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CMML - A rare diagnosis
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261
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6466
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8 May 2026
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A 36-year-old Mum diagnosed with high risk MDS
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7
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115
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20 April 2026
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MDS Diagnosis - bone marrow failure - genetic?
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1
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85
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23 March 2026
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Awaiting or considering or had a stem cell transplant, a place to share here
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1445
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19350
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11 March 2026
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Volunteer as an Blood Cancer UK Ambassador
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0
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48
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8 January 2026
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CMML & MDS/ MPN Overlap Media Opportunity
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3
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60
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4 December 2025
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MDS to AML
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5
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351
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11 November 2025
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Ask the Nurses - Managing fatigue
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59
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2567
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16 August 2025
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Rare blood cancer diagnosis? Connect, support and share here
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15
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682
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29 June 2025
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Blood Cancer UK Support Services
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1
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2290
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22 March 2025
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MDS & MPN overlap
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7
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758
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15 December 2024
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Dad’s treatment is being withdrawn
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28
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1843
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5 September 2024
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Dad diagnosed with MDS with 12% excess blasts - scared
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4
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883
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28 June 2024
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General talk about my recent CMML diagnosis-especially advice on travel
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15
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1477
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15 May 2024
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Chronic myelomonocytic leukaemia new diagnosis
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5
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484
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3 May 2024
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What reality should I expect as my dad’s MDS declines?
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2
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853
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17 April 2024
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MDS affecting healing
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5
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393
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14 April 2024
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Friends after diagnosis
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12
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505
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10 April 2024
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Ask the nurse - Have your say
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6
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339
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18 April 2024
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Chronic Myelomonocytic Leukaemia (CMML2)
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134
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3106
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2 April 2024
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Do’s & Dont’s & tips please before & after a stem cell treatment
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9
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2325
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26 March 2024
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The MDS Delphi survey (deadline Monday 8th February)
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1
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825
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4 February 2021
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Talking to a loved one about their cancer diagnosis
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5
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1015
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30 April 2019
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