Showing posts with label health care. Show all posts
Showing posts with label health care. Show all posts

Thursday, 7 October 2010

a must to read


Patience

Patience is a book which captures patients’ experiences and stories of staff on the wards in a very creative way. It shows how every patient is different and how everybody has a different view on their stay in hospital and their life in general.

The artists did an amazing job in engaging with people in a variety of ways meeting people’s interests and abilities e.g. by putting prescription messages for happiness on pharmaceutical packages, writing poems, making pictures of people’s views on their hospital stay and by designing personal postcards.

All pages in the book contain touching messages, give great insights and are often humorous too. It is an impressive piece of collaborative art describing something so common as a stay in hospital, which could also be sometimes frightening and frustrating, from a human perspective.

Patience is an excellent book to look through, to read, to talk about and to reflect upon. It is a must to read for everybody wanting to deliver personalised and dignified care.

A big thank you to all people who contributed and shared their experiences and wisdom and to Lois and Phillip for capturing these valuable messages!



Nicole Alkemade
Older People’s Joint Commissioning Manager
NHS Stockport



Friday, 24 September 2010

the minds of elderly patients


In response to our new book Patience, Advance Nurse Practitioner, Fiona Roscoe has written:


Who are we to know what is going on in the minds of elderly patients as they sit dutifully in their chairs waiting for the next ward round or cup of tea?

It is a time when many are at their most vulnerable and reflective but sometimes due to disability and ill health are unable to express themselves. The artists of 
arthur+martha have patiently sat with these souls and helped them to unlock their thoughts. In doing so, not only do we have examples of unique creative art but also a new dimension in our appreciation of our most senior citizens. (referring to Stages of grief 1950 and Parachute Landing by Albert Burrows)

Fiona Roscoe RN DN MSc BSc(Hons) is an Advanced Nurse Practitioner (Primary and Urgent Care)

Thursday, 13 May 2010

dementia support


Staff Nurse. Ruth Breslin

The dementia support we offer is for people of any age – here it’s given so that sufferers can stay in their own homes as long as possible, living their lives as fully as possible. At this day hospital we provide specialist assessment, nursing support and O.T activities for people with various types of dementia. We hope this will prevent the need for a hospital admission and allow relatives / carers some much needed respite.


There are many different types of dementia. Some are related to diseases such as Alzheimers or vascular conditions such as strokes. Depending on the illness, people might have short-term memory problems, disorientation, be anxious or agitated or develop problems such as disturbed patterns of sleep.


We also support people with less common illnesses such as fronto-temporal dementia which can involve very challenging symptoms such as obsessive-compulsive behaviours or marked personality changes. At all stages of the person's journey through dementia there are hurdles to overcome, for both the individual and their loved ones.


Our role is to help people understand what they are going through, and together find positive, constructive ways to look to the future. This may involve helping people to come to come to terms with their diagnosis and explore their feelings and anxieties. For example, some people may feel angry and need emotional counselling. Others may need practical support to understand their symptoms or treatment plan. Educational support is also vital. Certain dementia symptoms may require special consideration in carers; for instance, Alzheimers can cause problems with visuo-spatial awareness which affects a persons' recognition of depth, distance and what an object is. Someone with this problem might walk from a carpet onto lino and think that they should be taking a step up, when the two surfaces are actually flat beside each other. This can cause them to stumble or fall.


We also see many kinds of language difficulties. People might remember songs, or recite poetry, but be limited in other uses of words. I knew a gentleman who could recite Shakespeare in any accent you like, but his own self-expression was stunted.

Individuals can sometimes get lost in the illness and we fight that by helping them create books that tell the history of their own lives. The patient is transformed from an anonymous old lady into someone who has flown planes, who has lived an amazing life. A book like this is very valuable, especially when someone is in long-term care; it becomes a memory guide to the person and a prompt for staff. It’s an anchor for the patient and it’s a point of contact, a talking point.

You need background to understand people. Local history, personal reminiscences, things to hang a conversation on. From there you get to know them more deeply. Everyone’s needs are so different. Some people actively seek help, others are more reluctant to ask for it and we have to gradually earn their trust.

We achieve a lot once we’ve got trust. Its very rewarding to see people getting happier and growing in confidence every day.


