NHS scavenged for Profit by Health and Social Care Act 2012

hitler-quote lieOur media led us to believe the crisis in our NHS is due to a lack of funding and increasing private contracts with Virgin, Serco, Capita etc.

Its lies disguise the real sale of our NHS, by all political parties by the passing of the Health and Social Care Act 2012.

So our Public NHS, a hallowed bastion of altruistic public service, trusted to do what is in our best interests, our servant not our master.

Has been mendaciously converted to a cabal of monopoly ‘privatisation’ run by mangers for maximum profit, on a commercially aware basis, in secret, using the public as a  statistic for present and future profit.

With ever more media cries for more money to feed this profit, and harvest customers by preventative, innovative healthcare and medicalisation.

Is the NHS underfunded ?

No
https://www.kingsfund.org.uk/publications/nhs-myth-busters

The NHS was shown to be efficient and affordable and didn’t need this radical reform.

The Commonwealth Fund a private US foundation reported in 2010 ,using its own and other international data involving 20,000 patients in 11 developed countries found our NHS, one of the most cost effective systems with excellent access to care.

Who controls NHS money ?

By the Health and Social Care Act 2012, an all powerful national commissioning board- NHS England, whose head is Stevens an ex executive vice president of USA UHS international,took control of NHS England funds now in excess of £100 billion

Asked in 2012, the civil servant for the accountability of the NHS fund gave a battingly convoluted 300 word answer,

in 2014 Bernard Jenkin, Tory Chair of the Committee questioned the complex relationship the Act had established between the Department for Health and NHS England the ‘arms lenght’ commissioning board.

‘Vast amounts of money are involved here £95.6 billion( 2012) in the case of NHS England alone and it is simply not acceptable that there is no clarity or clear accountability for that kind of public expenditure… The architecture is not meant to be reminiscent of the film the Matrix where doors open on virtual worlds which are insulated from reality and hidden from the public and from those meant to be accountable for them’.

Social Care budget is also included in HSCA 12

HSCA also included the LA budget for care and destroyed the boundaries between medical healthcare,community and personal support for life, opening up huge areas of potential profit.

In Sheffield alone £464 million is available for health services and £107 million for social care and public health.

So the NHS is now our social carer usurping many LA roles and budgets.

So why did all parties vote for HSCA 12 ? Despite all professional bodies GMC GPs etc being opposed

Political expediency/party presure ,power could be devolved to local Common Purpose controlled CCGS, ignorance of effect

What is now the distinction between Private and Public NHS ?.

Despite what was proposed was within the definition of ‘privatisation’, this word was redefined by ministers to ignore whether health services were provided by a public or private

Few, as I didn’t, would know that the national MYDENTIST chain was run for profit as with most NHS and Community services.

Nor if their GP is employed by a private corporation.

Few in Sheffield will know the Health and Social Care Foundation Trust was converted to effectively a private company, its existing NHS managers made directors.

Nor how many more are now being run for profit not patients.

So the public have no way of finding out if the overriding duty of their services is to make profit and exploit them,

or to provide the best possible regulated NHS service, as they assume it is.

Worse still the public have no contract with service providers, their relationship dependent on trust in the NHS and so will find it impossible to sue for poor provision.

And their very vulnerability can be exploited in the ruthless commercial world.

As customers have no say/nor choice in their care. nor effect of outcomes on them.

https://www.nhsforsale.info/nhs-privatisation-overview-2/

The Myth of Competition by tender.

The lie of austerity,, resulting in the need for competive tendering of services, paved the way for monopoly cabal provision maximising profit and furthering globerlisation

S75 provides CCGs have to put out any services due for contractual renew to tender unless they prove there is only one provider capable of delivering the service ( How or who they prove this to is unknown )

If there is only one qualified provider in their estimation they will always get the NHS contract

In February 2019 NHS England produced a document outlining changes it wanted to see in legislation.

It is not only in control of NHS and social care funds, but our legislature

One of its main proposals was to remove the obligation to put services out to competitive tender if local commissioners considered a service would be best provided from within the NHS.

This has the mendacious appearence of avoiding further NHS/CARE privitisation by providing NHS public,

but allows monopoly private contracts, avoiding choice or competition.

