Duchenne Muscular Dystrophy (DMD) is a genetic muscle disease that causes progressive muscle degeneration and weakness. Sweet Dawson was diagnosed with Duchenne Muscular Dystrophy on July 11th, 2019 at the age of 8, and he is already requiring extensive medical care. The prognosis for those with DMD is poor but with good medical care the quality and length of life is significantly enhanced. The out of pocket costs for the daily medications he requires cost $2,500 per month, the braces he needs to stabilize his muscles cost $600 and the costs are building every single day.

Dawson is your typical 9 year old boy who loves to play video games and with his 3 brothers, Cody, Parker, and Mason. Dawson is the most genuinely sweet, kind, and caring little boy who is always thinking of others. Our wish for Dawson is that he can continue to do the things he loves and get the medical care he needs and deserves while we fight, hope, and pray for a cure for muscular dystrophy. 

Any donation helps Dawson and his family fight against this terrible disease and will be appreciated more than you could know. 

If you'd like to follow and support Dawson's fight against DMD, please go like his Facebook page Dawson Strong. 

Please keep Dawson in your prayers and help us raise awareness and funds for his cause.