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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
    7 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

  • Slightly Inconvenienced by Prostate Cancer
    Lemsip 11 hours ago
  • To Hop-on or Hop-off is the question?
    Mr U 21 hours ago
  • "It's Only Skin Cancer"
    A cautionary tale of personal experience and common misconception
    dolphin99 1 day ago
  • Peter's Blog
    A blog about bowel cancer at a young age
    HawkeyeBrown 1 day ago
  • Wittering away...
    Rowan8a3264 2 days ago
  • Living with Desdemona
    Desdemona 2 days ago
  • Kidney Not
    Mmum 3 days 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.
    Lizzie - Online Community Team 8 days ago
  • Looking after Mr. B
    Miranda t 8 days ago
  • One Life Live It
    Sadly not a LandRover road trip, but my journey through breast cancer
    Irishgirl16 9 days ago

Latest blog posts

  • my mum and me
    what next

    been a long day mums got a rash been for the bone scan but she had the rash before so it can't be that .went straight to the docs after hospital and she's unsure what it is and phoned the cemo unit as mums got to start taking her steroids tomorrow ready for thursday and she doesn't want her taking them if her treatment won't go ahead .so sat here now waiting for the call just hope its nothing that will delay her treatment any longer fingers crossed.

    Former Member over 16 years ago
  • Bowel C the fight, daily blog
    Day 1 the fight begins

    had the diagnosis, tomour in lower bowel, invasive, done CT/MRI scans, blood tests, go the schedule na hd the tatoo.

    Today base line blood test, then collected  Capecitabine (Xeloda®) tables, 1650m, twice daily, seems like rather heavy dosage to me, but what do I know. Apprehensive, oh yes, but prepared my body/soul with Bowen techniques, and assorted other treatments to be sure as relaxed as physically possible. Tomorrow is the first radium treatment, so another first. been through the side effects...

    Former Member over 16 years ago
  • 2 years
    2 years

    Dad has just called me to say he has been told he had 2 years to live.  I am determined to help him beat the ticking time-bomb!!  xxx

    His story so far....

    My dad is living with a brain tumour which until very recently was thought  to be benign.  It is now asuumed to be a higher grade.  Today he is meeting Dr Matt Grffin at Nottingham City to discuss radiotherapy.  Everything seems very scary at the moment.... 

    My father lives in Mansfield and I live in Southampton so its tough being so far away.

    How my jounrey...

    Former Member over 16 years ago
  • My breast cancer chemo diary
    Update on progress

    Hi all, well am having the day  off work today.  Had a sore throat this morning and since the period of low blood levels is starting tomorrow, I thought it best to have a rest.  I am not too bad otherwise.  Energy levels are fairly good.  I've had an on and off poppy tummy and that embarrassing burping, though I think that was down to the anti sickness drugs as certainly the last couple of days since I came off the drugs seems to have calmed that down a bit.

    So, just watching myself lots at the moment...

    Former Member over 16 years ago
  • Coping?
    D-Day Week!

    Not been posting progress of my Mum - just been to horrendous to try and put into words.

    She had 2-3 months in hospital for treatment and got home just before Christmas and gladly the tumour had reduced a lot, but then has had 3 x 4-weekly R-Chop treatments.  She has her scan today then her review next week - so scared and feel really selfish because my mum has fought the whole way and been so positive - has had some bad days but hardly any considering what she's been though.

    I suppose all we...

    Former Member over 16 years ago
  • my mum and me
    talking about funerals

    just sat on the sofa today having a coffee and chat to mum and she starts telling me what songs she want at her funeral nearly choked on my coffee i know she like's to be organized but this..... think maybe she's jumping the gun as yet we don't know the all the results .i know me and my dad used to talk about what he wanted when he past but he knew it would happen soon and didn't want to upset my mum and because we were so close it was just easier to tell me .but when it came too it my brothers and...

    Former Member over 16 years ago
  • geraldine23
    Leiomyosarcoma, just diagnosed.

    Had hysterectomy for heavy bleeding/fibriods on 2nd March 2010. Cancer cells found. Had result of first CT scan with oncologist today. There are signs of spots on my lungs and also a mass in my pelvis. They are not sure if this is cancer or post op fluids etc. I am having chemo on 12th April using doxorubicin. My consultant said chemo was not always effective against saracoma. I feel quite numb. I have 3 boys 16, 15, 12 and a lovely husband. Don't know how to start telling the boys about this. I...

    Former Member over 16 years ago
  • Hevvur's blog
    A small update......

    I spoke to the consultant at the Royal Free on Friday (26th March) - no update - we are STILL waiting for funding from my local PCT.

    I also had a meeting with the local Central Advocacy Services on Friday - and i'm hoping they can get in contact with my local PCT and find out whats happening. They agree that the time i've been waiting is too long, and not acceptable. So lets see if we get anywhere!

     

    I had my second dose of Vinblastine today. Once again 4 attempts to get the cannula in...

    Former Member over 16 years ago
  • gillydx2's blog
    Treatment starts tomorrow.....

    I have to be at the Royal Marsden at the crack of dawn tomorrow to have my mask made.  Then back in the afternoon for my first blast of radiotherapy to my brain.  Only five sesions in all but they have warned me that as it is my whole brain my hair may fall out!!!!.  The treatment MAY bring back the feeling in my left hand, but no promises.

    So if anyone else says "IT WAS ONLY a MOLE"  please may I thump them?

    Please wish me luck,

     

    Gill x

    Former Member over 16 years ago
  • Elaine On The Train's blog
    Jimbo/Jas34 UPDATE #3

    Jim's wife rang yesterday morning.  He's had some more problems that are keeping him in hospital still.  It sounds like its the same thing Mike had a while after he was discharged.  It might be rather fortuitous for Jim that this has happened while he is still in hospital, so they can fix him up before he goes home.  He's able to walk around OK using a stick and all of the hardware had been detatched from him too by the sounds of things.

    It seems he's a bit down in the dumps too poor thing...

    Former Member over 16 years ago
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