Quote from: girl you look fierce on March 12, 2013, 09:47:24 AM
Umm, afaik clotting risks are just related to E levels. So a low dose would not put you at any more risk than a cis girl... and would still give you changes long-term.
It's also related to how the E is initially metabolized, such as orally or straight into the bloodstream. Orally, ALL of it passes through the liver, where it is converted into Estrone (the form of estrogen that is BAD bad bad). Going straight into the bloodstream (transdermal patches, subdermal implants, or injections) only a bit of it passes through the liver once it is already in circulation, reducing the conversion to estrone to a negligible level.
What you need in order to feminize is Estradiol. When the liver converts Estradiol to Estrone, feminization is not nearly as effective- and it comes with the heavy price of unhealthy side effects- the same as birth control pills.
While describing this to me, my endocrinologist was literally getting red in the face with anger because so many Dr's use oral methods to administer E. As far as he is concerned, oral E is just bad for the body because of the Estrone coversion. On the other hand, when administered straight into the blood, Estradiol prevails and is extremely good for you AND the feminization process. You need much less of it in order to be effective. Besides increasing the risk of breast cancer, it reduces blood pressure, makes the heart healthier, greatly reduces risk of prostate disease, promotes life longevity, and there were more reasons but I forget all of them.
I have my next implant scheduled for April 1st, I will try to ask him if he has any good literature on the differences in the biological effects of oral vs trans/subdermal. The article I posted earlier I found myself and describes it vaguely, but I am definitely interested to know the details.