In part four of our series, we meet Matthew Congdon again—designer, sharp-tongued truth-teller, and stage-four cancer patient—still trying to make sense of a life that keeps blindsiding him. This chapter brings an unexpected turn: a new love that arrived just days after his diagnosis, in the form of a tall Dutchman in white pants named Ludo. Matthew reflects on allowing himself to be cared for, trusting life’s sudden shifts, stepping away from his work, finding joy in the small stuff, and the fears and imaginings that shape the way he’s approaching the end of life.

In part three of this series, designer Matthew Congdon, who is living with metastatic prostate cancer, reflects on what life feels like after the rush of tests and treatments fades. The fog begins to set in as he navigates the uncertain space between moving through treatment and finding acceptance in this new way of living. With his signature candor and dark humor, Matthew talks about how palliative care reshaped his idea of hope and the small rituals that help him feel in control—like freezing his bottle of morphine in a block of ice, saving it for when the time is right.

In part two of this series, designer Matthew Congdon shares the phone notification that changed everything for him. In this darkly funny conversation, Matthew recounts the chaos that followed: the shock, the breakup, the black moths, the medical missteps. But amid the turmoil, he begins to reclaim control–through design. From choosing his gravesite to curating the outfit he’ll be buried in, Matthew transforms fear into authorship and finds solace in beauty, ritual, and precision.

In this first part of a multi-episode conversation, designer Matthew Congdon speaks with raw humor and sharp wit about navigating life with metastatic prostate cancer. He reflects on growing up in the Midwest, his lifelong relationship with control, and the haunting parallels between his own diagnosis and his father’s cancer. With disarming honesty, Matthew shares what it’s like to inherit a sinking ship—and why he’s choosing to chart a very different course.

Have you ever had to make a decision that someone told you was 'life or death'? Maybe it's another round of chemo, a surgery, or an experimental treatment. The stress at these crossroads can be intense. In Part 2 of 'Death by a Thousand Cuts,' Jay Fishman faces a choice that is fundamental for patients with ALS, a choice that could either shorten or prolong his life. But at what cost? And what happens when people disagree about what to do? Jay explains his evolving thought process and how he ultimately decided what was right for him and his family.

When a diagnosis of ALS turned former Travelers Insurance CEO Jay Fishman's world upside down, he leaned into his disease. But acceptance never comes easily, and there was much to be learned in Jay's journey through his illness. In Part 1 of our premiere episode, Jay tells the story of how he's coped with his ALS and how he redefined his world to move forward after his difficult diagnosis. We also meet Jay's doctor and learn about the close partnership they formed, which allowed them to tackle tough medical decisions together. We learn that behind any well-considered medical decision is a series of dialogues with the people we hold dear about the things that matter most.

This is 'When I Die, Let Me Live,' a new podcast where we take up the taboo, fraught, delicate, but universal topic of death. We'll invite you into the lives of our guest, many of whom are patients, caregivers, and health professionals, as we try to understand what it means to live more fully as the end approaches. In these stories, we hope to find our own voices and feel moved to start having conversations with the people we care about. Because facing death isn't about dying but leaning into our living. Join us each month starting at the top of 2017, and subscribe to us on iTunes.