Skip to content
    • For Researchers
    • Blog
    The Global Foundation for Peroxisomal DisordersThe Global Foundation for Peroxisomal Disorders
    • Donate
    • Welcome
    • Peroxisomal Disorders
      • What are peroxisomal disorders
      • Types of peroxisomal disorders
      • Signs and Symptoms
      • How do I get a diagnosis?
      • Facts at a Glance
    • About Us
      • Our Work
      • Our Mission
      • Our History
      • Achievement Timeline
      • Board of Directors
      • Medical and Scientific Advisors
      • Our Team
      • Our Partners
      • Impact Reports
    • Support and Resources
      • Family Directory
      • A Letter to Newly Diagnosed Parents
      • Information for Newly Diagnosed Patients
      • Care Resources
      • Bereavement Resources
      • Support Groups
      • Meet our GFPD Warriors
      • Equipment Exchange
    • Research
      • Current Research
      • Clinical Trials
      • Scholarly Articles
      • Past Scientific Conferences
    • More
      • Walk Run Ride
      • Take Action
      • Advocate
      • Pause for The GFPD (old)
      • Fundraise
      • Donate
      • Join a Committee
      • News
      • Shop GFPD Gear
    • Donate

    Our Partners

    To view our partners’ corresponding pages, follow their logo.

    Newsletter Sign-Up

    Stay connected

      Read our privacy policy

      GFPD Values

      Our Mission

      To improve the lives of individuals with Peroxisomal Disorders by funding research, championing scientific collaboration, and empowering families and professionals through educational programs and support services.

      GFPD Diversity Statement

      Peroxisomal disorders impact individuals of every race, ethnicity, socio-economic status, sex, gender, sexual orientation, belief system, ability, and age. Using our values of inclusion and community as our guide, The GFPD is committed to promoting acceptance and advocating for equality and equity in healthcare and educational settings while combating prejudices, discrimination, and biases. We will engage in this important dialogue with our diverse community by listening and learning from our families, researchers, and professionals.

      CONTACT

      P.O. Box 33238
      Tulsa, OK 74153

      CONTACT US

      Email: contactus@thegfpd.org

      Phone: ‪(918) 998-5798‬

      Fax: (918) 516-0227

      logo-white
      © 2022 by The GFPD.

      Images on this site were contributed by families and may not be used without permission.

      Research & Resources --------->
      Rare Foundation Alliance
      Tulsa Regional Chamber
      NORD 2022
      RDDC logo
      • Welcome
      • Peroxisomal Disorders
        • What are peroxisomal disorders
        • Types of peroxisomal disorders
        • Signs and Symptoms
        • How do I get a diagnosis?
        • Facts at a Glance
      • About Us
        • Our Work
        • Our Mission
        • Our History
        • Achievement Timeline
        • Board of Directors
        • Medical and Scientific Advisors
        • Our Team
        • Our Partners
        • Impact Reports
      • Support and Resources
        • Family Directory
        • A Letter to Newly Diagnosed Parents
        • Information for Newly Diagnosed Patients
        • Care Resources
        • Bereavement Resources
        • Support Groups
        • Meet our GFPD Warriors
        • Equipment Exchange
      • Research
        • Current Research
        • Clinical Trials
        • Scholarly Articles
        • Past Scientific Conferences
      • More
        • Walk Run Ride
        • Take Action
        • Advocate
        • Pause for The GFPD (old)
        • Fundraise
        • Donate
        • Join a Committee
        • News
        • Shop GFPD Gear
      • For Researchers
      • Blog