Harvesting of the Disabled for Profit

A2013-09-20-15_36_14Parents of special educational needs children including those labelled autistic be warned this may be your fate.

The state are creating and labelling children as having a learning disability rather than a difficulty.

The renamed label is intellectual disability

See the latest number here.

http://schoolsweek.co.uk/schools-struggle-as-autism-diagnoses-rise-25-per-cent/

There are several databases used to share information illegally under Data Protection Act and s8 HRA to harvest children including future criminals.

http://databasemasterclass.blogspot.co.uk/

A learning (intellectual) ‘disability‘ is an impairment of mind, permanent, innate and evidenced by a low IQ  and is now  on the rise in the UK look at the statistics

http://chrishatton.blogspot.co.uk/2015/11/the-disappeared.html?spref=tw.

Whereas a learning ‘difficulty‘ is not inate, and  can be because  a child is autistic ( learns differently), a late developer,  has poor teaching/assessment or taught in a second language,  such a child will have at least an average IQ. .

So if your child is a late developer autistic, has inadequate teaching he labelled and doomed to be a cash cow for life.

Unless he is part of the labelling state cabal.

Or in private education as they do not have the EHC system.

Education, Health, and Care Statements replaced Special Educational Needs statements last year.

Education, Health and Care statements unlike SEN, require social services to monitor your child’s ‘welfare’.

A school protection officer/ social worker will now be part of your life.

And,  your  child’s name secretly notified to  MASH- Multi Agency, Safeguarding Hub

Invasive IT Databases are being provided by CAPITA at 2016 see link.

In breach of HRA and Data Protection, to target families at risk in schools without their permission or even knowledge.

Click to access capita_one_-_product_brochure_-_one_analytics_-_apr16.pdf

https://www.gov.uk/government/news/working-together-to-safeguard-children-multi-agency-safeguarding-hubs

Your child will be in this system and by it watched covertly by every  agent of the state.

Read here the law and databases used to target the ‘disabled’ and their families by all agents of the state.

http://databasemasterclass.blogspot.co.uk/

And, despite the inherent difficulties of coping with an autistic./ different child.

Any bruise, scratch, dirt, swear  word, behaviour issue, sexualised behaviour, weight loss/gain,  head lice, old /inappropriate/clothing, emotional problem, parents relationship, lateness, rearrangement of meeting, attitude,comments, will be noted.

But you will be unaware you are under their microscope.

And have no right of reply or correction of their databases.

You will be impressed everyone  is taking such an interest.

Ignorant of why, your child really is, so ‘special’.

In June 2016 the government announced millions would be given to provide early intervention before crisis point.

This means those merely ‘at risk’ will also be targeted ie the poor, or those with relatives with special needs.

Education ‘pathways‘ are  used to harvest as many as possible to private eventually venture capital education and care .

As it is highly profitable- £200,000 a year financed by NHS (health), LA ( social),  D of E ( education )

.http://www.manchestereveningnews.co.uk/business/acorn-care-acquires-pathway-care-9102370

All areas have similar Pathways as shown here for Nottingham

http://www.nottinghamshire.gov.uk/DMS/Document.ashx?czJKcaeAi5tUFL1DTL2UE4zNRBcoShgo=bSSB5VpG8vooSzX00hg%2FyPEcYUVxHpzqPrPXMJfEF%2BxGVODFeCYDfw%3D%3D&rUzwRPf%2BZ3zd4E7Ikn8Lyw%3D%3D=pwRE6AGJFLDNlh225F5QMaQWCtPHwdhUfCZ%2FLUQzgA2uL5jNRG4jdQ%3D%3D&mCTIbCubSFfXsDGW9IXnlg%3D%3D=hFflUdN3100%3D&kCx1AnS9%2FpWZQ40DXFvdEw%3D%3D=hFflUdN3100%3D&uJovDxwdjMPoYv%2BAJvYtyA%3D%3D=ctNJFf55vVA%3D&FgPlIEJYlotS%2BYGoBi5olA%3D%3D=NHdURQburHA%3D&d9Qjj0ag1Pd993jsyOJqFvmyB7X0CSQK=ctNJFf55vVA%3D&WGewmoAfeNR9xqBux0r1Q8Za60lavYmz=ctNJFf55vVA%3D&WGewmoAfeNQ16B2MHuCpMRKZMwaG1PaO=ctNJFf55vVA%3D

This intelligence gathering can be used to enforce any medication, therapy, schooling, or silence your complaints, via care proceeding or threat of them.

And serves as a file of historic ‘concerns’ of parental abuse/neglect/capacity, and/or future, Court of Protection LA evidence, that it is in your 18+ child’s ‘best interests’ to  be removed to community living for life, and your access limited and/or excluded.

Under EHC statements, your child can no longer attend a day school at 16, nor use overnight respite facilities.

His education, continues, by ad hoc, unaccountable, ‘independent’ living skills education packages

https://finolamoss.wordpress.com/2014/11/25/education-health-and-care-statements-emperors-clothes/

Consisting of agency workers,  escorting him to ad hoc skills facilities, overseen by a package boss.

Who, unknown to you are briefed on ‘your family’s file’ and will continue to monitor your child’s ‘welfare’.

Their goal,  is ‘independent’, away from home living and  is likely, to result, in a cash bonus, or, at least, more lucrative education packages from the LA.

‘Education’ will discuss leaving Mummy and Daddy, with your child.

Regardless of the effect or yours or his wishes.

And, you may not be told.

At 18, all services are funded by Adult Services.

Due to government cuts, these services are limited to assessment for state residential care for life- independent/ supported/community living,

A new private industry being bought up by monopoly venture capital US companies like Cygnet who own CAMBIAN with over 160 home sites.

http://www.local.gov.uk/documents/10180/5854661/Adult+social+care+funding+2014+state+of+the+nation+report/e32866fa-d512-4e77-9961-8861d2d93238.

This states,

‘The MODEL OF CARE, is increasingly one, which promotes INDEPENDENCE, and MANAGERS RISK.’ ( Code for ‘community’/supported living). 

Pressure, will be placed on the LA, to transfer adult funding to central government funding, which is only available, for residential Provision.

https://finolamoss.wordpress.com/2015/04/27/independent-living-disabled-penned-for-profit/

The LA’s standard  adult support plan criteria eludes to this in a question the Adult Social Worker must complete;

Does the plan promote independence including identifying goals that could result in reducing paid support within an agreed period ?

Your child because of his learning difficulty will be treated as a ‘child in need’ under s17 Childrens  Act.

