Laura from Sally

From: Sally Grigg (lostcst@mcn.org)
Sat Aug 10 16:23:04 2002


Welcome Laura, we are glad you found us. Please go to the home page for adhesions in the U.S. http://www.adhesions.org Then start reading some of other people's stories on the quilt. Then go back through the emails and read those from Helen Dynda, she has researched and explored the web to help us understand our bodies and our maladies.

You are not alone in being illtreated by the medical profession. For 33 years I was told it was all in my head, after my hysterectomy when they found an abdomen filled with dried pus from an infection, adhesions, and a little endometriosis, they still told me it was all in my head. I went to doctors with a letter from a pyschiatrist saying my head was normal and I was very well adjusted, but I had extreme pain in my abdomen probably from adhesions, the doctors said "well, if you have to walk around with a letter saying you are normal, then you must be really abnormal" and suggested counseling. Well, I don't mind counseling, I love to talk, but that doesn't help the pain.

You need to research and know that you are right and they are wrong. Don't give up. You have found a family here of fellow adhesions sufferers and we stick together. So hang on and start reading. I wish you well. Blessings and prayers to you, Love, Sally Grigg

>----- Original Message -----
From: "Laura" <sweetiepie42055423@yahoo.com> To: "Multiple recipients of list ADHESIONS" <adhesions@mail.medispecialty.com> Sent: Saturday, August 10, 2002 2:37 AM Subject: I am new here

> Hi my name is Laura, I am a 25 year old female,from Minnesota,I have
> been suffering from chronic lower abdomen pain off and on for several
> year's. It started getting much worse in April,when I started having
> severe constipation also. I went to a GI doc,and had 3
> colonoscopy's,which showed I had a bad case of colitis. They are also
> unsure if I have IBD or IBS. I have a lot of pain,which has landed me
> in the ER more time's then I can count. They are absolutely sick of me
> there. I was hospitalized,where they did a battery of test's,and can't
> seem to find what is causing this pain. I have a pelvic ultrasound
> coming up,and then we are going to do a Laprascopy. None of my doc's
> will treat my pain. I am on Ultram,but it make's me itch,and is not
> recomended for Epileptic's,which I am. They all seem to think this is
> in my head,or I am trying to milk them for drug's. I am truly
> frustrated. No one seem's to want to help me. I had to quit my
> job,because I never seem to feel good anymore,and I missed so much time
> for being sick. If they find nothing during the Laprascopy,then it has
> been suggested I go to a pain clinic. I just wonder what I can expect
> there? Does anyone have any suggestion's for me or know of any good
> doc's in the Twin Cities that could help me? I am scared,and frustrated.
> Thanks for listening to me vent. Laura.
>


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