greater than expected; 18% for eyes open (P =3D 0.03) and 23% for eyes closed  (P =3D 0.004). No significant relationships between balance and any of the quantitative descriptions of posture were demonstrated. Conclusion. A significant proportion of ankylosing spondylitis  patients have poorer balance than normal subjects. Copyright =A9 2000 British Society for Rheumatology.

Response:

Norman, What about poor balance and nausea? Are these symptoms of Spondylitis?

From what I’ve read elsewhere, and seen posted here, there are many possible symptoms of spondylitis, and most people only have a few of them. I haven’t had much trouble with balance itself, but I sometimes stumble a bit because of problems with my leg joints. Nausea could be caused by many things, including a reaction to medication, or to Irritable Bowel Syndrome, which many arthritis sufferers have. Whatever problems you are having, try to observe and understand possible connections and causes so that you can discuss them with your RD. My RD says that the patient’s understanding and observations are a very big part of the treatment. Take care and get lots of rest and spoil yourself now and then. — "Television is called a "medium" because it is neither rare nor well done."     Ernie Kovacs Norman Lampert mr-dot-bones-at-att-dot-net

Response:

– Hide quoted text — Show quoted text – I get "hot flashes" It’s not menopause. I am 27. (unless its very premature) My doc wants me taking my temp when I get em and tracking it along with symptoms so we can see if my actual temp changes or if it is a perception thing. I pour sweat and flush bright red (I have redhead skin to begin with…) and I get weak and nauseated. It usually lasts anywhere from 5 min to 30 min. I am also cold-sensitive. I just dont seem to regulate body temp well. I get very cold very easily and cant warm up. And if I am in cold air, especially a sudden change in environment, it sends me into a massive coughing fit. I am talking coughing till I hemorrhage the whites of my eyes, puke, burst blood vessels in my face, or all of the above. It is BAD. I have AS. No idea if these are all related directly, indirectly, or not at all. I think the lack of rib expansion doesnt help with the cough part. But the symptoms *did* all start about the same time…. Aim

Aim, I suspect that my father’s problems were caused by poor blood flow to his head. Blood vessels to your head pass through your neck where they are prone to being squeezed by inflammations. I suspect that Indomethacin relieved my fathers inflammations and restored blood supply. All of this is just conjecture, of course. Does your temperature sensitivity get better with your favourite NSAID? Have you tried Indomethacin itself? -T Before you buy.

Response:

– Hide quoted text — Show quoted text – Hi, My father was diagnosed with Spondylitis in his mid forties and has since (past 15 years) improved dramatically with exercise. His only symptom was lack of balance and nausea. According to his doctor this was caused by reduced blood flow to his head. Improved posture and neck exercises has made him near normal. A few years ago, he developed extreme sensitivity to heat and cold in his head. In summer of 1996 he started feeling cold, went under 3 <snip I have ankylosing spondylitis (diagnosed about 8? years ago) and I’ve never had the symptoms you describe. I’m not saying that it’s not possible to be a symptom of the spondylitis, but I would look for other causes also; Specifically if there are any "triggers" for the problem, such as a particular food or activity shortly before they occur, or any other problems which seem to occur at the same time. —

Norman, What about poor balance and nausea? Are these symptoms of Spondylitis? Thanks, Tripurari Before you buy.

Response:

Hi, My father was diagnosed with Spondylitis in his mid forties and has since (past 15 years) improved dramatically with exercise. His only symptom was lack of balance and nausea. According to his doctor this was caused by reduced blood flow to his head. Improved posture and neck exercises has made him near normal. A few years ago, he developed extreme sensitivity to heat and cold in his head. In summer of 1996 he started feeling cold, went under 3

<snip I have ankylosing spondylitis (diagnosed about 8? years ago) and I’ve never had the symptoms you describe. I’m not saying that it’s not possible to be a symptom of the spondylitis, but I would look for other causes also; Specifically if there are any "triggers" for the problem, such as a particular food or activity shortly before they occur, or any other problems which seem to occur at the same time. — "Television is called a "medium" because it is neither rare nor well done."     Ernie Kovacs Norman Lampert mr-dot-bones-at-att-dot-net

Response:

I get "hot flashes" It’s not menopause. I am 27. (unless its very premature) My doc wants me taking my temp when I get em and tracking it along with symptoms so we can see if my actual temp changes or if it is a perception thing. I pour sweat and flush bright red (I have redhead skin to begin with…) and I get weak and nauseated. It usually lasts anywhere from 5 min to 30 min. I am also cold-sensitive. I just dont seem to regulate body temp well. I get very cold very easily and cant warm up. And if I am in cold air, especially a sudden change in environment, it sends me into a massive coughing fit. I am talking coughing till I hemorrhage the whites of my eyes, puke, burst blood vessels in my face, or all of the above. It is BAD. I have AS. No idea if these are all related directly, indirectly, or not at all. I think the lack of rib expansion doesnt help with the cough part. But the symptoms *did* all start about the same time…. Aim – Hide quoted text — Show quoted text -Hi, My father was diagnosed with Spondylitis in his mid forties and has since (past 15 years) improved dramatically with exercise. His only symptom was lack of balance and nausea. According to his doctor this was caused by reduced blood flow to his head. Improved posture and neck exercises has made him near normal. A few years ago, he developed extreme sensitivity to heat and cold in his head. In summer of 1996 he started feeling cold, went under 3 <snip I have ankylosing spondylitis (diagnosed about 8? years ago) and I’ve never had the symptoms you describe. I’m not saying that it’s not possible to be a symptom of the spondylitis, but I would look for other causes also; Specifically if there are any "triggers" for the problem, such as a particular food or activity shortly before they occur, or any other problems which seem to occur at the same time.

Response:

more on my starving cat

Question:

Not sure who you’re replying to, but my kitty has food allergies.  I feed him Walthams products only.  Duck and Rice Dry along with Venison and Rice canned. Kelly – Hide quoted text — Show quoted text – I think my cat has this allergy too. What do you feed your two? Thanks, Kris

Response:

I agree with Ellen.  Nothing against your vet because he sounds like he is trying really hard.  I just think a second opinion is an excellent option. Gene

– Hide quoted text — Show quoted text – Have you had a second opinion yet?  It might be worth a shot. Good luck! Ellen A. Got questions?  Get answers over the phone at Keen.com. Up to 100 minutes free! http://www.keen.com

Response:

I think my cat has this allergy too. What do you feed your two? Thanks, Kris

Response:

I think my cat must have this allergy too. What do you feed your two? Thanks, Kris

Response:

Is it possible that he might have a food allergy??? some cats are allergic to corn glutten and are thin but all ways hungry. It is not very common, but I have two cats with the problem. Leslie                                                          "you can tell alot about a people or person in how they treat animals"

Response:

Have you had a second opinion yet?  It might be worth a shot. Good luck! Ellen A. Got questions?  Get answers over the phone at Keen.com. Up to 100 minutes free! http://www.keen.com

Response:

I certainly don’t like the idea of thyroid removal if the tests are showing no thyroid problems!

– Hide quoted text — Show quoted text – Hi folks, I got lots of great input from people here last week regarding my constantly hungry and weight losing cat. Yes, he shows the classic symptoms of thyroid problems, BUT three tests (over six months with different vets) have shown no thyroid problem. He has been x-rayed and there are no tumors or blockages. Blood sugar is normal. There is no evidence of parasites or GI inflammation. I made them check for all of these and they were all concerns registered on this board. Latest theory:  pancreatic problems: vet wants to treat with ongoing anti-biotics. Have been giving him Vikosay (sic? the pancreatic enzyme supplement) and he has continued to lose weight.  Vet also suggests that he could have thyroid problem but thyroid test isn’t showing it. (Anyone ever heard of this?) Vet says he attended recent workshop on feline pancreatitis and latest recommendation is ongoing anti-biotic treatment. This seems to be what we are going to try. Next choice might be thyroid removal (even with no evidence of thyroid malfunction). Might be noteworthy that this vet has about as good a reputation as any in our city. What do you folks think?  I don’t think vet likes me anymore as I have been very pushy with them. I did call his office Saturday morning and he was poring over my cats tests, so maybe "pushy" has gotten their attention. I have been through some hard times in my life and this pet has meant the world to me through it all. I am damn determined that I am not going to let him down. What do you folks think of these theories and plans? Bernie

Response:

