It was the summer of 2011. After many years of struggle, I had finally
accepted that mum’s dementia had progressed to a stage where I could no longer keep
her safe at home; encouraged by the social worker, I had found her a
residential place. But as mum believed there was nothing at all wrong with her, how could I persuade her to move?
I had spent the August
Bank Holiday with her at our family home as usual, but had returned to London
to make the final arrangements. This
might seem odd, given that the care home was in mum’s town; but I could not
visit it openly (or indeed go out by myself at all, except briefly to the shops),
neither could I use the computer or phone in mum’s presence, because, if I were
out of sight for even a moment, she would come looking for me, and would
interpret any outside communication as suspicious. She’d had paranoid symptoms for years; it was
a horrible irony that I was now really plotting behind her back.
I needed to wait a few
days to speak to the unit manager at the home, who was away on holiday. I was also waiting for the psychiatrist to return,
in order to assess mum’s mental capacity for my Court of Protection Deputyship application. This would give me legal
authority to manage her finances, which I would need to pay the care fees. The psychiatrist and I had agreed that I
would always stay away when she visited, so that she could see how mum was on
her own, and so that I would not be associated in mum’s mind with any unwelcome
professional approaches. She would usually
visit with Jenny, the independent care-worker mum liked, in order to maintain her trust.
A couple of days before
this visit was due, I was disturbed to receive a phone call from an old friend
of mum’s, whom she had not seen for a while. This friend told me that mum had
rung her out of the blue, and said some very strange and upsetting things. She did not go into detail, but the fact that
I never heard from her again, despite continuing to send Christmas cards, good
wishes, and letters of explanation, suggests that it must have been something
extremely offensive.
The psychiatrist’s visit
passed apparently without incident, although she did call me at the time to ask
some background details, such as whether our dog and various relatives were
dead; as so often the case, mum presented well verbally and socially, but what
she said and believed was highly delusional – something you would only know by checking the
facts.
I was reasonably assured
that all was proceeding to plan. The
next day, Jenny reported that she had looked in on mum and supervised her
eating an early supper, so I felt it was safe to go out for a few hours with
friends. Little did I know that mum’s
symptoms had been building to an acute psychotic episode…
It was on my way home that
I received a call from her Aid-Call alarm service, asking me to ring the
police, who were at our house. At the
time, all they could tell me was that some neighbours had found mum in distress
and called the police to take her home. It was not until later in the week that I learned the full story.
Desperate to find someone
to stay with mum until I could get there, I rang round her close friends and
next-door neighbours, who had often helped us in crisis – but they were all
away. Social services out of hours were
also unable to help, and I could not contemplate sending her anywhere alone in
an ambulance.
By this time, it was
nearly midnight and I knew I was over the alcohol driving limit, but even so, I
would have set off there and then, had I not needed to speak to the care home
manager the next morning, when she was due back. I knew that once I returned to
mum’s, all verbal communications would be impossible.
I shall never forget the
despair of that night, lying awake waiting for daylight, fearful that mum might
go out again in my absence and come to grief. In the morning, as soon as I had spoken to the care manager, I set off,
stopping at the petrol station to stock up on food, as I would not be able to
leave mum to go out shopping unless someone could sit with her.
En route, I also spoke to
the social worker and updated her on events. When I arrived, I found all the curtains drawn, every light in the house
blazing. In the living room, a cold cup
of tea and plate of toast that I had asked the kind policemen to prepare the
night before stood untouched on a side table. There was no response to my arrival.
I found mum upstairs in
bed, totally inert. Momentarily alarmed
that she might actually be unconscious, I woke her. She looked at me with no curiosity, as if
nothing had happened and I had been there all along.
For the rest of that week
until the date of her admission to the home, we were both prisoners in the
house. I had arranged for Jenny to come and sit with mum, while I went “to the
shops” – in reality, an appointment at the care home, to go through paperwork
with the manager. It was a nauseatingly stressful round-trip of a couple of
hours, culminating in a frantic “supermarket sweep”, as I had to return with
goods to support my cover story.
As the days ticked by,
tension mounted. How, how could I ever raise the subject of the impending move
with mum? Slipping out for another
supermarket trip (covered by the next-door neighbour), I called the home from
the car park. The room, they confirmed,
would be vacant in a couple of days; ready when you are. Amid the groceries, I had stashed away
toiletries and make-up for mum’s sponge bag; it seemed so pitifully underhand
and final. I broke down and sobbed in my car, as boisterous children scooted by
on trolleys and mothers loaded their weekly shop. I have lost count of the car-parks and lay-bys I have now wept in.
So how did I do it? What did I say? In the end, it was mum who raised it first.
Watching TV in silence, she suddenly turned to me and said: “What’s going to
happen to me?” It was a heart-stopping
moment. How did she know? What did she know? It seemed that somehow, despite having no
reasoned knowledge of the situation, she sensed that she was in crisis and that something was afoot. How could I answer? I had never lied to her, but neither could I
explain the full truth.
“I think you need to go
somewhere, where you can have people around you”, I said. “People to keep you company when I’m not here
and look after you at night, when you get frightened.” “I don’t get frightened”, she said, despite
having repeatedly told me that she was, without ever really knowing why. Miraculously, we managed to have a tentative
discussion along these lines and she didn’t go berserk at me, as I had feared for
so long - although there remained an uncomfortable silence at the end. I was hugely relieved to have it out in the
open at last. And yet…
By the time I had put the
kettle on to make a restorative cup of tea, the whole tortuous conversation had
of course been forgotten. I would have
to broach it again the next day – the very day of the move.
