by SADS Foundation | Mar 18, 2019 | Blog
After years of fainting episodes and misdiagnoses, Chevy’s family finally uncovered Catecholaminergic Polymorphic Ventricular Tachycardia—and began rebuilding his life with strength and hope. By Chelsi M. and The SADS FoundationUpdates February 19 2026 | 7 min read...
by SADS Foundation | Dec 4, 2017 | Blog
A mother with Long QT Syndrome shares how beginning beta blocker treatment at birth gave her family peace of mind—and helped her daughter thrive from the very start. By Kellie MooreUpdated February 19 2026 | 6 min read “I do not have a sick baby. Yes, my daughter has...
by SADS Foundation | Mar 6, 2009 | Blog
Jeff Stichler anxiously watched as emergency room doctors feverishly worked to get a steady heartbeat on his wife on Oct. 17, 2008. Even after numerous electric shocks to her chest, Melanie Stichler remained in a vegetative state and no one knew what caused her to...
