Survey Exploring Access to the Standards of Care for People who have SMA in the UK

28 August 2020

The John Walton Muscular Dystrophy Research Centre in Newcastle invites one respondent for each child / adult who has SMA to take part in gathering this important information that will help guide future practice. 

Invitations to respond are being sent out via the SMA registry, clinicians and social media.

You can find out more and take the survey, here.