Ebrahim’s story
Ebrahim was 6 years old when he was diagnosed with Duchenne muscular dystrophy, a genetic disorder that leads to progressive muscle weakness. Despite his condition, 16-year-old Ebrahim has always remained optimistic and determined. His older sister, just a year ahead of him in school, is his biggest supporter.
Ebrahim’s love for learning, especially in the field of biology, is unparalleled. He excels in school and dreams of a future where he can make groundbreaking discoveries in science. Football is another passion of his, but he can no longer play due to his inability to walk. Today, he revels in watching football games with his friends.
A new medication that slows the progression of the disease has brought renewed hope to Ebrahim and his family. This promising treatment could significantly improve his quality of life, enhancing his strength, mobility, and reducing his pain.
Unable to afford the treatment, his parents share their heartfelt plea: "Our beloved son Ebrahim has shown incredible strength and intelligence since his devastating diagnosis. He dreams of a future where he can live like any other child. This new medication offers a glimmer of hope that we desperately cling to."
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Get well soon ❤️