Congenital muscular dystrophy (CMD)
The congenital muscular dystrophies (CMDs) are a group of conditions which share an early presentation and a common muscle pathology. Congenital means 'from birth' and in the great majority of cases of congenital muscular dystrophy the initial symptoms are present at birth or in the first few months.
The Muscular Dystrophy Campaign leads the search for treatments and cures for congenital muscular dystrophies and other muscle-wasting conditions. We provide expert advice and support for individuals and families living with CMD, and for health professionals.
Our National Conference, taking place on 12 October 2013, will include a congenital muscular dystrophy specific workshop, led by Shirley Crosby. Find out more and book your place today.
The Muscular Dystrophy Campaign supports families by:
- funding research projects and providing regular information about research progress
- supporting the training and development of the next generation of scientists and funding clinical trials co-ordinators in the drive towards potential treatments
- collaborating with the American patient organisation CureCMD to support the international congenital muscular dystrophy registry (CMDIR).
- working with, and providing training and education for, NHS-funded care advisors
- taking a leading role in driving NHS support for neuromuscular networks and spearheading campaigns to improve access and quality of specialist care
- offering advice and information and enabling people to overcome difficulties through our advocacy service
- providing grants towards specialist equipment to help people to live as independently as possible
- helping people to connect with each other through our local Muscle Groups, online via TalkMD, at conferences and events; and through Trailblazers, our national network of young disabled people.
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There is a role for everyone in the fight against muscle-wasting conditions. We are a small but strong community of people in the UK and we are determined to win this fight, together.
There are opportunities to get involved in a variety of ways, such as:
- enrolling in the CMDIR patient registry
- connecting with others affected by CMD
- being an advocate for our campaigning and media work
- sharing your story to inspire others
- establishing a family fund
- participating in fundraising events
We are currently committed to supporting two research projects into congenital muscular dystrophy, for which we are seeking to raise £180,000. Please make a donation.
Support and information
We are here for you and your family. For more information about CMD please contact our freephone support line or send us an email (Monday to Friday 8.30am - 6pm): 0800 652 6352 (freephone) firstname.lastname@example.org.
- Find a clinical trial See an overview of current clinical trials into muscle-wasting conditions in the UK and around the world
- Research we are funding See the current world-class pioneering research into potential treatments and cures that we are funding
- Publications Read our free publications including our expert factsheets about medical conditions and comprehensive guides on adapting your home
- Your stories Read about families and individuals who are affected by muscle-wasting conditions