Wednesday 11 May 2016

Borderline cases: children falling into the gap

Hello guys. Let's get back to a serious topic today - I have an old friend from Singapore who has been in touch and we have had a really long conversation on Facebook discussing the condition of her son who is 5 years old (turning 6 this year). Let's call the boy Joe - not his real name and the mother Mrs V. She is very concerned about the development of her child and is running out of options, thus she wanted me to explore if he would be better off in the British education system. I will summarize what she has described to me about her son Joe and the challenges they face.
How will 'borderline cases' cope in the education system?

"Joe is turning 6 later this year but he doesn't have the mental age of a 5 year old - more like that of a 3 year old at best. He is really struggling at kindergarten and the teachers don't know what to do with him - we're not just talking about learning languages or mathematics, the boy struggles to even perform most simple tasks like getting dressed. I have tried everything: being nice, being strict, using rewards, being encouraging, punishing him - nothing works, nothing gets through to him. He is extremely slow to respond to even most basic instructions, like his IQ is very low and even the simplest of tasks are really big challenges. Most 3 year old would be capable of responding to instructions like that but Joe can't even function at that level - he can't do anything for himself, all he does is cry a lot and the teachers in the school in Singapore are telling me to send him to a special school for mentally disabled children. He cries a lot as well and often wets himself. The teachers don't know what to do with him.

My husband and I don't know what to do - we're both highly educated professionals with good jobs, graduates from good universities and we don't know why Joe is like this. Sure we have sought all kinds of professional help but every psychiatrist or expert has a different opinion and nobody has any solutions. There isn't anything drastically wrong with Joe apart from simply being, well, stupid and slow. The education system in Singapore has been a disaster for him as all the kids in his kindergarten are far more developed than him - he hasn't got the social skills to have any kind of meaningful social interaction with any of the other kids and I have observed him at school: whilst the other children play with each other, he either stares into space or just cries. I have been dreading the day I have to register him for primary one in Singapore as it would be a total disaster - he can't function and will fail everything for sure. I am wondering how the British system would treat a child like Joe because if it will make a difference, my husband and I are willing to try anything. Can you tell us more about how the British education deals with children like that please?"
Is the Singaporean education system just wrong for Joe?

Since Mrs V has presented me with a complex situation, I have turned to my friend Katie (not her real name, to protect her identity) who is a very experience primary school teacher. I have since put Katie directly in touch with Mrs V (yay, the power of social media) but I have turned our discussion into an interview to help present this to Mrs V and summarize what I have learnt about this rather complex issue.

Limpeh: Katie, could you tell me more about how the British education system copes when it comes to dealing with children with special needs? What have your experiences been like in this aspect?

Katie: I'm not sure the British system is any better with coping with children like that I'm afraid - we do get children like that in the school where I currently work, as well as with previous schools I have taught in. There is an evaluation done by medical experts to determine whether a child has special needs or not - this is not a job done by the teaching staff in the school, but the child is sent away to see this so-called expert and I'm not happy with that. You know, as teachers we spend most of the week with that child - we know the children so incredibly well, yet our opinion doesn't count because we're just teachers and it takes a doctor who has never met the child before to offer a professional diagnosis? Sometimes the results surprise me. You can have kids who are deemed to have special needs being surprisingly able to cope with the challenges of school; and then you have the opposite, you have kids who are clearly messed up one way or another, who have a below average IQ, but they are deemed to be 'borderline cases'. This is ludicrous of course, because it splits children up into two convenient groups: educationally normal vs special needs.

Limpeh: So you have kids who fall into the gap, when there is this dichotomy, ignoring the shades of grey.

Katie: Yes. I have seen a lot of kids who are deemed 'borderline cases' - that simply means that the experts recognize that the kids will need some help to adapt to life in school and some aspects of school will always be a challenge for the kids in question, but because they are not messed up enough, they are not deemed 'special needs' and so they are in the worst possible situation. The kids who are certified to have special needs, okay, they are then flagged up in the system and the school can then have right to ask for more resources from the government to help these kids. So for example, we can justify employing another teaching assistant if the child clearly needs more attention and help in the classroom. I'm not sure what the system is like in Singapore, but it does look like your friend is not given the help she needs because her son is probably not messed up enough. Being simply 'slow' is not a disability - to be perfectly blunt, we have always had people around us who are somewhat slower than the rest: we used to call them 'stupid', but it seems very un-PC to use that word these days. But resources are limited - some children are simply slow and for want of a better word, stupid: they don't have special needs. That refers to a certain set of medical conditions where the child is so severely affected that s/he is considered disabled and requires special assistance.

Limpeh: What happens then in these cases?

Katie: For the parents of these 'borderline cases', oh my - the onus is them placed on them to get the help their children need on the private market. If the parents are rich enough, then they will be able to buy the kind of extra therapy and help their children need. Not that there is any 'cure' or 'solution' - these experts help 'mitigate' the situation at best, really. You have to understand, these experts cannot 'cure' any of these kids, they can at best help them cope better with the challenges of life and make everyday tasks seem less of a challenge, so they can get through the day with less stress. Like in the case of Joe, you can't cure his condition and turn him into a straight A student. Get real. But there are cases where the parents are poor and don't have the money to pay for these expensive therapists and experts, so the kids are not given any extra help outside school and their situation often gets worse with time - the kids will struggle to stay in school or complete their education. Once they leave the school system, I shudder to imagine what happens to them. Most just end up living at home with their parents into adulthood, unable to get a job or integrate into society. I do feel sorry for the parents because I have seen the kind of stress they have to go through.
How will Mr & Mrs V cope with Joe's needs?

