Feb. 14, 2017

Tacoma Doctoral Student Studies Lupus to Empower Others

Cobi Silver has an impressive list of academic accomplishments. First, she graduated with honors from Arizona State. Then she published an anxiety workbook for her master’s degree at the University of Washington. Now she's working on her doctorate of behavioral health. To make these achievements even more impressive, Cobi has lupus.

Nov. 22, 2016

Wolf Pack Bakes Pies, Fights Lupus

Miranda Matchett’s professional life has run the gamut from firefighting to public relations and management. These experiences have made her comfortable approaching strangers, pitching ideas and getting other people excited about a goal. However, she never thought these skills would come in handy in the fight against lupus.

Nov. 07, 2016

Announcing the Cut it Out Challenge: A Crowdfunding Campaign for Lupus

Can you Cut it Out? Join the CrowdRise Challenge by cutting out one small thing – such as coffee or sweets – for 14 days and then donate the money you save to support life free of lupus.

Sep. 19, 2016

Walk to End Lupus Now Seattle and Portland 2016

The Lupus Foundation of America, Pacific Northwest Office welcomed nearly 800 participants to the Walk to End Lupus Now events in Seattle and Portland.

Aug. 24, 2016

SOCIAL SECURITY DISABILITY BENEFITS: Maximize Your Chances of Getting Disability Earlier

The Lupus Foundation of America estimates that approximately 40% of people with lupus will eventually have to stop working because of their condition. Attorney Anne Kysar has helped people with lupus gain their Social Security Disability Insurance benefits in the Pacific Northwest. Read what Kysar shared with the Foundation.

Jun. 23, 2016

2016 Lupus Insight Prize Presented to Dr. Ann Marshak-Rothstein

The 2016 Lupus Insight Prize was awarded today to Ann Marshak-Rothstein, PhD, University of Massachusetts Memorial Medical Center and Professor of Medicine/Rheumatology, University of Massachusetts Medical School, for a project with great promise to improve the treatment of lupus-related skin disease.

Jun. 15, 2016

Mother, Daughter Fight Lupus Together in Federal Way

Research shows that nearly two-thirds of the public knows little or nothing about lupus. However, when Keisha Nathan started experiencing pain in her joints and muscles in 2007, her mother—Althea Kemp—knew exactly what these symptoms could mean.

Jun. 01, 2016

Put on Purple 2016

Hundreds of participants gathered at the Seattle Great Wheel to enjoy an evening of speakers and performances and rally public attention to lupus and its terrible impact on approximately 1.5 million Americans.