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rarest.org
My little son is suffering from the world’s rarest disease SMA-1 ( Spinal Muscular Atrophy). His muscles are failing and he is losing the ability to even breathe. He is not able to sit straight. As per doctors the only possible cure for my son is a magical medicine named Risdiplam. But this magical medicine costs crores. An amount that is impossible to arrange for any family. He is running out of time. I need your help to save my son. Together we can achieve this triumph. Please donate and save
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