Many people who are referred to us understand that they have a diagnosis of dementia. Because of that you can be honest and trust can then build. People start to understand who you are, they open up to you, which is vital because dementia is in the mind.....unseen, it has to be talked about before we can treat it. It is so valuable for the person to know that the scary things that are happening to them, such as hallucinations, are part of their illness and that we will work hard to find the right medication to ease them. It is a partnership.


The care philosophy we use is based on the work of the late Tom Kitwood, who pioneered the person-centred care movement. Kitwood once said that to treat people as if they were objects or consumer durables like a TV is "grotesque". But, in the current ecconomic climate, it is easy for healthcare to reduce people to numbers or statistics. Dementia care nursing has, historically, been under-valued and overlooked as a specialist area of practice. But the nature of our patients' needs and their vulnerability demands that we need more - not less- skills to work in this area. There is a lot of emotional giving in dementia care. The reality of person-centred care is that we have to go the extra mile. Our client group need people to spend quality time with them and they deserve committed, compassionate, well-trained staff who understand their needs. That’s what keeps the patients safe and physically / emotionally well. We work hard to keep the atmosphere calm and uplifting, from the music we play to the activities we undertake. We also have good relationships with the people around the client too, relatives, doctors and other health workers. Close teamwork is essential.

When people move on, we miss them terribly because we’re very much a community. We get relatives coming to visit at our Christmas Fairs, people from the past pop in to say hello. I always say: “Have a cuppa if you’re near, let us know how you’re doing.”


There are days when the job can be tiring and demanding, but it’s never to do with the patients. They keep us going on the tough days! It is the politics, red tape and paperwork that causes the most frustration.


We never forget though, that however difficult our days can be, it is the carers who have the hardest job of all. They never cease to amaze us at how they keep going- sometimes under extreme pressures and even with their own health problems. When we come off duty, we can relax and re-charge our batteries. Our carers are on duty 24/7.

Tuesday, 11 May 2010

Caring and dementia


Anne Sadler and Anne Parry interviewed at Bluebell Ward Dementia Day Centre, The Meadows, Stockport, 2009


Ann Parry

Our job? Making life a little better, making it fun.

Anne Sadler

Treating people as you’d wish yourself or yours to be treated – as individuals. People aren’t a condition, it’s individualised for all of us. As health professionals we are in a privileged position to be with these people. Carers are often talked about as the ones who have to give their personal lives, their time, their caring, and so on. But the flipside is what we get from it- we get people’s histories, lives, wisdom.

Ann

We also get their trust. Making them feel wanted, because they might feel they don’t fit in anymore and they need reassurance. We can give that, among other things. You feel better about yourself because you have given something. I’ve never wanted praise, just that the patient feels settled and enjoys the group. If I can give that, I feel better.

Anne

You might not be having a great day, but if you catch glimpses of people, it brings you back to where you are and what you’re doing. It grounds you.

Ann

What we’re doing is caring for someone. We give life. We give choices, so they can make their mind up about things. We give them our attention.

Anne

Compassion fatigue can happen, I’ve seen it. The only thing I hope for is that if I burn out that I’m able to realise, because that is the time that I give up this job. If your compassion goes, you should go. A partner can lose compassion. They have to deal with it night and day, but we can go home at the end of the shift.

Anne

We try to keep sight of the fact that these people are made up of their own lives, which they can articulate and feel, despite the dementias. We need to keep listening, maybe listening more intently to people who are unwell. I liken it to day-to-day conversations where I will listen with half an ear. At work it’s very important that I give my full attention, truly listening.

Ann

Otherwise you make assumptions and they get frustrated.

Anne

The way people behave is explained partly by knowing their history, it helps you piece together what they’re saying now. I remember 30 years ago in residential care a lady with fists clenched, shouting. It didn’t make sense at first, but then it transpired that she was bothered about something that had happened from years gone by. That was the essence of it.

People cope with dementias the same way that people cope with physical issues. They get the strength from somewhere, faced with any illness.

Ann

With dementia, as with any illness there’s some who fight and some give in. Some want to be looked after, dependent. If the carer is fed up and doesn’t want to give care then these people have problems.

In the poem written in the workshop I liked the image of dementia being a bit like getting off a bus in the rain and not being able to tell where you are.

Anne

I like images of dementia to be more than just confusion. I like them to be lighter and brighter, that it isn’t all a dark journey. That’s what I’d like to get across to the general public. TV images of dementia as sadness I don’t agree with. You always get this awful chamber music and shots of gravestones. There is happiness too. It’s not all the time, but it is there. And are any of us happy all the time? No!

