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I Asked for Water—And Got So Much More

Parenting a child with chronic pain can feel isolating. Discover how one unexpected moment at camp became a reminder that no family walks this journey alone.

Federal Legislation Introduced: Better Pain Data for Better Treatments

In an important step forward for the chronic pain community, the bipartisan Advancing Research for Chronic Pain Act (ARCPA) was introduced into Congress on July 21.

When Acceptance Isn’t Giving Up

After years of searching for a cure, one mother discovers that acceptance doesn’t mean surrender—it means choosing to live fully despite chronic pain.

Storms Bring a Painful Reminder of Our Disability

When storms roll in, many people with chronic pain feel the effects long before the first raindrop falls. One advocate reflects on weather-related pain flares and the challenges of living with a disability.

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Pain Warrior of the Month: Jeannette Rotondi

Location: Jackson, New Jersey Age: 40 years old Pain Warrior Role: Ambassador since 2013 Conditions: I live with Chronic Migraine, and Ehlers-Danlos Syndrome, which has caused many co-morbidities including arthritis, TMJ, colonic dysmotility, POTS,...

Telemedicine: Breaking down barriers to care

Telemedicine is an exciting new frontier in health care that can provide more accessible, streamlined treatment by connecting patients and clinicians virtually. U.S. Pain Foundation is pleased to announce telemedicine as one of its new state...

NPS event provides encouraging update

Stakeholders in the pain community eagerly tuned in to “Implementation of the National Pain Strategy (NPS) Listening Session” on May 11. The daylong event was hosted by the Office of the Assistant Secretary for Health and the National Institutes of...

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