The cabal of NHS and community care provision- the real reason for the HSCA12

The HSCA was sold to Parliament, to promote patient and GP choice, but intended to produce the opposite.

Foundation Trusts are being privatised on the lie of sustainability.

https://www.sheffieldtelegraph.co.uk/news/health-how-bosses-are-facing-challenge-of-creating-a-sustainable-nhs-in-sheffield-57558

CCGs are being privatised and/or consolidated by government special measures and bought up by the very foundation trusts they commission .

The Foundation Trusts make/request the funding for the services they already own or are buying up or have financial interests in.

Such is the corruption such is the profit

and the love of money is the root of all evil.

A cry from every mother with an autistic child- please support

See plea for help from the Mother of an autistic son

https://www.crowdjustice.com/case/justice-for-my-autistic-son/?utm_source=case_page_social&utm_medium=facebook&utm_campaign=sumo_widget&fbclid=IwAR3bzu73ZSNyZu2402Ro7mPwJKjTuGUVZEPpoQCoCZXp6bCrCAcD-K_ZxG8

I’m a campaigning mother, fighting for the right care for my son and other autistic people as well.

Crowding funding for support, as no legal aid

Who am I?

I have a son who has autism and learning disabilities.

Five years ago when he was 16 years old, he was MHA sectioned

and placed in a hospital about 5 -6 hours driving distance from his home.

We only thought he would be gone a few weeks and it has been years.

He is traumatised by being away from home.

He has developed self harming behaviour in hospital. He has been regularly restrained and secluded, which has caused lots of injuries to himself.

We know that he doesn’t exhibit any challenging behaviours, which has been confirmed by over 200 times short controlled home visits now since 2016.

He is so much happier once he is home with us.

Case Background

My son has been out of hospital since June 2018 and is in supported living now in the community, however, with hospital model care still in place.

Despite support from professionals, and his own desperate desire to be back home living with us, there is a dispute with the Clinical Commissioning Group and the case has been referred to the Court of Protection to make a decision about his best interests.

They also set strict restrictions on our family contact time.

He can’t have even an additional few minutes longer with us – sometimes when he is halfway through eating dinner at our family home, staff will take away his dinner plate before he has finished as the visit is officially over.

It feels like psychological torture for us and we believe it is for him too. He still regularly being restrained on the floor and sedated. He constantly has unexplained injury marks in his body as well.

We don’t feel that he is safe to live in a the community like this that similar like another hospital.

The CCG believes that our son needs routine because he has autism. But being autistic shouldn’t mean you are excluded from family life: that is a basic human right.

Currently, the CCG has spent large amounts on his care team, which is 12 staff team. We believe it will save public money if he can return back to live with us. We need to make the human rights arguments to the court

How much we are raising and why?

We need a solicitor and barrister to put our case to court.

The CCG has a legal team and it feels unfair to fight this on our own. We need help to navigate the legal system and understand all of the evidence.

Currently, we can’t get legal aid. Despite the fact that we have lost a lot of earnings fighting the case in the court and that we are lower income family.

My solicitor has forecasted significant further costs.

The final hearing will be 4 days, which would need involvement of a solicitor and barrister. In addition, I need to pay lots of the cost of an independent experts assessment.

We can’t afford the legal costs, so we’re asking everybody who cares about this issue to make a little contribution. my son lacks capacity to instruct a solicitor but one has been appointed on his behalf

This isn’t just about my son.

I recently watched BBC1 Panorama’s “Undercover Hospital Abuse Scandal”. The documentary shows that this scandal is carrying on in many hospitals and it can happen to anybody, even in the supported living places.

“Panorama goes undercover inside a hospital for vulnerable adults and reveals patients being mocked, taunted and intimidated by abusive staff. In shocking footage, reporter Olivia Davies films patients with autism and learning difficulties being deliberately provoked by staff who then physically restrain them. The Panorama investigation comes eight years after the programme exposed the scandal of abuse at Winterbourne View, another specialist hospital. Then, the government promised to reform care for the most vulnerable. Now they stand accused of failing to keep that promise by families, campaigners and whistle-blowers.’”

