About this campaign
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Help us raise money for the National MPS Society for advocacy and research working towards a cure for the many MPS/ML disorders. Our son, Adam was only a newborn when he was diagnosed and has had to endure so may complex measures to give him the best chance to prolong the progression of this disease including a stem cell transplant on 8/14/20.
He is almost 6 years old and has come a long way. He goes through so much with a smile on his face the entire way!! We love him!
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