Limb-Girdle Muscular Dystrophy (LGMD) is a rare, progressive genetic disorder causing muscle atrophy in the hip and shoulder regions, with various subtypes distinguished by specific disease genes and inheritance patterns. Studies estimate its prevalence between 1 in 14,500 to 1 in 123,000 individuals, impacting millions worldwide.

We’re proud to support Rare Disease Hub and the Ministry of Health in raising awareness through the Limb Girdle Muscular Dystrophy Doctors-Family Gathering event, featuring expert insights to enhance understanding and support for those affected. Join us for LGMD awareness day and let’s “Show Your Colours” together! 🎗️ #LGMDAwareness #RareDiseaseHub #ShowYourColours