A 501(c)3 organization dedicated to raising awareness, funds, and family support for congenital central hypoventilation syndrome (CCHS), a rare orphan disease.
The 9th Annual International CCHS Day is exactly one month away. Let your light shine for our rare disease on September 23rd and help guarantee a brighter future for our community! For full details, click on the link in bio or go to https://t.co/zbvyXUdFcK.
Tomorrow is CCHS Day! Please help us deliver a unified message of advocacy by posting the following image on your social media accounts. #cchsnetwork#castalightoncchs#cchsday2022 https://t.co/xuWnUcZPdv
The CCHS Network is excited to launch our new logo and brand. Go to https://t.co/nnpFfokrnj for more information and to learn about CCHS Day 2022 happening on November 12th (including the sale of shirts and pins). #cchsnetwork#castalightoncchs#cchsday2022
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Happy CCHS Day! Watch our call to action video below, and post your own wave videos, or tag a friend for the #jointhewaveforcchs challenge. Go to https://t.co/9M6l94oue1 to donate and learn more about this heartbreaking disease