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Thank you everyone for another successful Walk & Roll weekend in Texas! Over 30 participants enjoyed the sunset & raised $13,000+ to support our work to #CureFSHD.

Read more updates & see additional photos on our blog: www.fshdsociety.org/2025/09/11/2025-walkroll...

#FSHD #WalkRoll

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🧡🍊 FSHD: Arretaz ikertzen den gaixotasun genetiko bat

Gaur, #FSHD|renMunduEgunean, #Biogipuzkoaren #DiagnostikoMolekularra|ren Plataformaren lana azpimarratu nahi dugu, distrofia #fazioeskapulohumerala ikertzen duena.

📰 https://f.mtr.cool/svthfvmsnv

#cureFSHD #WorldFSHDDay

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🧡🍊 Hoy 20 de junio, #DíaMundialFSHD: destacamos la investigación de la Plataforma de #DiagnósticoMolecular de #Biogipuzkoa. sobre la distrofia #facioescapulohumeral 🧬

📰 https://f.mtr.cool/jxluoahelp

#FSHD #OrangeSliceChallenge #cureFSHD #SalvaNuestraSonrisa #WorldFSHDDay @FSHDSociety

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The #CureFSHD muscular dystrophy campaign
The #CureFSHD muscular dystrophy campaign YouTube video by FSHD Society

#cureFSHD
www.youtube.com/watch?v=u1l_...

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Today is World Facioscapulohumeral muscular dystrophy (FSHD) Day. FSHD is a genetic disorder that causes weakening of skeletal muscle, affecting an estimated 870,000 people worldwide.

Learn more from @FSHDSociety at https://www.fshdsociety.org/world-fshd-day/

#CureFSHD...

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