Children in need meetings will be held  with the education package, and, safeguarding issues  raised,- hygiene, clothing, food, parenting, medical and dental attendance, physical, sexual emotional  abuse,  and, placed in social services core assessments.

As, the LA funding can only decide, it is in your child’s ‘best interests’, to live away from you, and, your access limited, little in your favour, will be recorded.

No matter, how unfairly skewed against you, even if factually incorrect, it appears impossible, to change these assessments, and, relay  the correct information to professionals, and agencies.

The difficultly posed by your child’s disability, or, the inadequacy of support will not be considered.

The LA commission the services, and, it is liable, if inadequate.

Your ability to safeguard, parent, clean your home, and not neglect your child, will be judged, as if your child, were not disabled.

And, any possible concerns, re cleanliness/safeguarding/emotional abuse, real, or contrived,

Will be reported back, by support workers.

Whilst, your child’s disability, will not be considered, in assessing your parental capacity.

It will be, grossly exaggerated, by the LA in  their assessments of him,

To enable the maximum to be claimed from public funds to be paid to private  independent/community living providers.

The worse your child’s behave becomes or is made to appear, the greater the income  the independent/supported living provider  can claim.

This also is used as evidence you are unable to cope, and it is  in his ‘best interests’ he to be removed.

If you do get support, it will not be charged to help you, other than engage with your child.

But, support will be charged, to assess your capability, as a parent, and, whether you have a safe, clean, adequate home environment.

But you again, will be unaware of this. https://finolamoss.wordpress.com/2014/10/14/gathering-evidence-from-social-https://finolamoss.wordpress.com/2014/10/14/gathering-evidence-from-social-care/

Regular meeting s behind your back, will be held, between the social services, education, and, agency worker provider, who  have ‘your file’.

Your family, and child, will be whatever, they, in secret, decide.

Any information, you provide to workers/professionals, about your child, that does not fit the cabal’s purpose, of abuse, and neglect, safeguarding concerns will be ignored.

Support workers, on zero hour, minimum wage contracts, will be briefed, on the questions, to ask, and, matters to look out for.

https://finolamoss.wordpress.com/2015/02/10/i-smell-a-rat/

Your family GP, will also  be part of the canal, and, despite confidentiality restrictions, both, your child’s medical records, and yours, will be shared.

Anything, that points to present or future parental physical, or mental incapacity, will be used to show, it is in your child’s ‘best interests’, to be removed to ‘independent’ living.

Any existent, or non-existent health, or mental concerns will be notified to your GP, by education, or, any agency, or social worker. https://finolamoss.wordpress.com/2014/08/24/my-complaint-and-unaccountable-services/

To possibly gain support, as a carer, or, any respite, cleaning   etc, you will have to undergo a Carer’s assessment.

This is used to probe, every aspect of your physical and mental ‘wellbeing’.

But, the LA are not under a duty, to provide support, and, have no funds to do so.

And, will only consider it, if the affect on a carer’s wellbeing, is ‘severe’, which would then make a carer, unfit, and/or a risk to their chargee. https://finolamoss.wordpress.com/2014/11/20/carers-act-2014-care-to-ensnare/

‘Concerns’, from support/education workers, are relayed to social services.

And sought expressly, by leading questioning.

And covertly, by tricks and grooming.

You will consider them all your friends, until without notice they disappear.

They will not raise their concerns with you.

https://finolamoss.wordpress.com/2015/01/31/education-report-a-red-mark-the-size-of-a-fist/

These ‘concerns’, will be placed in court statements,to prevent you representing your child in court as you are cast as abuser/neglector there is a conflict of interests between you and your child.,

And, show, it is in his ‘best interests’, to be removed from you and your contact limited.

You will only discover, their ‘concerns’, on reading your social worker’s  court statement, in support of s48 Mental Capacity Act Interim application to the Court of Protection.

Your child will be forced, if necessary, by a court order, to undergo a psychological assessment, paid for by the LA.

This will assess, any deemed emotional abuse your child is subjected to at home, and a blanket, illegal capacity test.

https://finolamoss.wordpress.com/2015/03/03/standard-capacity-assessments-stephen-hawking-would-fail-without-his-box/

This will state, that due to your child’s ‘intellectual disability’, he is, and has always been, unable to make any decisions.

It is now assumed that children subject to a SEN now EHC statement will be incapable under MCA and conferences for SEN families give presentations to that effect on Transition ie 16-18, see here

Click to access Transition%20seminar%20FINAL%20(2).pdf

Your child has now been made, the perfect commodity for life, for the multibillion pound, unaccountable, independent living industry.

https://finolamoss.wordpress.com/2015/05/31/the-mental-capacity-act-in-practice-emancipated-or-insentient/

Where he is safely behind the closed doors of the state where abuse  or even death is not investigated.

Your GP, will  look for signs of neglect, weight loss, bed sores, skin conditions, abuse, and self -harm.

https://finolamoss.wordpress.com/2014/09/25/a-voice-crying-in-the-wilderness/

If you proffer other causes, this may be evidence of fabricated disorder/ Munchausen.

Your GP, will be instructed by the Court of Protection, to do a  physical examination of your child, under s49 MCA, whether necessary, or not, and, any other assessments.

And, regardless of the distress, it causes.

His letter of instruction, will state, that the LA have concerns, and, that you have denied access, to your child, weather proved, or not.

Once the Court, becomes involved, any support workers, will become overt assessors.

All care agencies, and day centres, are funded by the LA, and therefore, controlled by them.

And as, ‘independent’ away from home living, is now the LA’s, only policy, for adult social care, all feed into it.

Despite, his EU, United Nations Rights not, to have the state remove his right to make decisions,http://www.un.org/disabilities/default.asp?id=279

Here is an OFSTED report in 2016 showing the shambles SEN is in there.

Click to access Joint_local_area_SEND_inspection_in_Surrey.pdf

You, and your child are flies in a sealed LA web.

The government’s Transforming Care document proposes early intervention for the autistic and learning disabled who evidence ‘challenging behaviour  and contains the following statistics;.

There are an estimated 1.2 million people in England, of which 286,000 are children and young people under the age of 18, with a learning disability (Emerson et al. 2012).

This means that roughly 20 people in every thousand have a learning disability (2-3% of the general population). The majority live their lives without support from specialist learning disability services – for instance, of the roughly 1 million adults with a learning disability, it is estimated that 189,000 (21%) (Emerson et al. 2012) are known to learning disability services.

