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Wednesday, 2 October 2024

Educating children with level 3 Autism

 


Some people do not like South Park, but it is a good example of genuine inclusion


The number of children with autism and intellectual disability continues to rise and this is putting a strain on government resources in many parts of the world. Increasing budgets can never match the increased perception of needs.

In spite of the vast amounts of money being spent very little attention is given to evaluating what gives the best results.

In the US it has long been put forward that the earlier the intervention starts the better the results will be and often it is stated that 40 hours a week of one-to-one therapy is needed.  This view is generally limited to the US.    

ABA therapy became a big business in the US and many providers are now owned by private equity investors.

I did point out that in the book the Politics of Autism, the author recounts her discussions with the founding father of ABA, Ivar Lovaas, that revealed he had rigged his clinical studies by excluding those children who did not respond to his 40 hours a week therapy from the final results. He just dropped them before the end of the trial. This would totally invalidate his conclusions.

There is a recent study on this very subject.


Rethinking the Gold Standard for Autism Treatment

Research shows some autistic children may get more treatment hours than needed.

The JAMA Pediatrics study looked at the relationship between the amount of intervention provided (hours per day, duration, and cumulative intensity) and the outcomes for young autistic children. Researchers analyzed data from 144 studies involving more than 9,000 children, making it one of the most comprehensive analyses of its kind.

Contrary to what many have long believed, the study found no significant association between the amount of intervention and improved developmental outcomes. As the authors write, “health professionals recommending interventions should be advised that there is little robust evidence supporting the provision of intensive intervention.”

Determining Associations Between Intervention Amount and Outcomes for Young Autistic Children A Meta-Analysis

A total of 144 studies including 9038 children (mean [SD] age, 49.3 [17.2] months; mean [SD] percent males, 82.6% [12.7%]) were included in this analysis. None of the meta-regression models evidenced a significant, positive association between any index of intervention amount and intervention effect size when considered within intervention type.

Conclusions and Relevance  Findings of this meta-analysis do not support the assertion that intervention effects increase with increasing amounts of intervention. Health professionals recommending interventions should be advised that there is little robust evidence supporting the provision of intensive intervention.


Some parents in the US get to the bizarre situation where their child can receive 40 hours of ABA for free, but if they say they want only 20 hours because they have other activities for the rest of the week, this is refused.  It is the full 40 hours or none.   


School segregation

Segregation is a word with negative connotations, but it is used when it comes to the merits of inclusive education versus special schools.

There are many ways in which schools are segregated, including

By sex

It is still very common to have separate boys' schools and girls' schools in many countries

By religion

Religious schools are common in both public and private sectors

By ethnicity

This was widely practiced in the United States and South Africa. The legacy of these policies is still evident today.

By ability

Selecting pupils by academic level is very common.

By disability

Segregation of those with learning disabilities into special schools or special classes within a mainstream school is widespread.

By socioeconomic status

Segregation by the ability to pay is common all over the world. In parts of the world there is no schooling for those whose family cannot afford it.

Homeschooling

In parts of the world homeschooling is legal and thriving. The US has by far the largest contingent, with 6% of children home-schooled.  In Germany it is illegal.


What is the best type of school for level 3 autism?

There is no “best” choice.

From the parents' perspective, some are desperate for their child to attend a special(ist) school and some are desperate not to attend such a school.

Some parents choose to home school.

Some parents look for some kind of hybrid solution.

Most parents just take what is given to them.


Inclusion vs segregation

The key issue here is whether the child is “includable”. It is fashionable in Western countries to be anti-segregation and pro inclusion.

Some children are not includable and some school environments are hostile rather than welcoming.  Even some children with level 1 autism struggle to cope in mainstream school.

Monty was lucky and completed all his schooling in a mainstream school with very small class sizes, about 12 pupils. He had his own teaching assistant throughout. Two of his former assistants later became class teachers at his school. We paid for the school and the assistants.

Had Monty attended a school with 30 children in the class with 3 other special needs kids, each with their own teaching assistant, the result would not have been so good.

As you can see it is a question of “inclusion in what” versus “segregation in what”.


What is the purpose of “school”

If you talk to parents of older children you will discover that over the years their view of schooling changes. It is an illusion, one grandfather told me. For many schooling is just daycare for the pupil and respite care for the parents.

Some parents do not want their child to be just taught daily living skills, they want the academic curriculum.

Some schools teach non-verbal children an alternative method of communication, whereas other do not bother.

It is not surprising that the result is often nobody is satisfied.


