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A rare disease called Hunter’s syndrome has taken these two little boys into its grasp and it is severely damaging their tissues throughout their bodies. At just 4 years, Kenit needs to go for regular enzyme replacement therapy, echo tests and MRIs. The doctors have said that he has to continue this routine for at least the next 3 years, while 2.9-year-old Medhansh needs an urgent nose and heart surgery. He is currently undergoing occupational and speech therapy, however, the child has a long wa
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