Throughout
the 1980’s and 1990’s, as well as being a social worker during the day, I also
used to do shifts on the emergency out of hours service.
You
were pretty much on your own, based at home, receiving calls via a deputising
service.
We
received every conceivable type of request, ranging from referrals for child
protection, through to Mental Health Act assessments and requests for night
sitters for elderly people.
You
also got requests that were so out of the ordinary that they didn’t readily fit
into any category, and required finding solutions by thinking out of the box.
One
night, I was contacted by the local police about a couple of New Age
travellers, who lived in a traditional horse drawn caravan and would tour the
commons and heaths of the county, camping for a few nights at a time before
moving on.
They
didn’t bother anyone, always clearing up their site before leaving, and no-one
bothered them.
Until
one night. They had a fire in their caravan, and although they had managed to
rescue most of their belongings, and the caravan had been burnt out.
The
police were asking for assistance to sort them out with emergency accommodation.
This was complicated by the fact that they had two horses and a dog.
As they didn’t have any children, and could not be regarded as vulnerable,
social services didnot really have any
responsibility for assisting them.
In
any case, finding accommodation for a couple of able bodied people at such
short notice, late in the evening, was a non starter. And finding emergency
accommodation for two horses, not to mention a dog, was virtually impossible.
But
being a social worker, I still felt that I should do something if I could. It called
for some lateral thinking.
I had an idea. I consulted my file of useful resources that I had compiled over
the years, and started to make phone calls.
Eventually,
I got hold of a local voluntary organisation and had a chat with them. They
were able, and willing, to help. It was arranged that they would provide a
large tarpaulin and deliver it to the site.
The
travellers were therefore able to construct a bender using the tarpaulin and
remain on the common, at least for the time being. This meant that they could
also continue to look after their dog and their horses. Problem solved.
From the early 80’s to the late 90’s I used to do out
of hours standby duty sessions. I covered nights and weekends, in addition to
the day job.
It always seemed to be that the most extraordinary and
perplexing cases turned up outside normal working hours. Nigel was certainly
one of those.
One Saturday, I received a call from the Samaritans in
a town in the county I covered. They needed the help of a social worker. But it
wasn’t the sort of problem they usually dealt with.
Nigel had just turned up at their offices in some
distress. It took a while to coax the story out of him. They eventually
gathered that Nigel had been living in some sort of residential facility in a
county 150 miles away. They thought he had learning difficulties. He told them
one of the staff had shouted at him, so he had decided to leave. He had packed
a few belongings in a bag and left.
He went to the local coach station and got on a random
coach, which had eventually dropped him off in the town. Lost and upset, he had
found the first place that seemed to offer help.
My first step was to try and find out more about him.
If he had left a residential care home, then he would have been reported as
missing. I rang the standby service for the area he had apparently come from to
see if they had an alert out on him. Unfortunately, they were unable to tell me
one way or the other.
I decided I would have to see Nigel, and make an
assessment. If he appeared to be a vulnerable person, I would then need either
to arrange bed and breakfast for him through the local housing authority, or if
necessary, try and find an emergency residential placement for him until we
could return him to his home area.
When I arrived, one of the volunteers took me through
to a side room where Nigel was ensconced with a cup of tea, milk three sugars,
and a sandwich.
Nigel appeared to be in his forties. He was wearing an
anorak zipped up to his neck and had a round face and rosy cheeks.
“Hello,” I said to him gently, and told him my name.
He peered up at me through the thick lenses of his glasses. “I Nigel,” he replied.
I attempted to find out his full name, his address,
and a contact phone number. He told me the place he had come from, but was
unable to give me any other information.
“The bad man did shout at me,” he said. “I didn’t like
it. So I wanted to leave. I got a coach. I got off here. Here I am.”
I asked him if he had any sort of identification. He
shook his head. I asked him if he had any medication with him. He took a bottle
of pills out of his duffel bag and showed them to me. They were anticonvulsants.
They came from a pharmacy in the town where he said he had run away from.
I decided that we would have to look after him until
he could be returned to his home county. He seemed far too vulnerable just to
arrange bed and breakfast.
In those days I didn’t have a mobile phone, so I was
reliant on the Samaritans to let me use their phone. They were only too pleased
to help. They showed me into a small cubicle which contained a small desk, a
phone, and a chair.
I made some calls to the local social services
residential homes that specialised in learning difficulties. Eventually, one of the homes called back, confirming that
they would accommodate Nigel over the weekend, until further enquiries could be
made.
I
went to see Nigel and explained to him what was happening. This seemed to
distress him.
“They
won’t hurt me? They won’t hurt me? I don’t like it when they hurt me!”
He
stood up and picked up his duffel bag.
“I
go to the bus station. I get a bus.”
“It’s
OK, Nigel, nothing’s going to happen. You’ll be safe.”
He
eventually calmed down and allowed me to take him to the care home.
The
next day being Sunday, I rang the next social worker on duty and explained the
situation to them. They would chase up the local authority where he came from
and get some more information, and hopefully arrange for his safe return.
I
saw my standby colleague a week or two later.
“Remember
Nigel?” he said. “I got through to his local authority. I managed to speak to
someone who knew him. They knew him all right. He wasn’t missing – but they did
accommodate him in one of their care homes a few weeks ago when he turned up one
weekend saying that he’d run off from somewhere in another county a long way
away. That is, until they made their own enquiries – and got the same story.
Then they sent him on his way! Once we found this out, we confronted him with
it and he left, rather quickly. I wonder where he is now?”
There
is a postscript to this story.
A
couple of years later I was speaking to a social worker in a neighbouring
county. I told him the story of Nigel. He immediately recognised him.
“We
put Nigel up in one of our mental health care homes for about 6 months,” he
said. “Then we had a full psychological assessment done, and it turned out he
had a completely normal IQ and everything. Then he mysteriously disappeared.”
