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Increasingly Difficult to Accept Peripheral Neuropathy

Neuropathy | Last Active: Aug 10 12:43pm | Replies (233)

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Profile picture for magrose45 @magrose45

Many moons ago a very eminent neurologist whilst trying to discover a problem I was having at that time came up. When he spoke to me what he said was in life there are simply things that we don’t have an answer or a name for not yet with peripheral neuropathy, I feel pretty much the same. I accept it I don’t like it and I’ve checked in England and I often go to the mayo clinic to see what if anything is out there so again zilch. I seldom if ever read medical ads preferring as I said earlier the advice of Doctor and looking into research let me know if you have any better luck than me thank you Margaret

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Replies to "Many moons ago a very eminent neurologist whilst trying to discover a problem I was having..."

I check Pub Med a couple times a year to see if any papers on PN have been published, and scan internet once a year to see if anyone looking for subjects to participate in Clinical trials (I’d def volunteer). It would be interesting to know what clinical and research orgs are focusing on PN treatment and research so I can narrow down what I have to wade through to those places that are actually conducting first rate research on humans. I’m not interested in reading about mouse studies. I don’t think Mayo is one of those orgs.