Tag Archives: Mental Health

Blimey……

…… I think my brain is full.  I and one of my work colleagues spent Friday and Saturday at the University of Essex on a 2-day workshop entitled: Capacity Assessments: Ethical, Political and Metaphysical issues.  Whilst it may sound like an indulgence, it was really useful and challenging to spend two days discussing and learning about the wider philosophical, medical and legal issues relating to current legislation on mental capacity.  The Essex Autonomy Project is a fantastic resource for anyone working in this sort of area (health and social care) and for anyone interested in the philosophical nature of self and autonomy.  I got to talk with all sorts of people that I normally wouldn’t have in-depth discussions with – lawyers, judges, psychiatrists, philosophers, social workers, researchers, students.  All interested in mental capacity and the ethical and moral issues around what happens when someone is deemed to lack capacity.  There were debates over the meanings of words, I learned about the ecology of capacity, we all struggled with the philosophical and legal implications of the UN Convention on Rights of Persons with Disabilities (especially article 12).

This last one was a difficult subject, because, if you choose to read the salient points of the Convention (to which the UK is a signatory), there are different ways in which Article 12 is being interpreted.  One of the implications of this is to potentially scrap the concept of “mental capacity” altogether when it comes to issues of law.  However, the UK is recognised as having a very progressive piece of legislation in the Mental Capacity Act (which is what I work with), which aims to provide a protective framework for individuals who lack the ability to protect themselves from harm or to take decisions for themselves (subject to a number of key conditions).  No-one in the room, or indeed that I know, would seek to reduce the rights of individuals with disabilities, and the UN CRPD contains some of the most comprehensive and clear statements hammering home the point that all are equal, and it builds on the UN’s Universal Declaration on Human Rights in a way that can only be beneficial for all persons with disabilities.  But I am still pondering over the implications of Article 12 and the fact that many of our laws will need to be looked at to see if they are compatible with the UN CRPD.

Tom O’Shea‘s presentation on the concept of an ecological model for capacity assessment intrigued me, and when looked at in conjunction with the idea of decision communities, is food for thought in my line of work.

The presentations and subsequent debates around the concept of “use or weigh” in the second part of the 2-stage MCA capacity assessment was really interesting, especially when exploring the concept of belief and the meanings of words like understand, appreciate, evaluate and reason.  It was a challenge for the three speakers to present their perspectives on this, but Neil Allen, Dr Gareth Owen and Dr Fabian Freyenhagen were clear, concise and fielded all subsequent questions and debate very well.

The Friday evening was the first time I have been in a Student Union bar for god-knows how long, and I got to have a really interesting conversation about historical psychiatry and the cultural differences between the US, England and Scotland, and about class prejudices with Dr Scott Kim (US) and Professor Peter Bartlett (Canadian) and others.  All very enlightening and good fun!  It was also really nice to meet Lucy Series, author of The Small Places blog, which is incredibly interesting and thought-provoking.

All in all, an excellent if knackering two days.  I will happily do it again.

One sentence that summarises each year of your life so far……

……um, gosh:

1974: Born in March, living in Langbank.

1975: Moved to Greenock.

1976: The Joyous One is born.

1977: No idea – who can remember being three?

1978: Big hairy caterpillars on Jura.

1979: Take a dead blue tit in for the nature table: Miss Armstrong was not impressed, but I am glad I am not in Miss Grant’s class because she was a scarey lady.

1980: I think Mum is embarrassed by Brian’s arrival as the baby Moses basket is located in a corner behind one of the living room chairs: I later discover this is probably to stop the dog knocking it over.

1981: No idea – a blank.

1982 : Also a blank.

1983: Blank – did I have a 3-year period of amnesia?!

1984: Kitten-heeled shoes :)

1985: TV!!!!!!

1986: Finish primary school – head for Greenock Academy.

1987: I get straight A-grades in my report card for everything apart from maths – I’m crap at maths.

1988: Arran, sausage sizzles and sea kayaking.

1989: Lots and lots of studying: seemed so important at the time.

1990: Pompeii, Herculaneum and pizza in Sorrento.

