IMAGINE being a child or a teenager and being told you have a degenerative muscle disease which will lead to a loss of muscle co-ordination, fatigue, vision impairment, hearing loss, slurred speech and then a serious heart condition - this is Friedreich Ataxia. 1 in every 30,000 affected. 1 in 90 are carriers. There is currently no cure.

Encouragingly, through the amazing work of researchers, our FA community and fundraisers around the world, SKYCLARYS, the first ever treatment for Friedreich Ataxia is now available in the United States. Biogen Australia has confirmed that they plan to make regulatory and reimbursement submissions for SKYCLARYS this year following the recent approval by the European Commission.

Upcoming events

  • Lend Us Some Muscle 2024

    GET INVOLVED IN THE LUSM GLOBAL CHALLENGE in 2024!

    Get running, take the dog for a walk, try your hand at yoga or even hit the gym! Whatever it is that you love to do. Or you can even set yourself a challenge to try something new in May. Help us raise funds and give hope to those living with FA.