The 2019 National Lupus Advocacy Summit will be held from March 4-5 at The Mayflower Hotel in Washington, DC. Join us as we urge legislators on Capitol Hill to support funding for programs to help us better understand lupus and move us closer to new treatments for the disease.Learn More
Lupus is an unpredictable and misunderstood autoimmune disease that ravages different parts of the body. It is difficult to diagnose, hard to live with, and a challenge to treat. Lupus is a cruel mystery because it is hidden from view and undefined, has a range of symptoms, strikes without warning, and has no known cause and no known cure.
Our mission is to improve the quality of life for all people affected by lupus through programs of research, education, and advocacy. In fulfilling our mission, we provide a variety of different programs and services for lupus patients and their support systems. If you need to speak with us, call the office at 1 (888) NO-LUPUS.
Less than 10 days left for our Annual Giving Campaign! Please resolve to help us do more to provide lupus patient support and physician education throughout the state by giving today!
Thanks to you- our generous donors - the LFA, GOC has accomplished so much this past year. Every dollar counts, and we would not be able to follow our mission without your support. You can click here to see an outline of the amazing impact of your gifts. Thank you!
No two people have the same lupus journey. But sharing your unique story can help all lupus patients know they are not alone. You can read Natalie and Kim's stories here.
Would you like to help others by sharing your story? Go to facebook.com/lupusreateroh and use the heading "My Life with Lupus" or submit your story to [email protected]
Have a safe and happy holiday season!
We are happy to announce that we were able to raise over $88,000!