This board has been the best resource I've been able to find and it's nice to know that I'm not alone in what I thought at first was some bizarre condition. I posted in another category but wanted to get more specific thoughts on managing my neuropathy which just won't go away.

I'm a 35 year old male in great shape and have never really had to go to the doctor much in my life. I'm active and eat well. The only thing that's really bothered me in the past is milk which I chalked up to lactose intolerance. About a year ago (I still remember exactly where I was), I started to have tingling in my face after eating at an Indian restaurant. Come to think of it, I had experienced a more mild version of it, always after eating, every once in a while for the decade before--just in the face. This time the tingling moved to my arms, then to my legs and began to change in sensation. First it was pins and needles and then turned to burning from my shins down (and electrical pulses in the feet and shins). For several months it was mostly in my legs and feet. After about 10 months the tingling (sometimes light pins and needles) basically started to evenly distribute itself throughout my body. I had a myriad of tests from Lymne, to B12, to cancer, to diabetes, etc. I saw a neurologist who did EMGs and had me do MRIs of the brain and upper and lower back. Everything turned out normal, except a finding of antiglaidines which my neuro assumed was a gluten allergy--celiac neuropathy. I had an endoscopy and it turned out negative for celiac and my GI doctor doesn't have a clue that PN could even be caused by something GI related (I basically had to educate him). I started taking Neurontin which took the edge off of the tingling but didn't make it go away. However, it made me feel very foggy with pressure behind my eyes so I stopped. Now the PN is back as usual. When I exercise it goes away but after it returns. I find myself shaking my leg constantly because the motion either makes it go away or distracts my brain into not registering the sensation.

I'm taking supplements now since the GI doctor and my Neuro basically don't know what to do. The supplements are:

- Multivitamin
- Vitamin E
- B-1 complex
- Vitamin D
- Probiotic
- Fish oil (stopped but am going to restart)

I'm trying the gluten free thing and it was suggested on another thread that I continue it for 6 months (it's been 2). However no change yet.

No other systems that I can tell.

My question is if there is anything else you would all suggest that I do or take to help? The condition is not debilitating but drives me CRAZY and I'm trying not to assume it's something that may turn worse (although, the uncertainty is the worst part of it). It doesn't help when the neuro says things like we may never know.

Your thoughts are greatly appreciated to help me manage the PN.

--like some molecular-mimicry autoimmune process, and it may very well be related to gluten sensitivity. That isolated anti-gliadin finding is often found in those whose gluten problems present neurologically, rather than gastrically (that anti-transglutaminase level is more correlated with degree of villous atrophy in frank celiac), as Dr. Hadjivassiliou has researched (you can find out a lot about this in The Gluten File: http://jccglutenfree.googlepages.com/).

Such people often have subclinical malabsorption issues that may lead to neurological symptoms as well--you should have your B- and D-vitamin levels checked, especially B12, B1, and B6, and mineral levels looked at.

Avoidance of gluten may enable the gut to start healing over time, and may help with neurological symptoms as both malabsorption and direct effects of gluten on neural epitoptes recede, but this may take a very long time. (Nerve healing in general is very slow). One may also find that one has multuiple sensitivities and may need to examine other foods (caesin is a freqeunt co-culprit) to get a full recovery effect. Even then, a number of people have reported that they have just arrested the neuroplogical progression rather than reversing it--inddividual results vary widely. People with zonulin dysregulation--zonulin regulates the cellular spacing in the gut, mediating what kinds/how many pathogens may pass through into the body for possible reaction--seem to have the most difficulty (the greater the dysregulation, the more likely that things will escape the gut and be reacted to, and the more likely one of these will start an autoimmune reaction through molecular similarity to some kind of body tissue).

I think you have to be REALLY strict about not eating gluten, and experiment with other food elimination. It might behoove you to revert to a very paleo-type diet--fruit, vegetables, nuts you're not allergic to, lean meats, minimal processed food--and see how that goes.

B-12 sublingual, METHYL cobalamin 2000-5000mcg/day wouldn't hurt,
and may help-over time. Halting PN progression is a start. It takes time.

Hi. Neurontin can take awhile and you have to get up to the correct dose. This may not me the med for you but I know in the past I tried it and did not find relief and also had severe pressure in my head. After 2 years I tried it again and the initial side effects wore off though I am still only on 1800 but am going to work on increasing again. Have you tried any other meds?I though that gi condition can cause pn like celiec. Have you looked on that board to see as well? I know you stated you were healthy before this but have you had any other illness,injury,etc.I am assuming you have had your blood sugar tested and what was your b12 number? Anything you can think of that has not happened to everyone? I hope you feel better and I wish I had more direction for you.

Before I started taking B12 supplements, the B12 result was 496. Reference range says 211-911. I've been taking a supplement since but haven't been tested again.

No injuries that I can think of.

Glucose, Serum result was 86 with a reference range of 65-99.

I'm going to try a test for lead, mercury, and arsenic poisoning. I do have the silver fillings in my teeth which I've heard can be problematic but I can't imagine that would cause this.

I went of the Neurontin yesterday to see and today I got a serious migraine. Not sure if it's connected or not. Although, the pressure is less behind my eyes so perhaps that was a neurontin symptom?

Are there any long-term side affects to taking Neurontin. I was at 900 per day.

You have only had it a year so now is the time to try and stop it and reverse the damage.

Have you looked at the sticky "Neuropathy does improve" at the top on the main page? There's great stuff in there. There's still a ton of tests that you can do. Look for lazy jane chart in the sticky. Also there's a great diet and exercise plan on the second page. You have to put your body in the optimum condition to give it a change. Body weight, sleep, diet, exersize, suppliments etc. There all there in the sticky. I think you could do more as far as your suppliments go. Here's what I was told to do by mrsD. I have notice some improvement. Not sure if it's healling or just that some of the suppliments help with the pain.

Good Luck,