Hi folks, I got lots of great input from people here last week regarding my constantly hungry and weight losing cat. Yes, he shows the classic symptoms of thyroid problems, BUT three tests (over six months with different vets) have shown no thyroid problem. He has been x-rayed and there are no tumors or blockages. Blood sugar is normal. There is no evidence of parasites or GI inflammation. I made them check for all of these and they were all concerns registered on this board. Latest theory:  pancreatic problems: vet wants to treat with ongoing anti-biotics. Have been giving him Vikosay (sic? the pancreatic enzyme supplement) and he has continued to lose weight.  Vet also suggests that he could have thyroid problem but thyroid test isn’t showing it. (Anyone ever heard of this?) Vet says he attended recent workshop on feline pancreatitis and latest recommendation is ongoing anti-biotic treatment. This seems to be what we are going to try. Next choice might be thyroid removal (even with no evidence of thyroid malfunction). Might be noteworthy that this vet has about as good a reputation as any in our city. What do you folks think?  I don’t think vet likes me anymore as I have been very pushy with them. I did call his office Saturday morning and he was poring over my cats tests, so maybe "pushy" has gotten their attention. I have been through some hard times in my life and this pet has meant the world to me through it all. I am damn determined that I am not going to let him down. What do you folks think of these theories and plans? Bernie

Response:

Not sure who you’re replying to, but my kitty has food allergies.  I feed him Walthams products only.  Duck and Rice Dry along with Venison and Rice canned. Kelly – Hide quoted text — Show quoted text – I think my cat has this allergy too. What do you feed your two? Thanks, Kris

Response:

I agree with Ellen.  Nothing against your vet because he sounds like he is trying really hard.  I just think a second opinion is an excellent option. Gene

– Hide quoted text — Show quoted text – Have you had a second opinion yet?  It might be worth a shot. Good luck! Ellen A. Got questions?  Get answers over the phone at Keen.com. Up to 100 minutes free! http://www.keen.com

Response:

I think my cat has this allergy too. What do you feed your two? Thanks, Kris

Response:

I think my cat must have this allergy too. What do you feed your two? Thanks, Kris

Response:

Is it possible that he might have a food allergy??? some cats are allergic to corn glutten and are thin but all ways hungry. It is not very common, but I have two cats with the problem. Leslie                                                          "you can tell alot about a people or person in how they treat animals"

Response:

Have you had a second opinion yet?  It might be worth a shot. Good luck! Ellen A. Got questions?  Get answers over the phone at Keen.com. Up to 100 minutes free! http://www.keen.com

Response:

I certainly don’t like the idea of thyroid removal if the tests are showing no thyroid problems!

– Hide quoted text — Show quoted text – Hi folks, I got lots of great input from people here last week regarding my constantly hungry and weight losing cat. Yes, he shows the classic symptoms of thyroid problems, BUT three tests (over six months with different vets) have shown no thyroid problem. He has been x-rayed and there are no tumors or blockages. Blood sugar is normal. There is no evidence of parasites or GI inflammation. I made them check for all of these and they were all concerns registered on this board. Latest theory:  pancreatic problems: vet wants to treat with ongoing anti-biotics. Have been giving him Vikosay (sic? the pancreatic enzyme supplement) and he has continued to lose weight.  Vet also suggests that he could have thyroid problem but thyroid test isn’t showing it. (Anyone ever heard of this?) Vet says he attended recent workshop on feline pancreatitis and latest recommendation is ongoing anti-biotic treatment. This seems to be what we are going to try. Next choice might be thyroid removal (even with no evidence of thyroid malfunction). Might be noteworthy that this vet has about as good a reputation as any in our city. What do you folks think?  I don’t think vet likes me anymore as I have been very pushy with them. I did call his office Saturday morning and he was poring over my cats tests, so maybe "pushy" has gotten their attention. I have been through some hard times in my life and this pet has meant the world to me through it all. I am damn determined that I am not going to let him down. What do you folks think of these theories and plans? Bernie

Response:

Hi folks, I got lots of great input from people here last week regarding my constantly hungry and weight losing cat. Yes, he shows the classic symptoms of thyroid problems, BUT three tests (over six months with different vets) have shown no thyroid problem. He has been x-rayed and there are no tumors or blockages. Blood sugar is normal. There is no evidence of parasites or GI inflammation. I made them check for all of these and they were all concerns registered on this board. Latest theory:  pancreatic problems: vet wants to treat with ongoing anti-biotics. Have been giving him Vikosay (sic? the pancreatic enzyme supplement) and he has continued to lose weight.  Vet also suggests that he could have thyroid problem but thyroid test isn’t showing it. (Anyone ever heard of this?) Vet says he attended recent workshop on feline pancreatitis and latest recommendation is ongoing anti-biotic treatment. This seems to be what we are going to try. Next choice might be thyroid removal (even with no evidence of thyroid malfunction). Might be noteworthy that this vet has about as good a reputation as any in our city. What do you folks think?  I don’t think vet likes me anymore as I have been very pushy with them. I did call his office Saturday morning and he was poring over my cats tests, so maybe "pushy" has gotten their attention. I have been through some hard times in my life and this pet has meant the world to me through it all. I am damn determined that I am not going to let him down. What do you folks think of these theories and plans? Bernie

Response:

Not sure who you’re replying to, but my kitty has food allergies.  I feed him Walthams products only.  Duck and Rice Dry along with Venison and Rice canned. Kelly – Hide quoted text — Show quoted text – I think my cat has this allergy too. What do you feed your two? Thanks, Kris

Response:

I agree with Ellen.  Nothing against your vet because he sounds like he is trying really hard.  I just think a second opinion is an excellent option. Gene

– Hide quoted text — Show quoted text – Have you had a second opinion yet?  It might be worth a shot. Good luck! Ellen A. Got questions?  Get answers over the phone at Keen.com. Up to 100 minutes free! http://www.keen.com

Response:

I think my cat has this allergy too. What do you feed your two? Thanks, Kris

Response:

I think my cat must have this allergy too. What do you feed your two? Thanks, Kris

Response:

Is it possible that he might have a food allergy??? some cats are allergic to corn glutten and are thin but all ways hungry. It is not very common, but I have two cats with the problem. Leslie                                                          "you can tell alot about a people or person in how they treat animals"

Response:

Have you had a second opinion yet?  It might be worth a shot. Good luck! Ellen A. Got questions?  Get answers over the phone at Keen.com. Up to 100 minutes free! http://www.keen.com

Response:

I certainly don’t like the idea of thyroid removal if the tests are showing no thyroid problems!

– Hide quoted text — Show quoted text – Hi folks, I got lots of great input from people here last week regarding my constantly hungry and weight losing cat. Yes, he shows the classic symptoms of thyroid problems, BUT three tests (over six months with different vets) have shown no thyroid problem. He has been x-rayed and there are no tumors or blockages. Blood sugar is normal. There is no evidence of parasites or GI inflammation. I made them check for all of these and they were all concerns registered on this board. Latest theory:  pancreatic problems: vet wants to treat with ongoing anti-biotics. Have been giving him Vikosay (sic? the pancreatic enzyme supplement) and he has continued to lose weight.  Vet also suggests that he could have thyroid problem but thyroid test isn’t showing it. (Anyone ever heard of this?) Vet says he attended recent workshop on feline pancreatitis and latest recommendation is ongoing anti-biotic treatment. This seems to be what we are going to try. Next choice might be thyroid removal (even with no evidence of thyroid malfunction). Might be noteworthy that this vet has about as good a reputation as any in our city. What do you folks think?  I don’t think vet likes me anymore as I have been very pushy with them. I did call his office Saturday morning and he was poring over my cats tests, so maybe "pushy" has gotten their attention. I have been through some hard times in my life and this pet has meant the world to me through it all. I am damn determined that I am not going to let him down. What do you folks think of these theories and plans? Bernie

Response:

Hi folks, I got lots of great input from people here last week regarding my constantly hungry and weight losing cat. Yes, he shows the classic symptoms of thyroid problems, BUT three tests (over six months with different vets) have shown no thyroid problem. He has been x-rayed and there are no tumors or blockages. Blood sugar is normal. There is no evidence of parasites or GI inflammation. I made them check for all of these and they were all concerns registered on this board. Latest theory:  pancreatic problems: vet wants to treat with ongoing anti-biotics. Have been giving him Vikosay (sic? the pancreatic enzyme supplement) and he has continued to lose weight.  Vet also suggests that he could have thyroid problem but thyroid test isn’t showing it. (Anyone ever heard of this?) Vet says he attended recent workshop on feline pancreatitis and latest recommendation is ongoing anti-biotic treatment. This seems to be what we are going to try. Next choice might be thyroid removal (even with no evidence of thyroid malfunction). Might be noteworthy that this vet has about as good a reputation as any in our city. What do you folks think?  I don’t think vet likes me anymore as I have been very pushy with them. I did call his office Saturday morning and he was poring over my cats tests, so maybe "pushy" has gotten their attention. I have been through some hard times in my life and this pet has meant the world to me through it all. I am damn determined that I am not going to let him down. What do you folks think of these theories and plans? Bernie

Response:

Confused!!!