From
time to time I think of Nigel, traveling the country, turning up in distress,
like a lost person with learning difficulties, in need of care and shelter,
being taken in and looked after, at least until the truth about him was found
out, then moving on again. What drives someone to live their life like that?
He’s
not the only one who does it. I knew of another case, of a young girl,
apparently in her early teens, who turned up one day, wearing a nightie and
clutching a teddy bear, claiming to have been abandoned. She was placed with
foster carers for several months, until it was discovered that she was actually
25 and had the tenancy of a flat in another part of the country.
Does
it constitute a mental disorder, or is it simply a means to an end, a way of
being looked after without any responsibilities? How many are there like Nigel
and the “little lost girl”? And how many are so successful that they’re never
found out?
There’s a whole chapter in the Code of Practice on the transport of
patients to hospital. Two of the particularly cogent paragraphs are as follows:
17.3
Patients should always be transported in the manner which is most likely to
preserve their dignity and privacy consistent with managing any risk to their
health and safety or to other people.
17.17
AMHPs should agree to a patient being transported by private vehicle only if
they are satisfied that the patient and others will be safe from risk of harm
and that it is the most appropriate way of transporting the person.
I am of course familiar with these paragraphs. I have at times found
myself in situations in which it seems necessary for the AMHP to take the
patient to hospital themselves. There just didn’t seem to be any alternative at
the time.
In both of the following cases, in which I found myself, shall we say,
in difficult osculatory situations, the patient was not being formally detained.
In my defence would submit that the Code does not specifically advise on
informal admissions.
Let this be a warning.
Leroy
Leroy had a very long history of bipolar affective disorder, which was
frequently made worse by his fondness for amphetamines. I had had to detain him
under the MHA on several occasions.
On this occasion he had been an informal patient, but when allowed leave
off the ward, he had not returned. I was asked to visit him at home to check
him out, and see if he could either be persuaded to return to hospital, or
whether he might need formally assessing.
I went out with Pam, one of the CMHT nurses, and knocked on his door.
He immediately opened the door and was unusually welcoming.
“Thank God you’ve come!” he said. “It’s terrible – the TV’s talking to
me, and I can’t stop it! I’m begging you, please take me back to hospital!”
We couldn’t really argue with that, and made the decision to take him
back straight away.
However, during the journey back, in which I was driving, and Pam was
sitting next to him in the back, we began to regret this decision.
Leroy was clearly very high, with marked pressure of speech. He was also
patently psychotic.
“Steve,” he suddenly said, for that is my name, “You’re scaring me.
You’re speaking with the voice of an alien from Alpha Centauri! Stop it
please.”
“I’ll do my best, Leroy,” I said, and decided not to speak at all.
At last we reached the hospital. I took him down the corridor towards the
ward, keen to get him into a safe place.
Halfway there, he suddenly stopped.
“I’m not gay, or anything, Steve,” he said, “but I really want to kiss
you. On the lips.”
With that, he put a hand round my throat and pushed me against the wall,
his lips wide open and his tongue moving rapidly from side to side like a conga
eel searching for prey.
I could suddenly see my whole life passing by. Could I survive a kiss
from Leroy?
I managed to extricate myself just as he was about to launch himself on
me, and hurried on down the corridor, with Leroy in close pursuit.
Once we were on the ward, I suggested that Leroy might need to be
detained under Sec.5(2), so that we could arrange a formal assessment.
Florence
Florence was a lady in her early 60’s. She, too, had a long history of
bipolar affective disorder. I had assessed, and detained her, on several
occasions in the past. Her typical presentation was to become hypomanic, with
grandiose ideas, and would spend money on irrational things.
Her long suffering husband called us, to let us know that she had “gone
off” again. I went out to conduct an initial assessment with Dave, her
community nurse.
Her husband met us at the door. He was a lot older that Florence, and
the strain was telling on him.
“She’s bought a first class one way ticket to the US,” he said in
despair. “She going to see the President to give him some advice.”
We found her in the sitting room, drinking a tumbler of sherry and
watching a pornographic video on the TV.
We politely asked her to turn the TV off.
“It’s just getting to the good bit,” she said, taking a large swig from her
glass.
We eventually persuaded her to turn off the TV. She abruptly got up and
wandered off into the kitchen. We followed her there.
She was quite plainly unwell, and her husband was unable to keep up with
her.
We tried to talk to her to assess quite how unwell she was, but she kept
jumping from one random topic to another.
I suddenly caught a glimpse of something peering out from the side
of their fridge. Curious, I pulled the fridge out to be confronted with a
fairly large furry animal, which looked up at me with appealing eyes.
“What is this, Florence?” I asked her.
“That’s my new chinchilla,” she said. “I got it yesterday. I was
wondering where it was. I’m planning to start a chinchilla farm.”
On this occasion, we managed to persuade her that it would be a good
idea to go to hospital. This time, Dave drove, while I sat in the back with
Florence.
Florence seemed to take a liking to me. She took off her shoes and put
her legs on my lap. Then she began to sing.
“Somewhere, over the rainbow, skies are blue...”
She continued to sing a medley of songs from 30’s and 40’s movies.
I decided to humour her with a rendition of my own. This was a mistake.
“You must remember this, a kiss is just a kiss –“
Florence looked at me with sudden affection.
Very well, my dear,” she interrupted, licking her lips, and without
warning lunged forward and planted her moist lips firmly on mine, attempting to
thrust her tongue down my throat at the same time.
“Need any help in the back there?” Dave enquired, seeing a commotion in
his rear view mirror.
On
28th May 2019 an inquest in Cornwall reported on the sad case of 23 year old
Amy Morby, who died as a result of an overdose.
