Saturday, June 9, 2012

Meet Mitchell Franzer

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Diagnosed with spina bifida as an infant, Mitchell was told he would never walk. Now, 11 years old, he is active in sports and farming. Mitchell Franzer was born September 15, 1997 to delighted parents Bill and Sandy Franzer. Sandy had a healthy pregnancy, yet when she delivered Mitchell doctors noticed immediately something was wrong. Mitchell was diagnosed with spina bifida. This was a shock to the Franzer family, but they had to focus on finding the best care for their son. Mitchell was transported to The Children's Medical Center of Dayton just hours after he was born. "When Mitchell was transported to Dayton Children's so many questions were racing through our minds. One of the nurses comforted us and answered our questions. Her daughter also has spina bifida and she gave us hope that Mitchell would be OK," says Bill. Mitchell spent 21 days at Dayton Children's Regional Level III Newborn Intensive Care Unit (NICU). "We were overwhelmed with taking care of a sick infant but the nurses and doctors were so caring," says Sandy. When Mitchell was just a baby, the doctors shared their concerns that Mitchell will likely never be able to walk on his own. He would be confined to a wheelchair indefinitely. "It was difficult to receive the news that your son will not be able to walk, but Dayton Children's gave us the tools to work with Mitchell to make him stronger." Sandy worked with Mitchell constantly by doing the exercises they learned at Dayton Children's. At 16 months old ...
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