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 | Jan 20, 2026 | Blog
Article by Amber S. Today, Monday 20th January 2026, is the International Day of Acceptance – a day dedicated to embracing life as it is, with all its challenges and changes. For those of us living with a chronic illness, acceptance isn’t just a word. It’s a daily...
by Nakita | Oct 30, 2025 | Blog
I’m now 24 years into my journey with Systemic Lupus Erythematosus (SLE). It began when I was just 18 — with rashes across my face in that well-known butterfly shape. At that time, I didn’t know what it was. I only knew that something inside me had changed. I was...
