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Celebrate Your (Purple) Power!
Let's celebrate the successes of 2022 and look forward to the opportunities in 2023!
Join Us!
NYC Power Party, May 16th at 6:30 PM
Register Here!
Questions?: Jessica Orr 917-675-2636, orr@lupus.org
Boston Power Party, May 4th at 6:30 PM
Register Here!
Questions? Michele Insley 617-686-8774, insley@lupus.org
Hartford Power Party, May 21st at 2 PM
Register Here!
Questions?: Michele Insley 617-686-8774, insley@lupus.org
Norwalk Power Party, May 25th at 6:30
Register Here!
Questions?: Alisha Scott 203-780-1697, scotta@lupus.org
Please join us for our upcoming online Lupus & You program: Living WELL with Lupus. This online education program will focus on the efficacy of yoga as a way to improve overall health and well-being. Ms. Long will lead you through a series of gentle yoga postures, breathing exercises, and meditation techniques that support the body, mind, and spirit of people managing lupus.
The Brigham and Women’s Hospital Lupus Center is happy to announce our Spring Community Lupus Forum. This annual community forum will be held on Saturday, May 6 from 11:00 am – 2:00 pm and is proudly sponsored by the Sportsmen’s Tennis and Enrichment Center and the Lupus Foundation of America.
Are you looking for more ways to get involved with LFA as part of your 2023 New Year's resolution?
Raise your voice to fight lupus. We are the leader in stimulating federal support for lupus, generating more than $684 million for lupus research and education in the past five years. Every day we fight to ensure the government is responsive to the needs of the 1.5 million Americans living with lupus, and your voice is one of the most powerful tools we have.
The Northeast hosts 5 walks throughout New York, New Jersey, Connecticut, and Massachusetts. Committee members help plan, organize and execute the walks. If you are interested in helping or joining the committee please visit our walk page.
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Check out the information below about how you can bring lupus awareness to your company.
We are honored to partner with all the Northeast Lupus Warriors, Families, and Friends.
Dr. Cynthia Aranow explains the impact of invisible symptoms in this episode of The Expert Series. Learn the difference between a sign and a symptom and how to discuss this topic with your healthcare team and loved ones.
For the first time since 2019, lupus advocates will come together in Washington, DC for the nation's largest lupus advocacy event! From April 23–25, Summit attendees will learn from experts in the field about the latest in lupus research, connect with hundreds of their fellow lupus advocates, and turn Capitol Hill purple by advocating for their members of Congress to join our fight against this terrible disease.
Could your symptoms be related to lupus?
Use this questionnaire to learn more.
Nearly 1.5 million Americans live with lupus, a chronic illness, yet those who suffer may not "look sick". Learn the facts about this cruel and mysterious disease and resources for managers, employees, and their family members. We'll share essential tools and information about how you can help the Lupus Foundation of America.
Contact usThe Lupus Foundation of America Northeast region is looking for corporate partners to help us reach our mission goals. Your company or organization has many ways your employees can make a difference in the lives of those living with lupus. Learn more here!
Please visit this landing page for information on the coronavirus and lupus. It contains information from the Lupus Foundation of America regarding the coronavirus, updated as needed, with additional FAQs from our National Health Educators.