Michael P Savoca Memorial Foundation

Mike Savoca was diagnosed with Pulmonary Fibrosis on March 17, 2009. Prior to his diagnosis, Mike and his family had never heard of Pulmonary Fibrosis. Over the next six months, his family watched as this horrific disease consumed Mike. Mike became easily winded and often, could not catch his breath. His breathing became labored. As Mike suffered, his family felt helpless that there was nothing they could do to help Mike. There is no cure, no treatment for Pulmonary Fibrosis. Mike passed away on September 25, 2009, just six short months after his initial diagnosis. Although Mike passed away from Pulmonary Fibrosis, the disease did not define him. Mike’s favorite movie was It’s a Wonderful Life. In his short life, Mike truly embodied George Bailey. Mike positively impacted many people during his life. He was a man of integrity, hard work and family values. Mike had a career of nearly forty years at the Chicago Mercantile Exchange. He was a mentor and friend to many of his people at the CME, always willing to listen and give advice. Mike had many lifelong friends and loved to laugh. Mike’s true passion in life was his family. The roles of husband, dad and grandpa are what truly made Mike happy. The Michael P. Savoca Foundation was founded by Mike’s six children who serve as the Board of Directors for the Foundation. Four of his friends and his wife serve as advisors to the Board. Although Mike is no longer with us, it is our sincere hope that we can keep Mike’s spirit alive through this foundation and the positive work we hope to accomplish catching a breath of hope for Pulmonary Fibrosis.