LHF Blog

We have a big announcement!

  Posted on March 25, 2024

We're expanding!

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Expert Physcian Testimonies on SRP-9001

  Posted on May 8, 2023

Hear directly from the SRP-9001 PI's expert views on treatment effect in their patients.

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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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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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