I'm 23 and I was diagnosed with adenomyosis, which is internal endometriosis (in which the endometriotic tissue grows within my uterine wall) I have been on Lupron since Nov 2007. I do not recommend this treatment to anyone unless they are in dire need. Though I am supposed to be on it for 6 months, I will not be continuing Lupron due to the negative side effects I have experienced. I've been experiencing extreme mood swings, from being enraged, on edge, anxious, emotional, or very depressed. I get intense head aches, very nauseas, swelling in my stomach at times as well as stomach pain, blurry vision, achy bones and joints, confusion, hard time concentrating, forgetfulness, insomnia, cramps and pressure...and the list goes on.
Please inform yourself and do lots of research before ever thinking of taking Lupron. I would never do this again, especially after realizing the harmful effects it has had on my body physically and mentally. I've learned to trust that the best people to listen to are those that have actually experienced this drug, rather than those that are trying to promote it. Everyone that I have talked to that has either taken Lupron or knows someone that has, have had the similar experiences to mine.
I'm disappointed about my experience with Lupron, and I would never recommend this treatment to anyone.