Lonely

Good morning like you said, I find the message platform hard. Loss of memory is hard especially went it so good before. I really I’m my kids to tell me how it all started and how, apparently was in hospital for three months. Was allowed to come home with a three months to live diagnosis. That was over three years ago. I think that’s also a reason for my wife to leave, go and live with one of her x boyfriends who’s wife just kicked him out. I cannot help thinking me out living my 3 months put a big spanner in her spokes. 
But starting to come terms with it and get on with my new life. It would be nice to communicate with you  Listen to your diagnosis and how you are coping with it.

Graham

Morning... I TOTALLY get it!!! I've just sent you a friend request

I think I’ve accepted, that is just another problem all this technology is getting harder all the time. Just taken five minutes to get back to this page. Plus my spelling is a problem, get a carer twice a day for a hour. But at the moment can get around my new flat with an aid walking stick, manage to cook and keep my flat clean. While I can do this I will, good to hear you are still working. I’ve had to give this up and driving. That’s why i rely on my kid to come and take me out, plus my six grandchildren keep me going.

Yes... I find getting round this site impossible with brain mets!! And my spelling and math is really bad! 

Sorry I meant I'm not working - being retired off this month.

Well done tho for managing life at home - I find domestic tasks really difficult and needed a cleaner... more costs!/money spent due to cancer hey 

Like you got a list of drugs to take, at the moment they seem to be keeping things in check. My consultant at the last scan said it’s not got any bigger, but his last words were it will and went that day comes it will be goodnight Charlie. 
Hope you are well, getting used living with this disease. Living now on benefits etc. 

Hi We me , so sorry for your loss, this horrible disease hopefully your husband will be at peace now. 
I still struggle with the web site and how it all works. All the best wishes for you and big virtual hugs for supporting your husband through this difficult experience.

Hopefully we can talk via this site in the future.

Thanks, One2many. 

I still plan to continue as a community champion even though G's journey ended last year. If sharing anything from our journey can help someone else then I'm happy to do so.

take care

love n hugs

Wee Me xx

Hi we me 

Good news that you are carrying on with helping others. At present I find my life has stopped and waiting for it to take me. Feel a burden for my family especially after wife has left. She has come up with a good story to tell people why she left, she knows I can’t remember anything for how all this started . I know at present can look after myself and cook, clean etc. Got a care company coming in twice a day, at present I’ve tell them to come have coffee and a good chat. Some of the ladies have been with me since I came out of Hospital. Hopefully we can chat on here.

All the best GT1/ one2may

Sorry it’s. late , how things for you. Been hailing trouble with catheter, nurse has been and fitted a new one. That’s another thing the cancer has affected. It’s good to have someone to talk too, that’s going through the same process. 
Talk again tomorrow?

Sorry I’ve not been in touch , have horrible cold plus another scan to see the mass on the other side of my first tumour was not waking up. Thankfully it showed everything was the same as last toy. Plus this website is horrible especially