This is a repost from the UK Daily Mail, Link Below
The consultant smiled at Mum. ‘I just
 want to ask you a few simple questions, Rose,’ he said. ‘Are you 
ready?’ Mum beamed back at him.
‘Tell me, what year is it now?’ asked the consultant. My mother frowned. ‘Let me think’, she said. ‘Is the war still on?’ ‘Do you mean the Second World War?’ he asked. Mum nodded. ‘No, that ended in 1945,’ said the consultant. ‘What year is it now?’ ‘Then it must be after that,’ she replied. ‘It’s 2002,’ he said. 
‘Yes,
 that’s right,’ said mum, who would have agreed if he’d told her it was 
1812, and that Napoleon was running the country. I squeezed her hand 
gently.
‘Who is the Prime Minister?’ continued the consultant. Mum
 was on firmer ground here. ‘Margaret Thatcher, the milk snatcher!’ she 
announced triumphantly. ‘No, it’s Tony Blair now,’ he replied. ‘Oh,’ 
said Mum. ‘I don’t like him.’ The consultant had stopped smiling. ‘I think we need to do some tests,’ he said. 
Alzheimer’s
 disease is the only medical condition that I know of which affects the 
family of the patient more than it appears to affect the patient 
themselves. If you break your leg, it’s your problem. You sit at home in
 plaster; you suffer and you deal with it. Your family have to fetch and
 carry for you a bit, but that’s it.
Alzheimer’s disease is the only 
medical condition that I know of which affects the family of the patient
 more than it appears to affect the patient themselves. If you break 
your leg, it’s your problem. You sit at home in plaster; you suffer and 
you deal with it. Your family have to fetch and carry for you a bit, but
 that’s it.
With 
Alzheimer’s, it’s the other way round. You behave as though nothing has 
changed, while everyone around you has to deal with the dramatically 
different person you’ve become.
‘It’s
 like rolling up a rug,’ the consultant had told me. ‘The end of the 
carpet nearest to you represents the present, and the other end 
represents your mother’s childhood. As we begin to roll up the rug, 
starting from the front, the memories inside the roll are erased and 
lost for ever, and her reality slips backwards in time. The more we 
roll, the further back in time Rose has to travel to find a point in her
 life that she remembers.’
I’d
 nodded slowly, trying to understand. So that was it, he seemed to be 
saying. Looking back on it now, I am convinced that my mother’s dementia
 began the day my father died.
My parents had been married for more than 50 years, during which time they had never been apart. 
Mum
 had nursed my dad devotedly through his final illness and when death 
eventually came, she had gone into a deep shock. It had been a difficult
 period for me too, with my own marriage coming to an end at the same 
time. 
Which was why I 
found myself, a year after Dad had gone, sitting in Mum’s kitchen and 
asking whether I could move back in with her. ‘Oh, that would be 
lovely!’ she cried. ‘We could have tea together every day!’
I
 hadn’t realised quite how much the dementia was starting to ebb and 
flow in her mind — already much worse than when we’d seen the consultant
 just a few months before. But once I’d moved back in, filling my 
childhood bedroom with the remnants of my marriage, her decline became 
all too apparent.
I stepped out of the shower one 
morning to find my bath towel cut into a series of neat strips, about 12
 in all. ‘What’s happened here, Mum? I’d called, holding the pieces up 
for her inspection. 
‘Ask Aunt Peggy,’ she said. ‘That’s just the kind of thing she’d do.’ ‘Aunt Peggy’s been dead for years,’ I replied.
 Mum looked at me if I’d hit her. ‘How could you say such a thing?’ she 
said, tears springing to her eyes. ‘I spoke to her only yesterday.’ 
That
 was the brutality of ignorance on my part. Later, when I understood a 
bit better how Alzheimer’s worked, I’d be much more tactful. 
Another
 time we’d been getting ready to go out and I’d told Mum she needed a 
coat. Like an obedient child, she went and got a lovely dark blue 
cashmere affair from the hall; I remembered my father buying it one year
 for her birthday. 
‘Now can we go?’ she said.
 I turned to look at her. The stitching around the left shoulder seam of
 the blue coat had been unpicked and the sleeve completely removed. 
‘For Christ’s sakes, Mother!’ I exclaimed. ‘It’s only got one f***ing sleeve!’ ‘Don’t you dare swear at me!’ she yelled back. ‘You wait until your father gets home!’
It
 took me a long time to understand why Mum kept cutting everything up. 
