Over 2 hours in clinic as they were running late and one consultant got called up to ward for something. Sister had to go and get him back. Sitting really worried wondering what was happening and trying to keep strong for Mr Mog. Everyone called in except us, we were last. Went in to be told had spread to bones, no more info as they hadn't had a meeting to discuss results and treatment. They will do that this Friday. We have to go back next Wednesday for full explanation and treatment options. I asked why they hadn't rung us to postpone meeting rather than keep us worrying and waiting. They couldn't answer that.
So another week of worry before the full details are known.
Keep a positive thought for Mr Mog please
The musings and meanderings of a mixed media artist and yarn junkie who loves to knit,spin, crochet, make a mess, write and enjoy life. I try to follow the wheel of the year and enjoy each day of it. My art reflects that spiritual journey.
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18 comments:
Of course. Lots of positive thoughts.
We are so sorry.
You know where we are if you want a chat, bugger about having to wait for news...
much love Sue & Neil xxx
....thinking you both....
you are both in my thoughts....
I've had a delay a couple of times there....they are always very good about it. Sorry to hear your news.
Thinking of you both...
Oh my dear, lots of love and thoughts to you both. Please pass on love from me and Mark.
I am thinking of you both.
I am thinking of you both.
Sending Mr. Mog lots of white light and good wishes. What a stressful time this must be for you both. Hugs, many hugs.
Methinks this isn't good enough.
I am so sorry you ave had this experience at such a crucial time.
Are you in touch with your local Macmillan branch? If not, do you think it might help speed things up? They usually have excellent connections - and if the Team are meeting on Friday and have mesed you about this much, then I think the least they can do is for one of them to find a few minutes to see you on Friday, rather than make you wait until next Wednesday... Macmillan should be able to facilitate this where you as patients won't be listened to. Also, I think their support right now might be a very good thing.
I think your nearest one isn't that near - Blackpool probably:
http://www.macmillan.org.uk/HowWeCanHelp/LocalInformationCentres/MacmillanInfoCentres.aspx
Or try their helpline: 0808 8080000
I have checked for you, but there is no NICE guidance on procedures at these times, and no up-to-date guidance on prostate cancer metastasising (2002 is the last, and 9 years in cancer research terms is a very long time).
Thinking of you, and do let me know if there is anything at all we can do to help.
So many hugs and healing thoughts for you all xxxxxxxxx
Positive thoughts on their way for both of you.
so sorry to hear, thoughts are with you both.
Mr BW
Well... my FL's cancer has always been in his bones and it's been 4 years now, so don't assume the worst, please! There are new drugs being developed all the time. I agree that the waiting is always the worst thing. The not-knowing is so hard. Hugs and more hugs.
Sending lots of positive and healing thoughts to you both, love and hugs xx
As soon as I heard this I went down the garden and rubbed the trunk of our Yew Tree.
Thinking of you both.
sending hugs and healing energy....
We're thinking of you both and send out love
Rosie & Graham x
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