This documentary and our son’s case shows that we need justice for autistic people’s human rights in hospitals and community care! We hope my son’s case can shed more light on this important issue and benefit other autistic people and children in their care in the community.
We want disabled people and their families to have more choices over their life and their care and for them to be able to enjoy their family life, as is a basic human right.

*I can’t disclose my name or my son’s name here on account of a court order.

Billions has been made from the autistic deemed also learning disabled

NAS its voice has made millions of recycled tax free profit from being its voice.

The Autism Act it canvassed for WAS surreptitiously stitched up so that it can/is being ignored

They, our most voiceless and vulnerable are made cash and pharma cows to fuel a bankrupt economy and immoral society,

LOVE and care, and the obvious, are ignored and suffering and death allowed.

In the name of humanity make this stop.

This mother can’t even show her name such is oppression in UK as her son is subject to as Thomas Rawnsley was the most secretive draconian Court of Protection.

These ATU EFFECTIVELY services for life, are run for private profit, bought up by venture capital, as paid £9,000 + a week for her son, and they can make any decision they deem in his best interests for life and noone can complain about their services even if they result in the service user’s death see Thomas.

As Thomas Rawnsley’s and my own plight’s non media cover showed this mother’s plight is not being taken up by media, which shows it is controlled by the gov’s agenda ie out of ATU to another effectively ATU near home

Debt used to bankrupt UK and make trillions profit.

national debt DCgSlArXkAARVkoGordon Brown eliminated ‘boom and bust’ omitting to say a false boom could be mendaciously manufactured from a bust

https://www.theguardian.com/politics/2008/sep/11/gordonbrown.economy

As debt and interest on it, and the asset stripping it allows makes power and profit.

The global crash a year later saw the realisation of this.

Allowing enslavement of the individual and State by debt, and the use of austerity to control and refashion society for profit.

Debt owned to banks, then and still qualitatively eased by the public purse, who bear the debt but not the profit.

Debt per se, makes huge profit from both interest rates, avoided unsecured creditors and the Administration industry

Debt also destroys competition, by take over, after insidious financial destruction of smaller competitors

A tool of avarice – Solicitors firms bought up by huge corporations leaving millions unpaid debt to unsecured creditors as DWF take over shows-

https://www.lawgazette.co.uk/practice/creditors-lose-5m-as-failing-law-firm-sold-at-knock-down-value/5059901.article

GP practices, building , care , NHS, retail suffered similar fates, to allow privatisation of public services, ever more multinational owners to increase their profit – also the face of globerlisation , the era of no competition, too big to fail, or oppose capitalism.

The Tories have won two elections on the back of the need for austerity to cut the UK deficit.

And more people than ever are in debt, three million excluding students will never be able to pay off their personal debt.

Yet NHS, schools, LAs, Prisons, Courts, Legal Aid, use the excuse of cost cutting to avoid the provision of any/adequate services.

http://www.telegraph.co.uk/news/general-election-2015/11339921/David-Cameron-and-the-national-debt-monster-in-three-charts.html

The Coalition took office in 2010 saying it would clear the deficit by 2015/16.

Having missed that target, Cameron planned to clear the deficit by 2018/19, more borrowing, that just added to the stock of public debt.

So what is happened to all the public money and why the cuts ?

The cuts/austerity has been used as a cynical tool of policy enforcement.

The only money available to support vulnerable/ disabled adults is to pay for enforced, no choice residential care.

Whilst the budget for family care is non existence the amount paid to the private residential care provider is effectively unlimited and unaccountable.

The NHS mental pays 3,000 a day in assessment, £13,000 a week in hospital and £8,000 + a week for life in community living all owned by private venture capital backed UHS/Acadia USA multinationals

Public-sector debt interest payments already represent the fourth-highest department for spending after social security, health education.

The same is true of schools, universities ,adoption and fostering agencies, mental health provision etc.

All soon along with our courts and all public services to be fully ‘privatised’.

But this is not ‘privatisation’ as we know it .

It is monopoly no choice , no accountability service for maximum profit.