That night, as I lay curled
up, weeping, in my bed, mum opened the door and looked at me, strangely
dispassionate, more bemused than upset.
“What’s the matter?”, she asked.
“Why are you crying?” What could I say?
That this was our last night together in our own home? The house we had moved into in Christmas 1973, when it was new and my father was still alive? Her last night in the outside world? The beginning of the end of a relationship
that had started with my birth?
Impatient at my inability
to respond, she chided: “Now come on! Stop
that.” Then: “I love you, you know. As if you were my own daughter.” As if? Then who did she think I was? Were we strangers already?
On the day of the move, I
surreptitiously packed an overnight bag, as instructed by the manager - best
not to take too many things at once, you can bring in more once she’s settled –
and put it ready in the back of the car. Mum came downstairs at lunchtime; I made us something to eat.
I had forwarded her “life
story” information (material facts, key events, likes and dislikes) to the home
from my phone, filling in the form in my bed overnight. Far from ideal, but the
best that I could manage in the circumstances. I had emailed the social worker to ask if she
could stand by to come with me if needed, but she had to be in a meeting that day. All that remained was to get mum into the
car.
After lunch, we sat in
silence, while I steeled myself to come out with it. And once again, mum took the lead. “What are we doing?”, she asked. “We’re going to look at this place”, I
replied. “What place?” “A place for you to stay in the week, when
I’m not here. Where they can take care
of you… Shall we go then? Just have a look? We can have a cup of tea…?”
And that was my biggest
lie. The only way I knew, to do what had
to be done. “Just a look… Just a cup of
tea…” When I knew it was forever.
She let me zip her into
her jacket and got into the car. The
staff, from the manager to the receptionist and finance controller, had been primed
to greet her as a visiting guest for tea.
I took her upstairs to the unit at tea-time, and, as instructed by the
manager, waited for her to be distracted in conversation, and slipped out
quickly without any fuss. Just like a
mother, taking a little child for her first day at school.
A move into residential
care is at least as much a watershed for the family carer, as for the person
with dementia – and the grief arguably greater, for we know the full story of
loss. No-one does this lightly. One might consider it similar to abortion: a
choice you make when it has become the only viable option. A similar stigma, maybe.
To carers, I say it may
seem an impossible decision, an overwhelming task. But sometimes you have to face it and you can survive.
To parents, I say please,
please don’t elicit impossible promises from your children; have the courage to
confront your own mortality before you lose capacity; have the discussions
while you can, be realistic, draw up power of attorney, put some plans of your own in place.
To everyone: don't fear care homes. The sector is woefully
underfunded and undervalued, yes; there are bad homes, true. But there are also many good ones and
wonderful people doing essential work to support the most vulnerable in
society. Don’t let’s stigmatise them. It
is not a fate worse than death.
Here are mum and I, as I
prefer to remember us, about twenty years ago, outside our home, now sold to pay mum's fees. (Not, by the way, a
“mansion”, as so often assumed of those liable for 100% self-funded care at circa £1,000 per week, just
an ordinary suburban house.)
So if anyone thinks it’s
easy to “put your mother in a home”, read this back. Imagine all those lonely years, when I had
dreaded having to break mum’s trust in me, her only child. I did it to save her. She is still alive today. I have no-one
left.
It will be a long time, if
ever, before I can think of August as a happy holiday season.
(This two-part post - read part one here - is a companion piece to an earlier post concerning the issue of "truth-telling" in dementia care.)
(This two-part post - read part one here - is a companion piece to an earlier post concerning the issue of "truth-telling" in dementia care.)
This is one of the most moving things I had ever read - thank you so much for having the courage to speak out about what clearly was an incredibly hard decision for you. When the time comes for me, as I know it will, to look at longer term care options for mum I will return to this piece and find strength from it. I'm sure it can't have been easy to write but sharing these experiences will help a great number of people in similar situations.
ReplyDeleteThank you. Yes, I had intended to write about this some time ago, in relation to the post '"Truth" or "Lies"?', but it is a painful episode to dwell on. I returned to it this week, because I had been discussing the issue of truth-telling again on Twitter, the novelist Penny Hancock had written a piece in the Independent about her experience of looking for a care home with her mother (link in 'My Biggest Lie: Part 1') - and because it's that time of year again.
ReplyDeleteWhen I was going through this, I found Alzheimer's Society Talking Point Forum useful for other first hand accounts of the same dilemmas. No-one has the ideal answer, but it can at least help to know that others have been there and survived it.
My advice would be a) don't wait endlessly to get support, in the hope that your loved one will one day be able to acknowledge and accept their declining capacity, as that may never happen; and b) don't leave it until you are already in crisis to start investigating care options. It's human nature not to want to think about this, but if there's a possibility that you may need to at some stage (as realistically there is for all of us), it is better to start the process when you have time to be objective about it and can make some advance preparations.
Thanks again. All the best with your journey.
Oh Ming, this is so sad and says such a lot about you. My story, as you probably know, is very similar. We too had to lie to my mum. But at least I had siblings to share the load (and the guilt). Well done for summoning the courage to write this. It will help others. Thank you.
ReplyDeleteThanks, Pippa.
ReplyDelete