The Lupus Foundation of America (LFA) is the largest national non-profit voluntary health organization dedicated to finding the causes of and cure for lupus and providing support, services and hope to all people affected by lupus.
The LFA was established in 1977 with the combination of several local lupus organizations. Since then, the LFA has evolved into the largest non-profit lupus organization with nearly 300 chapters and support groups nationwide. The LFA supports lupus research, education, advocacy and support services on the federal, state and local levels.
The Lupus Foundation of America focuses on five programs to achieve its objectives: 1. Through its national research program, Bringing Down the Barriers, the LFA is available to direct its financial aid to researchers 2. Rallies for support and advocacy in the public and private sector for Lupus 3. Help make new information about Lupus understandable and available to those suffering with the disease 4. Increase public awareness 5. Support individuals with the disease, their families and caregivers
With nearly 300 integrated chapters and support groups in 32 different states in the United States, the Lupus Foundation of America works on the national, state, and local level. The organization also works with nearly 100 international lupus organizations.
Some of the key accomplishments of the organization are:
The Butterfly Gala is an annual event held by the Lupus Foundation of America as a celebration by honoring those who act as champions for people living with lupus and their loved ones. This event also raises the profile of lupus and substantial funding. The Butterfly Gala is held bi-annually in New York and Washington D.C.