Policy and access to treatments
Giving a voice to myeloma patients is at the heart of our all of advocacy work
Myeloma patients and their carers are our top priority. We press for access to new treatments which can help patients live longer and with a better quality of life, as well as acting as advocates for patients when dealing with decision makers, such as politicians or senior figures in the NHS.
Our work has helped deliver the highest increase in survival rates of any cancer in the UK.
Here are some of the ways we make your voice heard.
Delivering access to the best treatments
We work with patients, doctors, the pharmaceutical industry, and drug approval bodies like NICE, the Scottish Medicines Consortium and the All Wales Medicines Strategy Group (AWMSG) to make sure myeloma patients receive the best possible treatments. We make sure that our submissions to drug approval bodies are evidence based by working closely with our Health Services Research Programme.
When it comes to influencing policy, we are focused on the following key areas:
- Improving diagnosis and reducing inequalities
- Access to treatment
- The pricing of medicines
- NHS cancer strategies and commissioning
- The myeloma research environment
- “Real world” data from treatments and results
We produce papers and reports to help inform government strategy.
Using our voice
We take a collaborative approach and work with the myeloma community to bring about positive change. We seek out opportunities for myeloma patients to have their voices heard – from clinical trial design, or appearing in the media, to speaking directly to decision makers to deliver change. We also work in partnership with a vast range of other cancer charities as members of campaigning coalitions.
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