by Nakita | Oct 30, 2026 | Blog
Lupus UK attends medical and research conferences throughout the year to learn about the latest updates in research and treatment, meet with healthcare professionals, and collaborate with other organisations. Unfortunately, many of these events don’t allow the general...
by Nakita | Oct 29, 2026 | Blog
It’s been eight years since I’ve attended an outdoor festival. Once upon a time in Cokerland, the party people of the place had an understanding; April was for arrangements. Blossom on trees signalled t’was summer schedule setting season. Messages would be flying...
by Nakita | Sep 25, 2026 | Blog
Government consultations are an opportunity for organisations and the public to share evidence, experiences and recommendations before decisions are made. For Lupus UK, they are an important way to ensure that the experiences of people living with lupus are included...
by Nakita | Aug 26, 2026 | Blog
Poetry can be a powerful way to express feelings and experiences that may be difficult to put into words. Bethany has written a poem “The Flow of Lupus” which reflects on the unpredictable nature of living with lupus. The flow of Lupus. As a fast-paced river, I...
by Nakita | Jun 18, 2026 | Blog, Latest News
We are delighted to welcome Eleanor and Ann-Marie to the Lupus UK Staff Team! Eleanor has joined the Fundraising & Marketing Development team as our Fundraising & Stewardship Officer, and Ann-Marie has joined the Community Services team as our Community...
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...