Rare Disease Day
“Rare diseases may be individually rare, but they are collectively common. There are millions of people living with rare diseases. Today and every day, doctors like me care for rare, and it’s our privilege.” - Dr. Wendy Chung
Growing Global Community
Our community is growing! We have nearly 900 followers across our platforms from at least 27 countries. Our social media
2023 Annual Update
On behalf of the entire Channeling Hope Foundation team, we extend our heartfelt gratitude for your support! Your contribution plays
Website Updates
In this edition: What's new on our website | Merchandise available for a limited time | Promotion for Giving Tuesday
Scientific Advisory Board
Introducing the CHF Scientific Advisory Board
We’re excited to announce our Scientific Advisory Board! We are fortunate to be
CHF Webinar Series Kickoff
In case you missed the webinar or want to revisit the content we shared, you can access the recording through the link provided.
CHF Family & Friends Webinar
You can access this past webinar and all webinars through the family resources page on our website. Subscription is required
Thank you for signing up & Greetings from Spain!
Thank you to everyone who has signed up with us! So that we can send you messages of most interest
Officially CHF!
After months of building connections with families and scientists over a shared hope for a world free from NALCN channel
Fundraising Update
🧬August 1, 2023: Our fundraising for NALCN genetic disorders was kicked off with two initial GoFundMes inspired by our children,
