Please contact us for:
- Information on lupus
- Names and contacts for leaders in lupus research
- Names and contacts for leaders in the care of people with lupus in NY, LA, and across the country
- Stories of people living with lupus, and contacts for follow-up
- Ideas for angles to cover
For this information and more, telephone our Communications or Public Relations Department at 212.685.4118 or email firstname.lastname@example.org.
Note: Spanish-language materials and doctor-researchers contacts available.
Press releases, health news, newsletters, and articles that feature our work
Find out what we do and where to reach us
Click to download a fact sheet about lupus
Learn about who is leading the Foundation
Programs on Lupus
We have special programs for kids with lupus, model community outreach programs in New York’s boroughs, and run various special programming throughout the year.
Public Service Campaigns
Our local and national PSAs have had tremendous impact.
We have a long history of helping young investigators focus on research in New York (and now Los Angeles), and were also a founding partner of the highly successful Lupus Research Institute.
The S.L.E. Lupus Foundation has cared for New Yorkers with lupus since 1970. Read about its founders and how the organization has evolved.
ING New York City Marathon 2013
The S.L.E. Lupus Foundation is an Official Charity Partner of the ING New York City Marathon 2013 on Sunday, November 3rd—the only lupus organization ever to host a team in the world’s most famous marathon. Our Team Life Without Lupus is proud to represent the lupus community in New York City, across the United States, and around the world.