First-time poster here. My mum has been diagnosed with Pseudomyxoma Peritonei and I am struggling to wrap my head around it as a whole. She has brain damage and is disabled (the bd covers memory loss, tiredness and her physical mobility isn't strong, needs a stick etc), so when in hospital, I act as her first point of contact and support along with 2 other family members.
I have to explain any diagnosis or information in layman's terms to my mum so she is able to digest it and I don't even know where to begin with understanding and explaining what this is to her.... Has anyone on here been through this or supported someone who has? If so, any advice or guidance on what to say or expect would be greatly appreciated!
