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Lupus is a complicated autoimmune disease that affects the lives of over 1 million Americans, each one facing their own battle, their own struggle. At Lupus LA, we fight to shift each narrative from pain to promise by providing patient services and programs, supporting medical research and sparking national advocacy. Lupus LA believes Your Story is Our Fight - a fight we can all win together. Watch full PSA
Lupus LA is a non-profit health organization dedicated to finding the causes of and a cure for lupus while providing support, services and hope to all who suffer from lupus. We raise funds to support our 3 core areas of focus: medical research, patient services, and awareness and advocacy initiatives.
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We offer a number of patient services to the lupus community in the greater Los Angeles area, including support groups for adults and pediatrics, doctor referrals, emergency grants, patient education and resources, as well as our newly diagnosed patient guide. If you are a patient or a caretaker to someone with lupus, our Patient Program is a great place to start your journey.
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Every life touched by lupus reveals a unique and important story. At Lupus LA, we are bringing these powerful stories to the forefront of lupus awareness in order to shine a light on this invisible illness.
Events are the cornerstone of funding for Lupus LA. Lupus LA hosts four fundraising events throughout the year to increase lupus awareness, organization visibility, and raise vital funds to support our mission. learn more
There are a variety of ways for you to make a difference in the lupus community. From corporate partnerships, event underwritings and individual gifts, we offer individualized opportunities for you to give. learn more
Lupus LA is powered by amazing volunteers. Join the Lupus LA volunteer email list to be included as volunteer needs and opportunities arise. Volunteers are needed at each fundraising event, and are used to help support key Lupus LA initiatives throughout the year.
learn moreSearch the Lupus Library for information about lupus, treatment, tips as well as patient stories and experiences. If you’re newly diagnosed, or simply looking to deepen your knowledge of lupus, this is a helpful content resource that we constantly update with new research, insights and community voices.
CULTIVATING CALM DURING CORONAVIRUS: AN “AT-HOME” SELF CARE RESOURCE GUIDE We know stress and anxiety from the spread of COVID19 deeply affects our community. During times like these, immune compromised individuals must be incredibly vigilant, which can cause even more anxiety. While this is a critical time for us all, we want you to know…
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Before the diagnosis of lupus, doctors look at lab tests, symptom records, and history of the disease in the family. Of course, the process for diagnosing the disease can be a long and challenging one. One of the tests conducted is the antinuclear antibodies (ANA) test. The ANA test is essential in lupus diagnosis as…
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Asking for Help Most of us don’t like to ask for help. The more stressed we feel, the more likely we are say (or feel): “Oh, I’ll just do it myself!” These are generally the reason people think they can’t ask for help: They fear looking “weak.” Asking for help is human. It is not a…
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Lupus LA will be a special guest at The Lupus Project on 2/23. This event is designed to bring together individuals living with lupus and their families for a convenient, fun, informative, and social affair, where health focused businesses and lupus organizations can share about their products/resources. Click Here for more information We look forward…
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Come join us at our next “Latest on Lupus” Patient Conference on Saturday, September 28th at the UCLA Medical Center in the Tamkin Auditorium. Registration is now open and we invite you to join us as we learn more about living with lupus and the latest updates in research. Latest on Lupus Patient Conference September 28, 2019 10:30…
continue reading view all Before the diagnosis of lupus, doctors look at lab tests, symptom records, and history of the disease in the family. Of course, the process for diagnosing the disease can be a long and challenging one. One of the tests conducted is the antinuclear antibodies (ANA) test. The ANA test is essential in lupus diagnosis as…
continue reading view all 
by: Sheba Family As Lupus sufferers, perhaps one of the hardest things to come to terms with is that we often do not look sick. People tend to assume that if we look fine, we are fine. It can be frustrating to experience a lack of empathy and compassion from the people who surround us….
continue reading view all Asking for Help Most of us don’t like to ask for help. The more stressed we feel, the more likely we are say (or feel): “Oh, I’ll just do it myself!” These are generally the reason people think they can’t ask for help: They fear looking “weak.” Asking for help is human. It is not a…
continue reading view all Come join us at our next “Latest on Lupus” Patient Conference on Saturday, September 28th at the UCLA Medical Center in the Tamkin Auditorium. Registration is now open and we invite you to join us as we learn more about living with lupus and the latest updates in research. Latest on Lupus Patient Conference September 28, 2019 10:30…
continue reading view all by: Sheba Family As Lupus sufferers, perhaps one of the hardest things to come to terms with is that we often do not look sick. People tend to assume that if we look fine, we are fine. It can be frustrating to experience a lack of empathy and compassion from the people who surround us….
continue reading view all 
NEW Digital 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 recommend downloading the Zoom App (if on your phone) or clicking a link below to download Zoom onto your laptop. For a fast, easy “How-To…
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What Lupus Patients Need to Know About Sunscreens and Sunblock For the last 20-30 years, Americans have become wiser about sun protection. Unfortunately, the sunscreens that received FDA approval at that time did not provide full-spectrum coverage. The emphasis was on protecting against ultraviolet B (the burning rays). For patients with lupus, protection against ultraviolet…
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You are invited to participate in our Live Facebook Chat Wednesday at 12pm! Lupus advocates will be LIVE on Facebook to answer your questions about living with lupus. Ask experts in your community support questions about living with lupus. This is a great opportunity to connect, receive support, and ask questions. Invite family and friends to…
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