Problems months after colon resection surgery: What Helps?

<p>Transanal flush post sigmoid colectomy for FREQUENT bm</p><p>I had 20 inches bowel resection sigmoid colectomy 10 months ago to remove a build up tissue blockage caused by repeated divirticulitis attacks. I currently have 9+ bm's a day- soft, not diarhea, just pencil like stool in the bowl. I wear a pad for leakage because if I dont use the bathroom about every 1.5-2 hours, I soil the pad. This is so frustrating to me because I am very active and athletic, and this has changed my life. The surgeon never mentioned this side effect. If I carry anything heavy or stress my body, I often have an accident. I rarely feel when I have soiled the pad, but if I feel the sensation to defecate, I usually only have 1-2 minutes to find a bathroom, or there is a disaster. I currently only eat 1 meal a day, but that doesnt seem to change anything, and have had gluten and lactose issues for a long time, so I am careful. Someone mentioned a transanal flush. Has anyone with my similar issue ever used this, and is it helpful?. I am a very fit 66 year old and cannot imagine tbe rest of my life being tethered to nearby bathroom facilities everywhere I go.</p>

I'm 44 years old . had an colon resection done about 2 months ago.. Everything was doing GRT.. Normal bv. Pain from surgery gone.. Woke up this morning with a sharp pain.. Almost like the first time.. Before they told me I had diverticulitis.. And removed the bad section.. Pain little lower than the first time.. But same.. No where near any of the surgery spots.. Should I get chk..

Hi I had sigmoid colectomy 2 months ago now I feel pain and pressure in rectum along with mucus discharge,wondering if anyoone has experienced this?

I had colon resection..laparoscopic AND open due to adhesions on Jan 4. I thought I was healing great. But now it has been 8 weeks and I have hot pains all across lower abdomen and stabbing pain where surgery was. I just had a THIRD cat scan and they say EVERYTHING looks fine...but I HURT and I BURN. I am SO frustrated!

It's been almost 3 years since my chemo treatments and I still have tingling in my hands and fingers. My Dr. told me the chemo would have this effect but it should subside with time but may never completely go away. It has subsided quite a bit, no more shocking feeling when I touch ice but they still feel somewhat numb at times. I also have Diabetes so I started out with peripheral neuropathy in my feet and it has gotten worse since the chemo too. At least my cancer is gone and I'll live a longer life because I decided to get it taken care of.

I’ve been having trouble with my big toe nails on both feet coming off read an article that was called chemo toe that said it was a result of the chemo treatments. Does anyone know anything about this

I'm also 3 months post op. I'm always having some kind of pain. I just had my 2nd CAT scan since the surgery. Everything looks fine, all my labs are fine. I'm still severely constipated. I know I needed this surgery, but I still can't help regretting it.