Keira's dreadful journey began September 17th, 2021, a High fever, foaming at the mouth brought us to BC Childrens Emergency and diagonsed with Brugada Syndrome Sept 21, 2021 at the age of 6.  Save Keira is dedicated to raising awareness about Brugada Syndrome. Keira is one of two pediactric females in the world with this rare syndrome where no cure and no treatment have taken lives. Join us as we work towards a future where families are informed and protected and we can gear towards treatment and a cure.

We're glad you're here to be a part of Keira's story, and helping her live her best life.