About Us

Faye, as a new mom; started up Bambini Co. with inspiration from her daughter, Adeline. Adeline was born with Glycogen Storage Disease, a genetic disorder where her liver is missing only one enzyme which is responsible for breaking down glycogen into the useable form of energy, glucose. Without the ability to metabolize sugars, Adeline lives life by the clock with a constant feeding regimen through her feeding tube and risk of severe hypoglycaemia. Adeline cannot have lactose, fructose and sucrose. Therefore, no dairy, fruits or candies for Adeline. GSD is a rare disease and effects 1 in 100,000 children around the world. There is no cure at the moment but hope is near. Human clinical trials with gene therapy commenced as of February of 2018 and 9 patients have been trialed for phase 1-3.  The research continues and it is Faye's dream for Adeline to one day have ice cream with all her GSD friends from around the world.

Our baby bandana bibs are handcrafted with love and gender neutral so it can be passed from siblings to friends; raising awareness along the way. A portion of all sales of Bambini products goes towards Adeline's fund for a cure. And all proceeds from the sales of Adeline's Awareness special edition baby bandana bibs are donated towards her cause.

Every dollar counts and every person that learns about this rare disease matters. For more information and to follow Adeline's GSD journey please visit adelinesawareness.com

Thank you for your generosity and support!