Her Pain Is Real. Every Single Day.
Shamila is 7. She has Epidermolysis Bullosa (EB), a rare disease where her skin tears and blisters from the slightest touch. A bath feels like boiling water on open wounds. Getting dressed rips her skin. At night, she cannot find a position that doesn't hurt, so she cries until exhaustion takes her.
Her mother changes her bandages for hours every morning, trying not to cause more pain. The specialized silicone dressings she needs cost more than the family earns in a month. They have already sold their furniture, borrowed from everyone they know, and skipped meals to buy pain medication. They have nothing left to sell.
This is not about a cure we cannot afford. This is about tonight. It's about giving a little girl the basic medical supplies to reduce her agony, to sleep for a few hours without screaming. All money goes DIRECTLY to her family. There is no organization taking a cut. Just a mother trying to keep her daughter alive and as comfortable as possible.
Join the Angels Who Are Helping Shamila
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