It is a rare inherited neurodegenerative disease that causes movement problems (impairs gross and fine motor skills and stability, called ataxia). Although rare, Friedreich's ataxia is the most common form of hereditary ataxia worldwide, affecting approximately 1 in every 50,000 people...

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Our goal is to spread awareness of FA and its manifestations among the public. First and foremost, we want to ensure that every patient who is not already in contact with us or with the Hereditary Ataxia Centre at the University Hospital in Motol receives all available information...

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We would be happy to welcome anyone who is willing and able to join our patient organisation. It can be someone whose life has been affected by Friedreich's ataxia or anyone else. Gender, age or health status is not a consideration. All that matters is the desire to support us...

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