Register now for our 5th Annual “Latest on Lupus” Patient Education Conference!
Saturday, September 26th
In addition to hearing from the best and the brightest in the field of lupus research and care, attendees will have the opportunity to speak with experts in the field during our roundtable lunch. View full program schedule and speakers.
Register online or call 310-657-5667 to reserve your space.
Six-Week Support Group for Kids Ages 10 - 13
This summer has been a time of networking, learning and sharing for teens and their parents who took part in our new six-week support group series presented with the Childrens Hospital of Los Angeles.
Now we’re building on the success of this series with a group for kids with lupus between the ages of 10 and 13. Starting Wednesday, September 9th and meeting weekly through October 21st, parents and children will tackle a different topic each session to help them cope with the challenges of managing a chronic disease. Sibling care will be provided. Details »
To participate, please email or call Elyse Reyes at firstname.lastname@example.org or 310-657-5667. Space is limited.
Lupus LA is heading to Capitol Hill!
We’re teaming up with the Lupus Research Institute’s National Coalition to share the needs of lupus community with our nation's lawmakers next month.
Interested? Contact Elyse Reyes at email@example.com or 310-657-5667.
Can’t attend? You can be a virtual advocate on Facebook and Twitter! Follow our updates:
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About Lupus LA
Lupus LA, the west coast division of the S.L.E. Lupus Foundation, was founded by renowned physician and author, Daniel J. Wallace, MD, and serves the needs of people with lupus and their families across southern California. Lupus LA raises lupus awareness and supports lupus research on the national level.