I have an 8 year old that was diagnosed with Down syndrome at birth. Her name is Miracle. The Dr.'s prognosis of her development was not very encouraging. She stopped breathing at birth and was rushed to NICU where she remained for 15 days. She also had two hospital stays with pneumonia and the flu. In 2016 she had brain surgery on both sides of her head for "Moya-Moya". Miracle is now in the 3rd grade and has defied all of the odds that were against. We started a Foundation in her name that is designed to help other families with Down syndrome children. It is called Miracle Mullen Downs Foundation and is a 501c3 organization. We help educate families about Down syndrome as well as assist them financially with tuition for places like the Bell Center. We have be fortunate enough to send 2 children to Bell Center for 1 year.