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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. 

Macmillan Information Blogs
  • Random act of kindness
    Random act of kindness
    8 months ago
  • The Changing Faces of Cancer- Scalp cooling, Hair loss and Regrowth.
    The Changing Faces of Cancer- Scalp cooling, Hair loss and Regrowth.
    over 2 years ago
  • If I could go back to the day of my cancer diagnosis
    If I could go back to the day of my cancer diagnosis
    over 2 years ago

Latest blog updates

  • 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.
    Wayne - Online Community Team 14 hours ago
  • To Hop-on or Hop-off is the question?
    Mr U 20 hours ago
  • Wittering away...
    Rowan8a3264 23 hours ago
  • "It's Only Skin Cancer"
    A cautionary tale of personal experience and common misconception
    dolphin99 1 day ago
  • Slightly Inconvenienced by Prostate Cancer
    Lemsip 3 days ago
  • Peter's Blog
    A blog about bowel cancer at a young age
    HawkeyeBrown 4 days ago
  • Living with Desdemona
    Desdemona 5 days ago
  • Kidney Not
    Mmum 6 days ago
  • Looking after Mr. B
    Miranda t 11 days ago
  • One Life Live It
    Sadly not a LandRover road trip, but my journey through breast cancer
    Irishgirl16 12 days ago

Latest blog posts

  • my big boy
    i think i might be losing the plot

    I took my girl upto school today a normal morning for me i looked across the road and i swear i saw my dad. i nearly shouted for him then a car drove past and he was away. I am missing him so much i really want him to hug me and tell everything is going to be ok. You dont relise how much you  miss something, you take for granted the stupid wee things like the hugs the laughs and the wee stares it breaks my heart  to think my dad will never make me feel safe again. sorry for being a pest again but i...

    Former Member over 15 years ago
  • How I feel
    Carrying on

    How on earth do you carry on without your soul mate, I am finding it really difficult and am really not sure what to do, i know its early days, its four weeks on Wednesday,  but i just can not imagine it will ever feel any better ever again.

    Former Member over 15 years ago
  • lisa j
    Mom's not well

    hi

    Its been a while since I blog,

    unfortunatley my mom was rushed into hosptial 10 days ago her remaining kidney wasn't working properly, at one point she had no renal function at all. Its been such a worrying time at one point I really thought she wouldn't pull through.

     She just went down ill so quickly we where even asked if we wanted her Resuscitate her, god that was such a shock, we couldn't answear because my brother was away and I didn't think it was far for us to make that d...

    Former Member over 15 years ago
  • Joycee's Blog
    Bit of a Down Day

    Felt a bit down today over my inability to eat ' normally ' - apart from my recent success in managing some bread with soup, I am still finding it quite difficult to move the food with my tongue. I realise that this may be largely due to the extensive surgery and radiation, but after almost three years I was hoping to be way further along. Maybe I am expecting too much - or do I have to come to terms with the fact that I may never eat ' normal ' food again and be grateful that at least I am...

    Former Member over 15 years ago
  • Tale of A Very Young Widow
    Last Words

    http://veryyoungwidow.blogspot.com/2011/06/last-words.html

    Last words are hugely important I think. Its nice to know that he was thinking about me in his last few hours, however hard that is to comprehend. 

    Keeping it short because I have to focus on my revision for my last exam on Tuesday!

     

    Former Member over 15 years ago
  • David's cancer story
    Day trip to Legoland

    I increased David's steriods upto 6mg, he stayed awake the whole day and we had a wonderful time.

    I borrowed my disabled sisters wheelchair so David didn't have to walk, though he still found it tiring watching the children running around.

    My other sister and her husband came with us, and she drove which was great as I didn't have to concentrate on driving and wasn't so tired and could relax and enjoy the day.

    I managed to get David on 3 rides, the Viking rapids where we get drenched...

    Former Member over 15 years ago
  • Joan2
    can't understand

    i haven't been on site for a few days but when i signed on a few minutes ago I seem to have joined the melanina group and the testicular cancer groups.  I have no reason or memory of joining these groups and was just wondering if this had happened to anyone else.

    Anyway best wishes to you all

    Take care

    Joan xx

    Former Member over 15 years ago
  • Juleshoneybunny
    Blue Day

    When i write here i want to be upbeat positive and maybe a little lighthearted.  As Sorry guys am on a downer today so i just want to rabble on for a bit to get it off my chest, I hope you dont mind....................

    Still sore from the biopsy sick of popping pain killers and I yearn for a long hot shower!  Other than that and the fact its dull outside and the family are in their beds for sat morn lie in what should I be moaning about.

    My man Gerald is busy in the garden bless him, he wants to...

    Former Member over 15 years ago
  • CarolD's blog
    Scan Results - 2nd June 2011

    What a way to celebrate the beginning of Summer!  After a long 7 day wait, received my scan results yesterday and its all good.  The drugs are continuing to do their job and there has been no further progression.  The one lymph node infected in my neck has not reduced or grown and there are no signs of cancer anywhere else.  The two hour wait at the hospital was worth the wait!!!!!

    Now all I have to do is continue to take the capcitabine for two weeks out of three, herceptin every three weeks, enjoy...

    Former Member over 15 years ago
  • leggy Griffs blog
    Enjoying the weather

    Improvements still happening.Doing jobs eating better,feeling ok,driving the car etc.Got appoi ntment through to see surgeon to see how i"m doing but certainly not gonna worry about that! So pleased for my wife Leanne and my boys Joe and Jack that they can see me improving (am actually moaning a bit to them, its hilarious as they dont take any notice of me) !!!!!! Eh even managed to sleep on my side as well which is good.

    Former Member over 15 years ago
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