#PAUSEforTheGFPD

Pause for The GFPD is officially 1 week away!

Below are 8 great ways you can participate leading up to and on Monday, October 5, 2020

Submit a Pause for GFPD Op Ed utilizing the GFPD template.
What is an Op-Ed? Click here to learn more!
Post a video or a picture online with our Pause for The GFPD sign here.
Make sure to tag: @thegfpd.org and use hashtag: #PauseForTheGFPD
Make a donation to The GFPD at thegfpd.org/donate
Share the GFPD Fundraiser on all your social media platforms to help us reach our goal https://www.facebook.com/donate/322172229039273/
Buy GFPD merchandise and share a picture or video of you wearing it to help raise awareness https://www.bonfire.com/store/the-gfpd/
Reach out to a local restaurant to host a curbside/to-go night with a percentage of proceeds benefitting the GFPD. Click here for the form!
Organize and host a Pause for GFPD celebration and fundraiser
Contact katie@thegfpd.org for more information.
Join our Facebook Event and share it with your community https://www.facebook.com/events/628749174700753/

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#PAUSEforTheGFPD

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#PAUSEforTheGFPD

Featured Posts

Anna Violet's journey to a peroxisomal disorder diagnosis | GFPD 2020 Patient Ambassador

Meet 2020 Patient Ambassador, Anna Violet

A bereaved mom's thoughts on grief during the Holidays.

PAUSE for PBD 2019! #PauseforPBD

What is Zellweger Syndrome? Why don’t we call it Zellweger syndrome anymore?

Scientific collaboration bringing GFPD Conference to Washington, DC this summer

Please join our family at the GFPD Conference in Washington, DC this summer

GFPD/STAIR Collaboration Invites Patient Input in Research

GFPD Fall 2016 Newsletter

My experience attending the 2016 Deafblind Symposium

Recent Posts

#PAUSEforTheGFPD

Happy First Day of Summer!!

Building our Little Room – Follow up from “Discovering Our Connections- GFPD Virtual Meetup”

History of peroxisome biogenesis disorder-Zellweger spectrum disorder (PBD-ZSD) Terminology

Mother's Day

Honoring Our Bereaved Mothers

GFPD "Sensing Connections" Grief Support Group | Remembrance & Support

Natalie and Gwendolyn's Rare Disease Week wrap up

Spring update from GFPD Patient Ambassador, Anna Violet

Anna Violet's journey to a peroxisomal disorder diagnosis | GFPD 2020 Patient Ambassador

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