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GFPD joins with over 100 rare disease organizations to support Accelerating Kids’ Access to Care Act

Rare Disease Orgs Letter

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Recent Posts

GFPD BACK TO SCHOOL SERIES: EXTENDED SCHOOL YEAR April 21, 2025
2024 #PAUSEfortheGFPD Op-Eds November 21, 2024
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

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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
Phone: 918-212-4815
Email: contactus@thegfpd.org

© 2025 by the GFPD.

Disclaimer: This website is not designed to diagnose, advise, or provide medical opinions, treatment, or services. It is for general knowledge purposes only. Please consult a licensed medical professional with all questions and concerns regarding a medical condition.

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

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Welcome
- Welcome from the Executive Director
Peroxisomal Disorders
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