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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
    8 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

  • Living with Desdemona
    Desdemona 1 hour ago
  • To Hop-on or Hop-off is the question?
    Mr U 3 hours ago
  • Wittering away...
    Rowan8a3264 5 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.
    Emma - Online Community Team 20 hours ago
  • time for a cuppa....
    hugs 1 day ago
  • Speaking to an empty room
    RedTree26 1 day ago
  • "It's Only Skin Cancer"
    A cautionary tale of personal experience and common misconception
    dolphin99 2 days ago
  • My Mengioma Brain Tumour Story
    GaryG298207 3 days ago
  • Looking after Mr. B
    Miranda t 7 days ago
  • Today my coffee tastes like Christmas in Costa Rica
    Beesuit 7 days ago

Latest blog posts

  • Valentinex2's blog
    Me and 11 platelets - out for a drink!
    Hi All again As some of you know I have AML and actually feel extremely well - I have been reading some of your blogs where you are worrying about platelets crashing to 200. Well - when I went for bloods last Wed my platelets were sitting at 11! I am going next Fri for blood transfusion which will probably put them up slightly. What I can't understand is how I am still alive - perhaps I am an alien? I went out tonight for a drink with friends and kept thinking - My God - my platelets are sitting...
    Former Member over 17 years ago
  • babydaisy's blog
    I would like to get in contact with other people who have had oesophegal cancer touch their lives in one way or another.
    I am hoping that this website is going to put me in touch with other people who have experienced oesophegal cancer in one way or another. I am interested to know and learn all there is to know and am hoping you lovely people on here can help.
    Former Member over 17 years ago
  • Trudy jayne's blog
    Sore & fed up :O(
    well after all the confusion during the past two weeks as to whether or not i was to have the op (right excision axillary nodes) it went ahead yesterday as planned. i was hoping it would be as quick and easy as the previous one ....i had an enlarged lymph node removed from my groin at the end of may when they found the cancer..... but i was very much mistaken i woke up from the general anaesthetic very weepy and in agony.i was given the maxium amount of morphine my consultant would allow which...
    Former Member over 17 years ago
  • babydaisy's blog
    at the beginning
    Hi all this is my 1st blog on here. Today my mum got results for her cat scan for her cancer in her oesophagus and was told that it hasn't spread which is good news but her lymph node gland things are enflammed which she is saying is normal due to where the cancer is which is near her stomach. There was talk a few weeks ago about an operation but she has now been told that there is no op and that chemo and radiotherapy works best with this type of cancer. She now has to have a Pet scan just waiting...
    Former Member over 17 years ago
  • Trishka's blog
    Side effects kick in
    ... it shouldn't really come as a surprise but it has... to hubby. He walks up a few steps and is out of breath. If life had gone to plan he would have been climbing Killimanjaro next week and here he is, struggling to get upstairs and nothing to do with altitude. He's also been feeling nauseaus alot. He's not actually sick but feels lousy. This last couple of days he has gone to bed for the afternoon - he probably would have slept through dinner too had I not woken him. He has to take medication...
    Former Member over 17 years ago
  • Valentinex2's blog
    Living with my unwelcome guest!
    As already I stated I was only diagnosed with AML a few weeks ago - fortunately my family although shattered are all grown up - must be so hard for those of you who are seriously ill and have young children to care for. Anyway I have decided to look on my illness as an unwelcome guest and call him Luke - I didn't want Luke here at all - but now I have to learn to live with him. The thing he hates most is me being happy and cheerful - so I am determined to be that as much as is possible. He loves...
    Former Member over 17 years ago
  • chrissiQx2's blog
    Is this real?
    I have just spent the morning at work providing beauty treatments for several clients, I'm now at home listening to my delightful children arguing and throwing cushions at each other. Its just gone very dark outside and a rumble of thunder just resounded near by. I can hear police sirens in the distance and the downpour of rain that has just begun. I'm wondering if my son is ok at his friends house and what I am going to do for dinner as I need to go shopping. I'm thinking about phoning mum to...
    Former Member over 17 years ago
  • Julesx2's blog
    Occupational Health - here we go again.
    Am off to OH this morning to discuss a phased return to work again. Tried before the summer hols to get back but after being back for a few days came down with a bug wich floored me- I guess this has knocked my confidence. Still trying to be positive but some days its hard as I feel I will never get back to the way I was before my diagnosis. Ive come through the worst ( I hope ) so why is everything so difficult now? I keep telling myself its only a job but ..... Hey ho! Have had a moan now gonna...
    Former Member over 17 years ago
  • Lari's blog
    TAC chemo
    Hi everyone I am a bit new to this blogging business. I am starting TAC chemo (breast cancer) tomorrow and although there is lots of info on side effects nobody tells you when they start. Can someone give me an idea as my daughter is having her twelve's birthday party on Saturday (she is having 30 friends for a barbeque). Thanks Lari
    Former Member over 17 years ago
  • LJane's blog
    Melanoma cancer stage 4
    This is my first blog so here goes... I had a malignant melanoma removed in 1993 and after years of regular check ups, and thinking it was all behind me, in April 2009 I discovered a lump and immediately went to my GP. After lots of checks, ultrasound, blood test and MRI scan I was devastated to be told the melanoma cancer had returned as secondary cancer in both lungs and both breasts. It was such a terrible shock! Iinitially I just wanted to cry, then felt angry, but what good would that do...
    Former Member over 17 years ago
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