There are an estimated 700,000 people with autism in England (Brugha et al. 2012) of which 125,000 are children and young people under the age of 18 (Baird et al. 2006).

This means that roughly 11 people in every thousand have autism (1.1% of the general population). It is estimated that 44%-52% of people with autism also have a learning disability (Emerson et al. 2010).

Those who display behaviour that challenges Challenging behaviours are generally understood to be exhibited by 10-15% of adults with learning disabilities known to services (approx. 22-34,000 people), whilst often peaking between the ages of 20-49 (Emerson et al. 2001).

A further 40,000 of children under the age of 18 are believed to display challenging behaviour (Emerson et al 2014).

As set out in Challenging Behaviour: A Unified Approach (Royal College of Psychiatrists, et al, 2007, p.14) challenging behaviour is behaviour

of such an intensity, frequency or duration as to threaten the quality of life and/or the physical safety of the individual or others and is likely to lead to responses that are restrictive, aversive or result in exclusion”.

Determined to harvest your child.spider-net-g8i1

Autism Epidemic the betrayal of the ‘different’ for profit.

Einstein_Tongue

What is autism?

The truth is startling.

No one has a clue.

There is no pathology, no gene, no biomarkers and little understanding .

It is an intrinsic part of an individual’s personality.

And as such, many maintain is not an ‘impairment of mind’, under the Mental Capacity Act.

And, it was not until recently  a mental disorder under the Mental Health Act.

It is a spectrum, we are all on.

Like quantum mechanics, it does not exist, until observed and labelled.

Only 70 years ago, it was merely a Greek word, meaning, ‘absorbed in self’.

Associated with loners, high intelligence, gifts, cold mothers, and, the children of academics.

Newton, Mozart and Einstein, who at 7, constantly repeated certain phrases, all showed autistic traits.

http://www.telegraph.co.uk/news/science/science-news/3326317/Albert-Einstein-found-genius-through-autism.html

On reading Plato’s description of Socrates, he could well have been autistic.

A study by University of Sterling this year shows it is associated with creativity

http://www.theguardian.com/society/2015/aug/22/autism-creative-thinking-study?CMP=share_btn_tw

Yet a ‘lack of imagination’ is one of its main diagnosis criteria.

Read this lady’s account of the genius of her autistic  son.

http://www.amazon.co.uk/The-Spark-Mothers-Nurturing-Genius/dp/0812983564

Scientists have urged it should not be treated as a disability but a different way of thinking with advantages

http://www.dailymail.co.uk/health/article-2056941/Autism-advantage-Valuable-traits-include-exceptional-memory-visual-skills.html

Here a mute autistic writes how wrong the experts are about him.

https://growingkidstherapy.wordpress.com/2017/01/05/diagnosis-disruption-debunking-the-myths-of-non-verbal-autism/

But today in the western world autistics are made the biggest cash cows .

anhttp://www.lse.ac.uk/newsAndMedia/news/archives/2014/06/Autism.aspxd educate,

They cost the UK more than cancer,or heart disease.

Yet a recent study shows, they are 2.5 more likely to die prematurely in comparison to the rest of the population.

http://www.medicalnewstoday.com/articles/308160.php

Why, as autism is not a physical illness ?

Is it because the autistic are huge pharma cash cows, earning billions for the autism and pharma industries, yet  receive little or no proper medical treatment.

And as a lucrative commodity the  number of autistic in the UK has increased ten fold, in the last 15 years, and 50% in the last 5 years.

http://www.telegraph.co.uk/news/health/9160322/Number-of-children-with-autism-soars-by-more-than-50-per-cent-in-five-years.html

In the US, study shows, it will cost one trillon billion dollars by 2025 http://consumer.healthday.com/cognitive-health-information-26/autism-news-51/u-s-autism-costs-could-reach-1-trillion-by-2025-study-701789.

Surveys increase the epidemic.

htmlhttp://www.bloomberg.com/news/articles/2015-11-13/autism-rate-nearly-doubles-on-paper-after-a-survey-is-changed

So there is an awful lot of money to be made out of autism.

It is likely, some disorders diagnosed as ‘autism’ is not but reaction/effect of vaccines- compulsory in USA, put under autism’s vague umbrella.

View at Medium.com

Autistics are now assessed,  as intellectually disabled, based unfairly/discriminatory on adeptive skills alone, irrespective of IQ.

And then  taught, medicated, and treated, as if mentally retarded.

This  allows inappropriate ‘special needs’ non- education, drug administration.

And, worse still, autistics being assessed, at 18, as being ‘incapable’ of  the most basic decisions, as to who they have a relationship with or where they live.

The Mental Capacity Act 2005 is being  illegally enforced, allowing the state to declare the autistic,  incapable of making any future or past decision.

Yet, educationally, autism, is a conditioning disability, not a learning one.

Autistics are not intellectually disabled.

Autistic children’s  IQs, have been shown, in recent research by Swansea University, to be underestimated, as IQ tests are designed for non autistic children.

https://finolamoss.wordpress.com/2015/09/10/profitable-retardation-of-the-autistic/

They merely have a different perception of reality, and therefore think, and  learn differently.

Autism, is explained and defined, as a difficulty with social imagination, communication, and interaction.

A  vague, expansive, meaningless definition.

What is social imagination ?

Autistics, once labelled, are perfunctorily and simplistically stereo typed, with little regard to the individual.

All like routine, all have sensory problems, all do not look you in the eyes, all hate transitions, all do not understand others emotions, and, the most damning  judgement, all are insentient, under the Mental Capacity Act.

And all this is wrong and discriminatory.

The different, are penalised, because they do not behave socially, learn or communicate as they should.

This, and, ever more blunted psychological diagnostic tools, make it, far too easy to label, a person, who merely, has an unknown, educational, communicational, and social ‘difference’ from the norm.

The diagnosis based on adeptive skills and misdiagnosed intellectual disability.

http://www.nytimes.com/2012/01/20/health/research/new-autism-definition-would-exclude-many-study-suggests.html?_r=2&pagewanted=1&hp

With such a cash cow, is it any wonder, more autistics are sought.

By awareness campaigns, in their best interests.

The latest is, to harvest autistic girls, on the basis, too few are being diagnosed.

Yet, the proportion of autistic girls, accords with the biology that the X chromosome masks the disorder in a female.

Who is merely a carrier of the ‘autism’ gene.

And a female will need both her X chromosomes to be affected, so an affected X from each parent, to manifest autism.

