The C4C was formed in 2013 to help support the family of Connor Olsen, a little boy who was diagnosed with Duchenne Muscular Dystrophy. This is a rare and incurable disease that is sadly always fatal. Connor is 5 years old and because of this disease he can expect to be wheelchair dependent by the age of 9 or 10 with a life expectancy of about 20 years. The C4C campaign is helping support vital research into DMD with the hope of finding a cure.
