In a life shaped by chronic pain, one woman discovers unexpected peace in quiet moments—watching birds, breathing deeply, and learning to truly savor life.
A powerful personal story of aging with chronic pain and Ehlers-Danlos syndrome—exploring loss, resilience, and finding new purpose and meaning in life.
After injury and chronic illness changed her life, one discovers that moving forward doesn’t mean going back—it means redefining purpose and self-worth.
On April 5, U.S. Pain Foundation’s Senior State Advocate, Wendy Foster, flew to D.C. for the joint meeting of the Anesthetics and Analgesic Drug Products Advisory Committee and Drug Safety and Risk Management at the Food and Drug Administration...
U.S. Pain urges its members to participate in livestreams of two major events about pain policy at the federal level happening this May. The first is a meeting at the U.S. Department of Health and Human Services entitled, “Implementation of the...
As a nonprofit, U.S. Pain Foundation runs solely on contributions from corporate sponsors as well as private donors. The organization is encouraging members to consider hosting fundraising events to help support its mission and services. “We rely...
Currently, 36 million Americans are living with migraine disease; four million of them have chronic migraine, meaning they have 15 or more attack days per month. There are many different ways you can help spread awareness and stop the stigma of...
The National Council on Patient Information and Education (NCPIE) recently announced that the U.S. Pain Foundation is among eight patient groups selected in the “consumer organization” board of directors category. U.S. Pain will serve on the board...
Medical cannabis activists had an exciting month in April: on April 19, West Virginia became the 29th state to legalize medical marijuana, and, from April 7 to 11, many activists attended the largest conference dedicated to improving access to...
