From: Susan Dahl <dahl_s@FORTLEWIS.EDU>

> To: vianet@i-2000.com

> Subject: I've go it too.

> Date: Thursday, May 08, 1997 8:00 PM

>

> Hello Kent and this amazing leiomyosarcoma support group,

>

> I continue to survivor a high-grade leiomyosarcoma found in 1991 in the

> fibroid walls of my now defunct-uterus (the cancer was discovered during

> an hysterectomy.)

>

> My doctor told me my prognosis was three years. That meant to me I had

> about 3 years to live. I walked out his door in a daze, smelling the

> just festering Spring greens, enjoying what I preceived to be the last

> years of my life. Six years later, and some difficult years at that, I

> am still alive.

>

> Unfortuantely, the cancer would returned almost three years to the day

> where it showed up as pain in my left hip bone. After chemotherapy and

> radiation treatments, (maybe a year, maybe only nine months, the time

> was too brief to remember, really) it appeared again in the lower lobes

> of my lungs: Hello Darkness my old friend. I left the doctor's office

> crying, defeated even though I'd spent the last years doing everything

> (Essiac, juicing, supplements, exercise, etc.) I could think of to keep

> those little beasties away.

>

> My husband and I then took a trip to France and Spain in late April

> early May. It was a a great trip. From the tranquill beaches of St.

> Jean du Luz I wrote my friends and relatives: "I'll probably be dead

> soon." I didn't expect to make it to my 47th birthday.

>

> Embarrassingly, I'm still here. Several friends who weren't even

> diagnosed with cancer in 1991 have since died from faster forms of the

> disease. Too many other friends and relative have died from accidents

> or illnesses.

>

> I tried chemo. again since September with no help, even attempitng us

> through the inovative Cancer TReatment Centers of American. I few

> months ago, the oncologist determined somthing was working. So, you can

> see I am still suffering from cancer, must use a crutches and pain pills

> to get by daily, but daily, through so many other good people's prayers

> and amazing discoveries like this "support group for leiomyosarcoma"

> patients I continue to work, tinker at my life's interests, and am quite

> happy.

>

> I would love to correspond with anyone with a similar type of uterus

> related cancer, or ANYONE, for that matter. I am looking into a gene

> P53 related genes just for leiomyosarcoma patients, but the information

> is at home. I am using my good friend S. Dahl's e-mail access, so will

> check back here soon for anybody interested in hearing more about this

> new gene. Or you can send e-mail to me directly to

> "SAUNDERS_R@FORTLEWIS.EDU" If this doesn't work please reply to address

> above. Or feel free to call (970) 247-7291 until May 15, 1997.

>

> Bless all of your struggles, and efforts to make this interesting site

> work. In my small town, no one has ever heard of this disease, much

> less know anyone with or have it.

Sincerely, Rebecca