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Research brings hope, but access to research opportunities remains a challenge for people living with PSC. Hear from Kerrie, President of PSC Support Australia, who highlights the challenges of securing research funding in an extremely competitive environment and the lack of clinical trial opportunities currently available to PSC patients in Australia. 💬 Her message reminds us that advancing PSC research requires sustained investment, international collaboration and equitable access to clinical trials. Every patient, regardless of where they live, deserves the opportunity to benefit from scientific progress. 🌍 Different countries, shared challenges, one global voice calling for more research and better treatment options for PSC. #PSCGlobalDay2026# #PSCawareness# #PSCResearch# #ClinicalTrials# #PatientAdvocacy# #ELPA#
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Different countries. Different journeys. One global voice for PSC.🌍 What does it really mean to live with Primary Sclerosing Cholangitis (PSC)? Behind every diagnosis is a person navigating uncertainty, making difficult decisions, adapting to everyday challenges and hoping for a better future. 🌍 This #PSCGlobalDay2026#, we are putting patients and their lived experiences at the heart of the conversation. 🎥 Over the coming days, hear directly from patients, families and caregivers around the world as they share their personal journeys — from diagnosis and daily life to transplantation, emotional wellbeing, treatment challenges and hopes for the future. 💬 Because patients are more than their diagnosis. Their experiences matter, their needs deserve to be understood, and their voices must be heard. Join us as we bring these voices together, raise awareness and remind the world that no one should face PSC alone. #PSCGlobalDay2026# #PSCawareness# #PatientVoices# #LivingWithPSC# #PatientCentredCare# #GlobalPSCCommunity# #ELPA# #PSCaware#
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Understanding PSC: the why, the how and what comes next. Hear from Jean-Philippe from @PSCPartnersSkeeingACureCanada , who highlights the importance of helping people understand their diagnosis, what is known about the disease, how to manage it in the long term and how to navigate the challenges ahead. 💬 His message reminds us that knowledge empowers patients. Clear information, open communication and ongoing support are essential to helping people make informed decisions and live well with PSC. 🌍 Different countries, shared experiences, one global voice for PSC awareness. #PSCGlobalDay2026# #PSCawareness# #PatientEducation# #HealthLiteracy# #PatientVoices# #ELPA# European Liver Patients' Association
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The power of community: no one should face PSC alone. Hear from Sarah from PSC Partners Seeking a Cure Canada, who highlights the importance of finding connection, understanding and support within the PSC community — especially for younger patients navigating life with a rare chronic disease. 💬 Her message reminds us that connecting with others who share similar experiences can make a real difference. A strong community provides not only information and support, but also a sense of belonging, encouragement and hope for the future. 🌍 Different countries, shared experiences, one global voice for PSC awareness. #PSCGlobalDay2026# #PSCawareness# #PowerOfCommunity# #YoungPatients# #PatientVoices# #ELPA# European Liver Patients' Association
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Living with PSC is about more than a diagnosis — it's about being seen, heard and understood as a whole person. Hear from Mark from PSC Support , who highlights the importance of recognising the symptom burden of PSC and understanding how the disease affects each individual's daily life, wellbeing and quality of life. 💬 His message reminds us that patient-centred care means looking beyond clinical results, listening to lived experiences and recognising the full impact of the disease on the person behind the diagnosis. 🌍 Different countries, shared experiences, one global voice for PSC awareness. #PSCGlobalDay2026# #PSCawareness# #SymptomBurden# #PatientVoices# #PatientCentredCare# #ELPA# @AircsOdv
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Different countries. Different journeys. One global voice for PSC.🌍 What does it really mean to live with Primary Sclerosing Cholangitis (PSC)? Behind every diagnosis is a person navigating uncertainty, making difficult decisions, adapting to everyday challenges and hoping for a better future. 🌍 This #PSCGlobalDay2026#, we are putting patients and their lived experiences at the heart of the conversation. 🎥 Over the coming days, hear directly from patients, families and caregivers around the world as they share their personal journeys — from diagnosis and daily life to transplantation, emotional wellbeing, treatment challenges and hopes for the future. 💬 Because patients are more than their diagnosis. Their experiences matter, their needs deserve to be understood, and their voices must be heard. Join us as we bring these voices together, raise awareness and remind the world that no one should face PSC alone. #PSCGlobalDay2026# #PSCawareness# #PatientVoices# #LivingWithPSC# #PatientCentredCare# #GlobalPSCCommunity# #ELPA# #PSCaware#
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