Just a reminder that the Vasculitis U.K. Helpline is open from 9am – 8pm, 7 days a week. Telephone 0300 365 0075 You can contact the Vasculitis UK Helpline for …

Vasculitis UK has produced a brief guide on Covid-19 vaccination and issues for vasculitis patients. (Updated 4 February 2021). UPDATE: Tuesday 9 February 2021 People living in England who are …

Jen Harper, married to GPA patient Charlie, has written a book to help explain vasculitis to children – and is selling it in aid of Vasculitis UK. Holly Helps Out …

Over 2 days in November, UKIVAS, the UK & Ireland Vasculitis Study Group, teamed up in partnership  with the Royal Society of Medicine (RSM) to lay on an educational webinar for 500 medical delegates. …

The Rare Autoimmune Rheumatic Disease Alliance (of which Vasculitis UK is a member) has produced a new report “Core NHS services during the pandemic: Latest report from Parliament and what …

Jane Edwards has Granulomatosis with Polyangiitis (GPA). Her story “Coming Out of Shielding” has been published on the Rare Disease UK and Genetic Alliance UK website.

Do you see a Rheumatologist for your Vasculitis? Has your care been affected by COVID-19? What do you want your future appointments to be like? Please complete this survey & share your …

The FIRST Immunoglobulin A vasculitis (Henoch Schonlein Purpura) Online Patient Information Video The University of Liverpool are offering a video of this online event – offering an opportunity to learn …

The PINPOINT trial needs your help! They are looking for 5 patients/families to help them design a study comparing which medicines work best for children with HSP – in a …

Rare Revolution magazine includes powerful individual stories highlighting the challenges of receiving a timely diagnosis and living with AAV, and describes the collaborative campaigns that are fusing science and art …