The Browns | Epidermolysis Bullosa Simplex
We hope this story encourages you.... Epidermolysis Bullosa is a condition that effects people of all ages across the world... its known as "The Worst Disease You've Never Heard Of." Our prayer is that as you watch this little glimpse into our lives that you would not just be moved emotionally but you would be inspired to become compassion in action to help support research and help families with similar challenges. Debra is a non-profit organisation dedicated to finding a cure for EB, which affects 1 out of every 20,000 live births in the United States. EB is a rare genetic connective tissue disorder. There are many genetic and symptomatic variations of EB, but all share the prominent symptom of extremely fragile skin that blisters and tears from minor friction or trauma.. EB is always painful, is often pervasive and debilitating, and is in some cases lethal before the age of 30. There is no treatment or cure. Daily wound care, pain management, and protective bandaging are the only options available. For more info or to donate Visit: www.debra.org Help find a cure and be the solution. Thanks Brenden Brown

A Kid with Butterfly Skin (Epidermolysis Bullosa Simplex)

Help change the future for kids like Ella with Epidermolysis Bullosa (EB)

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