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We understand that discussing Wills can feel daunting, which is why we’ve partnered with the National Free Wills Network to offer a free, easy-to-use service to help the PSC community gain peace of mind with confidence. Order your free wills pack today: www.pscsupport.org.uk/wills/ #LetsBeatPSC

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It’s been a month since #RareDiseaseDay, and while the hashtags might have slowed down, our community never does! Huge thank you to Jenny, Sophie and their entire community for raising awareness of PSC and vital funds for the PSC community.
#PSCSupport #LetsBeatPSC #RareDiseaseAwareness

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There are currently 5 PSC trials/studies recruiting. Could you be a match?

Claire has taken part in 8 trials to help find a cure. Read why she does it: pscsupport.org.uk/psc-and-me/c...

Have you taken part in a trial? Get in touch to share your experience. hello@pscsupport.org.uk #LetsBeatPSC

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The journey to a PSC diagnosis is rarely a straight line.
There's no single diagnostic blood test for PSC. Doctors need to piece together info from your medical history, blood tests, symptoms, colonoscopy and scans to make a diagnosis. ℹ️ buff.ly/6dzfdk6
#LetsBeatPSC

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Huge shout-out to Bill and the Plymouth Life Centre Indoor Bowls Club for their charity bowls day raising £1,700 for @PSCSupportUK, helping us provide a lifeline to patients and families navigating the challenges of PSC. Feeling inspired?
➡️ pscsupport.org.uk/fundraise/ #LetsBeatPSC

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because 4 slides just weren't enough 😊 #ThankyouThursday #LetsBeatPSC
See how you can get involved: buff.ly/cpcufF5 (2 of 2)

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Meet Becki: Healthcare strategist, MSc student, and PSC mum. She joins us as Research Project Lead Volunteer, bringing her professional expertise and lived experience of her daughter’s transplant journey to the heart of what we do. (1 of 2)
#LetsBeatPSC #RareDisease #PatientVoice

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What are the top 10 issues facing the PSC community? You tell us!
We’re running a quick survey to find out what matters most to those affected by PSC. It's open to anyone affected by PSC - patients, family, & friends.
➡️ buff.ly/9ktsU3N
#LetsBeatPSC

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To the mums navigating PSC themselves, the mothers supporting a loved one, and those remembering the mums they have lost... we see you, we hear you and we will not stop until we find the treatments and cure you deserve.
#MothersDay #LetsBeatPSC #RareDiseaseMums

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Dylan Carter takes on Bath Half Marathon 2026 On the 15th of March 2026, I am running the Bath Half Marathon for PSC Support. In the Spring of 2021, my eldest brother, Alex, was diagnosed with PSC (Primary Sclerosing Cholangitis), which is a rare

Join us in wishing Dylan the very best of luck this Sunday as he takes on the Bath Half Marathon to support his brother Alex, who was diagnosed with PSC in 2021.
pscsupport.enthuse.com/pf/dylan-car...

#LetsBeatPSC #BathHalf #PSCSupport #FundraisingHero #GoodLuckDylan

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Two Friday the 13ths in two months?! 😮 Statistically rare, just like PSC. But while the calendar relies on math, we rely on research. Luck won’t find a cure, science will.
Don't leave it to chance. Get involved: buff.ly/cpcufF5
#LetsBeatPSC #PSCResearch

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We’re recruiting new Trustees for the PSC Support board:
💰 Finance Trustee
🌟 Young Trustee
🤝 General Trustee
We welcome applications from all backgrounds & ages. Could you help shape the future of PSC care? Apply by 31 March: buff.ly/v7OFVW5
Please share #LetsBeatPSC

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What does a ‘PSC flare’ feel like for you? ✍️

Researchers need to understand the symptoms of acute cholangitis to develop better treatments. If you’ve experienced an attack please take 15 mins to help: ec.europa.eu/eusurvey/run...

Available in 11 languages. #LetsBeatPSC #PSCResearch

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Happy #InternationalWomensDay! Today we celebrate the women advancing PSC research and care. From clinicians and researchers to our brilliant volunteers and advocates. Their dedication offers hope to the PSC community.
#IWD2026 #LetsBeatPSC #WomenInScience #ThankYou

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Lucy is taking on @SemideParis this Sunday! 🇫🇷👟10 years after her first half, she’s feeling a bit "creaky" but motivated to run for a special young man & the whole #PSCcommunity. Wish her luck as she tackles 13.1 miles for a cure!
➡️ buff.ly/pvgpx1X #LetsBeatPSC

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Missed our live Ask the Expert on the Asp-PSC Clinical Trial? Don't worry, you can now watch (or re-watch) this expert break down one of the largest-ever #PSC trials.
➡️ buff.ly/uh5PrON
#LetsBeatPSC #ClinicalTrials #AspPSC #AskAboutAsp

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Our new multinational survey in @HepatologyComm highlights the severe impact of PSC itch (pruritus) 😫

Key findings:
✅ Itch significantly reduces quality of life & sleep.
⚠️ 75% of those on multiple meds get little or no relief.

