Surviving and Advocating for a Better Future for Those with Sickle Cell By Emil DeAndreis One night, seven-year-old...
Surviving and Advocating for a Better Future for Those with Sickle Cell By Emil DeAndreis One night, seven-year-old...
Racial Bias, Lack of Patient-Centered Care Delayed Diagnosis By Tara Bracco In 2020, Isiah Lineberry lost the use of...
By Kirsten BallardEveryone seeking emergency care navigates wait times, insurance, and harried medical staff, but for...
A statement from U.S. Pain Foundation As an organization, the U.S. Pain Foundation strongly condemns racism and...
The Pediatric Pain Warrior Program’s virtual retreat, which began in May, has been busy providing education,...
Pain Connection continues its interactive series, “Building Your Toolbox,” this Tuesday, July 7 at 7:30 pm ET. The...
City & state: Los Angeles, CA Age: 37 Role: U.S. Pain ambassador/advocate since 2019 Health conditions: Anxiety,...
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Approximately 5,400 individuals and organizations responded to the Centers for Disease Control and Prevention (CDC)’s...
U.S. Pain is pleased to share that Louisiana Governor John Bel Edwards has signed into law House Bill 819, which...
Throughout June as National Headache and Migraine Awareness Month (MHAM), the U.S. Pain Foundation and fellow patient...
While most in-person conferences and meetings have been canceled or postponed as a result of the pandemic, U.S. Pain...