She
had received treatment at the Emergency Department in Truro three times in 4
days in September 2018. A week later she died of a fourth overdose.
The
inquest reported that she was a patient of the local CMHT, and had also been
assessed by the hospital psychiatric liaison team. The hospital assessor stated
that Amy was treated at Treliske’s emergency department following deliberate
overdoses on five occasions during 2018, including three times between
September 2 and 6, just a week before she died.
He
said that: “She was not acutely mentally ill. Amy’s problems were psycho-social
stresses. Life was hard and she was going through a difficult time.”
The
manager of the Community Mental Health Team said the team were shocked by her
death as they did not consider the overdoses on September 2, 4 and 6 were
actual suicide attempts. It was concluded that Amy was probably suffering from
a borderline personality disorder.
There
is, unfortunately, nothing out of the ordinary in this narrative. Many people
suffering from a wide range of mental health problems make attempts to end
their lives, and some are successful. Mental Health Services do try to help
people at risk of suicide, but it is not always possible to achieve this.
Also
unfortunately, identifying that a patient has a “personality disorder”, in
particular, an emotionally unstable or borderline personality disorder, is
often used as an excuse not only not to compel treatment, but also to decline
to offer treatment.
However,
there was one sentence in this report that particularly struck me:
“The
inquest heard that Amy couldn’t be sectioned under the Mental Health Act as she
had full capacity and wanted to continue working with the mental health team.”
It
is not reported who said this in the inquest, but I know that many AMHPs would
disagree.
For
a start, I am reminded of the case of Kerry Wooltorton, who I have written about
several occasions on my blog. She was allowed to die in hospital after drinking
antifreeze, on the basis that she had made an advance decision to refuse
treatment. The coroner in her case stated: “Kerrie had capacity and she could
not therefore be treated”.
As
I have said before, it is not uncommon to assess someone under the MHA who is
either seriously planning suicide, or has taken an overdose of a noxious
substance and is refusing treatment.
Capacity
is not an essential factor in these assessments. Nowhere in the MHA is capacity
mentioned in this context. The requirement is for someone to have a mental
disorder within the meaning of the Act (which is very broad), and to be in need
of assessment and/or treatment.
Detention
under either s.2 or s.3 MHA would then provide a legal framework to provide assessment
and, if necessary, treatment against the will of the patient.
This
is not to suggest that mental capacity has no part in decision making about use
of the MHA. Indeed, there is an interface between the Mental Health Act, which
is about mental disorder, and the Mental Capacity Act, which is all about
mental capacity.
This
is reinforced by a considerable quantity of case law, including AM v SLAM, and
Cheshire West.
The
case law makes a distinction between objecting and non-objecting patients, and
capacitous and non-capacitous patients. A non-objecting, capacitous person can
be treated in hospital for mental disorder without recourse to the MHA. But
both an objecting capacitous person and an objecting non-capacitous person may
be detained for assessment and treatment under the MHA, and in many situations
should be, if it is the only means by which they can receive the assessment and
treatment they require.
Whether
deemed to be capacitous or not, Amy Morby could have been made subject to a section
of the MHA. The decision should perhaps have been allowed to have been made by
an AMHP and 2 psychiatrists.
One
thing I have learned as an AMHP is never to show patients that you are scared.
I have been in numerous situations over the years where I have anticipated
danger or been threatened with harm, but have in reality been physically
assaulted only rarely, and generally when I have misjudged a situation.
Derek,
however, was really scary.
I
was doing an out of hours shift in the early 1990’s when I got a call fairly
late in the evening from the city police station.
Derek,
a man in his mid 40’s, had been detained under S.136 after behaving bizarrely
and aggressively in a public place and I was called to assess him under the MHA.
He was apparently an intelligent man, with a degree in engineering, but had
convictions for a range of violent offences.
From
the comparatively bright and inviting reception area at the police station, I
was led down several flights of stairs to the custody suite, which was in the
subterranean bowels of the building with no natural light.
Derek
had already been seen by the duty doctor, who had left a medical recommendation
for s.2, and while I waited for the s.12 psychiatrist to arrive I decided to
see him.
I
followed the custody sergeant to Derek’s cell, at the end of a long corridor
lined with heating pipes and ducts with the cells opening off. The custody
sergeant looked uncomfortable.
“You’d
better watch this bloke,” he said uneasily. “Don’t trust him.”
Long
before we reached Derek’s cell, I could hear a loud and regular pounding sound
echoing down the corridor. The custody sergeant’s unease was rubbing off on me.
As we came nearer, I could see water flooding out from under the cell door. What
on earth was going on in there?
Derek
was monotonously pounding his cell door. The officer called through the grill
to him to back off and then unlocked the door and opened it. Looking into the
cell, I could see that Derek had tried to flush his shirt down the toilet in
the corner of the cell, blocking it and causing it to overflow, covering the
floor of the cell with water.
Derek
had his back to us when we entered. Since his shirt was halfway round the
U-bend, Derek was naked to the waist. He turned round and glared at us.
I
felt a surge of shock. He only had one
eye. He stared balefully at me with this one eye, but where the other
should have been was just an empty pink socket.
My
first thought was that he must have flushed his eye down the toilet. This did
not help me to maintain my composure. My voice probably sounded a little shaky
when I introduced myself.
He
put his hand in his pocket and brought out his second eye, which was made of
glass. He popped it into his mouth, sucked on it for a moment to remove any
fluff, and inserted it into the empty socket. He then examined me more closely,
as if this action had improved his vision. Although this went some way to
improving his appearance, it was hardly reassuring.
The
officer led him to an interview room. I stood on one side of the desk, with
Derek and the officer on the other side and tried to interview him. He was
hostile and asked me who I was. He did not appear impressed when I explained.
