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

Fourteen 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
Saturday, July 24th, 2021
Jack and Jill to End Duchenne
Jack and Jill Marathon in Seattle Washington – Jen’s 30th Marathon!
To date raising over $125k for Parent Project Muscular Dystrophy to End Duchenne

Saturday, October 31st, 2020
17th Annual Boo Run 5K raised over $10,000 to End Duchenne!
100% of the proceeds went to the Another Day for Gray Foundation

Upcoming Events

Saturday, October 30th, 2021 at 8am ET
18th Annual Boo Run 5K at Nathan Benderson Park
100% of the proceeds going to the Another Day for Gray Foundation
Sign up today at http://www.boorun.com

Monday, April 18th, 2022
126th Boston Marathon running for Parent Project Muscular Dystrophy
Donate today at http://join.parentprojectmd.org/site/TR?px=1689948&fr_id=4595&pg=personal