My name is Hashem Ayman Mohamed Abdelhamid, and I am the father of Ayman, a 3-year-old child fighting a rare, life-threatening genetic disease.

Ayman has been diagnosed with Iduronate-2-Sulfatase deficiency (MPS II – Hunter Syndrome), which requires lifelong enzyme replacement therapy to slow the progression of the disease and protect his organs.

The only approved treatment is Idursulfase (Elaprase). Unfortunately, this medication is not covered by government health insurance in Egypt, and the monthly cost reaches nearly 1,000,000 EGP, far beyond our family’s financial capacity.

I work in a small grocery shop and have no health insurance. Every day, my child’s condition worsens while the treatment he needs remains out of reach.

I kindly ask for your support to help:

Provide Ayman with his life-saving medication

Cover the cost of ongoing treatment

Give him a chance to live, grow, and smile like any other child

Medical reports and genetic test results have been uploaded to verify Ayman’s diagnosis.

Every donation, no matter how small, brings hope and gives my son a chance at life.