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votes are in, and well its not good news.
cancer in liver,spread to lungs
treatment= no treatment.
life expectancy months if lucky
was told to expect him to go downhill within the next couple of weeks
My life is shattered, he is my dad, and he is dying
A part of me died today as well.
HGello all
This is the third blog of my new fight with cancer,todat the District Nurse came,and then a little while later thy Physio came and she showed me some Breathing exercises and some others about getting out of the bed/chair saftly,also some other exercises to strengthen my leg muscles,I found it all very helpful even though after she left i found my self really hurting and having to lay down for a while she said that i probabaly would,,I cant wait to get some information on the meeting...
Phew, Ok In three and a half hours time, we will know for sure what it is and what they can do about it.
Endoscopy last week, drs reported a normal pancreas,normal bile ducts,Lyphomatous nodes not carcinomatous,6Cm diffuse mass adjacent to liver region
presuming they took biopsy of the liver mass,but report didnt go into details of where the biospy was taken.
Dad now doesnt believe it is cancer as he thinks they would had him in by now and "cut it out" Im thinking he may be slipping...
Evening All,
For me I have to say that the hardest part of this whole shitty journey is the fact that nearly three months later I am still completely confounded by the whole thing. I am suspended in this foggy painful disbelief that makes moving on completely impossible. It sounds normal doesn’t it – ‘oh, she’s in shock poor dear how could she comprehend such an awful thing’ but it feels different in reality, not nearly as simple and clean cut.
When someone you love...
It was lovely for the weekend to get away from all this "stuff" not that we had a quiet weekend. The bit I hated was when people ask you how you are getting on and you have to go over all the details. I skipped over them as I have to think about them in the week but wanted the weekend free of it all. I know they are being nice of course, but none of them, unless they have been here, will have the faintest inkling of what it's like.
Hubby did his gig without nerves which I am so, so...
I've used the same title to enter a discussion in the Prostate Cancer Group. Although my last blog entry was upbeat I now have worries for the future of this home with my wife and myself struggling to cope in it.
My pain is better from the pelvic fracture, I can walk about the house with one crutch, not two, so I can carry things in the free hand. But my wife is becoming much worse with joint pains and she sleeps a lot by day. We are due to see her consultant tomorrow and I'm going along with...
hello again,
i am finding this blog a lot of help as i can get out all of my thoughts and feelings,plus what happens when it happens,the mac support people contacted me again this afternoon,one to say that they had had the multi decipilnary meeting about me but due to the fact that they had not got all the information then they were going to have a meeting about me tomorrow,then the other support nurse phoned to say that,they are arranging for me to have a meeting with the physio to help with...
26/11/2013
hello again well i said that i would keep you all posted as to how things are going,the macmillan nurse came today she talked for over an hour trying to find out how was best to help me,well the first thing that she has told me to do is to up my morphine dose to sixty mg twice a day ,and try to help to hold the pain she also said that she will go see my drs and find out what went on in the multi decilipanry group meeting,and said that she would phone me later this afternoon.
so...
