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

Thirteen 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

Monday, April 17th, 2017 & Sunday, April 23rd 2017
The Boston Marathon and The London Marathon
Two Marathons, Two different countries, 6 days apart to Make a Difference for Duchenne!
Raised over $24,000 for Parent Project Muscular Dystrophy and Action Duchenne!

Saturday, February 27th, 2017
2nd Annual Doggies 4 Duchenne 5K
Raised over $12,000 for the Another Day for Gray Foundation and the LWR Humane Society!
Thanks to Monika Oberer & Rebekah Boos for hosting this awesome event!

Upcoming Events

Saturday, October 28th, 2017
14th Annual Boo Run 5k in Lakewood Ranch – 8:30 am
100% of the proceeds go to the Another Day for Gray Foundation

Register at www.boorun.com!