This blog has been set up to fill that gap in support that we all need. The individual support groups in the New England group have their own scheduled meetings. However, many people with Ataxia can not make it to these meetings. Therefore, this blog has been set up to serve as a way for all our NE members to keep in touch in between the times they can not meet face-to-face. So let’s share with each other those ideas we think others might benefit from, those questions we all have…Let’s not let anyone feel they’re alone in this. I know, for myself, that my biggest benefit from support groups has been learning the fact that “I am not the only one!”
– Donna
Ataxia Support 
How would i get information about this and help through this
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You could also contact John Mauro: john@ataxia.org and ask to be put on the e-mail list for the North East Ataxia groups.
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You can go into the NAF website and check out the support groups in your area. They’re a wonderful resource. http://www.ataxia.org/connect/support-groups.aspx
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