← Return to Anyone here dealing with peripheral neuropathy?

Discussion

Anyone here dealing with peripheral neuropathy?

Neuropathy | Last Active: Dec 8 11:43am | Replies (3052)

Comment receiving replies
@pinkmk

The skin biopsy says dermamyositis. That's what the muscle biopsy today was looking for. My other symptoms; dermagraphia, other unexplained rashes, COPD (I've never smoked), hiatal hernia, iratable bowel, uncontrollable acid reflux without disease, intestinal inflammation; are textbook.
Keep in mind I'm not a meat eater, I limit my vegetable intake to the ones my wholistic practitioner said were acceptable for me, I used digestive enzymes, vitamins, other supplements and no alcohol, no caffeine, no chemicals since I was 18...seriously. Because my migraines have been so bad since I was 8 and stomach pain has been so bad since I was 12 I had my first colonoscopy at 21.
You'd asked about MS before, I have increased hyper intense foci but they say it's due to migraines not MS. I'm no doctor but I think the Mayo clinic, I've never been but I have faith they are the best, will discover that people with chronic migraines are because of this white matter.

Jump to this post


Replies to "The skin biopsy says dermamyositis. That's what the muscle biopsy today was looking for. My other..."

Well that, like a lot of those I see on these boards, is a new one on me. It looks like the treatments are basically the same as those for other autoimmune conditions and it does look like they might slow it down. I assume that they did an double stranded dan antibody and anti-sm to maybe rule out lupus. All I can say is good luck and keep the faith. Apparently there are periods of remission so hopefully you'll get some prolonged ones.