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The latest news from PTC

  1. A Pioneering Advocate

    Kelly Heger became a nurse after her daughter, Jillian, was diagnosed with AADC deficiency.
    Rare Disease Community, Rare Journeys
    May 10, 2023
    reading time 2 minutes
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  2. Jenna’s Huntington’s Disease Story

    In this issue of Patient Voices, Jenna shares her journey with HD.
    Rare Disease Community, Rare Journeys
    May 8, 2023
    reading time 2 minutes
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  3. Meet Shalom: Writer, Advocate and Artist with Duchenne

    Shalom views Duchenne as a companion and source of inner strength.
    Rare Disease Community, Rare Journeys
    April 25, 2023
    reading time 2 minutes
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  4. Where Experience Can Make a Difference

    From global fellowship program to full-time at PTC: Luke's story.
    Rare Disease Community, Rare Journeys
    April 19, 2023
    reading time 2 minutes
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  5. International Women’s Day: Interview with Isabella Prada

    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…
    Our Culture
    March 8, 2023
    reading time 2 minutes
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  6. Duchenne & Sports: A Winning Combination

    Alexander & Tim share the positive effects of sports for the Duchenne community.
    Rare Disease Community, Rare Journeys
    March 8, 2023
    reading time 3 minutes
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  7. International Women’s Day 2023: Embrace Equity

    March 8 is International Women’s Day (IWD), a global celebration of the social, economic, cultural and political achievements of women around the world. IWD is also call to action for accelerating women’s equality; Embrace Equity is the 2023 theme. Per IWD: The aim of the IWD 2023 #EmbraceEquity campaign theme is to get the world…
    Our Culture
    March 7, 2023
    reading time 3 minutes
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  8. Meet Claudia: A Mompreneur and Duchenne Advocate

    Learn more about Claudia, a mother, caregiver, social media content creator & Duchenne advocate.
    Rare Disease Community, Rare Journeys
    February 21, 2023
    reading time 3 minutes
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  9. A Duchenne Dad and Esports Motivator

    Martin supports his son, who lives with Duchenne, and his passion for online gaming.
    Rare Disease Community, Rare Journeys
    February 2, 2023
    reading time 4 minutes
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  10. Lila Empowers Others to Embrace Who They Are

    Disability activist and performer living with Duchenne, Lila, encourages people to be themselves.
    Rare Disease Community, Rare Journeys
    December 20, 2022
    reading time 2 minutes
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