OUR WORK

Turning lived experience into lasting change.

Our early work is about building the relationships, evidence, and practical foundations needed for a responsive, accountable non-profit.

Community voice

We create opportunities for people with muscular dystrophy, families, and carers to influence the priorities that affect them.

Awareness and inclusion

We want to make it easier for wider communities to understand muscle-wasting conditions and remove barriers to participation.

Partnerships

We collaborate with people and organisations already doing valuable work, concentrating on the gaps where we can add something meaningful.