by SADS Foundation | May 28, 2026 | Blog
by Marsha Peterson After my sister, SM lost her last baby at birth, she was diagnosed with Long QT Syndrome. She had been passing out for unknown reasons. None of us knew anything about it and I didn’t have any literature about it. All I knew was that it was...
by SADS Foundation | May 27, 2026 | Blog
Age 25 · Massachusetts “I don’t want people to stop hearing her name. I want everyone to say her name.” – Rachel, Alyssa’s friend Alyssa Richardson was the kind of person who walked into a room and made it brighter. Her family and friends called her...
by SADS Foundation | Feb 27, 2026 | Blog
By Marie A. (Nana’s mother) Published February 27, 2026 | 5 minute read Delyth “Nana” Arthur was a bright, joyful little girl whose curiosity and love for her family lit up every room. After a mild illness, she suffered sudden cardiac arrest from myocarditis in...
by SADS Foundation | Dec 2, 2025 | Blog
By Jessica V. and the SADS Foundation Published December 2, 2025 | 15 minute read Jessica swings into the saddle and heads out with her daughter for a 50-mile endurance horseback ride. From the outside, it might look like any other long-distance ride – but Jessica is...
by SADS Foundation | Nov 11, 2025 | Blog
Growing up with photo albums, I discovered how my family moved through history – and how their stories still shape me. Even when memories are painful – especially with SADS and loss – looking back becomes an act of respect: acknowledging the whole...