If we can help channel the happiness – and the anger too - that’s our job. If we can take some of the anger it helps them. It’s not always pleasant, but it isn’t about us it’s about them. There’s a balance to be struck and people who attend as staff are aware of this. People’s emotions change as their illnesses progress. Some kind be insightful at times which can bring comfort, but at times can make them angry. “Why me?”

Ann

In the early stages a dementia can be awful, especially in young onset. People giving up jobs, big effect on the family.

Anne

Part of our job is to help people with that understanding. People can be angry, seem nasty, threatened. But it’s up to us to look beyond that. When I do home visits, very often it’s my job to help them maintain independence, not to take it. People worry about independence going.

When we talk about independence going, we often talk about this big whole. But there’s fractions of independence and they are important, little flags of independence. So for example, self-care might be very important to one person and not to someone else. Social independence – just the ability to socialise – can keep people going. If you chat to someone, that’s your choice and you’re exercising independence. A lot of it comes down to choice. It’s the same with our help. If we explain what we are doing and they give assent, then they are still showing a sign of independence.

Monday, 10 May 2010

Interview with Ian Clark, Healthcare Assistant

Cherry Tree Hospital, Stockport



Every morning I come in – and I’m the first person the patients see. I try to make sure it’s a friendly start. I’d hate to be woken with someone giving orders: “Wake up! Get showered!” People are poorly, frail, elderly, sometimes they’re forgetful, sometimes they’re not good at speaking… I always say: “I’ll give you 5-10 minutes to wake yourself.” It makes all the difference, a big smile, the expression on a face.


I ask them how they’re doing and I also check with the other staff to see how the patient is. Certain patients never get a good night’s sleep, they only sleep well in their own room. Here they’re out of their house, out of their routine, it’s totally alien.


Whatever help I give to patients, I ask myself first, “Would I like this situation?” I put myself in their shoes, it’s commonsense. People here are frail and you’ve got to support them all the time, keep asking them if they’re OK. My last shift was 12 hours and it was difficult, it drains you, all the little things. But you’ve got to give everyone the same care, it’s what they deserve. I think of my mum and dad and I hope they’d get good care. I hope someone looks after me when I’m in that situation.


From a patient’s point-of-view, hospital can be very frustrating. They’re hanging on for someone to take them to the toilet, for instance. It’s humbling. They might get in a mood and it can last all day. To change from independence to asking permission is confusing for people. Yes, some independence is lost, but we’re actually trying to help. Some folks look at us as if we’re the enemy and I have to reassure them WE ARE HERE FOR YOU.


Who copes best? Patients who have visitors seem better; they have something to talk about. Those who don’t get visits – well, it must feel heart-breaking, it’s going to play on the mind. A man here, he gets irate seeing others having visits. It’s doubly isolating because he won’t speak about it to us. If I’ve got a spare 10 minutes, I take people outside into the hospital gardens.

At the end of the day, it’s good to see them tucked up and safe. You can tell they’re happy and content. I can go home without worrying about them, knowing I’ve done a good job. Then if the patient’s better and they get back their own lives – all that effort and patience was worth it in the end.

Tuesday, 6 April 2010

a thousand times goodnight

sleeping daisies
waking up the senses
awaken upward the mind

nurses see the
touch
the

bitter scent
swash
the cuckoo buds

from the beds
floating petals
throw

lines dancing
white couplets
float over dead water

white life
paint the
meadows



Anonymous
2007

Tuesday, 23 March 2010

be patient




many patients
aren’t patient
if there’s waiting to be done
take your turn at

patience
nurses can’t give
everyone time
undivided

the vale of years turns
take turns to be patient, wiser
the main answer
what wound healed but by

patience visits
sits quiet with my own thoughts
I call myself
a quiet person

was a dressmaker
if a stitch went wrong
I set it right
in two words, two small words

Margaret Hargreaves

October 2009

Monday, 22 March 2010

Stepping Hill Hospital at Night (after Vosnesensky)


coughing at night

other breathing at night

people tend

droning to sleep

quietly

nurses’

footsteps

low light faces

the television

an adventure

of dark blue glass

constant

quiet breath engine

in their beds

three or four

calmed

safe



people

moving that’s the thing

I want to hear

people

X-ray photos of the soul

lonely

speak to me with dark tongues

lone

night

yawning




Ralph Starmer and Keith Philips

Stepping Hill

Monday, 15 March 2010

o lovely walls


seven months sorrow
been seven months
(o lovely walls!) its been hectic
times seven
nurses change the speed

lively nurseschange beds, lives
coming to you bones groan
brain on top spine down the back

