UPDATED: March 21, 2016 - also World EndoMarch 2016 day 5/23/14 I just stumbled across this article/post about the nightmare of Lupron, on Pinterest. I'm sharing it here because it is well written, factual, and it's a small sample of the insanity that has surrounded people with Endometriosis for decades. And because I'm so glad I didn't take Lupron or any of the other useless but dangerous drugs that were being promoted for endometriosis back when I was first diagnosed. (I have the Endometriosis Association , founded in 1980 by Mary Lou Ballweg, to thank for providing me with the knowledge and courage to buck the medical system from the beginning of my diagnoses.) The nightmare is that doctors are STILL prescribing Lupron for Endo. Hidden Clinical Trial Data About Lupron
