• Step away from Google. A PSC diagnosis is a lot to take in and it is natural to want to know more, but there’s a lot of outdated information out there. Ensure that your information source is reliable, accurate and evidence-based, and especially checked by medical experts, like the information from PSC Support.
  • There is no one size fits all for PSC - remember everyone is different - not everyone needs a transplant. In fact it’s only around half. Many people live a normal life with few or no symptoms, while others do progress to having advanced liver disease.
  • Don't bury your head in the sand and worry about things in silence. No one needs to face PSC alone - join our amazing Facebook group and come to our next PSC Information Day.
  • Live your life. PSC doesn’t need to define who you are, and we encourage everyone to live life, and not let the thought of PSC stop them. 
  • Go with the flow. Accept tougher times, listen to your body and do what is right for you. Rest when you need to. Get to know how fatigue affects you and how to manage it. Perhaps plan rest days after a busy day or activity. Know it is OK to be not OK!
  • Don’t expect your GP to know all about PSC. PSC is a rare disease. Only 7 in a million people are diagnosed with PSC per year. It’s unrealistic to expect our GPs to understand a rare and complex disease like PSC. Make sure your consultant keeps your GP in the loop about the care of your PSC, and do show them our website for links to the latest clinical care guidelines and best practice.
  • Don’t put up with itch! While there is not a cure for PSC (yet), there are treatments for symptoms such as itch. Speak to your PSC doctor about any new symptoms you experience and what medicine options you might have.
  • Know the signs of a bile duct infection so you can get medical treatment quickly. It’s very helpful to print off our bacterial cholangitis (bile duct infection) leaflet to show doctors who may not be experienced with PSC.
  • Embrace questions from others, but also accept that they won’t always understand. Your loved ones might be struggling with your diagnosis too, and that’s OK. You can use our'What is PSC?'  graphic to help explain PSC and share our information for friends and family. We've got some great tips for the people around you too!
  • Look for research and get involved! There is hope. PSC Support is working hard to support and fund PSC research to find a cure and we will not stop until we have one. 


Thanks to our PSC Support Facebook group for helping to compile these tips.

Quality information: this information has been reviewed by a panel (Q1) of patients and experts.
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