Peter’s idea about schooling for level 3 autism

I would require all children with level 3 autism to be taught at primary/elementary school a means of communication. Remarkably this is not done.

Proactive parents have been doing this for decades at home, but what if your parents are not proactive?

I read the other day that a mother commented that her non-verbal 7 year old daughter would greatly benefit from an augmentative communication device, but that the council/municipality did not want to provide one. In previous decades these were expensive devices, but nowadays these are just apps that you install on an iPad, or android device. Some of these apps are even free !!

Clearly, I would ensure all pupils with level 3 autism were screened and treated for any type of treatable intellectual disability, the most common one being elevated chloride inside neurons, which was the case for Monty.

I recently was contacted by a parent who, after trying to help his son for 7 years, has finally had success by increasing his dose of leucovorin (calcium folinate). Now his son responds to verbal instructions like "wash your hands".

Some of these children, once under medical treatment, will be able to follow much of the core academic curriculum and be genuinely included in mainstream classes. That was the outcome for Monty, now aged 21.

Children who remain with a lower IQ should not be in classes that teach academic concepts far above their level of understanding. This is pointless and will just lead to frustration.

One non-verbal child I know, who cannot read or write is “taught” a second language at school. How about teaching him a first language?

Children should be taught in groups of similar ability/functioning level, rather than grouping them by age. I thought this would be just common sense, but not in the world of education.

If the material has not been mastered there is no point moving forward, just repeat it. After 15 years at school there should have been measurable progress.

Beware of prompt-dependence and assistant-dependence. Skills learned at school need to be such that the child can apply them independently and can generalize them to new situations. Some wealthy schools provide very high levels of support and this risks that the child will become an adult dependent on a similar level of support. This is an example of “too much of a good thing”.

 

The services “cliff-edge”

Some people with autism, and their families, receive very considerable support for two decades and become dependent on it. At some point in early adulthood these supports may get abruptly withdrawn.

In other parts of the world, there was only ever very minimal support and the family became more self-reliant and so do not experience such a cliff-edge. The family and the young adult learnt to cope.


Level 1 autism / Asperger’s

This post is about level 3 autism, but I am always surprised how many people with level 1 autism write to me so here are some thoughts on them.

You would think that all people with level 1 autism should be able to thrive in mainstream education these days. There is so much in the media, or social media, about accommodating differences and promoting the “able disabled” who are featured everywhere, so how come kids at school are still bullying/tormenting their classmates who are 1% different. Times have not really changed as much as we might have thought.

Most kids with level 3 autism love going to school.  Monty adored it.

Many kids with level 1 autism clearly hate it.

During my time helping to run my children’s school one of the things teachers told me was that kids are actually very supportive of those who are clearly disabled but will delight in picking on kids who are a tiny bit different.

The net result is that many children with level 1 autism thoroughly enjoyed their on-line education during the pandemic away from all that awkwardness at school.

Many parents whose child goes to a special school for autism or Down syndrome are completely unaware that there are also some special schools for level 1 autism. It greatly surprised me.

 

Conclusion

The idea of trying to educate children with level 3 autism is relatively new. In the recent past they were just put aside in institutions and forgotten about.  Today much is possible, but a lot comes down to who the parents are and where they happen to live.

The Education for All Handicapped Children Act (EAHCA) of 1975 (later renamed the Individuals with Disabilities Education Act, or IDEA, in 1990) was the major turning point in the US. This ultimately opened the door to a flood of ABA, paid for by private health insurance, but only in the US.

My doctor mother once commented to me that we had shown that such children can be taught and can genuinely learn. This was a combination of personalized medicine and personalized learning.

Good things don’t just happen, you have to make them happen.

The outcome in level 3 autism is hugely variable and that is rather sad.




21 comments:

  1. Thank you for bringing up this topic, Peter. What concerns me about enrolling my daughter in a so-called mainstream school is the competitive nature at its core. The traditional education system fosters competition among students, and even among parents, who strive for their children to be faster, smarter, and more successful. From the very first day of school, the system and teaching methods encourage this competitive mindset. Is this really what our kids need? Should they have to face potential negativity from other children and parents in such a competitive environment? I'm not sure it could help to establish a good communication level for non-verbal children.
    Also what makes me think twice is an attitude toward AAC. There is an interest growing around spelling to communicate method, some practitioners create cool things to support education and lessons based on S2C boards. Would it be as one of priority for such schools to treat each communication need as something unique and respect as this is a right of a student to be understood? Maybe USA stands a step forward in this topic. But do you know of any European school with a good example of inclusion?