So is 50% less likely than a male to be autistic.

Mandatory  Universal Autism Screening has been called for.

http://www.medicalnewstoday.com/releases/309783.php

The ‘at risk’ who might not be autistic are sought, and research into genetic causes and biological processes paid for presumably to market drugs and vaccines but specific genes cannot be found.http://www.medicalnewstoday.com/releases/308185.php

It can now supposedly be detected in babies and now before symptoms appear.

http://www.disabledgo.com/blog/2017/02/autism-detectable-in-brain-long-before-symptoms-appear/#.WKYEtIXXJjo

An autism label has already proved devastating for over a million in the UK.

Who with America, form an epidemic in the western world, but not   in the East, and, autism, is virtually non-existent in the third world.

The, ‘in the know’, late developing eccentrics, with private means, can avoid detection, and labelling, research proper education, and, like the characters in the New York specialist school in the book, ‘Bring in the idiots’, become high flyers, in literature, and technology.

But not, the ever increasing majority, destined, to be cash cows, for the burgeoning autism industry.

Which spans charities, pharmaceutical, educational special needs, NHS, social care, and independent living.

74% are on anti-psychotic drugs, and, imprisoned for life in NHS ‘treatment’ centres, or ‘independent’ away from family living.

http://www.disabledgo.com/blog/2015/09/fears-that-antipsychotic-drugs-being-used-as-chemical-cosh-in-disability-care/?utm_source=DisabledGo+Blog&utm_medium=facebook

Autism is a social conduct development ‘disorder’ at most, and was not within the Mental Health Act until  recently.

It is not a mental illness.

But recent campaigns that autistics’ mental health was being neglected, enabled, autistic conduct to be perfunctorily diagnosed as separate mental disorders.

Even normal reactions of autistics to crowds, noise, muti stimuli has  now been labelled a separate disorder of Pathological Demand Disorder and Petitions supported by NAS have had it recognised in Scottish Parliament.

How can a mere facet of autism be recognised as a separate disorder, when this should have been appreciated as part of ASD and educated, treated cared for already ?

It serves to surreptitiously widens the net of cash cows by more diagnosis and will not improve care.

ASD has only be placed in the MHA fairly recently and is not a mental but a conduct disorder.

Continually government money is spent to show autistic are mental, the latest Cambridge and Coventry University report on their greater risk of suicide and depression January 2017.

https://www.learningdisabilitytoday.co.uk/study-launched-to-understand-why-autistic-people-may-be-more-at-risk-of-mental-health-issues.aspx

This is the worst form of discrimination and misrepresentation of the autistic and allows autism to be a mental disorder and other mental disorders to be added.

Each requiring profitable medication- OCD, psychosis, anxiety, depression, self-harm, OD, ADHD, and increasing the amount that can be claimed for their care.

https://www.autistica.org.uk/research/mental-health/

So they really are a useful, lucrative feed to the mental health industry and pharma.

How did this all happen? Is no one fighting for the autistic ?

In 2007, the National Autistic Society was the 8th largest charity in the UK, rich with government funding, and, 177,000 per annum residential school placements.

But,  was, strangely, precluded by its trust deed, from researching into the causes of autism.

Its campaign for autism rights, embodied in the Autism Act 2009.

Resulted in worthless, Local Authority Guidelines.

Which need expensive, complex, costs risky judicial reviews, by individuals to enforce.

To date I know of none.

So Local Authorities can ignore the Act.

As shown LA’s adult services policy of non-provision of specialist care.

But, the LA, commission, and the NHS pay, independent living providers, like the National Autistic Society, Autism Care UK, on the ‘severity’ of the individual’s disability.

Using the money available for disabled, and  family support, under the Chronically Sick and Disabled Act1970.

But now neither are given an option except private enforced secret care.

The autism industry, and venture capital, profit from creating ‘difference’.

The autistics have lost their lives, and, we have lost our visionaries, and eccentrics.

See here how a definition of autism allows  the state and care workers to decide all your decisions for life even when you are obviously capable and high functioning.

See fate of this 20 year old diagnosed  as autistic at 18, when Dimensions who own independent living support and the LA  got involved in her life. And an LA behavioural psychiatrist who decided she was MCA incapable of deciding, who she had relationships with and where she lived- terrifying stuff, happens nowhere else in the world.

http://www.bailii.org/ew/cases/EWCOP/2016/4.html

Read here latest book dispelling the myths about Autism by Steve Sliberman, The Legacy of Autism and the Future of Neurodiversity

http://www.npr.org/2016/09/09/493148713/neurotribes-examines-the-history-and-myths-of-the-autism-spectrum

Despite or because of being made cash cows a study revealed they die prematurely

Dr Hirvikoski says that she was “shocked and horrified” at the results.

Her team found that the mean age of death of somebody with autism was 54 – compared with 70 for the general population. For people with autism and a learning disability, life expectancy was a mere 40 years.

 

 

 

 

autism6

Acting out? – Dont worry we have medications for that!

This is a post from  Justice for Thomas Rawnsley’s blog.

With photos taken of Thomas,months before he died, in Cambian owned ;community living Kingdom House in Sheffield, where he was taken after a long history of care abuse involving one carer,who had said’ How many fingers can I break this time’, but was unable to as Thomas was double jointed.

After this, Thomas was found difficult to care for, so was sent to this ATU, where he was the only patient, and keeping it open, by his abuse, being used, to claim £12500 per week for the ‘treatment’, evidenced by the beyond shocking photos taken.

4

Thomas  on medication .

This is the unashamed use of the LA, and our government, of the most vulnerable for investment, and huge profit, using public funds, and breaching their statutory duty to care for them, but to claim the maximum money available under law for their ‘care’, on the basis of their ‘disbility’.

This is also 4 years after Winterbourne View was officially investigated.article-1392892-0C588EA900000578-684_468x286

Since then there has been more abuse, and death, for profit, of our most vulnerable.

The only move, via Norman Lamb, and LB Bill, is to move them out of NHS, MHA ‘care’/’treatment’, to LA, MCA ‘care’, for life in independent for profit living, with no reviews. And ASD/LD are now only being admitted to private hospitals like CYGNET/PRIORY group

Thomas, was placed in such independent living accommodation, where he was abused, and died.

Rip off social care.. the plight of the disabled family.

ghost

Friday 6th March

All is very bizarre,

All is very dire.

We, as always, are kept in the dark, until, whatever happens, happens.

As you can imagine, in between my waves of nausea, and caring for poor Issy, I have been kept, very busy, coping with officialdom.

I await the arrival of the other lady from the agency, who attends the social services’ weekly ‘surveillances’.

We had our 5 th ‘surveillance’, with our 2 social workers, two days ago, the sixth, next week, is the psychologist’s visit, to declare Issy a vegetable, and, observe her emotional state, and, no doubt, ours.

We are not told, nor dare ask, not that any definitive answer would be given, how long the ‘surveillances’ go on for.

It is now 11. 00 am, the lady was due at 10. 00am, so I assume, she is not coming.

She didn’t.

We have no timetable of hours.

Angel Eyes , has supported for three weeks, from 10-4 Monday, 10-3 Thursday.

We received an invoice, from the agency, for £710.50 for 50.75 hours support for February, at £14 per hour, yet Angel Eyes, is paid £8 per hour, and, no traveling expenses.

And, has to put her time sheets  online.

She also, appears, to organise support, and, inform us.

Personal ( direct payment ?) services, the basis, I assumed, this agency was paid on, allows £7.50 per hour, and a £30 per month administrative fee.

A little over half, of the agency invoice.

Adult services wouldn’t pay the £710.50, as the agency, is not approved by them

But, as the LA pay, are the source of all future lucrative, reliable business,and the piper that calls the tune.

The agency boss, assured us, he could have, our ‘pot of money’, held by the previous education package, (‘fist lady’ and co, no show), transferred over to his company.

Remember, the only alternative support, we were offered, was  ’ Fist Lady’, and,  new friend……

So, what can we do to be reimbursed this, and future support?

Sue the Local Authority, if we can find  the forms, pay the court fee, cope with the hassle, -service, posting etc, and  pay for the extra support, to attend court, and risk the LA’s legal costs, if we lose, which would be more, than the £720.

Courts are now profit making, and provide no legal advice, just an expensive, time consuming answering machine  service.

We have already paid out, £900 on officialdom.

No, we have no law, as, it cannot be enforced.

And complaints mechanisms are shut down on a court application.

So are living in the wild  west.

Just a reminder; the new agency support, is in lieu of Issy’s education, social care, respite, and NHS care.

Another reminder; we have had no overnight respite, other than, the three nights blogged in July 2014, and 3 evenings, in over 2 years.

The adult services lady told us, the insisted on, by social services agency  support, of 2 workers in the kitchen for  7 months, was to ‘interact’ with Isabel, as she fleetingly appeared in the kitchen for juice and food, and not to help me with cleaning  or even Issy’s personal care.

No one  knows, the role ‘support’ has, is it education, personal care, respite ?

Nor indeed, if they will turn up, or, leave, never, to be seen again.

Nor, more crucially,what the lies/spin, they report back to social services.

Do note, under the Chronically Sick and Disabled Act 1981, up to £82,000, can be claimed, legally, just for Isabel’s social care, and,a similar amount, from the NHS.

If Issy is in residential state care  over £4,000 will be paid to her private provider.

Hence, the push for Issy’s independent, away from family living, so this statutory entitlement,  in addition to  her benefits- housing, mobility, DLA, ILF, CA,can be claimed.

Clearly venture capitalists, have realised the autistic are a gold mine.

But has, or will, all this public money, help Issy ?

It hasn’t so far.

In fact it has caused her problems.

She is  still suffering, reignited post traumatic disorder, from her abuse in NAS care, exacerbated, by the fear of leaving her home, and, not returning, created by her first ‘education’ package, who informed her, she could not live with Mummy and Daddy.

As l write , Issy is echoing the words of the same NAS key worker, in the worker’s actual voice, replete with Yorkshire vowels, and, sneer.

Issy must have said to her, ‘Where is Mummy and Daddy?’,

the worker repeats this question, as Issy echoes, in the workers mocking voice,

‘Where’s Mummy and Daddy’, followed by a bellow of,

They’re not interested’.

What has been done about this abuse?

Nothing, as denied and usefully to justify antipsychotic medication, interpreted, as Issy  hearing voices.

Her 48 bruises in NAS residential school we declared and recorded for all time as self harm.

A National Autistic Society  claiming  £ 60,000 per annum, up until 24/5/2013, from the NHS, according to an NHS letter to me, despite the fact Isabel returned home, on the 29/1/2013, where she has never received any NHS care.

In addition, a further £60,000, for her education, as education and NHS paid 2/3rds of the £177,000,  ‘tax free’ per annum, paid to the National Autistic Society School as a charity.

There was no deduction the third of the year Issy was with us.

We paid NAS pocket money, and towards clothes.

All paid until May 2013, three and a half months, after Isabel returned home on 29 the January .

So much for cost cutting, value for money, and helping the disabled, and their family.

During these years, we were paid £20 per week Disability Living Allowance.

And still only this amount, for 4 months after Isabel had returned to live at home.

Isabel now receives £125 ( reduced to£105) DLA, and I receive £77 carer’s allowance ( reduced to £62.50p), no free nappies, no beds, no nothing….. Just the privilege now, of paying, through the nose,  for agency care.

Here are the statistics of number of hours of unpaid care by family.http://www.carersuk.org/news-and-campaigns/press-releases/facts-and-figures

Why can family carers not even claim any of their time caring, and worse still any  LA support is deducted from the disabled’s DLA.

Who’d  want to be a disabled family in this country, think of our plight, when ‘Pudsey Bear’ and ‘Children in Need’ come begging.

The door bell rings.

My heart leaps.

It’s difficult not to be paranoid, when you are secretly and silently surrounded.

But it’s just the nice post lady, a kind, familiar face.

And my fifth letter, 4 from the NHS hospital, and 1 personal one from the GP, about my failure to attend a Diabetic Eye Screening Appointment.

I have not got diabetes; even my 2 GP results 2 years ago were insufficiently raised.

I have no symptoms, but what does that matter.

Truth is irrelevant.

The box has been ticked.

Issy  in nursery

Standard Capacity Assessments, Stephen Hawking would fail, without his box.

The mental health industry is awash with captive consumers, who have never even engaged with their capacity assessment under the Mental Capacity Act.

This is illegal but this is how it happens.

Let us explore, what happens, on the day your loved one, is declared effectively, a vegetable and loses his right to make any decision. for the rest of his life.

The psychologist/ assessor, the MCA does not stipulate who can assess capacity it appears anyone can, will attend the autistic and or learning disabled young adult or confused granny.

And, most likely be ignored.

