Psoriasis Canada

05/12/2026

A great article in the Ottawa citizen on the dermatologist shortage in Canada…the Canadian Dermatology Association is taking action and shining a light on the issue - read how you can support their efforts!

Established in 1925, the Canadian Dermatology Association (CDA) is a member organization that advocates for dermatologists across Canada, underscoring their essential role in the health care system.

05/08/2026

À l'occasion de cette semaine de la santé mentale, nous souhaitons attirer l'attention sur le fait que le psoriasis ne se limite pas à la peau. Le psoriasis peut avoir un impact considérable sur la santé mentale, qui est tout aussi essentielle que la santé physique. Pour en savoir plus sur le lien entre votre corps et votre esprit, regardez l'enregistrement de notre webinaire: https://ow.ly/JoTa50YWyvc

05/08/2026

This Mental Health Week, we’re bringing attention to the fact that psoriasis is more than skin deep. Psoriasis can greatly impact mental health, which is just as vital as physical health. To learn more about how your mind and body are connected, check out our webinar replay: https://ow.ly/hzEq50YWysY

04/17/2026

📣 Our next English Online Support Program is just around the corner!
Living with psoriasis can feel isolating—but you don’t have to navigate it alone. Join a supportive community that understands what you’re going through.
🗓 April 29
⏰ 7:00 PM (Eastern Time)
💻 Online & accessible from anywhere
This session is a safe space to share experiences, ask questions, and connect with others who truly get it. Whether you’re newly diagnosed or have been managing psoriasis for years, your voice belongs here.

✨ Real conversations
✨ Shared support
✨ Practical insights
Spots are limited—secure yours today and take a step toward feeling more supported and understood.

👉 Register now and be part of the conversation.

https://psoriasiscanada.ca/online-support-program/

Online Support Program Welcome to Our Online Support Program for People Living with Psoriasis and Psoriatic Arthritis. Are you looking for a supportive space to connect, share experiences, and gain valuable insights about living with psoriasis and psoriatic arthritis (psoriatic disease)? You’re no...

04/08/2026

Are you 18–30 living with psoriasis, or a parent/caregiver of a child who is? We want to hear from you! Your input will help shape future programs, advocacy initiatives, and resources to better support young people living with psoriatic disease. Take our anonymous survey and make an impact today!

Vous avez entre 18 et 30 ans et vous souffrez de psoriasis, ou vous êtes parent ou aidant d'un enfant atteint de cette maladie ? Nous aimerions connaître votre avis ! Vos commentaires nous aideront à élaborer de futurs programmes, initiatives de défense des droits et ressources afin de mieux soutenir les jeunes atteints de psoriasis. Répondez à notre sondage anonyme et faites bouger les choses dès aujourd'hui !

Link to the survey: https://www.surveymonkey.com/r/2XFMZXV
Link to the survey in French: https://www.surveymonkey.com/r/2XFMZXV?lang=fr

03/24/2026

We want to hear from youth (18–30) and parents/caregivers of youth affected by psoriatic disease. Your input will help shape future programs, advocacy initiatives, and resources to better support young people living with psoriatic disease. Take our anonymous 15-minute survey and make an impact!

Link to the survey: https://www.surveymonkey.com/r/2XFMZXV
Link to the survey in French: https://www.surveymonkey.com/r/2XFMZXV?lang=fr

03/17/2026

Our next Online Support Group is online one week away.

Living with psoriasis isn’t just about the skin — it’s about the emotional weight, the questions, the moments you feel misunderstood.

You don’t have to carry that alone.

Join our next online support session — a safe, welcoming space where you can share, listen, and connect with people who truly get it. No judgment. No pressure. Just real support, real stories, and real strength.

💬 Whether you’re newly diagnosed or have been managing psoriasis for years, your voice matters here.

✨ Come as you are. Leave feeling heard, supported, and stronger.
📅 March 25th at 7pm EST
💻 https://psoriasiscanada.ca/online-support-program/

You are not alone — and you never have to be.

02/28/2026

Today we join the global community in recognizing Rare Disease Day — a day to raise awareness for those living with rare conditions like Generalized Pustular Psoriasis (GPP).
GPP is a rare and serious form of psoriasis that causes sudden flares of painful, pus-filled blisters on red, inflamed skin. These episodes can be life-threatening and often require urgent care.

Though rare, the impact is profound — physically, emotionally, and socially. Awareness means faster diagnoses, more research, and better care.

💜 Let’s stand with everyone living with psoriatic disease — common or rare — and amplify their voices today and every day.

02/20/2026

Living with psoriatic disease can feel isolating — but you don’t have to navigate it alone. 💙

Whether you’re managing psoriasis, psoriatic arthritis, or both, the physical and emotional challenges can be overwhelming. The flare-ups, the fatigue, the appointments, the explaining (and re-explaining) what you’re going through — it’s a lot. And sometimes, the people around you just don’t fully understand.

That’s why our Online Support Program for People Living with Psoriatic Disease exists.

✨ Find a community that truly gets it.
Connect with others who understand the ups and downs of flare days and remission days. Share your experiences in a safe, welcoming space. Learn practical tips for managing symptoms, advocating for yourself, and prioritizing your well-being.

✨ Feel heard and supported.
This is a judgment-free space where your story matters. Whether you’re newly diagnosed or have been living with psoriatic disease for years, your voice is valued.

Living with psoriatic disease can feel isolating — but you don’t have to go through it alone. 💙

Whether you’re living with psoriasis, psoriatic arthritis, or both, the challenges can be physical, emotional, and exhausting. Sometimes, the hardest part is feeling like no one truly understands.

Our Online Support Program for People Living with Psoriatic Disease connects you with a community that does. Share your experiences, s, and find encouragement in a safe, welcoming space.

There’s real strength in connecting with others who understand the journey.

You deserve support. You deserve community.

👉 Join us on Wednesday February 25th at 7pm EST and take the first step toward feeling less alone.

Register here: https://psoriasiscanada.ca/online-support-program/

02/09/2026

Do you have questions about navigating the healthcare system, or wondered what to do when faced with a challenge within the healthcare system? Our friends Canadian Arthritis Patient Alliance are hosting a Lived Experience Webinar on February 18th at 7PM EDT. Find out more about the webinar and how to register using the link.

https://ow.ly/pz3U50YbR2C

01/23/2026

There’s a lot to look forward to at Psoriasis Canada this year — and we don’t want you to miss out!

Be the first to hear about our expanded online support program ( with French sessions launching soon), new educational tools and webinars, and the launch of our new, extensive website — all designed to support Canadians living with psoriasis and psoriatic arthritis.

💌 Sign up for the Psoriasis Canada bilingual newsletter to stay up to date and connected with our community: http://eepurl.com/c6RN21