Meet Maximus Chum. He was born with a very rare disease that 1 in 12,000 babies get called cystic hygroma. His birth weight was approximately 6lbs 14 ounces 3 pounds of the weight being the mass itself. He was born July 23rd of this year and remains in the NICU in Seattle Washington. He is to weak for surgery at the time and the tumor continues to grow as he does. His parents must wait anxiously until he is ready for what could be a life threatening surgery. We pray for him everyday and hope that he makes a full recovery. However in the mean time his parents have been struggling to find the financial means to travel such long distances and spend the much needed quality time that a baby in the NICU needs for a full recovery. I know how important it is for the parents to be there for a child in NICU from my own experience. So I am asking you to please do whatever you can to help this struggling family. Please whatever you can donate will help this family that's in dyer need. Share this with all your friends and family and help bring awareness to this very rare disease.
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