Websites:
Lupus Foundation of America
National Resource Center on Lupus
National Institute of Arthritis and Musculoskeletal and Skin Diseases
Alliance for Lupus Research
Mayo Clinic
Caring.com (information for caregivers)Type your paragraph here.
Lupus and Allied Diseases Association
The Lupus and Allied Diseases Association, Inc. (LADA) is an all-volunteer national patient advocacy organization dedicated to enhancing quality of life by enlightening and empowering individuals impacted by lupus and allied diseases and other conditions of unmet need to become proactive in their medical care.
is a non-collegiate, disease oriented, professional and social organization that promotes sisterhood, advocacy, education and community outreach. Becoming a Glamorous Woman of Gamma Pi Rho Lupus Sorority, Inc. is a lifetime commitment. Each member plays an intricate role in ensuring that Gamma Pi Rho Lupus Sorority, Inc. thrives within the Lupus and Greek communities. Our primary goal is to “Unmask the Faces of Lupus” by being a voice for our fellow Lupus Warriors and making sure that the world as a whole gets to “KNOW Lupus to Say NO Lupus”.
Resources
Lupus Radio Broadcasts and Podcasts:
Live on Facebook via Streamyard
Join our Director, Autumn Austin, and other members of the Colors of Lupus for
Health, Wellness, & You
on the 2nd Friday of every month from 9-10:00 am (PST)
You can join live to interact via our Facebook page
Lupus, Science, and Medicine
Lupus Science and Medicine is an international online journal that publishes research on lupus and related diseases. It is a free-to-access journal where scientists from around the world can share their studies on different aspects of lupus. This journal was created to give researchers a platform to publish important findings without any barriers. It is the first journal of its kind dedicated specifically to lupus.
SickBoy Podcast
“Sickboy is determined to break down the stigma associated with illness and disease. Join Jeremie, Brian, and Taylor as they tackle health taboos with people who have experienced them firsthand. Taking the lead from Jeremie's lifelong battle with Cystic Fibrosis, the three best friends help us understand that sometimes the best way to deal with illness, disease, and life is simply to laugh.”