Personhood-focused relationships: a moral drive to get away from the transactional nature of care

In a way, the approach thus far has been very straightforward.

Even after abolishing ‘asylums’ for mental illness, Tom Kitwood pointed out the remains of the asylum days. That is, with all the best will in the world from all parties involved, a tendency towards ‘warehousing’ of people with later stages of dementia. In such places, often framed as microcosms apart from the rest of society, ‘care’ is meant to take place, but historically with an overdependence on drug rounds rather than a resident’s need to have a haircut, for example. Whilst many professionals do not wish to see care as transactional, there is recurrent use of this language by think tanks and policy makers. This managerial approach fragments life into processes which can be easily identified and, if need be, costed.

One of my biggest surprises is re-reading Tom Kitwood’s “Dementia reconsidered” was his prophecy about the impact that the hybrid market of the NHS and Community Care Act (1990) might place. Care should be care regardless of setting, and care does not necessarily have to be institutionalised. But there are simple ways in which care institutions do not have to be cut off from the rest of the society – why not have WiFi in these places?

But of course, this goes way beyond WiFi.

The drive towards ‘relationships centred care’ was a reconfiguration of person-centred care, but which did not ignore personhood. Reminding myself of Kitwood’s flower, known a decade before the travesty at Mid Staffs, it is clear to see how fundamental aspects of personhood could have mitigated against bad care.

The 'Kitwood flower'

Whilst there is a lot of extremely good care, there are some ‘spoiled apples’ such as Mid Staffs – which subsequently has tried a ‘clean break’ and Winterbourne. But it would be a danger to regard them simply as ‘spoiled apples’ or freak occurrences, as indeed Morecambe Bay pointed out. Markets involve transactions. What Tom Kitwood warned about, albeit subtlely, is very important in my view. What has gone wrong in recent years is care environments being run for a ‘surplus’ or ‘profit’, with budgetary pressures such as PFI loan repayments. Staff themselves have been viewed as a commodity, and the tendency to run a healthy budget sheet has to be run a minimum of staff with minimum time to care – which can render initiatives such as 6Cs ineffective.

A “health transaction” which is under-resourced and rushed is likely to be unsafe. But that is not to say money solves everything. And while we’re on the money there seems to be plenty of money elsewhere, for example in finding a ‘cure for dementia’, the ultimate nirvana which Kitwood indeed warned about.

fraud

Neither the person living with dementia nor caregiver wish to be involved in a ‘woe is me’ ‘victimhood’ race to the bottom, but the pressures for not being appreciated properly are huge for both parties. Despite think tanks and policy makers wanting to ‘measure it’, the quality of person-centred care has been hard to define. That’s because, I believe, personhood is fundamentally about relationships too, as well as the uniqueness of the person at that particular place and time.

Kitwood’s own definition on page 8 of ‘Dementia reconsidered’ pulls no punches.

“Thus we arrive at a definition of personhood, as I shall use the term in this book. It is a standing or status that is bestowed upon one human being, by others, in the relationship and social being. It implies recognition, respect and trust. Both the accoeding of personhood, and the failure to do so, have consequences that are empirically testable.”

A quality of care for dementia is not necessarily the same as the quality of medication. Take for example the lack of effects of the vast majority of ‘dementia drugs’ on quality of life. But quality of care, one would pretty readily concede, is linked to the quality of relationships. The idea that relationships involve emotion and affect, and reciprocal, is clearly defined in the construct of ‘relationships centred care‘.

But as a financial transaction, this is hard to measure; and Kitwood conceded there is not real competition for the market to be effective (p.44). And striking is Kitwood’s claim that ‘In particular, people do not know what they need and can be easily deceived by ‘experts’ who act for economic motives’. Another view of this would be to all embracing and for it to be reframed yet again as ‘patient and family-centred care’. But note the reference to ‘care transactions’ on this page, and the construct appears more like a service to sell rather a frame of mind arguably.  And not everyone has a family.

In my final book on residential care (including care homes and nursing homes), I will reset the direction of the compass of ‘person-centred care’, a term used by Kitwood himself, to orient it more to what I think Tom Kitwood himself meant: “personhood focused relationships”, which can indeed be applied to residential care settings.