The autistic may take an interest in their name, name tag, earrings, lipstick, pen, but then go back to their DVD, computer, or, just want juice.

The assessor may say words to the effect,

I have come to see whether, or not you want to represent yourself in court, so that your best interests/ what is best for you in the future, can be decided by an important person, called a judge’.

The first decision, an autistic, learning disabled or granny must be found ‘incapable’ of making.

The autistic will remain unresponsive with blank eyes, that hide so much, as would the author of, ‘Through The Eyes of Aliens’ a highly intelligent, mute autistic.

Who, most likely could be found ‘incapable’ had she not written an academic book.

By now, the vulnerable person, who rarely sees people will be feeling threatened by a stranger in his personal space asking him a question, which means little to a non- autistic.

He will want to be alone to comfort himself in the autistic world, where he alone resides.

So he will tell him to go away, get out of his room and become agitated.

The assessor will leave as his training is ever  risk  averse and he knows nothing, of this particular autistic’s behaviour or habits.

What will happen then?

The MCA Code of Practice provides;

4.57 There may be circumstances in which a person whose capacity is in doubt refuses to undergo an assessment of capacity or refuses to be examined by a doctor or other professional.

In these circumstances, it might help to explain to someone refusing an assessment, why it is needed, and  the consequences of refusal.

But threats, or attempts to force the person to agree to an assessment are not acceptable..

No one can force an assessment, unless, there are serious concerns about mental health, and the Mental Health Act can be invoked, as he is a danger to himself, or others’.

As by s1 MCA and the common law a person is capable and has autonomy over what happens to him.

But here is the shocker…

A person can be assessed as lacking capacity to refuse or agree to a capacity test.

As 4.58 Code of Practice provides, 

  ‘If the person lacks capacity to agree or refuse, the assessment can normally go ahead, as long as the person does not object to the assessment, and it is in their best interests’.

But how, is it possible for a person, to lack capacity to agree or refuse  an assessment but still  have sufficient capacity to object to the same assessment ?

Isn’t ‘objecting’ the same as ‘refusing’?

This makes no sense.

And surely if he refuses to engage is this not ‘objecting to the assessment’?

He has a right to refuse/object, as  he is presumed  capable under the Act.

But, despite this, the Code provides, ‘the assessment can then normally go ahead’.!

But, what is this ‘assessment’ that now goes ahead and what is it based on?

And, as consent, from a  capable person, must be obtained, to any assessment, this assessment would be a trespass to the person.

To say nothing of a breach of his human rights.

And, if it did go ahead, is effectively non existent.

As it, and the  assessment of the person’s incapacity to consent could  only be based under the MCA the functional test.

And, this,  in the circumstances,  as no questions have been asked of the assessee can only be based on, the autistic’s  general presentation and the condition , which is illegal, under the MCA.

And where does this fit in with s1 MCA which declares that there is a presumption of capacity until proved otherwise.

And highly discriminatory so likely illegal under the Equality Act.

And, in breach of the guidelines set out in statutory form in the Autism Act 2009, which would allow a judicial review of any assessment.

Also, this could only be a functional assessment, based on, the autistic’s failure to engage.

Also based on the autistic’s condition and presentation.

Ilegal under the MCA.

In fact this test, would not even. provide evidence, of suspected/alleged incapacity, let alone, amount to a formal capacity test, accepted by the court of protection, as rebutting evidence to  remove the presumption of capacity, given at common law, and in the Act.

In any event, the MCA capacity test per se, is not, applicable to the autistic mind, and is meaningless to the autistic.

And, thus proves nothing.

We also have the problem that many rightly believe autism is not an ‘impairment of the mind’ and therefore not covered by the MCA.

Yet, worryingly, and illegally, the Standard Assessment of Capacity Record to be completed by the Local Authority guidance allows for such assessments as it commences as follows;

The assessment should end if the person is unable to progress through the functional test. For example if a person cannot understand the decision they will not be able to retain it, weigh it in the balance or meaningfully communicate a decision’.

To obtain a Capacity Order, from the Court of Protection, the Local Authority need to show suspected incapacity by, stating the functional test, is satisfied.

Again, in respect to autistics, the suspicion, is normally based on the autistic’s condition, and presentation, and assessments, based on such evidence, are  not allowed, per se.

The guidance then continues,

The important point is to provide evidence that you have put the decision that needs to be made to the person,. and what their response is using direct quotes and or a description of their reaction.

If they cannot due to the level of impairment process the information there is nothing to be gained by continuing’.

Wow.

Local Authorities, do not even have to administer the functional test, to render a person incapable.

So back to our autistic/granny being assessed, the assessor can read out the questions, be ignored, and then state in his Record of Assessment Form, that the response was silence, and render this person, incapable of making any decision for the rest of his life.

And  it appears, from the guidance to the Standard Assessment Form, there is nothing about the fact, the assessment must be conducted under the best possible circumstances for the asssessee, having regard to, his state of mind, physical ease, to enable, the maximum possibility of capacity being found, as required by s1 MCA.

All  the assessor needs to show, by ticking the boxes on a standard form, is that a meaningless process, has taken place.

How easily assessors earn their money.

How shocking, effectively anyone, but particularly the autistic, could lose the right, to make any decision, for life on the basis of an illegal, meaningless, non assessment.

Even, Stephen Hawking, had he not been fitted with a voice box, would, it appears, have been deemed ‘incapable’.

memespp

But not if you are autistic.

Danger of EHCSs, and, Abuse of MCA Capacity for Adult Service Funding

blog-pictureSo let us explore, what appears, to be the Local Authorities practice, in relation to capacity assessments, since, the lucrative, ‘independent/community living’, away from family living industry was created.

Anyone, suspected of ‘incapacity’, all autistic, learning disabled, and, mentally disordered.

Including, potentially, anyone in need of ‘special’ education.

Funded under Education, Health, and Care statements.

Which unlike SEN, make the social services responsible for ‘protecting’ a child’s ‘welfare’.

So now, all ‘special needs’ children, are deemed  in need of the protection.

Discriminatory of parents and children,in breach of the Equality Act, and,s 8 Human Rights Act.

Strengthening a disabled’s  status, as a ‘child in need’, under the Children Act, see my article NLJ ‘The Disability Trap’.

EHCS,  also allow care, health, and educations distinct roles to overlap.

And,  their funding to be mixed and transparency even more obscured..

SEN/EHCS, do not apply to private schools.

So, the rich, can avoid, state intervention, and, are, allowed, their legal rights.

ECHS, do not fund schools after 16.

