We want to help you get the most of our your clinical appointments. We’ve put together ‘checklist’ to guide your conversations with your healthcare team. This will help you feel more prepared and confident to ask the right questions about the things that matter to you. Ultimately, we hope this will ensure you get the very best care you need.
We hope the checklist will help to shape discussions so there is greater consistency in the care that’s provided ensuring a high-quality care for everyone with WM.
Created by both patients and clinicians, this checklist is designed to help you:
This checklist was developed in collaboration with both clinicians and people living with WM. We’ve also put together a helpful ‘Newly Diagnosed Booklet’ to help you get to grips with what WM is and what you can expect on your journey.
It’s a helpful read for anyone who has just been diagnosed, but also for friends and family who are also keen to understand what the condition is all abouyt.
As you start using the checklist, we’d really value your thoughts. Let us know how it’s helping, and what could make it even better — we’re always listening.