At 5 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.

Michaela inspires our hope that a cure will be found so that other families will never have to endure the daily pain of MPS.  There have been significant break-throughs since this journey began that continue to renew our hope that our daughter will conquer MPS and live well beyond the prognosis of her teen years. 

 Any assistance that you could offer towards this very special effort would be greatly appreciated.

 With sincerest gratitude, 

 Ann and Glenn Kameka & Family