Well. after a year’s wait to get my Estradiol meds increased, my new patches came in approximately five days through the mail. There are several different methods of taking the meds.
You can take them by swallowing pills, taking shots or by applying stick on patches. My endocrinologist prefers the patch method due to possible blood clot issues. I know from talking to other transgender women, the other methods are preferred too. For many different reasons. Plus, I have to take the good and the bad in the Veterans Administration medical system. Obviously, the good is that it is free. The bad is that normally you are restricted in what the VA provides as far as hormone replacement therapy goes. An example is progesterone.
Progesterone as an additional hormone has never been mentioned to me. In the past, I have had some trans friends who took progesterone. One developed the annoying habit of lactating under her shirt while she was still dressing like a guy at work.
Believe me, I am not complaining. I understand my endocrinologist has always erred on the side of caution with me. I know, as well as she does, the threat of possible blood clots is always possible.
In fact, I had to go through several vascular and heart tests to even get approved for this increase.
I start the new patches on Tuesday and I am interested to see how it affects me. After all it’s a 25% increase.
We will see if it’s enough to induce hot flashes again.