The LCT Foundation

The Lauren Currie Twilight Foundation was set up in the memory of 15 year old Lauren Currie who died from vasculitis. Support/Awareness/Fundraising/Research.

[The LCT Foundation @LCTFoundation]

VOLUNTEER! If you've a bit of time you could use to help fight against Vasculitis, we'd love to hear from you! We rely on volunteers, and we always need help. So why not meet new people, do new (good) things, and help us help people with vasculitis?

See https://t.co/1Hw0AYek0P

[The LCT Foundation @LCTFoundation]

#VasculitisAwarenessMonth may be over for another year, but we’ll still be here. If you can donate anything, no matter how small, we’d really appreciate it. Thank you for helping us help people with vasculitis.

Give here: https://t.co/UthuoxZs7C

#LCTF #vasculitis

[The LCT Foundation @LCTFoundation]

THANK YOU for helping us help people with vasculitis! We couldn’t do what we do without your support and donations. ❤️🖤
#VasculitisAwarenessMonth is over for another year, but we’re still here. Please donate if you can: https://t.co/UthuoxZs7C

#vasculitis #LCTF

[The LCT Foundation @LCTFoundation]

Research funded by LCTF is leading to new insights into vasculitis treatment. Annie Peacock is a PhD student we fund. She’s halfway through a 3 year project on drug targets for Giant Cell Artheritis (GCA). This is her update:
https://t.co/1Zkti0fTAz

#Vasculitis #LCTF #research

[The LCT Foundation @LCTFoundation]

Get creative for vasculitis! Host a bake sale, fun run, or other event to support LCTF's vital work. From Chewbacca to cupcakes, our fundraisers are THE BEST ❤️🖤
Need ideas? Check out our fundraising guide: https://t.co/OiuWnDVORe
#FundraisingFriday #VasculitisAwareness #lctf

[The LCT Foundation @LCTFoundation]

Throwback to last year’s Black & Red ball celebrating 10 fab years of LCTF. Together we raised thousands for research & support services. Join us for this year’s, which will be EVEN BETTER! ❤️🖤
https://t.co/YIIIXig4dP

#ThrowbackThursday #VasculitisAwareness #LCTF #vasculitis

[The LCT Foundation @LCTFoundation]

At LCTF, we offer a range of support services for people living with vasculitis. Learn more about how we help and how you can get involved: https://t.co/zXKly3zhq3
#SupportServicesSpotlight #VasculitisAwareness #VasculitisSupport #vasculitis #weareLCTF #LCTF #vasculitisuk

[The LCT Foundation @LCTFoundation]

🎉 To date, we've donated £200,000 to vasculitis research - and it's all thanks to YOU! Let's keep making a difference – donate today: https://t.co/UthuoxZZXa

#VasculitisAwareness #VasculitisAwarenessMonth #LCTF #weareLCTF #vasculitis

[The LCT Foundation @LCTFoundation]

What are YOU up to this weekend…? 😴💤❤️🖤

[The LCT Foundation @LCTFoundation]

Fact Friday:
Do you know the signs of vasculitis? Learn about the symptoms, diagnosis, and treatments to help save lives. ❤️🖤 https://t.co/6NKMI2g0bs
#FactFriday #VasculitisAwareness #vasculitisawarenessmonth #vasculitis #weareLCTF #vasculitisuk #vasculitisscotland #LCTF

[The LCT Foundation @LCTFoundation]

Meet Tracey, a brave vasculitis warrior supported by LCTF. Read her inspiring story and see how your donation can make an impact. https://t.co/oyCotusuA1
❤️🖤
#TestimonialTuesday #VasculitisAwareness #wearelctf #lctf #vasculitis #vasculitiswarrior #vasculitisuk #vasculitissupport

[The LCT Foundation @LCTFoundation]

Share your experience: if you’ve been affected by Vasculitis, what's the one thing you wish you'd been told right at the start of your journey?

#VasculitisAwareness #LCTF #VasculitisAwarenessMonth #vasculitis #vasculitisuk #vasculitisscotland #vasculitissupport #weareLCTF

[The LCT Foundation @LCTFoundation]

Lauren Currie's tragic death at only 15 inspired the creation of LCTF. Read her story, learn about the importance of early diagnosis, and join us in making a difference. ❤️🖤 https://t.co/gSPk07GTnx

#LaurensLegacy #VasculitisAwareness #LCTF #VasculitisAwarenessMonth #vasculitis

[The LCT Foundation @LCTFoundation]

🎉 Welcome to Vasculitis Awareness Month! 🎉 Join us in raising awareness and supporting those affected by vasculitis. Your donations make a difference! ❤️🖤
Donate at: https://t.co/UthuoxZs7C
#VasculitisAwarenessMonth #LCTF #vasculitis #vasculitissupport #vasculitisuk

[ALARM, embrace risk @ALARMrisk]

We welcome Karen Locke as the new President of ALARM in July at the 2023 ALARM National Conference. Karen has chosen to support the @LCTFoundation, which is close to her heart. Read more.
https://t.co/loruranrHM
https://t.co/D3HiCqeAnf

[The LCT Foundation @LCTFoundation]

Today's #RareDiseaseDay. A day to recognise challenges faced by people with a rare disease. Like vasculitis. They're up against lack of knowledge, delayed diagnosis & inequalities in care & support. That’s why we do what we do.

Please help by donating: https://t.co/UthuoxZs7C

[The LCT Foundation @LCTFoundation]

Getting your head round a diagnosis of vasculitis can be hard. On our website we’ve got stories written by people who have vasculitis explaining what it means for them. Reading them can help.

See https://t.co/fOgh3oGfhO

#lctf #vasculitis #vasculitisuk #vasculitisstories

[The LCT Foundation @LCTFoundation]

This is Lizzie. Our counsellor. She’s great & has been working with us for years – helping people with vasculitis. Mental health is important for everyone, but especially if you have a chronic illness. Like vasculitis.

See more about our counselling: https://t.co/C3UqCEJqJS

[The LCT Foundation @LCTFoundation]

Live in the UK? Have vasculitis? We can help. We provide information & advice, and offer both practical and emotional support. Including support groups, online groups, counselling & courses.
Find out how LCTF can help you: https://t.co/AuqLv64T6n

#vasculitis #vasculitisuk #lctf