- News & Features
Diagnosed with rheumatoid arthritis, Jennifer Walker shares what compelled her to be a patient advocate and a Patient Governor for ArthritisPower.
"The war on RA rages all around. The outcome is uncertain, but things seem to be at a stalemate."
CreakyJoints is holding a three-day summit in Chicago, where the ArthritisPower Patient Governors and the CJ Patient Council will convene.
In an op-ed for the Daily News, Danielle Yevsa wrote about her experience with an insurer's step-therapy/fail first practices.
The designer's latest collection for his brand, Tumbler and Tipsy, was directly inspired by his own experience as an RA patient.
A look at the struggle patients face when dealing with insurance companies that deny coverage of vital, lifesaving medications which help manage chronic disease and pain.
Patient Advocate Joni’s voice made a difference: House Bill 1366 in Missouri passed!
Last week, fellow patients from more than two dozen U.S. states co-signed a letter with me to welcome the newly appointed (and confirmed!) Commissioner of the Food & Drug Administration (FDA).
It’s easy to poke fun at a community that is invisible. We saw the backlash after the opioid induced constipation ad aired bowl during Super 50. The chronic disease community become the punchline for comedians and also an easy way for politicians to score quick political points.
CJ Blogger Diane Talbert asks those who can to please join her in speaking at an FDA-sponsored public meeting on psoriasis patient perspectives in March
CJ Blogger Lene Andersen says as long as we use the word ‘patient’ to describe ourselves, we will not have meaningful participation in healthcare