Today, RAIRDA has released the Rare Care Matters report, which reveals that some individuals with rare autoimmune rheumatic diseases (RAIRDs) in the UK encounter major barriers in accessing care and treatment. Read the full report on our website 👉rairda.org/publication/re…

A very interesting read that provides food for thought, how can we improve the care of patients with rare rheumatic diseases in the UK #Vasculitis #RareDisease RAIRDA _ERNRITA UKIVAS VIA Vasculitis - In memory of John Mills MBE 💙💚 Jane L Edwards 📚

Vasculitis Awareness Month! Vasculitis is a rare rheumatic autoimmune illness and it can present in different ways. #vasculitis #vasculitisawareness #raredisease #livingwithvasculitis #visualisevasculitis _ERNRITA RAIRDA UKIVAS VIA Vasculitis - In memory of John Mills MBE 💙💚

During May 2025, #VasculitisUK will share what it is like to live with #Vasculitis We also ask those affected by vasculitis or their family members to hold an event on the 15th or 31st May (or any day that works for you) to celebrate the month of awareness vasculitis.org.uk/news/visualisi…

May is #VasculitisAwarenessMonth. We want to help you to visualise what it is like to live with #vasculitis. #Ears #Nose #Throat #Sinus

Vasculitis Awareness Month! One common initial symptom of vasculitis is joint pain, many times so severe it makes moving impossible. #vasculitis #vasculitisawareness #visualisevasculitis _ERNRITA RAIRDA UKIVAS Vasculitis - In memory of John Mills MBE 💙💚 VIA

Vasculitis Awareness Month! One common initial symptom of vasculitis is joint pain, many times so severe it makes moving impossible. #vasculitis #vasculitisawareness #visualisevasculitis _ERNRITA RAIRDA VIA Vasculitis - In memory of John Mills MBE 💙💚 Jane L Edwards 📚

The 3rd chick hatched at around 2.30 am this morning, but the first confirmation by visual was at 7.30 am when the falcon left to retrieve 'breakfast' - the tiercel then tried to sneak a peek at them but was quickly evacuated by the falcon returning.

#VolunteersWeek! Just want to say thank you to everyone who supports #VasculitisUK Everyone makes such a difference, all #volunteer in their own time - Trustees, #Volunteers, doctors, #vasculitis online support team, #helpline, #fundraisers, #newsletter vasculitis.org.uk/about

#CarersWeek #Vasculitis a #raredisease does not just affect the patient. It has consequences for #carers & families. Carers also face difficulties and problems. These vary depending on the stage at which the #patient is at any particular time. vasculitis.org.uk/living-with-va…