LHF Blog

Duchenne has long been a part of our family's past. But we don't have to unpack our things and live there.

  Posted on June 26, 2018

Read our latest blog post by one of our Personalized Access Team (PACT) Managers, Amy Aikins, whose long family history with Duchenne inspires her to help others, including her son, live their best lives by helping them get what they need.

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When your darkest day leads to a grown-up dream come true

  Posted on May 26, 2018

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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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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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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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