The EI Cure Project aims to fund research for children and adults affected with rare blistering skin disease Epidermolytic Ichthyosis (EI).

The EI Cure Project was founded by Helen and Tom Lill in 2023 to fund research into finding a cure for their daughter's 1 in 300,000 rare blistering skin disease Epidermolytic Ichthyosis (EI). The EI Cure Project is now a global organisation which joins patient advocates with world-class leading Doctors, Researchers, and Scientists working together to find better treatment choices for all those affected with Epidermolytic Ichthyosis (EI).