LHF Blog


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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