by Nakita | May 9, 2026 | Blog
People living with lupus face daily challenges depending on the severity of their flares and, along with other contributing factors, in my experience, most “good” days, need to be planned in advance. Spontaneity is a rare and wonderful thing, something most people...
by Nakita | May 9, 2026 | Blog
I live with Systemic Lupus Erythematosus (SLE), otherwise known as lupus. While it has changed my life in many ways, most people would never know it just by looking at me, and that is just the complicated reality of living with an invisible illness. “But you don’t...
by Nakita | Apr 30, 2026 | Blog
Within the last seven years, since receiving the lupus diagnosis, I’ve had to relearn, reinvent and re-love myself. I’ve researched and studied, educating myself about lupus and linked illnesses, in a way that I never did for my university degree. Being chronically...
by Nakita | Mar 27, 2026 | Blog
Article by Debbie Kinsey, Health Information, Policy, & Research Manager SLEuro is a conference for researchers and healthcare professionals across Europe to come together and share the latest research, treatment, and support for people with lupus. Although...
by Nakita | Mar 4, 2026 | Research Opportunities
The ADAPT TrialA team of researchers, patients and clinicians are looking at whether Pilates or Tai Chi online group classes can reduce fatigue and improve quality of life. Location: Online Deadline: Recruitment closes when the study is full. Spaces are limited, so...
