At just 24 weeks pregnant, Nicole and Jeremy learned their daughter, Blaire, had Congenital Pulmonary Airway Malformation (CPAM), a rare lung condition affecting 1 in 25,000 babies. What followed was months of monitoring, a referral to The Chicago Institute for Fetal Health, NICU stay, and life-saving surgery at just one week old. Today, Blaire is a thriving one-year-old who loves books, family walks, animals, and saying “Hi” to everyone she meets. Her family is participating in The Walk for Lurie Children’s on Sunday, June 7, to give back to the hospital that guided them through some of the hardest days of their lives. “[This event] is a time for us to talk about CPAM and spread awareness on such a rare thing,” said Nicole. They hope others will join them in supporting the hospital and helping make difficult days a little easier for families facing medical challenges. To read their full story and register for The Walk, click the link below. Register: https://lnkd.in/giJhEzwA Read: https://lnkd.in/gr5pZDiF
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