Your results should (by April, I think) become available over the internet.
Have a read of this:
https://www.england.nhs.uk/ourwork/pe/patient-online/about-the-prog/po-public/
Sorry I disappeared. The last couple of weeks have been a real roller-coaster. A lump formed under my jaw a couple of months after my wife passed away a year ago. For 8 months every test said it was benign. In December I insisted that I wanted it removed which was done on 5 January. On 14 January I was called to a meeting with the consultant who had removed it. It was cancerous - limphoma a very bad, aggressive strain. Since then I've had bloods taken, more bloods taken (I didn't know I had that much in an arm); a PECT scan (they inject you with radioactive glucose!); bone marrow samples taken and an echocardiograph.
Today was results day. I'M CLEAR!
Thank God I had it out!
They are still going to give me half a course (3 sessions) of half strength chemo just to be sure. Unlike diabetics, cancer patients really do get their moneys worth - I'm not saying they shouldn't, but there is a contrast.
The point of my original message was that between the Monday (I ring up for the HbA1c) and my Thursday DN appointment, I do a lot of work poring over meticulously taken blood glucose samples, looking where it may have gone wrong (if indeed it did). Of course my DN gives me the figures when I see her. I could book into my GP and get them too. But relative to a simple number in response to my telephone request doesn't that waste their time? Without the number and my review of my results it just wastes my time!
As it happens I was at the chemo clinic before my Thursday DN appointment. I asked them and they gave me the figure. On Thursday I complained at length to my DN who bought me off with a new meterOn Friday next I'm with my GP, pre-chemo. Yes...
J.
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