About this Blog

This blog started as an online diary and place for me to rant about annoyances in my family.

However since July it has become a place for me to catalogue and express my views and opinions on the treatment I have recieved following the diagnosis of a potentially cancerous tumor in my bowel.

On 3rd August 2011 I was told that it was cancerous. In April 2012 I was given the all clear.

October 15th 2013 I was diagnosed with peritoneal disease and liver metastases. The cancer was back and this time it is inoperable.

It is a little bit out of date as the NHS doesn't tend to have a WiFi connection in hospital and I can only post when I get home and posts take a while to write.

It is NOT about individuals or the nursing profession. It is about some of the inadequacies in the system and the way the NHS is failing some people.

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Friday, 20 July 2012

Cancer, one year on

Ok, so not strictly one year on as I didn't get the final diagnosis til 3rd August.
But never the less this last week has been really hard for me. I have been coming to terms with the fact that this time last year we knew there was something wrong but not what. In the last year I have undergone 8 hellish cycles of chemotherapy, been told that potentially I might not be able to have any more children and have lived with the very, very real fear that this might come back. 


It is certainly easy to say think positive but I defy even the most positive of people to not have their down days. This week has been a down week. 


There have been some lovely memories made this week. The olympic torch arrived in Crawley and we headed down to see that. A friend actually got to carry the torch in East Grinstead and Tony managed to get his hands on it too. It has also been Isaac's last week at pre school. 


Now that is quite significant for me. In my downest moments last summer I occasionally thought that I wouldn't get to see him start pre school, let alone graduate. But I did, I fought the cancer and saw my brave little boy graduate from pre school, and now we have the next big adventure, Infant School. He is so excited about the new challenges and adventures ahead and so am I. I am entering the world of lost jumpers, reading books, homework and lunch boxes. On top of all of that I am so proud of the way that he has coped over the last year. I don't know if the children understood how significantly ill mummy was, but I do know that last summer was probably a bit of a let down for them.


So this year we are going to have the summer of our lives. 


Tomorrow we are off to Scout Camp for a week, then there will be at least one trip on the Bluebell Railway, the Tulleys Farm Maize Maze, hopefully some picnics with some very good friends who have supported me massively over the last year. Then there are 2 massively significant events. 


Beautiful days Number 10. Last year it was all I kept asking my surgeon 'Can I go, Can I go?' So we went, it was hard work but I felt normal. This year will be awesome. I am planning heart bunting, heart t shirts and a fab menu.


Then there is Jo's Jump for Beating Bowel Cancer. If you haven't sponsored her yet, I urge you too. I will be there, albeit on the ground cheering, taking photos and generally being there for her as she has been there for me over the last year.


Beating Bowel Cancer have been a huge support to me and continue to support me even now and every penny raised goes towards raising awareness of this disease.