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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.

Growing Beyond the Lines I Thought Pain Drew: What Leading a Daily Support Group Has Taught Me

What happens when we step beyond the boundaries chronic pain seems to create? Michele Rice shares how community, purpose, and peer support changed her perspective.

It’s Only One Mile: What I’ve Learned About Pacing

What does “pace yourself” really mean when you live with chronic pain? A heartfelt reflection about limits, recovery, and self-awareness.

New EDS Patient: Where Do I Begin?

Just diagnosed with Ehlers-Danlos syndrome? Explore guidance, symptoms, and real-life strategies to help you navigate EDS and HSD with confidence.

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Read U.S. Pain’s letter to the FDA

Read U.S. Pain’s letter to the FDA

U.S. Pain Foundation was among several hundred organizations and individuals to weigh in on a recent Food and Drug Administration (FDA) comment period. Specifically, the FDA asked for the public's views on two main issues: What criteria the FDA...

How should the FDA evaluate new medications for pain?

How should the FDA evaluate new medications for pain?

We wanted to make you aware of an opportunity to submit public comments to the Food and Drug Administration (FDA). Specifically, the FDA would like the public's views on two main issues: What criteria the FDA should use to evaluate new opioids to...

Pain Warrior of the Month: LaSheila Yates

Pain Warrior of the Month: LaSheila Yates

Name: LaSheila Yates Location: Cedar Rapids, IA Age: 38 Pain warrior role: U.S. Pain advocate since 2019 Health conditions: ulcerative colitis, pelvic floor dysfunction, neuropathic pain, gastroesophageal reflux disease (GERD), pouchitis, cuffitis,...

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