But I finally found out that Alzheimer’s sufferers will often continue 
to carry out their once-familiar tasks as a way of anchoring themselves 
in the confusing sea of their new life.
Mum
 had been a seamstress all her adult life, so that when she found 
herself chopping up towels and clothes, in her own mind she was back in 
her  workshop, cutting up fabric for curtains and bedding.
Then,
 and many other times in the years I looked after her, I realised how 
often there is a perfectly simple explanation for the apparently 
inexplicable. It was around Christmas that year when I came home one 
evening to find Mum watching TV with a huge, headless bird in an 
armchair next to her. Its enormous drumstick legs were pointing 
downwards as it defrosted, creating a huge puddle on the chair seat.
‘What’s this, Mum?’ I asked.
 ‘It’s our Christmas turkey, of course,’ she replied, as though I were 
an idiot. ‘I bought him from the supermarket this morning. I couldn’t 
resist him.’ 
I read the label on the creature’s 
leg. ‘Giant Christmas goose,’ it announced. ‘Will feed 12 people’. We 
were just two for Christmas dinner. The day before Christmas Eve I’d got
 home to find all my socks pinned to the walls and ceilings of the 
house. ‘I’ve been putting up the decorations,’ cried Mum, dancing into 
the hallway.
And then 
there was the imaginary Irish band. I can’t remember quite when they 
appeared, only that there were six of them — an accordion player, a 
couple of guitarists, a violinist, perhaps a banjo player and a singer 
called Michael who had a lovely voice, according to Mum.
I
 was so grateful to those lads. They would keep Mum entertained for 
hours, her foot tapping and her body swaying as she listened in her 
imagination to the music she’d adored as a little girl growing up in 
Dublin.
And how she 
loved to look after those musicians! Whenever she made herself a cup of 
tea, which was often, she’d pour one out for each member of the band as 
well. It was the same with the sandwiches. 
As
 the months went by, I’d often get home to find every cup and plate in 
the house in use, with at least eight cold mugs of tea scattered round 
the house and plates of uneaten sandwiches everywhere. At one stage we 
were getting through several loaves of bread and three pints of milk 
every day.
One evening,
 when we were watching TV after supper, I saw Mum lean over and look at 
the radiator at the back of the living room. 
I
 watched as she smiled lovingly at it, and nodded once or twice. Her 
lips moved as though she were saying something, and then she nodded her 
head again.
‘What are you doing, Mum?’ I asked, gently. Her cheeks flushed in embarrassment. She shook her head but did not reply.  ‘Why are you talking to the radiator?’ I persisted.
‘She’s
 asked me not to say anything!’ exclaimed Mum, her eyes filling with 
tears. ‘It’s the little girl in the radiator.’ Tears were pouring from 
Mum’s eyes now. ‘She’s all alone in there,’ she explained. ‘She’s 
trapped and she’s frightened, and I don’t know how to help her.’
I went across the room and put my arm around her. She sobbed into my shoulder. ‘What can I do to help?’ I whispered. ‘You could let her out!’ she cried, and the tears came again. ‘Tell her I said it’s OK, she can come out,’ I replied.
It’s
 funny how easily you can get caught up in another person’s delusion. 
After that night, I found myself talking to the little girl in the 
radiator with Mum on many occasions.
I
 have no idea whether doing this was good for her mental wellbeing or 
not. A psychiatrist might say that I was strengthening the delusion by 
playing along with it, but what was my alternative? At least this way we
 were sharing precious time together. And for me, that had to be a good 
thing.
But things were 
worsening fast. ‘I’m off now!’ she called up the stairs to me one night,
 after putting on her raincoat, headscarf and gloves. ‘See you later.’
I knew she was going nowhere —her 
behaviour had been getting more and more erratic lately, and I was 
having to keep the front door locked and hide the key. ‘It’s quarter 
past three in the morning!’ I shouted, pulling the pillow over my head.
‘I have an appointment at the hairdresser’s!’ she shouted back. ‘I can’t get out!’ ‘The hairdresser’s doesn’t open for six hours,’ I yelled. ‘Go back to bed!’
 Half an hour later, Groundhog-Day-style, Mum was back by the front 
door. ‘I’ll see you later!’ she called, rattling the handle all over 
again.
With 
Alzheimer’s, it’s not just the patients that go crazy. But it was only 
when a friend found Mum wandering the streets at five in the morning 
wearing only her nightie and with a pair of broken sandals in her hand 
that I knew something had to be done. The truth was simple: I just 
couldn’t cope.
