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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

  • To Hop-on or Hop-off is the question?
    Mr U 17 hours ago
  • Living with Desdemona
    Desdemona 1 day 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 1 day ago
  • Benign Thymoma
    Jenz 2 days ago
  • One Step At A Time
    Phild26 4 days ago
  • Today my coffee tastes like Christmas in Costa Rica
    Beesuit 9 days ago
  • A trip with triple negative breast cancer
    Coddfish 9 days ago
  • Slightly Inconvenienced by Prostate Cancer
    Lemsip 13 days ago
  • Eunice77
    Eunice77 14 days ago
  • Prostate Cancer Recurrence - Triple Therapy
    excavator 18 days ago

Latest blog posts

  • Mell and Homer is going down!
    Key CT Scan tomorrow after 6 weeks on Trial!

    Well it's my 6 week check up tomorrow and the first view of a comparison scan that will show that we have shrunk these bastards down.  I'm feeling like I have a lot more energy and have just come off all my pain relief which must be showing that we're winning.

    Had a great family gathering at Norfolk at the weekend and it was wonderful to have so much support and encouragement.

    I'll let you know the full outcome of tomorrow's visit!  Keep fighting.....xx

    Former Member over 16 years ago
  • Let me be scared
    10 months from diagnosis and secondary tumour now removed.

    Well finally I have had surgery to remove the tumour in my liver and I am now at home recovering. It was all so much easier than my big op in March as I was lucky enough to have laparoscopic surgery and even though the op lasted just under 5 hours I feel I am improving day by day instead of week by week!

    What I am finding hard is getting my mind set to wait again - 6 weeks for follow up  with consultant and then I don't know how long till chemo starts. Even after 10 months of this drawn out treatment...

    aa22080868684372beb541e7268da1b9 over 16 years ago
  • I never expected that
    Treatment finally started - hurray!

    More or less two months after the initial diagnosis, I have today started the first phase of treatment: chemoradiation to shrink the tumour. My ECG was 'better' today and although neutrophil count a little lower than they would normally accept, I took my first Capecitibine this evening. No nausea yet, but this could be a cumulative thing.

    I was in Northampton for two hours this afternoon with the repeat ECG followed by first radiotherapy. B was with me which was welcome because there was...

    Former Member over 16 years ago
  • greybadger's blog
    our ruby anniversary.

    After the year I've had I was never sure I would reach our wedding anniversary - but I did, so had to celebrate with the family.  As they all live 100 miles away from us we decided the easiest thing to do was go to them, so Thursday we packed up the motorhome and took off to a rally at Abingdon, a site on the cricket field just by the river  Mick took the van and I drover the car (and suddenly realized after a little way that the furthest I had driven myself over the last 2 yeasr was about 10 miles...

    Former Member over 16 years ago
  • zoelaw's blog
    CDH1 (E-cadherin) anyone??

    Hi, just posting this on the off-chance that one of you may have come across this genetic mutation.  There's apparently only around 100 families worldwide with this but Im hoping just one of them comes on here. Just had Joe's DNA results back and been told this is the devil responsible.  I'd really like to speak with anyone that has this mutation and is having screening or has had a prophylactic gastrectomy - got a lot of very stressed relatives right now and could use all the help and advice...

    Former Member over 16 years ago
  • My journey with my Dad
    Begninning to feel it now

    It's been 7 weeks now since losing my Dad to this awful illness.  How I wish that he was still here with us but without the illness. 

    I'm normally quite a strong individual that can take issues head on and deal with them, but this time it seems like I've been caught out....

    I couldn't sleep lastnight, worst night in all, I must have fallen asleep about 5am ish.  When i got out of bed late morning I've just been feeling 'empty' inside, lost, and a whole lot of other feelings I can...

    Former Member over 16 years ago
  • sarahjc
    Third time unlucky?

    Hi

    I just need to write something to get it off my chest.  I am at work and cannoit concentrate.

    Twelve years ago I had ovarian cancer and am fine.  Five years ago I had thyroid cancer and again an fine.  Several weeks ago I experienced some changes in bowel habit, only for a week but long enough to make me think something was not quite right.  To cut a long story short, two weeks ago I had a rigid sigmoidoscopy and because the registrar could not see enough (apparently the suppository had not worked...

    Former Member over 16 years ago
  • Jim's Blog
    I never new Limbo would be so sticky

    Yes, wading through Limbo is truly energy-sapping, bit like being up to your shins in Grimpen Mire. I know there are people on this site who have spent much longer in Limbo than me, and my admiration knows no bounds. Keep wading folks! 

    Anyway, I spoke to Michelle, the surgeon's secretary again this a.m., and put the screws on a bit more than usual. (I am polite, but can be stern ). Anyway she is a lovely person, and said she was "more than certain" (I had to laugh) that I would be listed for Aug...

    Former Member over 16 years ago
  • jenni b
    Time to remember x

    Where do i start, im writing this as it helps to write things down ,

    I think half my trouble is ,when friends and family say are you ok ,i reply of course i am ,yet my heart will be breaking ,they dont understand so whats the point in telling them , if honest i cant even remember the last time my family asked me , but on here i can be honest at least as i know people will understand and it does make such a differance ,i dont feel so alone ,

    I want to just say thanx to my lovely friends on chat...

    Former Member over 16 years ago
  • My blog
    Unsure of what to do

    I am not sure if this will help me by writing this down on here but here goes :-).

    I moved in to my new house in June this year, two days later I found a lump after being in the shower. This lump was in my right testicle. I was quite shocked and scared as it was quite large and I was amazed that I hadnt found it earlier. I waited a week before going to the doctor - mainly because my work dont like it if you take time off to go to the doctor!

    I went that week and saw two doctors who examined me...

    Former Member over 16 years ago
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