Hi All. Does anyone out there got cerebellar ataxia (multiple syndrome atrophy) MSA. How long, what are symptoms you have n how you dealing with it. Anyone from Asia or Singapore. Rgds Jacob

Dear Jacob, Although I was diagnosed with Sporadic Cerebellar Ataxia (unknown cause/symptoms 24/7), it's not MSA. Hopefully, you'll hear from some others with MSA. The net has a lot of informaton, although I'm sure you realize this already. Also, the National Ataxia Foundation (NAF) in the US (where I live), and Ataxia UK (in the UK) are WONDERFUL sources for information on ataxia. My best to you..., ;o)