Skip to content
    • For Researchers
    • Blog
    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
    • Donate
    • DONATE
    Blog

    High School Robotics Team Creates Car for GFPD Kid

    A high school robotics team in Illinois built and donated a custom motorized car to Ethan, a child with PBD. Great work, Mars Wars team!

    http://www.centralillinoisproud.com/story/d/story/metamora-robotics-team-donates-car-to-easter-seals/28149/EtVsB6QB3EqBmaGfHsgPoA

    Recent Posts
    • THE GLOBAL FOUNDATION FOR PEROXISOMAL DISORDERS ANNOUNCES NEW EXECUTIVE DIRECTOR September 16, 2024
    • BACK TO SCHOOL SERIES: TACTILE TECHNIQUES FOR DEAFBLIND LEARNERS September 3, 2024
    • BACK TO SCHOOL SERIES: INDIVIDUALIZED EDUCATION PROGRAM (IEP) September 3, 2024
    • BACK TO SCHOOL SERIES: MODIFICATIONS AND ACCOMMODATIONS August 28, 2024
    • BACK TO SCHOOL SERIES: PYRAMID OF LEARNING August 22, 2024
    • The Impact of Community Connections for GFPD Warriors July 25, 2024
    • Developing Retinal Gene Therapy for Zellweger Spectrum Disorder Question and Answer with Catherine Argyriou, BSc (Hons.), MSc, PhD. July 10, 2024
    • (no title) May 15, 2024
    • Melissa Bryce, Executive Director, to step down in September 2024 March 14, 2024
    • Italian Family Making a Global Impact and Shines a Light on Rare Disease Day March 4, 2024
    Archives
    • September 2024 (3)
    • August 2024 (2)
    • July 2024 (2)
    • May 2024 (1)
    • March 2024 (2)
    • February 2024 (1)
    • December 2023 (6)
    • November 2023 (1)
    • October 2023 (1)
    • April 2023 (1)
    • March 2023 (3)
    • February 2023 (2)
    • January 2023 (1)
    • November 2022 (1)
    • October 2022 (1)
    • September 2022 (1)
    • August 2022 (3)
    • April 2022 (1)
    • March 2022 (1)
    • February 2022 (2)
    • January 2022 (2)
    • December 2021 (2)
    • November 2021 (1)
    • October 2021 (2)
    • May 2021 (2)
    • April 2021 (2)
    • March 2021 (3)
    • February 2021 (23)
    • October 2020 (1)
    • September 2020 (2)
    • June 2020 (2)
    • May 2020 (3)
    • April 2020 (1)
    • March 2020 (2)
    • February 2020 (3)
    • January 2020 (1)
    • December 2019 (3)
    • November 2019 (1)
    • September 2019 (1)
    • August 2019 (1)
    • April 2019 (1)
    • March 2019 (2)
    • February 2019 (2)
    • October 2018 (4)
    • July 2018 (3)
    • May 2018 (1)
    • April 2018 (4)
    • March 2018 (2)
    • February 2018 (4)
    • December 2017 (3)
    • November 2017 (4)
    • October 2017 (6)
    • September 2017 (2)
    • August 2017 (2)
    • July 2017 (2)
    • May 2017 (4)
    • March 2017 (1)
    • February 2017 (1)
    • January 2017 (2)
    • November 2016 (2)
    • October 2016 (2)
    • September 2016 (2)
    • August 2016 (1)
    • July 2016 (1)
    • June 2016 (1)
    • May 2016 (4)
    • April 2016 (1)
    • March 2016 (1)
    • February 2016 (2)
    • January 2016 (2)
    • December 2015 (2)
    • November 2015 (3)
    • October 2015 (1)
    • September 2015 (3)
    • August 2015 (2)
    • July 2015 (3)
    • May 2015 (3)
    • February 2015 (2)
    • October 2014 (3)
    • September 2014 (2)
    • August 2014 (3)
    • May 2014 (6)
    • April 2014 (1)
    • March 2014 (2)
    • February 2014 (3)
    • December 2013 (1)
    • November 2013 (1)
    • October 2013 (5)
    • September 2013 (1)
    • August 2013 (3)
    • July 2013 (1)
    • May 2013 (8)
    • April 2013 (2)
    • February 2013 (1)
    • January 2013 (1)
    • December 2012 (4)
    • November 2012 (1)
    • August 2012 (1)
    • January 2012 (1)
    • December 2011 (1)
    • October 2011 (2)
    • September 2011 (4)
    • May 2011 (2)

    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
    logo-white
    © 2024 by The GFPD.

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

    Newsletter Sign-Up

    Stay connected

      Read our privacy policy

      Tulsa Regional Chamber
      RDDC logo
      • 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

      Login

      Lost your password?