Question:

From a home medical advisor type book – For People Over 50: Under-active thyroid: (notice how many are totally contradictory signs) Signs: decreased tolerance for cold decreased sweating decreased appetite constipation chest pain coarse or slow growing hair slow, rapid or irregular heart beat weight gain or extreme thinness placidity or nervousness sleepiness or insomnia mental impairment, including depression, psychosis or poor memory fluid retention, esp around the eyes dull facial expression and droopy eyelids coarse skin anemia decreased tolerance  for medication decreased sex drive, infertility numbness and tingling in hands and feet deepened or hoarse voice Causes/Risk Factors: Auto-immune disease Radio-active iodine treatment Iodine deficiency in diet decreased pituitary activity use of drugs like lithium that suppress thyroid activity natural substances found in  some food like rutabegas, cabbage and cranberries obesity x-ray treatments

Response:

In article <6699AA19A32F5FF8.E050A59DBB0B95C0.FA476E7545198…@lp.airnews.net

, "Us"

<ho…@airmail.net

wrote: I believe it is because thyroid disease is being detected more often.  It was once accepted that women, who suffer from thyroid problems more than men, were old once they went through menopause. Therefore, no one looked into the possibility of something being wrong. Weight gain, tiredness, hair loss, being cold,menstrual irregularities, aches and pains were just normal things that happened to women.  If a woman complained of these symptoms, she was told it was where she was in her life now. Now, doctors know that it isn’t normal for women to age drastically after menopause.  They are still able to live energetic and full lives.

Right…and certain thyroid diseases like Hashimotos are hard to detect with the regular thyroid tests ( or so my sister who has Hashimotos tells me).

Response:

Exposure to radioactivity is by no means uniform around the globe.  An example that is painfully close to home is the "Downwinders", the folks who lived in a town in Nevada that was exposed to a lot of radiation on the day of an H-bomb test when the wind shifted unexpectedly.  The level of exposure was measured in the town, but covered up by the government folks until many years later, after the Freedom of Information act was passed.  And hey, I’m one who had more than normal exposure – I grew up in Los Alamos and worked in the labs one summer analyzing plutonium samples.  

I believe that I have recently read that the incidence of thyroid cancer , if not other thyroid disease is way up in the area around Chernobyl.

Response:

I want to thank you for those symtoms Joan. I am still having a lot of itching and swelling on my feet. I can’t sleep at night. I finally went to the doctor who gave me a antihistamine and some lotion. Nothing is working. I am going to tell him to give me a blood test for thyroid. I had one for glucose and my hormone level. Haven’t gotten the results yet. I am not on estrogen at this time. I want to rrule everything out and then deal with what I can do. My feet also get real hot and burning when I do any kind of exertion. I am really bummed out about this. It seems the doctors don’t want to say it is a estrogen deficiency. I think more doctors have to be aware as to what this does to us. But I am going to check the thyroid thing out. Thanks, Anita

Response:

In article <16219-38B9EBCD…@storefull-147.iap.bryant.webtv.net

,

Ben…@webtv.net (Anita L. Benjamin) wrote: – Hide quoted text — Show quoted text -

I want to thank you for those symtoms Joan. I am still having a lot of itching and swelling on my feet. I can’t sleep at night. I finally went to the doctor who gave me a antihistamine and some lotion. Nothing is working. I am going to tell him to give me a blood test for thyroid. I had one for glucose and my hormone level. Haven’t gotten the results yet. I am not on estrogen at this time. I want to rrule everything out and then deal with what I can do. My feet also get real hot and burning when I do any kind of exertion. I am really bummed out about this. It seems the doctors don’t want to say it is a estrogen deficiency. I think more doctors have to be aware as to what this does to us. But I am going to check the thyroid thing out. Thanks, Anita

hmmm….this is truly off the wall…but in 1974 I caught a case of Hepatitis A from contaminated food and one of the weird symptoms was itching hands and feet…apparently it had something to do with the bile not being broken down or the cholesterol levels going up or something. It was one of the first symptoms. I was seeing a therapist at the time who was convinced it was psychogenic. I took great pleasure in showing him my blood test results after he attempted to make the itching go away by hypnotizing me ( it didn’t work) . Oy, the therapist stories I could tell you…….. Anyhow, maybe get liver enzymes checked? what do you think docs out there?

Response:

- Hide quoted text — Show quoted text -FurPaw wrote in message <38B9B62A.DF5CD…@NOJUNKhome.com

… Joan Livingston wrote:   Plus, what goes wrong with so many women’s thyroids that besides having Synthroid being the Number 2 leading selling drug in the US right after Premarin as Number one, there seems to be this ready acceptance to investigate the thyroid gland?    Plus this gets tossed off as if it was some expected state of no consequence once it has been confirmed, with no curiosity why so many women’s thyroids "go bad".   And then there is that Johns Hopkins study

from

the 1970’s finding a "thyroid disease personality." Again, is mind/body getting treated only as body here? J Joan – Back up the horses a minute here, and let’s look at some basics for your proposition. Proposition:  more women are experiencing thyroid problems now than in the past – as evidenced by the observation that Synthroid is one of the top selling drugs.

  This is not my proposition. I don’t know if more women today are having "thyroid problems" than any other time .I am just surprised how many of them do ……relying on the incidence of thyroid medication use. And how readily posters suggest to have the "thyroid checked out " with the expectation that this is a commonly troublesome organ apparently.   Is it? Or is it getting over-treated or over-rated as a problem organ? It is a "master gland"? What is going so haywire in women’s bodies (more women than men have thyroid problems?) that this important gland goes wacko. This is serious, as Dr Sam says. Is this also true in other countries or is it again a US phenomenom?    If this alleged radiation/nuclear testing is the problem with thyroid glands, then does it show up equally in men and women? Plus the "thryoid personality" seems more skewed towards it being a female aka, a relationship or love issue problem …you just gotta read the book on the Johns Hopkins 1970’s studies on this to explore what more than a majority of experienced MDs intuited a "thyroid disease personality" was.    (I don’t accept this nuclear testing model, as I do not think this is a world-wide problems and the exposure has been world wide to these nuclear tests. Plus one MD in a CEU course claimed giving a woman a thyroid prescrition was called a "get out of my office diagnosis!" Shocking, eh?)   Does "thyroid disease" mask some other mind/body malaise that no one want to investigate, let alone face and treat? What are these commom characteristics that led a group of MDs to find a thyroid disease personality cluster? (Not 100% by any means, just more than average clustering of personality and symptomology.) J – Hide quoted text — Show quoted text -

First question:  do the data support a higher proportion of women with thyroid problems in 2000, than , say, 1950?  (Do the data support a higher proportion of men as well?) Second question:  If yes, is this due to a higher rate of incidence or better detection? Third question:  If it looks like a higher rate of incidence, what is the cause? One hypothesis re proposed relationship:  Something about mind/body, thyroid personality. (Sorry, I didn’t really understand what you were specifically proposing.) Another hypothesis re proposed relationship (one alternative): Increased rates of thyroid problems might be due to increased exposure to radioactivity over the past 54 years. We’ve had atomic testing, with its dispersal of strontium-90 and other radioactive compounds through the atmosphere, manufacture of uranium and plutonium for weapons, proliferation of nuclear power plants, Russia dumping its old nuclear subs in the oceans, etc.  We all have been exposed to more radioactivity in the past 50 years than our ancestors ever were.  Radioactive iodine, one of the elements dispersed by SOME of these activities, would probably be the top culprit, though other radionucleids can also cause thyroid problems. Immediate conclusion:  Need to get the basic data on the first three questions before either hypothesis becomes tenable. It is a proposition worth investigation. FurPaw PS There was a lot of hoo-hah about the "migraine personality" in the late 60’s and early 70’s, too. As the physiological roots of migraine become better understood, I don’t think too many folks still look at the migraine personality as causal, although different personality styles could make the _experience_ of migraine more or less awful.

