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logo MPE
  • Myeloma and AL Amyloidosis
    • About myeloma
    • About AL amyloidosis
  • What we do
      • Member and patient community programmes
        • Myeloma Awareness Month
        • MPE Masterclass
        • Scholarship programme
        • Care Connect Programme
        • Myeloma CABs
        • MPE Myeloma and AL amyloidosis Community Taskforce
        • Advocate Development Programme
        • European Young Myeloma Patients Group
        • Reasonable Agreements between Patient Advocates and Pharmaceutical Companies (RAPP)
      • Research
        • Patient Evidence
        • Horizon Europe
        • IMI
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        • Myeloma Access Atlas
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        • Myeloma and AL amyloidosis Clinical Trial Navigator
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      • Myeloma CABs
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      • European Young Myeloma Patients Group
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Charlotte Haynes

CHARLOTTE HAYNES

Charlotte joined MPE as Scientific and Patient Information Manager in January 2026.

Charlotte holds a PhD and BSc in Experimental Psychology from the University of Sussex, and a Postgraduate Certificate in Public Health from the University of Manchester. She has over 20 years of experience in healthcare research, evidence synthesis, and scientific communication.

Before joining MPE, Charlotte worked for 13 years at the National Institute for Health and Care Excellence (NICE), a public body that develops independent, evidence-based guidance to improve health and social care in England. She also worked for eight years as Research and Projects Lead at a UK NHS foundation trust hospital. In these roles, she worked at the interface of science, policy, and communication, ensuring that evidence was accurately interpreted and translated into clear, practical recommendations for health and social care professionals, commissioners and managers, patients, service users and carers.

Charlotte has a strong commitment to patient-centred communication and to ensuring that information is inclusive and accessible for all patient populations. She currently lives in the North West of England. She speaks English fluently and French at an upper-intermediate level.

 

Recent Posts

MPE team at IMS

Highlights from the International Myeloma Society (IMS) annual meeting

30 September 2026

From September 23-26, Myeloma Patients Europe (MPE) attended the 23rd International Myeloma Society (IMS) Annual Meeting in Glasgow, Scotland. The IMS Annual Meeting is one of the most important international…

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EMAs CHMP positive opinion image

EMA committee recommends melflufen label expansion to third-line myeloma treatment

22 September 2026

On September 17, 2026, the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) recommended extending the approved use of melphalan flufenamide (melflufen, Pepaxti®) to third-line myeloma…

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Faith Davies

Dr. Faith Davies interview on IMS 2026

17 September 2026

As the International Myeloma Society (IMS) Annual Meeting is taking place this week, we caught up with myeloma expert Dr. Faith Davies, from NYU Langone, about her expectations for the…

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Your views and experiences on myeloma, intimacy and sexual wellbeing

17 September 2026

We want to hear from people living with myeloma and their partners about how myeloma or its treatments have affected intimacy or sexual wellbeing and what information would be useful…

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Myeloma melodies is back in Paris

7 September 2026

Myeloma Melodies, an awareness concert for myeloma, returns to Paris on 24 September for an evening of singing, music and fun. The concert is organised by Sarah Tullamore, a professional…

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Preview to members September activities across Europe

2 September 2026

September is shaping up to be an extraordinary month for myeloma awareness and advocacy across MPE’s member network. From Portugal to Serbia, from Lithuania to Slovenia, our members are planning…

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      • Myeloma Awareness Month
      • MPE Masterclass
      • Scholarship programme
      • Care Connect Programme
      • Myeloma CABs
      • MPE Myeloma and AL amyloidosis Community Taskforce
      • Advocate Development Programme
      • Reasonable Agreements between Patient Advocates and Pharmaceutical Companies (RAPP)
      • European Young Myeloma Patients Group
    • Research
      • Patient Evidence
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      • IMI
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      • Myeloma Access Atlas
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