Support and advocacy information for individuals dealing with chronic pain.

Chronic Pain Management: Insights and Reflections When you live with chronic pain long enough, you learn quickly that it doesn’t just sit in your body. It weaves into your mind, your emotions, your spirit. And while I’ve tried every therapy, medication, and strategy under the sun, one of the most surprising tools I’ve come to…

Living with Chronic Pain When living with chronic pain, anger often lurks in the background. It can flare up quickly—sometimes with good reason, sometimes seemingly out of nowhere. Anger isn’t just an emotional reaction; it’s part of the way our brains and bodies cope with an ongoing assault. But if we don’t recognize and address…

Living Better with Chronic Pain When I first heard the phrase “the obstacle is the way,” I thought it was a clever slogan—something you’d see on a motivational coffee mug, or an ill-fitting tee shirt. But like so many things that seem simple, it stayed with me. It echoed through the toughest years of my…

Living Well with Chronic Pain On average, it takes 17 years for clinical trial results to reach routine practice. That’s not just a statistic—it’s a warning. This number comes from health policy research that’s been reviewed and confirmed across multiple studies. One of the most cited estimates is from Dr. Eugene Balas and colleagues, who…
Step Therapy, Prior Authorization, and What California’s Budget Means for People With Chronic Pain Co-author: Victoria Killian, BCPA, PCM, CDME Living with chronic pain is already a full-time job. Fighting for care shouldn’t be another one. If you’ve lived with pain for any length of time, then you’ve probably had to fight tooth and nail…

Putting People With Lived Experience at the center of research, guidelines, and health care One of the most common phrases I hear in patient engagement circles is PWLE — short for People With Lived Experience. What that really means is simple: people whose personal experiences with illness, chronic conditions, or caregiving make them experts in…
Putting People With Lived Experience at the center of research, guidelines, and health care. When I first entered the world of clinical trial research, I heard the term “stakeholders” over and over. It was the word everyone used—sometimes loosely, sometimes with precision. But over time, I realized that the phrase could blur the most important…

Putting People With Lived Experience at the center of research, guidelines, and health care. When we use the term PWLE – People With Lived Experience – it’s not just another acronym in health research or advocacy. It’s a way of honoring real lives, real stories, and real expertise that comes from walking through illness, injury,…
Every September we set aside time to highlight Chronic Pain Awareness Month. For those of us living with pain, it’s not just a campaign or a slogan—it’s our daily reality. This month is a reminder to speak up, stand together, and let the world know that chronic pain is real, it matters, and it cannot…

When we talk about caregiving, the focus is almost always on the person receiving care—their needs, their comfort, their well-being. That’s as it should be. But too often, what gets left out of the conversation is the caregiver’s health and resilience. I live every day with chronic pain. I know what it’s like to need…

Being a patient advocate is some of the most meaningful work I’ve ever done. It gives purpose, it connects me to others, and it helps turn pain into something that can help someone else. But here’s the truth: advocacy can also be exhausting. We carry not only our own stories, but the stories of everyone…

Living with chronic pain for over 37 years has taught me more than I ever thought I’d need to know about perseverance, adaptation, and self-discovery. Pain has shaped my days, my decisions, my relationships—and yet, it doesn’t define who I am. What defines me is how I’ve responded. This isn’t a guidebook or a prescription.…

What Works for Me While Traveling With Chronic Pain Travel and chronic pain don’t exactly make the best travel buddies. But over the years, I’ve figured out a few things that help make the process smoother, more manageable, and sometimes even enjoyable. I’m not saying it’s easy. But I’ve learned how to plan, stay flexible,…

A PWLE’s Guide to Asking the Right Questions Reading the results of a clinical trial shouldn’t feel like cracking a code. But too often, it does—especially for those of us living with the conditions being studied. If you’ve ever opened one of those reports and felt like you needed a translator, you’re not alone. I’ve…

A Patient-Friendly Look at the Latest Evidence “Just give me something that works—and doesn’t make me feel worse.”That’s the quiet hope so many of us carry into every doctor visit. If you live with neuropathic pain like I do, you know the drill: try a new prescription, wait it out, cope with side effects, maybe…