Macmillan Online Community
 
  • Cancer info and support
  • Online Community
  • Donate
  • Fundraise
  • Cost of living
  • Advocacy
  • Volunteering
  • Healthcare professionals
  • Shop
  • About Us
  • More
  • Cancel
  • User
  • Site
  • Search
  • User
  • Search
  • Forums
  • Blogs
  • Ask an Expert
  • News
  • Help
  • Guidelines
  • More
  • Cancel

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. 

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.
    Megan- Online Community Team 8 hours ago
  • To Hop-on or Hop-off is the question?
    Mr U 15 hours ago
  • One Step At A Time
    Phild26 1 day ago
  • Today my coffee tastes like Christmas in Costa Rica
    Beesuit 6 days ago
  • A trip with triple negative breast cancer
    Coddfish 6 days ago
  • Slightly Inconvenienced by Prostate Cancer
    Lemsip 10 days ago
  • Eunice77
    Eunice77 11 days ago
  • Living with Desdemona
    Desdemona 12 days ago
  • Prostate Cancer Recurrence - Triple Therapy
    excavator 15 days ago
  • WJ grade 3 Astrocytoma cdkn 2a/b non-deleted
    W J 15 days ago

Latest blog posts

  • 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
  • BronB's Radiotherapy Journey - treatment to the Salivary Gland
    Sessions 17 and 18 - 12 remaining
    I'm going to keep this brief because I need to get on with a small physical project 😳 Yesterday was clinic day so I met with my assigned Radiographer and my Oncologist. Onc has spoken with my neurologist, who enlightened him re Multiple Sclerosis. We are fine to continue though I have been advised to lower my Vit D to 4000 IU each day (from 6000). The Neurologist also suggested I see him once in have finished treatment. I was given a prescription for Senna (constipation) and also some dry...
    BronB over 12 years ago
  • BronB's Radiotherapy Journey - treatment to the Salivary Gland
    Session 16 and the weekend before - 14 remaining
    This weekend (after session 15) was hard. We went to friends for dinner on Saturday night - a well-planned mid-treatment evening with two really supportive couples who are really helping. The meal itself was perfect .... Nutritionally balanced and able to cool down to toddler temperature (goats cheese tart, salmon fillet with lovely veg, mascarpone ice cream). The friends hosting had bought several different types of fizzy water and so I was able to vary my drinks, just like they were doing....
    BronB over 12 years ago
<>
Help us do whatever it takes, because we’ve never been needed more.
Donate
Online Community
  • Cancer groups
  • Cancer blogs
  • Ask an expert
  • Cancer news
  • Help
  • Sitemap
More from us
  • Cancer information and support
  • Cost of living
  • Online Community
  • In your area
  • Fundraise
  • Donate
  • Advocacy
  • Volunteering
  • Healthcare professionals
  • Shop
  • About us
About us
  • Contact us
  • Jobs and careers
  • What we do
  • Our organisation
  • Corporate partners
  • Press office

Whatever cancer throws your way, we’re right there with you.

We’re here to provide physical, financial and emotional support.

0808 808 00 00
Macmillan Logo
Fundraising
PIF logo
  • Sitemap
  • Terms and conditions
  • Privacy policy
  • Cookies
  • About our information
  • Accessibility

© Macmillan Cancer Support 2026 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007