1991: Run amok in the Art Department and do nothing else but painting and classics for the whole academic year.

1992: Move to England.

1993: Went out for stamps, came back with tattoo.

1994: Fail Agricultural Biology, spend birthday on the White Horse at Uffington with Rob.

1995: Get pissed on by Apodemus sylvaticus and Clethrionomys glareolus a lot.

1996: Graduate and spend the summer identifying and surveying butterflies – the difference between small skipper and Essex skippers is the colour of the underside of their antennae.

1997: I win a village pub Christmas Eve fancy dress competition: I am not in fancy dress – this is how I normally dress.

1998: New Zealand & Australia – sea snakes and shark feeds off North Horn.

1999: GHP – I am overwhelmed by trees, polytunnels and an amazing team to work with.

2000: LARP.  That is all.

2001: Trees and seeds, lots of them.

2002: Buckingham Palace – the Queen is very small.

2003: The cows break down the fence and ravage the vegetable garden; one gooseberry and some onions are saved.

2004: Left conservation for mental health advocacy.

2005: Mental health advocacy work is both challenging and occasionally hilarious.

2006: New Zealand and Joy’s wedding.

2007: Egypt, lack of sharks, lots of lionfish and blue-spotted stingrays.

2008: Lots of camping.

2009: New Zealand, road trip, whales, albatrosses, and dolphins of the land.

2010: Hard work.

2011: not finished yet, but doing ok so far.

Food for thought……

…… found this today, published last month.  I am very pro-free legal representation for persons whom the state has seen fit to deprive of their liberty whether by use of the Mental Health Act, Mental Capacity Act or DOLS.  So I welcome the MHLAs concerns that funding cuts will impact on tribunal appeals and representations in relation to wrongful/unlawful detention and potential ECHR/HRA breaches for individuals.  We all have the right to swift recourse to justice and in the case of MHA/MCA impacted clients, I firmly believe in the right for this not to be means-tested.

However, what no-one has been able to tell me (and I work with mental health solicitors who echo much of what is printed below) is – how much to solicitors actually get paid for this work?  What is the financial cost per hour below which their work becomes financially unviable?  What does the cut mean in real live money terms?

I ask this because I imagine that one does not specialise in mental health law primarily to become rich, but because one believes in upholding the rights of the most disadvantaged and ensuring that all get access to fair hearings in a timely manner.

Love point 2.9, btw: appealing a DOLS authorisation is a lengthy, time consuming, impenetrable and inaccessible process for all but lawyers or solicitors.  Bringing the initial appeal process under the wing of the Tribunal system would mean a much easier recourse to challenging the authorisation, make it all much more cost effective, and be much more accessible for everyone. What a good idea. I like it.

Response of the Mental Health Lawyers Association to Legal Aid, Sentencing and Punishing of Offenders Bill “Destroying Representation for the Mental Unwell for £3million?”

1.
Introduction

The MHLA represents the majority of solicitors and solicitors firms who represent those detained in hospital. Our members have been involved in significant cases that have helped establish the rights of vulnerable people. The Association was founded in 2000and has contributed to many consultations on issues that concern our members and those we represent. The Association is recognised as the organisation representing specialist lawyers in the field by bodies including the Law Society, the Judiciary, the charity MIND and the Ministry of Justice itself. We have met with a range of Government and parliamentary figures, including Ministers. In addition a representative of the Conservative Party, Edward Garnier, addressed a recent MHLA conference, in November 2009.

 2.
10% Reduction in Fees

2.1. Introduction

The MHLA welcomes that the work of our members will generally remain in scope of the legal aid scheme. However we are greatly concerned with regards to the 10% reduction in fees which are still proposed, notwithstanding our particular earlier representations as to this jurisdiction, which were not addressed in your response. This will be disastrous for many of our members and therefore for the highly vulnerable clients that we represent. We see ourselves as a frontline service to our clients, but now consider that much of this service will collapse. This risk of collapse runs directly counter to the acceptance that this representation should remain within scope as a central plank of the legal aid scheme.

