Your journey with WM
Whether you’ve just been diagnosed, have been on active monitoring for a while or have just been told you need some treatment, we’re here to help. Your journey with Waldenstrom's macroglobulinaemia will be entirely personal to you, but we’ve tried to make this section as easy to navigate as possible so you can jump straight in and find the information you need, depending on where on your journey you are.
If you’ve just been diagnosed, or your clinician has mentioned WM and you’re looking for information, this is the section for you. You can find out everything you need to know about WM (without overloading yourself). We also have a Newly Diagnosed Support Group to offer support at the beginning of your WM journey.
Whilst treatments can lessen and even eliminate the symptoms of Waldenstrom's macroglobulinaemia for many years, unfortunately there is no cure and you’ll still be regularly monitored. Relapse can be detected before you may even feel unwell, so it’s important to attend your appointments regularly.
Living well with WM
Like any diagnosis, being told you are living with a rare cancer can be a shock. We’re here to support you every step of the way – and it’s important to learn to live well with Waldenstrom's macroglobulinaemia. We hope these pages give you a little insight into just how you can lead a healthy and active life with your new diagnosis.
We're here for you
Our Support Line will be open on Monday 9am-2pm and Thursday 1pm – 5pm – the number is 0300 373 8500. If you require support outside of those times, please email email@example.com we aim to respond to all enquiries within 48 hours.