It’s been a while since I last wrote about trans stuff on the blog; things have been chill, transition-wise, but here are some things worth telling. So firstly, medications. Last December I was switched to injections of Fensolvi which substitutes the Spironolactone. My doctor suggested this would be a good choice because I am forgetful with my doses, and with the injection I would only need a dose every six months. Also, Spiro might have been making my POTS worse, combined with the psych meds, I literally was about to pass out every time I stood up. And I guess this is a good time to say that I’m off psych meds; there’ll be a post on that soon. I had my second dose of Fensolvi a couple weeks ago but POTS symptoms never went away. My doctor wouldn’t believe I exhibited those symptoms for other reason other than the Spiro—I’ve had this since I was 13. We discussed increasing my Estradiol dose because I have not noticed many changes lately, but my labs show that my body is responding well...
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