24.7.15

Social Skills- Are they all they’re cracked up to be?


Social Skills- Are they all they’re cracked up to be?

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This article originally appeared as What About Social Skills at www.ntnoway.wordpress.com – Written by Richard Johnson Âû
Common process for young Autistic children is for them to head off to an occupational therapist, speech therapist or a team based social skills group program. Clearly this is a preferable option to an ABA program of compliance training and applied behaviour modification therapy delivered for hours on end as if it was dog training.
Generally it is safe to say that these programs are not dangerous to children, however they should still be questioned. Are they actually effective? Do they actually result in better outcomes for the children. Indeed, do these children go on to live better and happier lives, more fulfilled lives because of them. Does in fact make the social interaction in which they engage easier, more fulfilled and more successful.
Clearly here we are not considering the evils of ABA, CD, MMS, Chelation, GcMaf, Stem Cells and the like. But still we must consider the long term outcomes of these programs.
What exactly are these children learning and gaining in terms of their longer term success in negotiating life in a predominantly allistic world. A world that demands they interact in order to have successful educational and employment outcomes.
My personal experience was social skills pretty much taught at the end of a wooden spoon and a large amount of raised voices. Clearly the formerly mentioned approaches are preferably, nevertheless I learned many different social norms and rules. These equipped me supposedly to negotiate my way through life and provided an ability to attempt to fake an allistic life.
My two autistic children have received a thankfully more fun, caring and enjoyable program of learning such skills. But the big question of course is of what benefit are they. Has it actually been a positive experience in terms of the outcomes for the children. I guess in terms of my children that is a question awaiting answering.
In my case I can only say it has been an abysmal failure. Yes I managed to get through 40 odd years of life thinking and pretending to be an allistic member of society, but in reality this was an abject failure. On the education level my schooling was essentially a time of living through a fog. Consequently I was a very late starter to further education, which, of course, has had considerable impacts on my employment outcomes. My employment history is one of many different position of varying timeframes but never anything that could be considered of anything like long term.
Indeed the the positions have ended almost every time as a failure in the social context. Missing cues and being inappropriate. Misunderstanding cues and expressing things in such a way that left the employment situation to be untenable.
The big question of course is why has this been for me, and I would suggest a myriad of other autistic people, an abject failure. What is it about either the social skills training or the social context within which we live that is unable to be taught.
Greater minds than mine have considered these issues, but I would like to offer my take on it. Essentially this is that every social situation to be negotiated is different. They are in fact never the same even when they might look quite the same. The issue with this is that the social skills training is in effect like teaching a bunch of monkeys how to live as a tribe. Perhaps that is a little crass, but I think it is a fair analogy in terms of thinking about social settings like they are instinctual based situations rather than nuanced and varied from time to time, person to person and day to day.
It is my experience that in my Autistic mind that when faced in a social situation I am faced with having to draw on the rules I have learned, choose the correct rule or skill and apply it to the situation. So have a think about that for a moment. Consider, an Âûtistic person already in a state of stress due to being in a social situation. They meet someone and they have to assess, what comes next, oh that’s it I have to shake this persons hand, give them eye contact and make an appropriate greeting. Oh but wait this person is of a different ethnic culture and there rules are different, so what do I do, oh that’s it, I do all that but I don’t look them in the eye…


By this time the Âûtistic person is already looking a little out of place. Already the other person in the situation is possibly wondering, oh, this is odd, what’s the go with this person I wonder.
A gap in time, occurs. A gap in time that the Autistic person needs to think and work things out. However it is also a  gap in time that the allistic person is left to wonder and unfortunately often reason that this person is somewhat different, this person doesn’t fit in. I wonder what the go is here.
To make an apology, it is my view that social skills training and programs, whilst in many ways benign, teach a bunch of rules, skills, expectations and behaviours from which, the Âûtistic person can draw. Something like a filing cabinet from which to draw. Unfortunately this filing cabinet is a little more like a floppy disk at worst or a traditional platter based hard drive at best, a storage system that is far slower than the modern solid state drives which very quickly access information.
The Âûtistic person must run this storage system, find the correct folder, find the correct file, apply the correct file to the situation. This would be all very well if the files fit the situations correctly. The reality is though that they don’t. As described in the above the variations and nuances of the social context, whether it be due to facial expression, body language, tone or any other of a myriad of possibilities mean that the Âûtistic is often left attempting to apply a square peg into a round hole.

