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No Information on Endometriosis From: aileen (anonymous@obgyn.net) Thu Oct 14 23:12:53 2004 Messages sorted by: [ date ][ thread ][ subject ][ author ] Next message: anonymous: "Censorship" Previous message: Nise: "Re: lupron side effects--Ann" One more question...I wish I knew why I did not know what Endometriosis was before I was diagnosed? This DISEASE (THE ONE WITH NO CURE, CRONIC 24X7 PAIN, AND WHICH MAKES YOU FEEL INEPT, TIRED, FRUSTARTED and F-----d? I know I'm not the only one that had not heard of this disease. Most of my friends and family didn't even know this existed, and they didn't know it was a DISEASE that has no cure. They were also were unaware of the pain we feel 24X7. It seems there are a lot of women that suffer from this disease, but they are either mis-diagnosed or are told it's a "women thing". Is there any movement to change this? Next message: anonymous: "Censorship" Previous message: Nise: "Re: lupron side effects--Ann"

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