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When Longevity Meets Mortality

Publish Date: September 9, 2025
Author: Dr. Jeffrey A. Lieberman
Source: Shrink Speak substack

My Mother’s Death and America's Broken System of Elder Care

On May 9th, I flew from New York to Cleveland to spend Mother’s Day with my mother. She had turned 101 years old on March 7, 2025, but I was unable to attend her birthday due to a prior commitment to speak at the SXSW Conference (ironically on the topic of longevity) with my colleague, David Sinclair. She was in remarkable health: no chronic illnesses, mentally sharp, socially engaged, and living in her apartment. Her main concessions to age were frailty, requiring her to use a walker for mobility, short-term memory impairment, and pain from osteoarthritis.

When I arrived at her building, I rang up and was buzzed in. As I walked down the familiar hallway, I imagined greeting her at the door as I had so many times before. Upon entering, however, I found her collapsed on the floor, grimacing in pain, my sister crouched beside her. She had fallen and fractured her hip. Within hours, we were in the emergency department of the Cleveland Clinic’s community hospital, where a surgeon explained that she needed a relatively straightforward repair of her trochanteric fracture. “It shouldn’t take more than 40 minutes,” he commented blithely. The anesthesiologist painted a more ominous picture, however, saying there was a 1 in 5 chance that she would not survive the general anesthesia guided procedure.

We girded ourselves for the worst while we waited for the outcome of her surgery but were relieved and surprised to see her an hour later in the recovery room, lucid and chatting in the afterglow of the anesthesia, her resilience on full display. But by that evening, our optimism had faded. Transferred to a room on the trauma service floor, she developed a post-operative delirium and was in severe pain – both common but treatable complications. Yet the staff failed to provide the necessary care. When I pressed, I was told a physician wasn’t available. When I insisted, I was threatened with security and ultimately expelled from the hospital. It was the first, but not the last, indignity of her decline.

The Hidden Lethality of Hip Fractures
For the elderly, a fall is often the beginning of the end. Hip fractures are rarely fatal in themselves, but the recovery is punishing. Roughly 22% of seniors die within a year of surgery. Without surgery, mortality soars to 70%. The danger lies not in the fracture itself but in the cascade of complications that follow all too often: infection, immobility, delirium, muscle loss.

What determines survival is thus not the surgical skill of the repair but the quality of aftercare – rehabilitation, pain management, and attentive nursing. And here, as presciently described by Atul Gawande in his seminal book Being Mortal: Medicine and What Matters in the End (Gawande, 2014), America consistently fails.

From Rehab to Decline
48 hours after surgery, we were informed of my mother’s discharge, forcing my sisters and me to scramble to find a rehab facility. The one we secured was woefully inadequate: indifferent staff, poor communication, insufficient pain control, and limited rehab for my mother. Unsurprisingly, she deteriorated. Yet because she had no terminal diagnosis, she was ineligible for hospice. What she needed was not an immediate cure but compassionate, restorative care. Instead, she was shuttled from one underperforming facility to another, each with its own different policies and expectations.

Eventually, my mother developed a urinary tract infection that progressed to sepsis, requiring rehospitalization. After intravenous antibiotics, she returned, weaker than before, to the nursing home to resume her rehab. At that point, she was finally deemed hospice-eligible even though she still did not have a terminal diagnosis.

Hospice care was a relief in some ways. The staff were compassionate, and the environment was calm and nicely appointed. But hospice in the U.S. is not designed to help patients recover; it is designed to ease their final descent. My mother’s medications were limited to pain relief. She was no longer hydrated or nourished. The system had decided her life was over, and so recovery was no longer an option. The goal was to ease her passing.

On July 6th, less than two months after her fall, my mother died. She had survived 101 years of life with extraordinary vitality, only to be failed by the system meant to care for her in her final days.


My mother at her 100th birthday party, March 7, 2024

A National Problem, Not a Personal Tragedy
My mother’s ordeal is not unique. It is emblematic of a fractured, policy-oriented, and profit-driven system that too often subordinates the best interests of the elderly at their most vulnerable to actuarial algorithms and profit and loss statements. Facilities operate in silos, with little coordination between hospitals, nursing homes, rehab centers, and hospices. Policies are dictated by reimbursement formulas, not patient need. Families are left confused, powerless, and exhausted.

In 2021, the Lien Foundation published a global comparison of end-of-life care. The United States ranked 43rd out of 81 nations, earning a “C.” Wealthy countries like the U.K., Australia, and the Netherlands ranked far higher, not because they spend more resources on care, but because they focus on dignity, comfort, and family presence at the end of life.

Click image to enlarge (opens new window)

In America, Medicare rules often force impossible choices. To enter hospice, patients must relinquish curative care and accept a six-month terminal prognosis – an estimate often impossible to make. Meanwhile, more than 70% of U.S. hospice providers are for-profit, reimbursed at a flat daily rate that incentivizes doing less for patients. And even with insurance, costs remain high: nearly one-quarter of elderly Americans spend $2,000 a year out-of-pocket on medical care, far more than the costs required in Europe.

The Coming Wave
These systemic flaws will only grow more urgent. Today, 15% of Americans are over 65; by 2060, that number will climb to 24%. Roughly 2–3 million people are currently nearing the end of life, and half will die in hospice. Nearly a million live in assisted-living facilities, and hundreds of thousands cycle through rehab centers. Without reform, the suffering my mother endured will be multiplied across millions of families.

What Must Change
If America is to care for its elders with the dignity they deserve, we must:

  • Prioritize quality of life, not just longevity. Extending life is not enough if it means prolonging suffering.
  • Realign incentives. Facilities must be rewarded for improving outcomes, not for maximizing reimbursement.
  • Ensure seamless care. Transitions from hospital to rehab to hospice must be coordinated, not chaotic.
  • Empower families. Loved ones should be partners in care, not obstacles to be managed.
  • Invest in geriatrics and palliative care. These specialties remain undervalued, underfunded, and understaffed.

My mother’s passing was deeply personal. But it was also profoundly American: a story of resilience met with systemic indifference. Unless we confront these failures, we condemn millions more families to the same sad, senseless demise.

Jeffrey Lieberman, MD is the Constance and Stephen Lieber Professor of Psychiatry at Columbia University Vagelos College of Physicians and Surgeons and the president and co-founder of ARETÉ Science, an organization devoted to advancing mental health through science, social awareness, and policy reform. He also served as President of the American Psychiatric Association and is the author of Shrinks, The Untold Story of Psychiatry (Little Brown 2015) and MALADY OF THE MIND: Schizophrenia and the Path to Prevention (Scribners-Simon and Schuster 2023).

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