Canadian Pain Task Force released its final report An Action Plan for Pain in Canada. Add your voice to the call to #PrioritizePain. Read the report and learn how you can make your voices heard on the issue of pain in Canada.
Dr. Stephanie Garner will be holding a Zoom session for all rheumatology patients to answer your COVID Vaccine related questions.
On April 25th, CAPA hosted the webinar with rheumatologists Drs. Claire Barber and Glen Hazelwood and health researcher and occupational therapist, Dr. Karine Toupin April who are leading projects that support #shareddecisionmaking in rheumatology. Watch this video to learn more!
Are you considering talking to your healthcare provider about biosimilars or has your healthcare provider talked to you already about biosimilars? We have put together some questions that might be helpful to be part of a conversation with your healthcare provider about biosimilars and brand name biologics.
We invite you to complete the Global Rheumatology Alliance COVID-19 Vax Survey and help researchers in learning how people with rheumatic disease make decisions regarding the vaccines in light of their rheumatic disease.
CAPA’s Feedback to VCAG Recommendations on Exceptions to Extended Dose Intervals for COVID-19 vaccines
CAPA wrote this letter due to concerns about the time delay that the National Advisory Council on Immunization (NACI) has deemed acceptable between first and second doses of vaccinations for people living with forms of inflammatory arthritis and who are on immunosuppressants.
We continue introducing our new Board members and invite you to listen to Emily Sirotich’s story. Emily is a patient partner and a current PhD student in Health Research Methodology at McMaster University. “The COVID pandemic really pushed the real impact that patients can have not only as participants in research but people who lead [&
Please join us to try a new educational companion, a free, user-friendly tool Arthritis+Patient App that is designed to provide patient education and self-management. Learn more about its functionality and use here.
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.
This month CAPA Board members were involved in the guideline panel discussions on the new COVID-19 vaccination recommendation from the Canadian Rheumatology Association, attended and participated in the annual 2021 Canadian Arthritis Research Conference, contributed as panel moderators and presenters, and many more.
Welcome to 2021! "The 2020 was a year like no other where our homes have become the focus of our lives, our workplace, a classroom, and our sanctuarys", said the CAPA President Linda Wilhelm. January 2021 had been a very busy start of the new year for CAPA team, as we have been engaged in the development of the COVID-19 vaccine decision aid, writing a letter to NACI and public health officials across Canada, providing patient input to CADTH submissions for new drugs and many more.
2020 has been a challenging year for so many of us! As CAPA team, we have tried our best to support the arthritis community throughout the pandemic by addressing drug shortages, developing evidence-based resources, hosting a virtual fashion show and many more. To end the year on a lighter note, the CAPA Board of Directors wish you the best holiday season and best of luck in the year ahead!
This month CAPA has introduced its #ArthritisThenNow infographic designed to describe how arthritis treatments and life has changed for people living with inflammatory arthritis over the last 20 years! Read more about many other activities and projects we have been involved into!
This month CAPA has teamed up with CreakyJoints in the United States and Australia to bring our readers special content devoted to the World Arthritis Day for them to learn what it’s like to live with arthritis during the pandemic from a global perspective.
In this newsletter edition, we are celebrating the September Arthritis Awareness Month and presenting our new video with Board member and fashion designer, Michael Kuluva, as he speaks with 2nd VP, Laurie Proulx and...much more in this edition. Join us in raising awareness about arthritis!
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.