October 19, 2018 The Lupus Research Alliance Chief Financial Officer Debra Rose is quoted in an article in Consumers Advocate about nonprofits gaining accreditation by impartial organizations such as the BBB Wise Giving Alliance (WGA). BBB Wise Giving Alliance “is dedicated to evaluating national charities and reporting on their practices. Just as the Better Business Bureau focuses […] READ MORE
October 17, 2018 Winner of our most substantial grant, the Dr. William E. Paul Distinguished Innovator Awards in Lupus and Autoimmunity, Dr. Zhijian “James” Chen, Professor of Molecular Biology at UT Southwestern, just gained another prestigious award for that work from the Breakthrough Prize Foundation. He also recently received the 2018 Lurie Prize in Biomedical Sciences from the Foundation for the […] READ MORE
October 15, 2018 “For us, raising awareness about this awful disease isn’t limited to May. All year long, we are engaged in delivering discoveries that can transform lives. Because that is where real hope begins.” Kenneth M. Farber, President and CEO Lupus gained the attention it deserves throughout the month of May! Millions of people […] READ MORE
October 15, 2018 The Lupus Research Alliance’s Multi-cultural Outreach Task Force is out in full force to raise awareness among the African American communities, who face a higher risk of developing the disease, at health expos around the country, including the Essence Music Festival in New Orleans, LA this summer and Healthy Churches 2020 National […] READ MORE
The Lupus Research Alliance collaborated with the Lupus and Allied Diseases Association and the Lupus Foundation of America on a groundbreaking initiative in cooperation with the Food and Drug Administration’s (FDA) externally-led Patient-Focused Drug Development (PFDD) program. The well-attended meeting hosted by the three groups supplemented by a national survey of people with lupus resulted […] READ MORE
October, 2018 Certainly, advocacy is absolutely necessary to generate funding for the National Institutes of Health (NIH) and other federal organizations, as well as for groups that support and conduct lupus research. But patient involvement is also critical to opening pathways to discovery. “Just helping to raise money isn’t enough,” said Diane Gross, National Director of […] READ MORE
“Advocacy has many forms, including taking action for one’s own health. It’s self-advocacy — even though many would not think of their actions this way,” explains Diane Gross, National Director of Advocacy and Programs at the Lupus Research Alliance. “When patients hear that their insurance company is not going to pay for a medication and then […] READ MORE
Advocacy can mean different things to different people. Some seek to make changes in policy and funding at state and federal levels by helping Congress and government agencies better understand what it means to live with lupus. For others, advocacy is a way to take action with respect to their own health. Regardless of the […] READ MORE
2018 Awards Enable Promising Scientists to Bring Innovative Approaches to Lupus Research October 18, 2018 The Lupus Research Alliance announced six new Novel Research Grants to support paradigm-changing lupus research. To conquer the complexity of lupus, the Novel Research Grants support researchers who study lupus from many perspectives, testing new theories about what causes lupus and […] READ MORE
October 4, 2018 Abnormal immune cells invade the kidneys in patients with lupus and can damage the organs so severely that they stop working. But the kidneys defend themselves from these attacks by disabling these rogue cells, according to a new study from two scientists funded by the Lupus Research Alliance. Cancerous tumors similarly protect […] READ MORE
October 4, 2018 Immune cells called macrophages that normally clear away the body’s trash don’t do their jobs in lupus. Now, a study of cancer partly funded by the Lupus Research Alliance may explain how these macrophages promote lupus. Douglas Green, PhD, of St. Jude Children’s Research Hospital in Memphis, Tennessee, and colleagues found that […] READ MORE
NEW YORK, NY. Sept. 28 – Congratulations go out to the Lupus Research Alliance advocates! The 2019 spending bill was signed into law today, granting the two requests Lupus Research Alliance advocates made to legislators on “Capitol Hill Day” in March 2018. Approved by Congress earlier in the week, the bill provides $5 million for […] READ MORE
