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December 2011 Update

Follow the link below to read the GFPD’s year-end update letter from President Shannon Butalla:

December 2011 Update

Recent Posts

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
(no title) February 8, 2024
Minor changes to the Inflation Reduction Act (IRA) will make a big difference for rare disease patients. December 13, 2023
NIH grant establishes Mouse Mutant Peroxisome Research Resource December 5, 2023
Pause for the GFPD December 5, 2023
‘Pause’ for rare genetic disorder December 5, 2023
Letter to the editor: Oct. 5 is a day of remembrance for people with PBD December 4, 2023
GFPD Family And Scientific Conference: Warrior Camp Fellowship December 4, 2023
GFPD Family and Scientific Conference – Externally Led – Patient Focused Drug Development November 9, 2023

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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

© 2024 by The GFPD.

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Welcome
Peroxisomal Disorders
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For Researchers
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