โœฆ Fighting Duchenne Together

Another Day
for Gray.

Twenty years ago, three words changed everything: Duchenne Muscular Dystrophy. Today, our son Grayson is proof that hope, research, and community can move mountains. Join us in the fight! ๐Ÿ’™

Our Story

Twenty years of hope, heart & hustle.

Our lives would never be the same the day we received that call. Your son has Duchenne Muscular Dystrophy. The more we learned, the harder it was to accept.

"No cure. No way to stop it. No hope." โ€” but that was then. Now? There IS hope. ๐ŸŒŸ

Twenty years later, Grayson is benefiting from treatments that didn't exist when he was diagnosed. Researchers are closer than ever to a cure. But we can't stop now โ€” we won't stop until there's a cure for every boy with Duchenne.

Thank you for showing up. Every visit, every donation, every share gives Gray another day. ๐Ÿ’™

20+
Years FightingFrom diagnosis to hope โ€” two decades of advocacy, fundraising, and love.
36
Marathons RunJen has run 36 marathons (including Berlin โ€” twice!) to raise awareness for Duchenne.
1
MissionEnd Duchenne Muscular Dystrophy. Full stop. No boy should face this disease without hope.
About Duchenne

Know what we're fighting.

Duchenne Muscular Dystrophy (DMD) is a rare genetic disorder that causes progressive muscle weakness. It primarily affects boys and is caused by mutations in the gene that produces dystrophin โ€” a protein essential for muscle health.

1 in 3,500

Boys Affected Worldwide

Duchenne is the most common fatal genetic disorder in childhood โ€” making awareness and funding critical.

Ages 2โ€“5

Symptoms Begin Early

Children often show signs of muscle weakness very young โ€” delayed walking, difficulty climbing stairs, frequent falls.

๐Ÿ’ช

Research Is Working โ€” But We Need More

Recent FDA-approved therapies are slowing the progression of Duchenne. An entire generation of boys โ€” including Grayson โ€” are benefiting from treatments that simply didn't exist 15 years ago. But there is still no cure, and we must keep pushing until there is.

No Cure

Yet โ€” But Getting Closer

Gene therapy, exon skipping, and other breakthroughs are giving families real reason to hope.

$$$

Funding Changes Everything

Every dollar donated to Parent Project MD goes directly toward accelerating research and improving care.

Get Involved

Come run, walk & cheer with us! ๐ŸŽ‰

Sep 29
Marathon

Berlin Marathon 2024

Jen runs her 36th marathon โ€” her 2nd Berlin! Every mile is a mile closer to a cure. Cheer her on and donate to Parent Project MD through our page.

Support Jen's Run โ†’
Oct 26
5K Run/Walk

Annual Boo Run ๐ŸŽƒ

The 21st Annual Boo Run! Bring your furry friends for this 5K. Profits split 50/50 between Another Day for Gray Foundation and the Humane Society at Lakewood Ranch.

Register Now โ†’
Any ๐Ÿ’™
Ongoing

Direct Donation

Can't make it to an event? Your direct donation to Parent Project MD through our fundraising page makes a huge difference in the fight against Duchenne.

Donate Anytime โ†’
Say Hello!

We'd love to hear from you. ๐Ÿ‘‹

Have questions about Duchenne? Want to get involved with an upcoming event? Or just want to share some love? Reach out โ€” this community is everything to us.

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