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International SCN8A Awareness Day

Organized by Juliann Bradish
Po8736122 front
International SCN8A Awareness Day Fundraiser - unisex shirt design - front
International SCN8A Awareness Day shirt design - zoomed
International SCN8A Awareness Day Fundraiser - unisex shirt design - front
International SCN8A Awareness Day Fundraiser - unisex shirt design - back
International SCN8A Awareness Day Fundraiser - unisex shirt design - front
International SCN8A Awareness Day Fundraiser - unisex shirt design - back
International SCN8A Awareness Day Fundraiser - unisex shirt design - front
International SCN8A Awareness Day Fundraiser - unisex shirt design - front
International SCN8A Awareness Day Fundraiser - unisex shirt design - front
Next Level Tri-Blend Hooded Long Sleeve T-shirt

SCN8A Awareness Day Products Support The SCN8A Registry (www.scn8a.net)

verified-charity
All funds raised will go directly to The Cute Syndrome Foundation, Inc.
$1,060 raised
92 items sold of
150 goal
Thanks to our supporters!
$22
Next Level Tri-Blend Hooded Long Sleeve T-shirt, Next Level Hoodie - Heather White
Next Level Tri-Blend Hooded Long Sleeve T-shirt
Next Level Hoodie - Heather White
  • International SCN8A Awareness Day Fundraiser - unisex shirt design - small
  • International SCN8A Awareness Day Fundraiser - unisex shirt design - small
  • International SCN8A Awareness Day Fundraiser - unisex shirt design - small
  • International SCN8A Awareness Day Fundraiser - unisex shirt design - small
  • International SCN8A Awareness Day Fundraiser - unisex shirt design - small
  • International SCN8A Awareness Day Fundraiser - unisex shirt design - small
Organized by Juliann Bradish

About this campaign

SCN8A Epilepsy is a rare disorder that is known to affect around 150 individuals worldwide--causing severe epilepsy, developmental delay, and other medical challenges. The gene SCN8A was isolated in humans by Michael Hammer, PhD, a geneticist who found the gene in his own daughter, Shay, soon after her death in 2011. We celebrate SCN8A Awareness Day on February 9th, Shay Hammer's birthday. ​

This campaign was created by The Cute Syndrome Foundation and will 100% of the proceeds will be used to support the SCN8A Registry found at www.scn8a.net.

For more information and SCN8A resources, visit http://www.scn8aawarenessday.net/

Supporters

Mendy 1 item

for my daughter Lilly, who has the SCN8A mutation

Anonymous 4 items

For Leo and to support scientists who dedicate their life to finding a cure for SCN8A.

Carulla family 7 items

For María

Alejandra Encinas 1 item
Heather Christie 5 items

For my son, who inspires me with his happiness despite his daily battle.

Jolanda Laagwater 1 item

For my son Stijn

Shelley 2 items

For Nico xoxo

Dominic 1 item
Gina Bittner 1 item
Anonymous 1 item

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