SADS EL-PFDD Testimonials

We need to hear YOUR voice, YOUR story, YOUR experience with LQTS so we can represent the scope of impact this condition makes on families and individuals. We need the FDA to see how many families are impacted and how much of a difference new therapies would make –...

Chaunté’s LQTS Story

Chaunté and her daughter Kadence I’m a mom to three girls. When my second daughter, Kadence, was six months old, I took her to a pediatrician for a routine well-child check and immunizations. And when he was doing the initial examination, he noticed that her...

SADS Spotlight: Ruby

Can you tell me a little bit about your family’s SADS journey – from diagnosis to where you are today? Our journey starts with my husband’s daughter, who was having cardiac symptoms. The doctors didn’t know what was going on, so they did genetic testing, and found out...