I don’t have time for please
change the speed of the day

doing you good
change your window speed
good-doers do-gooders
throw your body puking
sorrow eat my body

the nurses change


anonymous
Stepping Hill Hospital
2008

Tuesday, 9 March 2010

Care of Nurses


I’ve seen a complete deterioration in care of the caring profession in terms of how well they are looked after by the administration - no place for staff to go and have something to eat. When I trained and you were on night duty you could go and have the same half hour off the ward as you would during the day. And a proper meal cooked in the middle of the night, now often they don’t have the opportunity. If you’re not looking after the staff, how are they going to be giving of themselves?

Staff rooms in the early days, doctors taking tea with Sister, and Sister had a big room and literally everyone could sit round and have tea. And where would you get that now? The staff are in cupboards, and they complain then about lack of communication between disciplines; doctors and nurses, or nurses and physios – but you have no means, no theatre.

Alison Creed. Retired

Thursday, 4 March 2010

night pains



I feel tight

feel clempt closed

always thinking trying

nighttime terror couldn’t tell you

a bit of a trouble-ful night

pains


hospital comforts: the beds are alright

the nurses are alright

the specialist said, “I can operate but…”


furious winter is in our stars


all the time many a time

I m always trying to look up

a-wondering what

to think of life itself

a bit of a trouble-ful night

pains


they do damn good work

specialist saved my legs for me

he was practically dancing


hope is a lot of things


group

Cherry Tree

2007

Monday, 1 March 2010

football



stanley matthews georgie best nobby stiles sammy much roger byrnes busby babes in packs in a set players 10 or 20 cigarettes on the back their age height history wifeswaps then in germany in munich early morn the takeoff

I do as best I can I do the journey from here to there is no different to any other journey more’s the difficulty is keeping your friends cos you cant get out the wheelchair

known as the munich crash the ground frosted fog photos of them on the runway matt busby sandy busby the son (good at spending money) when they emerged the babes were near unbeatable on £15 a week put edwards on he could cream the lot dog them clobber them sort em out

you cant get out the wheelchair and start getting angry telling the fellow where you want to go well lets say it does make you feel you’re not getting anywhere it’s just a question of administration

stanley matthews turned up at 8 in the morning running barefoot feels free blackpool sands (soak your feet in cold water you’ll walk a million miles) georgie best kidded the goalie banged it a brilliant shot but he done himself in daily brandy-soaked

you feel limited in the weight of this you’re not designing the journey the other person is I was an apprentice pro blackpool fc loved every minute gave back every penny

the footballs were heavier then leather soaked in rain describe a great god the best he was a tippler of everything two or three wives he had so many women over the weekend hundreds seen him train in the park a dangerous man a danger

you’ve got to be determined to stay alive otherwise this world will see you off falling into chaos somebody needs to mop the world up nurse sort the ends out I’m sat in a chair thinking literature I cant express

re-match: duncan edward he was only 19 in munich on the runway play was awhile ago you’ll hear them you’ll hear them a mile away no problem just a trick of the foot.

Allan Whittaker, Frank Wigley

Cherry Tree Hospital

2007

Tuesday, 23 February 2010

a locker



a locker is a sort of miniature you
haven’t much room on-ship
roll your mattress rope around
hammocks slung sausage-like

these curtain rails carrying

a coiled rope and a heaving line
panic at the dock everyone swearing
doesn’t bother me a cramped situation
eight fathoms for your morning wash

around the beds in the ward

a rough bloody outfit
you was on the frontline
some of the roughest buggers ever
I’ll take you all

remind me of

a good rough house in the pub
was a favourite occupation
thorough gentlemen
below decks

hammock rails

remind: dear me you don’t half meet characters
limbs and bits of heavy engineering
the place exploding
you hit the floor

the clews as they call em

undo them strings beg a kiss
the nurses
stealing sailors’
hatbands for ribbons


Allan Whittaker
Cherry Tree
2007

Wednesday, 17 February 2010

grit

you first come in you’re sick and that slows you can’t be mithered grit me teeth and bear it grit me teeth and keep me head down

