Lisa Deck is a mom of two living in North Attleboro, MA. As a multiple stroke survivor, Lisa was diagnosed with Moyamoya Disease after an 18-year diagnostic odyssey. She underwent two brain bypass surgeries in 2015 to restore blood flow to her brain. Lisa is a leading advocate and volunteer for the American Heart Association and served as a Go Red for Women National Spokeswomen 2014-2015. Today, she serves as an Advocacy Board Member for AHA Boston and Southern New England. Lisa also serves as a global ambassador and motivational speaker, sharing her personal experience and patient story and expertise with various groups. Lisa has become actively involved in rare disease advocacy. Lisa serves as a Board Member for the Moyamoya Foundation Co. and Rare New England. On behalf of Rare New England. Lisa produces and hosts a local healthcare talk show, The World of Rare Disease. Lisa also serves on RDLA’s Inaugural Advisory Committee. Lisa is proud to be a founder and director of Sisters@Heart.