So the question what about social skills?
Every person, whether Âûtistic or Allistic is unique. People are not a mass of uniformity. They do not walk in rows of conformity. People do not even act in the same way on repeat occasions of similar situations. They just don’t. It’s just that simple!
I have come to the view that we should dispense with these programs. There are many other things we can in fact do to assist Âûtistic children to grow to lead full lives and achieve successful outcomes in education employment and connection. There are many things that are not social skills training but in fact similar types of training that we already make an effort to teach our allistic children.
I would include in this efforts to teach our Âûtistic children Resilience, confidence and self-love. An understanding that regardless of anything they are valued, they are loved, they are worthwhile. In fact that yes you are a bit different, and that doesn’t matter because you are #DifferentNotLess. You’re #ActuallyAutistic. And most of all you are loved unconditionally by us your mother and father and brothers and sisters.
I wonder what your thoughts might be on this issue.

23.7.15

Spark Autism Talk 20/07/15 with Emma Dalmayne, Alan Borgas & Guest – 1


Spark Autism Talk 20/07/15 with Emma Dalmayne, Alan Borgas & Guest – 1

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Emma Dalmayne Radio interview on KTOK Radio


Emma Dalmayne Radio interview on KTOK Radio

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Emma Dalmayne Radio interview 11/07/2015 on KTOK Radio with Bantu and Alan re Autism abusive treatments such as MMS and GcMaf.

Seller of ‘miracle cure’ for cancer and HIV sold ‘potentially harmful chemicals used in bleach’


Seller of ‘miracle cure’ for cancer and HIV sold ‘potentially harmful chemicals used in bleach’

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Leonardo Edwards was filmed by the BBC selling the so-called “health items” to a reporter posing as a relative of an autistic child.
Leonardo Edwards' Healing Space
Selling: Leonardo Edwards’ Healing Space website advertises products
A man who sells solutions advertised to cure diseases like cancer and HIV has been accused of distributing potentially harmful chemicals used in household bleach.
Leonardo Edwards has a website called Leonardo’s Healing Space on which he sells so-called “health items” including chlorine dioxide solution, citric acid ‘activator’ and hydrochloric acid ‘activator’.
All of these can be dangerous if consumed by humans, reports Get West London.
Mr Edwards was filmed by the BBC selling the chemicals to a reporter posing as a relative of an autistic child.
Combined, the chemicals form bleach, but footage shows Mr Edwards claiming it can “purge” autism, HIV, cancer, arthritis and Alzeimer’s.
Campaigner Emma Dalmayne, 39, who used to live in South Acton but now lives in Plumstead, is fighting against such products being sold.
She claims they can cause seizures, vomiting, rashes, among many other health problems.
She says the products are sold for between £29.99 and £49.99 and there are conferences people can go to costing £285 which teach them how to make this solution.
Dalmayne said a closed Facebook group called CD Autism (chlorine dioxide) is made up of parents discussing the products for their children and claims Mr Edwards says he can ship chlorine dioxide to people.
The tagline on the group is: ‘Solving the Puzzle One…Drop…at a Time’ and the cover photo says ‘185 children now recovered from autism… and counting’.

Leonardo’s Healing SpaceLeonardo Edwards' Healing Space
Danger: When combined, some of the chemicals sold can form bleach

Ms Dalmayne, who has aspergers and runs a support group for people with autism, said: “’Miracle Mineral Solution’ is 28% sodium chlorite (household bleach), mixed with citric acid, it makes chlorine dioxide. You can only buy it online.
“Leonardo was previously exposed on the One Show making it and saying you can use it for Ebola, HIV, Hepatitis B and cancer.
“They [parents on the Facebook group] are administering it in enema form [administering a liquid through the rectum], straight up into the colon.
“It can cause seizures, rashes, vomiting, nose bleeds, diarrhoea and kidney problems.
“People [on the Facebook group] are saying ‘my child can’t walk’, ‘they are holding their stomach’.”
On a website called Leonardo’s Healing Space, he writes: “This is a place to provide effective Natural Health items suited to certain Healing Protocols found online, which may use CD, MMS and CDS.
“I seek alternative health items that are the most effective and I use them personally and in helping others.
“I do not offer any claims and prefer the people to educate themselves on the uses of the products found here.
“This is a path to empowerment and self improvement.”