He was clearly agitated and his mood was elevated. At a guess (I did not have
access to his medical records) I thought he might have bipolar affective
disorder and was probably hypomanic.
“Derek,”
I began after I’d introduced myself to him, “Could you tell me what led up to
you being here?”
He
leaned across the desk to get his face as close to mine as possible.
“What
business is it of yours?” he snarled. “I’ve met your sort before. You just want
to lock me up. Because you’ve got no bottle.”
He
raised his fist and made as if to punch me in the face, stopping just centimetres
from my nose. I don’t know how I didn’t involuntarily recoil.
I
asked him about his eye. He seemed happy to tell me that he had lost it at the
age of 12 while trying to make homemade fireworks in his bedroom. This seemed
to amuse him, and he continued to rattle on at some length about his childhood
exploits.
As
I continued to interview him it became clear that it was not possible to keep
him on track, and his thought processes darted tangentially from one subject to
another, often without any apparent relevance to what I was asking him.
“You’re
going to section me aren’t you?” he concluded. “I’ve slit bigger bastards than
you, and I promise you won’t get away with it.”
Deciding
to conclude the assessment, I indicated to the officer that he could return Derek
to the cell. I was relieved that I had survived the process without needing a
visit to A&E. When the officer came back to me, I could see that he was
trembling. It didn’t actually help to know that a police officer was even more
scared than I was.
“I
can stand a bit of aggression in this job,” he confided. “But these mental ones
– they really put the wind up me.”
Once
the psychiatrist had seen him (I decided not to take part in that interview) we
were in no doubt that he needed to be detained under S.2 for assessment. In
view of his volatility and potential for aggression, it was decided to
transport him in a police van. He was not happy about this, and swore at me as
he was led to the vehicle, each wrist cuffed to a police officer, with two
others as escorts.
I
went on to the hospital to alert them to his arrival, and got there before him.
I stood back as he was led down the corridor, but at least felt safe, since he
was handcuffed and flanked by two big policemen. I made sure that I was far
enough away to be out of danger should he decide to lunge at me.
But
as he passed, he turned to look at me balefully.
“Bastard!”
he hissed, and spat full in my face.
I
hadn’t anticipated that.
It
turned out I got off lightly. A couple of years later I was talking to a social
worker who worked in the regional secure unit. I discovered that Derek was a
patient there. He was detained under Sec.37/41 (a form of detention imposed by
the criminal court for serious offences, which means that a patient can only be
released with the consent of the Home Secretary). He had blinded someone by
throwing acid into their face.
As a social worker, it has always been my basic approach to believe what
service users tell me, unless and until I have evidence to the contrary. Having
worked with many people over the years with a history of childhood sexual
abuse, many of whom were doubted when they disclosed as children, I know that
it is of vital importance to them to be believed.
That does not mean I am gullible, but I am prepared to keep an open mind
and apply the Evidence Test. The Evidence Test is simple and straightforward –
is there any evidence which contradicts what a person is telling you?
I remember visiting an old lady who told me that her living room had
been full of girls singing and dancing the previous evening. She went on to say
that they had all disappeared into a hole in the wall – directly behind her TV.
Before coming to the conclusion that the lady was suffering from dementia, and
was no longer able to differentiate reality from television, I had a look
behind the TV just in case there was, however unlikely it might seem, a hole.
There wasn’t.
And there was another unfortunate old lady who was detained under the
MHA and admitted to hospital after repeatedly reporting the existence of
strange noises in her old terraced cottage. Following her admission, her
community nurse arranged to collect some personal effects from her home. She
entered the cottage and was disconcerted to hear loud noises emanating from
somewhere within the building. It was eventually traced to her next door
neighbour, who had decided to convert his cellar, and in the process had
extended his own cellar by knocking into the space beneath the old lady’s home.
So I initially had no reason to disbelieve Brenda.
Brenda’s GP’s referral letter catalogued the terrible experiences she
had had at the hands of her abusive husband who, even after she had left him,
had continued to stalk and harass her and had even broken into her house and
raped her on one occasion.
The consequence of this was that Brenda was afraid to leave her house.
She had difficulty sleeping, and reported frequent flashbacks to her ordeal.
She was afraid of being alone, and only slept with the light on. She reported a
full house of symptoms of post traumatic stress disorder.
I worked with her for several months. One of the first things I did was
to help her make a claim for disability benefits. I was surprised when she was
turned down for this, and helped her to appeal.
I put quite lot of work into this. She had a neighbour, who was often at
her house when I visited, who had told me the extent of the help she had had to
provide Brenda, as she lived alone, and had no supportive relatives. I prepared
an account of the daily assistance she provided Brenda, which included
encouraging her to eat properly, taking her to appointments, and even going
round to her house in the night when Brenda was too frightened to sleep. I sent
this statement off with the appeal documents, and arranged to take Brenda and
the neighbour to the appeal and to act as her advocate.
The members of the Appeal Tribunal were convinced by the evidence I had
prepared, and awarded Brenda full benefits, backdated 9 months. I was as
delighted as Brenda, and felt I had done a good job of social work.
A few months later, Brenda had more problems with benefits. This time,
she told me, she had had her housing benefit suspended because of an anonymous
tip off that she was fraudulently claiming. Someone had told the council that
she was working. She suspected that it was her ex-husband.
I again offered to write a supporting letter for her.
A week or so later, she told me that she had been summoned to an
interview, under caution, at the local council offices, in connection with
these allegations. I offered to attend with her as an appropriate adult.
We went into the interview room and the investigating council officers
began the formal interview.
The basic charge was that she had fraudulently claimed housing benefit
for a number of years while working full time, and that she had not disclosed
her earnings, or the existence of bank accounts into which these earnings had
gone, to the council.
Brenda denied these charges.
The interviewers listened patiently.
