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...
By: Ellen Lenox Smith Do you have an issue that you are concerned about? Do you see where change needs to be made? Are...
Congressional Budget Reports accompany the annual federal budget that Congress develops each year. In these...
The U.S. Pain Foundation is pleased to announce its new Director of Communications: Scott Rogers. Rogers joined the...
Migraine, headache, and cluster diseases affect more than 38 million Americans. To increase understanding and empathy...
By: Janet Jay The U.S. Pain Foundation is pleased to announce its virtual support group connecting veterans and active...
Our exploration of tools to help you reduce your pain and improve your overall health and well-being continues this...
City & State: Brooklyn, NY, and Trumbull, CT Age: 46 Pain warrior role: U.S. Pain advocate since 2019 What type of...
By: Brandy Garcia My son was 4-years old the first time he said, “Mom I have a headache.” At the time I did not think...
In an increasingly virtual world, many health-related support groups are moving online. But not all support groups are...