🎉 Introducing Our New Board Director: Bianca Zimperi

Bianca's decision to join the Lupus Canada Board of Directors stems from her desire to honour her mother's journey and advocate for greater awareness for those battling #lupus .

Learn more 👉 buff.ly/3ulscC6

Today we are spotlighting our partner, Lupus Canada

Executive Director, Leanne Mielczarek, shares why they support CIAN’s mission!

We’re always looking new partners. Visit us at immunocompromised.ca to learn more about our growing network. 🇨🇦💪

#Immunocompromised #CIAN

Exciting News! 🎉

Lupus Canada is thrilled to announce that #Saphnelo has been listed in Manitoba starting April 1, 2024! This progress represents a notable advancement in improving access to #lupus treatment across Canada. 🇨🇦

For more details, visit buff.ly/3W0sqNZ

We extend our heartfelt thanks to our dedicated Board of Directors and Ambassadors, whose commitment brings hope to Canadians impacted by #lupus .

To meet our team visit buff.ly/3ulscC6 💜

🌟 It's National Volunteer Week from April 14th to 20th! 🌟

This year's theme, 'Every Moment Matters', recognizes the invaluable contributions of volunteers in strengthening communities. Visit buff.ly/49A5Q1X to learn more.

#NationalVolunteerWeek #EveryMomentMatters

Meet Jolene Clark: Lupus Warrior and Co-founder of Creative Wanderings!

From battling #lupus alongside her mother to facing her own diagnosis, Jolene's journey has been one of resilience.

Read more about Jolene's story: buff.ly/3PS50Xn

Living with COVID-19 adds challenges for those with #lupus , making healthcare access tough amid fear & uncertainty. It's crucial to recognize not everyone can move on from COVID-19. Let's stand together for the immunocompromised community.

Read more: buff.ly/4azFNZK

Coinciding with World Lupus Day on May 10th, Lupus Canada is launching the “1,000 Laps for Lupus” campaign with Lupus Warriors Isaac & Kate who will be swimming 100 laps each day for 10 consecutive days, totalling 1,000 laps.

Stay tuned for more information.

🌍 World Health Day is on April 7th and this year's theme is, 'My health, my right'. This campaign reminds us of the fundamental rights we all deserve when it comes to our health.

For more information visit buff.ly/43DZc9l

Calling All Educators - Join The “Classroom for a Cause” Campaign!

Lupus is a complex autoimmune disease that impacts numerous individuals worldwide, and we believe it is crucial to educate the younger generations about #lupus .

Learn more: buff.ly/3TrACVJ

Join us in Raising Awareness and Inspiring Change for equitable access to care and treatment for #lupus !

Stay tuned for more updates on our Lupus Awareness Month initiatives and how you can make a difference.

We are delighted to announce that Lupus Canada has joined our Alliance!

They are dedicated to improving the lives of Canadians living with lupus through research, advocacy, public awareness & education.

Learn more about #lupus & their life-changing work: lupuscanada.org

Recent Canadian research found that direct healthcare costs for SLE averaged over $10,000/patient annually, with greater illness severity linked to higher expenses.

Let's continue to advocate for equitable access to care and treatment for all Canadians impacted by #lupus .

Introducing the Lupus Canada – William Birchall Foundation 2024 Scholarship Program.

We're offering ten one-time scholarships of $2,500 CAD each to support individuals with lupus pursuing post-secondary education; apply by May 31, 2024.

Read More: buff.ly/3TexxGy

Research from the First Affiliated Hospital of Xinjiang Medical University sheds light on the correlation between positive psychological capital, post-traumatic growth, social support, & quality of life in patients battling #SLE

Dive into the study here: buff.ly/49QoNOV

Reminder to participate in The World Lupus Federation Patient Survey. The survey closes on March 18th, 2024.

Your voice matters.

lupus.qualtrics.com/jfe/form/SV_dm…