Get West LondonEmma Delmayne
Campaigner: Emma Delmayne runs a support group for people with autism

On a Youtube video by Leon Edwards, his testimonial says: “In 2010 I saw a post on Facebook about MMS – Master Mineral Solution www.jimhumble.biz I began to read about it and it took over my life studying everything I could find on it.
“I then brought some and very quickly (around a week) the arthritis in my knee completely disappeared! I have had no symptoms ever since.”
“I then learnt Jim Humble was running seminars in the Dominican Republic to learn how to make MMS at home how to treat others and myself. So I travelled over there in February 2011.
“I spoke to Jim and he got a humidifier and put MMS in it and told me to breathe in two breaths which I did and he said come back tomorrow and breathe in three breaths which I did and in five breaths and two days I went from being very sick to completely healed it was miraculous.”
Edwards has an open Facebook group called MMS England with more than 1,700 members.
As well as various solutions, ‘enema items’ including syringes are on sale on the Leonardo’s Healing Space site.
Mr Edwards refused to comment when contacted by Get West London.
There is no suggestion that what Mr Edwards is doing is illegal.

21.7.15

Statement Regarding BANCDMMS


Statement Regarding BANCDMMS

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** STATEMENT REGARDING BANCD/MMS**
Dear all.
For the last 15 months I have been part of a worldwide campaign trying to ban abusive and unregulated Autism ‘Treatments ‘
We have had huge exposure worldwide on this awful issue and in some parts of the world we have seen convictions of those selling MMS and in Ireland criminal investigations have begun into parents using MMS on their Autistic children and also into those selling MMS.
We have seen Kerri Rivera banned from holding conferences and peddling her abusive ‘Treatments ‘ in Illinois Chicago.
We have educated thousands on this issue and brought the authorities to task with ongoing investigations into some of the biggest peddlers of MMS and GcMAF worldwide.
This has only happened because of the commitment and passion that has gone into this campaign and the many people that have put in hours of their time voluntarily to help us end the abuse of Autistic people.
However behind the scenes we have had some serious problems of late.
Events have unfolded which have threatened many aspects of our campaign.
Therefore after long discussions with my colleagues, including Emma Dalmayne , we have decided to disassociate ourselves from the BanCD/MMS Website and all Social Media groups connected to it.
This is not a decision we have come to lightly, however we feel this is the best way forward.
We are presently working on an alternative solution and will be updating everyone with new information soon.
We thank you for your support and our campaign will continue as strong as before !
We will fight until justice prevails!
Many thanks Fiona O’Leary.

20.7.15

Emma Dalmayne Ben TV


Emma Dalmayne Ben TV

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How to Help with Meltdowns and Stimming Needs