Our work with detained patients is seen by all, including the Ministry of Justice, as “core legal aid work”. Indeed when we were addressed by Edward Garnier, and in other dealings with the Conservative Party prior to the last election, we were impressed by the acceptance that our work was central to the operation of justice in a civilised society given our highly vulnerable clients.. However these proposals, and in particular the 10% cutback, do appear to directly contradict this assurance. 

The ability of those detained due to an alleged mental disorder to receive representation to challenge such detention is critical to the United Kingdom’s compliance to the ECHR. This is why such work it is one of the few non-means tested areas of legal aid. However, the effectiveness of such representation, as we pointed out to shadow conservative Ministers prior to the election, has been in decline for many years.

2.2.
Decline in Specialists in the field

The need for specialist representation for the most vulnerable in our community was the reason why the Law Society set up the first specialist Panel of lawyers in this area of practice. However, membership of this Panel has declined by around 25% sinc 2000, whilst the number of patients requiring representation has increased by around 30%; according to figures provided by the Tribunal Service. Furthermore a previous Law Society survey has shown that the average age of Panel members is middle age or above. Far fewer “young” entrants have been joining the Panel.
Our members directly report to us that the reason for leaving this area of
practice is the existing fee levels. The arbitrary proposals to reduce fees in
this area of representation by a further 10% will certainly rapidly accelerate
this process. 

The implications of the 10% reduction have been clearly depicted by a very longstanding and experienced practitioner in East Anglia who, when indicating he would have to leave this area of work, said: “This work is like being a minicab driver. You work Monday to Friday to cover your overheads: you make money that you can live off on Saturday. They now want to take away our Saturday”

 Our Association has been received numerous responses from members who will now no longer be able to carry out this work. It should also be born in mind that this cut is on the back of a lack of any recent increase and ongoing inflation, results in real cuts of around 15% in the last three years already.

A 10% reduction is therefore very much more than a simply shaving a few pounds off the budget. It is frequently the profit margin on which our members survive. And, as has been pointed out to the Conservative party previously, many of our members operate in small specialist practices. They have nothing to buffer their work and will simply go to the wall; notwithstanding their longstanding expertise.

2.3.
Judicial View of Mental Health Representation

The need for retaining such experience in the work we do has long been recognised by the judiciary. At the time of the introduction contracting Mr. Justice Brooke in the year 2000 (now Lord Justice Brooke) in the case of R v Legal Aid Board ex parte Mackintosh and Duncan (2000) gave the view of the Court on that occasion: “We are worried, however, that the Board (then the Legal Aid Board) has not yet appreciated how difficult Mental Health Law is, and how generally solicitors cannot pick up the expertise needed to serve the clients effectively, unless they have strong and practical grounding in this field of Law. We hope that the Board will now take urgent steps to identify the really skilled solicitors who are willing to serve their clients in this field at Legal Aid rates of pay ……………”. He also commented: “Reading the Report of a psychiatrist, identifying its areas of weakness, commissioning evidence and the appropriate expert challenge to it and representing a client at a Tribunal requires expert professional skills borne, as we have said, of education and practical experience. It is not like going down to the Magistrates Court as a Duty Solicitor, arduous though those duties are.”

Mr Stanley Burnton J. in KB & Others v MHRT [2003] made it clear that the MHRT is the most fundamentally important Tribunal in this country in that it deals with the liberty of the individual in circumstances where that liberty has been removed without having been sanctioned by a court. “The issues before MHRTs are probably the most important issues decided by any tribunals. The Tribunals make decisions as to the compulsory detention and treatment, and thus the liberty, of the individual. A wrong decision may lead on the one hand to the unnecessary detention of a patient, and, at the other extreme, to the release of a patient who is a danger to himself and may present a risk to the public. A patient will be the victim of a wrongful decision to detain him. Conversely, however, he may also suffer from a mistaken decision to direct his discharge.  The decisions of the MHRTs are as intrinsically important as many of those of the Crown Court……”

We are aware of the grave continuing concerns held by the Tribunal Judiciary relating to the decline in the quality of representation of patients in recent years and understand that they are looking to see how such decline can be addressed. Their particular concern is the continuing decline in availability of Panel members in relation to the rising amount of Legal Representation required. This has been greatly exacerbated by the effects of the MHA 2007 and the new Code of Practice attached to the MHA; coupled, of course, with the substantial decline in Panel Membership since 2000.

