The Muscular Dystrophy Campaign supports over sixty different neuromuscular conditions. These are all conditions that involve the weakening and/or wasting of muscles. Within this group lie the muscular dystrophies – genetic conditions that are either inherited or arise ‘out of the blue’.

More than 30,000 people in the UK have muscular dystrophy or a related condition. There are no cures or treatments which prevent the breakdown of muscle but increased knowledge has improved the quality or length of people’s lives.

The severity and impact on life varies considerably between neuromuscular conditions, although there is always some level of disability. Not all neuromuscular conditions are genetic, some are caused by a faulty immune system, and they can affect anyone of any age or race.

The Muscular Dystrophy Campaign is the only UK charity focusing on all muscular dystrophies and allied disorders. It has pioneered the search for treatments and cures for over 40 years.

The Muscular Dystrophy Campaign provides practical, medical and emotional support to people affected. In addition, the charity raises public awareness, campaigns to increase government spending on research and the provision of vital equipment and aims to empower the people affected along with their families and friends.