News

Today, September 7th is an international “Duchenne Awareness Day.” We took this opportunity to launch our video. It aims to inform the public about Duchenne muscular dystrophy and new [...]

The DMD community meets the FDA at the AdCom conference. Testimonial, part 2. Indeed, it was tough for me to attend the AdCom Conference. Throughout the day, monuments of data were built and [...]

On April 25, two representatives from the Force traveled to Washington, DC, to attend the AdCom Conference of the Food & Drug Administration (FDA), which focused on the approval of new [...]

La Force is proud to announce its participation in the funding of a promising research project on osteoprotegerin, also known as “OPG”. Invited to Boston by the Duchenne Alliance specialists [...]

Did you know that February is the Rare Disease Month? And that February 29th, a rare day that only happens four years is International Rare Disease Day? Read more DMD is also a Zebra Because it [...]

Marie-Catherine Du Berger, President Fondation La Force, Duchenne Muscular Dystrophy In our family, the diagnostic hit on October 2013: our son Anakin is stricken with DMD.  The only thing I can [...]