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    The Global Foundation for Peroxisomal DisordersThe Global Foundation for Peroxisomal Disorders
    • Welcome
      • Welcome from the Executive Director
    • Peroxisomal Disorders
      • Facts at a Glance
      • How do I get a diagnosis?
      • Signs and Symptoms
      • Types of peroxisomal disorders
      • What are peroxisomal disorders
    • About Us
      • Achievement Timeline
      • Board of Directors
      • Impact Report
      • Medical and Scientific Advisors
      • Our History
      • Our Mission
      • Our Partners
      • Our Team
      • Our Work
    • Support & Resources
      • A Letter to Newly Diagnosed Families
      • Bereavement Resources
      • Care Resources
      • Equipment Exchange
      • Family Directory
      • GFPD Support Groups
      • Information for Newly Diagnosed Patients
      • Meet our GFPD Warriors
      • Request Support
    • Research
      • Clinical Trials
      • Current Research
      • 2024 Externally-Led Patient-Focused Drug Development Meeting
      • Fellowships
      • Past Scientific Conferences
      • Scholarly Articles
      • GFPD Patient Registry
    • Events
      • Rare Disease Day
      • Past Conferences
      • Pause for the GFPD
      • Walk Run Ride
    • More
      • Advocate
      • Community Directory
      • Donate
      • Fundraise
      • Hope Hero
      • Join a Committee
      • News
      • Shop GFPD Gear
      • Take Action
      • Warrior’s Wish
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    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.

    • P.O. Box 33238 Tulsa, OK 74153
    • Email: contactus@thegfpd.org
    • Phone: ‪(918) 998-5798‬
    • Fax: (918) 516-0227
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    © 2024 by The GFPD.

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

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      Tulsa Regional Chamber
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      • Welcome
        • Welcome from the Executive Director
      • Peroxisomal Disorders
        • Facts at a Glance
        • How do I get a diagnosis?
        • Signs and Symptoms
        • Types of peroxisomal disorders
        • What are peroxisomal disorders
      • About Us
        • Achievement Timeline
        • Board of Directors
        • Impact Report
        • Medical and Scientific Advisors
        • Our History
        • Our Mission
        • Our Partners
        • Our Team
        • Our Work
      • Support & Resources
        • A Letter to Newly Diagnosed Families
        • Bereavement Resources
        • Care Resources
        • Equipment Exchange
        • Family Directory
        • GFPD Support Groups
        • Information for Newly Diagnosed Patients
        • Meet our GFPD Warriors
        • Request Support
      • Research
        • Clinical Trials
        • Current Research
        • 2024 Externally-Led Patient-Focused Drug Development Meeting
        • Fellowships
        • Past Scientific Conferences
        • Scholarly Articles
        • GFPD Patient Registry
      • Events
        • Rare Disease Day
        • Past Conferences
        • Pause for the GFPD
        • Walk Run Ride
      • More
        • Advocate
        • Community Directory
        • Donate
        • Fundraise
        • Hope Hero
        • Join a Committee
        • News
        • Shop GFPD Gear
        • Take Action
        • Warrior’s Wish
      • Donate
      • For Researchers
      • Blog