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Kathy G

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Dingle_dell
Dingle_dell

It is nearly 2023 I would like to hear from other people who suffer from small fibre neuropathy and if they have found out the cause and pain relief. I have had tests all negative but diagnoised with FM . But researching small fibre which can be missed by tests for large cell neurothopy. I have all the pains in feet my legs and creeping up to my shoulders and hands and getting worse. Has anyone seen a specialist for this in the south of England. Or is it just Manchester/London ? I would imagine the waiting list will be very long. Amerian research seem on the ball . I notice other replys on this disease are months old if not years. Things have moved on recently through new research on this subject. Would be interesting to hear from others who are suffering from small fibre neurothopy and how they cope with it. look forward to hearing from them .

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