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

  • To Hop-on or Hop-off is the question?
    Mr U 11 hours ago
  • Living with Desdemona
    Desdemona 1 day 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.
    Megan- Online Community Team 1 day ago
  • Benign Thymoma
    Jenz 2 days ago
  • One Step At A Time
    Phild26 4 days ago
  • Today my coffee tastes like Christmas in Costa Rica
    Beesuit 9 days ago
  • A trip with triple negative breast cancer
    Coddfish 9 days ago
  • Slightly Inconvenienced by Prostate Cancer
    Lemsip 13 days ago
  • Eunice77
    Eunice77 14 days ago
  • Prostate Cancer Recurrence - Triple Therapy
    excavator 17 days ago

Latest blog posts

  • AD-Cornwall
    Always so miserable.

    I was diagnosed with renal cancer 3 years ago, fortunately I had surgery and was given the all clear. I've been trialing a drug ever since called sorafenib and touch wood I've done ok . I had a scan at the end of last year and was told in January that the scan looked ok........BUT..........they were a bit concerned about my retro-crural node (haven't a clue but alledgely its in my chest) has grown by 0.5cm since my last scan. However seeing as I wasn't feeling unwell at all they would leave everything...

    Former Member over 15 years ago
  • jennifer52
    is this a wee moan!!!

    hi everyone

    think im about to have a moan because i have been wakened since haf 5 and its sunday morning this no sleeping is doing me in got 6 hours for the first time since wednesday

     bloody chemo is turning me into a zombie red eyes .....look like a lobster... hair falling out and i darent look in the mirror for fear it will crack into a million pieces ....on the up side if i can say there is one im eating for everyone in here and cant decide now what to have for breakfast ......my day is filled...

    Former Member over 15 years ago
  • Cherryl and Peter's blog
    Have signed in without crying!

    Hi Everyone, all too numerous to mention, but will get around to speaking to you soon.  I cannot tell you how many times I have tried to come on here.

    As with anyone who has lost someone so very dear to them, whether it be a child, partner, parent, sibbling or friend....time is essential in order for us to start getting a grip on life again.  There is so much to sort out, whether it be bills, banks, employment, pensions, clothes.....the list is endless.  My journey since Peter died in March is no different...

    Former Member over 15 years ago
  • lib
    my lovely dad has got cancer...

    Hi - the last 2 weeks have been just horrible. My dad has always suffered from sinus problems all his life, just allergies and infections etc. But around last October a lump appeared on his cheek, which the doc said was prob a blocked sinus. Gave dad beconase. But the lump grew, and started affecting his nose shape and eye socket and he couldnt breathe up his nose. I was pestering him relentlessly as I always have, to go to the Doc and get it checked. He eventually got referred, had a CT scan and...

    Former Member over 15 years ago
  • Jan
    Clairelouisjane

    How sad is this?

    Whilst away from chat for a short while the above person went it and was very abusive, will not repeat what i was told.  Regardless as to how ill a person is it does not give them the right to use such fowl language.  We are there to help people, if this person requires help we are all there for her, but dont tell folk they are all going to die etc..  i am being kind with my wording and do not wish to offend, but hearing what was said had to blog.  If you only wish to use chat to be...

    Former Member over 15 years ago
  • The Waiting Game
    The Waiting Game

    For any one that has been told they have cancer but not what one they have and it takes time to find out it can be very stress full to you and every one around you.you really do have to try and stay strong. i was told i had cancer b4 christmas  2010 and a week later after a pet scan told its spread to my spine so have a mass tumour aswell by my lung have had 2 biopsy's were some i now with a professor but im still waiting to find out what is got to see a doc on 7/2/2011 but ur find thay dont mean to...

    Former Member over 15 years ago
  • Trying To Deal With My Cancer
    help me

    hm

    Former Member over 15 years ago
  • rosie0207
    mri good news

    got results from mri today, told cancer hasnt spread and told more about my op on 25th. Feel good that it hasnt spread but bit scared of how close my op is.Cant remember half what specialist told me, had mixed emotions. Going to keep busy now and not think about it. No more hospital till next week so I am going to put a blank mind to my bladder and think about positive things.

    Former Member over 15 years ago
  • My Lovely Wife Julie
    My Lovely Wife Julie 2

    The Leicester Royal has restricted visiting hours to try and control flu viruses.  2-3pm and 7-8pm.  To get parked you have to arrive an hour early for the afternoon visit and then hang around waiting areas until the evening session.  We live 40 minits from the hospital so it doesn't make sense to go home.

    The old visiting times used to be 11am to 8pm and you were guaranteed to be there when the Onc visits or any other Healthcare professional stops by her bed.

    Today, while I was waiting to visit...

    Former Member over 15 years ago
  • ureter cancer tumor removal
    removal of carcanoma in the ureter

    I am new at this so bear with me, I had my operation for the removal of a tumor in the ureter some 14years ago however it has continued to come back in the bladder, these have happened some four times and been removed by laser. I was told by my surgeon that this is a very rare , ureter cancer that is, does anyone else out there have any experience of this look forward to hearing from you .jo

    Former Member over 15 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