People with autism detained for 20 years [UK]

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kaiouti12
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25 Nov 2021, 2:15 am

[WARNING: May induce rage, anger and or meltdowns (in the currently unstable)]

[Clip] More than 2,000 people with autism or learning difficulties are being detained in specialist secure unit hospitals across England, with precisely 100 people having been held for over 20 years.

Despite a pledge by the government to reduce the number of patients in such facilities by 35 per cent by March 2020, the data shows a drop of just 13 per cent, with 350 patients having been detained for more than a decade. [/Clip]

SOURCE -> https://www.thetimes.co.uk/article/auti ... 1637817186

I don't know how to feel about this, but I do think this needs to be shared and known. Systematic abuse from such a 'proper' society.



ASPartOfMe
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25 Nov 2021, 10:22 pm

From America the British have always seemed more accepting of eccentricities. This is the land of Monty Python, Benny Hill, and countless “different” pop music innovators. For Autism the UK is where Dr. Tony Attwood, Lorna wing, and Uta Frith come from. The UK media have usually been ahead of their American peers in covering autism in adults and females.

What they say and what they do are two different things. Be it this type of abuse or years long waits for diagnosis, or autistic services being cut during austerities the place seems to be a nightmare for a lot of UK autistics..


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Jakki
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25 Nov 2021, 11:05 pm

This is a bad situation, someone living under those conditions for extended periods might
not adjust wel to being back in normal society ? :cry:


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ASPartOfMe
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27 Nov 2021, 8:23 am

People with autism are being locked away in institutions. A radical change is needed
Lady Sheila Hollins is emeritus professor of psychiatry of learning disability at St George’s University, London and a crossbench member of the House of Lords. She is also the founder and chair of Beyond Words, the visual literacy charity

Quote:
Not many people have to worry that their children will be forcibly removed or locked away from society. Yet this is something I do worry about. My autistic son, who also has a learning disability, experiences the world differently. I am often in awe of his perspective, and he has inspired my more than 40 years of professional and voluntary effort advocating for better understanding, care and support.

When people like my son go into crisis there is a high chance they won’t be supported at home – not because they can’t be helped to live full, valuable and meaningful lives in their communities, but because our “system” doesn’t allow for it. Instead, they may be removed and taken, sometimes miles away, to an unfamiliar inpatient setting designed to treat mental illness, even though many are not mentally ill and do not need to be in hospital.

There are currently more than 2,000 people with learning disabilities and autistic children and adults in such settings in England and Wales. These often noisy and sensory-driven environments exacerbate the more troubling features of autism, instead of providing the routine, structure and predictability that autistic people need. It is little wonder that autistic people struggle to regulate themselves and fail to thrive in these places. Many get stuck, with the average length of stay for current inpatients being five and a half years, albeit skewed upwards by some long forensic detentions (those subject to legal or court proceedings).

This week we have seen shocking accounts of one man’s 20-year detention in such a setting, traumatised by a system that has failed him. Tony Hickmott’s brave, and now elderly, parents persuaded the judge in a court of protection hearing that his article 8 right to respect for family life had been breached – and that it was in the public interest for him to be named. They talked on national news about their 100-mile journey every week to see him. His father described having to break his journey on the way home to manage his own tearful distress. His mother said they don’t smile any more. The promise of his release by next spring offers some hope for Tony, who has spent nearly half of his life in hospital, but there have been promises before and it’s years too late.

Ryan, whose similar story featured in national news last year, recently moved back home to live near his parents. Neither Tony nor Ryan have forensic histories, but they are victims of inadequate planning and a lack of safe and adequate care and support in the community.

The sad truth is families are not routinely involved in the way that is the norm for patients with physical health conditions. Instead, distressed families are seen as somehow part of the problem. The families of Tony and Ryan describe being ignored and marginalised.

The reviews were intended to uncover the blocks in the way of getting people discharged more accurately. The reviews started just before the pandemic began and many had to take place virtually. Despite making urgent and achievable recommendations, there has been insufficient action to get people discharged even in cases where alleged rights violations have been reported. The numbers of people in long-term segregation have increased rather than gone down.

The independent reviews are continuing, and some people have been offered a senior “intervenor” as part of a pilot to speed up commissioners’ responses.

Shockingly, many of those responsible for implementing aspirational government policies and for making decisions about people’s care seem to have very low aspirations themselves. There is some good practice but too often the hopes and needs of autistic people and people with learning disabilities are misunderstood or considered marginal, and once out of sight in a psychiatric hospital they are literally out of mind.

A radical system change may be the only thing that will make the lasting difference needed to see all autistic people and people with learning disabilities fairly treated, with an urgent programme of high-quality service development in every localit

bolding=mine


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“My autism is not a superpower. It also isn’t some kind of god-forsaken, endless fountain of suffering inflicted on my family. It’s just part of who I am as a person”. - Sara Luterman