People living with dementia are the ones to listen to. They’re going to be the stars of the ADI Conference.

Perth

We’re nearly there. Between 15th and 18th April 2015, Perth Australia will be the host for the 30th International Conference of Alzheimer’s Disease International.

If you ever an opportunity to listen to Tommy Whitelaw for an hour, do it. It’s really easy for people interested in English and global policy like to me to become obsessed with the usual macro policy details, but many people aren’t interested in macro. They want to know how the organisation of health and care systems will affect them individually.

We need to face facts. That is, there are about a million unpaid caregivers often members of a family, like a child or a spouse, in some form of care or support rôle. They do not see themselves as being labelled ‘carers’, but are fully aware of the rewarding and demanding aspects. Invariably they describe how they’ve never been given any formal preparation, just chucked in ‘at the deep end’.

It’s still pretty amazing that there are people who, despite being incredibly busy, find time to go on courses such as my friend Charmaine.

And here’s another crucial ‘issue’. I know nothing about what it is like to live with dementia, nor to care for someone with dementia. I am not a fan of the term ‘co-production’. There is, however, nothing more important than research and service provision being designed around the needs of the people who want the system to help.

I of course like the idea of ‘primary care support workers’, but I do like the idea of GPs being able to diagnose dementias more confidently (particularly differentiating the younger onset dementias, such as frontal dementia, from psychiatric syndromes such as anxiety or depression).

I like the idea of trained specialist nurses being able to get to know a person living with dementia more. I would like greater clarity of how professionals, people in a care or support rôle, and people living with dementia can work together, share knowledge and views, come to a plan while managing beliefs, concerns, expectations and conflicts. I would like this without the bubblewrap of selling “person centred care” and policy wonks, managers and politicians getting fixated with their measurement and gaming.

There will be a few highlights for me in the Alzheimer’s Disease International conference coming up. Not least is Al Power who I’ve got to know reasonably well in the last few weeks – and who seems to be one of the guys who ‘gets it’.

The programme is amazing, with lots for everyone to get their teeth into.

The keynote speakers are stunning.

There are fewer things more humbling than to listen to Kate Swaffer or Helga Rohra. Of course, it is a tall ask to be able to be representative of any of the 47 million people living with dementia, but you get immediately a flavour of what these two view as important from them speaking. They want things better for other people living with dementia, and they are living in the here and now. They don’t deny making the world a better place for the future, but they want people with dementia to emerge from being hidden from view to being active people in society wherever possible.

Of course, the diagnosis of dementia itself is a big deal, and I personally feel, like Chris Roberts, living with mixed vascular and Alzheimer’s dementia in Rhuddlan Wales, and prominent Dementia Friends Champion,  that more care has to be paid to preparing the ground for the diagnosis, the diagnosis itself, and what happens after the diagnosis.

And pay attention to Kate Swaffer, Co-Chair of the Dementia Alliance International, who politely queries how her investigations were done without clear explanation. I find this approach from the medics ‘underhand’, but Kate would be far too polite to say so, I reckon.

Kate’s excellent personal blog, “Creating life with words: inspiration, love and truth”, is a must to look at.

People with dementia have human rights, and it’s become accepted, sadly, for people including professionals to abuse those rights, e.g. physical restraint in residential homes.

Helga, Chair of the European Working Group for People With Dementia (with Alzheimer Europe), doesn’t refer to ‘stages’ of dementia, and I agree with Helga; ‘stages’ is a very medical term, and I have never known such clear linearity (people varying at symptoms in different presentations and rates). But whatever ‘faces’ of dementia, people with dementia and those closest to them have an inalienable right to dignity.

I’ve been honoured to have advance notice of what will be in Truthful Kindness’ presentation. That too will also be a smorsborg of creative astonishment on how one person from California has successfully inspired others around the world to live with symptoms of a dementia.

I do not deny the incredible work being done in dementia friendly communities and young onset dementia around the world. I know, because I reviewed a lot of the abstracts for the conference in these categories, being on the advisory committee for the conference.

