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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

  • One Step At A Time
    Phild26 11 hours ago
  • To Hop-on or Hop-off is the question?
    Mr U 15 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
  • Today my coffee tastes like Christmas in Costa Rica
    Beesuit 5 days ago
  • A trip with triple negative breast cancer
    Coddfish 5 days ago
  • Slightly Inconvenienced by Prostate Cancer
    Lemsip 9 days ago
  • Eunice77
    Eunice77 10 days ago
  • Living with Desdemona
    Desdemona 11 days ago
  • Prostate Cancer Recurrence - Triple Therapy
    excavator 14 days ago
  • WJ grade 3 Astrocytoma cdkn 2a/b non-deleted
    W J 14 days ago

Latest blog posts

  • The next battle
    Day 4 - chemo free day

    So after completing his chemo yesterday. The sickness kicked in today. The staff have been fantastic & kept on top of it all day. Even had one nurse explain that its the brain that sends signals which create the sickness. It was really interesting. Other than this Pete is doing really well. Obviously dosed up with anti sickness orally & through syringe driver but he's eating little bits & has developed a liking for Costa Coffee & has even walked down to the shop 3 times today with me to get one lol...

    Former Member over 12 years ago
  • Dyad's second time around
    A small blip

    I suppose I couldn't really expect to get through this treatment scott-free, and so it has turned out.  The day before my Myto infusion I had a sore throat.  Spoke to the Christie hotline as I didn't want to traipse all the way up there only to be told they couldn't treat me.  But they said I'd have to go anyway as treatment would depend on the results of the blood test. So on Thurs morning we went to Manchester - by then I'd lost my voice.  Saw yet another registrar - it's a different...

    Former Member over 12 years ago
  • Will I get Superpowers?
    Friday 14 March, Levothyroxin Day 16. Spring is busting out all over!

    Is it Friday already? It's been a crazy-busy week!

    Spring arrived properly with a bang (Hooray!).  I've spent most of this week filming wildlife and taking photos of flowers as they pop their heads up in the garden. And I've finally seen a hedgehog (Hooray!).  I think it's me ol' mate Whiffle but he's HUGE. He's being all huffy, puffy and grumpy at me which means he's telling me that this is his garden and to s*d off unless I'm a lady hedgehog. And seeing as there is at least one lady hedgehog...

    Former Member over 12 years ago
  • BronB's Radiotherapy Journey - treatment to the Salivary Gland
    Day 4 - 26 remaining
    The treatment today required my mask to be refitted 3 times (to address the tiny mm difference). Eventually it seems that repositioning my hair and squiggling up towards the too if my mask made the difference. Side effects - none really as yet. I had a two hour kip earlier this evening but this is not really out if the ordinary for me. I am seeing my consultant next Thursday about the possibility if doubling up on one treatment week (rather than the Saturday session they have currently booked...
    BronB over 12 years ago
  • Smashing The Stragglers...
    Uncrossing Wires

    Well I have had the right runaround concerning whether or not I would be given a PET/CT scan to confirm if my treatment has been successful.  Fortunately the stars have aligned and I now will be having the scan on 28 March, instead of relying solely on monthly visual checks by my consultant.  I have as I am sure you understand now got a slightly anxious couple of weeks to wait and am keeping everything crossed that all has been a success...

    Former Member over 12 years ago
  • Smashing The Stragglers...
    Steps Forward

    Well finally today I have managed to be rid of my syringe driver and switch to oral medication for pain relief and anti sickness.  This means I am no longer reliant on being at home every day waiting for the 24 hour top ups from the brilliant community nurses.  Work are also in the process of sorting me out a laptop so that i can keep a watching brief but am still some way off going back to work yet as until i get off pain relief totally i cant even drive which is frustrating.  Still a day to remember...

    Former Member over 12 years ago
  • BronB's Radiotherapy Journey - treatment to the Salivary Gland
    Day 3 - 27 remaining

    This morning we arrived at the hospital with 45 minutes to spare and, having taken advantage of getting a free parking space for the first time, I decided to call into the Macmillan Information Centre. I asked about complimentary therapies and also brought away a leaflet about some therapies that are available locally for cancer patients - so I will definitely be calling them and arranging a session or two.

    On the journey to the hospital I had called BUPA to ask about the possibility of switching...

    BronB over 12 years ago
  • The next battle
    Today we begin

    So finely after a couple of false starts here we are at Southampton general about to begin what we hope will be the end of petes fight. Diagnosed with what is known in layman's terms as testicular cancer in his chest (none in his testicles) in may 2013 Pete underwent 4 lots of bep chemo. Each cycle lasted 2 days, with chemo being administered on days 1-5 & 13. This took us from July through to October & in November tumour was removed. This we had hoped was the end of petes journey. Unfortunately...

    Former Member over 12 years ago
  • BronB's Radiotherapy Journey - treatment to the Salivary Gland
    Day 2 - met the team and 28 to go
    I woke up at 4am this morning and so felt tired due to lack of sleep. I did manage 20 mins exercise (exercise bike and rowing machine) with just fourinternals of exertion and the rest at steady pace. My treatment today took longer, mainly because the imaging machine wouldn't recognise the 'bobbles' on my mask and kept refusing to take images. I had to keep repositioning my hands until the images were completed. I then had my clinic appt where I met my Macmillan nurse (Pauline); my clinician...
    BronB over 12 years ago
  • Scared feel lost
    Scared feel lost
    If anybody has any advice please email me as I really am struggling so many emotions that I have to control or try and understand everyday this on top of not feeling so great and hiding the pain from others so they don't hurt
    Former Member over 12 years ago
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