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...
by Erinsads | Oct 27, 2025 | Blog
From childhood fear to Ironman finisher and future physician, Alex’s journey with Wolff-Parkinson-White (WPW) Syndrome shows the power of early diagnosis, expert care, and determination to give back. By: The SADS Foundation and Alex G. Published October 30, 2025...
by SADS Foundation | Oct 23, 2025 | Blog
When 25-year-old Juliana from Switzerland was diagnosed with Brugada Syndrome – a rare heart condition that can cause sudden cardiac arrest – she turned her fear and uncertainty into purpose, finding strength through connection and raising awareness to...
by SADS Foundation | Oct 23, 2025 | Blog
Matt’s first symptom was Sudden Cardiac Arrest; his next act is resilience, as he learns to live – and dance – safely with ARVC. By: The SADS Foundation and Matt K. Published October 24, 2025 | 15 min read “You will be able to push the boulder over the...
by SADS Foundation | Oct 13, 2025 | Blog
After years of fainting episodes and misdiagnoses, Dalia discovered she was living with Long QT Syndrome – and turned her journey into one of resilience, advocacy, and hope. By: The SADS Foundation and Dalia B. Published October 20, 2025 | 10 min read “I don’t...
by SADS Foundation | Oct 8, 2025 | Blog
Ammon was diagnosed with a genetic heart condition called CPVT at just five years old after experiencing Sudden Cardiac Arrest (SCA) while playing outside with his brother. In July of 2025, he experienced SCA yet again while at a church youth camp. His family is...
