Quote:
Originally Posted by Conductor71
Jim,
Congress recently passed a law establishing a National Registry for both PWP and MS. It should help immensely to see patterns and make some connections on etiology or other variable that may serve as PD triggers. I believe that Parkinson Action Network played a key role in establishing this legislature.
23andMe is a means for also sharing data. If you have not gotten your "Spit Kit", please get to their web site to take advantage of highly discounted genomic analysis for PWP - it is for "normal" folks like $400 and for us only $25. It is well worth it!
Laura
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Laura, I've tried to get a kit, called with no response, sent email and was told that at this time they are not giving them out, it's been idled. What gives?????