Our Cause Drives Us

The Race is on

Life brings different challenges to everyone but we have to remember that they can often be turned into the greatest blessings. We consider Mason Keller one of them!
Mason & Katie Keller

Duchenne is the most common muscular dystrophy in children.

On September 12th 2017 we received the diagnosis that 1 in every 3500-5000 families with young boys receive each year. This news was the diagnosis of a disease called Duchenne Muscular Dystrophy (DMD). Our journey has just begun, but Mason like other boys with DMD, are in a race.

We aim to educate and support the disease until boys like Mason are left with hope. We invite you to help us!
Join the FIGHT
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PPMD is Making an Impact

10 yrs

Added to the average lifespan due to PPMD led advances in care

50mil

Invested by PPMD in Duchenne

3

U.S. Drug Approvals
The reason we are involved with PPMD is that it is one of the only organization whose focus is entirely on Duchenne Muscular Dystrophy.

This progressive disorder that causes muscles to become weaker over time until it affects the whole body leading to poor quality of life and premature death. This is the diagnosis our son received at the age of four.

PPMD presents optimal care standards and provides free genetic testing for Duchenne. They invest deeply in treatments for this generation of Duchenne patients and in research that will benefit future generations.

We have great hope for the future of these children!
-Rebecca Keller
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