called up 1939 went to France Dunkirk had a bad time a bad time

driven to distraction by all the waste of time getting angry doesn’t help you got to somehow slip into a lower gear get through these long days

in a truck for cover

get up when the nurses start clattering early habit of a lifetime bed late after the noise of the medicine the nurses overworking I’m surprised how cheerful they keep

tried to get in the little boat trousers round my neck and the trousers floated away

if you’ve got a decent book get what exercise you can push this wheelchair up and down

people fighting to get on the boat

that’s one thing I never do – give in

and keep a smile on the faces of the nurses

you’ve got to make your pleasure – is there anything that pleases me? - yes everything - grit me teeth and grin

E Wooley
2008

Thursday, 28 January 2010

a pox of this


gout is a condition that causes pain, inflammation and swelling in one or more of the joints. It usually affects the big toe, but can develop in any joint in

in here about four weeks
terrible state I was
knees useless
getting out of bed
wife standing by
couldn’t stop me flying
get paramedics
help me to stand
gentle s-l-i-d-e to the floor
didn’t bother me
knew I’d get up one day
wife not strong enough
(amazing how strong she is)
she was calm

often occurs in attacks that usually last for three to 10 days, after which the joint should feel normal and pain-free again. The attacks are almost impossible to predict and, if

‘if you go down
…’

just slide
gout inflammation of the blood
into the legs
try to pump them out
put a tube down the leg
and suck on it
not painful

not treated, can cause future attacks to be more frequent and last for longer

lack of power
most difficult getting to
the toilet
a gout of this pox


Gerald Manley
/Shakespeare/NHS Choices website
31st October 2008

Everyone has the right to be remembered



you have
more freedom when
you are away
but

the nurses put a limit

the atmosphere every year in
Wales Rhyll Llandudno or the Algarve
the pleasure to stop and go
a wideopen space, a beachfront
the smell is held
contained by things that are a pleasure
to eat doughnuts are sweet
pleasure constantly

cant look after myself proper

constantly seabirds on the headland
suspect or suggest the memory of places
a tram or a train from base to top
do and say what you want
a change of scenery

you’ve got to have someone to help
control


tremors
two shakes of a lambs tail to get to Llandudno
to get away to get home
you look around and see dust
look back and think I was doing such a thing
donkeys years in holiday camps
in tents men on one side women the other
the bane of my wife’s desire
the cheese was very

hard pleasure of these idle days


conversation poem
cherry tree hospital 2009

Wednesday, 30 September 2009

Interview with Fraser Burton, Diabetes specialist

Diabetes: explain it in user-friendly language. That’s my job. The first bit of news isn’t so friendly. Diabetes is a chronic condition, it’ll be the thing that probably kills you. But there are many things you can do. You want to get rid of that label. Stop putting that label DIABETIC on your forehead. We put you right back into the middle of your peer group. We do that but we keep you safe.


What are the myths? People say that it’s a disease that stops you eating sugar. People say they ‘fall over’ with it – they actually go unconscious and then fall. There’s a myth that you can’t eat bananas or grapes, that’s a misnomer. People can eat anything they want in moderation. We say: eat a handful size. The main myth is that someone who has diabetes is insulin dependent.


In hospital, 10% of people will have diabetes. Most people here in Stockport will know someone who has diabetes. These people will get injections in later life. Nowadays we’re proactive with medicine. People with diabetes are one of the best looked-after groups in the country. We deal with people as a team of doctors, nurses, dieticians, podiatrists, and we bring in other specialists. Our job is to allay fears. Reassurance.


I have Type 1 Diabetes, was seven years old when I was diagnosed. I’ve done all the things you do when being a manic teenager. That’s what I tell the youngsters – you can still have your life. For the older generation, it’s explaining that they can still operate quite normally. Fit the diabetes around your lifestyle.

Type 2 Diabetes will be treated with lifestyle measures and tablets, a whole menagerie of tablets, and insulin injection too. People think its bad because it’s an injection. Think it’s worse than it is – associate it with hypoglycaemia and weight gain and sticking a shard of metal into wherever. They expect an injection to be something big and medical Hattie Jakes would use. But our needles are tiny, we don’t inject insulin into veins.


