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Indeterminate colitis (IC) originally referred to those 10–15% of cases of inflammatory bowel disease (IBD) in which there was difficulty distinguishing between ulcerative colitis (UC) and Crohn's disease (CD) in the colectomy specimen.

(CD) Crohn’s Disease is a condition that causes inflammation of the digestive system or gut. Crohn’s can affect any part of the gut, though the most common area affected is the end of the ileum (the last part of the small intestine), or the colon.

(UC) Ulcerative Colitis is a condition that causes inflammation and ulceration of the inner lining of the rectum and colon (the large bowel). In UC, ulcers develop on the surface of the lining and these may bleed and produce mucus.

In simple terms, the small bowel (intestine) is rerouted across the abdomen internally and the end, the ileum, is put through a hole made in the abdominal wall and secured to the outside, the ileum is turned back on itself to form the stoma and stitched to the edge of the hole to hold it in place. This leaves an opening from the small bowel into to outside world where waste can then be collected and managed in a stoma bag. I have a full breakdown of this on my blog site.

hen the colon and rectum are removed (due to ulcerative colitis or familial adenomatous polyposis), another reservoir must be created for bowel contents (stool) to exit the body. Surgically creating a “J” shaped reservoir (called a J-pouch) is an option for selected patients to store and pass stool. A J pouch is created out of an individual’s own small bowel. Also see my blog: What is a JPouch for more information.

Cuffitis is inflammation at the anal transition zone or “cuff” created as a result of a JPouch (ileal pouch-anal anastomosis (IPAA)). It is similar to ulcerative colitis but occurs in the rectal cuff. Cuffitis is a common complication of IPAA, particularly when the lining of the cuff (the mucosa) has been left which in my expereince, most are, to give control of the output from the JPouch.

Pouchitis is inflammation of the Pouch (see other posts re What is a JPouch?)) that can happen when the pouch becomes irritated and inflamed. The inflammation can make you have to go to the bathroom more often, abdominal cramping or bloating, lower abdominal pain, or sometimes blood in the stool. This is a treatable condition and needs medical advice.

Infliximab belongs to a group of medicines called ‘biological drugs.’ It is also referred to as an ‘anti-TNF drug’ because it works by targeting a protein in the body called TNF-alpha. Your body naturally produces TNF-alpha as part of its immune response to help fight infections by temporarily causing inflammation in affected areas. Over-production of this protein is thought to be partly responsible for the type of chronic (ongoing) inflammation found in IBD. Infliximab binds to TNF-alpha, helping to prevent inflammation and relieve symptoms.

The gallbladder manages bile salts in the body and are needed to digest food amongst other things. However, the colon reabsorbs this to help maintain levels. If you don’t have any colon left, levels can often cause, or exaggerate, gas, urgency, watery output, urgency, explosive accidents. If it is a problem medication can help. I have also been researching this and found that long term antibiotics can also cause bile sat malabsorbtion (BAM). It can be treated by taking mediactions, normally Colestyramine in sachet form or Colesevelam Tablets.

Humira is a biologic drug. Scientists normally make biologics using protein antibodies from a living organism, such as humans, animals, microorganisms or yeast. They produce the proteins using DNA technology. It is a kind of genetic engineering. People normally take Humira at home, using a syringe or a pen device that already contains the medication. They cannot take it by mouth, because the human digestive system would destroy the active ingredient.

Sadly, that one was not answered with exact data which is what we all want to know! However, my specialist nurses advise me it’s a very small percentage. There are so many factors that affect each individual outcome.