    Best,
    Natalia

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    1. Natalia, there is a lot of luck in finding a good school.
      Monty had a very good experience all the way from nursery to the end of high school. Just a few years later and this same school refuses to enrol children with an autism diagnosis.

      There are small private schools in many countries where teachers actually do want to include children with special needs. Having small class sizes is the key.

      Regarding competition at school, the world has moved on since you were at school. Many schools nowadays seem to have very little academic competition going on and it is more about getting through with as little effort as possible. This attitude makes inclusion very possible and also means the teachers have more time for anyone that actually is interested to learn.

      Regarding how typical kids react to special needs kids, if you introduce them at nursery or early primary/elementary it actually works rather well. This is just like in the South Park TV show, which many kids also watch. This includes a virtually non verbal kid in a wheelchair.

      Some people start their own school and many resort to some degree of home schooling. The amount of effort required from the family can be very considerable – it was in our case.

      Delete
  2. Hi Peter,
    If you haven't already, I think you should read up a bit on Acetyl-Leucine / Tanganil / NALL at the Syngap1 website. This substance is likely useful for a range of other brain-related disorders, and seems -at least in the short run- to be free from bad side effects.
    Easy to read and understand:
    https://curesyngap1.org/blog/drug-repurpose-update-1-tanganil-acetyl-leucine-for-potential-management-of-syngap1-related-disorder-symptoms/
    and
    https://curesyngap1.org/blog/drug-repurposing-update-2-tanganil-acetyl-leucine-potential-mechanisms-of-drug-action/
    /Ling

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    1. Hi Ling, I think this came up once before. I remember noting that this product is OTC in France and cheap. If they prove it works in other neurological disorders beyond vertigo, it will become an ultra-expensive prescription only medicine.

      Did you try it?

      Delete
    2. Hi Ling, thanks for sharing, NALL looks interesting and tanganil in France is extreme chip. Definitely worth it to try. Natalia

      Delete
  3. Whenever autism is brought up in the media it’s nearly always followed about the importance of early intervention.

    Yet outside ABA it’s unclear what they mean by that?

    They dedicate whole federal research budgets to early intervention yet as highlighted by yourself the success was faked and they must know that by now

    In the UK they stress about the importance of early intervention yet they don’t even have ABA here. What difference does it make if a newborn baby is diagnosed what are they going to put in place?

    In the UK they have this autism research centre in Cambridge run by the controversial SBC. On their website it states they view autism as a difference that shouldn’t be cured. So that kind of begs the question what then do they do all day in this place apart from running surveys about autism and anxiety and depression, that water is indeed wet.

    All funded by the taxpayers some of whom are dealing with autism in their lives.

    Strange world we live in

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    1. In Europe early intervention usually means 4 hours of OT/speech therapy per week. And when you ask about progress they always mention the "developmental trajectory" of the child and how they can't do much about it. But still expect hundrends of euros at the end of the month by you.

      Strange world indeed.

      Delete
    2. The wider world certainly does look strange.

      Your own world can look much better, once you realize how much you can take control of it and improve it.

      Delete
  4. I went to a special school in Finland as an aspie. Our class was supposedly mainly for asperger’s people. Most classes however, were for kids with ”level 3” autism or down syndrome. This special school also had a section integrated with ”normal” kids, for the local kids for whom it was the closest school geographically. There was a special kids only school in our city as well for people with similar disabilities who were also physically ill/handicapped. Then there’s also a separate school for particularly violent and aggressive pupils, who dont suffer from major intellectual disability.

    I eventually moved on from there to normal education, and for me it was definately the right thing. It was an absolutely ”bubble”, and the world outside was totally different. Back there I felt depressed, when I went to a regular school this completely changed. Meeting ”normal” kids and other aspies who had managed in regular education and feeling like I’m not as retarded as I thought changed me forever. I almost cry as I’m writing this. HOWEVER, i often wonder if the special school saved me from a lot of bullying… It was certainly a very safe and caring environment. For some it certainly did, and I was one of those ”1% off kids” you describe. I was only discharged from there when I was thought to be ”mature” enough, and I tend to agree with the teachers on this. Maybe this was the best possible outcome.

    A lot of the staff there were very devoted to these special needs kids. They would know the ins and outs of aspergers behaviour having taught hundreds of them. In the end I was friends with many when I became an adult. Some of them said to me that my aspergers is essentially gone for the most part, that if they’d see me now, they couldnt tell anymore.

