Community saves young boy with rare disease

Published March 24th, 2024 - 08:58 GMT
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ALBAWABA - In a very touching display of kindness, a community of people in Oman has come together to support five-year-old Suleiman Al Maskari, who is battling Duchenne muscular dystrophy (DMD), a rare genetic disease. His treatment requires a single injection that costs around $2.1 million, which the community is determined to raise through donations.

The hashtag “#Save_Suleiman” is trending on social media in Oman, with calls for donations via the “Jood” platform to raise the necessary funds for Suleiman’s treatment. The goal is to raise one million Omani riyals (around $2.6 million) to purchase the specialized injection needed to combat this disease.

Community saves young boy with rare disease

Community

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Despite initial confusion about the fundraising target, the community has rallied around the cause, with people like Khalid bin Amer emphasizing the importance of supporting Suleiman. He spoke about how even small contributions can still make a large impact on the young boy’s life.

Local leader, Abdul Hakim Al-Salhi, has also decided to join the effort, urging citizens to donate and come together to help Suleiman in his time of need if they can. The community’s support has been crucial in providing the necessary treatment for the sick child, who is currently undergoing medical care in Oman.

Community

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In addition to raising funds for Suleiman’s treatment, medical professionals in Oman advise preventive measures such as genetic screening before marriage to identify potential risks of genetic diseases like DMD. By raising more awareness and taking proactive measures, the community hopes to support people like Suleiman and prevent the spread of such rare diseases to anyone in the future.

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