2.4.
Concerns of Care Quality Commission

We certainly consider that there is a link between the decline in the quality of representation; the decline in panel membership and the previous imposition of the fixed fee scheme in Mental Health Tribunal work. Indeed the link between the fixed fee scheme and declining standards has been raised in the last three Mental Health Act Commission/Care Quality Commission reports (those for 2005-7, 2007-9 and 2009-10). The CQC has reiterated the MHAC’s call for an independent review of the effects of the revised fee system, with a particular focus on Tribunal representation. It is of great regret that no steps appear to have been taken to set up such an enquiry. A further reduction of fees will only greatly worsen the concerns already raised by the Commission.

 2.5.
Ministry of Justice Research

Recent research by the Ministry of Justice itself in July 2010: Court Experience of adults with Mental Health Conditions, Learning Disability and Limited Mental Capacity confirmed the vulnerability of our client group. In particular it concluded the following findings:

Whilst across the board there was a range of awareness among legal
representatives of the particular needs of this client group, legal
representation was seen as a key support, particularly when the representative
was experienced in working with this client group, providing ”a unique
authority, perspective and understanding”;

Fixed fees were seen to be a barrier to good quality advice for this client
group who required more time spent on their case, for which the legal
representatives would not get paid; and

This client group had mixed success in accessing solicitors by telephone.

Again, a 10% cut, with its implications to specialists’ employment, appears to run directly counter to these findings.

 2.6.
Concerns of MIND

The Association has been contacted by the charity MIND. As you know this charity is frequently seen as the strongest voice for those suffering from a mental disorder. They are already aware of the research indicating a decline in the quality of representation and are greatly concerned as to the impact of the 10% reduction. We understand they are responding directly to your consultation. 

2.7.
Possible breach of the Disability Discrimination Act 1995

In the recent case of PIL & RMNJ Solicitors v Legal Services Commission (2010) the Court recognised there would be issues regarding detained patients with longstanding relationships with legal representatives. The Court was impressed particularly by medical evidence that the sudden breach of such relationships might well cause relapses in vulnerable patients’ mental health. The Court also noted that extensive psychiatric histories, including perhaps details of extreme abuse, would have to be re-counted at great length to new representatives. In the scenario resulting from a 10% cutback this situation is likely to be replicated as a number of long established practitioners suddenly leave the field. Although, of course, it would not be clear what representatives, particularly Panel members, who would be available to take over this role.

2.8.
Specialist Panel Membership Recognition

We have consistently argued for the need for good quality advice in the Mental Health category of law. We have in particular argued for recognition of membership of the Law Society’s specialist panel in this area, notwithstanding the decline in such membership since ten years ago. We feel that the failure of Government, to date, to link panel membership to fees has led to the decline in take up of the panel, with a knock-on effect on quality. We expressed concern about the imposition of the fixed fee scheme in 2008 given the effect we thought it would have. Again the 10% reduction in fees is a further leap in the wrong direction.

2.9.
Financial Implications

Our estimate is that would the financial implications of retaining the 10% would be very small. Our estimate is that the cost of provision of our work is around 1.6% of the total legal aid budget. Immediate savings made might be in the region of £3 million pounds however, the ultimate cost would be very much higher. Once specialists are lost to this area it is very unlikely they will return. Nevertheless the UK’s obligation to provide this representation will remain. Ultimately, therefore, the Government might be faced with a much higher bill to re-establish this “core” service.

2.10.
Proposals for savings

We consider that this process has already started because of more case management decisions following the 2008 Tribunal Rules. Adjournments have reduced over the last year.