We have the grieving – a recognised circle of feeling. Anger, denial, acceptance. Most people accept it and get on with it. But denial (‘I’ll eat what I want’) and anger are part of the circle and will continually come round. If you have had things taken away from you – like chocolate – you will feel anger sooner or later.

For instance, if you are on insulin you can no longer drive certain vehicles. We negotiate medication with bus and taxi drivers. They fear, ‘My god I’m going to lose my job.’ Self-help groups are excellent for dealing with these fears, they have a massive input. There’s a lot of support – it’s actually very costly – 8% of the NHS budget goes on diabetes.


I can remember my first injection, I sat on the Sister’s knee and did it. Fantastic, look at me! I self-injected for a week. Then I reacted – ‘I don’t want to do it anymore!’ That was my circle of grief, coming round the first time.


We’re getting better at treating it, but it’s getting more prevalent. Firstly because we screen more aggressively. Secondly, we’re all getting fatter through lack of exercise. Diabetes isn’t just something that’s restricted to older people. The kids are getting adult onset diabetes earlier, because they’re not exercising.

The patients are not being blamed, but we are trying to put in place things to increase exercise and improve diet. Diabetes is an easy thing to deal with, but to encourage patients to go with your suggestions is easier said than done. For example, smoking and diabetes go hand in hand, smoking makes you many times worse and vulnerable. How do you stop the bad habits? People who are motivated will flip out of that at some point. Who finds it hard to cope with the restrictions? The people who don’t cope is everybody – it’s just the length of time that they opt out of the diabetic system that alters with the individual.


I know someone who was a bad lad – a lot of naughty habits - didn’t make any allowance at all for being diabetic. Complete denial. Now he’s got holes in his feet and he’s at risk of amputation – and he’s the most responsible patient you could meet.


When I was younger, I went travelling. I was in Yugoslavia at a railway station and I needed to inject. I went to the ticket office to ask if there was somewhere I could do it, but they didn’t understand me. I didn’t speak their language. Eventually, I injected on the platform. Looked up and there was a circle of gun muzzles around me. They arrested me – and I was saying ‘I’ve got to eat something in half an hour!’ It was three and a half hours before the interpreter came and I was in a bad way by then. Travelling was a risk, but it was calculated. Fit the diabetes around your lifestyle.


For the rest of your life you go around the circle – anger, denial, acceptance. For most of your life we hope you’ll stay in the acceptance stage. Encouragement, support, good pharmaceuticals – that’s what people need and what we try to provide.


Research is key – improvement in diet, lifestyle, drugs, machinery to test blood and so on. Insulin has only been extractable since 1922. Before that, if you had Type 1 Diabetes you were dead. We treat it as a whole team: doctor, nurse, dietician, physiotherapist, wheelchair exercise people… It’s not just in every part of the body, it’s in the head. It’s global. A big, big jigsaw of attitudes. You have to take it apart and put it back together again.


The best patients take on information bit by bit, they’re prepared to wait. Ongoing diseases go on. The information, the research, changes. You can’t expect to have this information immediately, you have to be patient. People who have the time and resources to learn about it deal best with diabetes. The patients need patience to listen. But the care staff need patience to listen to the patients!


When I was diabetic as a kid I got given five needles a week. My dad was an engineer and used to sharpen them for me. My mum would boil the syringes on Sunday. I can still smell the surgical spirit.


Fraser Burton was interviewed by Lois Blackburn and Philip Davenport

Thursday, 24 September 2009

Interview with Sister Julie Hopwood. Rehabilitation Ward, Cherry Tree Hospital

I knew what I wanted to do this right from leaving school. I wanted to be a nurse, and I wanted to work with older people. I had always had a great affinity with my grandmothers and older adults. I knew it was a Cinderella Service, but I felt prepared to meet the challenge. I did an A-level pre-health course at Stockport College. At eighteen I started my nurse training at Withington Hospital. As a newly qualified staff nurse I went to Barnes Hospital and did stroke care. I was fortunate, and became a ward sister within a short period of time here at Stockport. I hope my early appointment was attributed to my enthusiasm and drive to make a difference in this area of care.


