Hunter Syndrome (MPS II) is a rare degenerative disorder that, when left untreated, affects all functions of the child’s body. Until recently, children with MPS II could expect to live into their early teenage years. But there is hope. Recent advances have resulted in two treatments that some children are able to access. We need more. We need a cure. We need approved treatment for every family affected because each of those children deserve life. That is what is at the heart of this charity: giving hope to the children and families who are, or will one day be, diagnosed with Hunter Syndrome.Read more »
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