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Re: EndometreosisFrom: Amy (anonymous@obgyn.net)Fri Apr 1 07:15:10 2005
Dawn, I have done the Lupron injections and for me, it helps a lot but the endo always comes back. I am lucky that I do well on Lupron and it usually provides me about a year of no pain and other endo symptoms. I can definitely relate to the painful intercourse. Has always been a problem for me but I am lucky that my husband understands and supports me. But that sure can play a lot of mental games with your head! It isn't that I don't want to have sex, but that my body doesn't cooperate. Sometimes depresses me and makes me feel like I am not a good wife. I have had three laps, two courses of Lupron, and I don't know how many different kinds of bc I have tried. Now take them continually which helps some, but doesn't keep the endo at bay. I almost had a hysto last summer and then decided to go for another lap and Lupron to buy time. I am 33 but have never wanted children (I have fur babies!) so fertility wasn't the issue. Just wasn't sure if I was ready for complete menopause. I have talked it over with my Doc, even went to a counselor for several sessions, and have decided I will have everything removed when the endo returns and gets really bad again. Two women I work with just had hysterectomies because of endo. So far, both of them say the endo pain, etc. is gone but they are having hormone issues. My Doc told me I can keep "band-aiding" things or remove my organs and hope it helps. I am at peace with the fact that I will one day have a hysto. If you ever want to talk more, feel free to email me privately. I can definitely relate and understand. Hope it helps to know you are not alone. Hang in there! Hugs to you! Amy Meyer
At Thu, 31 Mar 2005, Dawn wrote:
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