Hundreds of Ataxia Support Group meetings are held each year to connect people in the community and help them learn to live better with Ataxia. Donate now to show them they aren’t alone. Contributions will be matched by the Clementz Foundation – doubling your impact and increasing our ability to continue to offer important services like this. Donate now: http://bit.ly/2018SummerMatchChallenge | National Ataxia Foundation
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Hundreds of Ataxia Support Group meetings are held each year to co…
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People with rare diseases deserve to be part of the process that decides their future. Flexibility and the patient voice must be part of every decision for rare diseases. #PleaseListenFDA | National Ataxia Foundation
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Ataxia means different things to different people. But we all have one thing in common: we need better treatment options and a cure. Share this video and let your friends know what Ataxia means to you. ... Donate during the Summer Match Challenge to have your gift DOUBLED. Help us get the $100,000 match from The Michael and Patricia Clementz Family Fund! https://ataxia.org/summermatch/ | National Ataxia Foundation
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Get ready, Ataxia community! Next week, we’re launching the BIGGEST Ataxia awareness campaign ever, featuring a celebrity with over 20 million followers. Let’s make this our Ice Bucket Challenge moment and help it go viral! Can you guess who the mystery celebrity is that is leading the charge on the campaign? There’s a hint in this video. Stay tuned for the reveal and get ready to like, share, and comment! | National Ataxia Foundation
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The very first SCA Global Conference takes place tomorrow. More than 100 researchers from around the world will be collaborating in a 2-day scientific meeting that is focused on accelerating Ataxia research. Learn more about what SCA Global is and why it's a big deal. | National Ataxia Foundation
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