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After everything I have lived through as a patient, I can say this very simply: excellent providers make you feel safer, stronger, and more informed. They do not just treat illness. They help restore dignity.

As part of our interview series called “5 Things We Must Do To Improve the US Healthcare System”, we had the pleasure to interview Matt Toresco.
Matt Toresco is a patient advocacy expert and the founder of Archo Advocacy, a market research, training, and consulting firm, which aims to help healthcare companies understand the patient experience to improve outcomes. Matt is the editor-in-chief of ELAVAY, which ranks for-profit healthcare companies on their patient advocacy functions, and the co-founder of We The Patients, a non-profit lobbying for the rights of those with cancer in the United States. He is also a speaker and his TEDx talk on patient advocacy has been viewed more than 1.1 million times.
Thank you so much for joining us in this interview series! Before we dive into our interview, our readers would like to get to know you a bit. Can you tell us a story about what brought you to this specific career path?
I broke my neck in 2005. I was playing Division 1 lacrosse at Ohio State. One hit changed everything. I spent the next 20 years managing chronic pain and cycling through opiate prescriptions. I worked in healthcare that entire time. Pharma, genomics, consulting. I sat across the table from executives who talked about putting patients first. I built training programs, launched research reports, and became a partner at a consulting firm. I knew the system from the inside.
And the system still failed me as a patient.
After close to two decades of managing my own pain, an advocate helped me find the right physician. One person with lived experience and the right connections did what the entire industry around me could not. That moment rewired how I see healthcare. Those with lived experience possess knowledge that many in healthcare lack.
I had already been doing the work. I started what would become my advocacy intelligence research in 2017 at a consulting firm in West Chester, PA. I eventually became a partner there. Then, faced with my own mortality, a 14-hour surgery, and deep self-reflection, I decided to bet on myself and go off on my own. I left. I restarted the research from scratch.
That restart became Archo Advocacy. I founded it in 2022 with one conviction: the patient advocacy function inside a healthcare organization can serve as the beacon of hope in more ways than leadership understands. The complexity of the US healthcare system has outpaced the knowledge of many of its own industry experts, leaving patients in the dark. I build the tools, data, and training to change that.
The career path found me the same way it finds most people who end up doing meaningful work. Through pain, through failure, and through one person who showed me what was possible.
The most interesting story of my career did not happen in a boardroom. It happened in a hospital bed.
I suffered a cervical spine injury in 2005. That kicked off 18 years as a patient. I went through 8 spine surgeries. I lived on opioids for years. I saw healthcare from the inside at a level most people never do. My care costs reached roughly $20 million to $25 million over time. I learned what helps patients. I also learned what breaks them.
Then on May 15, 2023, I underwent a 13-hour cervical reconstruction. I woke up pain-free. That moment changed everything. I had spent nearly two decades surviving the healthcare system. Now I could finally build on what I had learned inside it.
That experience shaped my work at Archo Advocacy, ELAVAY, and everything I do around Advocacy Intelligence. I do not study healthcare from a distance. I lived it. I paid for the lessons in pain, time, and persistence. Now I use those lessons to help companies listen better, move faster, and create better outcomes for patients.
Can you share a story about the funniest mistake you made when you were first starting? Can you tell us what lesson you learned from that?
Quite frankly, I would say falling off the stage by missing the stairs. I cannot look down. It was an odd staircase. I was presenting at the Chief Patient Officer Summit, having just spoken to a crowd of about 200 healthcare executives, and the next thing I knew, I was staring at the floor.
That moment showed me a few things. It reminded me that people are willing to assist you if you only let them. It’s a major facet of the EMPWRD patient model, developing your support team. But I was reminded by those individuals who rushed to help me up that it still takes your acceptance of the help to change the circumstances. It was also a reminder of how far resilience can take you and that nobody will remember your falls if you continue with the mission. I got back up and shook hands with those who thanked me for the presentation and were seeking to work with the guy who had just fallen off the stage. So, remember, nobody else remembers your falls, as long as you keep pushing forward with a righteous mission.
Can you please give us your favorite “Life Lesson Quote”? Can you share how that was relevant to you in your life?
“Make Your Mess Your Message.”
I love that quote because it so clearly gave me my why when I was going through opiate withdrawal symptoms, preparing for my last surgery. The surgeon’s mandate was that I be off opiates for six months before he would schedule surgery. The hellish process left much to be desired, and I had plenty of time to think. It was this quote, along with my faith, that got me through it.
