The Canadian Arthritis Patient Alliance (CAPA) wrote a letter to the current Minister of Health Marjorie Michel regarding the importance of reintroducing federal legislation on health data interoperability, modeled on the former Bill C-72 (Connected Care for Canadians...
Canadian Arthritis Patient Alliance (CAPA) advocates for a coordinated, inclusive national approach that prioritizes fairness, equity, and meaningful patient involvement at every step. This letter highlights that ENP and TNP only address a narrow part of the broader...
By: Shanelle Gilman Makers Making Change, a program of the Canadian non-profit Neil Squire, connects people with disabilities, like arthritis, to a community of volunteer makers who can build affordable, open-source assistive devices. The platform serves as an online...
Chronic pain is more than just a number on a scale. For people living with arthritis and other persistent conditions, the question “What’s your pain level from 1 to 10?” often fails to capture what really matters: how pain affects sleep, mood, daily tasks, social life...
The CAPA Lived Experience Webinar will take place on Wednesday, November 19, 2025, at 6:00–7:30 PM Eastern Time as part of the Annual General Meeting (AGM). REGISTER HERE. This session explores the challenges, emotions, and lessons learned through the process of...
English 
Français du Canada