Then the main interviewer opened up a large dossier and began to show
Brenda some documents. Was this her bank account? Yes. How did
she account for regular sums of money going in on a monthly basis, of around
£1000 per month? She didn’t know what the money was for.
The interviewer showed Brenda the payrolls of several different
employers. Was this her name and address? Yes, it was. Was
this her National Insurance number? Yes, it was. Was this her
signature on the forms? It looked like her signature. Was the
employee therefore Brenda herself? No it wasn’t. It must have been
someone who had used her name and address. Was it the same person who
had then arranged for her monthly pay to be deposited in Brenda’s bank
account? It must have been. And this person was not, in fact,
Brenda? No, it wasn’t.
It was becoming blindingly clear to me that Brenda had, indeed, been
systematically claiming housing benefits and other benefits fraudulently for
several years, and that I had been an unwitting accomplice in this.
In the car on the way home, Brenda continued to maintain, in the face of
overwhelming evidence to the contrary, that she was entirely innocent. I
couldn’t look at her. I dropped her off at home and advised her to consult with
a solicitor. I said I would be in touch.
After consultation with my manager, I wrote to Brenda to say that we
would be discharging her from the service, as we could only work with people
with mental health problems. I never saw her again.
If you have been, thank you for listening. If you’ve
found this informative or entertaining, please don’t forget to like and subscribe.
People who follow my blog will know how exercised I can
become about S.117 after care entitlement, especially when that entitlement is
being concealed or misrepresented to patients by local authorities. Indeed, one
of the commonest enquiries I receive is from relatives of people entitled to
S.117 who are, to put it bluntly, being hoodwinked by local authorities who are
at best ignorant of their duties, and at worst seek to defraud patients out of
their money.
And so to Tinsley v Manchester City Council, a 2017 judgment
from the Court of Appeal concerning a case that had been meandering through the
courts for some considerable time, no doubt at considerable expense.
The case concerns a man called Damien Tinsley. Back in
1998 he was hit by a car while cycling which caused considerable brain damage
and left him with an organic personality disorder. He ended up being detained
under S.3 MHA, and was discharged to a mental health nursing home. In
accordance with the requirements of S.117, the costs were paid by Manchester
City Council.
In 2005 he was awarded damages approaching £3.5 million,
of which £2,890,257 represented the costs of future care.
Interestingly, it was successfully argued during this
court case that “the relevant authorities were entitled to have regard, when
deciding how the claimant’s needs were to be met, to the resources available to
them, and he concluded that they would not fund either a care regime which the
claimant was prepared to accept (namely, accommodation at home) or even the
care regime which the judge found to be reasonable.”
The consequence of this was that from that time Mr
Tinsley has been using the settlement to fund his care, which has included the
purchase of accommodation for him to live in.
After a number of years a new deputy was appointed for Mr
Tinsley by the Court of Protection, who took the view that the Manchester “has
always been obliged to provide him with appropriate after-care services” and in
2010 the deputy started to pursue Manchester for both a refund of the money Mr
Tinsley had paid as well as damages.
The case ended up in the High Court, where it was
concluded that it was unlawful for Manchester to refuse to pay for after care
“on the basis that Mr Tinsley had no need for such provision because he could
fund it himself from his personal injury damages.”
The case finally arrived at the Court of Appeal, which
issued a judgment in October 2017.
On the face of it, it would appear perfectly reasonable
for the money that Mr Tinsley had received in damages for disabling injuries
that were not his fault, and which were specifically identified to cover the
cost of his current and future care, to be spent on that care. After all, huge
sums are frequently paid by the NHS for damage to patients which is designed to
cover their long term care needs.
However, the issue here is that of entitlement to S.117
after-care, and the basic principle that after-care for the purpose of meeting
a person’s mental health needs cannot be charged for.
So what did the High Court conclude?
Manchester submitted that “the mere fact that an
obligation is imposed on it by s.117 to provide after-care services to persons
compulsorily detained pursuant to section 3 of the Act does not require it to
provide, or arrange for the provision of, such services if a claimant has funds
available for that purpose”.
In a lovely paragraph, the Court demolished that
argument:
This is an impossible argument… A refusal to pay for such
services is effectively the same as providing such services but charging for
them.The House of Lords has made it
clear in Stennett that charging persons such as the claimant is
impermissible.Manchester is effectively
seeking, in the teeth of the express obligation to provide s.117 services, to
recover by the back door what it cannot recover by the front”.
The appeal by Manchester was therefore dismissed.
This has to be a harsh reminder to local authorities of
their absolute duty to meet the expenses of patients entitled to after care
under S.117, tempting though it may be, in view of the severe cutbacks to local
authorities for social care, to seek to tap the person’s personal funds.
While it may seem perverse that even someone with unlimited
funds is entitled to free care if they have once been detained under S.3 MHA,
it is nevertheless the law.
Parliament had the opportunity when drawing up the Mental
Health Act 2007 to remove this absolute entitlement, but it did not.
Parliament again had the opportunity to change the law
when drawing up the Care Act 2014, which substantially amended S.117.
But it did not.
It remains to be seen whether the eventual reform of the
MHA decides to remove this duty.
This video is about another of my caseload back in
1976.
Aggie
was in her late 60’s. She lived with her 97 year old mother on a smallholding
in a particularly remote part of our area.
It
consisted of 10 acres of small fields and meadows enclosed by hedges, an oasis of
rural peace surrounded by the vast, open, intensively cultivated fields of an
industrial style farm.
To
reach her home, you had to drive a couple of hundred yards along a track across
one of these huge fields, in the summer swaying with wheat, or barley, or oats.
Once
through the gate of Aggie’s smallholding, you had to park up and walk the rest
of the way through meadows full of wild flowers where her small herd of cows
grazed, past ponds teaming with frogs and newts, until you reached what she
referred to as the farmhouse.
