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NAF has launched a petition on Change.org calling on the FDA to prioritize treatment options for rare diseases with urgent unmet needs, including Spinocerebellar Ataxia (SCA)
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Month: November 2021

Ewa Blonska

Hi! My name is Ewa 🙂 I live in a beautiful and green country – Poland. I am a recently diagnosed person whose story is probably quite unique, because almost Read More…


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