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.
Welcome dear readers.
I am now doing something that I never imagined in my wildest dreams that I would do - starting a blog. Unfortunately it is regarding a fight against incurable cancer. I hope that anything that I write provides some comfort/interest/curiosity ? for you. To be honest I do not really know if I am doing this for others. I suspect that in actual fact I am going to be using this so that the incessant voice in my head can be silenced for just a little while.
So, where should I start...
It has been a few days since my most recent chemo session so I thought a short update might be due?
This time the chemotherapy seems to have been just right, I had all the anti sickness medication available that was supposed to be and I for one was extremely grateful for it. It has made all the difference to my mood. I had been worrying, how was I going to physically drag myself through six cycles of what I had already experienced? It was horrendous. The nausea and the sheer pain and fatigue my body...
My husband finds it difficult to eat normal food after having chemoradiotherapy for head and neck cancer. It's now six months since his gastro tube was removed and is struggling. Can anyone give him an idea of how long this will last. His mouth is dry all the time also
thank you
twenty months after being diagnosed with throat cancer I a really happy to report that I am sat in a bar in Washington DC with a pint of beer having demolished a ribeye steak. They say you don't miss things until hey are gone(and I apologise for those reading this still struggling with the effects of throat cancer and radiotherapy treatment) but I needed to share this milestone on my blog. My tastebuds are still not back to normal yet the ones that have recovered seem to be supercharged, hypersensitive...
Hello readers,
What have I been up to? Well high in the agenda this week has been paperwork and putting affairs in order. That is the official wording for writing my will.
Who writes their will at 37 knowing it will be enacted in the not too distant future? Not many I hope. I had been thinking about writing a will anyway as an adult thing to do but little did I think I would be writing it because I HAD to. A long standing friend came and took us through the process, how we would set up any legacy...
Uk-wide vaccination of 12-13 year old girls against the Human Papillomavirus (HPV) began in 2008 and has achieved coverage of over 85% of this target population. As a result, prevalence of HPV 16 and 18, the particularly dangerous forms of the virus, has fallen significantly and we can look forward to a substantial reduction in HPV related cervical cancers. HPV can be considered a necessary but not sufficient cause of cervical cancer.
What has this got to with boys? Quite a lot, in fact. As Michael...
I am now halfway through my 6 week course of chemoradiotherapy. Hallelujah etc. But probably not half way through the side-effects yet, as they are cumulative - groan....
I went in to hospital yesterday for the second dose of chemo, only to discover that there had been some sort of muddle and that it was planned to start today instead. Grrrr. Not quite sure who muddled what, to what extent which side got the wrong end of the stick etc .... but have no choice but to let it go. Staff on duty were very...
I've been promising myself for almost two years now that I'd start a blog tomorrow.
Well, today's the day! I'm not going to write too much now but at least I've made a start! I read earlier that one of my friends from the Living with Incurable Cancer Group had died on Saturday morning, she was called Jane and her username was Dyad. Eamonn, Russell, Jane and myself had joined the Macaite around the same time and although we never actually met, it felt as if we had been friends all our lives...
Hi all,
It is one am here. I am still up. I often am at this time of day. It is the quiet times that get me.
I am struggling to process this mentally. I know there are cancer patients like me who have and are able to go forward with great positivity and know that they are fighting this disease all the way. I want to be like that I really do. But I am struggling.
I have no real hope to cling to. Obviously I have my family but that is different. I think I need something about this disease to hope for...
Hello dear readers.
Since my last post my emotions have settled a little but inevitably I still break down on occasion. I cannot help it. Often this is when I am faced with the stark reality of my disease, this cancer. This is when the Macmillan nurse comes or the district nurse or the health visitor. All these people want to help me, they are sad for me. I get that. I do. But I don't want them here. I don't like what they represent but accept them I must. Wasting time wallowing won't help...
