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Lauren’s Legacy Lives On — Help Us Support Vasculitis Patients

The Lauren Currie Twilight Foundation was created in memory of Lauren, who passed away at 15 from undiagnosed vasculitis. 💛 We support those living with this rare condition—but we need funding. Please donate or share to help us continue

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The Lauren Currie Twilight Foundation is dedicated to the support of Vasculitis. The charity was set up in memory of Lauren Currie who died of Vasculitis at the age of 15 in October 2010. The charity funds Awareness, Education, Research and Patient Support Services & Groups throughout the UK.

Story

The Lauren Currie Twilight Foundation was created in memory of Lauren Currie, who tragically passed away at just 15 years old from vasculitis—a rare autoimmune disease that went undiagnosed.

Her family turned their grief into action, creating a charity so that no one else has to face this condition alone.

Today, we support people living with vasculitis through:

• Support groups that reduce isolation

• Wellbeing courses that help people cope

• A respite cabin offering rest and recovery

We are entirely volunteer-run. Every donation goes directly to supporting patients.

Without funding, these vital services could disappear—leaving people without support, community, or a place to turn.

💛 £50 could help fund a support session

🏡 £100 could provide a night in our respite cabin

🌙 £500 could help keep our cabin running for a month

By donating, you are not just giving money—you are helping continue Lauren’s legacy and supporting people living with a life-changing condition.

Please donate if you can, or share this page to help us reach others.

Together, we can ensure Lauren’s legacy lives on.

Donation summary

Total
£180.00
+ £45.00 Gift Aid
Online
£180.00
Offline
£0.00
Direct
£180.00
Fundraisers
£0.00

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