The Lauren Currie Twilight Foundation

23/10/2026

❤️ Today has become that little bit lighter…

Today marks 16 years since we lost our beautiful Lauren.

For us, this is always an incredibly difficult day. A day when the memories of Lauren's time in hospital come flooding back, bringing with them thoughts and emotions that never really leave us.

But out of that heartbreak came something very special. The Lauren Currie Twilight Foundation was born, and for 16 years we have worked to create something positive from our loss, supporting people and families affected by vasculitis in Lauren's name.

The past few years have been particularly challenging for charities, with fundraising becoming increasingly difficult. But our passion for what we do, and our determination to continue Lauren's legacy, has never wavered.

And today, of all days, we have some wonderful news to share! ❤️

We are absolutely delighted to announce that The National Lottery Community Fund Scotland has awarded us £12,600 for our project:

🖤Empower: Living Well with Vasculitis❤️

This fantastic funding will allow us to get back out into our communities, bringing people together through support groups and wellbeing activities, helping those affected by vasculitis feel less isolated, more supported and better equipped to live well.

We are incredibly grateful to The National Lottery Community Fund Scotland for making this possible.

Lauren is at the heart of everything we do, and knowing that her legacy continues to make a difference to others means more than words can say.

Today will always be a difficult day. But thanks to this wonderful news, it has become that little bit lighter.❤️

10/09/2026

In just over a week, Tom, Ross and Catherine are taking on the Wee Westie - the first 22 miles of the West Highland Way, from Milngavie to Balmaha - to raise awareness and funds for the Lauren Currie Twilight Foundation. A fine looking trio! Thank you and good luck! 🖤❤️

https://www.justgiving.com/team/team-lctf-wee-westie?utm_medium=TE&utm_source=CL

29/08/2026

Happy National Cleaner Day! (Just made it!)
Today, I want to give a massive shout-out and a heartfelt thank you to and Graeme. They work tirelessly behind the scenes to keep The Twilight Cabin clean, safe, and welcoming. Their dedication, attention to detail, and hard work do not go unnoticed. We couldn’t do it without you! 🖤❤️
The Twilight Cabin from LCTF

16/08/2026

Good luck this morning to Martin Courtney who is striding out on the Dundee Kiltwalk by himself. There’s something pretty special about someone pulling on his walking boots and taking on the Dundee Kiltwalk completely on his own, simply to support people with vasculitis and the LCTF cause. We think you’re amazing Martin! Can’t thank you enough. 🖤❤️

You can still support him-
https://www.justgiving.com/page/martin-courtney-2?utm_medium=FR&utm_source=CL

10/08/2026

🥾 ONE MAN. ONE MISSION. ONE KILT.🥾

This Sunday, 16th August, the legendary Martin Courtney (he’s the one on the right!) is taking on the Dundee Kiltwalk for The Lauren Currie Twilight Foundation. 🖤❤️

There’s just one small problem…

He needs a gang!

Martin is currently preparing to stride heroically through Dundee, but we think he’d look far better surrounded by a team sharing the miles, the laughs and, quite possibly, the blisters.

You don’t need to be super-fit.
You don’t need to be fast.
You don’t even need particularly good knees for a kilt.

You just need to be up for a great day, a good laugh and helping us support people affected by vasculitis.

Dundee Kiltwalk
Sunday 16th August
Walking for LCTF

Who’s joining Team Martin?😂🥾❤️

https://www.justgiving.com/page/martin-courtney-2?utm_medium=FR&utm_source=CL

03/08/2026

Don't forget to support us every time you shop online!🛒

Did you know you can raise FREE donations for The Lauren Currie Twilight Foundation every time you shop online through easyfundraising?
With over 8,000 retailers taking part – including supermarkets, travel companies, fashion brands and more – it's an easy way to support our work at no extra cost to you.
If you haven't signed up yet, it only takes a couple of minutes. Then, simply remember to shop through easyfundraising and every eligible purchase could make a real difference to the families we support.
Every click. Every shop. Every donation counts.
Thank you for helping us continue our work.🖤❤️

30/07/2026

🖤❤️Happy Friendship Day to all of our wonderful supporters. 🖤❤️

One of the things we're most proud of at the Lauren Currie Twilight Foundation is bringing people together. Living with vasculitis can often feel lonely, but through our support groups, wellbeing weekends, ball and online community, so many lasting friendships have been formed by people who truly understand one another.