Response:

- Hide quoted text — Show quoted text -

One hypothesis re proposed relationship:  Something about mind/body, thyroid personality. (Sorry, I didn’t really understand what you were specifically proposing.) Another hypothesis re proposed relationship (one alternative):   Increased rates of thyroid problems might be due to increased exposure to radioactivity over the past 54 years. We’ve had atomic testing, with its dispersal of strontium-90 and other radioactive compounds through the atmosphere, manufacture of uranium and plutonium for weapons, proliferation of nuclear power plants, Russia dumping its old nuclear subs in the oceans, etc.  We all have been exposed to more radioactivity in the past 50 years than our ancestors ever were.  Radioactive iodine, one of the elements dispersed by SOME of these activities, would probably be the top culprit, though other radionucleids can also cause thyroid problems. Immediate conclusion:  Need to get the basic data on the first three questions before either hypothesis becomes tenable. It is a proposition worth investigation.

yup

FurPaw PS There was a lot of hoo-hah about the "migraine personality" in the late 60’s and early 70’s, too. As the physiological roots of migraine become better understood, I don’t think too many folks still look at the migraine personality as causal, although different personality styles could make the _experience_ of migraine more or less awful.

yup again.

Response:

I believe it is because thyroid disease is being detected more often.  It was once accepted that women, who suffer from thyroid problems more than men, were old once they went through menopause. Therefore, no one looked into the possibility of something being wrong. Weight gain, tiredness, hair loss, being cold,menstrual irregularities, aches and pains were just normal things that happened to women.  If a woman complained of these symptoms, she was told it was where she was in her life now. Now, doctors know that it isn’t normal for women to age drastically after menopause.  They are still able to live energetic and full lives.

Response:

Also a thank you to you…I will state what my doctor tells me back to the group.  I will ask for a thyroid test also.  Thank you so much… Cassie :) "Pat Kight" <kig…@peak.org

wrote in message

news:38B8626D.F1ED57@peak.org… – Hide quoted text — Show quoted text -

WhsprWulf wrote: Hello everyone,     Well, let me start my story off by stating my age.  I am 31 years

old

and for a couple of months now I was experiencing hot flashes (blushing)

and

my periods were really weird.  Just last month I had two periods but

they

only lasted for 2 days each.  This month I am very late for my period

and I

called my doctor and they gave me a preg. test but I had my tubes tied

along

time ago.  Now Monday I am trying to get an appt. for them to check my hormone levels because just yesterday and today I have been having like waves of heat going through my chest to my head and I feel like I am

burning

up.  My heart starts racing and that is not good for me since I tend to

have

anxiety attacks.  I am very moody (ask my poor husband) and feels like I

am

having a MAJOR Pms thing going on.  I hate this feeling and can’t wait

to

see what is going on with my body.  Thanks for listening to me and any

help

would be appreciated…. Cassie :) Cassie, if you were a few years older I might just say, "welcome to the club," but 31 is young enough that getting it checked out seems like a very smart idea. While your symptoms sound hormonal, there are a number of things that could cause them that aren’t menopause. Best to get those ruled out by a competent physician. You might want to ask the doctor, for instance, about thyroid tests – thyroid problems are relatively common in women, and because the thyroid is another hormone factory, problems with it can mimic some of the signs of meno. Meanwhile, try not to worry too much (yeah, I know, easier said than done). Some of us who have hot flashes have found that stress can trigger them (nasty little feedback loop there, eh?) Get some rest, drink plenty of water, and ask your husband to bear with you. Best wishes, –Pat Kight kig…@peak.org

Response:

Thanks…I am taking this info with me to see my gyn.  I am hoping I will find an answer to this problem. Cassie "Silver" <sil…@annburnett.fsnet.co.uk

wrote in message

news:89bj8q$46s$1@news7.svr.pol.co.uk… – Hide quoted text — Show quoted text -

Hi Cassie, and welcome  :-) Can’t add much to those who’ve already responded … except to suggest you check-out something called "post tubal syndrome".  I know very little about it but there is a site http://www.tubal.org/ which has lots of information (including a list of 41 symptoms which looks just like the peri list with some additions).  My grasp of the theory is that, in some women, the blood supply to the ovaries is affected by the tubal ligation and can result in varying degrees of damage to the ovaries and thus to oestrogen/progesterone production.  For reasons I haven’t quite got my head round, the resulting symptoms may not present until a few years after the tubal (I’m guessing that the damage is progressive, but don’t really understand this bit yet).  Anyway, might be worth your checking this out (another url on this is http://www.xtn.net/com/uppgobg/nbleed.htm ) (this latter is site more likely to be useful for discussion with your doctor as it is written by an MD). I’m interested in this myself because I had a tubal at 29 (ish, maybe 28, anyway) by my mid-30’s I was in peri.  Or so I think.  I’ve been reading up on PTS because I’m wondering if my early peri might not have been post tubal syndrome after all.  Who knows.  I tend to dislike diagnoses with the word "syndrome" in them as my personal experience is that these are dumping grounds for "I don’t know what’s wrong with you, but I’ll give it a name" …. but the idea that ovaries might by damaged by tubals does make some sense to me (a form of surgical menopause?).  Anyway, it’s something more for you to check out. All the best ….. I wish you luck and hope that you’re able to understand and find help for your problems. Silver "WhsprWulf" <pdqb…@mindspring.com wrote Hello everyone,     Well, let me start my story off by stating my age.  I am 31 years old and for a couple of months now I was experiencing hot flashes (blushing) and my periods were really weird.  Just last month I had two periods but they only lasted for 2 days each.  This month I am very late for my period and I called my doctor and they gave me a preg. test but I had my tubes tied along time ago.  Now Monday I am trying to get an appt. for them to check my hormone levels because just yesterday and today I have been having like waves of heat going through my chest to my head and I feel like I am burning up.  My heart starts racing and that is not good for me since I tend to have anxiety attacks.  I am very moody (ask my poor husband) and feels like I am having a MAJOR Pms thing going on.  I hate this feeling and can’t wait to see what is going on with my body.  Thanks for listening to me and any help would be appreciated…. Cassie :)

Response:

What goes wrong with so many women’s thyroid glands that make "Synthroid" the second leading selling drug in the US? Is there something more we need to know about what causes this need for medication and diagnosis of a failing thyroid gland     Do we need to investigate the "auto-immune" connection with thyroid diseases, as well as the "thyroid  disease personality" as suggested in the 1970’s Johns Hopkins studies? J Us wrote in message

<0C2B864DFE0B46AD.F048A270AB213709.42682CADF4B2C…@lp.airnews.net

– Hide quoted text — Show quoted text -

All hormones work with each other, and when one is depleted or low, it causes all the others to cease functioning correctly. It is very important for women to have  their thyroid hormone checked on a regular basis. The symptoms of underactive thryroid are similar to peri and menopause

symptoms.

Having a doctor question,and suggest a thyroid test is a blessing.  For years women have been told it was menopause.  My Mom died a year ago from

an

undiagnosed underactive thyroid.  I applaud doctors that will suggest a thyroid test.

Response:

Joan Livingston wrote:

  Plus, what goes wrong with so many women’s thyroids that besides having Synthroid being the Number 2 leading selling drug in the US right after Premarin as Number one, there seems to be this ready acceptance to investigate the thyroid gland?    Plus this gets tossed off as if it was some expected state of no consequence once it has been confirmed, with no curiosity why so many women’s thyroids "go bad".   And then there is that Johns Hopkins study from the 1970’s finding a "thyroid disease personality." Again, is mind/body getting treated only as body here? J

Joan – Back up the horses a minute here, and let’s look at some basics for your proposition. Proposition:  more women are experiencing thyroid problems now than in the past – as evidenced by the observation that Synthroid is one of the top selling drugs. First question:  do the data support a higher proportion of women with thyroid problems in 2000, than , say, 1950?  (Do the data support a higher proportion of men as well?) Second question:  If yes, is this due to a higher rate of incidence or better detection? Third question:  If it looks like a higher rate of incidence, what is the cause? One hypothesis re proposed relationship:  Something about mind/body, thyroid personality. (Sorry, I didn’t really understand what you were specifically proposing.) Another hypothesis re proposed relationship (one alternative):   Increased rates of thyroid problems might be due to increased exposure to radioactivity over the past 54 years. We’ve had atomic testing, with its dispersal of strontium-90 and other radioactive compounds through the atmosphere, manufacture of uranium and plutonium for weapons, proliferation of nuclear power plants, Russia dumping its old nuclear subs in the oceans, etc.  We all have been exposed to more radioactivity in the past 50 years than our ancestors ever were.  Radioactive iodine, one of the elements dispersed by SOME of these activities, would probably be the top culprit, though other radionucleids can also cause thyroid problems. Immediate conclusion:  Need to get the basic data on the first three questions before either hypothesis becomes tenable. It is a proposition worth investigation. FurPaw PS There was a lot of hoo-hah about the "migraine personality" in the late 60’s and early 70’s, too. As the physiological roots of migraine become better understood, I don’t think too many folks still look at the migraine personality as causal, although different personality styles could make the _experience_ of migraine more or less awful.

