Guest guest Posted September 21, 2006 Report Share Posted September 21, 2006 I am in Kent, Jill. Sama Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 21, 2006 Report Share Posted September 21, 2006 Welcome Sama, I too live near Manchester/Liverpool as Jill does. I have not been diagnosed yet, although I have seen a neurologist who thinks I may have " some form of Hereditary Motor and Sensory Neuoropathy (HMSN) " . I am now waiting for the EMG and NCV tests, but I have been told there is a 10 month waiting list. I have found out a lot of useful information from the people here just by reading the posts. I don't post very often as, I have said, I'm not even sure that what I have is CMT. Everyone here is very helpful and empathetic and they will try to give you the answers to any questions you may have and, although you are understandably petrified at the moment, I am sure they will do their best to allay your fears. Regards Quote Link to comment Share on other sites More sharing options...
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