Because I Can : Running for Hunter and Noah
My sons, Hunter (5) and Noah (3), were diagnosed with Duchenne in the winter of 2017. Since that time my wife Alison and I have made it our missiong to help spread awareness and raise money to find a treatment for all boys living with Duchenne.
We have moved from fun runs to 5ks and starting last year marathons. The support has been overwhelming and we are once again asking for your support as we run the Chicago marathon.
Please support me as I participate with the Race to End Duchenne team at the 2020Bank of America Chicago Marathon on October 11, 2020. Together, we will go the distance to end Duchenne.
Duchenne is the most common fatal genetic disorder among children. To date, there is no cure or treatment to stop the progression of Duchenne.
Those with Duchenne are truly in a race against time as their muscles deteriorate further each day. Please help us put an end to the devastating disorder by making a donation.
If you prefer, you may also mail a check, made payable to Parent Project Muscular Dystrophy, to:
Parent Project Muscular Dystrophy
401 Hackensack Avenue, 9th Floor
Hackensack, NJ 07601
(Please note that the check is in honor of my name/Chicago Marathon)
All funds raised will benefit Parent Project Muscular Dystrophy (parentprojectmd.org) and go directly toward researching a cure. Your contribution is 100% tax deductible.
Thank you for your support!
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