Anna Motyl

@dibbouk.bsky.social

PhD, MND/SMA Research programme manager @My Name'5 Doddie Foundation All views my own #ALS #MND #SMA #RareDisease 📍 Edinburgh

The fact that the UK still doesn't do newborn screening for SMA is nothing short of scandal. We have treatments we've known for years need to be administered as soon as possible. Spinal muscular atrophy in the UK: the human toll of slow decisions - The Lancet www.thelancet.com/journals/lan...

Spinal muscular atrophy in the UK: the human toll of slow decisions

Spinal muscular atrophy (SMA) is a recessive condition that affects globally one in 14 800 newborns.1 Infants with SMA type 1 do not acquire motor milestones and rarely survive beyond the first year o...

thelancet.com

After rolling in to Glenalmond College for the night, teams on the blue route of Doddie’s Grand Tour were greeted by Gerard Butler, who heard we were in the area and wanted to come along to support and hear about what we're up to 💪 Wonder if we can convince Gerard to join us on the ride next year?🤔

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