Hello all,

Quick update on where I am.

Gluten free diet seemed to work at first, but after a few months the PN was still there. Went back on gluten for a test and the symptoms didn't change.

One of the remaining big differences between my 'worst' symptoms and now (manageable, but very much still there) is my mood/attitude. Stressing about PN makes the symptoms infinitely worse (or does for me anyway).

The health service has spent 6 months doing various tests to tell me that a) It's not diabetes, and b) It's not my back (seemingly, they ignored me when I told them I had PN in my hands too).

Now I have a referal to a neurologist, which is a step in the right direction.

I've tried so many suppliments over the past 6 months it's unreal. However, my experience is that, outside of stress management, little touches my condition of burning pains in my hands and feet.

I'm just sort of getting on with things in the meantime. What else can you do?

Kev