2025 marks our 15th anniversary – help us make even more of a difference with our 15 for 15 campaign.
Lauren Currie had just turned 15 when she tragically died from what’s now known as Granulomatosis with Polyangiitis, a form of vasculitis. Had her symptoms been recognised in time, her illness could have been treated.
The Lauren Currie Twilight Foundation (LCTF) was set up in her memory by her parents, Adrienne and Grant. The charity raises awareness of vasculitis and supports those with the condition.
If you've just been diagnosed with vasculitis, we can help you with information about your condition and treatments.
If you're affected by vasculitis, we can help. We offer a range of practical and emotional support.
Donate, fundraise, volunteer or take part. Help us support people with vasculitis.