Jun 24, 202630 minS2
When Carmine was told he had hypertrophic cardiomyopathy, he thought he'd never see his kids grow up. Sixteen years later, he's living his best life. He spent years living in fear, isolating himself, and convinced his...
health
Let's Talk SADS Live
Hosted by Canadian SADS Foundation · health · EN
About this Podcast:
The Let’s Talk SADS Live Podcast is a highly accessible educational platform for patients and families navigating SADS conditions. Topics cover the spectrum of inherited arrhythmias, fostering a well informed and proactive patient community. Led by ARVC and heart failure patient Heather Cartwright, Let’s Talk SADS Live features monthly conversations with healthcare professionals, patients, and caregivers who share expert knowledge, practical advice, and lived experiences.To help us continue changing the lives of SADS patients and families, please consider donating at www.sads.ca/donate/.
Pitch Analysis
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Contact path
Verified email
Booking probability
32%
Guest openness
Selective
80/100
Required Score
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What is Let's Talk SADS Live about?
The Let’s Talk SADS Live Podcast is a highly accessible educational platform for patients and families navigating SADS conditions. Topics cover the spectrum of inherited arrhythmias, fostering a well informed and proactive patient community.
Who hosts Let's Talk SADS Live?
Let's Talk SADS Live is hosted by Canadian SADS Foundation. The show has published 53 episodes to date.
What has Let's Talk SADS Live covered recently?
Recent episodes include "Ep. 53 How Treatment for HCM Turned Fear Into Freedom" (24 June 2026, 30 minutes), "Ep. 52 Women, Inherited Heart Conditions, and the Care They Deserve with Dr. Danna Spears" (10 June 2026, 35 minutes), and "Ep. 51 When Patients Help Design Research, Healthcare Improves" (27 May 2026, 36 minutes).
How often does Let's Talk SADS Live publish?
Let's Talk SADS Live publishes roughly every two weeks, with episodes averaging 33 minutes across 53 episodes.
How hard is it to get booked on Let's Talk SADS Live?
Booking probability for Let's Talk SADS Live is 32%, and the host is rated Selective on guests. Let's Talk SADS Live requires a Pod Score of 80 or higher. Let's Talk SADS Live's contact route on record: verified email.
Who should pitch Let's Talk SADS Live?
The strongest fits for Let's Talk SADS Live are Health & Wellness Services. Let's Talk SADS Live has a health audience.
About the host
Canadian SADS Foundation hosts Let's Talk SADS Live, a health podcast with 53 episodes published.
Verified host email: ████████@████.comSign in to unlock →
Recent episodes
Our AI reads these to draft pitches. Use them as grounding for a pitch that cites a real guest and a specific topic.
Episode #17
Ep. 52 Women, Inherited Heart Conditions, and the Care They Deserve with Dr. Danna Spears
Jun 10, 202635 minS2Somewhere right now, a young woman is being told her heart palpitations are just anxiety. She is being sent home without an ECG. She is being told she is too young and too low risk for anything to be wrong. She might...
- May 27, 202636 minS2
When Patients Help Design Research, Outcomes Improve. No lab coat required. Just lived experience and a seat at the table. Anne Simard shares how patient partners have rewritten study protocols, redesigned unusable...
- May 12, 202640 minS2
We have a very special episode this week of Let's Talk SADS Live. Our host Heather is talking with someone she's known her whole life: her older sister, Meredith. They share a lot. Memories, jokes, the occasional family...
- Apr 28, 202629 minS2
You wouldn't expect a 16 year old with Congenital Heart Defect (CHD) to say a roller coaster is one of her favorite stories, but here we are! Amelia was born with Double Outlet Right Ventricle and has had three open...
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- Apr 14, 202636 minS2
Gene therapy. One injection. No going back. Brian O'Mahoney, the first person in Ireland to receive any gene therapy, has lived with severe hemophilia B his entire life. In this deeply personal conversation, Brian...
Episode #10
Ep. 47 A New Era of Remote Heart Monitoring and What It Means for Patients with Dr. Heather Ross
Mar 24, 202632 minS2Wearable technology that can predict heart failure hospitalizations days in advance is just one of the groundbreaking innovations Dr. Heather Ross, a world-renowned cardiologist and heart failure specialist, is bringing...
- Mar 10, 202633 minS2
Your story matters. And telling it might just help you heal.After surviving sudden cardiac arrest and a heart failure diagnosis herself, Dr. Sharon Bray discovered that writing wasn't just a creative outlet. It was a...
- Feb 24, 202632 minS2
What if a single treatment could change the future of your heart? This #HeartMonth, we are bringing you a conversation filled with hope, science, and the power of persistence. We sit down with Dr. Sheikh, a...
- Feb 10, 202629 minS2
This #HeartMonth, we are honoured to share a deeply moving conversation with a very special friend of The Canadian SADS Foundation, Walker Frahm, CEO of The US SADS (Sudden Arrhythmia Death Syndromes) Foundation...
- Jan 27, 202629 minS2
From unexpected heart failure at 23 to founding a national patient community. Today we are speaking with Marc Bains, co-founder of HeartLife Foundation. He shares his powerful journey from diagnosis to transplant and...
- Jan 13, 202631 minS2
What if we rebranded exercise with a SADS condition as play? Join us as health coach Janet Omstead shares her joyful approach to building a sustainable movement and exercise routine. This episode dives into practical...
- Dec 30, 202531 minS2
What if your diagnosis didn't mean you had to give up the sports and activities you love? Pediatric cardiologist Dr. Robert Hamilton challenges decades of fear with a new, empowering message for the SADS community...
- Dec 9, 202533 minS2
What if the greatest gift for your family wasn't something you could wrap? Yvonne Heath, author of "Live Your Life to Death", explains why preparing for the end of life is an essential act of love. She shares powerful...
- Nov 25, 202527 minS2
Having your life's dream taken away in an instant is a reality Brett MacLean faced at 23. A professional hockey player who had just scored in the NHL, Brett's career ended with a sudden cardiac arrest on the ice. In...
- Nov 11, 202533 minS2
For Lia Olmsted, the discovery that her children had Brugada Syndrome came after the devastating loss of her 21-month-old daughter, Reese. In this heartfelt conversation, Lia shares the realities of parenting a child...
- Oct 28, 202532 minS2
Meet Hannah Keime from HeartCharged. Diagnosed with a genetic heart condition at just 14, Hannah gets real about the challenges of an invisible illness and explains why she started HeartCharged. She opens up about...
- Oct 14, 202535 minS2
The Road to Recovery after a Cardiac Storm In this powerful first episode of the new patient-driven Let’s Talk SADS Live , Sally Gilbert shares her journey of living with exercise-induced ARVC and the emotional...
Let's Talk SADS Live
Ep 35. Past to Present and What Lies Ahead for Long QT Syndrome
Sep 16, 202545 minJoin the Canadian SADS Foundation for the 35th episode of Let’s Talk SADS Live with Dr. Andrew Krahn, as we take a closer look at Long QT Syndrome and what it means for patients and families.This episode will explore...
Let's Talk SADS Live
Ep 34. What Gene Therapy Means for Families Living with SADS
Aug 19, 202540 minJoin us for our first pre-recorded episode! In episode 34 of Let’s Talk SADS Live, we sit down with Dr. Andrew Landstrom to explore the promise and progress of gene therapy for inherited arrhythmia syndromes. This...
Recent guests
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