There should be a review of Schedule A1 MCA 2005. This provides a legal
framework for the detention of those lacking capacity but who are not receiving treatment in hospital for mental disorder under the MHA 1983. The DOL Safeguards are cumbersome and unpopular with nearly all those who have to deal with them. The only appeal avenue is to the Court of Protection at considerable expense. Often, the case has to be heard in London, a long way from where the person subject to the DOLS (and their family and the professionals concerned) is based. DOLS cases are mainly still heard before the senior judiciary, with the effect that counsel is often relied upon. The costs are often many times in excess of the costs of even the most complex tribunal. The Safeguards could be replaced by amendments to the Guardianship scheme under the MHA 1983, with the Tribunal service dealing with appeals rather than the Court.

Setting a limit on the hourly rate that NHS Trusts and other public bodies can
spend on legal advice which is equivalent to that which is spent on advising
detained citizens.

 2.11.
10% Reduction – Conclusion

The Association is greatly disappointed that this blanket reduction has been proposed for our work with detained patients, notwithstanding earlier assurances given. Ongoing departure of specialists from the field, in direct contrast to a rise in demand for their services, will turn into a torrent should this reduction be implemented. Such a decision will run directly counter to senior judicial concern, coupled with those of the leading mental health charity MIND and the Care Quality Commission; not to mention research work carried out by the Ministry of Justice itself. Its implications may also be unlawful in terms of the Disability Discrimination Act. Our members see ourselves as a front line service for our clients and very much hope that the Department and Central Government will re-think this 10% reduction for our members. We would welcome the opportunity to expand on, or clarify, our concerns

Mental Health Lawyers
Association 9th August 2011

And then it rained…..

In a rather biblical fashion on occasions today.  And it was cold.  How DARE the weather be so unsunny and not-springlike?!!  Oh well – as long as we don’t have a summer that’s as miserable as the last two have been, it’ll be ok.

Spent this afternoon trying to start writing a set of guidelines for non-instructional advocacy, and getting my brain tied in knots.  I kept coming back to the question “who gives me the authority to do this?” and for instructional work, it’s the client.  However, in the brave new world of the Independent Mental Health Act Advocate, non-instructional work is a necessity, and we need to have a clear framework to do it it.  I’ll cobble something reasonable together eventually……as long as we all know what we’re doing and why we’re doing it, it’ll be right.

An exciting week…….

….. of all sorts of things.  Had a really fun event over the weekend – one of those omigodwereallgoingtodie events which turned out to be just fine.  It was pretty cold on the Friday night, but we were camping and I had a really bad migraine, so I was a bit miserable.  Felt better by mid-Saturday, and was much warmer on Saturday night.  The two sleeping bags helped :)  

Monday was spent recovering and panic buying some lovely new shoes for an interview on Tuesday, which, I have to say, was not one of my better efforts.  I just kind of dried up and despite loads of preparation, didn’t really say all I should have done.  However, by some fluke of fate and luck, I was offered the job!  I haven’t got a start date sorted yet – that’ll get sorted out next week.  I’ll still have the same line manager, but for a different bit of the service, and I am now happy to say that when I move across, I will be one of three IMCAs covering the county.  I’m looking forward to the training, which I think will sort of happen as and when over the next few months until I officially finish my current post and take up this one.  I don’t think it’s really sunk in yet, as it’s business as usual at work until otherwise informed.

The weather’s absolutely beautiful at the moment – blue sunny skies and warm breezes.  I didn’t mind being stuck in a traffic jam on the way home from work today as there were several pairs of lapwings wheeling above a field I was stuck beside, and in a farm entrance way, there were several wee sparrows taking dust baths.

Wine and nibbles……..

Just been to a book promotional lecture with Professor Paul Gilbert launching his latest book, The Compassionate Mind.  Really enjoyable evening; met loads of people to talk with, including some people I haven’t seen for ages.  I bumped into an ex-client (from work) who looked really well, and it was very nice to see someone happier and better in themselves – I only really ever see people at their most depressed or manic, or psychotic, so it’s good to see someone well.

Time to Change?……….

