Raising Awareness for Lupus

Lupus is a disease of a thousand faces. We need your help to spread awareness and create change.

What is Lupus?

Lupus is a complex autoimmune disease that can affect any part of the body — including the skin, joints, kidneys, heart, lungs, and brain.

Its symptoms are often invisible, unpredictable, and unique to each person, which is why it’s often called the “disease of a thousand faces.”

There is no single test to diagnose lupus, and symptoms can mimic those of other conditions. Many individuals face significant delays in diagnosis and treatment, which is why raising awareness is so important.

Learn more about our mission to raise awareness and support Canadians affected by lupus on our About Us page.

The Symbolism Behind the Lupus Butterfly

The butterfly is one of the most recognized symbols of lupus, inspired by the butterfly-shaped rash that appears on the face of many individuals living with the disease. Beyond this physical symptom, the butterfly represents beauty, strength, and transformation — a powerful reminder of the resilience of those affected by lupus.

Our signature purple reflects the spirit of lupus warriors: clarity, hope, resilience, courage, and strength. It’s a bold and uplifting colour that unites our community in raising awareness and fighting for change.

Lupus is often misunderstood or overlooked. That’s why awareness is key. Public education helps foster empathy, push for earlier diagnoses, improve treatment outcomes, and drive funding for research.

At Lupus Canada, we believe that through awareness, we can build a more informed, supportive, and proactive community.

Current Awareness Campaigns

Let’s Talk Lupus: A Pathway to Progress

Bringing the latest insights from the LUPUS 2025 Congress directly to Canadians and advancing the conversation on global lupus research and innovation.

Lupus impacts more than 1 in 1,000 Canadians and an estimated 5 million people worldwide. It is a complex autoimmune disease with no known cure, impacting every aspect of life, including physical, emotional, and social.

Despite medical progress, too many Canadians face delayed diagnosis, inconsistent access to care, and limited treatment options. For many, living with lupus means navigating uncertainty every single day.

Let’s Talk Lupus: A Pathway to Progress brings together leading lupus researchers, experts, and advocates from across the globe to share breakthroughs in global lupus research, inspire hope, and connect international progress to the realities of living with lupus in Canada.

Conference panel at the LUPUS 2025 International Congress featuring global lupus experts presenting research insights. Text reads: “Let’s Talk Lupus: A Pathway to Progress — Connecting global innovation to national impact.”

Let’s Talk Lupus: Conversations with Macenzie

Real Stories. Real Impact.

Each month, Let’s Talk Lupus: Conversations with Macenzie shares uplifting interviews with Canadians affected by lupus. Hosted by Macenzie, a journalist living with lupus, the series explores real-life experiences, resilience, and strength.

Want to share your story? Email our National Digital Marketing Specialist, Ariana — we’d love to hear from you.

Person with dark hair sitting at a picnic table in a leafy park, resting their chin on one hand and smiling at the camera.

The Disease of a Thousand Faces

Help make lupus visible!

Lupus Canada is gathering 1,000 photos from people across the globe to reflect the diverse ways lupus affects individuals.

Through stories and photos, we shine a light on the real people behind the disease — and show that no two lupus journeys are the same.

Artwork featuring the word 'HOPE' intertwined with faces of people living with lupus, symbolizing strength and resilience

How You Can Get Involved

Follow us on social media to help raise awareness

Share your story or photo to help us reach 1,000 faces

 

Support our campaigns by making a donation and help drive research, education, and advocacy

More Awareness

Lupus affects everyone differently, and sharing real-life stories helps to shed light on the personal experiences of those living with the disease. Watch this powerful story from Heidi, who faced the challenges of photosensitivity, a common symptom of lupus. She shares how advocating for herself and working with her doctor has allowed her to enjoy the outdoors again.

Watch Heidi’s Story:

Past Lupus Awareness Initiatives: