Jillian McConnell, our guest host, speaks with the Dineen children: Justin, Rebecca, and Peter who were just 12, 10, and 8 at the time of their mom’s diagnosis (9 years ago), about their experiences as younger children learning about their mother’s bvFTD diagnosis and now as teenagers / young adults. They discuss the unique challenges they faced and offer perspectives and strategies that continue to help them as they navigate their mother’s diagnosis and their relationship with her.
Part 1 is a conversation with Matt Dineen, their father.
For more information:
"It Started with Oma"
Le rôle important des aidants et des ressources communautaires pour les personnes atteintes de troubles neurocognitifs majeurs.
Esprit en action
Mind over Matter: Game Changer
Circle of Music in Kitchener-Waterloo
L’importance de la communauté
Conversations That Matter: Talking About Dying and Dementia
Les defis de la proche aidance a distance
L’approche par le plaisir
Vivre le moment present et profiter de la vie
Dying & Dementia: Let’s Talk About It
Demystifying Dying: Stories from a Death Doula
Dementia and Indigenous Communities Part 2: A cultural perspective of dementia and dementia care
Taking it to the Streets: Reimagining Dementia
Dementia and Indigenous Communities Part 1: A cultural perspective of dementia and dementia care
Ruth and Maggie’s Story
2SLGBTQI & Dementia:From Research to Action
Modèles novateurs de résidences pour aînés vivant avec un trouble neurocognitif majeur: Conversation avec le professeur Philippe Voyer
Rainbow Wing in LTC and Emotion Based Care for 2SLGBTQ Residents
Les défis de la proche aidance à distance
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