At first I did not know what it was? I have now finally been diagnosed. But if the symptoms keep up there progression as they are so rapidly doing. What can I expect a year and a half from now?

They tell me it is Motor and Sensory Axonal Polyneuropathy, but my symptoms certainly feel far worst than mild. The Gabapentin does not really help.

Has anyone gone through a rapid decline? Do things ease off? Is it because it is a bad winter? Could living in a warmer climate help? Is stress making it worse?

The big question? How can you switch off thinking about it?