Bill Moore & his daughter Jessica Oberlin, two members of NAF, recently shared their stories of living with SCA3 as part of a feature for the Critical Path to Therapeutics for the Ataxias (CPTA). The CPTA aims to optimize clinical trials for inherited Ataxias. Impact stories like theirs can help researchers & drug developers understand the realities of living with Ataxia. You can read it here: c-path.org/impact_story/cpt...
A shared story of SCA3: Bill Moore & his daughter... - Ataxia UK
A shared story of SCA3
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wobblybee
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Ataxia sca3 
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Why am I a part of the Ataxia UK community?
My attempts at managing SCA3
