All About Unknown Ataxia Without Family History

[@lorraineophoff4984]

Thank you for all this important information!

[@alanscott4441]

Dr. Wilmott- Thanks kindly for your time and superb insight. So grateful for your help. Idiopathic at this point, extensive genetic testing 3 years ago. Slow progressing late- onset.

[@natasharoesch4470]

I was diagnosed after an MRI I was told. “You have Cerebellar Ataxia, there is nothing you can take, nothing you can do, and it will probably get worse.

[@argentinarodriguez4170]

How are you doing? That's what I was told in January 2023.

[@natasharoesch4470]

@@argentinarodriguez4170 Hi: turns out I do not have cerebellar ataxia! Have a second opinion-it could be a movement disorder of some kind. This diagnosis was made by a neurologist looking at an MRI but did not see me in person.

[@argentinarodriguez4170]

@@natasharoesch4470 , I am glad for you. Later, in June, I was diagnosed with ALS.

[@valariedemello745]

The neurologist said the same, he gave me no direction or hope. Very scary and depressing. Better after finding NAF.

[@ggbrait7140]

Thank you!!!

[@patdenman3887]

How do I find a knowledgeable doctor in North Idaho?😊

[@joshivrujesh4695]

Sir is there any hope of future complete treatment spinocerebellar ataxia3 available

[@truehuman9449]

Atlast nothing is shared to treat the sufferers

[@melissasmith2166]

How does this with athletics as we'll