Guest guest Posted February 11, 2002 Report Share Posted February 11, 2002 Hi all - I'm still put out about my chat with the doctor and since I had some time before I had to pick up my daughter at preschool, I stopped by the library (yes, I live there!) and within 10 minutes found the article which Elaine references in her Suite 101 article on TSH levels and how they can remained suppressed for long periods of time. Man, I am so tempted to mail it to my doc! It very clearly states exactly why the TSH level is an inadequate test for patients with GD and why. Here's just the abstract for anyone who cares: From Journal of Clinical Endocrinology and Metabolism, Oct 2001, pg 86(10) " Antithyroid treatment for Graves' hyperthyroidism restores euthyroidism clinically within 1-2 months, but it is well known " (I love how it says WELL KNOWN here...obviously not well known to MY doc) " that TSH levels can remain suppressed for many months despite normal free T(4) and T(3) levels. This has been attributed to a delayed recovery of the pituitary-thyroid axis. However, we recently showed that the pituitary contains a TSH receptor through which the TSH secretion may be down-regulated via a paracrine feedback loop. In Graves' disease, TSH receptor autoantibodies may also bind this pituitary receptor, thus causing continued TSH suppression. This hypothesis was tested in a rat model. " (Description of testing on rats deleted for length here) " We conclude that TSH receptor autoantibodies can directly suppress TSH levels independently of circulating thyroid hormone levels, suggesting a functioning pituitary TSH receptor. " Now I am full of righteous indignation that I was correct and my doctor was just un-knowledgeable! Sigh, not that it does me any good. He'll still probably want me to do RAI. I feel a little scared that I may actually know more than my doctor about this particular disease. I don't think that's necessarily a good thing, either. Anyway, it was an interesting article as well. Thought it may also come in handy for the Top 20 list references. Thanks for the cite, Elaine! Now it's a top 20 Top 17 Reasons Why I¹ll Never Have RAI 1. It¹s permanent; if you don¹t like the results, too bad 2. Since the science is inexact, it may have to be repeated 3. Graves disease is an auto-immune disease, not a disease of the thyroid, so killing the thyroid doesn¹t stop the disease 4. Who ever said hypothyroidism is easy to treat, lied 5. Being hypothyroid is neither less debilitating nor less dangerous than hyperthyroid 6. Increased antibody titers after RAI skew lab test results, adding to treatment difficulties 7. RAI is absorbed by other organs and can cause cell death or DNA mutations 8. For up to 4 weeks after dosage, we¹re exposing those around us to radioiodine 9. Studies show an increase in cancers, especially of the thyroid gland and small bowel, after RAI. 10. Possibility of damaging the parathyroid, causing hypoparathyroidism. 11. RAI can cause difficulty with future attempts to become pregnant and carry pregnancies to term 12. Chance of thyroid eye disease developing increases dramatically 13. Chance of significant, unhealthy weight gain is increased 14. Replacement hormone products currently on the market, both synthetic and pig, are not comparable to our own hormone, leading to 15. Reduced quality of life. For ever. 16. Ongoing problems as the gland gradually dies, necessitating close medical surveillance and replacement hormone dosage adjustments 17. Increased risk of developing fibromyalgia 18. For most GD patients, medication with ATD¹s creates a euthyroid state similar to " normal life " 19. As modern science explores the human genome, a cure for GD could be found, but after RAI kills the thyroid, it wouldn¹t work 20. I131 is so dangerous it¹s transported in a lead container and kept at the hospital only for the briefest time before being dispensed by a doctor shielded in lead from head to toe. Quote Link to comment Share on other sites More sharing options...
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