Who We Are
Our backstory
LCN was born out of a parent’s anguish.
In 2023, after 19 years of multiple endoscopic surgeries, our co-founder’s son underwent an open surgery for his type 3b laryngeal cleft. The surgery was tough: four days in a medically-induced coma on a ventilator, a new tracheostomy and G-tube, 18 days in the hospital, and five weeks relocated to a new city 2,700 miles away for the surgery. Upon returning home, the family then isolated for another six months to avoid exposure to any illnesses that could damage the healing repair. (Read Theo’s Journey of ultimate triumph.)
While difficult, that isolation brought time to reflect, and a realization started to grow. The realization that other children and parents were struggling around the world, on a daily basis, with the same birth defect. And the observation that no organization existed to support these families and work with medical professionals to help improve the lives of these children. That newfound awareness - along with the desire to offer resources, connection, and ultimately hope to other struggling families - gradually transformed into an organized effort, and LCN was born in early 2024.
Board of Directors
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Carolyn Schultz
President
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Deb Bachman
Secretary
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Baolu Korst
Treasurer
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Sandy Caputo
Beneficiary & Donor Services Director
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Landon Cotant
Marketing Director
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Cindy Schultz
Fundraising Director
Medical Advisory Board
LCN is proud to work with our esteemed Medical Advisory Board.
Our MAB reviews all educational medical content for accuracy and provides insights and guidance to LCN’s various programs.
LCN is an independent nonprofit organization, not affiliated with any specific provider or center.
All MAB members are volunteers and receive no financial incentives or compensation.
Content on our site does not reflect the individual opinions and views of our MAB members.
If you are interested in joining our MAB, please email info@laryngealcleft.org.
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Caetyn Groner | CCC-SLP
Midland, TX
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Reza Rahbar | DMD, MD
Boston Children's Hospital
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Mike Rutter | BHB, MBChB, FRACs
Cincinnati Children's Hospital
Patient Advisory Committee
LCN honors all laryngeal cleft heroes and is grateful to those who serve on our Patient Advisory Committee.
Through first-hand experience navigating life with a laryngeal cleft, our PAC members offer valuable insights to help guide and improve the work of LCN.
Content on our site does not reflect the individual opinions and views of our PAC members.
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Heather Bachman | MS, LPC
PAC Facilitator
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Markus Bachman
Minnesota
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Theo Schultz
Idaho
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Olivia
Australia