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

Nineteen 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
​Saturday, January 6, 2024
Team Tullio taking on the Disney Half marathon on Saturday, January 6th. Nick, Jen and Emma will all be running the half to raise funds to END Duchenne. You can donate at Another Day for Gray's Fundraising Page

Monday, April 15, 2024
2024 Boston 8 to END Duchenne. Jen will be taking on her 8th Boston Marathon to raise funds for Duchenne. Link coming soon to donate! 

Recent Events

Saturday, October 28, 2023
20th Annual Boo Run 5K Run/Walk with Four-Legged Friend Included!
50/50% split of the proceeds will be going to the Another Day for Gray Foundation AND The Humane Society at Lakewood Ranch
More details at http://www.boorun.com.