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Monthly Archives: November 2019

Family is at the heart of the GFPD

“You may often hear or see the phrase “GFPD is family,” and I fully and...

24
Nov

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

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

© 2024 by The GFPD.

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
About Us
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