Friedreich's Ataxia Research Alliance
FARA's Mission is to marshal and focus the resources and relationships needed to cure 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 (FA) is a debilitating, life-shortening, degenerative neuro-muscular disorder. About one in 50,000 people in the United States have Friedreich's ataxia.
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FARA Flash Talks 2024 Series - Session 2
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FARA Flash Talks 2024 Series - Session 1
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FA Community Conversations | May 2, 2024
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Applying for CDMRP/PRMRP Grants Training | April 25, 2024
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FARA Pediatric Research Initiatives Webinar | January 25, 2024
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FARA Wrapped 2023
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- 10 ай бұрын
Living with FA & Contributing to Research - The Impact of Two Sisters: Meet Scarlett & Lilah
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FA Community: We're Just Getting Started
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- 11 ай бұрын
FA Symposium 2023: Mental Wellness Workshop
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- 11 ай бұрын
FA Symposium 2023: Gene Therapy Panel-The Patient Experience in Rare Diseases (Part 7 of 7)
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- 11 ай бұрын
FA Symposium 2023: A Strategy for Funding Friedreich's Ataxia Research (Part 6 of 7)
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- 11 ай бұрын
FA Symposium 2023: Living with Friedreich's Ataxia (Part 4 of 7)
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- 11 ай бұрын
FA Symposium 2023: Friedreich's Ataxia Treatment Pipeline-Clinical Stage Programs (Part 3 of 7)
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FARA Flash Talks 2023 Series - Session 4
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FARA Flash Talks 2023 Series - Session 3
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FARA Flash Talks 2023 Series - Session 2
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FARA Flash Talks 2023 Series - Session 1
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2 Minute Mechanisms: omaveloxolone
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A History of Omav and the FA Community
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Thank You for giving The Gift of Research
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Episode 15: 2022 In Review
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Episode 14: Community Participation in Research
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