Samantha Lisle Muller
Muscular Dystrophy
Samantha Lisle Muller is a passionate advocate for people living with muscular dystrophy and neuromuscular disorders. Born with congenital myopathy, a rare genetic condition causing progressive muscle weakness, she has transformed personal challenges into a life of service, awareness, and inclusion through her work with the Muscular Dystrophy Foundation of South Africa. She enjoys building meaningful connections, travelling, and discovering new places. Participating in the Bold Beauty Project inspired Samantha to embrace her beauty and strength with renewed confidence. Guided by her faith, she hopes her journey encourages others to feel seen, valued, and empowered to embrace their own unique stories
