Showing posts with label NAS. Show all posts
Showing posts with label NAS. Show all posts

Friday, January 23, 2026

Hind Rajab whenever big organisations mess with you on the phone

The Voice of Hind Rajab is an era definingly important film, but in more ways than everyone knows.

Yes it's defining of a population under genocidal conditions and the personal humanitarian meaning of being in the middle of that level of destruction. That will always be, and it will always be with the importance of seeing this not only on one side, but on both sides of the Israel-Palestine tragedy, with parallel humanitarian horrors also for the Jews murdered in the Oct 7 massacres many of whose stories are getting told in Quora.

But the film has an impact outside the Israel-Palestine conflict, more globally on all fairness struggles and all problems and fights suffered in trying to solve unfair situations. It will be citable for all time as a moral statement on THE NATURE OF BUREAUCRACY. On every organisation you ever deal with that puts up difficult walls on the phone, is noncommittal and unpromissory and avoidant of the point, or wastes time with call links or unnecessary side points when the call is urgent or you are watching its cost. This is what, in the film's true story, the Red Crescent hq suffered when trying to organise a safe rescue of a 6 year old child trapped alone in a battle zone, making ihe effort fail after hours of mounting trauma for them and the child.

This experience can include from autistic big organisations like Autism Initiatives or NAS, or health and social services for parents pursuing a diagnosis when a child is getting maltreated by school and the system deliberately wants to drag its feet against stopping this. The Voice of Hind Rajab will now be a name to cite as an argument.

Using the phone can already be really difficult when you are aspie without a flowing voice or easy finding of words.

Recommendation to see it, from a member who already had, has been a success of ELAS's group meet. He was able to describe to me what it was like. He was clear, where cinema posters for it had not been, that being dramatised did not mean it contained any gratuitious fictional emotional twists, as too many films do. This one responsibly just tells a true story soberly to the factual record of the phone recordings as it happened.

Maurice Frank
23 Jan 2026

Wednesday, October 24, 2018

teach the teachers from the voices of all

At the now revived autism Cross Party Group in parliament, today Oct 23 the topic was education. Specifically, and nicely accountably, the follow-up to a report on rates of school exclusion, jointly by SA, the NAS, and Children in Scotland.

Among the report's list of "calls for action", enlarged on to us by Charlene Tait speaking for SA: is for more training up of the autism understanding level among teachers, and for schools. As has ever been so throughout the modern autistic scene's existence, here again the case evidence quoted and directly told by school leaver age autistics present, showed that schools widespreadly are brutally deficient in their understanding, and in their attitude towards having any.

There is a perfectly predictable explanation or that. Teachers are piece of shit tyrants by intentional design, and the authoritarian model of school is a disastrous destructive evil and one of the outstanding horrible tyrannies of history -site - Authoritarian Schooling a Catalogue of Damage.

My point given at CPG. After all the consequences they had heard of failed understanding, with even suicidality at issue, when they follow up this training up of teachers there will be an automatic duty to SHEER CHILD SAFETY, that the 3 organisations set up a facility for preventing the autism training from being incomplete by missing things. To date, clearly, teachers and schools have missed a lot of it. So they need a facility that ANYONE who has been part of an autistic school problems case can send in the itemisable school problems shown by the case details. Then the facility's responsibility would be to check whether the items are already recognised in the awareness program for the teacher retraining, and any items that are not already there, to add them in.

From anyone who comes forward with a case experience. Not just a selection of cases, which could miss something, but ALL who come forward. This proposed as explicitly being a duty to child safety. That is the govt's principle of "Getting it right for every child," GIRFEC. That is accountability. That is inclusive, against the problem mentioned by another contributor, of affected families feeling their cases invisible.

Monday, September 3, 2018

Breakthrough on adult diagnosis in Aberdeen

Aberdeen has been suffering for years a local unjust failure of service re such an important basic as adult access to diagnosis. Doctors have not been available for it, folks have needed to seek access to service from other regions unless they had the means for privately. This affecting such an essential life fairness as employment support.

NAS holding a conference there in 2015 budged nothing, nor even prevented the OSS there (which they ran) closing down! But now the local paper has budged the local NHS, as a follow-on benefit from a campaigning victory on ADHD. It reports this breakthrough in NHS acknowledgement of service duty: NHS Grampian commits to adult autism diagnosis.