I started my job as a ward sister at the same time as a newly appointed charge nurse. It was a good partnership. We had both been trained in the South Manchester at same school of nursing. The ward had both the benefit of a male and female perspective. Together we made changes – nurses were encouraged to owned the care they gave. We allocated specific nurses to specific people – it encouraged a deeper relationship – if you look after somebody day after day, you don’t just talk about the weather, you talk about real issues and what concerns them. Care needs to be personal and individual to give the greatest benefit. People think older peoples medicine is about incontinence and dementia. It’s not. It’s about adults who are ill – often with combinations of illness and complex care needs. We should adjust our ideas because people now stay well longer. We are more likely to give elderly care in all specialities of the healthcare. Care of the future cannot discriminate against age.


We offer dignity and respect, by discussing and offering patient’s options. It’s about control, offering choice, giving the patient control. Even as simple as: “ Do you want to wear this, or this?” At one time you did what the doctor ordered. Now, you get options, you are still an adult, not a lesser person because you’re elderly.


Older people have amazing life experiences. They’re an interesting group to work with. They saw the world when it was a different place. You can also ask the question: when are you old? A 65 year old can have an ‘older’ outlook than a 90 year old who is a fighter and has lasted through many changes in life. There was a lady I looked after who described how she used to chew the bed-sheets at night when she was a child, because she went to bed so hungry as a consequence of living in poverty with a very large family. How different times are now. Now we look after elderly people who carry mobile phones!


Even in my time of being a nurse, I’ve seen changes in care. If you were a patient with incontinence, you had to wear a pad and particular adapted clothing, almost a uniform. Pain management – now instead of injections, we have patches that absorb into the skin. We also have a more positive attitude towards death. With good management, you can have a good death experience, pain controlled, nausea managed, psychologically supported.


In elderly care, we assess for scales of depression, which can affect recovery – if you come in here thinking you’re going to die, it doesn’t help recovery. We discuss the need to use antidepressants if a low mood is identified. Lack of motivate hinders the recovery process. Treatment with antidepressants though may take two or three weeks to start a therapeutic effect and that can impact on the length of stay in hospital. The emphasis now is to get people out of the hospital as quickly as possible once they are medically fit.

The focus in rehabilitation has changed. It used to be non-acute care or convalescence in a hospital setting. Once rehabilitation patients were medically fit but frail and in need of therapy in a hospital setting. Now rehabilitation aims to happen out of hospital; in your own home, or in an intermediate placement at a residential home. Decisions about discharge destinations for rehabilitation are usually made considering night time safety and social circumstances. Hospitals are going to struggle with meeting care needs in the future as our population grows if it does not do things differently. Hospital stays aim to be about acute care, you come here if you are medically unwell and are in need of active medical intervention that cannot be met in the community.


Florence Nightingale said hospital should do you no harm. But if you put sick people together, you put them at risk. At home you are safer, if you can self-care. If people self-catheterise, they’re less likely to get infection. Same with self-care of emphysema, the emphasis now is training people to recognise they’re getting ill and to treat themselves with readily available steroids and antibiotics, so they don’t come into hospital and get recurrent infections. Kids with diabetes learn to monitor their own insulin levels.

Infection control is a big issue. We’re making advances in cleaning skin. Washing hands between patients, sterile gloves and aprons. There’s a lot of hand-washing. We wash hands before and after each person. But constantly hand-washing can make your hands dry and crack – which in turn carries risk of infection – so you need to moisturise hands too. Our hands are the tools of our trade so we have to look after them!

We use colour-coding: aprons are green for food, blue for dressings, yellow if a patient is infected, and white for general use. The mops and buckets are all colour-coded too to use in separate areas of the ward. Simple systems make a difference.


The public have been frightened by the news coverage of increasing numbers of MRSA and Clostridium Difficile in hospital settings. If you were to get on a bus full of everyday folk, a high percentage would have MRSA on their skin. That isn’t a problem as they are fit and well individuals. MRSA has a greater impact on un-well individuals especially those in hospital. Patients can become infected with the organism as a consequence of passing the skin barrier at wound dressing, catheterisation and cannulation and so hand washing and asepsis is vital practise.


Then there’s the bowel infection Clostridium Difficile, which is usually antibiotic induced. If you are frail and you’ve taken certain or multiple courses of antibiotics then you are susceptible to this infection. The antibiotics can destroy the good flora in your gut and the dormant toxin present in your gut can takeover giving you the drug induced colitis and subsequent diarrhoea which is clostridium difficile. This infection could then contribute further to increased frailty and an increased length of stay in hospital.


