Get the information and support you need, when you need it.
We understand you need more than medical treatment and care. You need information and support too. We’ve created a range of programmes and services designed specifically with myeloma patients, and their friends and family, in mind. We are here to help you cope with everything a myeloma diagnosis brings.
Speak to our team of specialists - on 0800 980 3332 - for information about myeloma, practical advice and a little extra support.
Prefer typing to talking about myeloma? Our team of specialists are also contactable by email.
Meet other patients, carers and family members at your local Myeloma Support Group for emotional support, friendship and the chance to share information and experiences.
We’re here to help you with the reality of living with myeloma, from talking to your friends and family, to looking after your physical and mental health.
Talk to someone who’s been through what you’re going through. The PEER (Patient Experience Exchange Resource) Network is a group of patients, carers and family members who are willing to talk, share experiences and offer support to people affected by myeloma via a one-to-one phone call. Call our Myeloma Information Specialists to be connected with a member of the PEER Network.
Join us in Southampton for a packed day of insights, information and meeting others affected by myeloma.
Choose from a morning session on an introduction to myeloma for newly diagnosed patients, or treatment strategies for relapsing and refractory myeloma, followed by a session on dealing with complications and common side effects of treatment. In the afternoon our breakout sessions will include living well with myeloma, ask the expert panel discussion and carer and family perspectives.
Book your place by downloading our booking form or completing the registration form below.
Caring for someone can take many forms, even if you are not the primary carer, you may still help in some way. It’s important to look after yourself as a carer.
Help & Support: Speak to one of our trained and qualifed Myeloma Information Specialists or email us
