Lupus Canada (@lupuscanada) 's Twitter Profile
Lupus Canada

@lupuscanada

Working to improve lives of Canadians living with lupus through advocacy, education, public awareness support & research | 1-800-661-1468 | [email protected]

ID: 311724571

linkhttps://www.lupuscanada.org/donation/ calendar_today05-06-2011 23:22:58

2,2K Tweet

1,1K Followers

187 Following

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Voting closes TOMORROW at noon (EST)! Nearly 300 votes in for the Patients’ Choice Award 🩺 Don’t miss your chance to honour a rheumatologist who’s made a difference in your lupus journey. 🗳 Vote now: forms.gle/dzmd7FKh4TyYYD… #LupusCanada #PatientsChoiceAward

Voting closes TOMORROW at noon (EST)!
Nearly 300 votes in for the Patients’ Choice Award 🩺

Don’t miss your chance to honour a rheumatologist who’s made a difference in your lupus journey.

🗳 Vote now: forms.gle/dzmd7FKh4TyYYD…

#LupusCanada #PatientsChoiceAward
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Are you a parent living with autoimmune arthritis? Researchers want to hear from you. 30–40 min survey $15 gift card Optional follow-up interview Must be 18+, have a child under 6, and live with an ARD. Learn more: ARDs-Parenthood.ca #Lupus #RheumatoidArthritis

Are you a parent living with autoimmune arthritis? Researchers want to hear from you.

30–40 min survey
$15 gift card
Optional follow-up interview
Must be 18+, have a child under 6, and live with an ARD.

Learn more: ARDs-Parenthood.ca

#Lupus #RheumatoidArthritis
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“Living with lupus can be isolating, but I’ve found a new sense of kinship through our shared dialogue.” — Macenzie Let’s Talk Lupus is a monthly series featuring real stories from Canadians living with lupus. 💬 Want to be featured? Email [email protected]

“Living with lupus can be isolating, but I’ve found a new sense of kinship through our shared dialogue.” — Macenzie

Let’s Talk Lupus is a monthly series featuring real stories from Canadians living with lupus.
💬 Want to be featured? Email ariana.ranjbar@lupuscanada.org
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🎓 Final reminder to apply for Lupus Canada's $2500 William Birchall Foundation Scholarship Deadline: May 31, 2025 Open to college, university, and trade students To learn more visit lupuscanada.org/scholarships/ #LupusScholarship #LupusCanada #StudentSupport #LupusAwareness

🎓 Final reminder to apply for Lupus Canada's $2500 William Birchall Foundation Scholarship

Deadline: May 31, 2025
Open to college, university, and trade students

To learn more visit lupuscanada.org/scholarships/

#LupusScholarship #LupusCanada #StudentSupport #LupusAwareness
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🔬 Get involved in #lupusresearch from the University of Cambridge Help improve understanding of flares in autoimmune diseases by completing a 45 min survey on your experiences Enter to win 1 of 4 £50 Amazon vouchers Survey closes early June Take part: bit.ly/4kOQeyg

🔬 Get involved in #lupusresearch from the University of Cambridge

Help improve understanding of flares in autoimmune diseases by completing a 45 min survey on your experiences

Enter to win 1 of 4 £50 Amazon vouchers
Survey closes early June

Take part: bit.ly/4kOQeyg
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Lupus Canada's CEO Leanne Mielczarek will be attending Unity Through Rheumatic Diseases on May 31 in Toronto. She looks forward to connecting with advocates, healthcare providers, and youth working to improve rheumatology care in Canada. #Rheumatology #LupusCanada

Lupus Canada's CEO Leanne Mielczarek will be attending Unity Through Rheumatic Diseases on May 31 in Toronto.

She looks forward to connecting with advocates, healthcare providers, and youth working to improve rheumatology care in Canada.

#Rheumatology #LupusCanada
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Are you a parent living with autoimmune arthritis? Researchers want to hear from you. 30–40 min survey $15 gift card Optional follow-up interview Must be 18+, have a child under 6, and live with an ARD. Learn more: ARDs-Parenthood.ca

Are you a parent living with autoimmune arthritis? Researchers want to hear from you.

30–40 min survey
$15 gift card
Optional follow-up interview
Must be 18+, have a child under 6, and live with an ARD.

Learn more: ARDs-Parenthood.ca
Lupus Canada (@lupuscanada) 's Twitter Profile Photo

#LUPUS2025 was a milestone for collaboration in care and #lupusresearch. For the first time, patient perspectives were integrated into the Congress agenda. We thank Dr. Zahi Touma for his leadership and all who contributed to this momentum. Together we can advance care.

