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.
Hi everyone, since past 2 weeks i felt some changes in my breast as one looks a bit larger than the other.went to the doctor yesterday n she goes its normal.you need to feel around your breast to check if there is a lump or sonething but i dont even know what a lump feels like.i had a check n i think there is a lump i dont know if i am right or not.please help me i am really stressing out.
I was diagnosed with terminal lung cancer - large lump both types mixed - in December this year. I was taken into hospital after a CTscan which showed a 6 cm tumour in my lung and a cluster of cancer cells on a vertebrae in my spine. I had a collapsed lung. I was in hospital for two and half weeks and started chemotherapy at the end of January. My oncologist told me I had a life expectancy of 6 months without the chemo and a year with the chemo. I am 66 years old and was previously fit and lively...
It's been 2 days since I've heard the ''news'' .... how am i dealing with it? not so good.. I find it hard to stop crying about it. He doesn't want me to feel this way, it must be difficult for him too. But, I tell him. I tell him everyday if I have to that I will always be there for him no matter what. Even if there's no cure for it now... I'll hope for a miracle. I'll pray everyday for the pain to slow down... As long as he knows how much I care and love for him despise everything and what others...
Im new to this so if wrong sorry I just feel so lost and alone my mum my wonderful mum as been told she has latter stages of liver cancer theres nothing they can do im no expert bit u know when the end ia not far seeing her today it wasnt my mum 6 months ago she was telling me off and im 46 wish she was telling me off shes not eating ahe cudnt even lift her own legs up today my younger was there to help I just wait for the phone or knock at door my children all grown moved away and I just have me...
Hello everyone,
It has been a few weeks since our news that currently there is no evidence of disease.
It has taken a while to digest it and only just are we beginning to get into some sort of routine.
How do I feel about it now?
I am not sure truth be told. Many people are so excited for us, which is great, really it is. But I find I am unable to get that excited. My brain has been quietly whispering to me again. It whispers that it will come back. Who knows where who knows when?
I also think that...
Day 4 to 6.
Well, it has been hard to adjust to doing practically nothing for 6 days, however, I think I could used to it! Actually,on second thoughts there is only so much Loose Women and Jeremy Kyle you can handle. healing has gone well so far, I have had no pain whatsoever in either my shoulder where the graft was taken or in my nose. Some general itching but apparently this means everything is healing. I have been able to shower, provided you don't direct the water on the areas concerned it is...
Well thought it was worth doing a quick update on this blog, incase anyone else has a similar journey to me.
I'm now 19 months post surgery and I'm supposed to be on 2 monthly check ups at the moment but a few Hic cups since August have meant it's gone back to every month.
Had a funny feeling in my throat in July/ August last year. Have had a few things looked at to try and see if there was any thing unpleasant causing It. I've had an MRI, barium swallow X ray and a camera...
Hi All & Hope Everyone is OK
Firstly apologies if I getting things messed up but this is the first time I've ever written any blog or anything else on line for that matter. Just a general question to all really but does anyone else suffer from cold hands after chemo. I have so far had 5 R-Chops (and have a teddy bear named "Chop" who keeps me company during treatment), 3 methotrexate treatments and five intrathecal lumber treatments. If anyone can please let me know if this normal I would...
Been thinking about doing this for a while now. I'm not someone who writes diaries and I've never done a blog before, but somehow it feels that the time is right, as things seem to be moving a little faster and I am finally coming to realise that we are very unlikely to walk away from this together. Perhaps up till now a little part of me has felt that writing things down would make them real?
I am hoping that my wife and I are unique in this, but we are both desperately disappointed with MacMillan services. The service is nothing like the lavish and presumably expensive adverts. So far in our experience, they are all self-marketed hype with no substance. Unfortunately they are the only Health Service support that we have been offered. My wife was diagnosed with liver cancer at the beginning of February, after the tumour was misdiagnosed as benign in June 2015. Consequentially the prognosis...
