Molecular changes after MECP2 loss may drive Rett syndrome traits
2 Articles
2 Articles
Aware That We’re Rare: The Power of Community in Rare Diseases | International Rett Syndrome Foundation
“You’re not alone. That’s what I want you to see. This is a community that understands you, a community that gets you, a community that knows what you are going through.” – James Griffin, Advocacy Chair, Rare Disease Week 2025 (sickle cell disease) For the past 14 years, the rare disease community has gathered on Capitol Hill for Rare Disease Week, hosted by the EveryLife Foundation for Rare Diseases. The week is designed to unite advocates, equ…
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