
Our strategy
Discover Myeloma UK’s 2024-2028 strategy
Together, with our dedicated community, we have transformed treatment and care for people affected by myeloma in the last 25 years.
But when you’re living with myeloma, every day counts.
We have more to do to find a cure and make sure that everyone can have the best life possible, today and tomorrow.
Our vision is the same as it has always been – a world where myeloma doesn’t exist.
But we need to go further, faster because people affected by myeloma can’t wait.
Three core areas will now define our work:

“Through my work as a Myeloma UK peer buddy, I have spoken with many fellow patients. Everyone has a different story about how their diagnosis came about – even those who are identified early are often spotted by chance, maybe through a blood test for a completely different issue.
But, ironically, myeloma and its precursor stages can be identified with a very simple blood test. The additional complications and difficulties faced by those patients who are diagnosed late are distressing and avoidable, and I believe Myeloma UK can make a big difference to life quality and expectancy through our focus on awareness and more timely diagnosis.”
Scott was diagnosed with myeloma in 2018.
He now volunteers with Myeloma UK as a peer buddy and patient advocate.

“Continued research into new treatments is crucial because it’s the only path towards discovering a cure. Organisations like Myeloma UK play a vital role in this quest by relentlessly seeking new treatments and bringing us closer to curing multiple myeloma – a journey I’ve seen progress significantly over the last 12 years.
Clinical trials hold immense significance for me because I firmly believe that, without my participation in the trials I’ve undergone, I might not be here today. I have exhausted standard treatment options. These trials offer not just extended survival chances and hope for others, but also pave the way towards discovering a cure for multiple myeloma.”
Antoinette was diagnosed with myeloma in 2012

“I was told myeloma was incurable but treatable, and that with treatment you can expect a life expectancy of seven years. That was in 2006. Now, with incredible advances in pioneering treatment, life expectancy has increased dramatically. I am one very lucky person – I have a loving wife, children, grandchildren and great grandchildren. Life is wonderful.
Myeloma UK increasing its focus on living well with myeloma means that thousands of patients never need to feel alone and can share their feelings and concerns with a team of trained professionals. Family members will benefit too, because it’s sometimes worse for the family seeing their loved one go through the journey of treatment.”
Andrew was diagnosed with myeloma in 2007

Download our 2024-2028 strategy
Download and read our full 2024-2028 strategy and find out more about how it was developed and what the myeloma community told us mattered most to them.

Change lives today
It’s only with the help of generous supporters that we can provide the best possible support and fund research that improves diagnoses, treatment and care.
Everything we do is funded by voluntary contributions, fundraising and gifts left in wills







