by admin | Jun 28, 2023 | Uncategorized
I’m Joe Schroeter and have had the honor of working with Jessies Heart Foundation, JC Heinen itsfounder and Kathy Lawless one of its key board members for several years. My involvement came inpart from my experience having a son with a congenital heart condition and...
by admin | Jun 4, 2019 | Uncategorized
On February 14, 2019 this year. Alex Schroeter, who was diagnosed with Long QT Syndrome in 2016 had the pleasure of being a speaker at the Jessie’s Heart Leadership Conference. I, his father was proud standing on the stage with Alex and his mother as he shared his...
by admin | Apr 21, 2018 | Uncategorized
Moments after you discover your child is born with a congenital heart defect, come the waves of emotions, instinctual responses, medical information and terminology, and subsequent confusion. Though your child is alive, fear, grief, and sadness crash into a family...
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