Lupus LA Lupus LA promotes lupus research, awareness, and education, and serves the needs of people with lupus and their families in Los Angeles County.

This page provides a forum for individuals to view materials, share information and engage in conversations about health, treatment, and support. It’s also a destination to learn about Lupus LA, our programs, services, conferences, and events. Safety Information
RULES OF USE:
Thank you for taking the time to visit our page. This is a place for people with lupus to become better informed,

actively participate in combating this condition, and find support through connections with others who have similar experiences. With your help and support, we hope to help bring about the next miracle treatment for those living with lupus. Since this is a public forum, there are a few rules for visitors to be aware of – and comply with. First, the basics:
• Comments and opinions that are posted by visitors don’t necessarily reflect the opinions of the Lupus LA page, or our employees and affiliates. This means that we assume no responsibility or liability arising from any content posted by visitors on our page.
• Lupus LA may post articles, commentary and opinions from other sources, that we believe may be of interest to our followers. These articles are not fact checked and do not necessarily reflect the opinions of the Lupus LA page, or our employees and affiliates. This means that we assume no responsibility or liability arising from any links posted on our page.
• We don’t verify or endorse any posts or content posted by visitors and don’t warrant their accuracy. Similarly, we don’t endorse any third-party websites or pages that may be linked from our page, and we aren’t responsible or liable for the content or accuracy of any other websites or third party pages. Visitors should read the terms and conditions and privacy policy of each third party website they visit.
• All comments posted here are subject to moderation, and may be edited or removed at any time to maintain community standards, to comply with these Rules of Use or for any other lawful reasons.
• We may use any comments posted and any other information shared on or through this page or other public pages for market research purposes, to further the goal of improving our outreach. Your privacy will always be protected.
• All posts must be courteous and respectful. We also would like for posts to be on-topic (that’s why we’re all here).
• Posts may not contain anything that is unlawful, threatening, libelous, accusatory, defamatory, obscene, offensive, inflammatory, pornographic or profane, or anything that we deem inappropriate.
• Posts may not contain anything that identifies or could be used to identify a specific person or company – we don’t want to hear about Dr. XYZ or Company 123.
• All visitors must be eighteen (18) years or older to post on this page.
• Everything on this page is intended only for people in the United States. And the not-so-basics:
• Our page may not be used to promote any products or services and we will remove any posts that we deem to be misleading or thinly disguised sales pitches.
• No medical or professional advice or diagnoses may be given – not by users of the site and not by us. Keep in mind that the contents of this page are for information purposes only and should never be relied on as the basis for making a decision or taking an action. Any health or medical information that’s posted here is not intended as a substitute for specific medical advice, and is not meant to replace the judgment of a healthcare professional. So if you do choose to rely on content that you see here, you are doing so at your own risk. Be smart: take your specific medical questions to a medical expert. Plus a very important additional point:
• If you have any questions or concerns about any medications you’re taking, or have an adverse reaction, contact your healthcare provider right away. Changes to these Rules of Use:
As new situations arise, we may need to change or add to these Rules of Use at any time. If we do make changes, we'll post a revision date to the bottom of this page. Updated: June 5, 2013

As   comes to a close, we want to say THANK YOU for helping us shine a light on this disease all May long!But the realit...
06/01/2026

As comes to a close, we want to say THANK YOU for helping us shine a light on this disease all May long!

But the reality is, lupus doesn’t disappear when June begins. Over 60,000 individuals in Los Angeles County (and 1.5 million in the U.S.) face this unpredictable, invisible illness every single day. That’s why Lupus LA is here to continue to provide critical emergency grants, support groups, patient resources and more - all year long.

Whether you have 5 minutes to share a post, or want to turn your next milestone birthday into a movement - you can help us change a life! Discover 9 simple ways to make a real difference with us year-round below, and get involved at LupusLA.org.

Which one are you committing to this month? Let us know in the comments below! 🧡


06/01/2026

The wait is over! We are officially back with Session 2 of The Autoimmune Beauty Protocol Series featuring the incredible Katherine Antequera! ✨

Living with an autoimmune condition can completely change how your skin behaves, from sudden butterfly rashes and intense inflammation to extreme sensitivity and puffiness. It takes a tools to navigate these changes, and Katherine is going live with us to break down her exact top techniques for contouring, and more!

Whether you want to learn how to hide "steroid moon face" with contouring or simply want to pick up tips from a pro who truly understands the chronic illness journey, this session is for you.

🗓 WHEN: Tuesday, June 2nd at 4pm PT / 7pm ET
📍 WHERE: Live at YouTube.com/LupusLA (Subscribe to get notified: https://bit.ly/LupusLA-Subscribe)

No registration required - just bring your questions - and yourself!

👉 Our DMs are always 100% open! Drop us a message anytime to submit a specific beauty question you want Katherine to answer live, or just to say hi to our team!

We can't wait to see you all there!


06/01/2026

The wait is over! We are officially back with Session 2 of The Autoimmune Beauty Protocol Series featuring the incredible Katherine Antequera! ✨

Living with an autoimmune condition can completely change how your skin behaves, from sudden butterfly rashes and intense inflammation to extreme sensitivity and puffiness. It takes a tools to navigate these changes, and Katherine is going live with us to break down her exact top techniques for contouring, and more!

Whether you want to learn how to hide “steroid moon face” with contouring or simply want to pick up tips from a pro who truly understands the chronic illness journey, this session is for you.

🗓 WHEN: Tuesday, June 2nd at 4pm PT / 7pm ET

📍 WHERE: Live at YouTube.com/LupusLA (Tap our link in bio to subscribe!)