How to Help with Meltdowns and Stimming Needs

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After my son was diagnosed with autism then subsequently myself I decided to do this piece for those who’s child may be diagnosed with autism or you may only have the suspicion that they are on the spectrum.
Apart from concerns about your child’s communication and social skills, they may also display self stimulating behaviours and melt downs. These behaviours may display as pacing, rocking, jumping and spinning. They may have oral stims they use to regulate themselves from humming, singing, shrieking, repetitive speech or screaming. They may sniff, lick and spit. They may also have self injurious behaviours such as chewing their hands and mouth, head banging, pinching themselves and punching solid objects.
The need for stimming is to regulate, ground and self calm.
Children with Autism will access stimming to trigger a part of their brain that releases endorphins to control their environment and also for enjoyment. Your child needs to exhibit these behaviours to make sense of the world around them and feed their vestibular, proprioceptive, olfactory, visual and auditory senses. Some of these will need to be re directed such as the spitting and chewing which can both be helped with chewy tubes specifically made for oral sensory seekers. Helmets to protect their head during a head banging episode will help as will crash mats and a punching bag with gloves for heavy priopreceptive seekers. Trampolines, spinning chairs, swings and exercise balls to bounce on help with the vestibular seeker.
A meltdown may occur for a number of reasons including frustration and sensory overload.
My child may sink to the ground screaming in a busy shop and there’s good reasons for this. It’s busy, bright and there’s lots of sounds. To help with this, I give him ear defenders or headphones with favourite music playing will cover the beeping and general background noise. Tinted-lensed glasses also help with the bright lights as will a low brimmed cap or a hooded top. Lastly a small handheld timer with an extra fifteen minutes added on to our approximate time shopping just in case I see a friend and stop to say hello. This helps him greatly as he feels slightly more in control. I also give him a shopping list written or with visuals.
Now if you’ve tried these things and they have not worked and your child is having a meltdown…I need you as a parent to remember this:
Disassociate yourself from their autism.
Sounds callous doesn’t it? It’s anything but.
Too often I read parents blogs where the parent is asking what should they do if people stare? Some parents feel embarrassed and their reaction is to drag their child out of the shop. By all means if your child is wanting to leave do so and swiftly. But if they need a minute to feel the solidness of the ground beneath them to ground them and if they need to scream to let it out, allow them that. It’s not about you, it’s about your child.
If your children hit you in a meltdown it’s not about you. It’s about THEM showing you the pain inside they cannot outwardly communicate any other way be it verbally or not. If they are outside having a meltdown and there’s muttering made by passers by and stares given…ignore them. If they are judging your parenting skills they do so out of ignorance and your only focus should be your child, block others out of your radar.
Your child in a meltdown state is angry, their flight or flight mechanism has kicked in and they may react violently if they believe they are threatened in any way. This is where you yourself come into your own as their guardian and advocator. Here’s what I recommend:
  • Do not touch your child unless they seek it as some children like to be held firmly when they are distressed.
  • If you can try not to touch them as in a meltdown touch can feel incredibly intrusive and cause your child to strike out indiscriminately.
  • If they are self injuring guide the hands down to their sides and only ever restrain your child of they are at risk of hurting themselves or others.
  • Try if possible to move them to a quiet place and keep language minimal as in this state it’s hard if not impossible to comprehend any communication attempted.
  • It’s not for you to take blame and wonder what you may have done wrong nor place the blame on your child.
  • Meltdowns can be brought on by a temper tantrum and feeling out of control can trigger one.
  • They are never intentional and the individual should not be reprimanded but rather advised how next time to avoid one.
It can be hard when you are on the spectrum yourself, like me, to deal with another’s meltdown as it can trigger a lot of anxiety and overload within yourself. I make time for myself to retune. I love to have a warm relaxing bath with bubbles and stim on the effects of the water. I also have a very soft teddy bear I like to stroke for tactile feedback to help ground and regulate myself. It’s about knowing when you are at your limit, breathing deeply, taking a step back, and reminding myself that this is my child’s issue. My responsibility is to keep him safe yet respect that he is feeling like this for a reason. It is not a reflection of my parenting.
Disassociate yourself from your children’s autism and act only in their interest. It’s their autism and their behaviours and your job is to help them cope.
*Emma Dalmayne is from London, UK. She is an autism advocate and keen campaigner against MMS. She has Aspergers and children on the autism spectrum. Emma loves to write and has a book in the works. She runs a helpful Facebook page for caregivers, parents and autists called Aspierations and Information.

How My Autistic Son Changed Since He Started Homeschool


How My Son With Autism Changed Since He Started Homeschool

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I smile as a little boy’s giggles ripple through the house.
At one time my son never laughed and rarely smiled.
But his confidence has come back in abundance since I withdrew him from school and began to home educate him. He was a stammering, nervous little boy back then.

unnamed-54When he first started mainstream school, I was concerned he wouldn’t be watched closely and asked for what was then a “statement of special needs.” But he was refused one-on-one support despite having three diagnoses: autism, expressive language disorder and dyspraxia. This left him vulnerable to bullying by children and a teacher’s aide. The day I found out how bad it had gotten, I pulled him out and deregistered him the following week.
It’s now been two years since he began his journey of home education, and he now has a glimmer in his eyes. He attends play therapy, music therapy, speech therapy and animal therapy. We read together, and he does online tutorials and lots of sensory play to calm and regulate him. His hobbies include photography and collecting little soccer player toy figures. He has an amazing knowledge of soccer scores and players and enjoys playing it every Wednesday on a team for children with special needs.
Every two weeks he goes to the National Autistic Society‘s Saturday club and enjoys socializing and playing with the other children. He adores his private tutor he sees once a week. We go to museums, the woods, the library and the park. He loves being with his little sister and older brothers who are also on the spectrum.
There are many things we already do with our children we don’t realize are educational: Playing with small figures and cars is small world play. Listening to a play on the radio is drama. Baking and cooking is science and math. Reading stories is literacy. Drawing is art. Playing with teddies and dolls is role play. I love the freedom of going for a walk in the woods with the children and watching it turn into an impromptu nature lesson: What plant is that? What sort of insect is that?

