Going to read up as much as I can, and of course ask my ReproEndoGuy (TM) as much as I can. I wonder about what percentage of PCOS "cysters" end up with this.
In the meantime, at least I have a good starting point for info and support. A person following me on Twitter provided this link. It is useful enough for me to ask about artery embolization.
http://www.adenomyosisadviceassociation.org
And on a related note: Not only was my sister diagnosed w/PCOS years before me and never mentioned it (so that I might, yanno, get tested and TREATED for it), she also allegedly has something "endometrial" going on, and again, no mention of it. I get diagnosed, I tell everyone to raise awareness. Keeping shit to yourself when it might help others is nothing more than a tacit fuck you, you're on your own.
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