I wasn’t
 in the house often enough, or long enough, to supervise my mother 
properly. Even when I was there, like now, she still wasn’t safe.
That
 afternoon, with a heavy sense of defeat and shame, I telephoned the 
social worker who had contacted me when mum had first been diagnosed. 
‘I’ll come out next week and have a chat,’ she said cheerily.
A
 few weeks later, after she’d been moved into a home, the staff advised I
 leave Mum a few days before going to visit her for the first time. 
When I did arrive, I found her wandering along a corridor hand in hand with an elderly male patient.
‘Storm’s coming up,’ he announced. ‘Going to be choppy.’ I later learned her new companion had been in the Navy for years. 
Mum broke into a huge smile. ‘I have something to tell you,’ she said. ‘I’m going to have a baby!’
For
some people, this sort of announcement might have been a  shock coming 
from their 80-year-old mother. But I’d been looking after Mum far too 
long to be surprised by anything.
‘Jesus,
Mum!’ I said. ‘You’ve only been here a week!’ ‘Terry and I are going to
call it Martin if it’s a boy and Peggy if it’s a girl,’ Mum continued. 
‘We’re very happy, aren’t we Terry?’
And so began a whole new chapter in 
Mum’s life, and mine too, as she moved between a succession of care 
homes and hospital wards.
But,
 the little girl in the radiator remained as firmly rooted in Mum’s 
consciousness as ever. Dropping in on her one evening, I found Mum 
kneeling in front of the radiator in her room with a box of chocolates 
on the floor in front of her. She was holding out a chocolate to the 
radiator, apparently trying to give it to the little girl.
‘Is she still in there, mum?’ I said. ‘She can’t get out,’ replied mum, over her shoulder. ‘She’s just lost in the dark, and she’s confused.’
 ‘Do you think she’s ever going to come out?’ I whispered. Mum looked at
 me, sadly. ‘I don’t see how she can. She comes from Dublin, you know. 
But she can’t ever go home, not now.’
‘What kind of things does she tell you?’ ‘She tells me how kind to me you are. She knows all about me, and I know all about her.’ ‘You’ve become very close then, you and this little girl,’ I said.
‘We’re
 the same,’ replied Mum, simply. I felt a lump swell in my throat as the
 penny began to drop. ‘Do you know her name?’ I asked, although I 
already knew the answer. 
‘Her
 name is Rose,’ replied mum. The last piece of the jigsaw had finally 
snapped into place. ‘She’s you, isn’t she?’ I whispered, my eyes filling
 with tears that I could not hold back. ‘You’re the little girl in the 
radiator, aren’t you?’
I
 thought my heart would break. I now knew why this delusion above all 
others had persisted through the years, and why the image of a small 
child, alone, frightened and abandoned in the dark, was the perfect 
description of the effects of Alzheimer’s itself.
I
 put my arm around Mum and she put her head against my shoulder. We both
 started to sob. We stayed there on the floor of her room for a long 
time like that, just holding each other.
I
 drove home that night with my soul in shreds. A deep understanding had 
been forged between my mum and me that day. I felt I might be able to 
reach her now at some deeper level, and that there was a new future for 
our relationship.
Sadly, it was not to be. Just days later Mum suffered a severe stroke, followed by two more. On 15 November, 2007, five years to the day after Dad’s death, I got the call to say that she’d gone.
 A few days later, when I stood at 
the graveside, I couldn’t help but smile as I remembered the mum I’d 
loved so much. I thought about the forest of socks pinned to the ceiling
 and walls. 
I thought 
about the giant Christmas goose. I thought about Michael and the Irish 
band, and how their ballads and jigs had transported Mum back to a 
happier, more romantic time.
And
 then, in my mind’s eye, I saw the little girl, standing on the other 
side of the grave. I recognised her straight away from a much-loved 
photograph of Mum. She was six years old or so, in a pretty pink dress 
with a matching bow in her hair, and clasping an armful of teddies.
There
 she was, little Rose, bejewelled with the magic of childhood. Here was 
the little girl, shining and new, before that vicious thief, 
Alzheimer’s, had stolen away her future, leaving her alone and 
frightened in the darkness.
She smiled, and waved, then she turned, and was gone. The little girl in the radiator was free at last.
- Extracted
 from the Little Girl In The Radiator by Martin Slevin, to be published 
by Monday Books on August 6 at £9.99. © 2012 Martin Slevin.
 
 
 
 
 
Taken from UK Daily Mail 
 
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