Instead, schools are replaced, by ad hoc education packages,consisting of skills for independent living, until 25..

These, combine support  at home.

And, these ‘education’ providers, unknown a family, will be charged  to notify social services, who approve them, of any ‘intervention issues’.

At 18, Adult Services fund everything.

As, the only  LA policy now, is life in  for profit, private residential care units.

All decisions are removed from the disabled, and their family by the MCA 05.

By showing  ‘incapacity’ to make  decisions.

So, the LA will insist,  a capacity test is carried out, before, providing any adult services.

So social services, will suggest, your young adult child see a psychologist.

This ‘seeing’ includes a capacity test, but, you are unlikely to be made aware of this and there appears, no duty on the local authority to inform you.

It can also provide, evidence of emotional abuse/neglect, to cut you out of your child’s life.

If you  ask for clarification of such assessments, and/or feel them unnecessary, the Local Authority, will apply to the Court of Protection, for an interim order under s 48 Mental Capacity Act 2005.

This application will be served, 24 hours before the court hearing.

Social services witness statements, in support, are not on oath, so not subject to the Perjury Act.

Matters to support this court intervention, can include any reported hearsay, from any source, care workers, GP, educators etc.

The first you may  know  of these ‘concerns’, will be 24 hours before the hearing.

No one is under a duty to discuss  concerns with you first and under a tightly prescribed, managed service will be told not to..

Despite Social Workers and Mental Capacity Act Codes of Conduct, and, the Human Rights Act.

The Local Authority will ask  the court for a list of expansive orders.

Including, any assessment and/or inspection, they wish.

If you do not agree, you may be warned your child could be taken that night.

So, you are given little choice.

This,  is all an abuse of the MCA, and its five overarching principles, and its Code of Conduct.

The MCA provides, ‘capacity’, must be assessed specifically, in terms of capacity to make a particular decision, at the time it needs to be made.

The LA,  will allege incapacity, in respect to the following decisions,

To litigate the proceedings

To make decisions about where they should live

To make decisions about the care they receive

To make decisions about the contact they receive from family members.

Clearly, only the first two, are in fact particular decisions, the others involve several particular decisions, should they have a bath, wash hair, brush teeth, depilate their arm pits etc.

Similarly, family members, are many decisions, to see mother, father, sister, brother, granny.

Remember the MCA provides an assessment should only take place,

‘At the time it (the decision) needs to be made’

But these decisions do not need to be made, at this, particular time.

Just because a person is 18, and now funded by adult services, a capacity test per se, is not allowed by MCA.

In relation, to the last three decisions, the disabled person, will have been making these decisions, all their life, whether to have a bath, sleep in thier home,  see their granny.

How can they suddenly become incapable of making these decisions, and, the LA make them for them for them, under the MCA?

How can an assessment be justified, when these disabled, have already made these decisions in the past.

And by making them, shown their ‘capacity’ to make them, just because LA funding, requires it?

In relation, to the remaining decision, capacity to litigate, no one, unversed in law, would have such capacity, and, in any event, it is not be necessary, if the other capacities  are present.

The MCA, was not drafted for the convenience of funding, only, independent living provision at 18, and enabling this by illegal removal from the family home.

The MCA was drafted, to protect a person, by allowing another person, to make a decision for them, in  the least restrictive way, and, as they thought, that person, would have made it, in that person’s best interests, if thought, that person, had become in capable of making that particular decision, and, it needed, to be made.

The MCA, was not drafted, to declare people ‘incapable’, and, allow all their future decisions to be made for them, for profit.

Or was it ?

Illegal MCA and Capacity Tests, and Lucrative Vegetables.

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The Mental Capacity Act was drafted to protect and empower.

Instead, it is illegally being used to remove all the rights of the deemed ‘incapable’.

To obtain a capacity order, all a Legal Authority needs is a box ticked by anyone, normally a GP,  that they ‘suspect’ a person, incapable.

Effectively, in their opinion, unable to retain information.

So beware of the Alzheimer tests, GPs are now paid, to provide.

Yet, if a person is autistic,  the assessor likely to be GP and/or social worker will only have physically examined, or seen the autistic, have no knowledge of autism and have based their opinion on a  discriminatory  view, of the autistic’s appearance and condition, such an assessment illegal under the MCA.

So much for the National Autistic campaigns and expensive education.

To say nothing, of all our high flown rhetoric, on diversity and equality.

The Court of Protection, on the basis of this perfunctory over sight, will then issue a  48 MCA capacity order without sight of the autistic, or information from those, he has lived with all his life.

This order will be enforced on an interim basis on threat of removal of the alleged incapable despite this being illegal under the MCA, which only has jurisdiction, if a person is incapacitated.

A psychiatrist, or more likely a psychologist,titles matter, will perform another standard tick box test, family might be consulted, but will not take part in the decision making process, despite assisting, and witnessing their child make such decisions, all their life.

Unlike his family, the ‘experts’, will not have seen, the soon to be incapacitated, before the assessment day, and, will know little of the autistic mind, or even, autism.

Actions of the autistic in the past, that show ability to want, and be able, to make decisions, like living at home, will be ignored.

We have no statistics, of how many, if any, manage to pass the test.

Assessors,are paid, chosen, and remitted by the Local Authority, who now, only provide adult services for those in, or destined for, independent living, where the maximum profit can be made, from them.

A clear conflict of interests.

If the LA fail to find an assessor, the official solicitor will then find one, and deem it even more credible, as independent.

Once tick boxed, ‘incapable’.

You’re loving, full of personality and fun son, daughter or granny, becomes a non-person.

A vegetable.

Non sentient.

Incapable, in law, of even being aware of what is happening to them.

Incapable of remembering, anything.

The perfect victim.

But capable of making millions for their encaging private corporations.

Lady Hale, chillingly alluded to this, when she said, just because a person cannot appreciate, they are living in a cupboard, does not mean, it is not a deprivation of liberty.

But can a court remove all a disabled persons rights?

Yes.

Is this, not the worst form, of disability discrimination?

Yes.

Is it not in breach of the person’s Magna Carta right not to lose his liberty except by trial by his peers?

Yes.

The Committee on the Rights of Persons with Disabilities Art 12 provides, that states party to it, UK is, should replace legislation that provides for substitute decision-making for incapacitated adults based on, ‘what is believed to be in the objective ‘best interests’ of the person concerned, as opposed to being based, on the person’s own will, and preference.