Response:

Cassie wrote:

Well, let me start my story off by stating my age.  I am 31

years old and for a couple of months now I was experiencing hot flashes (blushing) and my periods were really weird.  Just last month I had two periods but they only lasted for 2 days each.  This month I am very late for my period and I called my doctor and they gave me a preg. test but I had my tubes tied along time ago.  Now Monday I am trying to get an appt. for them to check my hormone levels because just yesterday and today I have been having like waves of heat going through my chest to my head and I feel like I am burning up.  My heart starts racing and that is not good for me since I tend to have anxiety attacks.  I am very moody (ask my poor husband) and feels like I am having a MAJOR Pms thing going on.  I hate this feeling and can’t wait to see what is going on with my body.  Thanks for listening to me and any help would be appreciated…. Cassie :) ————— Haven’t heard the name in years,I think it’s so neat.As I read your post I first though because of your age to get your thyroid check and that may be a good idea still. But we have heard from younger ladies in preimenopause too,keep us up-dated. Kit

Response:

Pat wrote:

Cassie, if you were a few years older I might just say, "welcome

to the club," but 31 is young enough that getting it checked out seems like a very smart idea. While your symptoms sound hormonal, there are a number of things that could cause them that aren’t menopause. Best to get those ruled out by a competent physician. You might want to ask the doctor, for instance, about thyroid tests – thyroid problems are relatively common in women, and because the thyroid is another hormone factory, problems with it can mimic some of the signs of meno. Meanwhile, try not to worry too much (yeah, I know, easier said than done). Some of us who have hot flashes have found that stress can trigger them (nasty little feedback loop there, eh?) Get some rest, drink plenty of water, and ask your husband to bear with you. Best wishes, –Pat Kight kig…@peak.org —————- Cassie : I wrote in an earlier post to check thyroid please ask your doctor for TSH,T4 and T3 that way you will get a full picture of the thyroid.If you have other symptoms such as weight gain or loss,shaky hands,brittle nail’s etc.. Let us know.I will try to help you further with this if I can. Thanks Kit

Response:

- Hide quoted text — Show quoted text -Sam Saidi <54…@doctor.com

wrote in message … Joan Livingston <joan.livingst…@gte.net wrote in message news:0pcu4.3128$oO6.45150@dfiatx1-snr1.gtei.net…   Plus, what goes wrong with so many women’s thyroids that besides having Synthroid being the Number 2 leading selling drug in the US right after Premarin as Number one, there seems to be this ready acceptance to investigate the thyroid gland? That is worrying    Plus this gets tossed off I would hate to tell you what that means in colloquial English, but I bet Jo’s chuckling

     We "toss cookies" in the US ……is this what you mean? (regurgitate) J – Hide quoted text — Show quoted text -

Sam

Response:

Joan Livingston <joan.livingst…@gte.net

wrote in message

news:0pcu4.3128$oO6.45150@dfiatx1-snr1.gtei.net…

  Plus, what goes wrong with so many women’s thyroids that besides having Synthroid being the Number 2 leading selling drug in the US right after Premarin as Number one, there seems to be this ready acceptance to investigate the thyroid gland?

That is worrying

   Plus this gets tossed off

I would hate to tell you what that means in colloquial English, but I bet Jo’s chuckling Sam

Response:

- Hide quoted text — Show quoted text -"J.Prescott" wrote:

On Sun, 27 Feb 2000 17:33:23 GMT, "Joan Livingston" <joan.livingst…@gte.net wrote: Sam Saidi <54…@doctor.com wrote in message … Joan Livingston <joan.livingst…@gte.net wrote in message news:0pcu4.3128$oO6.45150@dfiatx1-snr1.gtei.net…   Plus, what goes wrong with so many women’s thyroids that besides having Synthroid being the Number 2 leading selling drug in the US right after Premarin as Number one, there seems to be this ready acceptance to investigate the thyroid gland? That is worrying    Plus this gets tossed off I would hate to tell you what that means in colloquial English, but I bet Jo’s chuckling     We "toss cookies" in the US ……is this what you mean? (regurgitate) ROFLMAO! Sorry. No Joan, but here might be a small mess involved….. PS. I’d have thought that to toss cookies would have been a US baking expression

Is "toss" in British slang synonymous with "jerk" in American slang, in this context? Or am I guessing the wrong anatomical system entirely? FurPaw

Response:

Yes, it seems the US  medical industry "jerks-off" thyroid disease diagnoses, as if it was some form of  desirable indoor recreation …….;-) J – Hide quoted text — Show quoted text -FurPaw wrote in message <38B9A8BC.97964…@NOJUNKhome.com

… "J.Prescott" wrote: On Sun, 27 Feb 2000 17:33:23 GMT, "Joan Livingston" <joan.livingst…@gte.net wrote: Sam Saidi <54…@doctor.com wrote in message … Joan Livingston <joan.livingst…@gte.net wrote in message news:0pcu4.3128$oO6.45150@dfiatx1-snr1.gtei.net…   Plus, what goes wrong with so many women’s thyroids that besides

having

Synthroid being the Number 2 leading selling drug in the US right

after

Premarin as Number one, there seems to be this ready acceptance to investigate the thyroid gland? That is worrying    Plus this gets tossed off I would hate to tell you what that means in colloquial English, but I

bet

Jo’s chuckling     We "toss cookies" in the US ……is this what you mean?

(regurgitate)

ROFLMAO! Sorry. No Joan, but here might be a small mess involved….. PS. I’d have thought that to toss cookies would have been a US baking expression Is "toss" in British slang synonymous with "jerk" in American slang, in this context? Or am I guessing the wrong anatomical system entirely? FurPaw

Response:

Hello everyone,     Well, let me start my story off by stating my age.  I am 31 years old and for a couple of months now I was experiencing hot flashes (blushing) and my periods were really weird.  Just last month I had two periods but they only lasted for 2 days each.  This month I am very late for my period and I called my doctor and they gave me a preg. test but I had my tubes tied along time ago.  Now Monday I am trying to get an appt. for them to check my hormone levels because just yesterday and today I have been having like waves of heat going through my chest to my head and I feel like I am burning up.  My heart starts racing and that is not good for me since I tend to have anxiety attacks.  I am very moody (ask my poor husband) and feels like I am having a MAJOR Pms thing going on.  I hate this feeling and can’t wait to see what is going on with my body.  Thanks for listening to me and any help would be appreciated…. Cassie :)

Response:

