CAPA
@CAPA_Arthritis
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The Canadian Arthritis Patient Alliance (CAPA) is a grass-roots, patient-driven, independent, national advocacy organization with members across Canada.
Canada
Joined October 2015
Parents with inflammatory arthritis, we want to hear from you!. You can participate if you:.• Have inflammatory arthritis.• Have at least one child under 13 years old . Complete an online survey You’ll receive compensation for your time
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RT @earlyarthritis: Saviez-vous que notre site, est entièrement disponible en français ? .Explorez dès aujourd’hui….
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Earlier this year, CAPA President and Managing Director, Linda Wilhelm and Laurie Proulx, hosted an event called DMARD Dialogues in Calgary, Alberta. This event explored the impact of biologics on RA in preventing joint surgeries. Read the report here. 🔗
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Laughter is the best medicine. Join @TNOtoronto if you want to have a little break from your stress, worries or loneliness. This program is for residents in Ontario; all ages are welcome. Please register from the link below. . #Yoga #LaughterYoga
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RT @earlyarthritis: Did you know that most people with early rheumatoid arthritis experience significant improvement—often 50–70%—in pain,….
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RT @Arthritis_ARC: Living with inflammatory #arthritis? Want to move more and live life to the fullest? Check out this awesome resource cre….
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“Patient and/or community engagement as an essential evaluation criterion for these grants, and inclusion of a Knowledge User or Patient Partner as a Principal Applicant or Co-applicant aligns with the Knowledge to Action Framework.”.
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RT @Susanbartlett12: Your input is vital as we look to transform arthritis care in Canada. Please consider completing this brief survey.
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RT @Arthritis_ARC: People with rheumatoid arthritis often lose muscle strength, making daily tasks harder to manage. This research is testi….
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Did you know that Sjögren’s disease can cause dry mouth, dry eyes, or arthritis, painful and weak muscles, neuropathy, and fatigue?. Check out Sjögren’s Society of Canada @SjogrensCa to learn more. #Sjögrens #SjögrensDisease #SjögrensAwareness #SjögrensAwarenessMonth
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RT @takeapaincheck: Join Take a Pain Check today in raising awareness for Sjögren's Syndrome! #SjogrensSyndrome #Sjogrens #SjogrensSyndrome….
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Do you live with rheumatoid arthritis? Share about your experiences in a short survey!. Use the following link or scan the QR code. #RheumatoidArthritis #RA #CanadianArthritisPatientAlliance #CAPA #Survey #Research
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RT @CIHR_IRSC: Congratulations to the 2025 #VanierCanada Graduate Scholars, Canada’s future research leaders! . Meet the awardees: https://….
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RT @TO_dpr: 📢Patient Partners! Been asked to write a Letter of Support (LOS) and not entirely sure what that is? We co-created a resource w….
pxphub.org
Written by Deb Baranec, Jim Kempster, and Dawn Richards Graphic Created by Tianna Magel What is a Letter of Support […]
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RT @fibrocanada: Fibro Chat with Trudy & Janice. When ❓July 8th @ 12PM EDT .Where❓ This Fibro Chat will focus o….
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RT @PutrinoLab: In honor of #PrideMonth2025, I just wanted to take a moment to discuss the crucial role of intersectionality, gender and in….
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June 29 is recognized globally as World Scleroderma Day. Scleroderma is a rare, progressive and chronic autoimmune connective tissue disorder that causes excess collagen accumulation. @SclerodermaCAN.@scleroderma_sso. #Scleroderma #SclerodermaAwareness #AutoimmuneDisease #CAPA
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It's Pride Month!🏳️🌈 . Learn more in this blog post from Anna Samson, a CAPA community member and self-identifying queer person living with axial spondyloarthritis #Pride #PrideMonth #Pride2025 #Inclusivity #Arthritis #InflammatoryArthritis #Osteoarthritis
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