I agreed I would give it a year, however I am now exactly 1-year post surgery and although struggling still, I am still fighting as the good days are amazing, the bad days are all due to my acidic output and Cuffitis. I am now under a top consultant, Professor Hart at St Marks Hospital (London specialist bowel hospital) and undergoing various investigations including Bile Salt Malabsorption to try to sort me out at last! Aug 2018

My surgeon warned me that if you have 3 stage surgery (Iloestomy, Jpouch creation then takedown) some patients have some output from the rectum, mucus or very rarely some stool but that’s not likely. However, from experience, even with a temporary stoma, you still experience some output of mucus this is because the rectum produces it and until that is removed when a JPouch is made (or its removed if permanent Ileostomy) the mucosa will still be present. I had a weird pressure and feeling of needing a poop about 3 months after my temporary ileostomy, this totally freaked me out as no one warned me! It happened every week or so until my JPouch was completed. It didn’t hurt at all and after getting over the anger of now having to manage my bag and still poop passed, It didn’t cause and trouble. I was very lucky and had my JPouch created and connected all in one surgery so for me it made no difference.

You can have internal hemorrhoids in the anal canal. Painful (and painless) lumps are frequently hemorrhoids. painful lumps can also be other things, like abscesses and fistulae. I have not suffered but do struggle with a skin tag from previous problems. As far as butt burn… well when it hits you will know about it! I had it about 3 months after my JPouch surgery, once my diet was re-established, and WOW did I know it! I swapped from using any form of wipes and used Epsom Salt baths and washed after each BM, Metanium baby nappy cream became my best friend. On the occasion it really hit, I was struggling with output and was going about 20/25 times a day, it was that acidic watery output that killed me, my bottom was red raw, burning and bought tears to my eyes. I switched to a plain white food diet of rice, chicken, bread and pasta and after a few days using Metanium and regular Imodium, it passed. Each time I have had an attack since it has been milder and now I can manage. I installed a bidet and use a barrier cream if I feel it’s getting irritated.

No, there is no reason you should suffer Pouchitis, it can happen to anyone and there is no higher risk as the infected rectum will be removed when the JPouch is created. Only a very small area of cuff is left to maintain control (between 1-5cm typically). I have 1.5cm of Cuff left and unfortunately, I am suffering chronic Cuffitis. I always suspected as would as I had historically suffered extreme Proctitis*, however, the surgeon did not feel I was at any higher risk than others without Proctitis. *(Proctitis is an inflammation of the lining of the rectum. The rectum is a muscular tube that's connected to the end of your colon.)

I was given a patient-controlled Oxycodone drip must the same way as the morphine was given, but I was also given a dose of antihistamine to back me up against an immediate reaction. I was fine on this and remained on this whilst I was in hospital, shortly before I went home was moved to Oxynorm and Oxycontin tablets which I used for the first 6 weeks and then slowly withdrew them. I was also given Gabapentin for spasms and pain relief, I was on this for 4 months as I had nerve pain around the site where my Ileostomy was removed. This managed it very well. These were both backed up with Paracetamol and Codine Phosphate as needed. I occasionally use Codine Phosphate now to help with output consistency if I feel the loperamide is not being as effective when I am suffering Cuffitis and more recently, Pouchitis.

In short yes! Initially I found with the JPouch, I felt the need to run to the loo, this lasted literally a few days, then I would get pressure and take myself off to the loo without too much panic. After about a month I gained confidence and as the area healed from surgery, I started training my new Pouch to hold, when I had the urge (which literally felt like a bit of pressure in my anus) I would wait 5, then 10, then 15 mins and it has now, a year on, progressed to at least an hour when I am healthy (with Cuffitis I can still hold it but in extreme flare ups I have had 2 accidents where I didn’t make it in time, that’s the only accidents I have had). Taking into account I had my JPouch created and connected in one single operation, and via my anus, it meant I was pooping through where I was healing, although this may have made it more tender, it didn’t effect the control. I feel I have more control now than ever before, even if my output is liquid, which it often can be. I have had no leakages or accidents when well. Obviously, this isn’t always the case and others may not be as lucky, this is just my experience.

