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  • About Us
    • Our Mission
    • News
    • Who is who at MPN Voice – meet the teams
    • Videos
      • MPN Voice YouTube videos
      • Living with MPNs Day Saturday 16th November 2024 in London
      • Living with MPNs Day Saturday 18th November 2023 in London
      • All Other Videos
    • Newsletters
    • How your money helps
    • Epidemiology Study
    • Young People and MPNs Blog
    • MPN Voice Vlogcasts – In Conversation With …..
  • About MPNs
    • About MPNs
      • Diagnosed with MPN?
      • What do blood counts mean?
      • What are MPNs?
      • What causes MPNs?
      • Essential thrombocythaemia (ET)
      • Myelofibrosis (MF)
      • Polycythaemia vera
      • A-Z of terminology
    • Treatments
      • General Info
      • Treatment leaflets
      • Anagrelide
      • Integrative treatment
      • Aspirin
      • Cytarabine
      • Hydroxycarbamide
      • Inrebic
      • Interferon alpha
      • Melphalan, busulfan and P32
      • Ruxolitinib
      • Thalidomide
      • Venesection (phlebotomy)
      • Bone marrow transplant
      • Additional treatments
    • Trials and Research
      • Trials and Research
      • Going on a Trial
      • Current UK MPN trials
      • Guy’s Hospital, London, MPN Clinical Trials Portfolio
      • MPN Voice supported trials
      • Mosaicc
      • Vorinostat Phase II Study Results
      • CMML (Chronic Myelomonocytic Leukaemia) MONOCLE Study
    • For Health care professionals
  • Living With MPNs
    • Real Stories
    • I Am…
    • Treatment decisions
    • Talking with your doctor
    • Everyday Challenges
      • Everyday Challenges
      • Contraceptives and HRT
      • Deep Vein Thrombosis
      • Fighting fatigue
      • Renewing Intimacy
      • Coping with side effects
      • If you need surgery
      • Itchy skin
    • Your state of mind
      • Your state of mind
      • What you may be feeling
      • Looking well but feeling awful
      • Communicating feelings
      • Coping long-term
    • Blood Clots
      • After a blood clot
      • After a serious clot
      • End-of-life
      • Hospice care
      • Reducing pain and symptoms – palliative care
    • Ways to feel better
      • Ways to feel better
      • Complementary therapies
      • Reflexology and massage therapy
      • Relaxation podcasts for people with MPNs
      • Staying active
      • Eating well
      • Keeping track of symptoms
      • Reducing stress
      • Know the warning signs
      • Staying well
    • Pregnancy
      • MPNs in pregnancy
      • Planning before pregnancy
      • During pregnancy
      • Miscarriage
    • Practical advice
      • Practical advice
      • Cost of medications – exemption certificate
      • Employment rights
      • Travel information
      • Planning for travel
      • MPN Alert Cards
      • Living abroad
    • GSK’s MPN Time To Be Seen
  • Get Involved
    • How To Get Involved
    • Events
    • Patients forums
    • Buddy Programme
      • About the Buddy Programme
      • Join the programme
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      • HealthUnlocked
  • My MPN Voice App
    • Learn more about MY MPN VOICE APP
    • Overview of the My MPN Voice App – with Study and without Study
    • Next Steps – Stages, Sign Up & Support
    • FAQs – GSTT Study App and Wearables
  • Contact
    • Contact Us
    • Submit a story
    • Join our mailing list
  • COVID-19
    • Fast access to COVID medicines for people with blood cancer
    • 4th dose COVID vaccination for people with MPNs
      • COVID-19 Vaccine for people with MPNs
    • Coronavirus (COVID-19) Advice and Information
    • COVID-19 and Day-to-Day Life: making decisions about your risk of exposure
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Category Archives: Myelofibrosis

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  4. Category "Myelofibrosis"

Being a buddy

Buddies, Living with MPNs, MyelofibrosisBy Tim EllisMarch 10, 2016

Chris talks about being a buddy and giving support to others.

Update from The 56th American Society of Hematology (ASH) December 2014 meeting held in San Francisco – part 2

MyelofibrosisBy Tim EllisDecember 16, 2014

Video 2 – Myelofibrosis update https://youtu.be/94MrWefhAmk

Bone marrow transplant (BMT) as a treatment option for patients with Myelofibrosis (MF)

Bone marrow/stem cell transplant, Myelofibrosis, Treatment and Management of MPNsBy Tim EllisJuly 19, 2012

Dr Ruben Mesa and Dr Veena Fauble, haematologists at the Mayo Clinic discuss bone marrow transplant (BMT) as a treatment option for patients diagnosed with Myelofibrosis. https://youtu.be/DJNQOIkdYQw

What Do Patients with Myelofibrosis (MF) Need to Know?

Myelofibrosis, Treatment and Management of MPNsBy Tim EllisAugust 19, 2011

An Overview of Myelofibrosis (MF)

MyelofibrosisBy Tim EllisAugust 19, 2011

Leading MPN specialists give an overview of the symptoms patients with MF may suffer from.

What are Myeloproliferative Neoplasms (MPNs)?

Essential Thrombocythaemia, Myelofibrosis, Polycythaemia vera, What are MPNsBy Tim EllisAugust 17, 2011

Myelofibrosis, A Patient’s Story

MyelofibrosisBy Tim EllisAugust 17, 2011

Myelofibrosis, A Patient’s Story

Myelofibrosis

MyelofibrosisBy Tim EllisNovember 7, 2010

Albert talks about living with myelofibrosis (MF) and taking a JAK2 inhibitor drug currently under trial.

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