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Friedreich ataxia (FA) is a genetic, debilitating and life-shortening neuromuscular disease. People living with FA experience progressive loss of coordination, muscle weakness, and fatigue, which progresses to muscle incapacitation and wheelchair rel

Friedreich ataksi (FA) er en arvelig, svekkende og livsforkortende nevromuskulær sykdom. Mennesker som lever med sykdommen, opplever gradvis koordinasjonstap, ustødig gange og muskelsvakhet, som utvikler seg til fullstendig tap av gangfunksjon.

Friedreich ataksi (FA) er en arvelig, invaliderende og livsforkortende neuromuskulær sygdom. Mennesker, der lever med sygdommen, oplever gradvist tab af koordinationsevne, ustabil gangfunktion og muskelsvaghed, som udvikler sig til fuldstændigt tab a

Friedreich ataxia (FA) is a genetic, debilitating and life-shortening neuromuscular disease. People living with FA experience progressive loss of coordination, muscle weakness, and fatigue, which progresses to muscle incapacitation and wheelchair rel

Friedreich ataxia (FA) is a genetic, debilitating and life-shortening neurodegenerative disease. People living with FA experience progressive loss of coordination, muscle weakness, and fatigue, which progresses to wheelchair use and incapacitation.

Friedreich ataxia (FA) is a rare, serious, and progressive neurodegenerative disease with a profound impact on patients and their families. People living with FA experience progressive loss of coordination, muscle weakness, and fatigue, which progres