How does Spondyloarthritis Pain Affect Your Quality of Life?

The results of our Quality of Life Survey are in! 

We asked Spondyloarthritis (Spa) patients from across Canada to share their experiences of how Spa pain affects their lives. Over 850 of you raised your voice to be included in our national survey, and we have compiled your responses into our 2021 Quality of Life Survey Report. Your experiences are helping us learn how we can best support you in your journey with SpA.

Your responses affirm the significant impact Spondyloarthritis has on patients’ quality of life. They also reveal what patients need to live a better life with SpA. Things like a better awareness and understanding of symptoms, an early diagnosis and access to effective treatment options, the essentials of helping Canadians living with SpA and their families.

Our team has combed through the data to develop five recommendations to help patients that we can use in our mission to advocate and support SpA patients. Check out our recommendations below to find resources you can use today to take control and start living a better life with SpA. 

What we learned about SpA and Quality of Life

We learned that chronic SpA pain affects a patient’s:

  • Sleep  :  89% of respondents said that Spondyloarthritis impacts their sleep.
  • Mental Health : 56% of respondents said they lived with anxiety and depression. 
  • Relationships:  37% of respondents said that they do not feel they have a good support network.
  • Livelihoods:  Only 41% of respondents felt their employer would accommodate their illness, and many are afraid to tell their employer about their condition.

Can you live a better life with Spondyloarthritis?

Yes! Although living with SpA can have an impact on your quality of life, patients just like you are taking control and living a full life. It’s not easy, but our goal is to help you have more good days. Every day will not be easy, but we’ve come up with 5 recommendations to help patients like you: 

We recommend: 

What’s Next? 

We are committed to boldly sharing the impact of SpA on all patients. Surveys like this help the CSA continue raising awareness and advocating for better care and health outcomes, and developing resources to support the SpA community in Canada. 

Join our mailing list or our community on Facebook for further updates

Share & Download the report & our Infographics!

You can download the full report here (right click -> save as in your browser).


Click on any of the below infographics to view in full size. You can right click -> “Save As” to save locally to your device, or you can click on the appropriate social media icon in the top left corner of each image to share to your preferred social media platform!