We have partnered with other Lupus organizations and have events scheduled. See link below:http://peoplewithempathy.org
Let's Advocate with International Support Fibromyalgia Network March 2020 in DC. click on link: http://supportfibromyalgia.org
The Lupus and Allied Diseases Association, Inc., was founded in 1978 and is a national non-profit organization dedicated to enhancing quality of life by enlightening and empowering individuals impacted by lupus and allied diseases and other conditions of unmet need. As a passion-driven, patient-focused charity led by individuals with lupus and their loved ones, we work to ensure that the patient perspective is included and recognized as an equal voice in the healthcare and public policy arenas and across the research continuum. It is our goal to improve access to care and quality of life by fostering collaboration among stakeholders and promoting innovative advocacy, education, awareness and biomedical research initiatives that will identify causes, advance better diagnostics, and discover superior treatments, and cures.
315-829-4272 or 1-866-2-LUPUS-4
Lupus Research Alliance is the world’s leading private funder of lupus research. Established in 2016 – from the merger of the Alliance for Lupus Research, the Lupus Research Institute, and the S.L.E.
Research and Clinical Trials
Online Community Patient and Caregivers Portal and so much more information about Lupus.
For more information visit:
Lupus LA is a non-profit health organization dedicated to finding the causes of and a cure for lupus while providing support, services and hope to all who suffer from lupus. They raise funds to support 3 core areas of focus: medical research, patient services, and awareness and advocacy initiatives.
Lupus LA offers patient services to the lupus community in the greater Los Angeles area, including support groups for adults and pediatrics, doctor referrals, emergency grants, patient education and resources, as well as our newly diagnosed patient guide.
International Support Fibromyalgia Network is a 501 (c)(3) global patient organization with a mission to bring the fibromyalgia community together through education, awareness, research and advocacy.
To learn more please visit https://supportfibromyalgia.org