But, above all, it’s a chance to meet up with people I like, and whose work I respect, like Simone Willig. There is a real sense of global solidarity I feel currently, including of course the traditional work being done in translationary neuroscience.

I will be looking forward to bumping into Marc Wortmann while dunking my biscuits, as usual; and I look forward immensely to meeting Glenn Rees, the incoming elected Chair elect of Alzheimer’s Disease International.

I reckon I’m all set – I’ve only got this far in organisation for this ‘trip of a lifetime’, thanks to Jayne Goodrick.

We are only a week ago. Am I excited? Very.

Anything can happen to anyone at any time

let life go

 

When I woke up on the top floor of the Royal Free in North London at about 10 pm, it was left to a junior night-duty nurse to explain to me that I had been in a coma for six weeks.

I was later to be told that Tony Blair was no longer Prime Minister; and that there had been a foot and mouth health crisis.

I had a very brief medical career, but it always struck me how life-challenging diagnoses seemed regularly to be given to the nicest of people.

While I ‘get’ the current drive towards compassion in the NHS, any person who has been a doctor or nurse on a medical ward will tell you about how you do have to park emotions elsewhere when you’re confronted with emotionally very challenging issues.

What I do not think is acceptable is politicians of all parties, imposing neoliberal austerity, airbrushing under-resourced secondary care wards with the ‘fault’ of clinicians who do not have the time or resources to care.

You see, following my cardiac arrest and epileptic seizure in the summer of 2007, heralding my period unconscious on the ITU of the Royal Free, I believe that anything can happen to anyone at any time.

I then spent two months as an inpatient of a neurorehabilitation ward of the National Hospital for Neurology and Neurosurgery, where indeed I had been a junior doctor.

One of my best friends was a man about my age who had accidentally fallen down a pothole, had been admitted as a neurosurgical  emergency, and had an entirely new titanium skull fitted.

I have already been dead in a sense; but in my subsequent life, I live each day as it comes. This totally changes my perspective on life.

I don’t have time for ‘woe is me’ stories, not because I am a heartless bastard; but because it will surprise you with the amount of personal pains people have in private.

I think there are dangers with adopting a ‘victimhood’ stance. I don’t spend time thinking about how I could’ve avoided becoming physically disabled in adult life. But likewise the people I have seen who have out of the blue decided ‘enough is enough’ have taken their decisions out of the blue.

One close friend of mine killed herself, also a medical student but who had a housing crisis, drank two bottles of wine and drove her car off a cliff in Cornwall. I remember tidying up her room when her parents came to clear up all her belongings in student accommodation before the funeral.

Only weeks earlier, she had been telling me about her wish to be a neurophysiologist.

If we all concentrate on the past or future, we lose neglecting what is happening today. But today we can do things and will be surrounded by people who won’t be there one day.

I think we are all on a learning curve, and no matter how senior you are, nor how many qualifications you have, you must always be willing to listen, and sometimes admit you have failed. But likewise when things go well things how they went well, and what can be learnt from them.

I feel mistakes have been made in English dementia policy, like having incentives for diagnoses in dementia without addressing requirements of the workforce, but I have no involvement with the machinery of NHS England. My ‘ambition’ is to carry on what I am doing, with the people I want to do it, and expect nothing in return.

How to get tickets for the pre-launches celebration of our dementia books in Camden on 11 July 2015

Kate Swaffer (@KateSwaffer) and I, Dr Shibley Rahman (@legalaware), intend to do a joint book launch later this year.

Both books are being published by Jessica Kingsley Publishers later this year.

We request the pleasure of your company.

Tucked away in the heart of Camden Town, our hosts, the Arlington Centre, are known to be a very popular venue for community events like ours.

Details of the Arlington Centre are here.

The event will start at 2 pm on Saturday 11th July 2105.

The hashtag for the event is #KateShibBooks.

talk

Please note that this is the final and settled date and venue for this event. Thanks very much for your patience while we have been resolving this.

This event is strictly by invitation only – so we do request that you sign up in advance. We have tried to avoid this event clashing with the RCN Congress to be held in Bournemouth this year.