As we get ready to kick off our support groups again, we hope to see familiar faces and welcome plenty of new ones too. Whether you're newly diagnosed, a long-time patient, a family member or a carer, you'll find a warm welcome, understanding and the chance to connect with others who simply "get it."

Because no one should have to face vasculitis alone.

Happy Friendship Day! 🥰

07/07/2026

🖤Talk to Us Month
The Power of a Conversation ❤️

One conversation can make all the difference.
After being diagnosed with a lifelong illness, Pam found support, friendship, and understanding through The Lauren Currie Twilight Foundation. The foundation gave Pam and her husband the chance to enjoy a wellbeing weekend, a respite cabin stay, and opportunities to take part in fundraising events.
This Talk to Us Month, we're celebrating the power of talking. Reaching out, sharing your story, or simply listening can lead to connection, support, and hope.
🖤No one should face life's challenges alone.❤️
http://bit.ly/4y8DHwq

Despite usually being fit and healthy, Pam was diagnosed with GPA after experiencing joint pain and eye issues. This is her vasculitis story.

01/07/2026

July is national Talk To Us Month

A vasculitis diagnosis can bring a whirlwind of emotions. You might feel frightened, uncertain, isolated, or overwhelmed—and that's completely understandable.
Whether you're newly diagnosed, supporting someone you love, or have been living with vasculitis for years, you don't have to face it alone.
This 'Talk To Us' Month, we're encouraging everyone in our community to start the conversation. Share what's on your mind, ask questions, or simply let someone know how you're feeling.
🖤We're here to listen❤️

📩 Send us a message, call or join one of our online support group, or tell us how you're doing in the comments.

[email protected]
0141 404 1184

25/06/2026

🖤Small Charity Week. Shining a Light on 16 Years of Impact❤️

For the past 16 years, The Lauren Currie Twilight Foundation has been making a real difference to people affected by vasculitis. As a small, volunteer-run charity, we've shown that a dedicated community can achieve extraordinary things.

Together, we have:

💜 Supported over 500 families through our respite cabin, providing much-needed time away to rest, reconnect and recover.

💜 Hosted 14 Charity Balls, raising vital funds and increasing awareness of vasculitis.

💜 Delivered 9 Wellbeing Weekends, supporting more than 300 patients and family members with education, therapies and peer support.

💜 Been there for countless people through our helpline and counselling services when they needed someone to listen.

💜 Brought the vasculitis community together through 126 support groups, helping to reduce isolation and build lifelong friendships.

💜 Launched the first-ever TV advert dedicated to raising awareness of vasculitis, alongside four radio campaigns that reached thousands of people and introduced many new supporters to our charity.

💜 Helped establish the Scottish Systemic Vasculitis Network, working alongside outstanding healthcare professionals to improve care for patients across Scotland.

💜 Built an incredible LCTF family, meeting some of the most courageous, resilient and inspiring patients, families and supporters imaginable.

💜 Even created our own beautiful LCTF tartan and range of merchandise, giving our community something unique to wear with pride.

When we look back, it's incredible to see just how much a small charity can achieve.

And it all started because of one amazing young lady who we could never, ever forget… our wee Lauren. Her legacy lives on in every family we support, every friendship that's formed, every life that's touched and every moment of hope we help create.

But our work is far from over.

We are entirely volunteer-run, and every support group, wellbeing weekend, respite break, counselling session and phone call is only possible because people choose to support us.

To everyone who has donated, volunteered, fundraised, attended an event or simply shared our story—thank you. You are part of Lauren's legacy.

And if you'd like to help us continue making a difference for the next 16 years, please consider supporting our fundraising or making a donation. Together, we can ensure that no one faces vasculitis alone. 🖤❤️