Thanks again for responding,

My story: In march of this year I was prescribed levaquin by my urologist, a low dose 40 day course. I developed tingling and burning in my feet and pain and weakness in my shoulder, nausea, dry mouth, and general malaise and had to stop at 20 days. I ingested alot of levaquin by that time. I was referred to a neurologist who put me on prednisone and followed up in 2 weeks to see if it was helping. It had not stopped the symptoms but they had not gotten significantly worse. He then sent me to the University of Michigan for evaluation. They did an EMG which showed what they thought was a brachial plexopathy. (I had a similar episode with my right shoulder 15 years earlier but no SFN symptoms presented themselves and it resolved in 6 months or so. I never even went to a neurologist) They also did a lot of blood work which came back normal. They told me to get off the prednisone so I did a taper and once I got below 10 mg a day things flared up again. I told the people at U of M about this and they still said to get off. I decided at that time to get a second opinion and consulted with a neurologist at Cleveland Clinic who after reviewing my information said to try the prednisone again. I'm thinking, Hmmmm. I reported this back to my local neurologist who first seen me and he suggested I go for 2 out of 3 and be a walk in at Mayo to find some sort of consensus. So I did. They did a bunch of blood work, another EMG, autonomic testing Etc. The EMG results were similar, the autonomic testing showed slight abnormalities, and the blood work was normal. They also did a gastro workup with tests, scopes, a MRI, and biopsies only to find that I had high fecal fat for an unknown reason. They told me to get off the prednisone so I had a consensus. I started to taper the same result with things flaring up under 10 mg. I continued the taper and got off. I did have stomach damage from the prednisone and NSAIDS I was on which eventually go better. The shoulder got better. The burning and other neuropathic symptoms eventually leveled off but definately did not cease. I have tried Neurontin, Klonopin, and Antidepressants and either could not tolerate them or they did no good. Basically I was just trying to eat right and do some of the supplements shown here when a couple of weeks ago the burning and stuff went from irritating and localized to extreme and all over in a matter of days. I told the guy at U of M (whom I like more than the guy at mayo and consult with regularly) and he just gave me more suggestions for pain and was not going to do any thing else. I do not know why this has flared like this worse than ever when it had been fairly stable for a few months and perhaps even improving in some ways. Is this a common thing with SFN and can it go back to what it was before it flared up? I have been thinking about trying the neurontin again, I have tried it twice and it gave me backaches but this is so intense that it may be worth it. I also have some Norco but I hesitate to use it too much. I smoked some marijuana the last week or so(I am not a regular user) and it did take the edge of but only for a short while. Of course I have all the other junk like extreme fatigue, sleep problems, eating problems and etc. I do not know if any of you good people have any advice but I am open to anything or if you want to know more please ask. Thank you very much for reading my story