Around 140,000 or more healthy people in the United States have C9orf72 repeat expansions, a few thousand more with a current ALS or FTD diagnosis – what research is available for them to participate in? It can be hard to understand what research participation is available. It can be even harder to picture what participating in research is like! Hear from experts about what research is available, and from everyday people with the mutation about what participating looks like for them.
Family Learning Opportunity
End the Legacy thinks Inherited Diseases are best understood in concert with other family members. To facilitate this, we are offering a chance for a shared meal for families learning together. Apply by emailing info@endthelegacy.org with why you are interested and who you will be viewing with.