CMS announced their intention to improve pain care for Americans over 65 or disabled by paying separately for...
Blog Articles
Understanding Life With Pain
Research tells us that 50 million Americans live with chronic pain, or pain that lasts most days or every day for...
Two U.S. Pain Foundation Support Group Leaders’ Books Published
U.S. Pain Foundation is proud of its constantly expanding network of chronic pain support groups. There are now over...
Announcing 2019’s Ambassador of the Year: Ernie Merritt
U.S. Pain Foundation is pleased to announce that the 2019 Joselynn Badman Ambassador of the Year is Ernie Merritt....
A Q&A with the newest member of the Board of Directors: Marv Turner
U.S. Pain Foundation is pleased to announce the newest member of its Board of Directors: Marv Turner. Turner is the...
Saco resident receives prestigious pain advocacy award
For immediate release Contact: Emily Lemiska 860-748-1349 emily@uspainfoundation.org Middletown, Conn. (Feb. 4,...
Pediatric Pain Warrior Program reveals new video; Points for Pain game scheduled for Feb. 20
The Pediatric Pain Warrior Program is dedicated to helping kids with pain and their families feel less alone and...
Iowa: Bill that keeps you on your medications headed to hearing
Iowa State Rep. Tom Moore has proposed legislation that would keep individuals with chronic conditions medically...
Take these surveys to help expand understanding of CRPS and chronic migraine disease
No matter what health issue you deal with, your experience is unique. Sharing your reality and your feelings about it...
U.S. Pain spearheads joint letter to Congress from 30 patient and professional groups
U.S. Pain Foundation recently spearheaded a joint letter to the U.S. House Energy and Commerce (E&C) Committee and...
Hearing on medical cannabis important progress; take action to ask for second hearing
On Jan. 15, the House Energy and Commerce Subcommittee on Health held a hearing on discrepancies between state and...
How I manage EDS, part three: ER and inpatient tips
By Ellen Lenox Smith People living with Ehlers-Danlos Syndrome (EDS) are often afraid to go to the hospital, due to a...