There is no tendering for health and social care by NHS as there is only one ‘specialist/qualified provider that CCGs fund under the Health and Social Care Act 2012.

On the back of this public bonanza, investment companies like Ontario’s Municipal pensions pay 207 million for Lifeways residential homes, UHS 379 million for Cygnet hospitals

It starts with smaller providers taken over by the large multinationals, Cultistish , all hidden behind commercial confidentiality and too big to fail or be made accountable.

This is not competitive, best and cheapest service but the most expensive and worst provision.

It fuels GDP. at increase of our deficit.

It is a means of siphoning off/ripping off the Country and its people who are harvested as commodities to multi nations, venture capital investment trusts with offshore tax havens and no accountability.

Universities are now unaccountable cabals, all charging the same, whilst students are captive consumers who will never pay off their ever increasing debt, which is an annual bill of £9 billion for the tax payer another unseen , unpaid country debt..

http://www.thisismoney.co.uk/money/cardsloans/article-2326560/Debt-timebomb-85-cent-students-pay-loans.html

£36,000 per year is paid per prisoner to private prisons and they are not fit for purpose.

£30,000 minimum/ max discretionary. is paid to private adoption agencies per adoption, minimum £900/max discretionary per child fostered to private fostering.

Adoption- Cameron’s flagship policy is a billion pound, unaccountable industry which has not helped child protection, as Rotherham/ Rochdale rapes testify, as does the attempt by LAs recent statutory attempt to exonerate themselves from liability for child protection.

Mental Health , another Cameron and now May flagship with now nearly a quarter of the NHS budget ploughed into provides worse services.

https://finolamoss.wordpress.com/2017/02/14/what-is-happening-in-662600-a-year-mental-hospitals-cqc-reports-2011-2016/

billions of public money is being poured into monopoly private enforced by courts in secret private services which are not supporting but abusing.

NHS England nor our LAs are accountable.

Professions and vocations Nurses, Social Workers, Psychatrists ,GPs, Dentists, Solicitors, Barristers are empolyed by ever larger corporations on an itinerant, prescribed basis for corporate profit.

Even the USA do not employ the alternative business structures for their lawyers

Yet we do and for our GPs/dentists, as NHS pay £136 per 10 minute consultation.

http://www.lawsociety.org.uk/support-services/advice/practice-notes/alternative-business-structures/

10 years of austerity has resulted in a trillion pound deficit

https://www.thenational.scot/news/17537879.has-no-one-noticed-the-uk-national-debt-has-topped-2-trillion/?ref=fbshr&fbclid=IwAR0WxEOD_6-Uf9MIkfcwQNWKY_K2S1WLBkyfMFCBIWEXJ2_5o_gS-_6igj0

loadsofmoney2And unprecedented personal debt

https://www.mirror.co.uk/money/great-british-borrowing-binge-sends-7166258?utm_source=facebook.com&utm_medium=social&utm_campaign=sharebar&fbclid=IwAR0HPN4azIKj-mEYBGTvmuTflOoKVhxVUlojEjIrcnCZF4QN5NuxYp7aQG8

So what can be done ?

The UK has been refashioned,and is personally and publically bankrupt

Debt and its power is all that remains.

Sister Eleanor’s cry for Issy

issy photo fb‘I would be very grateful to those who take the time to read this

A lot of you may have caught onto the fact I have a severely Autistic sister, Isabel (Issy), 22.

Issy decided to remain at home one weekend and not return to her NAS residential care school, enforced upon her by care court application after attempts to MHA section, without any assessment at the age of 10.

After being so abused in NAS  (pulling her hair out, 48 bruises one weekend noted as ‘self-harm’, far too skinny (no period for a yr, not noted), undetected potentially fatal fecial impaction, an unexplained cauliflower ear, two bites, verbal abuse from a carer and witnessing the distress of other residents, all compiling to cause her to suffer intense physical and emotional suffering for most of her time there.

All at the cost of £177,000/yr ,paid by the LA with taxpayer money. At the age of 15 she couldn’t even write her name ( when she could at 5), brush her teeth or wipe her bottom.

Since her return we’ve received an interminable series of ever-changing pairs of LA care and education workers visiting our house.

