By: Jennifer Burt, BScPT AHPA Past President St. John’s, Newfoundland and Labrador Attempts to start a professional body of allied health professionals working in rheumatology in Ontario began in the 1970’s. Planning began in earnest in the early 1980s and was supported by The Arthritis Society (TAS), Ontario Division. In her capacity as Di
by: Linda Wilhelm As October 2014 was winding down, members of the Canadian Arthritis community, including the entire Board of The Canadian Arthritis Patient Alliance, gathered in Toronto for the 2nd Annual Arthritis Alliance of Canada (AAC) Conference and Research Symposium. The three day conference was jam packed, beginning on Thursday, October 3
On October 18, 2014, I had the pleasure of attending the 1st Forum on Arthritis organized by Québec division of The Arthritis Society. The event gathered 940 participants, speakers, vendors and partners. In addition to sessions for the general public, continuing education sessions were offered to health professionals. Topics discussed were chosen
by: Laurie Proulx Like so many of you, I’ve learned to deal with this disease. I was diagnosed with Juvenile Idiopathic Arthritis at the age of 14. Hardly a day goes by where I don’t feel pain in some part of my body. But I’ve learned that there are always a few more surprises this […]
by Marie-Eve Veilleux Montreal is one of the least accessible cities in Canada. Among the challenges faced by disabled people is that the metro system only has 7 accessible stations out of 68, all located on one single metro line (see map of the accessible metro). At the current rate, the Montreal Metro would be fully accessible by 2090. [&hell
By Laurie Proulx People living with arthritis have to take medications (often many!) to control their disease. I’ve had to take medications for the last 20 years in order to control the Juvenile Idiopathic Arthritis (JIA) that struck me when I was 14 years old. I have usually taken for granted that these medications go […]
I don’t remember a lot of the battles my mom had to fight before I could take over to fight my own, but I know one thing: she always made sure I would grow up in a regular environment and that’s probably the greatest gift she ever gave me. I have juvenile arthritis, so I […]
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!
This newsletter edition highlights CAPA's activities during the summer season. We kept on contributing patient perspectives to research, health policy and education. Read our summer newsletter to find out more.
This month CAPA team have been actively participated in various initiatives while pandemic is moving into a new stage. CAPA's #ArthritisAtWork social media campaign video presentation was the highlight of the international EULAR e-Congress held on June 6, 2020. Read more about what we have been up to!
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.