On Every Journey, There is a Story...

It all started with a rash...

Welcome To The LupieGirl!


Lupus is a profound illness that often lacks the attention and understanding it deserves. It's crucial to advocate for Lupus awareness beyond a designated month and raise awareness year-round. Many individuals face life-threatening complications due to Lupus, and as of now, there is no cure. Nevertheless, The LupieGirl remains committed to motivating, uplifting, and inspiring those affected by Lupus to live fulfilling lives. We aim to challenge misconceptions about what "being sick" appears to be and empower individuals to pursue their dreams and aspirations.


For further information and Lupus statistics, please visit www.Lupus.org.

tHE lUPIEgIRL'S BOARD OF DIRECTORS IS OPEN!

WE ARE CALLING FOR PASSIONATE LEADERS TO JOIN OUR TEAM!

Please click button below for more information about joining the LupieGirl, Inc. Board of directors!

COVID-19 Lupus Advice 

Since March 2020, many of us have been working from home, furloughed, and teachers (not our profession) due to this pandemic that had taken the world by storm. It appears that the world has now reopened and The LupieGirl wants to remind you to be safe and continue to practice healthy hygiene. 
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​ Lupies, if you are unsure,  Lupie Advice remains below as a reminder. 

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About the LupieGirl

Lupus is a devastating disease that still is not discussed enough and many times misunderstood. We have to advocate past Lupus Awareness month and bring attention to this illness year round. Individuals are dying from complications of this illness and to date, no cure has been found for Lupus. In the meantime, The LupieGirl will continue to motivate, encourage and inspire Lupies to live their best lives, debunking the stigma of what "sick" looks like, as well as accomplishing their wishes and goals.

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