The Sel de Vie Story
Sel de Vie, or Salt of Life, is a jewelry line inspired by the need to find a cure for Cystic Fibrosis (CF).
Thirty thousand children and young adults in the United States fight this challenging and life-threatening genetic disease, affecting mostly the lungs and GI system by clogging important organs with thick, sticky mucus.
The name Sel de Vie comes from the fact that salt plays such an important role for those affected by CF.
Each necklace in our collections are named after children in the Charlotte, North Carolina, area who fight Cystic Fibrosis.
Sel de Vie is proud to give 25% of all proceeds towards important CF research with the hopes of increasing the life expectancy and improving the quality of life for those living with CF. Each necklace you buy gets us one step closer to the hopeful reality of people with CF living normal, healthy lives.
Meet the Team
Mallery Horton is our jewelry designer and mom to Sel de Vie inspiration, Palmer. Palmer was born with Cystic Fibrosis in January 2014. Since Palmer was born, Mallery has become an active advocate for advancing CF research and educating people about the genetic disease.
Ashley Sullivan manages Sel de Vie's online content. She is inspired and awed by Palmer's resiliency and loves having the opportunity to partner with one of her closest friends for something so meaningful.