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Increasingly Difficult to Accept Peripheral Neuropathy
Neuropathy | Last Active: Nov 29 9:52am | Replies (169)Comment receiving replies
I went through a similar issue. One neurologist said I had neuropathy and another one said I had MS. Eventually you will get to the bottom of this and find out what you have. Finding a physician that deals specifically with neuropathy would be your best solution at this time. They will know usually on your first visit. They know the disease very well.
Hope you find out soon. But don’t let either of those diseases define you. You can get through this.
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Thank you what did you eventually have? I can't see a neurologist who specialises in neuropathy because that is difficult in the UK unless you go private I did go semi private and was told it was likely small nerve fibre Neuropathy. Now to be told I don't have it makes no sense. I have all the hallmarks of it I should know. A DAT scan to test for Parkinsons is very depressing and doubtful as well. Probably be a complete waste of time.