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Monthly Archives: November 2012

GFPD Fall 2012 Newsletter

November 3, 2012

The GFPD celebrated its second birthday in October 2012! Check out the GFPD Fall 2012...

Recent Posts

GFPD and the Financial Impact of Rare Disease October 1, 2022
GFPD joins with over 100 rare disease organizations to support Accelerating Kids’ Access to Care Act September 8, 2022
F2FC Groups Now Enrolling August 23, 2022
The third annual GFPD Warrior Walk Run Ride on September 30th – October 2nd August 8, 2022
The GFPD’s Corin Chapman and Catherine Argyriou present at the World Orphan Drug Congress in Boston August 2, 2022
The GFPD and the Rare Disease Community Urges States to Take Advantage of Funding to Screen More Babies April 8, 2022
Governor Youngkin Announces Addition of Two New Disorders to Virginia’s Newborn Screening Program March 23, 2022
Rare Disease Day February 23, 2022
GFPD Supports Legislation for Newborn Screening in Iowa February 20, 2022
The GFPD Creates a Diversity Committee to Promote Greater Health Equity for Warriors and their Families. January 28, 2022

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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.

CONTACT

P.O. Box 33238
Tulsa, OK 74153

Email: contactus@thegfpd.org

Phone: ‪(918) 998-5798‬

Fax: (918) 516-0227

© 2022 by The GFPD.

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

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Welcome
Peroxisomal Disorders
About Us
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Research
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For Researchers
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