Insights

Community Outreach Expansion The S.L.E. Lupus Foundation actively engages in public service campaigns and community outreach in both New York City and Los Angeles, indicating opportunities for partnership in health awareness programs and local community initiatives.

Focus on Disadvantaged Areas With a strong emphasis on supporting minority and low-income populations through tailored programs, there is potential to offer solutions that enhance patient education, support services, and health management tailored for underserved communities.

Research & Education Funding The Foundation funds research grants and fellowships, opening possibilities for collaborations in research technologies, grant management platforms, or educational content delivery to empower investigators and clinicians.

Targeted Demographics Focusing on minority women affected by lupus, the Foundation offers an opportunity to develop specialized health communication, patient engagement tools, or culturally sensitive digital platforms.

Regional Presence & Growth With operations in New York and Los Angeles and a revenue range of up to 10 million dollars, there is potential to scale services, technological solutions, or funding platforms that support regional expansion and program effectiveness.

S.L.E. Lupus Foundation Email Formats	Example	Percentage
FLast@lupusny.org	JDoe@lupusny.org	33%
First.Last@lupusny.org	John.Doe@lupusny.org	17%
FLast@lupusny.org	JDoe@lupusny.org	33%
First.Last@lupusny.org	John.Doe@lupusny.org	17%

S.L.E. Lupus Foundation Email Formats

Example

Percentage

FLast@lupusny.org

JDoe@lupusny.org

33%

First.Last@lupusny.org

John.Doe@lupusny.org

17%

FLast@lupusny.org

JDoe@lupusny.org

33%

First.Last@lupusny.org

John.Doe@lupusny.org

17%

Frequently Asked Questions

Where is S.L.E. Lupus Foundation's headquarters located?

S.L.E. Lupus Foundation's main headquarters is located at 330 Seventh Avenue, New York, NY 10001, US. The company has employees across 2 continents, including North AmericaOceania.

What is S.L.E. Lupus Foundation's phone number?

You can contact S.L.E. Lupus Foundation's main corporate office by phone at

+1-212-685-****

. For more prospecting data, LeadIQ has access to up-to-date and accurate contact information within our platform. Find, capture, and sync contact data to your CRM and sales tools in one click.

What is S.L.E. Lupus Foundation's official website and social media links?

S.L.E. Lupus Foundation's official website is lupusny.org and has social profiles on LinkedIn.

How much revenue does S.L.E. Lupus Foundation generate?

As of October 2025, S.L.E. Lupus Foundation's annual revenue is estimated to be $1M.

What is S.L.E. Lupus Foundation's SIC code NAICS code?

S.L.E. Lupus Foundation's SIC code is 8399 - Social Services, Not Elsewhere Classified NAICS code is 71394 - Fitness and Recreational Sports Centers.

How many employees does S.L.E. Lupus Foundation have currently?

As of October 2025, S.L.E. Lupus Foundation has approximately 11 employees across 2 continents, including North AmericaOceania. Key team members include Vice President Of Development: S. O.National Director Of Major Gifts: D. N.College Transfer Office Director: M. L.. Explore S.L.E. Lupus Foundation's employee directory with LeadIQ.

What industry does S.L.E. Lupus Foundation belong to?

S.L.E. Lupus Foundation operates in the Wellness and Fitness Services industry.

What is S.L.E. Lupus Foundation's email format?

S.L.E. Lupus Foundation's email format typically follows the pattern of FLast@lupusny.org. Find more S.L.E. Lupus Foundation email formats with LeadIQ.

S.L.E. Lupus Foundation

Q: What is S.L.E. Lupus Foundation's official website and social media links?

S.L.E. Lupus Foundation's official website is lupusny.org. S.L.E. Lupus Foundation has social profiles on LinkedIn.

Q: How many employees does S.L.E. Lupus Foundation have currently?

S.L.E. Lupus Foundation has approximately 11 employees.

Wellness and Fitness ServicesUnited States11-50 Employees

The S.L.E. Lupus Foundation helps people with lupus and their families and friends to cope with the anxieties and confusion that accompany daily living with a complex and dangerous chronic illness.

The S.L.E. Lupus Foundation is headquartered in New York City and has a West Coast division in Los Angeles. Through public service campaigns, public education programs and community outreach, the Foundation promotes early diagnosis of lupus and provides support especially in disadvantaged neighborhoods of New York City and Los Angeles.

The Foundation vigorously addresses racial disparities in lupus through its community based model programs demonstrating the effective management of chronic disease among minority women.

The Foundation funds lupus research grants and fellowship awards for new investigators in the New York region and in southern California, and in partnership with the Lupus Research Institute, supports innovative novel research nationwide.

Insights

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