unnamed-53

Since being home, my little boy has come a long way from the melting down, upset and angry child he once was. He sleeps now, and occasionally almost through the night! He takes his own “time out,” going to the bedroom to play and chill out with his football cards and sensory toys. With the pressure to interact constantly in public school, he would have never been able to take this time. Now, he engages on his own terms, and knows when he needs to walk away.
Would I ever send my son back into the mainstream school system?
No.
Of course, with the right support, children with autism can thrive in a school setting. But I often notice some children on the spectrum find schools too overwhelming and the endless interaction exhausting. Children with autism and sensory problems might be told to hold in their feelings, only to erupt at home.
If your children are unhappy, you are not failing by withdrawing them from school. It’s simply a different way of educating. Not every peg will fit a round hole.
Pound a peg hard enough, and you will chip the paint and eventually splinter the wood. My peg is a bouncy, cheeky one, and his paint is now shiny and vibrant.
That’s all you can ever want for your peg.
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Applied Behavioural Analysis – First Hand Accounts


Applied Behavioural Analysis – First Hand Accounts

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pinocchioApplied Behaviour Analysis (ABA), one of the first things mentioned when your child receives a diagnosis of Autism.
The paediatrician may recommend it and you are sure to read glowing reports about it.
The ultimate goal of ABA? To make your child indistinguishable from their peers. To stop all self stimulating behaviour and enforce eye contact whether it be uncomfortable or not.
Children complying and a therapist fully in control of the child’s every action, even down to where they look. Try searching ABA harm or tantrums. You will see a very different view then, children screaming and forced to do the same thing repeatedly till the therapist is satisfied that her commands have been followed. Restraining while in meltdown for no other reason then an intense desire to make the child obey, comply.
The Autistic community’s view is predominantly against and after researching I found its not only Autistics but also other professionals and parents who have a dim view of it.
I have spoken to Jane Johnstone who is an Integrative Psychotherapist for her opinion both as a professional and as a mother of two sons Evan and Daniel who are both on the Autistic spectrum.
On asking Jane how she first came to hear of ABA:

“I first heard of ABA when a home tuition grant was sanctioned when my eldest son was diagnosed. Other parents of Autistic children spoke very highly of it and it seemed the answer to our prayers. Evan was just three years old at the time and we wanted to optimise his potential. We heard many pros at the time, we heard stories of non verbal children learning to talk under an ABA programme. ABA at the time offered us hope. Evan was non verbal and we were desperate to chat to our little boy. At the time it was the only firm of communication we knew and we couldn’t foresee how he could progress through life in absence of speech. Little did we know!”

