by SADS Foundation | Feb 24, 2025 | Blog
In May of 2020, Elizabeth’s close friend passed away suddenly and unexpectedly. She tried to think of a way to support his family after this tragic loss – and wanted to give them a gift that didn’t involve food or flowers, since both are temporary. That’s when...
by SADS Foundation | Feb 24, 2025 | Blog
Morgan was diagnosed with CPVT after passing out on the playground just before her tenth birthday. Morgan – an active, loving, and beautiful little girl with a huge heart – pivoted from playing basketball and soccer to sewing, cooking, and playing the piano. Morgan...
by SADS Foundation | Feb 18, 2025 | Blog
written by Landri My day-to-day life generally consists of school, friends, playing video games, and participating in activities that interest me. Unlike the average teenager, one of my favorite things about school is learning new things and applying that knowledge in...
by SADS Foundation | Feb 13, 2025 | Blog
Running your first marathon while raising money for the SADS Foundation is no easy feat; neither is figuring out how to tell your 9-year-old she has Brugada Syndrome, so Camila “Mila” did something inventive. She used the marathon as a vehicle to tell her daughter,...
by SADS Foundation | Dec 20, 2024 | Blog
by Kiersten Rock-Torcivia Who is this girl? What is on her chest? On her chest, just below her left collarbone, is a black oval outline shadowed with gray. Slashing diagonally through the upper part of the shape sits a vibrant raw pink scar. From the upper part of the...
