In this episode, we hear from Trina O'Brien Leggott, a heart patient with inherited hypertrophic cardiomyopathy (HCM). Trina's familial journey with HCM began when her youngest brother experienced unusual symptoms, leading to his diagnosis of HCM. This discovery led to family screenings that traced the condition back to their father, 40 years previous.
In this episode, host Ann-Marie delves into the complexities of Atrial Fibrillation (AF) with Dr. Robert Rose, a scientist and professor in the departments of Cardiac Sciences, Physiology and Pharmacology at the Cumming School of Medicine, Libin Cardiovascular Institute at the University of Calgary.
In this episode, we delve into the deeply personal and transformative journey of Marc Bains, who was catapulted onto a life-changing path following a heart failure diagnosis at the age of 23.
In this episode, we speak to Dr. Ratika Parkash, a cardiologist based in Halifax, Nova Scotia. Dr. Parkash is a Professor and Director of Research in the Division of Cardiology in the Faculty of Medicine at Dalhousie University, and the Associate Scientific Director at the Cardiovascular Network of Canada (CANet). Her research is focused on cardiovascular disease prevention, cardiac implantable electrical devices, and atrial fibrillation.
In this episode, host Ann-Marie is joined by Sue Armstrong, a patient with lived experience, who discusses her emotional journey with heart failure and how it has shaped her approach to life. Sue recounts the impact of heart disease in her family spanning generations, her personal heart health journey, and the importance of embracing joy in everyday moments.
In this episode, Dr. Venk discusses the development of the Canadian Syncope Risk Score (CSRS) to guide the management of patients with syncope in emergency departments. The CSRS simplifies the approach for evaluating patients and determining the risk of adverse outcomes. The score also guides physicians in deciding whether further investigation, ongoing monitoring and or hospitalization is necessary for patients, or if they can be safely discharged home.
In this episode of Ticker Talk, host Ann-Marie speaks with Cyrena Ferreira, a caregiver, mother, and advocate of cardiac health and research. Cyrena shares her journey of discovering her son Alessio’s heart condition shortly after his birth, and the challenges they have faced as a family following diagnosis.
In this episode, we speak with Dr. Jennifer Reed who is the Program Chair of Cardiac Rehabilitation, a Scientist in the Division of Cardiac Prevention and Rehabilitation, Director of the Exercise Physiology and Cardiovascular Laboratory, and serves as Program Chair at the University of Ottawa Heart Institute. She is also Associate Professor at the School of Epidemiology and Public Health Faculty of Medicine and Adjunct Professor at the School of Human Kinetics in the Faculty of Health Sciences at the University of Ottawa.
Susan McLaren shares her lived experience as a caregiver for her husband and children living with Hypertrophic Cardiomyopathy (HCM), an inherited cardiac condition affecting the heart muscle. She discusses the gaps in support and counselling for families dealing with genetic cardiac disease, the impact on her husband and children’s lives after their diagnosis, and the importance of finding ways to cope and take care of oneself as a caregiver.
In this episode, we speak with Dr. Robert Hamilton, children's cardiologist, heart rhythm specialist and senior associate scientist at the Hospital for Sick Children and Research Institute in Toronto, Canada. He is a CANet Network Investigator and senior electrophysiologist managing an inherited arrhythmia clinic and has gained a unique perspective on the clinical impact of hereditary heart rhythm conditions on children and families.