They’ve also let Issy down one way or another, abruptly leaving her and/ or telling her she was to go to independent living and never see mummy or daddy again.

This threat, Issy repeated herself through her daily short repetitive mantras of distress.

A particularly awful statement, considering she was then and still is suffering from PTSD as a rational reaction to her previous treatment of care, which is furthermore exacerbated, due to her autism, that makes her innately more sensitive to nastiness anyway, especially from those she trusts, as Issy had shown that she wanted to live with her family.

As a consequence, she’s barely stepped a toe outside our house since May 2014, for fear of never returning.

To this day, we’ve had no support. No respite from 24/7 care, often endless nights, and just weekly supervision by Sheffield Health and Social Care, a private company, run for profit.

Two workers come in and never even encourage her to brush her teeth, which are rotting, nor try to take her out for walks.

If she says “go now”, (one or her common sayings). After an average of 15 minutes of unproductivity, two/ three times a week they leave

Not asking my parents and I how we are, and even being quite confrontational at times during periods of intermittent hostile silences.

Our 24/7 support allowance is £62.50/week.

Her DLA has been stopped and we’ve yet to receive PIP, where a private company funded by the NHS owning community/independent living whose providers would receive £8,000/week.

If we wish to discontinue the Health and Social Care visits, which amount to nothing no help with Issy’s basic needs, and actually make her regress, we would have to go to court, seen as the state would deem us to be interfering with Issy’s rights even though they’ve written her off as having no capacity following the MCA act anyway, and are blatantly disregarding her wishes to stay at home so much so she daren’t ever leave the house threshold.

I haven’t written this as a means to exercise my ‘cynicism’ or for scare-mongering. Nor have I given much care for the perfunctory need to preserve the dignity and privacy of my family and most significantly Issy, as might be interpreted. We are far past that point.

It has been driven by a compulsion to provide a brief glimpse that doesn’t even touch the sides into my sister’s suffering inflicted by the state and our oppression and bullying – not only to inform people but to expose what countless severely disabled individuals and their family’s suffer in this system but are overlooked and dismissed. The odd exceptional case publicised.

Through this little amount of exposure, I want to chip a little into the path to tempering the pervading state control and detrimental interference of family life for the sake of venture capitalist profit. To try and help all autistic and their families, from their daily oppression, not least our own.

I cannot coerce anyone to A) give this time of day or B) believe the entirety of what I have just written. It is the people’s choice as much as the profit makers for this flagrant breach of human rights to continue through public acquiescence and indifference.
Ultimately, this post has come about because I love my sister, and am sick of her and my family being hounded.

Thank you.’

My daughter posted this in her facebook received over 200 comments but now effectively forgotten.

we as a family are beyond fed up, but who cares ?

Billions profit from Institutions – 8 attempts to get Issy

Investment Company Omers bought Lifeways in 2012 for 207 million, UHS Cygnet in 2016 bought Cambian Adult services for 379 million.

Such is the guaranteed profit from the lifelong care of our most vulnerable that
All agency developmental support plans lead to the institutionalisation of the autistic/learning disabled/vulnerable.

It is the only funded support at 18.

The net of avaricious State harvesting of these lucrative commodities, made ever wider by the State’s definition and assessment of those that qualify.

The State’s web is honed to perfection via safeguarding, statute and all agencies.

Now under Liberty Safeguards ( Newspeak for removal to institution) at 16.

Millions will, and are being imprisoned for life without oversight, or even family contact, against their and their families wishes for profit.

All illegal under Autism Act, HRA, MHA and MCA.
.
Our most vulnerable are commodities- non persons – worse than slaves- rendered ‘incapable’ of any decision under the MCA

All agencies conspire in secret to this end – GPs, LAs, NHS, Care agencies, charities, companies.

Institutions are the only funded support at 18.

paid £8,000+ a week per person, £13,000 if sectioned to a mental hospital, fuel our economy, boost our GDP, at huge expense to our trillion pound deficit, and result in a life of torture and early death for our most vulnerable.

All achieved on the most audacious lie of austerity.

The State pounds by bureaucratic foot, the most loving families and society’s most vulnerable

Whilst it is charged and paid to support, it feeds it into private untaxed profit coffers.