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Lupus Canada’s 2025 Patients’ Choice Award for Canadian Rheumatologist of the Year goes to Dr. Deborah Levy of SickKids Hospital! Thank you to everyone who shared their stories and helped us honour excellence in lupus care 💜 Read more: lupuscanada.org/patients-choic…

Lupus Canada’s 2025 Patients’ Choice Award for Canadian Rheumatologist of the Year goes to Dr. Deborah Levy of SickKids Hospital!

Thank you to everyone who shared their stories and helped us honour excellence in lupus care 💜

Read more: lupuscanada.org/patients-choic…
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Lupus in men is rare but serious. It often appears with kidney, blood, or nervous system issues Men report poor support and fewer resources Stigma adds another layer of challenge We are raising awareness this Men’s Health Month #MensHealthMonth #LupusAwareness #MenWithLupus

Lupus in men is rare but serious.

It often appears with kidney, blood, or nervous system issues
Men report poor support and fewer resources
Stigma adds another layer of challenge

We are raising awareness this Men’s Health Month

#MensHealthMonth #LupusAwareness #MenWithLupus
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Anifrolumab (Saphnelo) is now listed under BC PharmaCare’s Limited Coverage formulary for adults with moderate to severe SLE Learn more: lupuscanada.org/resources-anif…

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Students and educators across Canada joined #ClassroomsForACause to raise awareness for lupus—through art, empathy, and action. From purple butterflies to school-wide displays, classrooms made lupus visible. 💜 See how: lupuscanada.org/classrooms-for… #LupusAwareness #YouthInitiative

Students and educators across Canada joined #ClassroomsForACause to raise awareness for lupus—through art, empathy, and action.

From purple butterflies to school-wide displays, classrooms made lupus visible. 💜

See how: lupuscanada.org/classrooms-for…

#LupusAwareness #YouthInitiative
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Men experience lupus differently. Regular care and support are essential. Without treatment, lupus can progress quickly and impact vital organs. Learn more: lupuscanada.org/men-and-lupus/

Men experience lupus differently.
Regular care and support are essential.
Without treatment, lupus can progress quickly and impact vital organs.

Learn more: lupuscanada.org/men-and-lupus/
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DJ Prosper Laguerre, Canadian DJ, father, and lupus warrior, opens up about his journey and the strength he’s found in speaking out. This #FathersDay, we honour men living with lupus. Read his journey: lupuscanada.org/living-with-lu… #MensHealthMonth #LupusAwareness #MenWithLupus

DJ Prosper Laguerre, Canadian DJ, father, and lupus warrior, opens up about his journey and the strength he’s found in speaking out.

This #FathersDay, we honour men living with lupus.

Read his journey: lupuscanada.org/living-with-lu…

#MensHealthMonth #LupusAwareness #MenWithLupus
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60% of Canadian employees live with a chronic illness. 70% say they find purpose through their work. Lupus Canada and Health Partners are helping employers support their teams through workplace giving campaigns. Contact us at [email protected] to learn more

60% of Canadian employees live with a chronic illness.
70% say they find purpose through their work.

Lupus Canada and Health Partners are helping employers support their teams through workplace giving campaigns.

Contact us at info@lupuscanada.org to learn more
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New findings from #LUPUS2025: 89% of lupus patients treated with Acthar® Gel saw symptom improvements Many also reduced steroid use Encouraging real-world data for those with hard-to-manage lupus. Read more: prnewswire.com/news-releases/… #LupusResearch #SLE

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At Lupus Canada, we are committed to fostering a sense of belonging for everyone impacted by lupus. We are committed to fostering spaces where every voice is heard and every story matters. We wish all those celebrating a joyful and safe #PrideMonth! 🏳️‍🌈

At Lupus Canada, we are committed to fostering a sense of belonging for everyone impacted by lupus.

We are committed to fostering spaces where every voice is heard and every story matters.
We wish all those celebrating a joyful and safe #PrideMonth! 🏳️‍🌈
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The Canada Disability Benefit launches June 20, 2025! Eligible Canadians aged 18–64 can apply for monthly support. Apply online, by phone, or in person First payments begin July 2025 More info: canada.ca/en/services/be… #DisabilitySupport #LupusCanada

The Canada Disability Benefit launches June 20, 2025! Eligible Canadians aged 18–64 can apply for monthly support.

Apply online, by phone, or in person
First payments begin July 2025

More info: canada.ca/en/services/be…

#DisabilitySupport #LupusCanada