Guest guest Posted August 28, 2003 Report Share Posted August 28, 2003 Man has it gotten heated lately. For what it is worth, I was diagnosed 7 yrs ago with GD post partum, and was only been treated with ATD's. My numbers were very high at first and I was put on beta blockers and PTU. I got pregnant two times without difficulty while on low dose PTU and had more problems with the hypo aspect of pregnancy than the hyper. I had two yrs of remission in between the next pregnancy before needing to go back on PTU. I haven't been on beta blockers in years. I seldom have GD related rage. More like craziness of just being a mom of five children. I am on low dose PTU with normal numbers except the TSH and antibodies. ly I would not care if I had to take the PTU for the long term. At least I know the thyroid hormone is being produced by my body. I also have some control in telling the docs if my dose appears to be too high if my hypo symptoms return. I was in hypo hell for 6 months at one time due to over dosing of the PTU and you couldn't pay me to be in that state, letting alone allowing a doc to purposely make me hypo. It was so much more difficult to function hypo than hyper. At the time I couldn't find one endo who believed I was hypo because of low TSH. I gained 40 lbs. lost my eyebrows, developed terrible joint pain, lived with a sweater on even in the heat of summer, and slept more than my toddler child at the time. I refuse to place my thyroid hormone needs in the hand of physician who determines my needs based on lab statistics and books. I want to control my health. God forbid I would end up with an endo who doesn't believe in T3 replacement, and I would end up hypo forever. The so called anti RAI people on this forum have made educated decisions as to what is best for them. Many have had GD for years and know their disease well. I assure you I know more about my body than an endo I have seen only a few times. I know three people personally who have had RAI and are miserable for it. Each one has said to me they wanted the GD to end quickly and went through with the RAI. Now 3 to 5 yrs later they struggle constantly with their doses and are frequently at odds with their endos over prescribing the proper doses of replacement meds. I can tell you I have felt a whole lot better than them. They are always complaining about their hypo symptoms. These are not inflated claims just facts from the patients not from books. I am a RN as well as a GD patient. I have access to many resources and have chosen my course with great thought. Other people on this board are also in the health care profession and understand fully the repercussions for their decisions. I am getting a little of a feeling that because one chooses against RAI that we are not educated or informed enough. On the contrary I think that we have chosen wisely before going the extreme root and making a very permanent decision which puts us at the mercy of physicians the rest of our lives. Iannuzzi Quote Link to comment Share on other sites More sharing options...
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