Hello everyone.

I am new to the site and am very happy to have found it!

I have recently been diagnosed with Charot Marie Tooth Syndrome. This is a genetic neuropathy.

I will be meeting with my neurologist in two weeks to discuss this diagnosis.

If anyone out there has CMT, do you have any suggestions regarding what types of questions I should ask, or give me some advice on your experiences? How are you dealing with the symptoms? I would be grateful for the help.

Di