I followed the advice I was given which was, to have a *low residue diet for approx 4 weeks, then start reintroducing foods slowly, see how I react to each before progressing to the next. I think it was about 8 wks before I was back on a varied diet, however, I didn’t reintroduce vegetables, salad, nuts etc for at least 12 weeks. Alcohol and any juice were at about 15 weeks but that was more due to the fact I was on medication that would react until then. It was at approx. 14 weeks my specialist nurse suggested I try Imodium to thicken up and slow down my output, I started on 1-2 once or twice a day and have progressed now to 3 half an hour before each meal and 3 at night, this is because I am now on a full varied diet without avoiding any foods or drinks except Cheese (as it causes me to have extreme bloating, cramps and discomfort), and my output remains typically liquid and acidic. *The low residue diet I used consisted mainly of white foods such as; chicken, white bread, white rice and pasta, egg, dairy and potatoes. I drank mainly herbal teas and water.

Little did I know that the stitching was actually where they had secured my remaining rectum when they carried out the temporary Ileostomy and colon removal, this made sure it maintained blood supply so the JPouch could be connected at a later stage to my anus, and the rectum would then be removed, thus freeing up the stitching.

My consultant at the time did not feel this was related, I still suffer both now and believe I get water warts and ulcers when I am run down, but anyone can suffer either or both of these without bowel disease.

I was told this would be located where the current stoma sat and would not protrude far from the skin, this can cause the stoma to be prone to leakages and may patients need convex bags to manage but its not normally an issue. I never had a loop ileostomy as my surgery was done in a single step, from temporary Ileostomy to functioning JPouch.

When I had my temporary Ileostomy, my recovery lasted approx. 4 months, this was because I was extremely ill at the time it was performed. My JPouch surgery that created the pouch and connected it removing all stomas, took 31/2 months to recover and return to work, I have had periods of trouble since caused by cuffitis but have managed to remain working with time off for a few days when needed.

From very early stages of having my Ileostomy created I started doing pelvic floor exercises, similar to those before child birth (Kelgel exercises**), to strengthen the muscles. I kept these up and as soon as I could after my JPouch surgery I started doing them again, just tensing my pelvic muscles, holding them and relaxing, I have found this has helped hugely with all the above concern as well as the control I have now over my bowel and bladder. Intimacy is a very personal choice, I found I could resume intercourse after about 5 weeks of surgery, however it was not an easy task, especially emotionally as my body had changed yet again and I was petrified about accidents, leakage etc. I discussed all of this with my partner whom was completely understanding and probably as worried about hurting me as I was worried about my issues. I am pleased to say all was fine, nothing bad happened and we both adjusted slowly and learnt to feel totally comfortable with each other again with the new ‘improved’ me. (**Kegel exercise, also known as pelvic floor exercise, consists of repeatedly contracting and relaxing the muscles that form part of the pelvic floor, now sometimes colloquially referred to as the "Kegel muscles". Wikipedia)

It took me 14 weeks to return to work after my JPouch surgery, on a phased return basis, I started swimming once the wound from my stoma site had healed at approx 5 weeks. I started walking and doing very light exercise and built it up slowly being careful not to cause any hernia or injuries after about 6 weeks, but I did take a several months for me to feel any energy or strength again, it was a hard time as I was in fact a Zumba Fitness Instructor before all this surgery started 2 years prior!

Sadly, the hospital I was dealing with at this time offered no support network and it was suggested my GP refer me. I didn’t feel this would be beneficial as people outside the world of IBD often don’t understand what it is or what’s involved etc. I helped myself by talking to friends and loved ones as well as taking the next step into my own hands! One of the nurses at the first hospital I was operated on suggested to me that I had the option to choose who and where I go for my next step. I had such a terrible time in the hospital I was at and that was causing much of the stress and anxiety. I researched and found St Marks Foundation, A Bowel specialist hospital in Harrow, Middlesex, UK. They have top surgeons and dealt with my problems on a daily basis. I was lucky enough to persuade my GP to refer me and after waiting 13 months at Brighton Hospital for a referral, I was seen, consulted and operated on within 3 months of being sent to St Marks! It was the best move I ever made, despite the 2 hours travel, I continue to be managed by them and would not want to go anywhere else! The removal of the first hospital from the equation gave me the strength to deal with my trauma and stress and heal!

NO! In the UK you have the freedom of choice when it comes to where and whom you are treated by in hospital.

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