Lookfar out of the water and cleaned off. It looks cleaner than it is. |
Saturday, 25 February 2012
Friday, 24 February 2012
Tuesday, 21 February 2012
Lookfar - March 2011 launch. Admire the crane. |
I am still fatigued - but perhaps slightly better. I am trying to tidy the junk in my flat. Unsure whether I will ever get to use Lookfar again - but intend to get her sorted out - incase - - - .
Saturday, 18 February 2012
Matilda in St Andrews outer harbour as the tide goes out. 2004 |
The horrible symptoms are due to fatigue - induced by a combination of the cancer and the chemo. I feel a lot better today and yesterday - but not leaping around yet. Thanks again for your good thoughts, cards, support and much else. xx
Wednesday, 15 February 2012
Tuesday, 14 February 2012
wolf fish - another metaphor (picture from J.J.Greenfield. Taken at St Abbs Head nature reserve. |
I am not sure what they are metaphors for exactly - whatever seems to fit. I find them truly hideous and therefore refer to my present condition. (BTW - they eat shell fish - not people.)
Update - still zapped-out. But part of it seems to have been a lung infection - I started anti-biotics a day ago. Obviously have enough energy to locate the fish!
Saturday, 11 February 2012
Friday, 10 February 2012
Wednesday, 8 February 2012
I did get into Ipswich hospital - (a bed came available) - in ice and cold on Monday evening - ready for the chemo on Tuesday.
Tuesday - a heavy day. The complex infusions started mid afternoon and ended at half-past midnight. The morning a nightmare of wondering whether it would happen and being seen by various (helpful) people. For example - a palliative care doctor. Exhausting. The afternoon and evening - a nightmare of boredom and exhaustion, especially as the machine that handles it appeared to malfunction - in fact it was the cannula - adding an extra 2 hours to the 7 that it takes in theory.
Today - I was released in the afternoon - after various tests. Good (if somewhat exhausting) to be home.
Tuesday - a heavy day. The complex infusions started mid afternoon and ended at half-past midnight. The morning a nightmare of wondering whether it would happen and being seen by various (helpful) people. For example - a palliative care doctor. Exhausting. The afternoon and evening - a nightmare of boredom and exhaustion, especially as the machine that handles it appeared to malfunction - in fact it was the cannula - adding an extra 2 hours to the 7 that it takes in theory.
Today - I was released in the afternoon - after various tests. Good (if somewhat exhausting) to be home.
Monday, 6 February 2012
I have felt actually ill for over a week and since my visit to the caravan cafe last week I have not been able to go out at all.
Add to that - I have yet to get chemotherapy (which involves an overnight stay) because there are no beds in the ward. I was hyped up yesterday for getting in and spent an unhappy day here instead - one of the darkest I have had. It seems as if it might take some time for a bed to be availabe - I guess I am in a queue - and meantime I still feel ill.
Add to that - I have yet to get chemotherapy (which involves an overnight stay) because there are no beds in the ward. I was hyped up yesterday for getting in and spent an unhappy day here instead - one of the darkest I have had. It seems as if it might take some time for a bed to be availabe - I guess I am in a queue - and meantime I still feel ill.
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