Helping people living with autoimmune disease inspires our work.
Aurinia’s goal is to foster a coalition of aligned communities: understanding the disease, monitoring for signs and symptoms, and making the best, most informed treatment decisions for long-term health. We have built meaningful relationships and developed pioneering resources to make this happen.
We always keep line of sight to the urgency of our mission: With a chronic, degenerative disease, early intervention is critical. We believe we have the potential to change the course of autoimmune disease and make a difference for people with LN.
We are building out an educational program for healthcare professionals to help them understand and diagnose the condition, as well as improve its management. For the LN community and their caregivers, we are focused on helping them understand the risk factors for the disease, how to assist in getting rapid diagnosis and how to best take care of themselves. We listen closely to how this community accesses care and feed that into our future planning. In every case, we focus on grasping challenges and helping draw lines of clear understanding.
Time is Nephrons, sponsored by Aurinia, is a lupus nephritis (LN) disease-state awareness campaign for healthcare professionals (HCPs). The initiative aims to highlight the importance of active screening for early diagnosis to potentially minimize the impact on kidney function and improve long-term outcomes for every patient with LN.
The ALL IN program and website, sponsored by Aurinia, is a source of information, resources, and support for those affected by lupus nephritis. If you or a loved one are living with LN and would like to learn more, please visit www.allinforlupusnephritis.com.
For additional information, you may also visit the following independent organizations.
The Lupus and Allied Diseases Association (LADA) is a national organization dedicated to enhancing quality of life for those impacted by lupus and allied diseases and other conditions of unmet need by fostering collaboration among stakeholders, promoting unity in the community, supporting innovative advocacy, education, awareness and biomedical research program initiatives, and ensuring the patient viewpoint is present and heard in the healthcare, regulatory, policy and research communities.
A national organization devoted to improving the quality of life for all people affected by lupus through programs of research, education, support, and advocacy.
National Resource Center on Lupus: Developed by the Lupus Foundation of America, the National Resource Center on Lupus provides up-to-date information and resources for the lupus community.
Local Chapters: Find support and connect in your community with regional offices and chapters of the Lupus Foundation of America.
The Lupus Research Alliance is the largest non-governmental, non-profit funder of lupus research worldwide. Together, the Lupus Research Alliance and its affiliate Lupus Therapeutics support the entire research continuum from basic research into the causes of lupus and lupus nephritis through conducting clinical trials on innovative drug treatments.
The organization aims to transform lives of people with lupus by driving discovery toward better diagnostics, improved treatments and ultimately, a cure. Because the Lupus Research Alliance’s Board of Directors funds all administrative and fundraising costs, 100% of all donations goes to support lupus research programs.
An organization in the U.S. dedicated to the awareness, prevention, and treatment of kidney disease for hundreds of thousands of healthcare professionals, millions of patients and their families, and tens of millions of Americans at risk.
Please note that Aurinia Pharmaceuticals does not endorse or monitor the activities and content of advocacy groups, their websites or third-party online communities.