One fifth of Canadians live with some form of chronic pain and the impact of pain on people varies significantly. Do you live with chronic pain? Take part in the Circa Pain study today!
"2022 is feeling a lot like 2021! The past few years have been even more challenging for those of us living with autoimmune disease." Read a message from our President Linda Wilhelm.
This month, we would like to introduce you to Lupus Ontario - an organization that supports people living with Systemic Lupus Erythematosus in the province.
On November 12, 2021, in celebration of the #NationalPainAwarenessWeek, the Facebook live event was hosted by an arthritis blogger and advocate Lene Andersen (The Seated View) with guests Michael Kuluva and Linda Wilhelm who shared their experience on how Canadians living with arthritis cope with pain in their everyday life. Check out this Facebook
The Research Team at the University of Waterloo is working on the development of an evidence-based deprescribing guideline for opioid medications for persons over 55 years of age. This project is led by Dr. Feng Chang, a clinical pharmacist at the School of Pharmacy, University of Waterloo. For this project, they are recruiting participants with [&
Join us to celebrate the National Arthritis National Pain Awareness Week on November 7-13, 2021!
CAPA is participating in the upcoming CADTH Symposium on Tuesday, November 2, 2021 at 10:00-4:00 pm EDT. Our President, Linda Wilhelm, Vice-President Dawn Richards and 2nd Vice-President Laurie Proulx are presenting on and participating in the panel discussions on such important important issues as Accessing Care During a Pandemic, Rapid Living Rev
Welcome to 2022! "2022 is feeling a lot like 2021!" said CAPA President Linda Wilhelm. January 2022 had been a busy start of the new year for CAPA team, as we have been engaged in providing patient input to CADTH submission for new lupus drug, preparing for a poster presentation at the CRA annual meeting and many more.
This month CAPA has been participated in numerous events in support of the National Pain Awareness Week. Learn what we have done by reading our newsletter!
CAPA had been busy with various activities over the month of October including involvement in the release of the Baring It All final report, Fashion Show, compiling information on the 3rd dose vaccine access in provinces and many more.
Over the summer, CAPA had participated in the development of a CRA virtual care statement, voiced the patient perspective on proposed drug pricing changes on patients and did an extensive survey on sexual and reproductive health in collaboration with other patient groups. We had planned lots of fun activities for September, the Arthritis Awareness month!
This month, CAPA team has been involved in the development of the video on a biosimilar medication. launching the new parenting resources, speaking at the webinar on an action plan for pain in Canada and many more!
This month CAPA team has been busy advocating for the second dose of the COVID-19 vaccine for people with autoimmune rheumatic conditions, updating and launching our pregnancy resources and being at the forefront of "A call for action to #PrioritizePain" campaign. Learn more by reading our newsletter!
In this newsletter edition, we invite you to provide input to the three very important surveys on the sexual and reproductive health in arthritis care, the COVID-19 vaccine access and the COVID-19 Global Rheumatology Alliance. Register and join us for the Shared decision making webinar on April 25th to be hosted by Dr. Claire Barber, Dr. Glen Hazlewood and Dr. Karine Toupin April.
This month we continue informing you about the rollout of the COVID-19 vaccine which is currently underway and what this means to many people living with rheumatic diseases. Read more.
When you live with arthritis,
information is your most important tool.
The Canadian Arthritis Patient Alliance (CAPA) works with various groups in the arthiritis community to ensure the voice of people living with arthritis is heard and to bring you up-to-date information on issues that affect the arthritis community. We work with healthcare professionals, health organizations, clinicians, industry, health charities, researchers, and various levels of government.
We keep Canadian people living with arthritis and their support groups understand more about their disease and have a voice in managing it.