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.
learn moreWe 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.
learn moreEvery 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.
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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.
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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.
PATIENT VOICES Patient Voices | Lupus: The Positive Effects and Growth In My Life One thing I really have to focus on while I’m on this chronic illness journey is…
continue readingLupus LA is dedicated to promoting and protecting the health and wellbeing of our lupus patients. We know that many in our community are struggling to find support and resources…
continue readingBefore 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…
continue readingWatch the replay of our most recent Live Expert Q&A: “Lupus and Eye Care” with board-certified ophthalmologist, Dr. David Lazar of Lazar Retina! 👁 Did you know that a prominent…
continue readingMy Advice to Teens Adjusting to Living Life With Lupus From personal experience, I know that it is very difficult to adjust to life living with lupus in high school….
continue readingLATEST ON LUPUS PATIENT WEBINAR Saturday, December 5th 2020 from 10:00 a.m. – 11:15 a.m. You can join our next patient conference from the comfort of your home as we…
continue readingNEW 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…
continue readingLATEST ON LUPUS PATIENT WEBINAR Saturday, December 5th 2020 from 10:00 a.m. – 11:15 a.m. You can join our next patient conference from the comfort of your home as we…
continue readingA Day in the Life of a Teen Living With Lupus On a typical day, I wake up to my alarm blaring at 7:20 am. Immediately, I hit snooze on…
continue readingNEW 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…
continue readingLATEST ON LUPUS PATIENT WEBINAR Saturday, December 5th 2020 from 10:00 a.m. – 11:15 a.m. You can join our next patient conference from the comfort of your home as we…
continue readingLIVING WITH INVISIBLE ILLNESS Why being told “but, you don’t look sick” or “you’re too young” is not helpful, and can be detrimental to getting the treatment invisibly ill patients…
continue readingNEW 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…
continue readingLupus LA is excited to announce our newest adult support group, to be held in the Koreatown area at the Karsh Center! This group will be held on the First Tuesday of each…
continue readingWhat 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…
continue readingWatch “Lupus and the Kidneys” with Dr. Bevra Hahn below! Listen as Lupus LA’s Medical Advisory Board member and expert rheumatologist, Dr. Bevra Hahn, answers patients’ top questions about how…
continue readingYou 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…
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