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Re: EndometrisosFrom: Reshenda (anonymous@obgyn.net)Mon Dec 31 00:55:58 2007
At Fri, 5 Dec 2003, Rhonda wrote: > >Hi I'm Rhonda and I have Endometrisos and I'm only 22 years old. I was >diagnosed with it in the year 2000 and sence then I have had 2 surgerys, >nothing has changed. My first surgery consisted of a cyst that grew >from 17mm to the size of a grapefruit with in 3 days. It incased my >left ovary and caused tremendous pain in my abdominal area. The surgery >lasted 3 hours and recovery was 3 months long. It was the most horrific >pain ever, I couldn't even get out of bed. Coughing, snezzing, and >laughing was a mission, I had to put a pillow on my stomach and lean >down for my stomach not to hurt. Sleeping was another painful thing I >had to do, roll up into a ball and have my best friend hold my knees to >my chest for the pain to be tolerable. >6 months after my 1st surgery I was in the hospital for another one. >Laposcopy surgery lasted 1 day but recovery was long and hard. Sence >then I have been on real harsh pain pills like, Oxycodone, Perasets, >vioxx, etc... >I'm presently on YASMEN for Birthcontrol and Naproxen for pain but still >nothing is helping. My doctor wants me to consider the Lupron shot, I >go see him today @1:00pm. I don't like the side effects and the stories >I read about of the internet. Some one please help me.
-- Hi, My name is Reshenda and I've had Endometrisos since 2004,and i'm 23 year old. I had the laposcopy examine and they lasered the endometrisos off but the pain returned a year later and worst than ever. Just recently I went to the ER I was in so much pain for about and hour I couldn't even get out of the bed and when I did arrive at the hosptial they just treated me with pain meds after they finally got around to me . It's like the doctors are clueless about what is going on I need help I personally think that the endometrisos has spread to my bowel area from the amount of pain I have in that area. I can't go thru life like this I need help.
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