Living with FA & Contributing to Research – The Impact of Two Sisters: Meet Scarlett & Lilah
Give the Gift of Research at give.curefa.org/campaign/gift-of-research-2023/c542072 FARA's Mission is to marshal and focus the resources and relationships needed to cure Friedreich's Ataxia (FA) by raising funds for research, promoting public awareness, and aligning scientists, patients, clinicians, government agencies, pharmaceutical companies, and other organizations dedicated to curing FA and related diseases. Friedreich’s Ataxia is a debilitating, life-shortening, degenerative neuro-muscular disorder. About one in 50,000 people in the United States have Friedreich's Ataxia. Subscribe to FARA's YouTube channel / fara1998 Follow FARA on Facebook / curefa Follow FARA on Instagram / curefa_org

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"This is our FAmily": Meet the Juips

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Behind the Mystery: Friedreich’s Ataxia

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The French Do Not Care About Work

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The Un-Ending Struggle: I Can't Stop Sleeping | Living Differently

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Give the Gift of Research

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She’s 12. She Sings Aretha Franklin… Until Simon TELLS Her to Do It Acapella! 😳

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My Second Life - Living With ALS

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Friedreich's Ataxia v4 6 3

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NERVOUS 12-Year-Old Who Can Sing Without Opening Her Mouth Earns Mel B's GOLDEN BUZZER!

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How To Think SO CLEARLY People Assume You're A Genius

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Living with Friedreich Ataxia: Carla, Maria, and Nuria

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Die teuerste Schule der Welt: Hinter den Toren von Le Rosey | Y-Kollektiv

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'Listen Like You Might Be Wrong': Harvard Student Goes Viral For Stunning Speech On Trump Amid Feud

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I Lived Another Life In a Coma | It Happened to Me

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ALS at 21? I Hope Not, My Story (full video)

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Life with a Friedreich's Ataxia Diagnosis | Proof Bread

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Living with Friedreich Ataxia: Sean's Story

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FARA Flash Talks 2026 – Session 2

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How I Set Myself Free | Keke Palmer | TED

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