How do I know if I have Wartenberg's migratory sensory neuropathy?
What signs or symptoms may make you suspect you may have Wartenberg's migratory sensory neuropathy. People who have experience in Wartenberg's migratory sensory neuropathy offer advice of what things may make you suspicious and which doctor you should go to to receive treatment
WMSN is whats left when everything else has been ruled out. You will probably have MRI’s, nerve conduction tests, bloodtests, medical history review and maybe others. A neurologist will diagnose this condition.
Find people with Wartenberg's migratory sensory neuropathy through the map. Connect with them and share experiences. Join the Wartenberg's migratory sensory neuropathy community.
5 years ago, 32 years old, I was walking up a hill an noticed that I had a stretching pain in my lower right ankle and the outside of my heel. As I was always active, I thought I strained something, but the area became more sensitive and then began g...
I had a massive reaction to some bad mosquito bites on holiday where I got eaten alive in Italy. I was left with some numb patches which my GP dismissed. A few years later, I suddenly realised my finger was numb in a small area. Suddenly I was whiske...