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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
        • 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
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        • IMI
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        • Myeloma Access Atlas
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Solène Clavreul Head of Medical Education and Scientific Engagement at Myeloma Patients Europe MPE

SOLÈNE CLAVREUL

Solène is Head of Medical Education and Scientific Engagement. She joined the team in January 2021.

Solène holds a PhD in Neuroscience and a Master of Biology and Physiology from Sorbonne University (Paris). She studied brain development during her PhD and then worked on brain cellular diversity as a researcher at the Helmholtz Zentrum München (Germany). Early involved in education, she has been leading holiday camps for children for many years and worked in a science museum during her studies to promote science, design exhibitions and lead workshops.

Interested in science policy and particularly in the health field, she trained herself in European policy implementation, clinical data management and industrial pharma management before joining MPE.
Solène comes from France and currently lives and works in Munich, Germany. She speaks French, English and German.

Recent Posts

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Join our webinar “The generics market in Europe and implications for cancer treatment and care”

5 March 2026

Myeloma Patients Europe (MPE) will hold a webinar on the generics market in Europe and implications for cancer treatment and care on Monday 30th March from 17:00 – 18:30 CET.…

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Highlights from the Myeloma Cure Summit

25 February 2026

Myeloma has always been an incurable cancer which is becoming increasingly chronic with treatment advances and access. Whilst the community remains cautious talking about myeloma as a curable cancer there…

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#FacesOfMyeloma: Zvika’s story of living well with myeloma

24 February 2026

  Zvika’s journey with myeloma began sixteen years ago with monoclonal gammopathy of undetermined significance (MGUS). Over time, it progressed to smouldering myeloma, and eventually to myeloma. He’s experienced a…

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#FacesOfMyeloma: Kayleigh’s story of living well with myeloma, as a carer

24 February 2026

  When Kayleigh’s husband was diagnosed with myeloma in October 2020, everything changed overnight. The couple are from Basingstoke, UK, about an hour from London. They both worked together in…

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#FacesOfMyeloma: Maria’s story of living well with myeloma

24 February 2026

Maria is Greek-Australian and moved from Sydney to London with her adult daughter. A former research centre director, she had always lived an active, independent life.  Three years ago, at…

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#FacesOfMyeloma: Sandra’s story of living well with myeloma

24 February 2026

Sandra, 50, lives in Belgrade, Serbia. She’s a mother to two teenagers and worked as an interpreter until recently. “I worked long hours,” she recalls. “Sometimes ten, twelve hours on…

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      • Scholarship 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
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      • Patient Evidence
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