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Re: Endometrisos

From: 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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