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Blogs

Create a blog

Blogging can be a great way to journal your experiences and share with others. Why not create your own cancer journey blog, or have a read of other blogs created by our members?

Unsure how to get started? Take a look at our help pages on blogs. 

Latest blog updates

  • Living with Desdemona
    Desdemona 14 hours ago
  • Community News
    This is a place where you can read about everything that's happening on Macmillan's Community. From guest stories, to sharing awareness months, here is where you'll hear about all of the latest from Macmillan's Community.
    Megan- Online Community Team 19 hours ago
  • To Hop-on or Hop-off is the question?
    Mr U 1 day ago
  • Benign Thymoma
    Jenz 1 day ago
  • One Step At A Time
    Phild26 3 days ago
  • Today my coffee tastes like Christmas in Costa Rica
    Beesuit 8 days ago
  • A trip with triple negative breast cancer
    Coddfish 8 days ago
  • Slightly Inconvenienced by Prostate Cancer
    Lemsip 12 days ago
  • Eunice77
    Eunice77 14 days ago
  • Prostate Cancer Recurrence - Triple Therapy
    excavator 17 days ago

Latest blog posts

  • Madmadge's life without John
    My first visit to John's grave

    I visited John's grave today for the first time since the funeral on Monday.  It's only been five days but most of the flowers were flattened and blemished from the rain and nibbled by slugs.  However, my simple sheaf of Arum Lilies were almost perfect and, maybe I'm being silly, but I took it as a sign that our love goes on.  We'd arranged for a simple vase to be sunk into the ground and I placed a dozen red roses in it for my darling man - I hope they stay as fresh as the lilies.

    ...
    Former Member over 15 years ago
  • captains blog stardate chemo +8days
    strange days.

     hi folks,

     I honestly haven't got a clue what i'm going on about in this one, so bare with me. well i had my chemo 8 days ago, the first 4 days i've decided to bury in the deepest darkest pit of my mind,never to be opened (yes it was that bad).

       So 2 intravenous injections followed by 21days of tablets,(to be repeated nonstop til feb 2012), and this is the strange part.

       DAY 2- no pain at all, now considering that you could set the speaking clock to within 10 seconds of me needing pain...

    Former Member over 15 years ago
  • A week in the lives of Shaz & Dave
    A week in the lives of Shaz & Dave !!!!!!!

    I just wanted to see it in writing what a "normal" week we have had, well just over a week......

    It started last Friday 2nd Sept, it was our old friends funeral.....actually a day of celebration as lots of people came, people that we have known for over 35yrs.......don't need to explain about funerals and meeting up with long lost friends. We hadn't been to a funeral since the death of Daves brother just before his diagnosis so were both a bit apprehensive, me more so as it always brings...

    Former Member over 15 years ago
  • The mysteries of Mo
    September 10th (pt 2)

    Mo had a bad day today even though she slept all night from 9.30pm-6.30pm without getting up she woke up with pain in her head,belly and legs,bless! She had her meds this morning,9 tablets all told same as every morning after a piece of toast,not a lot for brkfast. After her meds she usually has a rest for an hour or two then I help her get washed & dressed. Today though she spent the rest of the day until 2-2.30ish in bed which is unusual for her. The only reason she got up was because her son...

    Former Member over 15 years ago
  • Working?
    child-free day

    Lurched out of bed at 5.40am, managed to get one 6 yr old and two 13 yr olds out of the house by 6.40 in time to get on a bus at 6.50, all excitedly off to legoland.

    Back to bed then for me til 9.30, then lay on sofa drinking tea. Managed to get my glad rags on in time to meet my friend L for lunch... baguettes and chips yumyum! Then we drifted about the village and peered into various shops, and then I found what I have been after for weeks - a mac. LOL! I have winter coat, wool coats, cardigans...

    Former Member over 15 years ago
  • The mysteries of Mo
    September 10th 2011 (pt 1)

    Rang the St Michaels hospice helpline this morning didn'y go well.I was trying to arrange for someone to come to the bungalow & give Mo a wash,probably hasnt had a 'proper' wash in a week,she tries but its hard.Hopefully they could wash her hair also as i was worried about doing it myself because of the biopsy scarring.The person i spoke to,whether it was intentional or not,said something along the lines about the service only being available to 'end of life' patients.You have to be aware,Mo was...

    Former Member over 15 years ago
  • advice/similar experiences welcomed-kidney,brain,lung
    new to site.family member with kidney,brain,lung tumours

    New to site & looking for as much info/similar experiences/suggestions. Family member  diagnosed 6 weeks ago with grade 4 kidney cancer. He is 70, has high blood pressure (controlled by medication), a pacemaker to regulate his atrial fibrilation. Had one cancerous kidney removed 15 years ago (without complications or need of any other treatment/medication) and subsequently had yearly checks for a period of 10 years where no further sign of cancer appeared.

    However, at Easter of this year he...

    Former Member over 15 years ago
  • Working?
    YAWNING!!!!!!!!!!! And waiting nervously for LM....

    That is all I have done today. Well, not literally, otherwise I would be sat here having not got dressed or gone to work or eaten or used the loo... :) AND, I have been on tenterhooks until could get onto my laptop this evening and see what LM's results were - PHEW!! (HUGS LM TIGHTLY)

    But yes, yawning took up a large amount of my time. So, why stay in work I hear you cry? I asked myself that and the response was, they are giving you 3 days off a fortnight so TRY to go in when you can to...

    Former Member over 15 years ago
  • Daisybun
    Limbo anyone?

    I have not had a bad day. In fact i have felt quite normal at times. I am trying to stay positive.

    However, there are times in the day when I just feel alone. Even in a room full of people and family - I am in my own world - I have to deal with this and my thoughts.

    I think the gap between being told there might be a problem and when you go to see someone seems like forever. This is a kind of limbo - not that I intend on doing the limbo - I am not that flexible anymore!

    So I stay here in limbo...

    Former Member over 15 years ago
  • just so gutted !!!!
    post stem cell

    Nige been out 3 weeks now !!!  He doing really well white cell count normal platletts over a hundred !!!   :) x  Line was removed on Wednsday he said it hurt more coming out than going in but is all ok !!! 

    just waiting for the 3 month scan to see if stem cell has worked already over a month post stem cell so not much longer to wait now  :) x

    love to all

    Maxine xxxxx

    Former Member over 15 years ago
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