Here, I describe what my family went through from years of support, after their 16 year old vulnerable daughter had been abused for a million by the very advocate for autism- the National Autistic Society , and desparately wanted to remain with her family.

Reflect on the horror caused to that vulnerable child, the family, and the mother that writes this and the public money spent.

And the modus of gov and their agencies to feed private venture untaxed profit.

First attempt was by social services in December 2012 when Issy was 15, depressed, not eating and pooh impacted, with rotten teeth in NAS residential , under MHA section to St Andrews , Northampton but the psychiatrist, refused to section without our knowledge.

So Issy, pooh impacted fed risperidone and build up drinks might as many have died an agonising death at 15, unseen in St Andrews.

Issy refused to go back to her NAS home after her weekend with us.

Without support we cleared her impaction, got her eating and took her out for walks.

We could get no support until we had innumerable meetings with our social worker and Reed agency, and funding was available after the NAS notice period expired on her placement .

costing a quarter of £177,000 for one 4 hour babysitting of Issy in May 2013.

Issy’s NAS worker abuser and large burly male baby sat but refused to take Issy out for a walk, despite her demands, as not insured.

In June 2013 Reed support commenced thanks to Zoe an excellent carer Issy went via bus all over Sheffield and Darbyshire put on a lot of weight and was happy.
We had tickets to watch Wimbledon so requested a weekend respite and underwent more innumerable meetings and emails with Reed

Social services offered Issy a stay in what appeared to be an independent living complex apartment in the city.

Worried that Issy would think she’d never return home, be distressed in a strange environment, and stop going out, I rejected the offer,

Reed at the last moment notified us that the LA respite request had been too late to organise staff, and I decided not to go worrying Issy would be distressed left alone.

The support appeared to be unaware that I would be at home.

Reed support was a bureaucratic exercise to produce a body, some complete strangers, to cover the hours paid at huge expense -estimated at over£3,000 pounds, Reed charged 3 times the worker’s £7.50 an hour to provide them.

Here I describe it
https://finolamoss.wordpress.com/2014/07/09/respite-care-and-a-secret-social-worker/

One overnight worker, I found out later, was an experienced Social Worker paid £30 an hour for an 8 hour overnight shift- £240, costing LA £720 to Reed , a worker £7,50 costing £168.

Why this extra provision for a social worker, if not anticipated that any problem with Issy could result in a phonecall for police aid and MHA section ?

The third, and one would think most unlikely attempt, was then by an education package funded by the LA to a charity New Routes 2,

Issy had regressed – hardly read, couldn’t write,didn’t wipe her bum or brush her teeth, despite NAS paid million
.
Issy had refused to go into a classroom in NAS for over a year, there and now since January 2013 no attempt at educational provision, despite the LA’s duty to provide.

A teacher from the local Bents Green special needs school arrived in my kitchen and assessed Issy in August 2013.

By October, having been told Issy could not attend any local school – Bents Green, Talbot, we were offered New Routes 2

The package consisted of an assistant teacher from Bents Green , her Reed workers and New Routes manager, eventually taking Issy to a room in ad hoc provision in Sheffield, full of computers and storage and often locked.
The two four hour a week provision was factored into Reed support.

I have to add the stress caused by yet inderminable meetings with SW and education package head, who appeared disinterested in Issy’s needs,.

New Routes 2 and our social worker started to create safeguarding intervention issues.

In January 2014, I was informed by a rker, that the education workers, were meeting up in Costa Coffee each week, and being quizzed for negative comments about me, my home, and care of Issy.

When workers were in our kitchen their boss would ring asking what I was doing

In April 2014 Issy whilst having lunch out with the education workers refused to leave the cafe and eventually after hours she arrived home in the managers car rather than usual bus.

She then refused to go out and started repeating ‘you can’t live with mummy and daddy’

The page of this incident were removed from Reed Daily log book kept on our kitchen table.

Our new social worker drafted a critical assessment with many serious inaccuracies which I complained about.

A rather hostile Children in Need Meeting of 8, including a note taker was convened in our kitchen, the social worker commencing with ‘Isabel started to pull her hair out when she returned home’, when in fact she had had bald patches on arriving home which had now regrown, so quite the reverse.

