Canadian Skin Patient Alliance

Are you unsure about how to navigate life with a skin condition? If so, check out our Self-Empowerment Toolkit for useful tips and strategies to assist you throughout your journey. Find the full Self-Empowerment Toolkit here: ow.ly/lZq250QIs2r

CSPA’s Skin Patient Charter of Rights is a key document that was developed to educate & empower patients to take an active role in their care and treatment, as well as to safeguard the respect of society, government, & workplace as a result of a diagnosis. canadianskin.ca/advocacy/skin-…

Do you live in Canada and have vitiligo? Would you like to share your story in an upcoming issue of Canadian Skin Magazine? Your experience can help raise awareness, inspire others, and shine a light on life with vitiligo. Contact info@ canadianskin.ca to learn more.

Have you noticed changes to your skin, hair, or nails after being exposed to wildfire smoke? CSPA is inviting you to share your personal experiences so we can better understand the impact of wildfire smoke and climate change. Reach out today and let your voice be heard!

Living with bullous pemphigoid isn’t always easy — and it’s often misunderstood. If you have BP and would like to help raise awareness through patient advocacy, we’d love to hear from you. 📩 Connect with us: info@canadianskin.ca

We Want to Hear Your Story! Are you a patient with an inspiring journey or unique experience related to your skin health? Whether it’s overcoming challenges, navigating treatments, or advocating for awareness, your story can inspire and educate others!

Want to keep up to date with CSPA? Sign up for Beneath the Surface, our monthly newsletter to stay in the loop on our projects, advocacy initiatives, news from our Affiliate Members network, & more! Subscribe: ow.ly/w53z50TtNcP Abonnez-vous ici : ow.ly/w53z50TtNcP

We Want to Hear Your Story! Are you a patient with an inspiring journey or unique experience related to your skin health? Whether it’s overcoming challenges, navigating treatments, or advocating for awareness, your story can inspire and educate others!

Nous voulons entendre votre histoire ! Êtes-vous un(e) patient(e) qui a un parcours inspirant ou une expérience unique liée à la santé de sa peau ?

"Some days, every step is painful and I have to be very careful with how many steps I take so I don’t miss the things that are important. Despite carefully planning and saving steps, there are days when the pain makes me miss what is important". Eliza, Pachyonychia Congenita

Today is #RareDiseaseDay! >300 million people around the world are living with a rare disease, including many rare dermatological diseases. CSPA strives for a world where people living with rare dermatological conditions lead healthy and fulfilling lives. #RareDERM #MySkinIsRare

🏆 Nominate a Dermatologist Who’s Made a Difference! CSPA is accepting nominations for Dermatologist of the Year 2025. This award recognizes dermatologists who’ve made a profound impact on their patients and the dermatology community. Deadline: Feb 28 2026

Living with bullous pemphigoid isn’t always easy — and it’s often misunderstood. If you have BP and would like to help raise awareness through patient advocacy, we’d love to hear from you. 📩 Connect with us: info@canadianskin.ca

Rare skin diseases can be life-altering, yet they often go unrecognized❗️ This February 28 is #RareDiseaseDay, let's take the opportunity to learn about conditions including Epidermolysis Bullosa, Pityriasis Rubra Pilaris, and Hailey-Hailey Disease. #MySkinIsRare #RareDERM

If you have been diagnosed with a rare skin disease, you are not alone! 💜 This#RareDiseaseDay (Feb 28), we are supporting those impacted by rare skin diseases. CSPA has developed the Self-Empowerment Toolkit, learn more about this toolkit here: canadianskin.ca/education/self… #RareDERM

🏆 Nominate a Dermatologist Who’s Made a Difference! CSPA is accepting nominations for Dermatologist of the Year 2025. This award recognizes dermatologists who’ve made a profound impact on their patients and the dermatology community. Deadline: Feb 28 2026

Nearly 1/20 people will live with a rare disease at some point in their lives—many of which affect the skin. This February 28 is #RareDiseaseDay, CSPA is partnerting with the RareDERM community to raise awareness for rare dermatological diseases worldwide. #MySkinIsRare #RareDERM

Winter Canadian Skin Magazine explores: 🔹 HS, AD & psoriasis & their systemic connections 🔹 Seborrheic dermatitis & urticaria 🔹 Innovative burn care research @ LOEX Don’t miss this must-read issue for patients, caregivers, & advocates. Read it today: canadianskin.ca/magazine/canad…

The month of February is known for Valentine's Day, but what you might not know is that this February 28th is International Rare Disease Day! While conditions such as Congenital Ichthyosis may be uncommon, they have significant impacts on life of individuals that are affected.

Do you live in Canada and have vitiligo? Would you like to share your story in an upcoming issue of Canadian Skin Magazine? Your experience can help raise awareness, inspire others, and shine a light on life with vitiligo. Contact info@ canadianskin.ca to learn more.

Do you live with prurigo nodularis (PN)? Want to help shape future initiatives that support people living with PN? We’re inviting people with lived experience to join our project advisory team. Your voice and insights will help guide research, education, and advocacy efforts.