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Angelman Syndrome is a rare genetic condition, affecting around 1 in 15,000 individuals. It often shapes how a child communicates, moves, and experiences the world — requiring lifelong care and support. For Belinda, motherhood also means becoming a translator of silent joy, learning to navigate a world that wasn’t designed with her son in mind. This is a glimpse into that everyday journey. #AngelmanSyndrome #Caregiving #EverydayLife | Give.Asia
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