Hunter Syndrome (MPSII) Foundation – Bravelets

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Hunter Syndrome (MPSII) Foundation

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About this cause:

The Hunter Syndrome Foundation aims to fund and find a cure for Hunter Syndrome. Hunter Syndrome or Mucopolysaccharidosis Type II (MPS II) is a rare genetic disorder that slowly destroys the body’s cells. This is a rare condition affecting 1 in 150,000 males. There is currently no cure, and the disease is progressive and life-limiting.

This is a disease that is very close and dear to my heart as my two grandson pictured both have this incurable disease. I would love nothing more that to find a cure in their lifetime.