*** REMEMBERING RUTH *** TAUNTON EDITION ***
There will be a second celebration of Ruth's life on the 30th August between 4-6pm at St Andrews Church Hall in Taunton.
All friends and family are welcome.
It would be really nice if you have any photos to share of yourselves with Ruth at a young age (or older!), please write your name and where and when it was taken on the back - this can then be passed onto the children.
More information closer to the time, or contact Sharon Kinloch for anything more urgent.
We look forward to seeing you there, love from Ruth's Family.
xxx
This started as a blog to rant frustrations in parenting my 2 'adorable' children. It is now my way of dealing with my diagnosis of Bowel Cancer in August 2011 & the subsequent chemotherapy experience. In April 2013, we were blessed with the arrival of Baby Hope and are feeling very lucky. In October 2013, I was diagnosed with peritoneal disease and liver mets, which are inoperable and require aggressive chemotherapy.
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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It is a little bit out of date as the NHS doesn't tend to have a WiFi connection in hospital and I can only post when I get home and posts take a while to write.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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