Ataxia Patient Research Registry

[Beryl_Park]

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

Please see - sanfordresearch.org/cords/cordsregistryform for more information.

[Alan_T]

Thanks

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 http://www.terrapinn.com/conference/world-orphan-drug-congress/index.stm

Alan

[Beryl_Park]

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