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Re: lupron useFrom: Ana (anonymous@obgyn.net)Thu Apr 11 02:40:36 2002
Cheri, I was wondering what exactly the website said was the problem with lupron. Lupron is basically the only thing that ever helped me. Granted it sucked. I remember my first office visit after the first lupron injection my dr looked at me and said how is it going? gotten any hot flashes? he said i looked like i was about to jump across his desk and punch him. I was having horrendous hot flashes, but it was much better than the constant pelvic pain, back pain, vomiting, etc. Not just that but I enjoyed not getting my period. HAHA! I am sorry you are having such a hard time. I will be thinking about you. *hugs* ~ANA
>----- Original Message ----- hi ladies, wishing everyone is having as many pain free days as possible.. i hope someone could comment on my dilema.. i am about to start taking lupron (as ordered by my doctor) I JUST HAD MY 8TH LAPOROSCOPY..and was told that they could only see adhesions wich they burnt away, and informed me that my endometriosis was underlying and could not be seen nor burnt away (are only hope of getting pregnant is IVF) so he tells me to take lupron as it will deminish the pain and that for ivf there is a three month time on lupron..so my doctor tells me (i was just diagnosed with skin cancer) that while i am getting my face hacked up, to go on the lupron and then when the cancer and treatment are well on thier way i will also be on my way to ivf..well the stress and pain was enough to deal with from the cancer so i left the lupron shot till i was feeling better, wich would be now. so i was going to call my local clinic for an appointment to get my shot administered by the doctor...so i crawl out of bed and think i will get a little info on the lupron as i have started my period and was not shure when to take the shot ..and in my search i found a site called lupron victims, anyway with all kinds of scary stuff..in bold letters it said that if your doctor is prescibing it you chould find another doctor who cares... i am feeling soooo confused and frustrated, this disease may not be killing me physically, but i am so frusturated and during these times i would love to have it all out. it is bad enough that endo ate at my two tubes so i am infertile..and the next most important thing, i cry almost every time we make love.this is not healthy i am not happy and feeling so scared and alone about the decissions i have to make..i know there is alot of crap on the internet, but there is also some great stuff (this site for one) the feeling of disparity form a desease they say doesn't kill you..a labodomy doesn't kill you either.. i am pobably too emotional and babbing alot.. thanks to anyone whose listening, i already feel a bit better.. hoping everyone finds what they need to get better :-) cheri
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