Welcome to the Myeloma UK Blog

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Patient Advocacy
Amy Capper
17 September 2021

What the Government’s new Health and Care Bill means for myeloma patients

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Patient Advocacy
Laura Kerby
06 July 2021

Mask removal exposes the need for greater support for myeloma patients

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Patient Advocacy
Laura Kerby
31 March 2021

Making your voices count: navigating the COVID-19 vaccine programme

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Patient Advocacy
Shelagh McKinlay
29 January 2021

Lenalidomide maintenance – the journey to a “yes”

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Patient Advocacy
Shelagh McKinlay
21 December 2020

What do the Cancer Recovery Plans mean for myeloma?

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Patient Advocacy
Laura Kerby
30 November 2020

Making your voice count: Myeloma moved up priority list for COVID-19 vaccine

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Patient Advocacy
Shelagh McKinlay
20 November 2020

Behind the Headlines – Vaccine Priorities?

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Patient Advocacy
Laura Kerby
29 October 2020

Myeloma UK COVID-19 Patient Survey 2: Our call to action

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Patient Advocacy
Daniel Cairns
08 September 2020

What happens after a draft ‘no’ from NICE?

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Patient Advocacy
Daniel Cairns
01 September 2020

Patients are positive about the benefits of lenalidomide maintenance

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Patient Advocacy
Shelagh McKinlay
23 June 2020

We are one myeloma community: ensuring myeloma patients are not forgotten