The latest news from PTC

Our passionate colleagues from Northern Europe cycled 40km this June to raise money and awareness for Duchenne muscular dystrophy (Duchenne). The initiative supported ‘De Duchenne 40’, organized by Duchenne Parent Project Netherlands, to further research and better care for young adults with Duchenne, so that they live to be at least 40 years old. Camilla…

Through recumbent trike riding, Kyle was able to approach the roadblock that was his FA diagnosis.

Imagine being unable to experience the delight of eating food in a restaurant without fear. For people living with the rare disease familial chylomicronemia syndrome (FCS), this is their unfortunate reality. FCS, which affects one in 700,000 to one million people, prevents the body from breaking down fat, or triglycerides, leading to an accumulation in…

Ethan’s passion for astronomy and physics is “out of this world.”

Kelly Heger became a nurse after her daughter, Jillian, was diagnosed with AADC deficiency.

In this issue of Patient Voices, Jenna shares her journey with HD.

Shalom views Duchenne as a companion and source of inner strength.

From global fellowship program to full-time at PTC: Luke's story.

Sorority and team spirit Today, International Women’s Day, we’re sharing the story of a PTC employee that we are proud to have as part of our team: Isabella Prada, Executive Director, Associate General Counsel & Compliance – LATAM and Data Protection Officer LATAM. Isabella has been with us for four years, leading a department made…

Alexander & Tim share the positive effects of sports for the Duchenne community.