Time to Change is a relatively new campaign which is aiming to reduce the stigma that surrounds mental ill health.  Backed by Mind, Rethink and Mental Health Media, the national campaign looks to challenge discrimination in all areas of life in relation to expereices of mental illness.  Go on – have a look.  The might be something local happening in your area!  In Derby, there’s Derbyshire Mind’s Enjoying Derby project, which aims to get people out and about in their local area by joining organised walks – the aim is to reduce the impact that illness can have,as well as giving you a whole heap of other health benefits.  The walks are open to anyone who thinks that they might benefit from them, and let’s face it, most of us could do with getting up of our arses and being outdoors more :)

And in other news…….

…… my lovely and sympathetic boss said that work would possibly pay the parking fine I accrued the other week!  Hooray!!  How kind.  I like it when stuff like this happens.

Elsewhere in the sunny world of Fairy Basslet, work is all a bit up in the air whilst stuff changes with the new provisions of the Mental Health Act 2007 (yeah, I know it’s 2009 – that’s law implementation for you).  Things will settle soon, and then we’ll see how much it’s altered who we work with (not much I hope).  There’s been lots of conferences and talks and workshops, but still lots of unanswered questions, which I guess will only be answered when the service starts to actually be delivered.  We’re all trying not to get too stressed about it.

New Stuff……

Spent the day at a conference at Eastwood Hall (posh conference facility) looking at changes to the Mental Health Act and more specifically, the introduction of the role of the IMHAA.  For those of you who don’t take even a passing interest in the exciting world of mental health legislation (woo!), this is the all new all singing all dancing Independent Mental Health Act Advocates.  Of which I shall be one come first of April.  The fact that this is April Fool’s Day is not lost on me, when I consider how long everyone’s had to prepare for this and how woefully underprepared for it everyone actually is.

Basically, the Mental Health Act 2007 amended the 1983 Act to bring in a variety of new statutory rights, duties and instruments, and certain categories of detained patients will shortly have the right to independent advocacy.  Up till now, advocacy provision in the UK’s been patchy and it all really depended on what your local PCT or Health Authority wanted to fund.  So it’s all a bit of a postcode lottery in respects of specialist mental health advocacy.  This new provision will end this (finally) and has loads of implications for us working with detained patients.  It also has implications for our current voluntary inpatient and community clients, as there is no statutory right for them.  What our funding will look like for them remains to be seen. 

It means that I have four weeks to become much more familiar with the legislation, so lots of reading for me.  It also means that at some point, we’ll all be taking the relevant modules on the new national advocacy qualification to ensure that all IMHAA’s have the same baseline of training.  Top marks to Eastwood Hall for having the best food I have ever had at a conference (not that I go to many……).

On a more frivolous note, I went to the dentists and all is well with the teeth.  Thank god.  The thought of the trauma and cost of dental work fills me with dread – I’m a bit crap when it comes to fillings and suchlike.  For the time being, I don’t need to worry about that!!

CTO’s……

Since Monday (3rd November), the new/revised Mental Health Act introduced the concept of Supervised Community Treatment as implemented by Community Treatment Orders.  As you can imagine, not everyone is delighted about further measures designed to impose treatment on people in the community.  I’m in two minds about this.  All the reading I’ve done about the use of CTOs in other countries hasn’t really proved that they’re effective in preventing illness relapse.  They are, however, good at placating the Daily Mail type readers who howl and wail about psychiatric patients being Loose In The Community Murdering Us. I can think of a few people I work with who will be assessed and transferred to CTOs, but I can’t imagine for a moment that they’ll be effective at making them take their medication or engaging in any other form of treatment (not that there’s much available locally if you don’t want to wait an eon).  I’m not sure why they just didn’t stick with the original S25 of the 1983 Act and actually use it properly.  Anyhoo, the new Act brings in the concept of treatability – your condition must be treatable, and that treatment must be available.  That’s you buggered if you’ve got a personality disorder diagnosis then, or an eating disorder with a BMI above 16 (or something). Or a combination of diagnoses.  Unless you’re happy to be shipped off to a therapy unit/community out of area.

http://mhact.csip.org.uk/

http://www.mentalhealthalliance.org.uk/news/prpowersusedwisely.html

http://www.rethink.org/how_we_can_help/campaigning_for_change/mental_health_act_20.html

Here’s some reading to keep you going. Hehehe.