No registration required - just bring your questions - and yourself!

👉 Our DMs are always 100% open! Drop us a message anytime to submit a specific beauty question you want Katherine to answer live, or just to say hi to our team!

We can’t wait to see you all there!



05/30/2026

Our June 2026 virtual support groups are open for registration! If you’ve been looking for a safe, understanding space to navigate your lupus journey, this is your sign to join us.

🌎 Join from anywhere in the world (you do NOT need to live in LA or CA!). We have participants joining us internationally.

📷 Come as you are. Join with your camera off, or just listen in. There is never any pressure to speak or share your story until you are ready.

💬 Share your story or just listen in. There is no pressure to share - just show up how you feel comfortable.

✨ Our moderators are highly knowledgeable and bring the kind of warm, positive energy that turns a room full of strangers into a community.

➜ What To Expect: bit.ly/lupusla-supportgroups

➜ Meet Our Facilitators: bit.ly/lupusla-facilitators

🔗 Find Your Group and Register Today: LupusLA.org/supportgroups



Our June 2026 virtual support groups are open for registration! If you’ve been looking for a safe, understanding space t...
05/30/2026

Our June 2026 virtual support groups are open for registration! If you’ve been looking for a safe, understanding space to navigate your lupus journey, this is your sign to join us.

🌎 Join from anywhere in the world (you do NOT need to live in LA or CA!). We have participants joining us internationally.

📷 Come as you are. Join with your camera off, or just listen in. There is never any pressure to speak or share your story until you are ready.

💬 Share your story or just listen in. There is no pressure to share - just show up how you feel comfortable.

✨ Our moderators are highly knowledgeable and bring the kind of warm, positive energy that turns a room full of strangers into a community.

➜ What To Expect: https://www.youtube.com/watch?v=C3UVt030PWg

➜ Meet Our Facilitators: https://www.youtube.com/watch?v=h2n8cGWPB08

🔗 Find Your Group and Register Today: https://lupusla.org/supportgroups



Global Virtual Support Group Information: We are currently using the Zoom platform to conduct our Support Group Sessions. If you have never used Zoom on your laptop or device, we...

05/30/2026

We're keeping in the spotlight! 🌟 As comes to a close, we want to thank Extra TV for bring lupus to light and supporting Lupus LA! We are so proud to see our phenomenal Board Member, Donna Jordan, and Extra TV’s own Terri Seymour (our recent 2026 Loop Award Recipient from ) teaming up to spread awareness about the invisible realities of this disease. 🧡

Thank you, Donna and Terri, for your powerful advocacy, and thank you to the team at Extra for using your platform to support our critical mission.

🔗 Learn More: https://bit.ly/extratv-lupusla

05/26/2026

NOW LIVE! 🎙️Watch Season 5 Ep 14 of the Podcast featuring lead singer and guitarist of The Detours, Brett Kohler!

In this episode, Brett opens up about navigating the shock of getting diagnosed with lupus as a young adult, how music pulled him through the emotional weight of those early days, and why he hopes sharing his journey today will bring comfort to others when they need it most.

If you’ve ever had to pivot your life or find strength in a creative passion - tap our link in bio to watch the full episode! 🎥



A life-altering diagnosis in your 20s can feel like the ultimate roadblock. For Brett Kohler, it became a detour that le...
05/26/2026

A life-altering diagnosis in your 20s can feel like the ultimate roadblock. For Brett Kohler, it became a detour that led straight to his purpose. 🎸 Tomorrow on ®, host Adam Selkowitz sits down with the lead singer and guitarist of The Detours, Brett Kohler.

Brett opens up about navigating the shock of getting diagnosed with lupus as a young adult, how music pulled him through the emotional weight of those early days, and why he hopes sharing his journey today will bring comfort to others when they need it most.

If you’ve ever had to pivot your life or find strength in a creative passion, you won’t want to miss this conversation.

🔗💻 Set your reminders! Episode 14 drops tomorrow. Make sure you’re subscribed: https://www.youtube.com/?sub_confirmation=1

05/23/2026

Welcome to today's Live Session "Clear The Fog: Practical Executive Functioning Skills For Lupus & Low Capacity Days" with Lupus LA Medical Advisory Board member, Clinical Psychologist, Adjunct Professor of Psychology at Pepperdine University, wife, mother of three, and founder of Faces of Health in Claremont, California - dr.blied, PhD, MACL, BSP!

Lupus can impact the way a person thinks, plans, remembers, prioritizes, and moves through daily life especially during periods of fatigue, pain, and flare activity. 🧡

Watch this session for an affirming, research-informed conversation with Dr. Monica Blied on executive functioning and lupus as we explore practical strategies to help everyday life feel more manageable and sustainable!

Lupus can impact the way a person thinks, plans, remembers, prioritizes, and moves through daily life especially during ...
05/20/2026

Lupus can impact the way a person thinks, plans, remembers, prioritizes, and moves through daily life especially during periods of fatigue, pain, and flare activity. 🧡

Join us Friday, May 22nd at 4pm PT on our YouTube channel for an affirming, research-informed conversation with dr.blied on executive functioning and lupus. We’ll explore practical strategies to help everyday life feel more manageable and sustainable.

📅 Friday, May 22, 2026
⏰ 4:00-4:45 PM PT
📍 YouTube Live with Lupus LA

🔔 Get notified when the live event begins! Subscribe: https://www.youtube.com/?sub_confirmation=1

Address

C/o Emerge, 16000 Ventura Boulevard, Suite 630
Beverly Hills, CA
91436

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

Telephone

+13106575667

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