Thank you to everyone who has signed up with us! So that we can send you messages of most interest to you, please tell us who are (family member, scientist, etc.) by completing this survey. A handful of NALCN families and 40+ researchers and physicians are only a few days

After months of building connections with families and scientists over a shared hope for a world free from NALCN channel diseases, we officially launched as the Channeling Hope Foundation on July 12, 2023. We're looking forward to making more connections at the first-ever workshop on NALCN, bringing

🧬August 1, 2023: Our fundraising for NALCN genetic disorders was kicked off with two initial GoFundMes inspired by our children, Cora and Amanda. We are grateful to our friends and family who have believed in our cause from the very beginning. We look forward to continuing our fundraising efforts as