A small change in one gene can influence how the body develops.
Every scientific discovery can help to create better care and future treatments.
Even a single act of support has far-reaching effects.
Our 2026 Quest for a Cure gala will celebrate the extraordinary impact that our community has had on Kabuki syndrome research.
Your presence may seem like a small step, but it is not. You will help move this work forward in extraordinary ways.
6:00 PM - Cocktail Hour
7:00 PM - Dinner and Program
Leila Zegna
Roya's Mom
Founding Partner, Kindred Capital
Dr. Margaret Adam
Physician, Seattle Children's Hospital
Professor, University of Washington School of Medicine
Kevin Brassil
Student, Elmhurst College
Stephanie Manning
Joey's Mom
Operating Partner, Lerer Hippeau
Email Mackay Gunn for more info:
mackay@kabukisyndromefoundation.org