He suffers from a genetic disease .. And he needs 42 thousand to complete the treatment

4 Donors Contribute 60,000 Dirhams for Medicines for "Muhammad"

Four donors paid 60 thousand dirhams out of a total of 102 thousand and 340 dirhams for the cost of medicines for the child (Muhammad - 6 years old - Pakistani), who suffers from a genetic genetic disease.

The first donor paid 30,000 dirhams, while another guaranteed the payment of 15,000 dirhams, and three 10,000 dirhams, while the latter was charged with 5,000 dirhams, and the child's father is still appealing to someone to help him find the remaining amount of 42,000 dirhams.

The "hotline" coordinated between the donors and the Department of Islamic Affairs and Charitable Activities in Dubai to transfer the donation amount to the patient's account at the hospital.

The patient’s father expressed his happiness with the generous donation, and the donors ’standing with his son in his suffering, in light of the circumstances he is going through, and he hopes to complete the amount of medicines he needs.

On the ninth of September, Emirates Today published the story of Muhammad’s suffering with a genetic disease since his birth, which is an acute disorder in bone growth and curvature in the spine. According to Tawam Hospital, the patient needs to take an enzyme Al-vein route, weekly, for four months, at a cost of 102,340 dirhams.

Abu Muhammed said: “My son has been suffering from the disease since birth that has caused him many health problems, such as a curvature in the spine, and one of his legs is shorter than the other, as well as his hands, and he has undergone medical examinations and analyzes at Tawam Hospital, and doctors confirmed that he has a disease Jenny, what causes skeletal dysplasia, which is a severe disturbance in bone growth, and abnormal curvature of the spine, and if he does not undergo treatment, his condition will worsen, and his bone growth will not be corrected properly.

He added: “Doctors have confirmed that my child needs an enzyme that is given to him intravenously every week, and needs treatment for a period of four months, at a cost above my modest financial capabilities, knowing that my child has a (Aounak) card, and he has consumed the amount allocated to him in the card, which requires completion of his treatment with payment. Personal, as I need to cover the costs of his treatment for a period of four months until the (Aounak) card is renewed at the beginning of next year, and his health condition requires him to take regular therapeutic doses before the disease worsens. ”

He continued: “I do not know how to manage my life's affairs from the living expenses of my family, so how can I manage the costs of treating my child, as I have previously approached foundations and charities to help me, and I did not find any response, and I do not know what to do in light of my son’s need for treatment, so I appeal to good people. Kind-hearted people help me to heal my son. ''

“I used to work in a private sector company, and due to the outbreak of the (Corona) pandemic, I stopped working, and a living salary of 900 dirhams is being paid, and I have children studying in schools,” Abu Muhammad reported. "I have fees that I do not know how to pay, in addition to the monthly rent of 1400 dirhams."

- The

hereditary disease caused "Muhammad" an acute disorder of bone growth and a curvature of the spine.