JULY IS CHRONIC DISEASE MONTH!
Now is the perfect time to shine a light on the ongoing struggles and triumphs of those living with the wide range of chronic conditions including Lupus and too many others. This month, we’re focusing on and raising awareness about all chronic diseases, highlighting the daily battles people face, and pushing for more research and support. By spreading the word, we can help create a kinder and more understanding world for everyone dealing with these challenges.
To help with this, the Chronic Disease Coalition has put together some fantastic Advocacy Toolkits. These toolkits are packed with everything you need to become a strong advocate for better healthcare policies and more awareness. Give them a look, think about how you might be able to help and let’s make a difference together!
NEXT COMMUNITY FUNDRAISING EVENT:
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NEXT SUPPORT GROUP MEETING:
Come to our free monthly support groups where we meet, talk, network, and share stories and information. These are free events and everyone is welcome – lupus patients, family members, and friends.
NEXT BOARD MEETING:
Attend our bi-monthly board of directors meetings where we discuss Lupus Foundation of Southern California business, past and upcoming events, and new ideas. We will also open up the floor to the public for comments towards the end of the meeting (please submit comments no later than 10:00 a.m. one week prior to the meeting you plan to attend by email at [email protected] or phone at 858-278-2788.
Upcoming Events
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- 16Board of Directors Meeting January 20246:30 pm - 7:30 pm
Attend our bi-monthly Board of Directors meetings where we discuss Lupus Foundation of Southern California business, past and upcoming events, and new ideas. We will also open up the floor to the public for comments toward the end of the meeting (see below for details about how to participate). Location: United W , ...Board of Directors Meeting July6:30 pm - 7:30 pmAttend our bi-monthly Board of Directors meetings where we discuss Lupus Foundation of Southern California business, past and upcoming events, and new ideas. We will also open up the floor to the public for comments toward the end of the meeting (see below for details about how to participate). Location: United W , ... - 17Virtual Support Group5:30 pm - 6:30 pm
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- 20San Diego In-Person Support Group10:30 am - 12:00 amRegister Here , ...
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OUR APPROACH
The Lupus Foundation of Southern California (LFSC) originated as a small support group for local lupus patients, growing to become the Lupus Foundation of Southern California, an independent, patient-oriented 501(c)(3) nonprofit organization. We are made up primarily of volunteers, providing service and support for the lupus community in San Diego and beyond.
SHOP USING AMAZON SMILE AND HELP LFSC!
All you need to do is visit smile.amazon.com and search for the Lupus Foundation of Southern California, and every time you make an Amazon purchase through smile.amazon.com, you will be raising money for the LFSC!
It’s that simple. Plus, it’s free to you, the consumer. The sooner you enroll, the more it helps the cause!
How You Can Get Involved
Call 858-278-2788 to Donate Or Contact Us to get Involved
Volunteer Program
Become a Member
The Lupus Foundation of Southern California (LFSC) is a 501(c)(3) nonprofit organization so all contributions are tax-deductible. Making a donation or becoming a member helps ensure the LFSC will be able to maintain its ongoing efforts to educate and support the community about lupus.
DONATE
Your donation of any amount helps us provide valuable services and support to the lupus community in San Diego and beyond. With a minimum donation of $35, you will become a member of the Lupus Foundation of Southern California.
DONATE
Your donation of any amount helps us provide valuable services and support to the lupus community in San Diego and beyond. With a minimum donation of $35, you will become a member of the Lupus Foundation of Southern California.
News & Updates
Exciting news from LRA about a potential new treatment for Lupus Nephritis
LRA Applauds Aurinia on Priority Review of Voclosporin by U.S. FDA for Lupus Nephritis Great news from the Lupus Research Alliance came out this week and we had to share it with you all. The U.S. Food and Drug Administration recently accepted the New Drug Application...
Lupus Patients Invited to Attend Free Doctors Panel Discussion
Lupus Foundation of Southern California Hosting Informational and Q&A Event for Patients and Supporters San Diego, CA – April 25, 2020 The Lupus Foundation of Southern California (LFSC) is a patient-oriented, nonprofit group made up primarily of volunteers....
Lupus Foundation of Southern California 2019 Sip for the Cause Wine Tasting Fundraiser
Attendees Will Enjoy Wine and Hors D’oeuvres at the 2nd Annual Fundraiser at Gianni Buonomo Vintners San Diego, CA – August 5, 2019 The Lupus Foundation of Southern California (LFSC) strives to enhance the quality of life for the local lupus community through...
Get in Touch. Get Involved.
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