Why does it say it is important that folks cease to need to present to mental health service? Of course it's important that autistics are not mental, but that service is long established one of the commonest sources for diagnoses. GP referral to it. If Aberdeen folks have been referrable to mental health, and have been diagnosable by it, then there is no form of words that makes sense, that they could use to reject diagnosing the folks who were not going to stay on the mental health service for something else. Yet that is what the article reads like saying they used to do.

The principle of accessing adult diagnosis is importantly universal everywhere, Aberdeen's experience this far into the autism aware era has been staggering. This is the turning point of their acknowledging this principle for a maltreated place.

Saturday, September 24, 2016

NAS slaps aspie grassroots in the face again

The multiple signed letter to the NAS's trustees, just last year, on ordinary aspies' dissatisfaction with NAS's lack of accountability and responsiveness towards us, us on whose behalf NAS supposedly exists, might never have happened. NAS's Scottish director Jenny Paterson has shown, openly in her emailed reply to an enquiry from ELAS, that the big charity culture continues as determined as ever to seek to get away with arrogance.

This is a one-off answer, which an ELAS enquiry on their general standard of responding to contacts extracted. It followed 7 months of total silence from her towards the personal contact previously made. Hence it does not follow a spurt of correspondence. Yet she is rude enough to write a bureaucrats’ closure, a proclamation of final answer:
"this is my final position on our campaigning plans and priorities, and I am unable to offer any further assistance regarding child authorship."

Even nasty bureaucrats usually only do that after a spurt of correspondence when they have run out of evasions. She does it in her one-off late answer to something she had simply sat silent on for 7 months. See how aggressive that is? Hostile to an issue of maltreated aspie kids, an agenda the whole time against them and doing anything for them. Also she does this deviously so as never to actually answer what she was asked! For she was asked simply to mention that wronged child authors exist, in every literature that mentions or advertises successful child authors. That is not campaigning that needs any resources or time priorities allocated to it. She answers only to the practicality of big extra campaigning then rudely shuts down all contact with her on child authors at all, KNOWINGLY LEAVING NEVER ANSWERED THE SIMPLE NO-EFFORT ACTION THEY CAN TAKE!

Even her timing is sneaky: she sent this email on Sep 20, just 2 days AFTER the Autism Europe conference here in Edinburgh, which had NAS involvement, had ended. Avoiding this being out as an issue at conference time.

All autism workers and projects: you can’t ethically afford any connection with NAS, with an organisation that behaves like this.

Monday, August 29, 2016

The hidden wave of women with undiagnosed Asperger’s

A new story on increase of aspie self-awareness in women. seventhvoice.wordpress.com/2013/10/01/the-hidden-wave-of-women-with-undiagnosed-aspergers-syndrome

But it agonisingly says some of them are getting rejected diagnoses and interpreted to have personality disorders instead, by closed minded conservative psychologists, likely men. THIS LONG INTO AUTISM AWARENESS.

I have commented there on what support we the whole aspie scene need to give to these women. It's simply what I have always said is what all the undiagnosed newcomers need, as remembered from when I was one: and clearly the NAS is still doing nothing to provide or advise them on this. Simply, they should join the aspie scene in some form, first, while they are still undiagnosed. So that they are backed up by our perception of them before they go for diagnosis. Before the diagnoser can say no, he is landed with having to explain that backing from other aspies to the grounds for why you are one.

Maurice Frank

Monday, July 25, 2016

30 degrees and where is the NAS?

A petition for Boys to be able to wear shorts in hot weather instead of trousers at secondary schools has my fervent solidarity, that can't surprise anyone.

But look at the obvious fact: such a petition should not still be necessary, after at least c15 years of sensory issues being openly known about through the autism scene. The continued existence of school uniforms at all, and of this gender discriminatory cruelty in them, is a mass maltreatment of kids by all the autism charities that have not chosen to campaign against them. The NAS, all this time, has said nothing opposing school unforms at all. Its leaders have sought to hobnob around with politicians and enjoy careers for thenselves based on the NAS just being formulaic and unchallenging in the stuff it says. By it leaving aspie boys, both diagnosed and missed, suffering a bodily abuse. Including in 30 degree heat, as the parent making this petition cites.

This when at the NAS's own conference in Aberdeen on 27 Mar 15, Luke Beardon described personally knowing a case, again through the NAS! of a man whose school coping and outcomes had been unjustly entirely wrecked by this uniform abuse, which made him totally unable to focus in exams.

