Peristomal ulcers

I would love to know what has worked for those of you who have dealt with peristomal ulcers.

I currently have a handful of ulcers that I just can't get rid of despite trying everything that has worked in the past. I can usually clear them up by putting a piece of tape (sticky side against sticky side of pouch) on the back of the pouch where the ulcer would be touching but it isn't working this time and is causing me to have leaks. =(
H E L P!!

Yes, they are excruciatingly painful and will usually cause blood to come through the opening of the pouch.
I've been getting these since 2000 and even had to have my stoma moved to my left side because the skin around my stoma was so scarred up from the deep ulcers.
If I could figure out how to post a picture here then I could show you exactly what they look like.

At one point, I had seen every WOCN within a 100 mile radius and had even gone to the Wound clinic at Duke Hospital where they ended up having to cauterize a couple of the ulcers.
I'm allergic to latex so some products are out of the question for me to even try.
I've been informed, a couple of times, that they can't move my stoma again because there would be no place to put it and they can't build me an internal bladder (j pouch) because of the Interstitial Cystitis (IC). My next option, they say, would be to bring both ureters up to the surface of my skin, suture in place and then I would have to cath myself throughout the day to empty my kidneys. Problem with that is that your kidneys do not last long and I would be on dialysis fairly quickly. So, I need to figure out how/what to do to get this current location to last as long as possible.

No one knows for sure what is causing them. Some have suggested that since IC is an auto-immune disease (much like Lupus) that could be why I keep getting them.
However, I have a different theory. . .because the bud on my stoma is flush with my abdomen AND the opening is now in the upper corner of the stoma, it causes urine to go behind the pouch and just sit on the skin.
This greatly irritates my skin so when I remove the pouch I have a bloody hole starting. Also, I'm getting a lot of areas that are looking like the top layer of skin has been burned off.
I take a picture at each pouch change so that I can keep up with the improvements and any new ulcers.

:::sigh::: it really shouldn't be this difficult!

Also, pulling the pouch off is so much nicer and less painful with that method. I was also advised to change my pouch every other days long as the Aquacel was getting soakedwith blood/pus. Then decrease the changings.

Aloha Sunee,
When I was discharged from the hospital, I had 1/2 & 3/4 inch blisters under and around the adhesive. After 3 weeks of this my doc suggested taking 500 mg of C/day. Several weeks later, the blisters had reduced to pin head size.
I had also tried several different appliance manufactures, but no luck. It appeared to be a skin problem.
Don't know if it will help, and it would not hurt to try.
Keep bugging the Doc's & nurses till you get some relief,
Joe