After a long time and misdiagnosis after misdiagnosis, my mum Margaret was finally diagnosed with large cell vasculitis in 2018. It is a rare little understood autoimmune disease which left untreated can be fatal.

Through my mum’s diagnosis we heard about the Lauren Currie Twilight Foundation a charity dedicated to fund patient support, awareness campaigning, and medical research. There isn’t much out there for those with a diagnosis - so the LCTF is vital which is why I’m raising money. Any contribution would be appreciated. Thank you!