A New Dawn for EB: The 2024 debra of America Benefit in LA
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In Loving Memory of Chance Walker (2018-2020)
Travis and LaKeisha Walker are in Mississippi. Chance was our only child and he was 21 months.
Simply put, living with EB hurts, but as cliché as it may sound you need to take the good with the bad. My daughter, Sarah, was born with Recessive Dystrophic Epidermolysis Bullosa (RDEB). She turns 12 this September, and we’re having a sleepover birthday party at a local hotel. We planned early because that’s part of the fun. We pore over party supply catalogs, pick out decorations and favors.