drob31
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I think it was the fasting sugar test. I should know the results by Tuesday hopefully.
Any news?
I think it was the fasting sugar test. I should know the results by Tuesday hopefully.
Yes, I don't have diabetes. My TSH is very low, however, and I'm taking the same amount of synthroid I have been taking for years. For the last 3 years my TSH has been between 1 and 2 and now it is almost 0. It has never been this low. It has always slowly gone up and I've had to increase my synthroid every few years. The doctor wants me to get a thyroid ultrasound. The nerve pain in the feet seems to be subsiding however. That's good news!Any news?
Yes, I don't have diabetes. My TSH is very low, however, and I'm taking the same amount of synthroid I have been taking for years. For the last 3 years my TSH has been between 1 and 2 and now it is almost 0. It has never been this low. It has always slowly gone up and I've had to increase my synthroid every few years. The doctor wants me to get a thyroid ultrasound. The nerve pain in the feet seems to be subsiding however. That's good news!
What I'm learning is that the adrenal glands and thyroid, or at least inconsistent levels of the hormones they supply can cause dysglycemia, which makes it seem like you have blood sugar issues. I think I'm putting allot of peices together, i'll start a new thread with my theory, but I'm borrowing part of what Dr. Kharazzian has concluded.
Is your synthroid for a deficiency caused by hashimoto's? Also, I would wonder how well your t4 is converting to t3, as adrenal issues and blood sugar issues have a huge impact on that.
Yes, I have Hashimoto's. Unfortunately, I can't find a doctor who cares about t4 converting to t3. They only worry about TSH. I think this new doctor I am seeing is finally noticing that the synthroid is not stopping the Hashimoto's antibodies. This is a nice change from many doctors who are in denial that synthroid doesn't always solve all thyroid problems. I think I will ask her about the t4/t3 conversion test. Maybe she's different.
Thanks for the information.
I have seen 4 or 5 endocrinologists since 2011. Last year I finally found one who thought it was a good idea to put me on hormone replacement despite "low" TSH of 4. He said that my high antibodies were causing too much inflammation and that HR would help with that. Then he prescribed me levothyroxine. One week later I had to run to a psychiatrist who put me on citalopram.Yes, I have Hashimoto's. Unfortunately, I can't find a doctor who cares about t4 converting to t3. They only worry about TSH.
I have seen 4 or 5 endocrinologists since 2011. Last year I finally found one who thought it was a good idea to put me on hormone replacement despite "low" TSH of 4. He said that my high antibodies were causing too much inflammation and that HR would help with that. Then he prescribed me levothyroxine. One week later I had to run to a psychiatrist who put me on citalopram.
My antibodies decreased slightly, and TSH decreased to 2. The endo was very statisfied, and said that my constant low BP (90/60) was just excellent, and ignored other complaints of mine.
I finally found an integrative dr who put me on compounded T4/T3. Even so, my reverse T3 has been pretty high (the integrative dr checks for it!), and after increasing the T3 replacement I had to titrate the citalopram down very quickly and quit it. BP is now 11/7 and antibodies are going down more quickly, head is much more clear
We tried increasing the T3 again, but it didn't work out. I still have a need for something else, and am going to look into pregnenolone next. I take a homeopathy that gives me a light adrenal support, so I will try to improve something on that direction.
What makes it harder is the fact that blood tests don't accurately match the symptoms. I guess I will have to chart my body temperature after all to know what I really need.
It is highish to very high in the morning after a bad night's sleep.How does your cortisol look? Ever consider cortef?
I am suspecting that tyramine plays some role in inflammation for MAO-Aers.Since you know it's an autoimmune attack, I would first treat it from an autoimmune perspective:
Autoimmune paleo diet (most important): http://www.phoenixhelix.com/paleo-autoimmune-protocol/
Fish Oil + Tumeric + Resveratrol + Vitamin D
Sunlight as much as possible to reinforce Vitamin D
Focus on gut: probiotics (primal defense), glutamine, (AIP diet above),
Read this: http://www.amazon.com/Still-Thyroid-Symptoms-Tests-Normal/dp/0985690402
If that doesn't cut it, then if you use t3 or slow release t3. I know it works for some with hashimoto's. At a high enough dose you will supress TSH, and the activity of the gland, and I know allot have lowered their anitbodies this way.
