Welcome to our vasculitis blog

Welcome and thanks for checking out our blog. This is where we will be sharing our thoughts on how we can fund vasculitis research, raise awareness and support people and their loved ones living with a life-changing illness.

We set up the The Lauren Currie Twilight Foundation in October 2010 in the memory of Lauren Currie who died from vasculitis and specifically the rare variant, Wegener’s Granulomatosis. Lauren was only 15 and highlighted that vasculitis can strike at any age, gender or race.

Since then we have been trying our very best to raise awareness of this rare disease. Our events section has all our details of upcoming webinars, support groups in your area and our vasculitis 5k in April this year.

Please do leave any comments and check back on our stories that we’ll be updating you with on here.

Thanks for reading,

The Lauren Currie Twilight Foundation x

More Articles

22nd May 2023
Giant Cells in GCA update
Read Article
6th May 2023
Vasculitis Awareness Month 2023
Read Article
21st December 2022
The LCTF Tartan
Read Article