Your support WILL make a difference.
Every day, thousands of Southern Californians live with the unpredictability of lupus, a disease without a cure which often causes debilitating affects. Remember how it feels to have the flu? Now multiply that by a thousand and that is just a slight glimpse as to have someone feels when they have lupus.
There is HOPE.
With your support, new treatments and cure can be found, patients will have access to support services and college students with lupus will be able to continue their education through assistance with Pocket Relief. We are hoping to add 100 new students to our program.
Since 1983, Lupus International continues to stand rock solid beside those who are afflicted with Systemic Lupus Erythematous (SLE).
Our mission is to alleviate suffering and improve prognosis for children, women and men living with lupus by providing information, support, doctor/patient exchanges and dialogues, by training pediatric Fellows, by contributing to research for novel treatment and cure for this chronic life threatening disease and by assisting college students with lupus through our program Pocket Relief.
Lupus International expands our content and enhances the delivery of information interactively through the Internet and social network platforms. Only a keystroke away, we bring knowledge and ideas for living with lupus to patients, their families and their support teams. Whether in rural communities or in the hub of big cities, we reach across America, and around the world.