Welcome to the Canadian Psoriasis Network

I am proud and honoured to assume the role of President of the Canadian Psoriasis Network. I am a passionate advocate for the inclusion of people living with psoriasis and psoriatic arthritis in our community. Over one million Canadians suffer from the disease and it is my goal to work with our Board to continue to build a strong Network to raise awareness and increase the understanding of our disease. The ultimate goal is to reduce the suffering and help people live their lives to the fullest.

Today, we have treatment options unavailable to us previously. There are new treatment options becoming available frequently as research progresses however, it is important for us to continue to collaborate with stakeholders in the ongoing quest for a cure. I hope you will join me in this mission. It will happen with the strategic focus of dedicated Canadians who are impacted by the disease. If you have any suggestions or questions, please contact me at president@cpn-rcp.com.

Simmie Smith, B.A, M.B.A.

Président, Réseau canadien du psoriasis

Qui Sommes-Nous?

Nous sommes le Réseau canadien du psoriasis (RCP). Notre objectif est d’améliorer la qualité de vie de tous les Canadiens qui vivent avec le psoriasis et l’arthrite psoriasique, tout en recherchant vigoureusement une cure. Notre mission est de fournir toutes les informations actuelles sur le traitement et les soins continus grâce à l’éducation, la sensibilisation, la recherche et en donnant l’exemple.

INVISIBLE MAN tells the inspiring story of Andrew Gosse’s journey to treatment after suffering from severe psoriasis for 18 years.

What do I do Now?

If you are newly diagnosed it can be overwhelming to plan the next steps.

We have been down this road. Let us help you.

We suggest you start with the psoriasis section, and then check resources. If this looks helpful, please consider joining CPN to stay up to date on upcoming events.

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Nous sommes maintenant complet! Désolé.

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What’s Happening at the CPN?

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Dear Members, Directors, Sponsors and Friends:
In January 2012, I had no idea what I was venturing into when founding the Canadian Psoriasis Network. What I did know, was 24 years of struggling with psoriasis and just how life-changing the right treatment can be. Read Andrew’s letter

biologics and biosimilars

Biologics and Biosimilars
Learn more about biologics and biosimilars, their similarities and differences.

WHO report

WHO Global report on PSORIASIS
The World Health Organization has released its Global report on psoriasis.
Click to open the WHO Report (PDF)

Thank you to our Sponsors!

We couldn’t do it without you.

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