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The latest news from PTC

  1. Supporting and Empowering the Rare Disease Community

    When you speak with our Global Patient Engagement (PE) Team, you can feel the passion and care they have for the patients they serve. At PTC, we have dedicated PE teams covering the U.S., Latin America, and EMEA (Europe, Middle East and Africa). The PE team is an incredibly important function of PTC, as they…
    Rare Disease Community
    August 30, 2023
    3 minutes
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  2. Take on Duchenne Podcast: A Scientist’s Quest to Solve Duchenne Muscular Dystrophy

    Dr. Ellen Welch is the Chief Scientific Officer at PTC who has been researching and tackling Duchenne for more than 20 years. In this podcast episode, Dr. Welch reflects on scientific advances in the last two decades and how it has contributed to progress in the Duchenne space.    She also explains the growing appreciation…
    Rare Disease Community
    August 18, 2023
    2 minutes
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  3. Continuum of Development

    Investing in future PTC leaders and establishing a path for their successful growth was foundational to the creation of the Emerging Leaders (EL) program at PTC. The PTC Leadership Team recognized that it was essential to create a continuum of development and community for future leaders within PTC, with the goal of establishing a healthy…
    Our Culture
    August 2, 2023
    2 minutes
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  4. Living Independently Gives Philip a New Perspective

    For Philip, "everything is possible if you look at it from a different lens."
    Rare Disease Community, Rare Journeys
    July 17, 2023
    2 minutes
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  5. PTC Northern Europe team Raises Money and Awareness for Duchenne with Cycling for De Duchenne 40

    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…
    Rare Disease Community
    July 12, 2023
    2 minutes
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  6. Riding Through Roadblocks

    Through recumbent trike riding, Kyle was able to approach the roadblock that was his FA diagnosis.
    Rare Disease Community, Rare Journeys
    July 12, 2023
    3 minutes
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  7. PTC Partners with FIPFA to Support Powerchair Football World Cup 2023

    People living with rare diseases have many strengths, abilities and ambitions. One of them is playing and engaging in sports. This October, the 2023 FIPFA Powerchair Football World Cup is taking place in Sydney, Australia and the world’s best powerchair footballers are coming together to compete for the 2023 trophy. PTC is proud to support…
    Rare Disease Community
    June 19, 2023
    2 minutes
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  8. Eat Without Fear

    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…
    Rare Disease Community
    June 7, 2023
    3 minutes
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  9. Ethan Shares His Passion for Astrophysics

    Ethan’s passion for astronomy and physics is “out of this world.”
    Rare Disease Community, Rare Journeys
    May 18, 2023
    2 minutes
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  10. Tenacious Ferocity

    Jonathan and his entire family’s advocacy efforts are driven by what he calls “tenacious ferocity”.
    Rare Disease Community, Rare Journeys
    May 17, 2023
    3 minutes
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