Ataxia Patient Research Registry

The National Ataxia Foundation urge people diagnosed with Ataxia to participate in research by registering with CoRDS ( Coordination of Rare Diseases).

Please see - for more information.


I have met Liz from Sanford Cords many times, at many events and meetings

the Orphan Drug Congress, in Brussels have our picture on their website header


I followed the link, they had the nerve to block your face :-)xB