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Read conversations, start a discussion, and connect with others about Lupus.

Advocates, Ya'll OK?

I not only have a heart for our community, but there's a special place in my heart for fellow advocates. We're not only patients ourselves, but I feel there's an...

Calling all Lupus Warrior Moms! Let's discuss motherhood!

Being a lupus warrior is hard, being a lupus warrior mom is super tough! Let's come together and share our joys, challenges, frustrations, whatever to help one another. If you...

Question for the ladies

Good Evening All: I am new to this forum. I am blessed to report my sle lupus is in remission. I truly thank God!! Ladies, I am working on a...

Do you get to share your opinion about lupus care?

Many living with lupus feel misunderstood by their providers. Last year, the survey this community responded to revealed important findings on the struggle to get a diagnosis, issues related to...

Facial Rash

Hi, I have been diagnosed with Lupus after having a biopsy done on my face due to a facial rash. Would anyone be able tell me the name of the...

Lupus Awareness Month 2021

What is the most important thing you can think of to share about lupus awareness? What do you need people to know about your lupus journey?...

What Do You Wish People Knew About Lupus?

The Significance of Lupus Awareness

Why is Lupus awareness important to you? What should others know about living with lupus?...

To Vax or not to Vax

Good Evening Warriors! Has it not been the craziest 2 years? Seriously!? I have Lupus, 2 different kidney diseases (nephrocalcinosis, and polycystic kidney disease) and as of May 2020, have...

Share your lupus story

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