|
|
|
|
Register
to post messages
|
|
|
|
|
|
|
|
|
Register
to post messages
|
|
|
|
|
|
Go
|
New
|
Find
|
Notify
|
Tools
|
Reply
|
|
| Oregonians?
| Login/Join |
Anyone from Oregon? Portland? Never met in person anyone with GS or FAP... just curious...
  Diagnosed FAP/Gardner's Syndrome and Desmoids 4/1992 Colectomy 6/1992 ileoanal anastomosis 10/1992 17 surgeries for desmoids and infections in 17 years |
|||
|
 |
Not Orgeon, but we drive up through Portland now and again. We live in Northern California and have family in Portland, Lake Oswega areas... plus, we just plain like Oregon (and Washington). Hubby (38) and son (15) have FAP.
|
|||
|
 |
Tigard,OR here ... J-Pouch for close to two years now.
Mark. Diagnosed with ulcerative colitis 1995 Step 1: May 25,2006 - ileostomy Step 2: Nov 13,2007- J-pouch / temp ileo Step 3: Feb 28,2008 - Take down |
|||
|
 |
I live in Redmond but had my first surgery in Bellevue, Washington. I had some subsequent surgeries in Portland Providence with Dr. Breen. We get to Portland frequently as we do have relatives there.
Jim |
|||
|
I am from Lebanon OR. Was misdiagnosed 20 years ago and two years ago finally got so ill that I was admitted to the hospital. Tried 2 years of meds and this last September had surgery with my takedown being in Dec.'09.
|
||||
|
 |
I live in Spanaway, WA, just south of Tacoma. I have FAP, too. Haven't met anybody else with FAP either, other than family.
Wondering if anybody here knows the Ails family from Yakima, WA? That's my mother's family. Lost touch with them years ago. The FAP comes through them. Diagnosed FAP 6/1981 Colectomy 8/1981 Takedown 11/1981 |
|||
|
| Powered by Social Strata |
|
