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Cancer is a funny thing. It puts your life into perspective and in my world, a lot of good has come from it. I thought it might be nice to share the ‘Silver Lining’ of my dark days and this arduous journey.
https://theartofsuffering.wordpress.com/2015/02/15/silver-linings/
Liz
last throw of the dice, saw.my consultant last friday who conformed there plan,
wait till the end of march rescan and see if surgery is still an option, if not then not good, this is all very well having it explainec to me its the best plan as if they wait till march
they get all th active disease out in one go, trouble is thats in 6 weeks time, an awful lot can happen in 6 weeks time, like umpteen more tumors appear and what could of been curative surgery becomes no surgery
Can anyone tell me how and if it is possible to get a copy of my pathology report from the hospital as I was not offered it when I was diagnosed back in 2010. I am absolutely fine at present and would just like to see it for myself.
Since being diagnosed with Breast Cancer I have become a little obsessed with learning about nutrition and trying to use it as a tool to avoid the side effects of Chemo. So far so good... but I am always adapting it.
Since writing my initial blog about what I do on a daily basis to help myself, I have just updated it.
I am just about to have my fourth EC treatment.
Anyway I just thought it might help someone else - https://theartofsuffering.wordpress.com/2015/02/08/february-nutrition-take-two...
does the above seem a familar phase ? Yep im not syre how many times ive heard this said to me, i know the people mean well and dont know what to say , but really why that phase , i hate it i really do i mean what am i suppossed to do stay asleep till its all over? Tell the sun it cant come up any,ore to start a new day?
i have no choice but to get up eat, try and do things, wait for my wife to come home, maybe when it gets warmer we do more
any suggestions?
In case you didn’t see my comment attached to the previous blog post, I would like to thank all those who have commented so kindly on what I write. I am very touched by the support I am receiving here, especially from the other ladies in the AC group. Some have said that I’m ‘an inspiration’: I can’t say that I recognise myself in that description, but if I do inspire others that can only be a positive thing. I simply say it like it is. Now, I must warn you that this...
you guys on this forum must be getting fed up with my winges, but i am a tad worried, upset and scared, back in april i was worried but optemistic that i would get though this ordeal and go on to get on with my life with out the prospect of a terminal verdict, in june we knew it was a challenge as for some reason they decided not to give me a chance at a third collection of stem cells, but straight to hdc whoopie i thought i skip an extra week of chemo, not relising it may of been better to have...
So I've been meaning to write here again for a while but as usual the stress of work started again and honestly, it's easier to try and avoid all things cancer when I'm feeling the pressure, despite the fact that it still seems to be everywhere. I'm not sure whether that feeling ever leaves you.
A couple of people I work with have had reason to consider the possibility of cancer and it brings it back to me when I'm trying to support them. I work in the health service and so there...
Well its now febuary and im still in cancer limbo land, well not exactly limbo land as i know i have a 5mm tumor in my right lung, well it was 5mm a month ago so by now would of grown, plus a very small spot in my lower left lobe, the thing is am i terminal or curable, i thought a month ago i was curable with surgery but the surgery has been delayed for at least three months, i have an xray next week and a follow up consultation will they tell me im terminal?