Hi Cassie,  Good timing. We are currently having a discussion about whether a tubal ligation can accelerate the onset of menopause. There seems to be some studies supporting this, and then other experience to the contrary. So it could be that you indeed are maybe getting some early menopause signs, which do not necessarily mean that your periods will stop for many years as this pre-peri-menopause stage can last 7 or so years.     Don’t worry, the signs you are experiencing can come and go for years before one’s periods stop so what you may be feeling now may disappear in a few months, and then get replaced with something else, and then come back for a few months. Just some tweaks of early warning ….if in fact this is "menopause". Always be sure you are comfortable  with this conclusion atfter discussing this with your health care provider, however.    Also for many women, age 35 is normal for their menopause regardless of a prior tubal ligation so you may be one of those whose history may put you in this catagory. Many doctors keep saying that age 35 is "too young" for menopause, but we have heard too many stories from perfectly normal women who report indeed this is their time for menopause. So be careful if your doctor may want to experiment with a lot of drugs in case your situation does not meet his/her version of "normal." You may want to discuss this with the group here if you have any further questions after you visit a doctor, if you feel it is needed. It may not be. This is your choice.    The best thing to do right now in any case is to start reading up on menopause and get aquainted with its many manifestations and understandings. The best books I have found are in this order: 1. "The Menopause Industry" by Sandra Coney     Excellent introduction explaining both common sense information and the marketing and politics that have too often dominated this time in our lives. Leaves one with a positive feeling rather than a doom and gloom book. This book will immediately take a lot of the confusion away about this topic and tell you how things got to appear so confused in the first place .Can’t recommend this book enough. 2. Dr Susan Love’s Hormone Book: Making Informed Choices About Menopause    A very comprehensive book that you may eventually want to get as it covers just about everything that could be researched about menopause at the time this book was written. Lots about the pros and cons of different ways of looking at the medical aspects. 3. "Woman: An Intimate Geography" by Natalie Angier     This is a great book in a very conversational style that imparts a lot of the "scicence" about how our female bodies work, and what myths still surround them that through this author get replaced with current facts. It is more than just about menopause. It is about all of us.   And by all means please visit Tishy’s Website which is a volunteer website put together by several of the members of this newsgroup over time with research, links, commentary, resources and a place where women new to this can touch base and get some basics. www.oxford.net/~tishy/beyond.html Welcome and best wishes. J – Hide quoted text — Show quoted text -WhsprWulf wrote in message <899lrd$ng…@nntp3.atl.mindspring.net

… Hello everyone,    Well, let me start my story off by stating my age.  I am 31 years old and for a couple of months now I was experiencing hot flashes (blushing)

and

my periods were really weird.  Just last month I had two periods but they only lasted for 2 days each.  This month I am very late for my period and I called my doctor and they gave me a preg. test but I had my tubes tied

along

time ago.  Now Monday I am trying to get an appt. for them to check my hormone levels because just yesterday and today I have been having like waves of heat going through my chest to my head and I feel like I am

burning

up.  My heart starts racing and that is not good for me since I tend to

have

anxiety attacks.  I am very moody (ask my poor husband) and feels like I am having a MAJOR Pms thing going on.  I hate this feeling and can’t wait to see what is going on with my body.  Thanks for listening to me and any help would be appreciated…. Cassie :)

Response:

- Hide quoted text — Show quoted text -WhsprWulf wrote:

Hello everyone,     Well, let me start my story off by stating my age.  I am 31 years old and for a couple of months now I was experiencing hot flashes (blushing) and my periods were really weird.  Just last month I had two periods but they only lasted for 2 days each.  This month I am very late for my period and I called my doctor and they gave me a preg. test but I had my tubes tied along time ago.  Now Monday I am trying to get an appt. for them to check my hormone levels because just yesterday and today I have been having like waves of heat going through my chest to my head and I feel like I am burning up.  My heart starts racing and that is not good for me since I tend to have anxiety attacks.  I am very moody (ask my poor husband) and feels like I am having a MAJOR Pms thing going on.  I hate this feeling and can’t wait to see what is going on with my body.  Thanks for listening to me and any help would be appreciated…. Cassie :)

Cassie, if you were a few years older I might just say, "welcome to the club," but 31 is young enough that getting it checked out seems like a very smart idea. While your symptoms sound hormonal, there are a number of things that could cause them that aren’t menopause. Best to get those ruled out by a competent physician. You might want to ask the doctor, for instance, about thyroid tests – thyroid problems are relatively common in women, and because the thyroid is another hormone factory, problems with it can mimic some of the signs of meno. Meanwhile, try not to worry too much (yeah, I know, easier said than done). Some of us who have hot flashes have found that stress can trigger them (nasty little feedback loop there, eh?) Get some rest, drink plenty of water, and ask your husband to bear with you. Best wishes, –Pat Kight kig…@peak.org

Response:

Welcome Cassie.  At 31 you may be a little young to be starting perimenopause, but not unheard of.  I think the average age is about 35 and a woman can go about 15 years or so before actually hitting menopause.  Most changes are so suttle that we often don’t really notice them at first or write them off to stress or other things. Most women, I think, really start noticing the differences around their mid 40’s. Hormone tests, I feel, are not a good indication of what is going on as you only get a picture of what they are at that moment and hormones fluctuate up and down all the time. I would suggest that you have your Thyroid tested though, because some of the symptoms of Thyroid problems mimic perimenopause. I am sure that you will get lots of good advice from people here and the best thing that all of us can do is research.  Don’t take 1 person’s opinion.  Check things out and do your homework. Karen Marshall kar…@yosemite.net On Sat, 26 Feb 2000 17:58:33 -0500, "WhsprWulf" – Hide quoted text — Show quoted text -<pdqb…@mindspring.com

wrote: Hello everyone,    Well, let me start my story off by stating my age.  I am 31 years old and for a couple of months now I was experiencing hot flashes (blushing) and my periods were really weird.  Just last month I had two periods but they only lasted for 2 days each.  This month I am very late for my period and I called my doctor and they gave me a preg. test but I had my tubes tied along time ago.  Now Monday I am trying to get an appt. for them to check my hormone levels because just yesterday and today I have been having like waves of heat going through my chest to my head and I feel like I am burning up.  My heart starts racing and that is not good for me since I tend to have anxiety attacks.  I am very moody (ask my poor husband) and feels like I am having a MAJOR Pms thing going on.  I hate this feeling and can’t wait to see what is going on with my body.  Thanks for listening to me and any help would be appreciated…. Cassie :)

Response:

All hormones work with each other, and when one is depleted or low, it causes all the others to cease functioning correctly. It is very important for women to have  their thyroid hormone checked on a regular basis. The symptoms of underactive thryroid are similar to peri and menopause symptoms. Having a doctor question,and suggest a thyroid test is a blessing.  For years women have been told it was menopause.  My Mom died a year ago from an undiagnosed underactive thyroid.  I applaud doctors that will suggest a thyroid test.

Response:

Yes, I had my tubes tied in my early 20’s.  Yes, sometimes I regret it since I am married to a different man but those were my decisions.  I know what it feels like to go through anxiety and panic attacks….they have never stopped my period and have given me waves of heat.  If it is…its a new one on me. :)  It may be stress but I don’t feel stressed….maybe its due to I am getting over a sinus infection and I am on my second antibiotic and I strained my pec muscles and I am on motrin for that.  This is all new to me…I wish my period would just start and I wouldn’t have all these pms feelings all the time. "Sam Saidi" <54…@doctor.com

wrote in message

news:cgau4.9093$74.249030@nnrp3.clara.net… – Hide quoted text — Show quoted text -

BUt Joan, she’s 31, a long way off what would be expected of perimenopause even in the younger age groups that you quote. Don’t these symptoms more resemble an anxiety state than perimenopause? Common things are common and I can bet anxiety state is a damn site more common at 31 than premature perimenopause! The prior tubal ligation does pose a worry here though, the fact that it

was

"a long time ago", that means that Cassie had her tubal in her 20’s, a notorious age group associated with a high regret rate. I assume the pregnancy test was negative? (the failure rate of sterilisation, as with any form of contraception, is higher in the younger age groups) As regards blood tests, an estradiol level may be more help than the standard FSH test, although it may need to be repeated once your periods

get > back to a more normal pattern. Thyroid check may also be suitable. > Sam > Joan Livingston <joan.livingst…@gte.net

wrote in message

> news:vcZt4.1465$oO6.18970@dfiatx1-snr1.gtei.net… > >    Also for many women, age 35 is normal for their menopause regardless of

a prior tubal ligation so you may be one of those whose history may put

you

in this catagory. Many doctors keep saying that age 35 is "too young" for menopause, but we have heard too many stories from perfectly normal

women

who report indeed this is their time for menopause. So be careful if

your

doctor may want to experiment with a lot of drugs in case your situation does not meet his/her version of "normal." You may want to discuss this with the group here if you have any further questions after you visit a

doctor,

if you feel it is needed. It may not be. This is your choice.

