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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

  • Wittering away...
    Rowan8a3264 16 hours ago
  • To Hop-on or Hop-off is the question?
    Mr U 19 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 3 days ago
  • Looking after Mr. B
    Miranda t 3 days ago
  • One Life Live It
    Sadly not a LandRover road trip, but my journey through breast cancer
    Irishgirl16 3 days ago
  • One Step At A Time
    Phild26 5 days ago
  • Speaking to an empty room
    RedTree26 5 days ago
  • Today my coffee tastes like Christmas in Costa Rica
    Beesuit 5 days ago
  • Slightly Inconvenienced by Prostate Cancer
    Lemsip 6 days ago
  • My mum 86yrs
    Julie17 8 days ago

Latest blog posts

  • mums lung cancer
    3rd Cycle of Chemo is here

    To see this blog as it is intended please visit http://mumslungcancer.blogspot.com

    How fast is this coming around? We are up to the 3rd cycle of chemo already, I think they have scheduled 6 in total, then a blast of radio therapy on the brain, as a safe guard measure as is likely to spread there next. I have brought my computer and am typing this while we are here! Up to now they have put her arms in water to make her veins more visable and also suggested that she has a top up of blood when she...

    Former Member over 16 years ago
  • Riding the bus is so hard.........
    Riding the bus is so very hard...........

    As a non cancer person (at least up to now!) I thought I'd write something about a very good friend of mine who I learnt this morning has lost her struggle against cancer.

    Linda MacVev is a lovely lady and I count it very much a privelage to know her, even though she lost her battle last month she is and always will be a 'present-tense' person because she is in my memory and always will be.

    I cried so hard for her this morning again, and it made me think of the one's riding the bus...

    Former Member over 16 years ago
  • Duchessx2's blog
    My darling Bobbie has lost his fight.

    My darling husband passed away on Sunday 1st August. He fought so very hard right up until the bitter end.. I feel so numb just do not know what to do. He was the most wonderful husband  and father that anyone could wish for. Our lives will never ever be the same, my very best friend is not here any more. I feel so lost, people say stay strong for all the children. I shall try my utmost for them but other than that I feel my world has ended.  I cradled him in my arms until the very end and shall never...

    Former Member over 16 years ago
  • Dad, cancer and me
    The beginning

    So here I am, catching up to the sort of technical stuff most people take for granted, personally I'm much happier with pen and paper but there you go!

    When Dad was diagnosed with cancer in his right lung and duodenum just before Easter this year I went into shock.  He had been ill with various things for years, sadly most of it as a result of self infliction, but the reality was that this was now something a short stay in hospital or some pills couldn't solve. 

    Mum had had cancer when I...

    Former Member over 16 years ago
  • Scared Win
    Best Results i could of Hoped for !

    Had good day yesterday after having pet scan last week went to see oncologist yesterday and he amazed me by telling me the cancer in my lyphnodes in neck and chest are inactive !!!!   i do still have `1 node which he thinks maybe slighlty active in my chest he is looking to seee if he shoul;d do a ultrasound biiopsy and if it is a new drug which is a ten minute infuusion!! i am over the moon !!  best news i could of wished for he said i had responded very well to treatment i went through really bad...

    Former Member over 16 years ago
  • Ramblings of a Bad Fairy
    Woe is me.....

    …..but don’t despair!

     

    It was the weekly jaunt to see the consultant today to get the ok for chemo this week and woe is me ….the little toe-rag is on holiday! Fancy that, holidays in August tut tut, how dare he. Mr Bad Fairy muttered under his breath about Dr Socks probably being on a yacht sailing to and fro between exotic islands. I was thinking more caravan at Cromer maybe?

    After a mere two hour wait and numerous cups of tea I was summoned in to see the covering doctor...

    Former Member over 16 years ago
  • Babybear's Blog
    Re Protocols for Lung Cancer

    Hi Re my post earlier in the week asking about protocols for Lung Cancer.

    I was asking as my sister had told my mum that she had Lung Cancer, However the pieces did not fit and I was questioning what the Dr had told her apparently according to her the Consultant just told her it was there without doing any further tests. don't know whether to be relieved at the fact she does not have it or angry for the lies she told my mum who thought it would be a good idea to tell me. I have spent the past 2...

    Former Member over 16 years ago
  • 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
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