Maurice Frank

Sunday, August 23, 2015

Open letter to NAS on accountability

www.autangel.org.uk/letter-to-nas-trustees.html


This link is an open letter to the NAS, about its standards towards us: "trying to adapt to what it thinks its audience of the moment may prefer" and "We are concerned that the NAS is a charity that is not listening to the very people – autistic people – it purports to support and address the needs of". Which has always been my feeling, and why we needed ANS to emerge instead.

It's a UK scale action, it's written by an aspie in London, David Mery,gizmonaut.net. He is gathering signatures, by emailing him if you want to sign it.

NAS reply of Sep 11 is just a businesslike holding acknowledgement, says nothing of substance.

Monday, April 6, 2015

NO UNIFORM. There is a place that has learnt.

Apr 6:THERE IS NO SCHOOL UNIFORM IN THE SHETLAND ISLANDS, ACCORDING TO THEIR OWN COUNCIL !!

Question remains how effectively they have prevented there being informal uniforms effected by peer pressure. But as regards formal uniforms, their own Executive Manager of Additional Support Needs and Early Years says "we do not have a school uniform policy in our schools, and pupils are free to wear what they wish.

Our teachers receive training on strategies to support our pupils with autism, which includes awareness of sensory issues."

Like the case of sensory issue which Luke Beardon cited in his address to the NAS conference in Aberdeen on Mar 27, of an autistic man with a shorts sensitivity who he had met through the NAS, who was prevented being able to focus on any exams and had his school outcome destroyed entirely by a trousers uniform that made his knees feel "on fire." A so clear obvious abuse that I am circulating it as the inescapable clincher against uniforms.

Apr 27: Glasgow too. "confirm we have no policy or school rule that would prevent the wearing of shorts". But again NO WORD on the critical biggie of preventing of PEER GROUP oppression, by allowing every pupil to opt out of any class or social circle who would persecute their personal choice by the undemocratic ape means of RIBALDRY.

Wednesday, November 12, 2014

None out of 3

Besides an NAS social group discriminatorily only for aged under 35, and how is that legal? there is still no adult aspie support in Clackmannanshire. The Forth Valley's position with small council areas has left it as a void in the national coverage, left on the sidelines whle the bigger more prominent conurbations get to set up services. What about a job placing service equivalent to Edinburgh's Intowork, which should be particularly important in this economically oppressive era?

The services that Autism Initiatives has developed in a wide spread across Scotland, Borders, Perth, Highlands, are being missed in the Forth Valley. The perception of why is alarming. It is perceived locally there, that the local dominance by Scottish Autism, headquartered in Alloa, is a discouragement to AI from setting up any projects in the Forth Valley void. That the 3 national autism charities are behaving territorially with each other, allowing each other to be the big boy in certain localities and not intervening in their patch.

Who does that fail to help? The autistic folks ourselves, who are supposed to be the point of all 3 charities' existence. If SA has not set something up in that locality, which AI can set up and has done in many other places, then AI should. Ain't that common sense?

Unless the charities function by common sense and not by mutual politicking, all their supporters and donors must ask themselves who the charities actually care about? Whose interests they work in?

Maurice Frank

Monday, December 9, 2013

a famous aspie does not mean all is right for us.

