
Hello Pain Peeps...To my "old" chronic pain pals and some newbies that have joined the club nobody wants to enter!
WISH I were on a good roll, but unfortunately it feels more like I've rolled into a ditch. Someone please throw some dirt over me before the buzzards show up!

I've submitted surgical records to endometriosis surgeon in St. Louis, which was my last best hope. He seems to think that GI issues are due to adhesions from multiple surgeries...duh?
FFS, endometriosis causes uterine cells to mutate throughout the abdominal/peritoneal cavity. Those lesions BLEED monthly. The body makes every effort to heal those lesions, by forming scar tissue. The scar tissue contorts the pelvic/abdominal organs, literally "clumping them" together.
Think Super Glue poured into your gut, causing organs to become one large mass. It chokes bowels, bladder, rectal/vaginal canal.
Because my FSH level is 136, he discounts new disease (I have stage 4). He recommended I see a general surgeon locally for my bowel obstruction issues. I would never allow a "general surgeon" surgical access. I was not
eager to submit to laparoscopy with St. Louis specialist, but feared for my so-called life, if next bowel obstruction were total.
Devastation and darkness do not skim the surface of what I am feeling right now. I had such hopes that HE would help me, somehow. It brings up some memories of the years I tried to conceive, but couldn't. I begged OB/GYNs to help me, they wouldn't. I suffered more than any human deserved for YEARS before diagnosis of stage 4. The surgeries/treatments were as brutal as the disease. My bones have the density of a 90 year old because the chemo devoured them. I tell myself to quityerbitchin' and get on with it...I have for DECADES, actually.
Cosmic...Thank you for asking. Lord, yes, I've used enemas when the blockage was in the lower colon. I still do, when that's the case. The OTC bottles don't do the job for me. I have to use the hospital issue quart bag enemas, repeatedly while lying in the floor writhing in agony.
TMI (always with me) but this disease ain't pretty. Recent CTs with/without contrast/barium have shown that the current partial obstruction is above my left splenic flexure. The stool cannot make the transition from transverse colon due to a crimped effect (think crimped garden hose...water can't pass). It builds up in my left side, distending my intestines like a helium balloon.
Words cannot describe the pain. Enemas won't reach the blockage when it's that high up.
Linzess 290 isn't really working, as I still MUST take softeners and/or stimulants. What's the point? Plus, Linzess is CRAZY expensive!
Funny thing, though I'm not laughing, is that I'm not taking the Oxycodone. It's not the opioid that's causing the slow bowel. So...I continue to suffer with the pelvic/vaginal/rectal pain that is mind-bending, along with the bowel pain, oh and extensive spinal/bone/joint pain. I'm taking Toradol since hospitalization, which helps with internal inflammation. However, it's not a permanent solution.

I think it's time to brew a pot of Hemlock tea and take a nice, long nap.
My sincere gratitude to all of you for your care and concern.
Closeau, RTP, Anna, SKR, Steph, etal...I think of you often! My wish for all of us is for better or
forget it!