Response:

Thanks for your support….I will come back to this group and let you know what my doctor says.  My husband is so pleased that I have found a group of women that can help me through this. Thanks so much, Cassie :) "Joan Livingston" <joan.livingst…@gte.net

wrote in message

news:vcZt4.1465$oO6.18970@dfiatx1-snr1.gtei.net… – Hide quoted text — Show quoted text -

Hi Cassie,  Good timing. We are currently having a discussion about whether a tubal ligation can accelerate the onset of menopause. There seems to be some studies supporting this, and then other experience to the contrary. So it could be that you indeed are maybe getting some early menopause signs,

which

do not necessarily mean that your periods will stop for many years as this pre-peri-menopause stage can last 7 or so years.     Don’t worry, the signs you are experiencing can come and go for years before one’s periods stop so what you may be feeling now may disappear in

a

few months, and then get replaced with something else, and then come back for a few months. Just some tweaks of early warning ….if in fact this is "menopause". Always be sure you are comfortable  with this conclusion

atfter

discussing this with your health care provider, however.    Also for many women, age 35 is normal for their menopause regardless of

a

prior tubal ligation so you may be one of those whose history may put you

in

this catagory. Many doctors keep saying that age 35 is "too young" for menopause, but we have heard too many stories from perfectly normal women who report indeed this is their time for menopause. So be careful if your doctor may want to experiment with a lot of drugs in case your situation does not meet his/her version of "normal." You may want to discuss this

with

the group here if you have any further questions after you visit a doctor, if you feel it is needed. It may not be. This is your choice.    The best thing to do right now in any case is to start reading up on menopause and get aquainted with its many manifestations and

understandings.

The best books I have found are in this order: 1. "The Menopause Industry" by Sandra Coney     Excellent introduction explaining both common sense information and

the

marketing and politics that have too often dominated this time in our

lives.

Leaves one with a positive feeling rather than a doom and gloom book. This book will immediately take a lot of the confusion away about this topic

and

tell you how things got to appear so confused in the first place .Can’t recommend this book enough. 2. Dr Susan Love’s Hormone Book: Making Informed Choices About Menopause    A very comprehensive book that you may eventually want to get as it covers just about everything that could be researched about menopause at

the

time this book was written. Lots about the pros and cons of different ways of looking at the medical aspects. 3. "Woman: An Intimate Geography" by Natalie Angier     This is a great book in a very conversational style that imparts a lot of the "scicence" about how our female bodies work, and what myths still surround them that through this author get replaced with current facts. It is more than just about menopause. It is about all of us.   And by all means please visit Tishy’s Website which is a volunteer

website

put together by several of the members of this newsgroup over time with research, links, commentary, resources and a place where women new to this can touch base and get some basics. www.oxford.net/~tishy/beyond.html Welcome and best wishes. J WhsprWulf wrote in message <899lrd$ng…@nntp3.atl.mindspring.net… Hello everyone,    Well, let me start my story off by stating my age.  I am 31 years old and for a couple of months now I was experiencing hot flashes (blushing) and my periods were really weird.  Just last month I had two periods but they only lasted for 2 days each.  This month I am very late for my period and

I

called my doctor and they gave me a preg. test but I had my tubes tied along time ago.  Now Monday I am trying to get an appt. for them to check my hormone levels because just yesterday and today I have been having like waves of heat going through my chest to my head and I feel like I am burning up.  My heart starts racing and that is not good for me since I tend to have anxiety attacks.  I am very moody (ask my poor husband) and feels like I

am

having a MAJOR Pms thing going on.  I hate this feeling and can’t wait to see what is going on with my body.  Thanks for listening to me and any

help

would be appreciated…. Cassie :)

Response:

Psychiatric Medication & POF and Premature Menopause

Question:

Hello All ;-) I would like to know whether Paxil (for depression) and Zyprexa (for anxiety) can cause POF and Premature Menopause.  I take both medications and haven’t ‘bled’ for about 2 1/2 months.  My primary doctor says the 2 meds can cause my menstrual periods to be ‘off’ but I would like a second opinion, if necessary. Any help is appreciated; thanks in advance. Christine Geary

Response:

On Wed, 17 Nov 1999 20:55:04 GMT, Christine Geary <cge…@epix.net

wrote:

Hello All ;-) I would like to know whether Paxil (for depression) and Zyprexa (for anxiety) can cause POF and Premature Menopause.  I take both medications and haven’t ‘bled’ for about 2 1/2 months.  My primary doctor says the 2 meds can cause my menstrual periods to be ‘off’ but I would like a second opinion, if necessary. Any help is appreciated; thanks in advance. Christine Geary

How old are you, Christine? While some antidepressants and such may disrupt menstrual cycles, it is also possible that you are beginning perimenopause, something which is entirely normal after about age 35 or so. This is not POF or premature menopause – it’s normal and not a disease condition. Terri

Response:

- Hide quoted text — Show quoted text -Terri wrote:

On Wed, 17 Nov 1999 20:55:04 GMT, Christine Geary <cge…@epix.net wrote: Hello All ;-) I would like to know whether Paxil (for depression) and Zyprexa (for anxiety) can cause POF and Premature Menopause.  I take both medications and haven’t ‘bled’ for about 2 1/2 months.  My primary doctor says the 2 meds can cause my menstrual periods to be ‘off’ but I would like a second opinion, if necessary. Any help is appreciated; thanks in advance. Christine Geary How old are you, Christine? While some antidepressants and such may disrupt menstrual cycles, it is also possible that you are beginning perimenopause, something which is entirely normal after about age 35 or so. This is not POF or premature menopause – it’s normal and not a disease condition. Terri

Terri, I’m 37 years old and started having irregular periods earlier this year.  I was on Mellaril (for anxiety) earlier in the year before I started having irregular periods.   My periods started to become irregular this year, so my psychiatrist switched me Zyprexa.  I kind of had regular periods for a while then 1 month I was spotting for almost an entire month then I stopped spotting for a few weeks.  After that,  I had kind of normal periods for about 2-3 months until now when I didn’t have a period since the 1st week of September.  Also I was adopted so I don’t know whether my ‘birth’ mom went through early menopause or not. I hope this helps. Christine

Response:

Christine Geary <cge…@epix.net

wrote in message

news:38335CFC.3D67@epix.net…

Terri wrote: On Wed, 17 Nov 1999 20:55:04 GMT, Christine Geary <cge…@epix.net wrote: Hello All ;-) I would like to know whether Paxil (for depression) and Zyprexa (for

anxiety) can cause

POF and Premature Menopause.  I take both medications and haven’t

‘bled’ for about 2 1/2 – Hide quoted text — Show quoted text -

months.  My primary doctor says the 2 meds can cause my menstrual

periods to be ‘off’

but I would like a second opinion, if necessary. Any help is appreciated; thanks in advance. Christine Geary How old are you, Christine? While some antidepressants and such may disrupt menstrual cycles, it is also possible that you are beginning perimenopause, something which is entirely normal after about age 35 or so. This is not POF or premature menopause – it’s normal and not a disease condition. Terri Terri, I’m 37 years old and started having irregular periods earlier this year.

I was on

Mellaril (for anxiety) earlier in the year before I started having

irregular periods.

My periods started to become irregular this year, so my psychiatrist

switched me

Zyprexa.  I kind of had regular periods for a while then 1 month I was

spotting for

almost an entire month then I stopped spotting for a few weeks.  After

that,  I had kind

of normal periods for about 2-3 months until now when I didn’t have a

period since the

1st week of September.  Also I was adopted so I don’t know whether my

‘birth’ mom went

through early menopause or not. I hope this helps. Christine

Christine, You may want to have a doctor check you for any physical issues.  I started having very severe PMS at about age 38 the day before I started my periods. I was absolutely exhausted for no apparent reason, weepy, and heard rushing noise in my ears all night long and couldn’t sleep.  Moodswings, gastrointestinal disorders (including food intolerance), and insomnia have been my worst symptoms.  Kit and others may have some comments about thyroid for you. Welcome! –Jane

Response:

I’m 37 years old and started having irregular periods earlier this year.  I was on Mellaril (for anxiety) earlier in the year before I started having irregular periods. My periods started to become irregular this year, so my psychiatrist switched me Zyprexa.  I kind of had regular periods for a while then 1 month I was spotting for almost an entire month then I stopped spotting for a few weeks.  After that, I had kind of normal periods for about 2-3 months until now when I didn’t have a period since the 1st week of September. Hi Christine: Do you have thyroid problems that you know off ? Are you having trouble losing weight or are gaining weight ? Do you have any symptoms of body heat all over the body not just the face and neck ? Do you have trouble with your bowel’s ? Is your hair dry and brittle and are your finger nail’s pealing or breaking,Are you losing hair ? Do you find it easy to swallow or hard to swallow ? Are you very tired or very hyper ? Depression fit’s with hypo-thyroid not a hyper one.Many symptoms of thyroid problems are the same as menopause if you like answer the questions,I will try and help that way, if not have your thyroid checked first and go from there.Test’s for thyroid are TSH.T4,T3 Take Care kit

Response:

I Hope This Doesn't Sound Silly

Question:

Just because I’m having anxiety attacks does necessarily mean I have a panic disorder, right?