It
took a leap of imagination to see this structure as a “farmhouse”. In reality,
it was a single storey timber clad barn with a corrugated iron roof, a few
small windows, and a dilapidated door that led into what passed as her kitchen
cum living room.
It
had been built by her father 60 or more years previously. After surviving the 1st
World War he had bought a few acres in the tiny hamlet and decided to raise his
family there. He had died many years previously, but his daughter and wife lived
on there.
Aggie
and her mother lived in the most primitive conditions imaginable. They had no
electricity or running water. All their water was obtained from a well just
outside the back door. The toilet was a tiny corrugated iron outbuilding with a
plank of wood with a large hole in it and a bucket underneath the hole.
The
interior of the “farmhouse” consisted of the kitchen cum sitting room, which
contained an ancient and inefficient coal fired range that was kept alight all
the time. It was the only heating or cooking facility they had. In the winter,
the temperature rarely rose above 10C.
Unaccountably,
the room was furnished with a range of fine antique furniture, all of it now
very dilapidated and wormy. There was also a piano, and on the walls, in the
dim light, could be seen huge Victorian oil paintings, some of them reaching
from floor to ceiling. It was almost impossible to tell what the subjects of
these paintings were, as they were covered in a film of soot from the oil lamps
which were Aggie’s only source of light.
There
was what Aggie called a parlour, but which she mainly used as a store room, and
there were two bedrooms. Aggie slept in one, and her mother slept in another.
Aggie
always took pride in introducing me to Mother during my visits. This meant a
visit to the bedroom, where Mother appeared to spend her entire life.
Mother
had had a number of strokes. This had left her almost completely immobile, and
apparently incapable of speech. I certainly never heard her say a coherent
word.
It
is very difficult to adequately describe Mother’s appearance. She was very
obese, and very pale. Folds of flesh covered her face. Her eyes rarely opened. Her
body was covered in tattered and ragged layers of old fashioned nightdresses,
which remiknded me of Miss Havisham in David Copperfield. In fact, the entire
experience of visiting Aggie and her mother was exactly like stepping into a
Dickens novel.
Mother
was incontinent, and Aggie’s solution to this was to cover the mattress with
roofing felt. As well as protecting the mattress, this also served the
function, she told me, of preventing Mother from slipping too far down in the
bed.
During
these visits, Aggie would introduce me to Mother, and then prop her up in a
sitting position. Mother would open one eye to examine me, and might make some
sort of noise in response. I was never sure she had any idea what was going on,
but Aggie would delightedly interpret these possibly random utterances as
insightful comments about the weather or current events.
Aggie
tried to keep alive the dream her father had of living the good life off the
land, but to be honest, she was not very good at this. She kept chickens, and tried to grow
vegetables. She had a grape vine and would attempt to make wine out of the
juice come the Autumn. She once offered me a bottle, but I could not bring
myself to try it.
She
used to make jam, with a minimum of sugar, as it was expensive, which meant
that a layer of mould would soon appear on the top. She also made various medicinal
preparations using traditional recipes. One of my predecessors had once been
reckless enough to try one of Aggie’s special complexion ointments, and had
come out in a rash.
She
and her mother lived a life of most extreme poverty. Their main source of
income was their pensions, and although periodically Aggie would arrange for
one or two of the cows or calves to go off to market, I suspected that the herd
cost her more to maintain than the income she received from it.
Because
of their isolation, several miles from the nearest shop, Aggie relied on a
local grocer to deliver her weekly groceries. She had a standing order which
she was fearful of changing for fear of upsetting the grocer and losing their
lifeline.
A
consequence of this was that she had a pack of salt delivered every week. She
once showed me the stockpile of salt in the parlour. It occupied nearly half of
the room. She would not entertain cancelling this part of the order “just in
case”.
Aggie
was very frugal and economical. If she wore out the cuffs of a shirt or blouse,
she would simply cut off the sleeves up to the elbow and then attach some other
sleeves using large stitches of wool. It didn’t matter whether or not the
fabric matched in any way.
Despite
apparently living life in the past, Aggie had a portable radio and would listen
to Radio 4 constantly, so she was always up to date on national and world
events, and actually had a keen and intelligent mind.
Although
she had never had a formal diagnosis, Aggie probably had schizophrenia. She
would often suddenly start whispering in the middle of a conversation, pointing
to the ceiling and muttering under her breath about how the neighbouring farmer
had fitted listening devices and was spying on her.
You
may be wondering exactly what good a social worker was doing for Aggie and
Mother. If I had a plan, it was to preserve the lifestyle they had chosen, and
at times to deflect demands for “something to be done”. I would make sure that
they had the benefits to which they were entitled, and my regular visits also monitored
Aggie’s needs as a carer and provided Aggie with an outlet in which she could
engage in an adult conversation.
One
day, I had a phone call from Aggie. This took quite an effort for her. It meant
she had to cycle the mile to the nearest public phone box.
She
was beside herself. Mother had had another stroke. She needed a doctor.
I
phoned Mother’s GP. I arranged to do a home visit with him.
I
met him at the farmhouse and he examined Mother.
He
agreed that she had had a stroke and that she needed to be in hospital.
This
horrified Aggie.
“Mother
won’t like it in hospital!” she wailed. “She won’t be able to hear the lowing
of the cows, and the dawn chorus! She’ll pine away! She needs to stay here!”
But
the doctor was clear. She was ill and needed to be in hospital. He was off to
the nearest phone box to call them.
But
I was thinking. What was in Mother’s best interests?
I
knew for a fact that, once she was in hospital, she would never be allowed to
return to the Victorian hovel that Aggie regarded as home. A district nurse
would take one look at their living conditions and would refuse to allow it.
I
was convinced that Mother would die in hospital if she were to be admitted.
