‘Raze out the written troubles of the brain’. The Myth and Horror of Mental Disease

Mquote-canst-thou-not-minster-to-a-mind-diseased-pluck-from-the-memory-a-rooted-sorrow-raze-out-the-william-shakespeare-384568

Psychiatry, is defined, as.

the diagnosis and treatment of mental diseases’.

‘Disease’ as a concept can only be defined in terms of its pathology.

Pathology  diagnoses disease from changes in cells, tissues, and body fluids.

Not even Schizophrenia, or psychosis, let alone, the recently created 375 mental ‘disorders’ have any pathology and therefore cannot be ‘diseases’.

And psychiatrists have had to admit  to this.

The difference between a medical diagnosis and a psychiatric diagnosis

Many academic and influential psychiatrists have written extensively on the non existence of mental illness per se, in books like ‘The Myth of Mental Illness’ by Thomas Szasz

https://en.wikipedia.org/wiki/Thomas_Szasz

Once a putative disease,  that has a pathology like neurosyphilis, is diagnosed, it then becomes a physical not a mental disease.

The use today, of socially ‘acceptable’ conduct/behaviour, as the main  diagnosis of  mental ‘diseases’, is akin to its historic use, that categorised homosexuality as a disease of the brain.

And institutionalised unmarried mothers as social deviants.

It would appear, social control, and profit, are the reason for our third largest, burgeoning pharma industry, and mental health services, soon to be totally privatised. https://finolamoss.wordpress.com/2014/12/16/mental-health-big-pharma-big-profits-big-danger/

It  is now possible, to label almost anything, as  a mental ‘disease’/disorder,- alcoholism, shyness, terrible twos, removing social responsibility, maintaining social control, and make profit from these new diseases, by fixing them with expensive, dangerous magic bullets, that cause more harm, than good

.http://www.cchrint.org/2011/07/29/harvard-expert-ties-mental-illness-epidemic-to-big-pharmas-agenda/

And, the side effects of this ‘disease cure’, itself, then causes pathological changes  in brain and body and even death.

We are insidiously brainwashed by TV soap operas, like Coronation St to believe, that these ‘diseases’, like depression/ADHD  are common, and can be miraculously cured by drugs.

Such medication, at best turn us into human robots, unable to emphasise or feel, or, at worst, has side effects, that will then be treated, with more dangerous magic bullets.

Rarely, are they the solution, except for a very short time preferably with counselling.

And their use, boosting the pharma industry, and our economy,  motivated, by unregulated profit.

The following blog comments, received from two mothers are just two of the millions affected.

Theirs, and their child’s horror, speaks for itself.

Pauline Thomas writes of her son’s medication

‘My son has been taking Carbamazepine for 25 years, and Lamotrogine for 19 years.

Both are anticonvulsants. Both also used has mood enhancers for people suffering with Bi-Polar My son has cerebral palsy, mostly down his left side and a learning disability.

My son was 17 when he was diagnosed with epilepsy after a hip operation. He was medicated on Carbamazapine, and for 5 years was seizure free.

We were coming to the decision to start taking them away, when he started having startle jumps whenever there was a loud noise or someone knocked against him. Sometimes these jumps led into a full blown seizure (tonic clonic).

It was then that he was medicated with Lamotrigine. Six months later he was getting moody and distressed. We did not realize then that Lamotrigine effected peoples moods. We were given help from psychologists.

In 2008 his seizures stopped. About the same time he was having aggressive outbursts and refusing to do anything or go anywhere. Sometimes they lasted for a few days, sometimes longer. At this time the day services in our borough were being pared down and outsourced to private companies. A disaster for him and many others.

Anyway in late 2012 we started to reduce his carbamazepine (he was on 1000mg daily).

Carbamazepine is an enzyme inducer. Any drug taken with Carbamazepine (Lamotrigine) would automatically begin to get stronger when you start to reduce CBZ.

I reminded the psychiatrist of this but he ignored me. Perhaps he thought I was talking out of turn?

The result was that a month after he was free of CBZ (in Jan 2014) he started to have terrible frightening hallucinations. He was terrified. He could not sleep. He was so scared.

We contacted his psychiatrist who said that he had never come across this type of reaction before but he believed my son was having a interictal reaction to his withdrawal of CBZ. I argued that he was most probably having a toxic reaction to Lamotrigine. His psychiatrist reinstated 400mg of carbamazepine.in two weeks. He recoverd for 3 weeks and then went back to be psychotic again but this time with the added side effect of ‘freeezing’ in the middle of doing anything. He would suddenly stop like a statue.

Telemetry showed no sign of any seizure activity. We have now began the long haul of getting rid all his medication. Lamotrigine is gone. We are now down to 400mg of CBZ.

