We will be gathering at Jacobs Pavilion at Nautica on September 7th, 2019! Join us in Cleveland to raise money for lupus research, increase awareness of lupus, and rally public support for the estimated 1.5 million Americans who suffer from its brutal impact.
Many thanks to our presenting sponsor, GSK!
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.
This series of live educational teleconferences webcasts on a variety of topics is designed to provide you with important information about living with lupus. Click here to RSVP.
We will be holding multiple educational programs across the state. Registration is now open in select cities. The summits are free, but space is limited. Click here to reserve your seat.
Are you interested in advocating for patients? We are looking to build an army of lupus advocates across Ohio who we can call when advocacy needs arise. Let your voice be heard by signing up to be an advocate.
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.
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]