Aggie
offered Mother love and uncomplaining round the clock care in the environment that
Mother had always known. So far, she had managed to keep her alive despite her
poor health and extreme age. It wasn’t all about the physical environment.
I
argued this case to the GP. Although he was looking at the situation from a
purely medical point of view, he did nevertheless listen to me. He could see my
point.
In
the end, it was agreed that he would call in on Mother over the next few days
to observe her progress. She would not be admitted to hospital after all.
I
felt pleased. I told Aggie the good news. But she was so distressed by the
threat that she felt she needed to focus this on someone.
“It’s
your fault!” she said. “You’ve come here wearing grey. Grey is an unlucky
colour! You’ve put a jinx on Mother! This would never have happened if it
wasn’t for you!”
And
despite my efforts to produce an outcome that would be best for Mother and for
Aggie, she refused to see me again.
You
don’t often get thanks as a social worker. But that’s all part of the job.
Social work has changed a lot
since I started in 1976, in many ways for the better, in some ways for the
worse.
Back in 1976 the local social
services office would receive a request for assistance, the case would be
allocated to a social worker – and, er, that was about it. Unless there were
very clear identified needs, for example a need for residential care, for aids
to daily living, or a child subject to some form of abuse, the social worker
would just tend to, sort of, bumble along, visiting the client, developing a
relationship, maybe sometimes doing something practical, like helping them
claim benefits.
Most clients did not have any
sort of formal care plan. Occasionally, in supervision, your team leader would
ask you what you were doing with a particular person. Then you had to think
hard and say something that sounded worthy and useful.
My first caseload was very
mixed. I had a few children and family cases, some elderly people, some people
with physical disabilities, a few people with learning difficulties or mental
health problems, and one or two who defied categorisation.
Margaret was one of the
latter. She was in her early sixties, and lived alone in a local authority
house in a small village a few miles outside town.
I was never clear about how
she ended up a client of the social services department. It may have been a
referral from the local housing authority, who was certainly concerned about
her ability to manage her tenancy. It may have been because of complaints from
neighbours.
It’s possible she may have
had mild learning difficulties, although she had no formal diagnosis. She had
lived all her life in that house, taking over the tenancy when her parents had
died over twenty years previously, and perhaps they had been her carers. She
certainly had no obvious mental illness. But she was deemed to be a vulnerable
person, and hence worthy of having a social worker, even if that social worker
was unqualified and completely inexperienced.
Or maybe it was because she
was a witch.
She certainly looked like a
witch. She had uneven and discoloured teeth, a long nose with a wart on the
end, and matted hair. It was thought that the last time her hair had been
washed was 20 years ago, when she had had to go into hospital when she’d had a
fall. I could believe it; her hair had become felted. She had probably also not
had a bath for twenty years, and her face and hands were black with dirt.
And she had cats. I never
knew how quite many cats she had, and I don’t think she knew either, but there
must have been as many as 40. They lived in the house, never leaving it, and
freely interbreeding. She seemed to have no arrangements for their toileting,
with the result that they defecated anywhere and everywhere.
Let me describe the
experience of visiting her house.
I always went in through the
back door, which was never locked. The hallway was comparatively free of cat
faeces, as she tended to keep them in the living room and kitchen area. But she
made up for this omission by having piles of newspapers at least 4 feet high
lining both walls of the hall. As she lived and slept in the living room, she
never went upstairs. I have no idea what the bedrooms were like, as it was
impossible to go up the stairs because each step was piled high with old
newspapers.
I was told that a previous
social worker had attempted to clear the house of newspapers by diligently
putting them into an outhouse, but Margaret had then brought them all back in
because she was afraid they’d get damp outside.
Festoons of ancient cobwebs
hung from the ceiling, some hanging so low you risked getting them in your hair
unless you ducked.
Having negotiated the
hallway, you finally entered the living room. Winter or summer, Margaret never
opened the windows, so the temperature in there could get quite high during the
summer months. But not as high as the stench.
It was impossible to tell
what the original floor covering in the living room was, as it was completely
covered with cat faeces to an unknown depth. My shoes tended to stick to the
floor as I walked through. There was an audible noise as I picked my feet up
step by cautious step.
The smell was almost
unbearable. In those days I smoked a pipe, and used to smoke furiously
throughout my visits in a futile effort to mask the ghastly smell.
Margaret would be sitting at
the head of a table covered with old papers and cats. Her matted and filthy
hair was partly covered with an equally filthy headscarf. She generally ate
white bread straight from a bag during my visits, tearing it into smaller
pieces with her black hands before putting it into her mouth. Sometimes she
would offer me a biscuit. I always declined.
During the summer months she
would be surrounded by a halo of flies.
I never sat down in her
house. This was partly because any seats were always covered with cats, but
mainly because they were so filthy that I would have needed a change of clothes
afterwards.
So what social work tasks was
I undertaking with Margaret?
Did I try to improve her
living conditions? Not really. Her file catalogued the efforts previous social
workers had made, all of which were futile. Margaret did not want to change.
Did I support her within her
community? I guess so; people seemed reassured that a social worker was
visiting her. But if they hoped that it would effect any perceptible change,
they were sadly disappointed
Issues of capacity were barely
talked about back then. Apart from her appalling living conditions, I never had
any feeling that Margaret was not mentally able to make decisions about her
lifestyle. Nowadays I could make an explicit assessment of her capacity, and would
probably conclude that she had the right to make unwise decisions, but there
was no legislation that covered Margaret’s situation in the 1970’s.
She appreciated my visits,
and liked to talk to me, so I suppose I fulfilled some welfare purpose. Again,
nowadays that befriending role could either be provided by a voluntary
organisation or supplied via a personal budget under the Care Act. But back
then, the main resource was social workers.
