In April 2009 our friend Alfie, at the age of 4 was diagnosed with Duchenne muscular dystrophy. Put simply this means that his genetic make-up prevents his body from producing the stuff needed by the muscles to repair and rebuild themselves. Progressive muscular degeneration means that the condition has a catastrophic impact on the quantity and quality of life that can be enjoyed by those who suffer with it.

There is no cure, but the Muscular Dystrophy Campaign (MDC) works tirelessly to promote research into treating the condition. The MDC also provides a precious lifeline of information, guidance and solidarity for all families that have to learn to deal with MD. The support and care that our friends Sam, Rachael and their family have received so far has been invaluable; they would not have had this help without the specialist services sponsored by MDC and the efforts of the campaign to co-ordinate and fund work on the medical front.

Supporting the work of the Muscular Dystrophy Campaign is one small thing that we can do immediately to fight the frustration of not being able to make things better for all who are affected by the cruel disease. This is why we are targeting our appeal to benefit MDC.