Moving to Virtual

To continue to provide up-to-date information about COVID-19 and to bring our essential services to the lupus community we are converting our programs and services to virtual platforms wherever possible. Here's what we're working on:

COVID-19 EXPERT Q&A SESSIONS
We are talking with physicians and experts to answer the most pressing questions lupus and autoimmune patients have been asking us. Watch them all on YouTube.

• Virtual Lupus Office Hours with Dr. Sean Parsa (ongoing, live every other Saturday)
• Q&A with Rheumatologist, Thomas M. Bush M.D. (retired) (English)

• Q&A with Rheumatologist, Dr. Cristina Lanata (Spanish)

COVID-19 RESOURCE CENTER
We've collected reliable and helpful resources and novel coronavirus COVID-19 information for people living with lupus and autoimmune conditions. We'll be adding and updating this page often, so check back frequently during this time. COVID-19 Information

VIRTUAL SUPPORT GROUPS
We are working with our support group leaders to convert and set up virtual support groups and several groups are already hosting virtual meetings this weekend! We will publish information to our website and in our social media channels about how to attend. Support Groups

LIVING WELL WITH LUPUS, WHILE AT HOME
We are working on new virtual Living Well with Lupus activities, such as virtual walks (from your own neighborhood or home!), online wellness sessions, and online resources. See our living well with lupus page and follow us on social media to hear about the latest program updates and virtual events.

STAYING CONNECTED
Stay connnected with others in the lupus community during this time—we are sharing important information social media. Join our community!

• Facebook, Instagram, YouTube, LinkedIn, Twitter

OPEN FOR BUSINESS
We are still open to serve the lupus community—though not at our physical office.
We can be reached at 408-954-8600, and at communications@lfnc.org or outreach@lfnc.org.

THANK YOU for your patience while we convert programs, and for your critically needed support of the Lupus Foundation of Northern California and all of the patients and families we serve—we are ever-grateful for your contributions at this urgent time. If you're able, please consider a donation to help us sustain and convert our programs to virtual platforms, so we may reach lupus patients where they are during this time.