I spent 18 years fighting through pain, setbacks, surgeries, dependence on opioids, and a healthcare journey that could have broken me. Instead, it built my conviction. It sharpened my empathy. It gave me a level of resilience I could not have learned any other way. Better yet, it prepared me to give back to the patient I once was and to build a career helping the patient I used to be.
I do not glorify suffering. But I do respect what struggle can produce when you refuse to quit. I say it often; I wouldn’t change a thing about my past. It’s what’s prepared me to take on the mission I have today.
How would you define an “excellent healthcare provider”?
An excellent healthcare provider combines skill, judgment, humility, and humanity. They don’t see the individual across from them as a patient, but rather a customer they can learn from.
They know their craft. They communicate clearly. They tell the truth even when the truth feels hard. They listen without rushing. They look at the whole person, not just the chart, the scan, or the billing code.
For me, excellence in healthcare starts with trust. Patients need to feel seen, heard, and respected. They need a provider who can say, “I believe you. I understand what is at stake. Here is the plan.”
The best providers also stay curious. They do not let ego drive the room. They ask better questions. They work across teams. They understand that great care does not stop at diagnosis. Great care helps people navigate what comes next. Great providers recognize that what the patient has not told them cannot be used to generate their diagnosis and understand that effective conversations are paramount to better patient outcomes.
After everything I have lived through as a patient, I can say this very simply: excellent providers make you feel safer, stronger, and more informed. They do not just treat illness. They help restore dignity.
What are your favorite books, podcasts, or resources that inspire you to be a better healthcare leader? Can you explain why you like them?
A few resources have shaped how I think and lead.
First, I value patient communities more than almost any formal resource. Real patients tell you what market reports often miss. They tell you where the friction lives. They tell you what language lands and what language fails. If you want to lead well in healthcare, listen to where people speak honestly.
Second, I gravitate toward books about resilience, leadership, clear thinking, and, of course, my Christian faith. I appreciate voices like Simon Sinek because they push leaders to start with purpose, not ego. I also like thinkers who can make hard ideas simple and useful for the masses.
Third, I learn a lot from operator-driven podcasts and founder conversations, even outside healthcare. Good business is good business. I want to hear how smart people make decisions, build trust, cut waste, and create momentum.
That said, my biggest source of insight is still lived experience. Eighteen years as a patient taught me to lead with urgency, empathy, and accountability. That perspective shapes every article I write, every client conversation I have, and every framework I build.
Are you working on any exciting new projects now? How do you think that will help people?
Yes. I am building several things that all connect to one core mission: Ensure the patient voice is at the center of all healthcare organizations and healthcare decision-making. Whether empowering patients to be heard or assisting healthcare professionals and companies in listening and acting, the patient voice is paramount to successful healthcare outcomes.
One major focus is growing ELAVAY and the BIOADVOCATE Benchmark Report. That work gives pharma and biotech leaders real data on how patient advocacy functions operate, where the gaps are, and what strong execution looks like.
I am also expanding Archo Advocacy’s consulting and training work, especially around the ACE Model: Access, Credibility, and Execution. I built that model to help teams move advocacy from a nice idea to an operational discipline and ensure market access and key account management teams maximize their success in a highly integrated world.
Other projects I am excited about are the AdvocateBridge and the EMPWRD Patient Record. AdvocateBridge aims to connect patients with organizations that can support. The EMPWRD Patient Masterclass and Record are focused on educating and empowering patients to be better prepared to engage in the healthcare economy through both a structured training program and smartphone application. The Record allows patients to track symptoms daily, summarize their own data, and synthesize questions to ask their physician about their health. When you can come alongside a patient early in the process, it’s amazing to see how different their reality can be.
At the highest level, all of this supports the same goal. I want to help build a healthcare system where educated patients and responsible organizations (companies or hospitals/health systems) work together to remove barriers to care. If we do that well, we help people get access sooner, make better decisions, and live better lives.
Ok, thank you for that. Let’s now jump to the main focus of our interview. According to this study cited by NBC, the US healthcare system is ranked as the worst among high-income nations. This seems shocking. Can you share with us a few reasons why you think the US is ranked so poorly?
I do not find that ranking shocking. I find it honest.
The United States spends more on healthcare than countries of similar size, yet still ranks last among the top 10 high-income countries. That gap tells you the problem is not effort alone. It is design.
First, we built a system that makes access too hard. Too many people delay care because of cost. Too many people carry insurance yet cannot afford to use. As I like to say, “these days, paying your insurance premium only gives you the opportunity to pay your deductible. For a family of four, that could be $40,000- $50,000 before insurance even kicks in. So, we have a pervasive insurance system that is increasingly expensive and still too costly to use when you need it, leaving patients underinsured or uninsured. Gone are the days of truly affordable health insurance. As with the government’s involvement in student loans, government guarantees only lead to higher prices.
