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Alpaslan has Spinal Muscular Atrophy (SMA). SMA is a rare, genetic, & progressive disease that affects nerves & muscles, causing muscles to become increasingly weak. This may affect crawling, walking ability, breathing, swallowing, & the movements of the arm, hand, head & neck. There are different forms of SMA & a wide spectrum of how severely children, young people & adults are affected. The most common form of SMA is broadly known as ‘5q SMA’. This condition can affect infants & children but the milder forms can also affect adults. There are four main types of SMA: 1, 2, 3 & 4 based on the age that symptoms begin & highest physical milestone achieved. Thankfully there is a solution for SMA. But its only at Dubai and U.S. Alpaslan lives at Turkey but this is not the only problem. The SMA medicine costs 1.8 MILLON US DOLLARS and in Alpaslan’s contury(Turkey) you need afford money the money by yourself. If you understand SMA, I am going to tell how can you help Alpaslan; You can send the YouTube videos to your family and friends ( https://youtu.be/3Uhy5DXEHCQ and https://youtu.be/bbuCopdV_u8 )
Or you can join instagram live videos ( instagram: @arparslanyasasin ) Or you can give a signature
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