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SHOW YOUR STRIPES

Organized by National Organization for Rare Disorders
Front large extended
SHOW YOUR STRIPES Fundraiser - unisex shirt design - front
SHOW YOUR STRIPES Fundraiser - unisex shirt design - back
SHOW YOUR STRIPES shirt design - zoomed
SHOW YOUR STRIPES Fundraiser - unisex shirt design - front
SHOW YOUR STRIPES Fundraiser - unisex shirt design - back
SHOW YOUR STRIPES shirt design - zoomed
SHOW YOUR STRIPES Fundraiser - unisex shirt design - front
SHOW YOUR STRIPES Fundraiser - unisex shirt design - back
SHOW YOUR STRIPES shirt design - zoomed
SHOW YOUR STRIPES Fundraiser - unisex shirt design - front
SHOW YOUR STRIPES Fundraiser - unisex shirt design - back
SHOW YOUR STRIPES shirt design - zoomed
SHOW YOUR STRIPES Fundraiser - unisex shirt design - front
SHOW YOUR STRIPES Fundraiser - unisex shirt design - back
SHOW YOUR STRIPES shirt design - zoomed
Gildan Softstyle Jersey T-shirt

1 in 10 Americans are living with a rare disease

verified-charity
All funds raised will go directly to National Organization for Rare Disorders, Inc.
$1,230 raised
174 items sold of
150 goal
Thanks to our supporters!
$20
Gildan Softstyle Jersey T-shirt, Unisex - Heather Sapphire
Gildan Softstyle Jersey T-shirt
Unisex - Heather Sapphire
  • SHOW YOUR STRIPES Fundraiser - unisex shirt design - small
  • SHOW YOUR STRIPES Fundraiser - unisex shirt design - small
  • SHOW YOUR STRIPES Fundraiser - unisex shirt design - small
  • SHOW YOUR STRIPES Fundraiser - unisex shirt design - small
  • SHOW YOUR STRIPES Fundraiser - unisex shirt design - small
Organized by National Organization for Rare Disorders

About this campaign

About Rare Disease Day® It’s a day to raise awareness of the over 7,000 rare diseases that impact over 300 million people globally!

The National Organization for Rare Disorders (NORD) is proud to be the official US partner for Rare Disease Day. We work with our sister organization EURORDIS (Rare Diseases – Europe) and others all around the world to drive an international campaign that shines a light on rare diseases and advocates for health equity for all those living with a rare disease. Visit the international Rare Disease Day site for additional information and resources at rarediseaseday.org.

Join us as we support and celebrate Rare Disease Day 2024!

Supporters

Susan Medalie 1 item

I have a rare disease

Amanda 3 items

For our son

Anonymous 2 items

Born with a rare disability

Kelly Dinoia 1 item
Terri Whisenhunt 2 items

My son has WAGR Syndrome.

Meghan Dominick 1 item

My son Luciano was diagnosed with Cardiofaciocutaneous syndrome

Anonymous 1 item
Anita Russell 1 item
Elise Faulk 1 item
Anonymous 1 item

GAD65 autoimmunity, eosinophilic esophagitis, empty sella syndrome, trigeminal neuralgia

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