Our Southern California region is working hard to provide the educational and emotional support you may need. We are currently offering both virtual and hybrid options. Please feel free to email the support groups for more information or questions.
Hybrid - Meets 1st Wednesday of the month 6:30pm - 7:30pm Pacific Time LFAchulavista@gmail.com Hablamos Espanol
Virtual - Meets 2nd Tuesday of the month 6pm - 7:00pm Pacific Time LFAsdcgroup@gmail.com
Support group for the active lupus warrior. In-person meet-ups in San Diego area; Click for more details! lfalupusactive@gmail.com
Virtual - Meets 3rd Thursday of the month 6pm - 7:30pm Pacific Time lfaasiangroup@gmail.com
Virtual - Meets 1st Saturday of the month 9am-10:00am Pacific Time LFAcaregivers@gmail.com
Hybrid - Meets 1st Saturday of the month 12:30pm-1:30pm Pacific Time LFAespanolgroup@gmail.com
Virtual - Meets 4th Tuesday of the month 5pm-6:00pm Pacific Time lfamancave@gmail.com
Virtual - Meets 3rd Thursday of the month 4pm-5:15pm Pacific Time LFAsistercircle@gmail.com
Virtual - Meets 1st Saturday of the month 10am-11:30am Pacific Time LFAyouthgroup@gmail.com
In-person - Meets 4th Monday of the month 10:30am - 11:30am PT Optum Hemet Community Center 1850 W. Florida Ave., Hemet CA 951-438-2222 for more information
An online lupus community where individuals with lupus and their loved ones can engage with others like them to share experiences, find emotional support and discuss practical insights for coping with the daily challenges of the disease.
An online and multi-media collection of resources and information for all things lupus, for people with lupus, their families and health professionals.
Our health educators are available to answer your questions and provide the help you need.
RAY is a lupus data platform where people with lupus and caregivers share information about their lupus experience to help researchers accelerate the development of new treatments and improve disease outcomes. You can be a ray of hope to ensure a bright future for lupus research by sharing your lupus experience.