Lupus Foundation of America

06/17/2026

🆕 A new podcast episode of The Expert Series is live!

Dr. Megan Lockwood breaks down everything you need to know about steroids in treatment — why they're essential, the risks of long-term use, and how to work with your doctor to build a plan that's right for you.

🎧 Listen now: https://buff.ly/VOQ6MgX

06/17/2026

That's a wrap! Last month's brought together more than 215 streamers across the globe, raising over $230K for research, education, and support.

To every content creator, supporter, and viewer: thank you. 💜 See you next May!

06/16/2026

💜 Keeping track of your medications and symptoms with can feel overwhelming — but our free SELF app is here to help,

With a built-in medication tracker, SELF helps you know your options, stay organized, and track your symptoms before and after starting a new medication.

Download the SELF app today: https://buff.ly/fXNCTeK

06/16/2026

👟💜 Like Bri, you could be walking this summer in your very own customizable baseball jersey. Two weeks left — raise $500 by June 30, rally your community, and make it yours.

Sign up now: https://buff.ly/BGdTAmf

06/15/2026

Meet Rina. 💜 At 16, she thought the pain after soccer practice was just soreness — it wasn't. After multiple visits, she was diagnosed with , and her life changed in ways she never expected.

Today, she shows up for her middle school students every day, even when her body is fighting against her. Read her full story: https://buff.ly/tWDJHLA

💬 Comment a 💜 to show Rina support.

06/14/2026

💜 We're halfway through — and we want to make sure every man living with knows he's not alone. From support groups to expert resources and personalized guidance from our Health Educators, our latest blog has everything you need in one place.

Learn more: https://buff.ly/kzmAzLe

06/14/2026

Today is . 💜 Did you know tends to be more aggressive and severe in children than in adults?

We're thinking of children living with lupus and the parents and caregivers showing up for them.

Find resources and information about lupus in children: https://buff.ly/3mvBV7b

06/13/2026

What is your life with like? 💜 We're looking for photos that show the real, unfiltered experiences of people living with lupus — the ups, the downs and everything in between. From doctor visits to butterfly rashes to quiet victories and big accomplishments— we want to honor your journey.

📷 Submit your photos here: https://buff.ly/zHx4a5V

💬 Comment 💜 to show support! Let’s show the world what life with lupus looks like.

06/12/2026

💜 Meet Yousselyn. Diagnosed with at 8 years old, she shares the reality of life with lupus — the hard days in the infusion chair and the moments of joy with family in between.

Share your life with lupus: https://buff.ly/zHx4a5V

💬 Comment a 💜 to show Yousselyn support!

06/12/2026

Help Prevent Lupus. If you live with , your family members could make a difference in preventing lupus for future generations.

CARE Lupus is a research study focused on women (18–49) who have a parent, sibling, or child with lupus — but do not have lupus themselves. Participation is easy and can be done from your home.

It’s groundbreaking research aimed at prevention.

Learn more: https://buff.ly/YuJULjC

CARE Lupus is a groundbreaking research study designed specifically for people who do not have lupus but have a close family member who does. The