The government has so far done nothing, to repeal the MCA, but, the Court of Appeal has endorsed the Article, as having persuasive authority, as an aid to interpretation of it.

A study of the implementation of article 12 on the decisions of the learning disabled which usually includes the autistic shows it is not being implemented in UK in health or care settings.

Instead, substitute decision making takes http://www.publichealthreviews.eu/upload/pdf_files/12/00_Werner_S.pdf place.

http://www.publichealthreviews.eu/upload/pdf_files/12/00_Werner_S.pdf place.

And even without considering  Article 12, particular weight, must be placed, upon the incapacitated wishes and feelings, in determining where their best interests may lie, Peter Jackson J  Re M (Best Interests: deprivation of liberty order [2013] EWHC 3456 (COP).

So why is it happening to millions?

Profit.

OLYMPUS DIGITAL CAMERA Is this the photo of a vegetable ? Does she look non sentient?

Corruption, and abuse of Autistics for Profit

This is a tale of two young autistics in Sheffield.

One living at home with loving parents

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The other ripped from his parents, to face abuse, alone, and isolated,

in independent living.

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And to die, of unexplained injuries, and a heart attack, after huge doses of anti-psychotic drugs, were pumped into him,in a private cAmbian  owned community living placement, charging  at least £6,500 per week.

This is a tale of evil, and corruption.

Of  profits, for a privatised NHS, and, independent living providers.

Of colluding  courts, and Local Authorities.

This is a tale of me, a mother, sick with worry.

And another mother, who had warned, they would kill her son, with their ‘treatment’, but they continued, gagged her with a court order and he died two weeks later.

Thomas Rawnsley, was transferred, via a deprivation of liberty order, granted by the Court of Protection, under the Mental Capacity Act, against his parents wishes, from his home in Bradford, to a hospital in Peterborough, and then, to a privately run, ‘independent’/ supported living facility in Sheffield.

His loving mother was replaced by itinerant carers.

One of whom, a large man, would kick him into his room,

and, regularly threaten, ‘How many fingers can I break this time ?’, and then bend Thomas’ fingers back, but they did not break, only because, Thomas was double jointed.

Thankfully for Thomas, there was a witness, prepared to risk all to whistle blow.

How much violence, and, verbal abuse goes unseen, ignored, or blamed on self harm, or mental illness ?

Thomas’ ‘carer’, received a suspended prison sentence in February 2014.

Despite this desperately traumatic abuse, Thomas was not returned to the love, and care of his parents, and familiarly of this friends, and community.

But forced to remain, in the same independent living unit, as Thomas was earning more than £6,000 a week.

Understandably,Thomas’ trauma, and unhappiness, made him difficult to care for.

And, his carers warned him, that he was, ‘Acting out, and they had medications for that.’

See, the Justice For Thomas Post reblogged later. Now disappeared.

The independent living provider now also owned by Cambian sent  Thomas, to an A T Unit for his ‘medication’.

Fortuitously, for this new ATU, as it had been threatened with closure, and, for a long time, Thomas was its only patient.

This appears to be the same group of  multimillion pound assessment centres, build on the back of my daughters illegal, off label Risperidone trial in 2007, when our complaint to CAMHS,  lead to the LA taking court proceedings against us.

It is where, her National Autistic Society wanted to send Issy in 2013, just before she, refused to return to their care, with a faecal impaction, 7 stone in weight, with 2 rotten teeth, and suffering PTSD from their carers abuse.

The only ‘treatment’ in these centres, is high dosage antipsychotics.

No dentist, no clearing out of impaction, no peace with her family to get over her PTSD, just more emotional abuse.

It is also where Issy would be sent if there had ever been any violent/uncontrollable incidents. See my post Respite and the secret social worker.

They promised Thomas, he could go home for Christmas.

At the last minute, permission was withdrawn on the grounds, he would not want to return, and, his subsequent behaviour,might be difficult.

So much for disabled person’s  independent autonomy, human rights, and best interests.

And the mockery of his supposed ‘independent’ living as an adult.

The Unit only eventually agreed to let Thomas go home, after realising he knew about the trip, and someone would have to tell him it was off.

Thomas’ poor mother described him in the ATUnit;

He can’t eat, he can’t talk – he just dribbles. He’s been turned into a junkie; he’s addicted to his anti-psychotic drugs because he’s kept on the maximum dose to make it easier for them to cope. It breaks my heart. He sits naked in a corridor just wrapped in a quilt. He has no modesty or dignity in there. He is my beautiful, beautiful little boy. When I ask the unit why he’s left naked like that they tell me it’s what he wants. I ask them lots of questions, I don’t get real answers. I think they see me as a trouble-maker but I’m not, I’m Thomas’s mum.

Thomas in ATU on medication .

Thomas in ATU on medication .

http://www.blogistan.co.uk/blog/mt.php/2015/02/03/thomas-rawnsley-abuse-separation-unexplained-injuries-heart-attack

On the very day Thomas lay dying,a few miles away, social workers,  sat in my kitchen, inspecting clothes, already photographed by teacher/care workers. a day after the hearing of the LA’s mca application to remove my daughter to the same home Kingdom House where Thomas had  effectively died.

and the LA Service Manager, AFTER we complained held meetings on her ‘concern’, that she had seen Issy, naked in the kitchen, on the way to her bath.

No one saw, or cared, about Thomas’ abuse, this was the ATU’s purpose, he was keeping it open, making huge profits for its corporate owners.

Thomas was earning £6,500 ( and drugs and kickbacks ) per week, for our privatised NHS ie Cambian Group.

So much for budget restrictions, these on only placed on support at home.

They are the excuse, for enforced away from home living and big bucks for the privatised monopoly ‘care’ services, from central government.

The weekend before Thomas died, his parents noticed ‘unexplained injuries’, including carpet burns, and he was ‘’struggling with a chest infection that they knew was serious’.

There is little medical attention in COMMUNITY LIVING, as in Issy’s  £9,000 per week National Autistic School.

He collapsed, and died shortly afterwards of a massive heart attack.

He was just 20.

And had spent the last two years of his life in hell.

Will there be an inquest?

Unlikely, and if there is, all experts, providers,  have financial/career/systemic interests in covering up the truth, and continuing their income and investment source.

Will the Unit be closed down now, as it is at present under used, and serves no purpose, but to torture, and drug those who cause any problems, to their itinerant carers, in their 3,000 per week independence.?

Not, if the state, can steal more autistics from loving families.

Thomas. collapsed, and became brain dead on the 3rd February 2015.

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