She also complained Isabel was now overweight at 12 stone, up from 7 when she arrived home, including her periods restarting, and was not eating healthily.

I noticed parental consent was needed for the educational support funded to March 2015, so withdrew it, at which point New Routes manger angrily withdrew the workers at the end of the meeting midway through their shift.

Zoe, issy’s main worker arrived days later but could not get her out and refused any information on the education incident that appeared to have caused this , and left never to be seen again, a great loss for Issy.

Eventually. with the help of another worker X, we got Issy out all day in May 2014, but then she again became housebound as this worker was not sent again by Reed.

There then appeared a fourth attempt to get Issy with the help of Reed support.

A new Reed regular worker was, unknown to me, a trainee social worker, and, she asked me without reason, ’What are you going to do to keep Issy? ‘Stop her slipping when she got out of the bath, when she never had.

By September 2014, most support was by this lady, and a newly qualified social worker, who wrote a very unfair, negative, spun daily log, which was corrected and part of a formal complaint.

I was told by a worker, that one of the regular support, had refused to support Issy, at the end of September. We were told she was ill, but I was told, she knew what they were doing, and, did not want to be part of it, and, has since left social care altogether

I think a Warrior Mum’s blog post- Michelle Daly published in net on Issy 28 /9, put heat on Reed a reputable international agency,

So much so, on October 6th, Reed withdrew their extremely lucrative support, and ended their contract with LA without explanation.

The fifth apparent attempt was by a family comany, a second education package recommended by the LA, paid for by use by our direct payments,the LA funding lady met in the kitchen to inform us it was our money, jet LA chose the package and we never saw the money, nor amount paid.

They initially, messed us around for months with no support arriving when scheduled, until they seconded an LA education worker, who falsely claimed, that IB had a red mark on her stomach, and other lies, and disappeared, only a week after Issy had for the first time, put on her outside clothes, and had gone out for a walk.

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

https://finolamoss.wordpress.com/2014/12/05/meeting-with-personalised-education-provider/

I now understand why the only other company worker who appeared family stated ‘I don’t like working with education’ and revealed ‘They are rounding them up and making pin cushions of them’

The sixth attempt was when the COP knocked on our door and the next day told us Issy would be removed from our house in her MCA ‘best interests’, if we did not agree any order.

We needed support, so ‘Got Friends together’, one worker Gail, from internet
We privately paid.

But our private efforts resulted in an apparent seventh attempt to find safeguarding issues to exclude us from Issy’s life.

Gail, our only support worker, didn’t want to continue to support after only 2 weeks, no indication she was unhappy, her excuse was loss of tax credits, an unknown lady suggested by agency owner , we refused. Gail came back supporting.
We found Burton street day centre for Issy.

https://finolamoss.wordpress.com/2015/03/07/rip-off-social-care-the-plight-of-the-disabled-family/

Plan by Social Services, to get her up,’ mentors’ to be sent into kitchen, to bring Burton Street to Issy.

But no explanation, as to how this would encourage IB out of the house, and, how they would get IB to engage with such workers.

Issy went out walking with me and photos taken by Gail put on Friends Together Facebook, were removed by the Social Services.

By April Gail had become a stepford care worker , formal with prescribed communication.

What do you drink ? How does Eleanor get on with Issy ? –
worn bath flannels removed from bathroom and she disappeared.

When we informed social worker, Gail rang had had a migraine for 2 weeks at the beginning of June 2015.

‘Friends Together’s owner informed our social worker

’ No concerns have been raised by any staff member with regards to Isabel’s choice not to engage with them and where interaction has occurred Isabel has appeared happy and contented’

But 5 months later on contacting Gail,sent a very different report by email on the day of his meeting with SHSC on the 15th October.

I spoke to Gail on Tuesday night about how she felt working with the family. She said that she Felt that Finola regularly ran interference when she was interacting with IB, that Finola was sarcastic towards her and that Finola was at her happiest when Gail was doing housework/decorating rather that working with Isabel’

A never before stated lie, which did not save Friends Together being put into special measures by the CQC.

