New Developments in Vasculitis by Prof Neil Basu

Vasculitis doctors and scientists are pushing the boundaries of knowledge in order to address the many challenges which people with vasculitis continue to experience. In recent times there has [...]

The Black and Red Ball is back! Help us raise funds and awareness of vasculitis by joining us at a fabulous evening of entertainment on the 17th September 2022 at the Radisson Blu Hotel, Glasgow. [...]

Annie Peacock is the PhD student who will be contributing to the discovery of next generation drug targets for GCA. This is a 3 year project which has been funded by LCTF. Congratulations to [...]

28th February marked Rare Disease Day. East Ayrshire Council lit up the Viaducts in Kilmarnock town centre in recognition of Rare Disease Day and in memory of Lauren who died from vasculitis at [...]

We are looking for feedback for the Clinical Care working group of the SSVN (Scottish Systemic Vasculitis Network) where The Lauren Currie Twilight Foundation is a patient representitive. [...]

Goodbye 2020. Will we be sad to see you go? Not one little bit! In fact, we might adopt the custom of opening the door at midnight to usher out the past year…just to make sure it actually goes! [...]

          Cat Walker Art from Aberdeenshire painted this beautiful winter scene for LCTF’s Christmas card selection. It’s proven to be one of the most popular designs and a repeat [...]

Sleep Well During The Covid-19 Pandemic   For the first time for many people they are experiencing unsettling vivid dreams, nightmares, and often wakening during the night with feelings of [...]

It’s normal to feel worried and anxious when financial uncertainty is looming or the prospect of unemployment is pending. Debt and financial problems can all cause significant emotional [...]

Now more than ever it’s essential to look after your wellbeing. Being diagnosed with a life-changing condition alongside the stress of living through a pandemic can easily exacerbate your [...]