Isla's legacy: Long QT Syndrome awareness

Sharing knowledge about Long QT Syndrome, raising awareness and supporting patients.

About Me

Who am I?

Hi, I'm David. My daughter, Isla, was diagnosed with Long QT Type 3 when she was born back in 2015. Since then I have dedicated my life to learning as much as I can about it; talking with cardiologists, electrophysiologists, researchers, industry experts and patients from around the world. Despite all the medications and precautions, Isla died in 2022. She inspired a team of scientists in Canada to begin developing new treatments for Long QT Syndrome and I have been working alongside Thryv Therapeutics to help share stories and raise awareness.

What I Do

Video Diary

Patient Stories

Patient Stories

My thoughts about Long QT and my personal journey and struggles as a parent of a Long Cutie

Patient Stories

Patient Stories

Patient Stories

Shared stories of people around the world living with Long QT Syndrome

Information

Patient Stories

Information

Some informative posts I have made about Long QT Syndrome, explaining different aspects of the condition.

Want to share your story or learn more about Long QT?

Message me and lets raise some awareness