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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

  • To Hop-on or Hop-off is the question?
    Mr U 16 hours ago
  • Wittering away...
    Rowan8a3264 17 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.
    Lizzie - Online Community Team 2 days ago
  • Looking after Mr. B
    Miranda t 2 days ago
  • One Life Live It
    Sadly not a LandRover road trip, but my journey through breast cancer
    Irishgirl16 2 days ago
  • Silly
    Bbbb 2 days ago
  • One Step At A Time
    Phild26 3 days ago
  • Speaking to an empty room
    RedTree26 4 days ago
  • Today my coffee tastes like Christmas in Costa Rica
    Beesuit 4 days ago
  • Slightly Inconvenienced by Prostate Cancer
    Lemsip 5 days ago

Latest blog posts

  • Living with SCLC
    Scan Results
    Went for CT scan on Wednesday. Went for clinic appointment today and got results.
    Tumor on lung, central lymph glands in chest and liver have all shrunk - so that's really good and I will now get more chemo.
    Tumor in brain has grown slightly - now 9 mm (was 7 mm). Might have grown before I started the chemo. So they have decided I will get another CT in six weeks rather than twelve to check what its doing.
    Also got results of bone scan that I had a few weeks ago. Apparently they always can...
    Former Member over 15 years ago
  • AnnieR's Journey
    Radiotherapy & chemo tablets

    Hi,

    I am now halfway through my treatment for rectal cancer. To my surprise i have had few side effects form the ongoing treatment.

    There was some real discomfort from the tumour area after 2 weeks radiotherapy, i sometimes felt like I was going to pass out, particularly when sitting on the loo. mentioned it to radiotherapists & they held me back after that day's zapping & I met with a Dr from the oncology dept. She prescribed me codeine/morphine pills to be taken regularly throughout the day alongside...

    Former Member over 15 years ago
  • pinkvicki
    My Birthday.

    Today is my Birthday and i was awaken to the sound of my phone going off and i was convinced that it was dad, he is always the first one to text or call me on my birthday. i was convinced it was him and was overcome with grief when i realised it wasn't. Oh well another first i guess.  

     

     

    Former Member over 15 years ago
  • IainP
    Too young for this
    I am very very worried about having advanced stages of Prostate Cancer that hasn’t been diagnosed yet. I am only 35 Years old and have two beautiful little children ages 4 and 7 as well as a gorgeous wife. I Know the statistical likelihood of me having this awful disease is very slim but given my symptoms I am petrified.
     
    I first went to the GP complaining of Backache about four weeks age and he gave me anti-immflamatories and pain killers. I have had a bad back for months now and it just...
    Former Member over 15 years ago
  • teresaeth
    it doesnt seem real

    Its been a week since errol's funeral and all went well there were so many people there, made me smile knowing how many friends he had.

    And now i have to carry on but my life has changed so much i don't know where to start,, i have kept myself busy because the minute i stop i cry but i feel bad for being busy if that make any sense. I know there are so many on here who have lost someone and we are all different and cope in different ways there is no right way i am sure ??

    When errol was...

    Former Member over 15 years ago
  • what now
    did it change

    we saw the consutant yesterday and they said that the tumour had not grown or decreased in size. so it is good news or is it bad news im not sure

    Former Member over 15 years ago
  • greybadger's blog
    making the most of my time

    Hi,

    Here I am sitting on my daughters computer, after I have done my 'grandma' bit, and taken the girls to school.  My daughter is doing teaching practice, and has had to find child care to cope with the extra time it takes to be a 'teacher' rather than a TA, and each time she needed help over the last two years I have been having treatment, so this time I'm pulling my weight.  How do you fill your time in somebody elses house during school hours?  I don't like to interfere too...

    Former Member over 15 years ago
  • wood
    Mum

    This week my mum goes for her three months scan. She has had chemo and has been on a drugs trial. I have read that chemo does not seem to work fro people with advanced Pancreatic cancer but I am keeping my fingers crossed as she is fitter than when she was diagnosed, I hope its not just a false hope. I cant believe the last three months have gone so quickly.

    Former Member over 16 years ago
  • Hevvur's blog
    In Patient and it begins...

    Well, i've been admitted to The Christie today to start my chemo.

    Not even been here that long and i've lost count of how many drips i've had!

    I'm connected to 3 pumps at the moment - what a pain to get to the toilet lol

    Former Member over 16 years ago
  • baps54
    nodding head/tingling feet

    has anyone in macland had any experience of this....when i nod my head i get this strange tingling sensation in  both my feet. went to docs today and she is getting in urgently  touch with my oncologist  for an appt. she wants to rule out  that  mets havent attatched themselves to my spinal cord but as you can imagine this is a bit disturbing.  i would be grateful for any info .

    Former Member over 16 years ago
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