There is often confusion around what palliative care is, who it is meant for, and at what stage of life. In this episode, Allison and Justin interview Dr. Drew Rosielle, who provides the history, describes the model, and outlines the goals and benefits of palliative care.
Caregiving can impact our friendships in a variety of ways. Some friends disappear. Others stick around, but disappoint. Others we find and connect with because of our caregiving role. Listen in as Allison and Justin dig into these different types of relationships.
One of the few things we can count on in this life is death and yet our culture is not good at talking about or preparing us for it. In this episode, Justin and Allison speak with Jane Whitlock, an end of life doula and former spousal caregiver, about her role, the stages of death, and the questions we can start asking and conversations we can start having now about this important and inevitable topic.
There’s no question that the life of a caregiver is hard and that feelings of disappointment, comparison, and unfairness can be pervasive. So how do caregivers move through their days as they deal with the weight of it all? In this episode, Justin and Allison talk about how to keep going even when everything is terrible.
When someone in our life has an acute injury or medical situation, it makes sense for us to focus solely on their needs. But when an illness becomes longer-lasting or chronic, caregivers need to find ways to balance the needs of their loved ones with their own. In this episode, Allison and Justin talk about why that can be challenging, ways that can look, and what might happen if we don’t.
Allison and Justin talk about how caregivers need community care in order to practice self care, how they each practice acts of micro-care throughout the day, and what supporters can do and say instead of, “Are you taking care of yourself?”