We NEED better treatments NOW. buff.ly/XQ1FlTA #LetsBeatPSC #PSCItch

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Did you know there's such a thing as #WorldComplimentDay? A simple, genuine compliment can brighten someone’s spirit.
💬 Share your favourite compliment (one you’ve given or received) in the comments.
🏷️ Tag someone below who deserves a boost today!
#RareDisease #LetsBeatPSC

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15 years into her journey, Parastoo shares what it means to be a mother, professional, and #AutoimmuneWarrior while living with a #RareDisease.

Read her story for #RareDiseaseDay: pscsupport.org.uk/parastoo/

#PSCSupport #ChronicIllness #PSC #LetsBeatPSC #LiverDisease

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Rare is many. Rare is strong. Rare is Lindsay.
Diagnosed with PSC aged 24, Lindsay has navigated 2 pregnancies, 2 countries, and 2 biliary drains. This #RareDiseaseDay, we’re sharing her story in her own words.
➡️ buff.ly/MnkobfV
#LetsBeatPSC #RareDiseaseDay2026 #PSC

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This #HelplinesAwarenessDay, we’re celebrating the people behind crucial support services, like our Helpline Nurse, Loren. Whether you have a question, are worried about something, or just need someone to listen, we’re here for you.
➡️ pscsupport.org.uk/helpline/
#LetsBeatPSC

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A liver transplant is a gift of life, but it is not a cure.

1 in 3 people with PSC need a transplant within 10 yrs. Even after surgery, patients face lifelong medication, rejection risks, and the potential for PSC to recur.

Help us find a cure: pscsupport.org.uk/donate/
#LetsBeatPSC #PSCResearch

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Let’s talk Vitamin D! ☀️ The UK’s "sunshine vitamin" is hard to come by in February. Most people are advised to supplement for bone and muscle health. For those with PSC, malabsorption is a common hurdle in PSC.
How are you getting your Vitamin D? Daily spray, tablet, or a sunny window? #LetsBeatPSC

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Can aspirin lower the risk of cancer in PSC? 💊
Join our FREE Ask the Expert live webinar to explore the #AspPSCTrial.
✅ The Science
✅ The Participant Journey
✅ Live Q&A with experts
Open to anyone affected by PSC. Register 👉 buff.ly/mVHkRzm
#LetsBeatPSC #AskAboutAsp

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Flat, fluffy, or full of fruit...pancakes are as varied as PSC. 🥞
Whilst we need more research into PSC and diet, many of you have told us that dietary changes help you feel & function better. Have changes to your diet made a difference? pscsupport.org.uk/psc-eating-f...
#PancakeDay #LetsBeatPSC

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Last week in Prague, Martine Walmsley and Dr. Nora Cazzagon presented the ERN RARE-LIVER PSC Working Group’s achievements and 2026 strategy.
Read the full report:
🔗 pscsupport.org.uk/progress-and...
#PSCSupport #ERNRareLiver #RareDisease #PatientAdvocacy #LetsBeatPSC

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Roses are red, violets are blue..we’re funding research to find a cure for you. 🌹🔬
Okay, we’re definitely better at science than poetry. This Valentine's Day consider showing your love by sharing your story, or making a donation. pscsupport.org.uk/donate/ #RareDisease #LetsBeatPSC

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At #PSCSupport, we leave the superstitions at the door, focusing on:
🟣 Fact-checked, evidence-based information
🟢 Quality-assured resources you can trust
🟠 The latest clinical research and medical guidance
ℹ️ buff.ly/Yn1QQhE #FridayThe13th #LiverDisease #LetsBeatPSC

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If you could go back to the day you were diagnosed with #PSC, what is ONE thing you wish someone had told you? We often here that the biggest game-changers are 1️⃣ finding a PSC specialist 2️⃣ connecting with the PSC community.
Quote tweet or reply with your thoughts #LetsBeatPSC

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PSC affects everyone differently and treatment should reflect that. Seeing talk about Urso (UDCA) in the community? The decision to take it rests with you and your medical team. We’re here to help with fact-checked, quality-assured info. 👉 pscsupport.org.uk/treatments-f...
#LetsBeatPSC

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