One thing I learned from
Margaret was not to be phased by extreme housing conditions. In later years,
when people complained of patients living in squalor, I set Margaret as the
benchmark. That was squalor.
During the two years Margaret was on my caseload,
I achieved one traditional social work task; I arranged for a neighbour to be
paid as a home help in order to do her shopping once a week. So I suppose I did
do something to improve her life.
This is a 30 minute guided visualisation exercise It includes ambient natural sounds of forest rain. The exercise has no wake up ending, and may assist with sleep.
When I worked in a Community Mental Health Team, I used to run relaxation sessions and produced several relaxation exercises for distribution on CD. This is one of them. It features natural ambient sounds, and is specifically designed to aid sleep.
While it’s an occupational hazard for the police,
ambulance crews, doctors and nurses to have to deal with dead and dying people,
it’s fairly unusual for social workers to have such experiences. In over 40
years of being a social worker, I’ve been in the unfortunate position of being
directly involved in the discovery of a recently deceased person on only four
occasions. You don’t tend to forget about them.
I’ve told you about Robina and Cyril in a previous
video. I’m going to tell you about two other incidents.
George
George was in his 50’s and a longstanding patient of
the Community Mental Health Team. He had a very long history of chronic
paranoid schizophrenia, and had a fortnightly depot injection. Although I was
not his care coordinator, I had had to detain him under the Mental Health Act
on a couple of occasions.
One day, Jim, his community nurse, went round to his
house, where he lived alone, to give him his injection. He had been unable to
get a reply. Jim returned to the CMHT and discussed this with me. It was not
like George to be out on the day his injection was due, or not to answer the
door. We decided to go out together to investigate further.
We rang the bell and knocked on the door, but there
was no reply. The curtains were drawn, but we could hear the television. Jim
knelt down and peered though the letter box.
“Oh, God,” I heard him say, as he backed away.
“What is it?”
“I can see him. He’s sitting in his chair in the
living room at the end of the hallway. He’s not moving. I think he’s dead.”
I had a look. His profile could be seen clearly
through the open door of his living room. His head lolled to one side,
supported by the wings of the armchair. I called, but there was no movement. I
feared the worst.
We decided to call the police.
When they arrived, we explained the situation to them.
They too had a look through the letterbox, then tried to find an open window or
unlocked door, without success.
One of the police then revealed an arcane piece of
knowledge. The windows on this particular estate all slid within a groove in
order to open them. There was a way to jiggle the window so that it could be
slid back a little way, even though there was a window lock, and then it was
possible to reach through and release the catch so that the window could be
opened enough for a person to get through.
The police officer climbed into George’s house and
opened the front door. We all entered and went into the living room. Goerge’s
eyes gazed sightlessly at the morning TV programme. He appeared to have been
dead for at least a day or so.
Once we had formally identified the body, we returned
to the CMHT.
Jim was pale. He was badly shaken. He was looking at
something far away.
“So lonely,” he said. “So alone. Looking down that
long hall through the letter box, there he was. He died on his own. He was so
alone.” A tear rolled down his cheek.
Gordon
One morning I had a call from one of my service users.
Beth was a middle aged woman whom I had known for several years.
Not long before I first started to see her, she had
finally escaped a long, abusive marriage to Gordon. Gordon was an alcoholic. Throughout
the marriage he had terrorised her, undermined her, hit her, and sponged off
her. I had helped her through the aftermath of this, including aiding her
resolve not to return to him, affirming her decision, and assisting her to go
ahead with a divorce. Over time, she had adjusted to being a single parent, and
her confidence in her own ability to be a parent for her children slowly
increased.
In recent months, after a long time with no contact,
she had started to see him again – not because there was any prospect she would
return to him but through pity. Because of his drinking, he was in very poor
physical shape. For the sake of the children, who still had contact with him,
she wanted him to get help for his drinking and also tried to persuade him to
see his doctor, as he had lost weight and was physically quite frail, even
though he was only in her early 50’s.
“I’ve been
round to Gordon’s flat,” Beth said, “but I can’t get any reply. I was going to do
his shopping for him. I’m sure he’s dead. I’m convinced of it.” She began to
cry.
I arranged to pick her up and go round to the flat
again. Sure enough, there was no reply. She has last seen him a couple of days
previously, when she had done some shopping for him. He never left the flat. So
I called the police.
The police managed to get a key from the housing
association, and I arranged to meet them at the flat. I persuaded Beth not to
come. I didn’t want her to be in the position of having to identify the body,
if our worst suspicions were realised. She didn’t want to, anyway.
I went into the flat with the police officer. We found
Gordon curled up on a sofa. He was dead. He looked tiny, emaciated, desiccated,
almost mummified; there was hardly any weight to him. He didn’t look as if he
could ever have been alive, somehow.
His skin was a deep yellow, almost mahogany. I had
never seen anything quite like it. He
had clearly been in the last stages of liver failure.
On the floor beside him, in a carrier bag, was the
last shopping that Beth had done for him. Still in the bag was a 3 litre bottle
of white cider.
I went to see Beth at her home. She was crying
profusely. I told her the basic facts. I didn’t give her the details of his
appearance.
“I killed him, you know,” she said in between gulps of
air.
“What do you mean, Beth?” I asked her.
“I didn’t want to. He made me.”
“What do you mean?” I asked again.
“He made me buy him alcohol, that last time,” she
wailed. “I knew I shouldn’t have. I killed him.”
“Beth,” I said quietly, “he never opened the bottle.
He didn’t have a drink before he died. It was drink that killed him. But not
that particular drink.”
Over the months following this incident, I had to
spend many sessions helping her to work through her bereavement and guilt
issues. But the fact that I had gone in that day, and had found that bottle,
and had seen that it hadn’t been touched, and could tell her this, certainly
helped to absolve her of at least some of her guilt.