    Eventually the aspergers classes were actually integrated with the regular school I was doing my last years in. I could definately see some downsides to this as well. One of the pupils got punched in the face due to being your typical over honest aspie and reporting some ”normal” bad boys smoking cigarettes outside.

    However, there was also one abusive thing, which really can’t be blamed on any single person. I had a lot of behavioural issues which were mostly down to the fact that I didn’t eat properly. I would be hungry all the time. Despite being aware of this, child psychiatrists recommended risperdal for these issues. I never took this drug. The Finnish adolescent psychiatry community at least used to be totally infiltrated by risperdal (marketing?). I do not know why. They even seem to go as far to think it is a medication for ”aspergers” and not for specific issues. I have the fact that I know about twenty aspies and 90% of them have been suggested or tried specifically risperdal, so it’s systematic. My current adult psychiatrist was also of the opinion that this was highly inappropriate. It’s very hard to comprehend, since a lot of the young docs at the clinic were certainly very intelligent, AND fully aware of the side effects when I asked. Despite this they happily recommended it to me when I didnt even have behavioural issues anymore but I didn’t respond well to methylphenidate.

    Cheers,
    Julius

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  5. Julius, Risperdal is approved for irritability associated with autism.

    Doctors have interpreted this as meaning Risperdal is good for autism and because it has official approval you will never get in trouble for prescribing it. Never mind if it can do harm or is appropriate.

    I am glad that you survived school pretty much intact and your autism has faded. This is often the case and is aided by the fact that as your NT peers get older they also change their behavior and it becomes more like yours.

    Having been closely involved in my son's school, I always thought it should be much easier to coach/mentor the level 1 autistics than the really hard level 3 cases. There would be a big payback for very little input, but instead there was no input and kids got ostracized. My son was very well included by his 1:1 aides and had a great time throughout his schooling.

    Good luck

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  6. Dear Peter,

    I’d like your opinion on my son’s education. He is now 5 years old. Since his diagnosis at 2.5, he has followed the standard care funded by the state here in Greece: two 1.5-hour sessions of speech and occupational therapy per week. He also goes to a mainstream preschool with a private assistant we hire ourselves.

    Unfortunately, he hasn’t made much progress. He isn’t toilet trained, speaks only single words when he needs something, and can’t follow the other kids. Now we have to decide what to do for next year.

    Since we cannot afford both a private assistant and intensive therapy, we are considering these options:

    Option 1: Stay in the mainstream preschool for another year, keep everything the same, and hope for the best.

    Option 2: Switch to a special needs school and put our budget into a full ABA program. I feel that if a teacher pushes him just enough, he could make progress. In the OT/ST world here, "pushing" is seen as too much, but I worry the current approach is too little. However, I am very concerned that in a special school he might start copying aggressive behaviors from other children, behaviors he doesn't have right now.

    Option 3: Go full ABA, but send him to the mainstream preschool 1 or 2 days a week just for socialization. The teachers say they can handle him for those few days without an assistant.

    What is your take on this? Is it better to keep him in a mainstream environment for the social aspect, or should we pivot to a more "pushy" and intensive structure since the current path isn't working?

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    1. Konstantinos, it is highly individual, it depends on your son, the mainstream school, the special needs school and the assistant.

      A good assistant is worth a great deal. In our case the assistant was really a combined teacher and ABA therapist. We combined mornings at school with an assistant in a mainstream school with tiny class sizes, with afternoons home schooling/ABA with the same assistant. During school holidays it was all-day home program with the assistant. This worked really well, but you have to train/coach the assistant. Two of our assistants later went on to be class teachers at our school.

      I think being in a large mainstream class has little value - with or without an assistant.

      Some special schools are very good, but some really are not. You want more than your child to be happy and get party invitations, you want them to learn. Fun is great, but breaking through to kids with severe autism requires a great of effort and repetition and this is often lacking.

      Ideally, you first treat the child’s autism biologically to maximize their potential to learn. It is good to learn socialization, but you do need basic functional skills first, which methods like ABA focus on.

      You have to adapt a solution to fit your specific situation. The easiest option is rarely the best one. "Pushy" is best.

      Delete
    2. Dear Peter,

      Thank you. We are working on the biological interventions, but slowly. I want to keep only what makes a consistent difference.

      So far, the only thing that consistently helps is low-dose melatonin, which completely normalizes his sleep. I know it works because we tested it: we stop it, the issue re-emerges; we restart, and the issue vanishes. I haven't seen such a clear result with anything else yet. Only on the negative side. Since he had a major regression around age 2, I have tried several mitochondrial interventions. They all consistenly send him to crazy town, and it is not something temporary.

