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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 13 hours ago
  • Slightly Inconvenienced by Prostate Cancer
    Lemsip 3 days ago
  • Eunice77
    Eunice77 4 days ago
  • Living with Desdemona
    Desdemona 5 days ago
  • Today my coffee tastes like Christmas in Costa Rica
    Beesuit 6 days ago
  • Prostate Cancer Recurrence - Triple Therapy
    excavator 7 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.
    Emma - Online Community Team 8 days ago
  • WJ grade 3 Astrocytoma cdkn 2a/b non-deleted
    W J 8 days ago
  • Cool Cap Relief
    TerryB 11 days ago
  • One Step At A Time
    Phild26 13 days ago

Latest blog posts

  • The next battle
    SCT 2 last day of chemo
    So today completes the 3 days of chemo. 2 days of no treatment to follow before he gets his cells back. He has slept most of the day bless him. Waking only for the toilet and to eat. Not sure he's done all his mouth washes so hoping he doesn't get a sore mouth. Nurses changed the way anti sickness is given as apparently he can't have it through syringe driver whilst on fluids. So half of it (nonsa sonething) is given via injection. Pete thinks this is there name for the levopromazine. Odd cause...
    Former Member over 12 years ago
  • Life without Hubby - Missing Him
    Now supporting mum

    Now my mum is a widow, the other day she said to me "I should have supported you more, I didn't realise what you were going through".

    Only now that she has lost her husband, does she understand the emotional anguish that I had to deal with while maintaining routines and supporting my children through the loss of their father.

    What frustrates me is that as I know what she is going through and support her, she has no consideration to the fact that I am also dealing with the fact that...

    Former Member over 12 years ago
  • The next battle
    SCT 2 things moving faster
    So it looks like things are moving quicker this time round. Pete is doing OK in himself, still eating & no sore mouth etc.. although he has slept all day. Not sure if it's the anti sickness meds or chemo causing this. Metroclopramide and levopromazine in syringe driver. Metroclopramide, Ondansatron and cyclozine orally. The reason I say things are moving faster is he was told today he now has to stay in his room as his neutrophils are 0.3 this is only day 2 of chemo. He has 3 days then a 2 day break...
    Former Member over 12 years ago
  • Dyad's second time around
    Platelets

    I went up to The Christie on Thursday for my 3-weekly review (no Mytomycin this time).  My friend  from York met me at the station and we grabbed a nice lunch and a quick tour of the art gallery, as we usually do, before going to the hospital.  The blood test revealed that my neutrophils are back to normal but unfortunately my platelets are low.  I'm certainly getting to know a bit about all the different white blood cells!  The oncologist I saw was a bit concerned.  He said that because I'd had a fair...

    Former Member over 12 years ago
  • BronB's Radiotherapy Journey - treatment to the Salivary Gland
    Sessions 19, 20, 21 - 9 remaining

    Last time I wrote about my issue with constipation and I didn't write until today because this blog post might have ended up being about nothing more.

    However, following a brief meeting with the on-call doctor on Wednesday and a prescription for Movicol (and also 14!!!! enemas just in case) some movement has happened - woohoo - it's these little but important things that are the focus at the moment. I have stopped taking Cocodamol and until last night (Friday) have been getting by on paracetamol...

    BronB over 12 years ago
  • The next battle
    Chemo started today
    So today Pete started his chemo again. He seems more tired this time & has slept most of the day. I am hoping this is due to the levopromazine & other anti sickness they have him on & not a sign that he's gonna be as well as last time
    Former Member over 12 years ago
  • Salvage radiotherapy - another journey
    Radiotherapy underway 4/33 to day 8/33

    4/33, Monday 31 March, and a new week. Coughing less but London pollution and the Sahara desert sands are making me cough, especially with my asthma. A scan was included today. Whilst waiting for the water to filter through to my bladder (4 cups, my decision), one of the team tool me aside for chat. Her name was Mitch, and she told me I would be given the chance to talk to her, or a colleague, each week. She wore a grey uniform but her two colleagues wore blue, one the ‘large, Polish lady’ named...

    Former Member over 12 years ago
  • The next battle
    SCT 1 done now starting 2
    So I guess I got carried away with Petes well being with his 1st transplant. He was so well & no real side effects. Phew. He was discharged 10 days after having his cells replaced & we have just had a fantastic week of being lazy, choosing new bedroom furniture & decor & a lovely day on the beach. Bless he even had an urge for a beer or 2 for the 1st time in months, so I took him to the pub for a few. Today we are back in a very cloudy Southampton ready for sct number 2. Fingers crossed this will...
    Former Member over 12 years ago
  • Smashing The Stragglers...
    Back Home...at last
    After two weeks of going stir crazy in hospital I finally made it home this Tuesday only to have the paramedics called out at 2.30 in the morning when some of my overnight feed had somehow gone on to my lungs causing me to choke. After quite a panic and several tests carried out I had calmed down and was given the all clear. So now at home after being knocked back for six I am slowly starting to eat other foods such as soup, taste buds still not working and dry mouth all the time. Family continue...
    Former Member over 12 years ago
  • IVF treatment before chemotherapy - funding problems
    Problems with NHS IVF funding before chemotherapy

    Hi I start chemotherapy soon and have had one cycle of IVF treatment which was not successful. My oncologist recommended I have one more cycle of IVF before the chemo to give it another chance. However the fertility dept has said I will need to pay £5000+ for this as only one cycle is funded on the NHS. Does anyone have any advice please?

    Former Member over 12 years ago
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