One of the cancer forums calls it Fairy Dust. I'm trying to decide how much it bothers me and what I might be able to treat it with.
Spoke with Dr Patt's nurse on Friday. Apparently my e-mail had overwhelmed them and they thought maybe I should have another appointment with her to discuss all my questions. She's out for Spring Break and I didn't think I was asking anything extraordinary that required a $300.00/15 minute appointment so I cleared most of it with nurse Candy.
The biggest news for me was that based on my blood test hormone levels I am now post menopausal so instead of Tamoxifen I'll be starting on the drug Femara. I read all about it yesterday and will start on it this week. The biggest SE most people report is joint pain. Fingers crossed hoping I don't experience that.
Blood results for the thyroid Dr. came in and I am reducing my dosage of synthroid. In 3 months I've gone from 100mcg to 75 then to 50 and now to 35. The body chemistry continues to fascinate me.
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