      Also, due to an abnormal sleep EEG, he was prescribed VPA. It initially normalized his mood and the EEG. Our neurologist suggested tapering it off since there was no other change, so we are currently on a very low dose. His mood is still good, and we will see about the next EEG. It feels like a marathon.

      Regarding the personalised education, may I ask what resources you used to train your assistant?

      It seems to me that the hardest part is finding someone who will accept that setup. So far, all the professionals I have talked to have an "expert" attitude and do not welcome parents interfering with their "field of expertise."

      Delete
    3. Konstantinos, a very good source we used (and still exists) is

      https://difflearn.com/

      They are based in New York. They have the curriculum and teaching materials and much more.

      In the world of ABA and even speech therapy all the "good stuff" is English. If you are going to teach your son Greek, this adds another complexity. It can be done.

      I ended up learning ABA myself. We did have some coaching from experts, but minimal. It really is not that hard to learn about it, the massive issue is implementing it for 1,000s of hours. Some people use psychology students as part time therapists. It is a big job and most people give up unless they are getting it all paid for by someone else. We ended up paying for full time assistants for 15 years. So it is a major undertaking.

      Delete
  7. Hi, sorry to jump in.
    We learned about ABA therapy in this course on Udemy. On sales days it costs about $10. You have to keep looking when they have deals.
    It's in Polish but has English subtitles.

    https://www.udemy.com/course/15-minutes-for-treatment/

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    1. Also note that some parents end up as big ABA fans, others end up very disappointed.

      It has become a big business and you may not be getting a good service if the actual therapist is poorly trained. There are some really great people doing this, but I think they may not always be the majority. We used a great Greek American ABA consultant.

      Delete
    2. I totally agree with you. After sending our son to two ABA clinics, we were fortunate to find a place which worked for our son (DTT trial method with mostly table time than naturalistic approach with floor time).
      As you mentioned it's really important to find a well experienced RBT and again in our case, my kid is able to sit down and learn with his RBT (it was impossible to teach him anything with stimming and running around about a year ago).
      We followed the ABA course I mentioned above, to work with our son in the weekends.

      I also wanted to mention that in our case, the public school system didn't help. There are special education programs for preschoolers here in the US where we sent our son when he was 2 years old but it didn't help him at all. He really needed and improved with 1on1 teaching approach which ABA offers.

      Also we know many parents here in the US are homeschooling even their NT kids to avoid being bullied and the quality of the educational system in public schools is not as it used to be (we see in the news that there are NT highshoolers who are unable to read)
      Sue

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    3. Peter, thank you for the link to Different Roads. I will check their materials. The language is indeed a hurdle since we speak Greek at home, but I assume the teaching principles (breaking skills down) remain the same even if I have to translate the words for him.

      You mentioned you used a Greek-American ABA consultant. I was actually able to find her ABA center here, but it's a 1.5h distance from our home, not very practical for daily intensive sessions. However I did schedule an appointment with an ABA center nearby who belongs to a former student and partner of her.

      I appreciate the warning about the "business" side of ABA. That is my fear—spending our limited budget on a therapist who isn't actually effective.

      To Sue: Sue, thank you for the Udemy link and for sharing your experience. It is very validating to hear that the public preschool didn't help your son either. It makes me feel less guilty about my decision to pull him out and focus on 1-on-1 work. My son is exactly as you described—unable to sit or learn in a group right now, so hearing that DTT helped you gives me hope.

      Delete
    4. Konstantinos, there are different ways of implementing this kind of therapy. Sometimes you take the child to the center and in others the therapist comes to your house. We did the second, which is much better in my opinion. It all depends on your family circumstances and how ther therapist works.

      I think you will get much better therapists in Athens than in the US. Demand there is huge, pay is low and they take just about anyone. It used to be much better.

      Delete
    5. Thank you for this perspective, Peter. I will contact your former teacher's center to see if they can support a home-based program.

      Regarding the quality of therapists, unfortunately, the situation you describe in the US has arrived here as well, specifically with OT and Speech Therapy centers. They have mushroomed and there are now multiple centers in every neighborhood in Athens. The turnover is incredibly high, and the therapists keep changing all the time, which makes building a relationship with the child almost impossible. ABA, on the other hand, is not popular at all here. It is actually quite hard to find, which is a different kind of problem.

      Delete
    6. Konstantinos, Lillian is a really nice person. I would suggest you take your son and go have a coffee with her. She will give you plenty of useful advice. Send her my regards.

      Delete

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