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Today there is no cure for Duchenne muscular dystrophy…

Today there is no cure for Duchenne muscular dystrophy…

But with your help,
there can be one tomorrow

Our Mission

Funding to cure DMD. image

We are 100% focused on raising money to fund research toward a treatment and cure for Duchenne muscular dystrophy.

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Our Story

The moms of sons with DMD. image

The Little Hercules Foundation was created by three moms, two of which have 3 sons—Jake, Noah and Jackson—living with Duchenne MD.

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Our Gift

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Help us fund the research to find a cure for Duchenne Muscular Dystrophy and start saving lives.

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Nov 15

Little Hercules Foundation advocates for Right to Try Bill in Ohio

Today, Kelly Maynard provided proponent testimony on HB 290, Ohio Right to Try Bill.  This bill, if enacted into law, gives patients suffering from terminal illnesses and their doctors a chance to utilize unapproved drugs and/or treatments when no other options exist.  This bill protects doctors from sanctions or penalties when attempting to utilize all therapeutic resources to save a patient’s life – even those that are still in the clinical trial process and not yet approved by the FDA.  Read my testimony HERE.

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