X the lady worker who had previously managed to get Isabel out, contacted by Facebook, was then privately paid by us for care and got Issy walking 3 times round close on her first visit in August 2015.

Meetings with our social workers recommenced where our social worker denied any contact with X but could not explain why X was only available for social services meetings and on the odd occasion cared in a stepford manner for Issy .
It was stated by social worker that she, not us, was the only person who had a relationship with Issy.

She stopped attempting to take Issy out.

We decided only to employ her without social workers being in the house and she was unavailable

Issy has never been out since except for one walk up our drive.

Was all this costing millions, making huge profit and not in Issy’s ‘best interests’

The Risperidone Scandal

Written nearly 5 years ago, and this drug is still the main treatment for ASD/LD as it zombifies, to allow ever more profit from ‘care’ enforced by State.

The number of deaths it has caused in the UK is unknown. Deaths are not investigated as certified from ‘natural causes’.

From MENCAP 4 years ago 3 a day were dying.

Billions has been paid in US for its damage in court actions,https://www.bbc.co.uk/news/business-49982237?fbclid=IwAR0h1G5tJFum6wC9-Ogs16UlBPOch8ONv_Xnejn6w3tQ8IsiqgvDjDCsnP0

but it continues to be used in UK as we have no lawyers, experts or courts all are controlled by a State that promotes its use.

See affect on my 10 year old daughter and use as ‘treatment’ after £80,000 CAMHS assessment CENTRES,with millions NHS money spent to build assessment centres in Sheffield like Ruby Lodge CAMHS.

When will we wake up to how dangerous NHS for profit, is to us and our children.

The use of this drug is enforced in UK BY Care and MCA order .

IT costs NHS billons and causes untold torture and physical damage and death yet we can do nothing…………

finolamoss

100_0074

The above was published by the American Federal Drug Agency in 2008.

It shows the adverse side effects, of the anti-psychotic drug risperidone, trade name risperidol, since licencing.

http://www.fda.gov/ohrms/dockets/ac/08/slides/2008-4399s1-04%20%28Risperidone%29.pdf.

Well over $5 billion, in damages, and fines has been paid to plaintiffs, state, and local government agencies by the manufacturer.

http://www.drugdangers.com/risperdal/

Please read in link the legal actions, against Johnson &Johnson in respect to Risperidone damage.

http://highline.huffingtonpost.com/miracleindustry/americas-most-admired-lawbreaker/

In   the UK, we do not have an insurance based system of healthcare, so  such actions are effectively impossible.

Read here the shocking expose of history of Risperidal in USA, and effect on children.

http://highline.huffingtonpost.com/miracleindustry/americas-most-admired-lawbreaker/chapter-2.html

I was unable to find similar information as obtained from FDA, from the UK Medicines & Healthcare Regulatory Agency (MHRA).

Our UK’s system of censured, patient led, ad hoc yellow card warnings, and under used coroners inquests, make it difficult to even record a drug’s adverse.

As a…

View original post 2,297 more words

Sorrento: Sant’Anna Scuola di Lingue

My daughter’s blog post on her recent two week language course and her many experiences worth a read particularly on Sorrento

My life as a young artist

Sorrento, or rather ‘Sirento’, named after the ‘Sirens’ -mythical women/bird hybrid creatures who lured sailors with their sweet song to their peril as foretold in Homer’s epic, the ‘Odyssey’. Whose neighbour city, Pompeii was destroyed by Mt Vesuvius 2,000 years ago, offers a wealth of History.

My earliest memories were in Sorrento, from my holiday there with my family when I was two. The pinocchio puppets, innumerous alleys scintillating with the glow from little stalls and shops, and simpatico Italians all imprinted on my little dawdily mind instilling in me a fondness for the place that had prompted my return at the age of 20.66424467_873526553014747_6868097338498351104_n

Recently, I attended a language course at the Sant’Anna institute which is situated in a Program_3529_Photo__d2c8relatively secluded yet still rather central speck away from a lot of the summer bussle of Sorrento, in a tranquil place known as Marina Grande.

The initial orientation meeting marked a…

View original post 1,507 more words