Response:

Hi- If your having anxiety attacks, what that means is you need to get to the doctor and make sure it isn’t something more serious.  Oh I know that anxiety attacks are no day at the beach.  But other diseases have similar symptoms, namely thyroid problems, diabetes, and MS. It is very important to rule this stuff out.   Wishing you the best. Jess

Response:

Just because I’m having anxiety attacks does necessarily mean I have a panic disorder, right?

Yes, that’s right. Philip

Response:

Blood pressure

Question:

The best way to find websites on hypothyroidism is to just do a search for it…there’s tons of stuff as it’s very common and affects men, women, and kids. My main symptoms were chronic fatigue and inability to lose weight…though I may have also had PCOS at the time and not known it, who knows? Jessica

Response:

Liezl van Zyl wrote:

Any good sites or articles you could recommend?

http://www.brodabarnes.org   It lists symptoms of thyroid disease, has a recommended book list, and if you call them, will send an info. packet and doctor referrals for your area for $15. http://www.personal.u-net.com/~my4tune/appto_treatment.txt This is an excellant article on thryoid and related disorders. Darlene

Response:

In a message dated 6/2/99 7:16:50 PM Eastern Daylight Time, li…@waikato.ac.nz writes: << You wrote: You seem to know the thyroid connection. Have you been tested?

I had been tested annually because of my family members.  <<I’ve heard of the thyroid connection, but don’t know anything about it.  I  don’t even understand the difference between hypo- and hyperthyroidism.

Hypo is underactive and the symptoms mimic PCOS with the added symptom of slow heart beat.  The slow pulse makes me wonder about you. <<My gp ran a test last year, which seemed normal, but I heard that these tests  can be deceptive. Apart from the symptoms I mentioned before, I’m a bit  worried about thyroid because my mother developed problems with an  overactive thyroid a few years ago and had part of it removed.

There is one kind, I think called Hashimoto’s (or something like that) that one girl on the board had and all her levels showed normal, she had to have a biopsy to discover this was her problem.  <<What are the symptoms of thyroid problems?

For hypo, the symptoms for  a woman are much like PCO-facial hair, irregular periods, weight that won’t come off for nothing.  Sometimes periods that are more like hermorraging.  <<I had some awfully heavy bleeding during my teens, as well as periods that  went on and on – impossible to distinguish between different visits form  AF. This was never investigated. (My concern was not with my health back  then, I was only afraid that someone might find out – which was really  quite hard since I lost what felt like litres of blood a day).  The last  few years (I’m 30) my periods have been few and far between and very light,  and occasionally they tend to go on for too long (2 weeks or so).

This could be from either PCO or hypo or even both.  There are some women who post to our board who have both problems, unfortunately.  I<< also have brown lines under my eyes, which I thought was from hayfever,  but I still have them, minus the hayfever.  I’ve had a number of tests done earlier this week, but don’t have the  results back yet. My next appointment with my endo is only in August  (public system), so I’d like to figure things out for myself in the meantime.  

I hope that some of the women on the board who are also hypo get in touch with you.  Perhaps they can tell you some of what they went through.  I myself will probably have more testing soon and I plan to mention the Hashimoto or whatever it is to my RE since you never can tell. I wish you all the luck in the world.

Any good sites or articles you could recommend?

I bet some of the other Cysters here know of some.  I am not so sure about the thyroid thing but I know there is one Cyster here that posted that was quite knowledgeable.  Perhaps she will see this post and respond  ^–^ { ‘.’}cathy-to send e-mail, delete edyclub    `   <A HREF="http://www.geocities.com/Heartland/Cottage/8060/index.html"

My~WEB!</A<BR<A

HREF="http://www.geocities.com/Heartland/Cottage/8060/PCOS.html"

PCO-HOPE FOR

CYSTERS</A

</HTML

Response:

Is IR necessarily accompanied by high blood pressure and obesity? Someone said something about low pulse and thyroid? Any ideas?

You seem to know the thyroid connection.  Have you been tested? One friend of mine some years ago had symptoms that we would call classic PCO, but it turned out to be her thyroid.  She had one of those never-ending periods and almost hemmoraged to death.  They had to remove her thyroid and she is on Synthoid (I have no idea if I spelled this right, please forgive) for life. Please have it checked, though many drs. should have checked your thyroid from the beginning–though problems can develop later  on.  I have tested normal, but am still at risk because my oldest brother is hypothyroid (and type 2 diabetic) and a first cousin is too (both hypo and diabetic like my bro)  ^–^ { ‘.’}cathy-to send e-mail, delete edyclub    `   <A HREF="http://www.geocities.com/Heartland/Cottage/8060/index.html"

My~WEB!</A<BR<A

HREF="http://www.geocities.com/Heartland/Cottage/8060/PCOS.html"

PCO-HOPE FOR

CYSTERS</A

</HTML

Response:

Cystercat wrote: You seem to know the thyroid connection. Have you been

tested?
I’ve heard of the thyroid connection, but don’t know anything about it.  I don’t even understand the difference between hypo- and hyperthyroidism. My gp ran a test last year, which seemed normal, but I heard that these tests can be deceptive. Apart from the symptoms I mentioned before, I’m a bit worried about thyroid because my mother developed problems with an overactive thyroid a few years ago and had part of it removed.
What are the symptoms of thyroid problems?
I had some awfully heavy bleeding during my teens, as well as periods that went on and on – impossible to distinguish between different visits form AF. This was never investigated. (My concern was not with my health back then, I was only afraid that someone might find out – which was really quite hard since I lost what felt like litres of blood a day).  The last few years (I’m 30) my periods have been few and far between and very light, and occasionally they tend to go on for too long (2 weeks or so).
I also have brown lines under my eyes, which I thought was from hayfever, but I still have them, minus the hayfever.
I’ve had a number of tests done earlier this week, but don’t have the results back yet. My next appointment with my endo is only in August (public system), so I’d like to figure things out for myself in the meantime.
Any good sites or articles you could recommend?
Thanks,
Liezl    -**** Posted from RemarQ, http://www.remarq.com/?a ****-  Search and Read Usenet Discussions in your Browser – FREE –

Response:

I also have low blood pressure…the worst part of it is that I weigh like 325 lbs…and so when I go to the Dr.’s office and they take my vitals…they pump up the cuff until I think that my arm is going to burst…Only to have them let it back down….and take it several times, since they can’t believe that at my weight (I’m only 5′3") my blood pressure is like 80/120 or so!!!  I HATE IT!!!  I don’t know about my IR but my Dr. keeps taking my BG & thyroid levels at every appt. since there is a STRONG family history of diabetes & thyroid problems. All of my sisters are Cysters.  And all of them except me have diabetes. And all of us belong to the ‘hair bear club’…   :) Love to all, Mary McK Sent via Deja.com http://www.deja.com/ Share what you know. Learn what you don’t.

Response:

Something that’s been mystifying me:
I have LOW blood pressure. Have always had it, not abnormally low, but doctors always say its on the lowest side of normal. I’ve always thought that my fainting, dizzy spells and fatigue, especially in summer, can be ascribed to this.
Now I’m not so sure. Insulin resistence produces the same effects, if I understand it correctly, and a low-carb diet has done wonders in alleviating these dizzy spells.
I’ve no idea as yet whether I am IR, was just wondering whether low blood pressure throws me off the waggon of those who’ll benefit from insulin sensitising drugs.
Apart from the low blood pressure, I have a very slow heart rate (60 per minute, around 45 first thing in the morning), although I’m decidedly unfit. Normal weight. And before you begin to wonder whether I’m an alien: I do have most of the other PCO symptoms (acne, infertility, hair, male pattern hair loss, etc.)
 Is IR necessarily accompanied by high blood pressure and obesity? Someone said something about low pulse and thyroid? Any ideas?
   -**** Posted from RemarQ, http://www.remarq.com/?a ****-  Search and Read Usenet Discussions in your Browser – FREE –

Response: