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From Barriers to Bridges: Making Pain Research More Inclusive
Pain research is strongest when it is inclusive and accessible to every group and population that can benefit from it—but many individuals still face barriers to participating in clinical trials and research. The obstacles inhibiting greater...
From Overlooked to Understood: Why Research Must Reflect Real Lives
Every November, the U.S. Pain Foundation brings our community together to spotlight something powerful: knowledge. We call it KNOWvember—a month-long campaign amplifying a theme that matters deeply to the pain community. This year, we’re focusing...
Staying in the Know: Why Disease Awareness Matters for Diabetes and Diabetic Peripheral Neuropathy
Learn why disease awareness is essential for diabetes and diabetic peripheral neuropathy (DPN)—from recognizing symptoms to treatment and research options.
Licensed to Treat, Unprepared for Pain
Chronic pain is the top reason Americans seek care—yet providers feel unprepared. Here’s what a new U.S. Pain Foundation report uncovers.
My Daughter’s Pain Is Invisible – She Is Not
Behind every chart is a life. One mother’s story of pediatric chronic pain exposes the heartbreak, resilience, and hope in the face of invisibility.
Parents of Kids with Pain: Burned Out, Broke, and Desperate for Support
Parents of children with chronic pain face burnout, job loss, and crushing costs—revealing urgent gaps in support, coverage, and caregiver protections.