Is there anyone out there with a cerebellar disorder, ataxia, shrinking cereballar gland?

I am starting to think that my sister and I are the only ones in the world going through this. I guess it is really rare.

Anyone?

Julie, this is the community for you both: http://www.livingwithataxia.org/

There are over 1,500 members, so perhaps it is not as rare as you think. :)