Something has been bothering me for the last couple days, and I thought maybe I might ask you all for some feedback. A while ago I went to my doctor and asked her for hormone prescriptions. She said not without a letter. Ok, fine, I can live with that. (therapy has actually proved to be way more productive than I thought it would be anyway) About a month later I managed to get her to write me a prescription for spironolactone. Well, I have a letter now. I went back to her and we started the blood drawing blah blah blah you know the procedure.
All this while, I've been educating myself on hormones and the various options and this and that and what does what. The other day I stumbled across an article which stated that food increases the bioavailability of spironolactone by almost 100%, and helps minimise side effects.
Basically, take it with food.
At first, I was like woo hoo and sure enough it worked. This is a tremendous relief too, I took my dose earlier and after about an hour I realised I didn't have a headache. Wonderful! The thing that is bothering me, is why didn't she tell me to take it with food? On the one hand, I have done everything I said I would and met her conditions, and she is providing lab testing and prescriptions. On the other hand, she seems almost hostile. She's made little comments, given me little looks...It's hard to explain, and I'm afraid it might be all in my head. I know that Doctors have issues with fooling around with otherwise "healthy" individuals. I also know that hormone therapy is relatively clear cut compared to most of the other things she studied in medical school. So why didn't she tell me. It's really bothering me. What else might come up over the next two years? Her attitude toward dvt is almost dismissive, like if I get one, well, I deserved it didn't I?
So I don't know. She IS providing the lab testing but literally no advice or guidance as I take these powerful medications. I had to tell her, from my own research, where I wanted to try and get my testosterone level at. That bothered me a little, but at the time I thought maybe it was a trick question to see if I'd done my homework.
So what are your relationships with your physicians like? Should I just be greatful for what I have? It's fair to say that she does not encounter transexual people often, so I don't expect to be her area of expertise. Spironolactone and it's side effects aren't exactly rare though. The thing is, if I call her out on this, she'll most likely feel threatened and I'll probably lose her. My health plan only pays for her in this area, the next doc on their list is 3 hours away. I am inclined to kep her, since it's easier than finding someone else, disclosing, waiting for them to look at you like youre crazy, and say yes or no to prescribing and monitoring. I am also inclined to wonder what else might come up that she won't tell me, simply because I didn't know to ask.
Thanks for listening