Last
week I started a deliberate project of being thankful for small things, because
so many of the big things seemed out of my hands.
Also,
I just got so sick of being permanently angry and complaining, so worn down by continual
difficulties and obstacles, that I felt utterly defeated. What was the point of all this effort?
I just started expecting the worst. When that
happens, you become brittle, angry and permanently on the defensive. Even when
you truly believe that the next transaction will go smoothly, it’s as if you
give off an invisible signal inviting trouble. I can’t help thinking that the
expectation of conflict can become a self-fulfilling prophecy.
There
had to be another way to deal with it all.
I
made this list of reasons to be grateful to Nick’s carers, and it was an
interesting thing to do because I started appreciating them more.
I am grateful that they
come three times a day to give Nick his tablets so he gets the regular
medication he needs.
I am grateful that they
nearly always make his bed nicely.
I am grateful that
their visits break up his day when he might otherwise be alone.
I am grateful that they
feed the cat.
I am grateful that they
are (mostly) reading the menu book now and following the food preparation
requests.
I am grateful that they
do the washing up and vacuum the carpet.
I am grateful that they
are starting to put card and plastics etc. in the recycling bag.
I am grateful that it
takes some of the load off my shoulders.
I am grateful that Nick
seems to like them.
I am grateful that
things seem to be gradually improving.
Have
they suddenly picked up their feet and transformed magically overnight? No, not
really. When I visited yesterday evening they had not switched off the washing
machine or taken the damp clothes out and hang them to dry, as politely
requested the night before.
They seem to have a problem with giving Nick a pudding (which I have called by various names, “dessert” “sweet” and even specifically named, “chocolate mousse” or “trifle”, all to no avail)
It just seems to be an alien concept to them.
They seem to have a problem with giving Nick a pudding (which I have called by various names, “dessert” “sweet” and even specifically named, “chocolate mousse” or “trifle”, all to no avail)
It just seems to be an alien concept to them.
He
has developed a really sweet tooth over the last couple of years and craves
chocolate; left to his own devices he would polish off a four-pack of Snickers
bars after tea every night. It’s weird for me to see this when chocolate bought
for the children used to sit mouldering in his cupboards for months at a time
because he just wasn’t bothered himself. Now he loves it, but those big chocolate bars
are a choking hazard as well as terrible for his teeth.
Luckily
he also loves sweet, creamy desserts, which are actually something that
dieticians recommend for HD because they are calorific and easier to swallow.
So
we buy lots of these and I write it in the menu book every time asking the
carers to give him a dessert after his main meal but it’s hit or miss whether
he gets something or not.
One
day last week I saw the lunch that they had prepared for Nick with a slice of
blackcurrant cheesecake nestled carefully in the same bowl as his fish pie and chopped broccoli.
I
had to add something to the list:
Just when I thought I
had seen it all, I am grateful to the carers for surprising me.