<div>Ben Süleyman Akın 20 şubat 2024 de Burdur'da doğdum. Ağlasun ilçesinin Yeşilbaşköy köyünde yaşıyorum doğduktan 3 ay sonra soğuk algınlığı şikayetiyle hastaneye başvurdum. Yapılan kan tahlilleri sonucunda DMD (Duchenne Musküler Distrofi) tanısı aldım. 1 yıldır fizik tedavi görüyorum. Bu ilacı alamazsam ileride daha büyük sağlık sorunlarıyla karşılaşacağım. DMD, kasları zamanla zayıflatan, ilerleyici bir kas hastalığıdır. Gün geçtikçe basit görünen hareketler bile zorlaşır. 
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<div>Süleyman için bu hastalık; koşarken çabuk yorulmak, merdivenleri çıkamamak ve yaşıtlarıyla aynı şeyleri yapamamanın verdiği sessiz bir mücadeledir. O, her gün biraz daha zorlaşan bir hayatta gülümsemeyi ve güçlü kalmayı öğreniyor. Süleyman'ın mücadelesi, DMD ile mücadele eden tüm çocukların sesi olmaya devam ediyor. Süleyman'ın sağlıklı bir gelecek için ELEVİDYS ilacına ihtiyacı var, bu ilaç Süleyman'ın hayatında dönüm noktası olacak ama bu zorlu yolda senin desteğin çok önemli.

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<div>My name is Süleyman Akın, I was born on February 20, 2024, in Burdur. I live in Yeşilbaşköy village of Ağlasun district. Three months after my birth, I went to the hospital with complaints of a cold, and as a result of blood tests, I was diagnosed with DMD (Duchenne Muscular Dystrophy). I have been receiving physical therapy for a year. If I cannot take this medication, I will face more serious health problems in the future. DMD is a progressive muscle disease that weakens muscles over time. Even seemingly simple movements become increasingly difficult. 
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<div>For Süleyman, this disease is a silent struggle; tiring quickly while running, being unable to climb stairs, and not being able to do the same things as his peers. He is learning to smile and stay strong in a life that gets harder every day. Süleyman's struggle continues to be a voice for all children fighting DMD. Süleyman needs ELEVİDYS medication for a healthy future; this medication will be a turning point in his life, but your support is crucial on this difficult journey.

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