We campaign across the UK to bring about change and make a difference to people affected muscle-wasting conditions
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Campaigning in parliament

We greatly value cross-party support from parliamentarians across the UK. This is vital in our fight for improved neuromuscular services. We provide detailed briefings for our parliamentary supporters ahead of meetings, debates and questions.

Paul Maynard, John Bercow, Fiona Mactaggart and Graham Evans at APPG for Young Disabled People Launch

How members of parliament can support us

Supported by the Muscular Dystrophy Campaign, cross-party groups in Westminster, the Welsh Assembly, the Scottish Parliament and the Northern Ireland Assembly have been investigating access to specialist neuromuscular care and social care across the UK. The four reports produced, with their recommendations, provide a focal point for the continued battle to ensure that action is taken to address the significant gaps in the provision of specialist neuromuscular care and to implement service improvements.

Walton Report (All Party Parliamentary Group for Muscular Dystrophy, August 2009)

Thomas Report (Welsh Assembly's Cross Party Group on Muscular Dystrophy, July 2010)

Mackie Report (Scottish Parliament's Cross Party Group on Muscular Dystrophy, September 2010)

McCollum Report (Northern Ireland Assembly's All Party Group on Muscular Dystrophy, July 2012)

Supporters at the launch of the McCollum Report by the All Party Group on Muscular Dystrophy

For any queries or for advice on parliamentary activity in support of people living with muscular dystrophy and related neuromuscular conditions, please get in touch on 020 7803 4839 or by email at campaigns@muscular-dystrophy.org