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CCHS Day 2019 - Teddy Joe Fox T-Shirt Fundraiser

Organized by Teddy Joe Fox CCHS Day 2019 Fundraiser
CCHS Day 2019 - Teddy Joe Fox T-Shirt Fundraiser Fundraiser - unisex shirt design - front
CCHS Day 2019 - Teddy Joe Fox T-Shirt Fundraiser Fundraiser - unisex shirt design - back
CCHS Day 2019 - Teddy Joe Fox T-Shirt Fundraiser shirt design - zoomed
CCHS Day 2019 - Teddy Joe Fox T-Shirt Fundraiser Fundraiser - unisex shirt design - front
CCHS Day 2019 - Teddy Joe Fox T-Shirt Fundraiser Fundraiser - unisex shirt design - back
CCHS Day 2019 - Teddy Joe Fox T-Shirt Fundraiser shirt design - zoomed
Bella + Canvas Ultra Soft Pullover Hoodie

Buy a TJF Shirt or Hoodie to raise funds now and raise awareness year round!

verified-charity
All funds raised will go directly to CCHS Family Network
$2,230 raised
46 items sold of
100 goal
Thanks to our supporters!
$55
Bella + Canvas Ultra Soft Pullover Hoodie, Unisex - Deep Heather
Bella + Canvas Ultra Soft Pullover Hoodie
Unisex - Deep Heather
  • CCHS Day 2019 - Teddy Joe Fox T-Shirt Fundraiser Fundraiser - unisex shirt design - small
  • CCHS Day 2019 - Teddy Joe Fox T-Shirt Fundraiser Fundraiser - unisex shirt design - small
Organized by Teddy Joe Fox CCHS Day 2019 Fundraiser

About this campaign

Our Son Teddy Joe Fox was diagnosed with an incredibly rare disease called CCHS (Congenital Central Hypoventilation Syndrome) in February. There are only around 1200 cases diagnosed worldwide, and almost all research funding for treatment or a cure comes from private donations. We have made it our mission to help the CCHS Network raise these much needed funds. There are many ways to donate for CCHS Day. The easiest is going directly to the CCHS Network website :

https://www.cchsnetwork.org/get-involved/donate/

So many of Teddy's friends have already been so generous with donations already. For anyone who wants to spread the word and raise funds now for research, and spread the word/awareness year round, we have created TJF CCHS Day T-shirts and Hoodies. All proceeds will go to the CCHS Network.

The 5th annual CCHS (Congenital Central Hypoventilation Syndrome) day is on Nov 9th.The CCHS Family Network is a non-profit, tax-exempt organization registered in the United States. Our efforts focus primarily on education and support of our families and CCHS patients, inter-family and family-physician communication, and supporting and facilitating CCHS research.

Supporters

Susie garcia 1 item
Bruno Memme 2 items

Let’s find a cure!

Maxwell Shapiro 1 item
Anonymous 1 item
Noah Fox 2 items
Jen B 1 item

For my favorite little CCHS warrior, Teddy Joe

Joshua Olstein 1 item

For my guy Teddy Joe Fox

Amy Fox 1 item
Sheroum Kim 1 item
Shane Malach 1 item + $50

Bestest boy! ❤️

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