Fragile X Syndrome (FXS) is a genetic condition, affecting around 1 in 4000 males and 1 in 6000 females. It can cause a wide range of difficulties with learning, as well as social, language, attentional, emotional, and behavioural problems. Some may experience connective tissue issues such as difficulty breast-feeding, hypotonia, hyperflexibility, flat feet, recurrent ear infections and mitral valve prolapse. FXS is the most common inherited cause of learning disability.

Support our three peaks challenge team as we take on the ultimate adventure for the Fragile X Society! Inspired by the incredible story of Ernie, a little boy with Fragile X Syndrome, we're pushing ourselves to new heights to make a difference. Your sponsorship will help fund vital support, resources, and research into this rare genetic condition. Every step we take, every pound raised, will bring hope to families like Ernie's. Join us on this epic journey and help us conquer the three peaks for Fragile X