“My son remains non verbal but communicates through an iPad app. Evan did have some ABA tutoring in the early years but it was too difficult for him and was clearly not the right approach for him. We moved him to another school which suited him better and he was much happier. My training in Psychotherapy is based on a humanistic model, working with a holistic approach to the human condition of the mind, body and soul.
“ABA is cognitive based and considers only the science if the mind to the exclusion of the individuals body and soul or essence. One part of our human condition does not operate as a lone ranger, each part of us-body, mind and soul impact on each other whether negatively or positively but to work exclusively with just one part of our humanness can only ultimately harness damage to our other parts. “I completely understand when parents first learn their children have Autism their first instinct is to “fix” them, I’ve been there myself and it is often down to how the diagnosis is delivered by a practitioner in diagnosis which leaves parents feeling as though their child are in someway flawed or broken. “Of course what they need to hear is more of the positive and less of the negative and be encouraged to accept their child’s Autism”. After speaking to fellow Aspergien Frank L. Ludwig and reading his article “Why Applied Behaviour Analysis Harms Your Autistic Child” I am including this quote with permission:
“You will find that the majority of parents who subjected their Autistic children to ABA swear by it while the majority of Autistic individuals absolutely abhor it.
“The reason for this is perfectly simple: while ABA makes life easier for parents and caregivers (at least for the time being) by getting rid of undesirable behaviours and enabling them to pass their child off as ‘ more normal ‘, the child is put under unbearable pressure to conform, perform and obey without any consideration for their feelings, needs, desires, abilities and emotional safety.”
I also was lucky enough to speak to Em Scott, a woman with Autism who gave me an introduction of herself , her experience of ABA and the effects it has had on her.
Brain confused
“My name is Em, I am 31 and transgender. I am also on the severe end of the spectrum of Autism and up until being sectioned in a learning disability hospital I was very low functioning. I live in a group home for people with complex needs, require two to one support staffing and have a mobility car because my Autism and learning disability greatly affect my mobility and getting around.
“I also happen to get padded helmets prescribed on the NHS because I am what you would call typical head banger out of frustration when I can’t communicate something in a communicable language. I am an adult that gets spoken for time and time again when I am able to do so myself in different ways including echolalic speech, PECS and MaKaTon.
“I don’t need treating like I’m invisible and my support staff spoken to instead, I need someone to recognise my voice and stop assuming I can’t communicate because I behave in a stereotypical way. When I was in infant school I had what I now know was a form of ABA. The people who did it were brutes and I am still affected by their behaviour every day as it comes up in my memory. They had me forcibly held into a chair with one staff on each arm and another staff staring into my eyes shouting at me to repeat after them. I had no understanding of what they were saying and was extremely shocked and upset by the eye contact which was ultimately painful and burnt through my soul.
“I bit and and hit staff which made their behaviour harder and faster. I never learnt any speech and until early high school and in fact I’m sure it stopped my speech from developing properly. I only have echolalic speech.
“Another time I experienced ABA was in the disability hospital I got sectioned in due to being bullied online I had such challenging behaviour that three psychiatrists said I needed to go to a specialised hospital for people with learning disability.
“I was kept there for four months and during that time I experienced a brutal form of ABA.
“I was in agony every day at the treatment I suffered. I was thrown to the floor and pinned so many times that I now suffer from sciatica.
“Yes ABA and its extreme variants helped me function in a world I was unable to function in but at what cost? I have regular flashbacks throughout the day back to the hospital and my treatment there. No one knows, it’s hidden away in my brain. It only comes out when I type like this”.
After hearing Em’s account of ABA I decided to go on Google and have a look for clinics practicing ABA here in the UK. I came upon Blooming Tree ABA Clinic for Autism and Related a Developmental Disorders. On going into their website I clicked on About Autism then into ABA Autism Treatment. There I found this information, under the heading
‘What is Applied Behavioural Analysis (ABA)?’
behavioral therapy


“ Applied Behavioural Analysis is probably the best-known, best researched, and the only treatment for children that has produced significant and comprehensive improvements, up to and including recovery.”
Recovery?
Further down:
“ABA involves the breakdown of all skills into small, discrete tasks, taught in a highly structured and hierarchical manner … In an ABA program, lessons to be taught are broken down into their simplest elements. ABA focuses on teaching small, measurable units of behaviour systematically.
“At first, the child may be rewarded for doing something close to the desired response. Over time, as the child masters the lesson expectations are raised and primary reinforcers (like bits of food) are replaced with social reinforcers ( hugs, praise, etc.)”
One could be forgiven for thinking they were reading about dog training.
The fact that if the child does what is asked be it placing a puzzle piece, building block or the possibly uncomfortable if not painful task of making forced eye contact to be rewarded by food or physical contact is questionable.
Does that train the child to believe that if an adult commands them to do something no matter how nonsensical to them or uncomfortable they must obey believing they will be rewarded by titbits and pleasurable psychical contact?
Lastly under the heading ‘Is ABA effective?’
“It should be noted, however, that intensive behavioural is by no means a “ cure “ for Autism. No amount of behavioural therapy can cure the underlying and so far unknown etiology of Autism. Intensive behavioural interaction is effective in re mediating many symptoms of autism thereby recovering children in that their behaviour may become “ indistinguishable from their peers.”
Indistinguishable from their peers.
No longer distinguishable.
To close I leave you with the fully accepting parental view of Jane Johnstone.
“In my view once you embrace and accept your children as they are, the journey becomes life changing for everyone. My late husband and I always said that we would be very different people if the boys weren’t Autistic and we honestly believed that they made us better people. Our boys, like other human’s consist of a mind, body and soul. To change or work with just one element just simply cannot be consistent with accepting and respecting the Autistic person as a whole.”

Brit parents with autistic children paying thousands for 'scam dolphin therapy'

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