It’s about being human, coming into hospital. You are faced with your frailties. You’re the new kid at school again. You want someone to show you round, make you welcome. We’re preparing your journey, whatever it is. We have a duty of care and we try to engage family and friends too, for help. It’s not just about us who are the carers or experts in care. The family contribution is vital, as they know the particular person and how they behave when they are well. If they are concerned about something, I seek a medical review. They can’t necessarily say what is troubling them about the state of their relative, but they have a perception and it should be taken seriously, not dismissed because they aren’t professionals. Working together with the family unit is important to achieve the best outcome for the patient.


Complaints shouldn’t be dismissed either. They shouldn’t be seen in a negative light, because they help us to improve our service when we get it wrong. We are all human and capable of getting it wrong sometimes; as the saying goes “By the grace of God there go I”. If we don’t reflect, review and change, then we’ll make the same mistakes over and over again.


Who deals with hospital best? It is hard to say. Some people present well, but they will not share their experiences – they could be anxious or depressed. Men especially try to put on a brave face. You could line up five people with the same illness and they’d all present differently. It’s about how people deal with it, there’s not a right fix for everyone.


Accident and Emergency focus on illness first, but in rehabilitation we need to consider the physical, psychological, spiritual, social aspects. We determine how you were living before your illness, what are achievable goals, what goals are too big. People sometimes get disappointed if they measure themselves against others. But we are all different and can respond differently according to our life conditioning.

The physical and mental are interlocked. Some people believe that faith helps them. But you can also turn that on its head. Others see illness as a punishment from God.


Motivation and following instruction has a lot to do with recovery. I cared for a man who had a stroke, a bad one. By his motivation, his diligence, he recovered more than he ‘should’ have done. And the converse can happen. If a stroke damages part of the brain that affects understanding and you can’t follow instructions, then your recovery isn’t going to be as good. You also have people getting aggressive towards staff because of misunderstandings. If a nurse is doing something to you that you don’t understand, then you defend yourself. And that can get you labelled as difficult, or disturbed… If you have a diagnosis of dementia, people tend to stand back from you. But dementia doesn’t necessarily bring behaviour difficulties.


For staff, is it possible to have compassion, fatigue, burn-out? I’ve had burnout because I care passionately about what I do and understand my responsibility as a registered nurse and ward manager. I often stay after hours if the service requires it for a better patient outcome or to ensure management goals are met. But sometimes it does become expected that you will stay on and sometimes you have to draw a line that you balance your work and home life. Care can fluctuate at the end of shift, so you might stay on if you have the skills others haven’t. I’m the manager of the ward, so I need to have an overview of all the ward issues to lead effectively. I need support and good communication from the ward staff. I ask for feedback on their workload & how the shift was, to enable me to delegate appropriately & protect them from fatigue and risk of injury. I try to be fair & balanced with my decision making but I am mindful that we have to meet the service needs.


You’ve got to get a team that works well together – a 24 hour service. People cannot be left packed up in bed with incontinence pads. A pressure sore only takes a couple of hours to develop. You can’t sit and read or knit – you’re being paid to be a nurse. You are always on the go assessing, anticipating and meeting patients care needs.


If you’re a patient with dementia, you might need the prompt of sitting at a table with others in order to eat. People coming together makes them interact. People with dementia in that situation will perhaps pick up knives and forks when otherwise they might not have done if left to themselves. New wards are designed for bed to chair existence with no dayroom or dining facilities. This is the design for acute care and not rehabilitation. Almost like battery nursing on a conveyor belt- quick in quick out. Time will tell if this new design will change to again encourage patients to interact.


People need to understand their illness – for instance, a stroke is not a quick fix. They need a strategy, things to occupy them, to entertain them. Everyone is individual in this, recovery time is individual. And even their personal coping strategies have to change – using same coping strategy repeatedly doesn’t work. The family can help get people re-engaged into the community. Going out into the grounds in a wheelchair, go for a drive with your family. Achievable goals must be given to motivate recovery. Prognosis & progress should be discussed honestly. You have the right to the information first, if it’s about you.


We all become vulnerable at some time in our lives. This might be for physical, or mental, reasons. Or it might be emotional, a relationship break-up for instance. We hear a lot about ‘vulnerable adults’ and we have changed our practice because of that.


Changes always come, turning what we previously knew on its head. Nursing changes, it spirals, moving on. We should take the good with us, looking always with new eyes.


Interview with Philip Davenport, 2nd September 2009