Bill Nye is back in his lab with NAF and Biogen—breaking down the science of Friedreich Ataxia in a new video series. WATCH NOW
The Annual Rare Disease Week on Capitol Hill brings together advocates united by one goal: driving change for the rare disease community. As individuals living with rare diseases, we understand the power of advocacy and the impact we can make when we raise our voices together.
Learn more: https://everylifefoundation.org/rare-advocates/rare-disease-week/