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Monthly Archive for: "September, 2016"
An unprecedented decision by the FDA
By Marie
In News
Posted 19 September 2016

An unprecedented decision by the FDA

The FDA has just announced an unprecedented decision… The children with Duchenne muscular dystrophy were heard because it’s “yes” to Eteplirsen! Eteplirsen was approved! This is absolutely [...]

Duchenne muscular dystrophy (DMD) won’t stop Samuel…
By La Force DMD
In Testimonial
Posted 15 September 2016

Duchenne muscular dystrophy (DMD) won’t stop Samuel…

“When you focus on your dreams and objectives, the disease disappears!” At 22 years old, Samuel Lachaine recently completed his Bachelor’s degree in journalism at UQAM. He also got his first job [...]

Hope for Duchenne muscular dystrophy
By La Force DMD
In News
Posted 6 September 2016

Hope for Duchenne muscular dystrophy

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 [...]

Articles récents

  • The global day of giving
  • EMBARK, gene therapy for the treatment of DMD
  • Part B of MOMENTUM study of SRP-5051 in patients with DMD
  • World Duchenne Awareness Day 2021
  • ENDEAVOR, gene therapy for DMD

Catégories

  • Fundraising
  • in the Medias
  • News
  • Research
  • Testimonial
  • Treatments

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