Histoire
Since birth, Saleh and his brother have been living with a rare genetic condition known as epidermolysis bullosa, a disease that causes painful wounds and blisters across their skin, making everyday life a constant struggle. Saleh frequently requires esophageal dilation procedures due to complications from the disease, along with continuous use of medications, disinfectants, sterile dressings, and specialized medical supplies to protect his fragile skin from infection. His situation became even more difficult after the loss of his father, leaving the family in worsening financial conditions and unable to meet the ongoing cost of his care. Today, Saleh urgently needs support to continue his treatment and manage this painful condition with dignity and hope.

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