It is highish to very high in the morning after a bad night's sleep.
When I upped my T3 again I started biting very hard the insides of my mouth at bed time, then backed off.
I don't think I need to test that one - high for sureI'll be super curious to see what the 4 AM sample says
When I upped my T3 again I started biting very hard the insides of my mouth at bed time, then backed off.
I have what you are describing sometimes and to me it is when I have too much salicylates, then the mucosa inside my cheeks and mouth gets swollen (allergic reaction). That is why I avoid tooth paste and use CaCO3 and MgO with water to brush my teeth.Do you mean the insides of your cheeks, because the skin seems to be loose? I am getting that at the moment but am not taking anything different from usual, and don't take any thyroid meds.
I have what you are describing sometimes and to me it is when I have too much salicylates, then the mucosa inside my cheeks and mouth gets swollen (allergic reaction). That is why I avoid tooth paste and use CaCO3 and MgO with water to brush my teeth.
What I meant as related to too much T3 was that just before falling asleep I get a sudden muscle contraction in my jaw and it will close very tightly, painfully biting my mouth lining and making a noise when the lower teeth meet the upper teeth
The mouth swelling isn't specifically at night, on the contrary. It apparently happens randomly, but I suspect it is when something allergy-wise builds up, be it too much of a certain food or a slower Phenolsulfotransferase function (details in my salicylate link). Coconut oil pulling makes for a big time swelling, so it's no-no.I see. I sometimes get that too but not for some time, and not usually at night - it could happen at any time. I haven't eaten different foods from usual, so it can't be that causing my current problem, but it's not as bad as it was - not really a problem now.
Since you know it's an autoimmune attack, I would first treat it from an autoimmune perspective:
Autoimmune paleo diet (most important): http://www.phoenixhelix.com/paleo-autoimmune-protocol/
Fish Oil + Tumeric + Resveratrol + Vitamin D
Sunlight as much as possible to reinforce Vitamin D
Focus on gut: probiotics (primal defense), glutamine, (AIP diet above),
Read this: http://www.amazon.com/Still-Thyroid-Symptoms-Tests-Normal/dp/0985690402
If that doesn't cut it, then if you use t3 or slow release t3. I know it works for some with hashimoto's. At a high enough dose you will supress TSH, and the activity of the gland, and I know allot have lowered their anitbodies this way.
The adrenal glands complicates it because if there is dysglycemia or hpa-axis dysfunction, you can't proceed with the t3 until that is resolved.
I have seen 4 or 5 endocrinologists since 2011. Last year I finally found one who thought it was a good idea to put me on hormone replacement despite "low" TSH of 4. He said that my high antibodies were causing too much inflammation and that HR would help with that. Then he prescribed me levothyroxine. One week later I had to run to a psychiatrist who put me on citalopram.
My antibodies decreased slightly, and TSH decreased to 2. The endo was very statisfied, and said that my constant low BP (90/60) was just excellent, and ignored other complaints of mine.
I finally found an integrative dr who put me on compounded T4/T3. Even so, my reverse T3 has been pretty high (the integrative dr checks for it!), and after increasing the T3 replacement I had to titrate the citalopram down very quickly and quit it. BP is now 11/7 and antibodies are going down more quickly, head is much more clear
We tried increasing the T3 again, but it didn't work out. I still have a need for something else, and am going to look into pregnenolone next. I take a homeopathy that gives me a light adrenal support, so I will try to improve something on that direction.
What makes it harder is the fact that blood tests don't accurately match the symptoms. I guess I will have to chart my body temperature after all to know what I really need.
Drob, thanks again for the information. I take most of these supplements through the Pall Protocol. I can't take curcumin or Tumeric, however, because it boosts my Sjogren's antibodies. I think it strengthens my immune system too much. I would love to find a doctor willing to prescribe T3 (Cytomel), but, unfortunately, I live in Wyoming. The doctor choices here are limited.
If anyone knows of a doctor who prescribes T3 in Colorado, I would be willing to travel.