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Our lives would never be the same the day we received that call twenty 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.

Twenty 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.
​Upcoming Events
Sunday, September 29, 2024 - Berlin Marathon
Jen will be running her 36th marathon and 2nd Berlin Marathon to raise funds and awareness for Duchenne.
You can donate directly to Parent Project Muscular Dystrophy at Another Day for Gray's Fundraising Page

Saturday, October 26, 2024 - Boo Run
21st Annual Boo Run 5k Run/walk with four legged furry friends included! Profits will be split 50/50 between Another Day for Gray Foundation AND the Humane Society at Lakewood Ranch. Sign up directly or donate at the Boo Run site.