[Anonymous]

#1163058

Hi! I know how you feel. It took a good 3 weeks for my Tapazole to kick in, and I’m beginning to feel semi-normal (as normal as I guess I can get!) most days. I, too, was SO relieved to know that it wasn’t just me going crazy. I was diagnosed in December, saw my endo on January 10th, and he’s stabilized me with the Tapazole. I go for my first RAI on Tuesday. He assures me this process will take 6 to 8 more months, but at least now the path is predicable and explainable! Keep showin’ up here, there’s a lot of inspiration goin’ around, and it helps more than anything to have other people who understand what it’s like. Love and Peace to you this day. Sharon T.

[Anonymous]

#1056313

Thank you so much for the response. I’m going to check out the free t-3 and t-4 test. The Cytomel that I mentioned in my last message is a T-3 drug and that’s what pushed me over the edge. Thanks again, Valerie

[Anonymous]

#1163059

Valerie, Welcome! I was also just diagnosed so I don’t have any answers. But I have many of the same sypmtoms you have:

MVP, unrecognizable handwriting, chest pains (just recently), hot, headaches. etc.

I guess we can learn this stuff together karylinn

[Author]

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