SMA Europe is a non-profit umbrella organisation of 30 spinal muscular atrophy (SMA) patient organisations from 28 European countries. We work to bring effective treatments and optimal care to everyone living with SMA.

Our members are national patient organisations, led by people living with SMA and their families, who put the voice of those living with SMA at the heart of everything they do. They advocate and campaign at the national level while also engaging and influencing all stakeholders and decisions at the European level, through SMA Europe.

Together, through greater understanding, we will create a better world for all those living with SMA.

We work to bring breakthrough research, effective treatments and optimal care to everyone living with SMA.

All together. One goal.

Find out more about SMA Europe here.