Let's see. You've come for a look at what aspies are all about because you heard the news about Susan Boyle? Splendid: here's what the media should be telling you. Are they?
  • Our heightened physical sensitivities, including to fabric and heat, are biologically incompatible with dress codes and make them an assault on our physical wellbeing. Our existence abolishes all work dress codes and school uniforms. This has been known for years and the big charities have not been choosing to push it.
  • Because some aspies find it easier to focus on the written word than the spoken, there is a correlation between aspies and child authors. There is a succession of books by aspie child authors, and there is a child cruelty offence done in long history of big charities' total avoidance and failiure to publicise that there are WRONGED child authors, like me, whose chance to write was destroyed by harmful school pressures and homework.
  • With the big charities' big failings to speak for us where needed, you can see how seriously we have needed the voice developed for us, to contribute into professional awareness and policymaking, by the AUTISM NETWORK SCOTLAND, developed out of Strathclyde University and now a part of the national strategy. It's invaluable, and its creation is the great success of the scene in Scotland. So IT NEEDS COPYING IN EVERY COUNTRY. If you are outside Scotland do you think your aspies deserve not to have any ANS?
  • The NAS is to be complimented on attending properly to striking off its contact list a bent autism legal service that advised me to surrender in a dispute with a council tax malpractice where I was in the right by statute law and won. There needs to be a media consumer exposee of bent services that will prey on their clients instead of stand up to councils - you want to know more, you need it publicised.
  • Likewise you want to know that aspies' local groups can't be corrupted and seized control of by malpractisers bent on hushing up emotional abuses, as happened to a group near us, defunct since stood up to by an earlier post on this blog describing its malpractises: 28 Feb 2011, Invitation to an autocratically restricted group's members to escape it and join us.
  • It's only the same common sense that all the details should be published of the ways we have been harmed by schools and by child psychiatry. Aspie kids not safe until these things stopped, and how do you stop them unless you have heard widely what they are? In a safely non-deletable way on paper: for it's no good putting them in an Amazon e-book where the site's lawyers reserve a power to turn round and say, no no no, delete to be on the safe side. So the media are turning their backs on child safety unless they read this and chase after these things' publishing.
  • Where competitive jobsearch utterly has never worked for us, the approach that works is to have aspie employment services who talk through both our strengths and our limitations with an employer to work out a working niche for us. But more ethical accountability upon these services is needed, to prevent the malpractice of them turning round and claiming that a third party problem that arises after you are in a job is not in their remit to deal with. By obvious definition, a remit to support employment automatically includes any problem that affects the work's doability or the work environment's justice in any way. This an item I am holding Edinburgh's new local Autism Plan responsible to put right locally.
Maurice Frank

Thursday, January 13, 2011

now uniforms take life, preventably

Many papers today carry a child death story that challenges anyone willing to persist in believing there is any good at all in the physical world. In the Australian floods, a boy aged 13 was swept away and killed, along with his mum, when the floodwaters swamped their car, the reason why they narrowly missed rescue by a truck driver was because this boy made said rescuer save his younger brother first !

Now, there is more to this horror than accident. Here is the twist to make you angry, that adds to this story an element of human evil which our scene could have prevented: quoting from the Metro's story, "Ms Rice and her sons were returning from a trip to buy school uniforms when they were caught up in what police called an "inland instant tsunami."""

This is a child's life actually ended, entirely by reason of the prison badge of children's enslavement, and the obligation on families to actually buy with their own money the chains of their own oppression. To make this purchase mattered enough to go driving in the middle of a flood crisis for specifically this purpose, to buy a degrading slave costume whose communist purpose as openly declared by the nutty professor - see last post - is to airbrush away children's personal identity and give physical form to a state of possessed subjection.

For a century we have been told school uniforms do all these wonderful things. Anyone who defends them now is seen to defend costing lives and intentionally to be willing to cost more lives, and this is for a purpose of destroying liberty.

This includes any big autism organisation that continues not to speak out against them, and against all uniforms ever, as they owe to adult workers too. For years the big organisations have known this need exists. For years they have kept themselves on hobnobbing terms with employers and teachers. This boy most likely was not one of us, and there is no need for him to have been. Remember, acting on aspies' biological needs will get rid of uniforms, not just for aspies, but for everyone. If the big autism organisations had done this, then thanks to autism knowledge, uniforms could have been eradicated all over the democratic world years before now, for everyone. Then, by the reported facts, this family's fatal car journey would not have happened.

This be on the head of all limits to publishing of facts, all control and filtering of issues, that has existed in the autism scene. In the media too.

Meanwhile, yesterday, here, parliament threw out Hugh O'Donnell's bill for an autism strategy, at first stage, by 109 votes to 5. I watched them in the public gallery, all jumping on the momentum to say oh it's not proven what difference this would make oh we need less obligations for service users to run around trying to enforce and we need more time muddling along as we are. The way they seized on the committee report to criticise the bill for being too noncommittal! is an irony howling against the way all law is practised at present. All of them every day are in the political class's game of always being noncommittal, and now they have damned a bill for the same thing.

It is an indictment of the NAS for its insistence on legalese drafting of the bill. In the consultations last year, we put in for using ordinary language, and through it, for having some committality about what the bill would definitely make happen. The NAS have dominated this entire campaign, and their aversion to committal obligations to any issues that come from us to them, has delivered this rubbish outcome for them and us alike.

Maurice Frank