Second, we reward volume, complexity, and middlemen more than clarity, prevention, and outcomes. We built a machine that moves money well but does not always care well. Patients feel that every day. They spend hours chasing prior authorizations, refills, appointments, and answers when they should spend that energy getting better.
Third, we do a poor job connecting medical care to real life. Health does not live inside a hospital or clinic. Social determinants of health are pervasive and often ignored. That includes Poverty, food insecurity, transportation gaps, unstable housing, addiction, and violence, all of which shape outcomes. Yet hospitals and physicians do not involve themselves in the personal lives of their patients to even know what could be impacting their health where they live.

Fourth, we burn out the people we need most. A strained system cannot produce great care at scale. When physicians and nurses work short-staffed, overloaded, and buried in bureaucracy, patient care suffers. That is not a character flaw in clinicians. That is a system failure. The average length of a patient visit with a physician is 7–8 minutes. How can you gather enough information about a patient in that timeframe to make an accurate diagnosis that a patient can understand, not to mention treat it appropriately in that short a time window?
At the highest level, I think the U.S. ranks poorly because we confuse activity with performance. We do a lot. We spend a lot. We bill a lot. But we do not consistently make care easier, faster, more humane, or more effective for the person living with the problem. As you will hear, we do not have healthcare; we have sick care.
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As a “healthcare insider”, if you had the power to make a change, can you share 5 changes that need to be made to improve the overall US healthcare system? Please share a story or example for each.
1. Make care easier to access and more affordable.
I spent years living through a system where every next step felt like a fight. When a patient with serious pain or a complex condition has to weigh a bill, call an insurer three times, and still wonder if treatment will get approved, the system has already failed.
2. Rebuild primary care and patient navigation.
Most patients do not need more noise. They need a trusted quarterback. They need one person or team who helps them understand the plan, sequence the next steps, and catch problems early. During my own healthcare journey, the hardest moments often came between visits, not during them. A scan might be done. A referral might get placed. Then the patient goes home and sits in fear, pain, and uncertainty while nobody connects the dots. That space between appointments can wreck people. Strong primary care and navigation can close that gap.
Unfortunately, primary care physicians are the lowest-compensated provider type, yet they are in the greatest need these days. You cannot have effective healthcare when 80% of physicians are specialists. It’s supposed to be the 80/20 mix in the other way!
3. Remove administrative waste, especially focused on prior authorization reform.
Prior authorizations, duplicate forms, fragmented records, and endless back-and-forth crush patients and clinicians alike. I have lived the patient side of that friction. I know what it feels like to need an answer now and get a form instead. It creates a delay when people need speed. It creates confusion when families need clarity. It creates exhaustion when teams need focus. We need a system that treats time as a clinical asset, not as free raw material to burn. We not only spend the most on healthcare in the US, but we also spend the most on administrative services like prior authorization, as well, with about 25% of spending going to administrative tasks, costing US citizens tens of billions of dollars annually.
4. Tie incentives to outcomes that matter to patients.
I would ask better questions. Did the patient get access faster? Did pain drop? Did the function improve? Did the treatment plan hold up in real life? Did the family understand what came next? Too often, the system celebrates completion of a process while the patient still struggles. I have seen patients hit every compliance checkbox and still feel lost, blocked, or sicker. I want incentives tied to real-world progress.
5. Treat the patient voice as operating intelligence, not as a marketing prop.
That belief drives much of my current work. Patients can tell you where access breaks, where language confuses, where trust falls apart, and where support disappears. For example, if ten patients tell you they got lost after a diagnosis because nobody explained the next step in plain English, that is not anecdotal noise. That is operational data. If leaders listen early and act quickly, they can fix issues before they lead to denials, abandonment, worsening disease, or avoidable costs.
What concrete steps would have to be done to actually manifest these changes? What can a) individuals, b) corporations, c) communities and d) leaders do to help?
Change happens when people stop talking in slogans and start owning a lane.
Individuals need to ask better questions, keep records, challenge vague answers, and advocate early. Patients and families should document symptoms, denials, delays, and costs. That creates clarity and leverage.
Corporations need to stop treating patient centricity like a branding exercise. Pharma, biotech, payers, health systems, and vendors should map where patients lose time, drop out, get denied, or give up. Then they need to fix those points with measurable accountability. Fund navigation. Simplify support. Reduce friction. Pay for outcomes that matter.
