LHF Blog

Disco For Duchenne

  Posted on April 23, 2018

When I first heard of Duchenne Muscular Dystrophy (DMD) and The Little Hercules Foundation (LHF), I was surprised by how close to home it really was. The first thought in my mind was… I can’t even imagine.

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2018 Little Hercules Golf Classic

  Posted on March 30, 2018

“We want to do a golf outing but we don’t know anything about golf.” And with those words in February of 2016 the Little Hercules Golf Classic was born.

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Oregon Fulfills Its Obligations to Duchenne Patients (For Now)

  Posted on October 14, 2017

Little Hercules Foundation continues to organize patients and advocates in our Duchenne community to educate state Medicaid boards on DMD and the critical need for them to allow access to FDA approved treatments.

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A Wake Up Call For Millions With A Rare Disease

  Posted on July 12, 2017

Just a year ago, there was not a single FDA-approved treatment option available to patients with Duchenne muscular dystrophy. However, thanks to the FDA’s Accelerated Approval Program, a 25-year old FDA process that Congress expanded in 2012, treatments can now get to market faster than the traditional approval process.

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New website, renewed commitment to fight Duchenne...

  Posted on June 19, 2017

Here we are, 4 years after launching Little Hercules Foundation.  What started as a desire to raise money to fund research that would hopefully save my son’s life, has expanded into so much more.  

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Little Hercules Foundation relies on the generosity of individuals around the world, like you, who believe in our mission and in the power to make a difference in the lives of those diagnosed with — and families fighting against — Duchenne muscular dystrophy.






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