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I am surprised a numbing cream will not work. At least that is what I was told. I asked my Dr.. Surgeon for some lidocaine cream it was so bad this week I was not getting more than three hours of sleep a night. I finally collapsed Thursday nite and got some sleep but it's not a way to get it.
Can anyone answer why a numbing cream is not out there for us?
Richard.
I can't understand why the Canasa does not stop the burn. I was told that I had cuffitis by my surgeon, and I thought that might be the reason for the irritation but quite frankly, I see no improvement while using them, and they cost a fortune.
I do appreciate all of your responses. There has to be something that we can all use, the question is WHAT?
The theory behind this is that the pouchitis could come from bacterial overgrowth (which is why antibiotics "work"), which itself comes from stool statis in the pouch, which itself comes from incomplete emptying of the pouch.
See my posts in the topic "Irrigation tube .. Anyone ?" by Fosty for articles/details about how to use a catheter with your pouch.
Good luck, keep us posted !
A
It helped me way more than the canasa ever did. It's definitely worth a try, and was exactly what I needed to get over my reoccurring cuffitis.
Hope this helps!
C-jay
I'm from Canada, but I can tell you that one month of canasa (Salofalk, here in Canada) for 30 suppositories cost me $65.29. A one month supply of the proctofoam cost me $45. But that was for one dose per day. Two doses a day would cost $90 a month.
I always responded well to prednisone when I had colitis, so I wasn't that surprised at how well this medication ended up working for me.
I was on Salofalk on and off for almost 8 months, but one month on proctofoam and I am back to normal. I have been off it now for more than 3 months. Everybody reacts differently to the different meds available to us, and this is what worked (finally!) for me.
C-jay
Richard.
It's a shock when you first use it.. a cold sensation (hard to describe). Some people refuse to keep trying it and give it a chance. My husband brought me everything under the sun during my first three months of J-Pouch life. And THEN I found Calmoseptine (I think I learned about it on this site). Thank you!!!
A bath w Epsom salts provides some relief too.
I don't like when this happens to me (I'm 14 yrs post takedown, too) and all the creams make it so my rectal skin cant properly heal w air (or so I surmise, I don't usually look!), and I need a cream (I rotate w calmiseptine, aquaphor, and a few others) for relief. The Epsom salt bath is great - old fashioned but it is real nice!
So... I can't give any "for sure" answers. However, I believe that taking an acid reducer has helped me immensely with butt burn issues. I take Prilosec daily. And probably 90% of the time, I have no issues with the burn. If I get a touch of pouchitis I may still have burn, and antibiotics do help. But whether you take a 12-hour acid reducer or a PPI, it should help with the burn.
Questran is a powder that you mix with water and drink. It binds the acid in your stool so no more burn. It is kind of a pain to take as it also binds your meds, so it needs to be timed just right. When things get really bad for me, I take it. It gives things time to heal as the stool no longer burns. Good luck.
Use Dibucaine it is the stuff dreams are made of. Let me know how it helps. I could kiss the maker!!
PEOPLE BIDET!!!! Best money you will ever spend. Search online mount to any toliet and cost between 300-500
Last year after experiencing many more close calls and burning episodes then in the previous two decades with the J-pouch, I decided to go with my gut and do an illumination of items and low an behold once I eliminated drinking wine & certain fatty foods I had an amazing improvement, also downsizing intake during the summer months when I usually over due the menu with all the extra fruits & vegetables coming from the garden.
I also take a tablespoon of Metamucil & tablet of Imodium in both AM & PM, I take a Florastor (probiotic) after dinner and now I rarely experience those previous challenging times of burning bottoms. But, I will say with the holidays around the corner I know those extra fats found in gravy's, pumpkin pies, cheese cakes, apple cider, eggnog... will be again a huge challenge, and the burning bottom effects will definitely be present afterwards if I choose to again enjoy these favorites. I'm thinking pick your battles.
As far as lotion to the bottom redness & soreness, I'm pretty old school with what my surgeon advised A & D ointment (walgreen's my choice) and Desitin. Hope this helps.
To get around the burning...I use something called the Blue Bidet...you can purchase at Lowes online or Amazon...I fill with very warm water and use as a bidet would function and use toilet paper or wipes after area is cleaned with warm water. It has been a life saver.
My pouch is going on 8 years gold, and I get bad flare ups of butt burn at least once a month, which includes bleeding on the toilet paper at times. Unfortunately Canasa suppositories (called Salofalk in Canada) only seemed to cause me more irritation, so I had to stop using them. I use Calmoseptine and vaseline, and when it's really bad I've used hydrocortisone. It doesn't seem to be diet specific for me, though I believe it's related to hemorrhoids at least to some extent, and it also seems to flare up around my period which is probably another factor. I try to avoid excess wiping if I can and use the detachable shower head to rinse whenever possible. A bidet would be an option - it's something I may look into. Otherwise, I feel like I've tried pretty much everything. I have the same concerns about cancer, although my surgeon didn't seem exceptionally concerned. I am due for a scope next year since my last one was in 2014. I'm wondering if it might be a better idea for those of us with this problem to be scoped annually instead of every other year. I definitely plan to discuss that with my surgeon the next time I see him.
I have had my pouch since 2010. Seriously I had many issues, incontinence, butt burn the worst. I finally went to the doctor and he prescribed Questran it’s taste nasty but it binds to the bile acids and stops the burning. Believe it started working right away. Doctor told me that the Ileum ( the part of the small intestine that the pouch is made of) is where the bile acids are absorbed with j pouches that cane be a problem with absorption thereby causing the burn. I also use Critic aid, it’s the best. I tried them all believe me. Hope this all makes sense.
Do either of these help fissures?
Hi there! Just wanted to comment on some of the things that people have mentioned. I believe that the Proctofoam is now banned in the US. I was using it last year and then my insurance company informed me that the FDA no longer approves it. I have used the Questran and I do think it works. But what I really wanted to recommend is a bidet. I know it sounds crazy, but it is literally what has saved my life. If you do not have one....please Make the investment. I've had others that I've recommended it to thank me wholeheartedly. It will greatly decrease the irritation!!
Laurie
Any recommendation on the biget? Also, the possible tooth damage makes me unlikely to try questran.
We bought a Biobidet toilet seat online. Saved my life!! When we vacation, I'm miserable by the end without it.
Thank you!
Since my October input, another product I use for painful irritations Which included pouchitus is an OTC lotion called Tronolane. It 's works like Prep H but it takes care of the pain an discomfort immediately. And my go to (bottom burn) OTC standards are still Desitin, A&D , (system slow down)OTC Metamucil & Loperamide 2mg. Hope this helps!
I have a Coco bidet. I bought it through the company. It's the complete one, not the attachment style. It has temperature controls for the water, a heated seat if you want, and a dryer as well. We did have to have an electrician install an extra outlet for it.
Calmoseptine - the only answer to butt burn. I use it several times per day.