Attendance is, needless to say, completely free of charge.

Please sign up HERE – first come first served. 

 

 

light bulbs

 

Kate Swaffer (@KateSwaffer) and I, Dr Shibley Rahman (@legalaware), intend to do a joint book launch later this year.

Both books are being published by Jessica Kingsley Publishers later this year.

We request the pleasure of your company.

Please note that this is the final and settled date and venue for this event. Thanks very much for your patience while we have been resolving this.

There is, as such, no programme for this event; but attendance is by invitation only.

To request a ticket please sign up.

 

Please note that the last day for application for a ticket/tickets is June 27th; but the event will take place on July 11th 2015.

Refreshments will be available throughout.

We are in the very comfortable Arlington Centre which holds regularly such professional events.

 

The aim of this event is to launch two separate books by Kate Swafffer and Shibley Rahman.

 

It will be informal in approach. People from a diverse range of backgrounds have expressed an interest to attend, and this will be reflected on the day when guests will be encouraged to introduce themselves to one another.

 

While the programme is flexible, the afternoon will have two complementary prongs of attack.

 

One will be to establish the ‘macro’ environment of dementia policy around the world, as discussed in Shibley’s new book (currently schedule for July 21st 2015 publication date).

 

The other one is a personal experience of life by Kate Swaffer. Kate’s book is wideranging, including a life expereince after receiving a diagnosis of dementia, but will reflect Kate’s much wider knowledge and other interests too.

 

We are hopeful that ‘highlights’ may include contributions by Dr Richard Taylor, a world ‘champion’ in issues to do with dementia living with dementia and who has written a Foreword to Kate’s book; and Chris Roberts, a ‘Dementia Friends Champion’, ambassador and who has written a Foreword to Shibley’s book. 

 

Also, Kate herself will be doing selected readings from her book (details below). This, I anticipate, will be a popular focus of the afternoon.

Please let Shibley (srahman@doctors.org.uk) know of any special requests for this afternoon, and they will be considered by both Kate and Shibley. 

 

 

best wishes, shibley

 

6 April 2015

 

Notes:

 

Kate’s book is called, “What the hell happened to my brain?

Details are here.

Information about this book:

“Kate Swaffer was 49 years old when she was diagnosed with a rare form of young onset dementia. Here, she insightfully explores issues relating to that experience, such as giving up employment and driving, breaking the news to family, having a suddenly reduced social circle, stigma surrounding dementia and inadequacies in care and support. Kate also shares her experiences in dementia activism and advocacy, highlighting the important role of social media in combatting isolation post-diagnosis. Kate’s empowering words will challenge preconceptions on dementia, highlight the issues that impact individuals living with a dementia diagnosis, and act as a source of comfort for them and their loved ones. The book will also be of interest to dementia care professionals.”

Shibley’s book is called “Living better with dementia: looking forward to the future“, as a follow-up to his irst book “Living well with the dementia: the importance of the person and the environment” which was received with critical acclaim.

Details are here.

Information about this book:

What do national dementia strategies, constantly evolving policy and ongoing funding difficulties mean for people living well with dementia? Adopting a broad and inclusive approach, Shibley Rahman presents a thorough critical analysis of existing dementia policy, and tackles head-on current and controversial topics at the forefront of public and political debate, such as diagnosis in primary care, access to services for marginalised groups, stigma and discrimination, integrated care, personal health budgets, personalised medicine and the use of GPS tracking. Drawing on a wealth of diverse research, and including voices from all reaches of the globe, he identifies current policy challenges for living well with dementia, and highlights pockets of innovation and good practice to inform practical solutions for living better with dementia in the future. A unique and cohesive account of where dementia care practice and policy needs to head, and why, and how this can be achieved, this is crucial reading for dementia care professionals, service commissioners, public health officials and policy makers, as well as academics and students in these fields.”

Kate and Shibley have decided to make a limited number of tickets for this free event for this book launch available to all, but the event is generally by invitation only.

If you’d like you to be considered for one of these limited number of tickets, please do let us know.

Thanks and best wishes!