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Lupus Office Hours with Dr. Parsa

Lupus Foundation of Northern California

Lupus Office Hours with Dr. Parsa
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Office Hours with Dr. Parsa
No ticket is required to attend the live office hours on YouTube, however you can purchase a free ticket to RSVP to the event, add yourself to our newsletter for upcoming event information and foundation updates, to receive follow up materials from Dr. Parsa or the Lupus Foundation of Northern California, and so you can add this office hour session to your calendar. Note: your ticket is not used to join the free, live session—just join us on Youtube at the scheduled time and you'll be able to hear Dr. Parsa, live and add your questions in the comments.
5 min before event ends Free  

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Event Details

Lupus Office Hours with Dr. Parsa | LIVE, VIRTUAL MEETINGS


Please send us your questions to before Saturday morning.  

TO JOIN: Go to the Lupus Foundation of Northern California’s YouTube Channel at 10:00AM PDT, on the scheduled Saturdays.


Registration is free, and not required, though you can share your email to receive updates about future events and add the office hours to your calendar easily when registering.

About Dr. Parsa: Dr. Sean Parsa has over 20 years of practicing medicine all over the world and is a board-certified in wound reconstructive surgery. He is passionate about helping his patients live better, healthier lives. He is a student of medicine reading every medical journal and research paper he can get his hands on. Sean received his MD from SBMU, residency at the University of Hawaii in 2004, and visiting scholar for 2 years at Stanford School of Medicine, Department of Surgery.  Most recently Dr. Parsa has advised thousands of doctors across Europe and the Middle East around the COVID-19 pandemic.

Have questions about Lupus Office Hours with Dr. Parsa? Contact Lupus Foundation of Northern California

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Lupus Foundation of Northern California

With a mission to improve lives impacted by lupus, the Lupus Foundation of Northern California has served the Northern California lupus community for almost 40 year. The Lupus Foundation of Northern California was founded as the Bay Area Lupus Foundation in 1978 by Jo Dewhirst. Jo was elected to be the first Chairperson  of the Board and served in this position from 1978 - 1982. She was hired by the Board to be the first Executive Director of the Foundation and held this position from 1982 - 2009.

Dedicated to serving an ethnically and economically diverse population and to providing the widest possible access to services, the Lupus Foundation of Northern California offers programs designed to meet both social and educational needs of patients and their families in English and Spanish, both in-person and online.Focused on those living with lupus as well as on research and advocacy to find a cure, we are proud to be the voice of the northern California lupus community of patients, families, friends and caregivers. Our Mission is  to be a premier source of information on lupus by providing programs and services designed to educate and increase the knowledge of those affected by lupus, promote lupus awareness, and support external lupus research efforts.

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