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Our lives would never be the same the day we received that call eighteen years ago...

Your son has Duchenne Muscular Dystrophy.

The more we learned about the disease, the more difficult it was to accept.

No cure.
No way to stop it.
No hope.

Eighteen years after that initial diagnosis, I am happy to say that there is hope.  Tremendous strides have been made in research, awareness, and improving standards of care and treatments.

An entire generation of boys, including our son Grayson, are benefiting from these advancements.  But it's not enough.

There still is no cure, and we must continue the fight until one is found.  The lives of Grayson of other boys affected by this disease depend on it.

Thank you for visiting our site.  Together we can help overcome Duchenne Muscular Dystrophy, and provide Grayson and other boys another day.
Recent Events
Sunday, September 11th, 2022 and Sunday, October 2nd, 2022
Erie Marathon on September 11th, 2022 and London Marathon on October 2nd, 2022
2 Marathons, 3 weeks apart on separate continents to End Duchenne!
100% of the proceeds went to Muscular Dystrophy UK towards research across the globe to put an END to Duchenne!

Monday, April 18th, 2022
126th Boston Marathon running for Parent Project Muscular Dystrophy
To date raising over $127,500 for Parent Project to END Duchenne!

Upcoming Events

Saturday, October 29th, 2022 at 8am ET in Lakewood Ranch
19th Annual Boo Run 5K Run or Walk with Four-Legged Friend Included!
50/50% split of the proceeds going to the Another Day for Gray Foundation AND The Humane Society at Lakewood Ranch
Sign up today at http://www.boorun.com