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.
My mum is 68, she was diagnosed with breast cancer 13 years ago. She had the lumpremoved and recieved chemo and radiation. She was then on Tamoifen for a number of years.
6 years ago she was diagnosed with secondary breast cancer in the lungs and bones. She received chemo and radiation again and worked her way through the hormone cancer drugs until none of them worked any longer. This bought us to October 2010.
The cancer had got worse and she was in a lot of pain walking. By December she washaving...
I lost my Dad on the 3rd August 2009 when i was just 17 years old. It was only 6 weeks after he was diagnosed and it all happened so quick.
He collapsed one night and i was forced to do CPR. Nothing helped and no one could help him, even the paramedics. He was pronounced dead 2 and a half hours after he collapsed.
I was always a Daddy's girl. My brother and sister are a lot older and had moved out of the family home. It was my Dad who was always there for me when i came home from school and who...
I am very scared and very lost. My Husband was diagnosed with bowel cancer 2 years ago, he has had several different treatments but nothing seems to be able to stop his cancer growing and making him iller. He turned 40 this year and the Dr's don't think he will make it to 41 in fact they don't think he will see my birthday in October when I will be 32, I am so scared at the thought of being a widow at 31, we have a 2 year old. I try not to think about it as it's too heartbreaking to think...
Hi
Not sure if anyone will read this blog but I'll give it a go anyway,
My mom was told she had renal cancer in december 2009, she came out of the operation fairly well but then had to start a form of Chemo called sunitineb which she took for around 12 months. She also had to have some radiotherpy on her lumbar spine and most recently on her T-spine.
The radiotherpy this time round really knocked her about she was in a lot of pain and had to go onto some pain patches, which also had there...
Next week I have an appointment for a check-up and, as always, I am getting a bit nervous and apprehensive. It is almost three years since I was diagnosed with mouth cancer but somehow the fear comes back when I have to go to the hospital. My mind plays games and I am back on the table with the mask firmly in place having the radiotherapy..........but I should be grateful for the fact that this cancer has been destroyed. I shall strive be positive and keep smiling !
One week in and not so bad yet!!!!!!!
A few mouth ulcers, a little bit of nausea and an overwhemlming feeling of tiredness but otherwise ok. Oh and the body rash from the antibiotics that makes me look like a 17th century pox victim lol, but if it keeps bugs at bay i can live with it. Adelaide is behaving herself rather well and even the teenage son is doing housework wihout being asked, yes i must be ill lol.
So in all not a bad start to chemo!!!!
Didn't I say my holidays are a disaster. Just come back from my hospital appointment for blood results ready for last session of chemo next week. Last month (the day I came back) the CA125 had gone up 12, this month it has gone up to 617, and that is on treatment! The doctor listened to me saying I thought things were not right, but he didn't have the results, just said have the chemo then the regular post chemo CT scan, come back in 6 weeks. I insisted he got the blood results, and he didn...
Hi all,
My wonderful boyfriend Andrew died of cancer on 28th March 2011. To help with my grief and other people I am writing down my experiences in my blog:
http://veryyoungwidow.blogspot.com/
Please feel free to read it, follow it, and comment. I update it regularly so keep checking to see how I'm doing.
Thank you
Louise
Well after being told by someone on Tuesday ( who by the way needs to be strike of ) that they couldn't do anything for my mum. That chemo wasn't an option. We have had the worst 2 years.... did I really say 2 years I meant 2 days although it feels like years of our lives. My family have just gone through hell only to be told by someone different they are doing chemo although it wont shrink it it will contain it.. To say I am confused is an understatement. We seem to be getting conflicting...
Can't believe how quickly it has gone but finally I can say last chemo next week, can't wait to get it over with. When I was first diagnosed with breast cancer I read a ladies blog from America in the chemo unit where she had her treatment they had a bell that people rang at the end of their last chemo, so I've ordered a ships bell for my chemo unit which I will ring then donate next week.
Its not the easiest of journeys but as most of you brave lovely people know we can get through...
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© 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