At 9 years old, Michaela should be meeting new friends, instead she is fighting for her life.
Please help Michaela’s fight against MPS IIIB
Our nightmare began in September 2008 when we received the paralyzing news that our then, 4 year old daughter, Michaela has Mucopolysaccharidoses (MPS) type III B which threatens to take her life. Current research has the potential to be translated into a treatment leading to a cure within a three year period if we can raise the needed funds.
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