Communities need stronger local support systems. That means patient groups, faith communities, schools, employers, and local leaders working together to improve health literacy, transportation, trust, and access. Good care does not start at the specialist’s office. Good care starts where people live.
Leaders need to make fewer speeches and more decisions. Expand access. Simplify benefits. Build primary care capacity. Measure delays. Publish denial and abandonment patterns. Reward teams that solve real problems for patients. If leaders want a better system, they need to stop protecting the maze.
How do you think we can address the problem of physician shortages?
We need to treat physician shortages like a national security issue, because it is.
First, expand graduate medical education. If we do not increase residency slots, we will keep training talent in a bottleneck. Far too many med students are left out of the match system. Usher those folks into the primary care field! When it comes to primary care, increase the reimbursement for E&M codes, your standard well individual visit. Value the work of the primary care provider in keeping the community health, rather than paying exorbitant amounts to specialists only, who are needed when the initial problem has exacerbated.
Second, build stronger pipelines into medicine from rural, underserved, and nontraditional communities. People often stay close to where they train and where they feel rooted.
Third, use team-based care better. Let physicians practice at the top of their license and let advanced practice providers, navigators, pharmacists, and care coordinators carry the work they can carry well. Better yet, ensure the work of care navigation is billable to insurance so that hospitals stop cutting those roles due to the balance sheet!
Fourth, reduce the nonsense that wastes physician time. A clinician who spends hours on bureaucracy every week does not actually have full clinical capacity.
I would also add one more point. We cannot fix physician shortages if we ignore trust and working conditions. You do not keep talent by making the job feel impossible.
How do you think we can address the issue of physician and nurse burnout?
We need to stop acting like burnout lives inside individual weakness. Burnout usually grows in broken environments. 80% of providers are now owned by the hospitals they once sent patients to, or even insurance companies.
The American Hospital Association highlighted several major drivers of burnout in a 2024 review of clinician data. Staffing shortages stood out as the top factor for both physicians and nurses.
Bureaucratic tasks, chaotic workplaces, lack of workload control, and after-hours work due to an overly booked schedule all contribute to burnout. None of those problems gets solved by telling a nurse to meditate harder.
I would start with staffing and technology as ways to alleviate burnout. Lean into technology and AI to minimize the administrative tasks for providers and healthcare practitioners. While we are at it, ensure that the administrative work of fighting to appeal a denial is billable to a physician by the hospital, the health system, or the insurance company. Time is money. Frontline tools at the dawn of AI, if provided to these practitioners, can provide immense support and allow the providers to focus on the patient.
Finally, I would put control back in providers’ hands. Burnout happens when there is responsibility without control. Let providers control their schedules, how many patients they can effectively see per day, and how to develop workflows to reduce administrative burden. But also ensure that, in safe working environments, providers feel comfortable speaking up without being punished by leadership. That support needs to be real, accessible, and stigma-free. Burnout is not just a numbers issue; it’s a patient care issue, an economic issue, and a national security issue.
You are a person of great influence. If you could inspire a movement that would bring the most amount of good to the most amount of people, what would that be? You never know what your idea can trigger. :-)
I would build a movement around educated patients and accountable systems, exactly what I am building with the EMPWRD Patient Method & the Fusion Formula.
That is the heart of what I believe. When patients understand their condition, their options, and their rights, they make better decisions. When companies, providers, and institutions face real accountability for access, communication, and outcomes, they perform better. Put those two forces together, and you can lower barriers to care at scale.
That movement would push for clearer communication, faster access, stronger advocacy, better use of patient insight, and more responsibility from every player in healthcare. I believe patient education is one of the highest leverage moves in the entire system. An informed patient asks better questions. Better questions force better answers. Better answers lead to better decisions. Teach the EMPWRD Model, or at least healthcare and healthcare-economics & incentives 101, in high school.
If I could help normalize one idea, it would be this: the patient voice is not soft intelligence. It is strategic intelligence. It should shape how healthcare gets designed, delivered, measured, and improved. Stop treating patients like a side effect of healthcare! They are the customer and the reason the system exists in the first place.
How can our readers further follow your work online?
Readers can follow my work in a few places.
For my company, consulting work, market research, and publishing, visit archo.io. For my personal platform, the EMPWRD Patient, FUSION Formula, speaking, and broader thought leadership, visit matttoresco.com.
I also share ideas and commentary on LinkedIn, X, Instagram, and TikTok at @matttoresco, where I often opine on patient advocacy, healthcare friction, and the business case for what I call Advocacy Intelligence.
Thank you so much for these insights! This was very inspirational and we wish you continued success in your great work.

