Live from Stage 4 | Episode # 022| 3/31/2026 | S**t We Deal With

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Host

Dr. Jill N. Tirabassi, MD, MPH

sports and family medicine specialist, researcher, and educator based in Buffalo, NY. She is a Clinical Assistant Professor at the Jacobs School of Medicine and Biomedical Sciences and serves as the Health and Wellness Thread Leader at the University at Buffalo. 

Professional Background

  • Specialties: Dr. Tirabassi focuses on Sports MedicineFamily Medicine, and Preventive Medicine.

  • Education:

    • MD: SUNY Upstate Medical University (2012).

    • MPH: University of Massachusetts (2019).

Research & Advocacy

Dr. Tirabassi is a researcher with a strong emphasis on Lifestyle Medicine and nutrition. 

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  • Key Projects: She has led initiatives such as "Developing School-based Food Literacy Initiatives for Buffalo Teens" and research into Food Prescription Programs for older adults.

  • Awards: She recently received the Food as Medicine Clinical Leadership Award(November 2025) for her work in primary care and implementation science.

  • Community Work: She is an advocate for those with Metastatic Breast Cancer (MBC), having served as a mentor with Project Life and an alumna of the Hear My Voice MBC Leadership program. She also co-hosts podcasts/discussions focused on breast cancer support. 

Summary

How much time does living with metastatic breast cancer actually take? In this episode, Dr. Jill Tirabassi dives into recent research that puts real numbers to what many in the MBC community instinctively know: managing advanced cancer is incredibly time-consuming.


Jill examines a December 2025 JAMA Network Open Prospective Study which used a validated smartphone app (Daynamica) to track every cancer-related episode of care, travel, waiting, and at-home tasks for 78 adults with metastatic breast or advanced ovarian cancer over 28 consecutive days.

The research used mobile technology to document:

  • Out-of-home care: Patients averaged 4 cancer-related trips over 28 days (roughly once weekly), primarily for clinic visits and lab work

  • Wait times: While half experienced waits under 15 minutes, 14% waited over an hour—with some extreme cases reaching 2.5 hours

  • Travel burden: Average travel time was 35 minutes per appointment, often exceeding actual care time

  • Home tasks: Patients spent a median of 209 minutes weekly on cancer-related activities—medications, scheduling, billing, symptom monitoring

  • Daily disruption: Over one-third of participants reported cancer tasks disrupted their daily activities more than half the time

The Reality Check

Most participants spent 5-15 hours per week managing their cancer care—not quite the "full-time job" metaphor often used, but a substantial commitment nonetheless. Only two patients exceeded 25 hours weekly, though the burden varied significantly depending on treatment line and side effects.

Why This Matters

This study validates the invisible labor of living with metastatic cancer. Beyond scans and treatments, patients navigate complex logistics, financial administration, and constant health monitoring. Jill reflects on her own experience across multiple treatment lines—from easier oral medication periods to more demanding IV infusion schedules.

By documenting these realities, researchers help healthcare systems and policymakers understand what patients truly face—and hopefully identify ways to reduce these burdens.

Study Citation: "Time Burden in Patients with Metastatic Breast and Ovarian Cancer From Clinic and Home Demands," JAMA Network Open, December 2025

Figure. Weekly Total Time Spent on Each Health Care, Travel Waiting, and Home Cancer-Related Task by Participant.

Each column represents an individual participant. Care time included all time spent out of home at a medical facility and labeled as cancer care; travel and waiting time were associated with these cancer care visits. All other types (taking medications or injections, self care and symptom management, scheduling appointments, monitoring health status, managing medical claims and bills, and arranging help or support for cancer care) were reported in the end-of-day survey as occurring outside of a health care facility.


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Stage 4 Living: Palliative Care is Not Hospice with Dr. Mary Busowski

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