LHF Blog

2019 Little Hercules Golf Classic Event Details

  Posted on September 28, 2019

We are excited to see each of you on Monday morning.  

Please take a moment to read through the information below this weekend.  It includes information for those playing golf or those wishing to attend the after-party or bid on silent auction items.


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Let's Talk....

  Posted on August 2, 2018

Read our latest blog post about how simply starting a conversation leads to meaningful change.

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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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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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