A miraculous life deserves a resounding tribute... this is mine. My 54-year-old autistic and developmentally delayed brother, John, is battling colorectal cancer for the third time in his life. This time, he will lose; it has metastasized, and it is terminal. John knows this, as do I, and yet he lives. I don't mean that he survives; I mean he lives with a passion that can only be described as... odd. I suppose the easiest way to break it down is to say that he is not living like he is dying. John is living a simple, quiet life, the life he always wanted. As his caregiver and sister, I have spent my life surveilling my brother, from trying to figure out why he is the way he is to bearing the brunt of the punishment for childhood misbehaviors that were usually his idea... I swear. This man has been the forerunner of my own existence. I rightfully inherited all of the ridicule and cruelty heaped upon him because in the 1970s, in rural Missouri, no one knew what autism was. It was something more lethal than a gunshot wound to the it was misunderstood and different, and it was seemingly neverending. At least the gunshot wound, if positioned correctly, would kill you quickly. But something happened that changed all of that. As I fought tooth and nail to get out of that town and never come back, John found a rhythm to living there, sharing a home with our mother. He became a member of the community, a contributing member, volunteering his time to help in community projects, attending church regularly, even procuring a golf cart so that he could go fishing out at the community lake. He mowed yards, helped Mom take care of the house, even went on a trip to Washington, D.C., as a chaperone with the high school. And as he was changed, it changed me as well. When John received the first diagnosis of cancer, it was stage four. John not only lived through it, he thrived. The doctors were stumped. I had an idea that it was his autism that saved him. There was no emotionality, no anger, no pleading with the universe, no giving up. There was only cancer and the battle against it. And he won for nine straight years. It came back three years ago with a horrifying vengeance. It is more extensive, uglier, and more malicious than before, wrapped around bones, settling in his lungs. And yet, John lives, through radiation, through chemo, through COVID-19. Most people spend their lives trying to figure out their ministry to the world, the gift that they can give and leave behind as a legacy. John's ministry is living as John does. Simply living, and living simply, but living as if he understands the complexity of finding joy in every single day, every single task, every single breath. Everyone is born with a question, my mother would say. They spend their life trying to find the answer. But John, my mother insisted, was born with his response and would thus live his life accordingly. As a writer, I feel a deep obligation to tell not only John's story but the story of those of us who have been so intersected by his life. Finally, as a sister, I feel it is my purpose to settle my own odds at the universe, so to speak. This book has an accompanying podcast where I interview my brother. At the end of some of the chapters, you will find QR codes that, when scanned, will take you to one of the podcasts where I interview John, and he tells his story in his words. This project was started as part of my thesis project for my MFA at Lindenwood University, the blending of writing as storytelling and audio from the primary source as a structural scaffolding to make the story more alive. In the middle of it, I was interviewed by some veteran podcasters who told me that what John and I were doing was actually creating a new genre of the legacy podcast. We hope you find something useful in this unexpected legacy.