“Your Team, One Dream, A Cure”
As a member you help provide those with ataxia a better life and hope for a brighter tomorrow. NAF is a membership based nonprofit organization dedicated to serving ataxia families. We are grateful for the support of our members and welcome others to also join.
As a thank you for being a valued member, you will receive discounts in attending the annual membership meeting as well as a subscription to the NAF’s in-depth quarterly ataxia news publication, Generations.
Be Part of Team NAF…become a member today! Please ask your friends, family, co-workers, and neighbors to also become a member. Thank you!
New: Ataxia Research Studies
Awarded Funding for FY 2015
The National Ataxia Foundation (NAF) is pleased to announce that 23 promising ataxia research studies from the United States, Belgium, Mexico, United Kingdom, Portugal, and Germany were awarded funding at the December 2014 NAF Board of Directors meeting for fiscal year 2015. With the funding of these 23 research studies and the previous research studies funded earlier in 2014, nearly one million dollars were committed for ataxia research. Click here for more information.
NEW NAF PRESIDENT
|The National Ataxia Foundation welcomes William “Bill” Sweeney as the newly elected President of the National Ataxia Foundation. Bill joined the NAF Board of Directors in 2007, became a member of the Executive Committee in 2009, served as Treasurer from 2012-2015 and was elected as President in March 2015. Bill has also been active in the Twin Cities Support Group and helped start the Twin Cities Walk, Stroll ‘n Roll in 2010.|
Myra KRAFT Community MVP Award
John Mauro was one of the 26 recipients of the Myra KRAFT Community MVP Award on June 9th, 2015. He was also awarded a $5,000 grant for the National Ataxia Foundation.
Saturday, August 29, 2015