Family Resources
We’re Here For You
LCN recognizes the many struggles that come with having a child with a rare or complex disorder. Check out the pages listed in the menu above for a variety of resources that can help families navigate through their laryngeal cleft journey.
Downloadable and Printable One-Pagers
Looking for information to reference or share with medical providers/your community? Check out LCN’s growing list of informational one-pagers. They’re easy to print, share, and use in any way you’d like.
LCN has its own Facebook community where parents, patients, family members, and providers can all share concerns and information.
Laryngeal cleft is a challenging condition for patients, families, and providers. We believe it is important for all community stakeholders to be able to communicate about this birth defect in order to improve the lives of people born with it.
Didn’t Find What You Need?
Please email us at info@laryngealcleft.org and let us know how we can help!