John Hudson lives with epidermolysis bullosa (EB), a rare condition that makes his skin incredibly fragile and turns everyday life into a constant battle of care and pain. Through Special Books by Special Kids, his story has touched millions, not just for his resilience, but for the unwavering devotion of his father. From daily bandage changes to endless hospital visits, his dad has never left his side, carrying both the physical and emotional weight with quiet strength. Their bond has become a
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John Hudson lives with epidermolysis bullosa (EB), a rare condition that makes his skin incredibly fragile and turns everyday life into a constant battle of care and pain. Through Special Books by Special Kids, his story has touched millions, not just for his resilience, but for the unwavering devotion of his father. From daily bandage changes to endless hospital visits, his dad has never left his side, carrying both the physical and emotional weight with quiet strength. Their bond has become a
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Grab a tissue: The family of John Hudson Dilgen, a 16-year-old living with a rare skin disease, received the keys to a brand new, mortgage-free, handicapped-accessible home in Tottenville -- courtesy of the Tunnel to Towers Foundation. https://www.silive.com/news/2018/11/cheers-tears-as-staten-island-teen-with-rare-disease-receives-new-home.html | Staten Island Advance
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