For 13 years, Moza has endured unimaginable pain from a rare skin disease that leaves her body covered in blisters and open wounds. Her skin oozes and emits a foul odor, making each day a fight for survival.

Even as a newborn, Moza showed early signs of the condition – small rashes that spread across her delicate body. Doctors diagnosed her with GEA Disentriform, mild dehydration, and malnutrition. What started as minor symptoms quickly escalated into a devastating illness, leaving her skin fragile and vulnerable.

As Moza grew, the disease worsened. Her body became covered in painful sores, and the constant discomfort left her unable to move freely. Over time, her condition caused developmental delays, leaving her unable to walk or care for herself.

Despite the worsening state of her health, Moza’s father, a humble school janitor, does everything he can to ease her suffering. But his small income is not enough to cover the long-term treatment Moza desperately needs. With each passing day, her wounds deepen, increasing the risk of severe infection.

Moza’s fight is far from over. She needs urgent medical care to prevent further deterioration. Your support can bring hope and healing to Moza, giving her a chance to live free from pain.

Stand with Moza and help her take the next step towards recovery.

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