The withdrawl symptoms are horrendous. Completely in a world of his own. Keeps talking about his days st college (20 years ago) with a focus on the same person. Her name and her parents and her sister going over and over in his head. It is like living with a completely different person

Carbamazepine has wrecked my son’s bones. He has osteoporosis. He has reduced white blood cells. (leucopenia). Both known side effects. He has little purple mauve spots on his body. Another known side effect which has been ignored by his psychiatrist. His psychiatrist suggested a while ago that my son should take biphosphonates to strengthen his bones. We refused, as we said we would not know if the drug would harm him, or if he was experiencing any side effects.

In America the drug company Merck was being sued by patients suffering with necrosis of the jaw and cancer of the oesophagus  after being on this drug.

We were threatened with the MCA

The doctor said if it could be proved that my son lacked capacity it could be taken out of our hands. This is why we cannot trust or like this doctor.

The doctor claims that my son is not suffering from withdrawal symptoms because antiepileptics have no known withdrawal symptoms.

He has reminded us however that they are mood enhancers.

We reminded him that our son was not mentally ill when he was given antiepileptic drugs.

My research tells me that Carbamazapine is related to the tricyclic group of drugs, which are antidepressants. There are withdrawal symptoms with antidepressants, especially if you have been on them for many years.

I recently purchased a book by American Dr. Peter Breggin called Psychiatric Drug Withdrawal, and one of his arguments is that

prescribers identify drugs according to the conditions that they are being used to treat rather than by their pharmacological category or characteristics, including their impact on the brain.

He also in his book refers to articles by Dr. Joanna Moncrieff.

I deplore that many of our children and loved ones are being used by the pharma and psychiatrist world as some sort of learning curve.

My son and many like him cannot fully explain what side effects they are having. Thank you Finola for exposing these cruel practices… ‘.

Another Mother, Cynthia Bartlett, wrote tragically of her son Charlie;.

‘ My son, Charlie, died two years ago of what I believe to be side effects from Risperdal given from age 15 until a few months before his death ay age 24.

I am really trying to start and do an investigative journalism piece on just this…Risperdal is routinely handed out here in Canada to children with autism.

I see one boy (on risperdal since age eight) in our small town, going down, exactly as my son did, starting with a strange gait and then rapid onset dystonia, losing swallowing and then dying from choking in the middle of the night.

I have accompanied the family to the neurologist to no avail’.

Our government, is at present debating, and, determined to introduce, an Assisted Suicide Act, legalising euthanasia.

One of  its clauses, could be, that if, all the MCA ‘incapable’, would have decided, to end their life, were they capable, the state can end it, for them.

Even, their body parts, can be used under MCA regulations.

This will mean no inquests, into why they died, even court deracinated family, need not be told of their death.

Parents of the MCA disappeared are not even afforded notification and a funeral.

There is no closure on parents’ lifetime horror of wondering what is happening or has happened to their child.

Today, literally by now thousands  of autistics and LD  are holed up in private NHS ‘hospitals’ and private care homes like Winterbourne View some managing to survive for decades.

All a statistic earning £4,500, for 24/7 surveillance, and medication.

What physical and mental state will they be in by now?

Imagine, the permanent effects of the long term drugs, they have been pumped full of, the horror is too much to contemplate but they and their families must daily.

https://finolamoss.wordpress.com/2015/01/01/the-risperidone-scandal/

There are no future services/ life, for autistics, and, mentally disordered, except, as such encaged, cash cows.

The corporate/charity ‘independent’ living providers, need drugs, to enforce their ‘support’, as the system, does not allow, for individual care.

Shakespeare knew over 400 years ago no doctor could,

Raze out the written troubles of the brain.

As, Therein the patient Must minister to himself.’

And the autistic and learning disabled are not mentally ill.

But, these wise words were before big pharma and the realisation of the gold mine of mental disability.

Scientology_psychiatry_kills

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Harvesting of the Disabled for Profit

A2013-09-20-15_36_14Parents of special educational needs children be warned this will be your fate.

The state are creating and labelling children as learning disabled instead of having learning difficulty.

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 in breach of s8 HRA to harvest children including future deemed criminals.

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

A learning ‘disability‘ is an impairment of mind, is permanent, innate and evidenced by a low IQ,  and is now inexplicably,  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, a late developer,  has poor teaching/assessment or is taught in a second language,  such a child will have at least an average IQ. .

So if your child is a late developer and/or has inadequate teaching he may be doomed to be made a cash cow for life.

Unless he is part of the labelling state cabal.

Or in private education.

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 and social worker will now be part of your life.

And,  your  child’s name will  be 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 knowledge.

http://www.capita-one.co.uk/files/one/attachments/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 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 a disabled 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 from school to venture capital education and care .

.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/ community living,

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.,

And, show, it is in his ‘best interests’, to be removed from home 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 https://www.ambitiousaboutautism.org.uk/sites/default/files/Transition%20seminar%20FINAL%20(2).pdf

Your child has now been made, the perfect commodity, 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.

https://www.gov.uk/government/uploads/system/uploads/attachment_data/file/575666/Joint_local_area_SEND_inspection_in_Surrey.pdf

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

Determined to harvest your child.spider-net-g8i1