Limpeh: What happens then in your classroom, when you have to teach a 'borderline case' child?

Katie: (Sighs) Goodness me. It is like walking a tight rope in terms of establishing the right balance: when you have a child like that in the class, you can be tempted to spend 50%, even 60% or more of your attention on that child because that child just can't learn as fast as the others. But then in a class of 30 students, that means one child gets more than half my attention and the other 29 children have to share less than half of my time, attention and energy. That's not right - the parents of the other children have paid school fees just like everyone else, why should the quality of their children's education suffer just because they have a 'borderline case' like that in their class? If they were in the next class which doesn't have a 'borderline case' child, then they are able to learn a lot more effectively. You think the child suffers, the other classmates suffer as well, because if I am trying my best to help that 'borderline case' child, I am inevitably neglecting the other children who are more capable - that's not right, is it? Why should they be punished or penalized like that? But who do we blame then - the system? The government?

I have to discipline myself - I set myself goals to achieve: I have to cover this much of the syllabus within this lesson. I am not going to allow myself to slow down and miss my targets just because I have a 'borderline case' child in my class. Once I know I am on schedule and am not going to miss my target for the day, then I can give the 'borderline case' child more attention and help. If I am behind schedule, then I just have to tell myself, "tough, that kid is going to stare into space, not understand what the hell is going on and I can't go over there and help him. Not today. Too bad." I don't like doing that, because if you allow the child to fall too far behind, then the child will fail the exams and end up retained a year. It's not like these children don't have the IQ to learn anything - they can learn something, give them a chance and they will learn. But we have to recognize that they learn a lot more slowly than normal children and trying to then integrate them into a classroom full of normal students with the best of intentions is a total disaster at times.
Katie has to teach a mixed-ability class.

Limpeh: Well, I would have thought that a solution would be to put the 'borderline cases' in a class of their own and then the teacher can teach the same lessons at a much slower pace, a pace which is appropriate to the learning ability of the students.  I guess that's a rather Singaporean approach to the matter as we regularly stream students to group them according to ability. That's why I am wondering if the British system is better?

Katie: That is not done in the UK - I am not saying that the British system works better or am I condoning it. I'm just saying that it is not done in the British system and you tend to have mixed ability classes, at least in primary school anyway. Well, I can see the benefits of our system - you can't dump the borderline cases in a class where the expectations are so low that the teacher teaches so little that the kids walk away barely literate. You simply have to integrate these kids into mainstream society at some point, at some level and it is easier to start at primary school. How do you expect these 'borderline cases' to live and work alongside others in society if you start isolating them away from everyone else at such a young age? What is the alternative then? Do you have an alternative?

Limpeh: So is Mrs V going to be better off moving her child to the British system? Would it help their situation?
Mrs V has little faith in the Singaporean system.

Katie: Not really. To be honest, I can't tell for sure as I have never met her child, if her child can be diagnosed as 'special needs' then there will be resources in the British system to enable children like that to get a decent education. But if the child is classified as a 'borderline case', then quite frankly, pulling her child out of Singapore where everything is familiar and putting the child in a British school, where everything foreign, different - that's a massive shock to the system for any child. I'm not sure how well her child would be able to cope with this kind of transition and you are removing the child from an existing network of family members: grandparents, uncles, aunties, family friends etc. That is probably a far bigger factor for me to recommend against uprooting the child as the British system would not be any kinder to the child. The solution is ultimately money: if your child is a 'borderline case', then money can buy you a lot of the extra help the child needs and would make some difference.

Limpeh: Tell me please about some of your experiences with borderline cases.

Katie: Well, I have taught a child who was very sick - he had MS (multiple sclerosis) and also suffered from epilepsy. His spine was also deformed so he had a long list of medical conditions. When I was first assigned to teach the class he was in, I was given this long list and told, "you should be aware of this" and I was shocked at what I saw on that list. But I was told that the boy was educationally normal - that means that whilst he was very sick, he should be able to learn like everyone else. That was not the case at all. The medicines he has been prescribed had some very strong side effects on him - there was a period when he was given some medicine to reduce the incidence of epileptic seizures, that meant he was dozy, unable to focus in class, awake but barely lucid. There are good days and bad days. And there were very, very bad days when we couldn't do anything with him because of those side effects of the medicines. On top of all that, he was also being bullied by some of the other children in the school as well. He was a very unhappy boy at school, to say the least with all of these different factors that prevented him from learning well.
What is the right way to deal with such borderline cases?

After a few years of going through school like that, he fell behind the rest of his class so much that he couldn't follow the lessons. He hated the lessons - because it left him feeling confused and stupid, so he would get very distracted and he lost all interest in learning. The teachers struggled to deal with his behavioural issues - he became very disruptive in class and whenever the teacher got angry with him for misbehaving in class, he would claim, "I'm not feeling well. I feel sick." He knew the moment he played that card, the teachers would allow him to go rest instead of forcing him to say, participate in a maths lessons. All those problems, they are all connected, they compound each other - yet the child is certified educationally normal and thus not 'special needs'. We get told all these stories about Stephen Hawking being physically disabled and has ALS, yet he has a most brilliant mind - well, this child is no Stephen Hawking. His IQ may be normal, but there's just no way he can learn in a normal school but what do you do with a child like that? Put him in a padded cell with loads of sweets and chocolates? I don't know. I have no answers. His parents don't know what to do with him as his behaviour has become totally impossible as he gets older and I'm worried about that child. I'm also worried about his mother - she is a little lady: he has been hitting her and I've seen the bruises on her. How can children like that be classed as 'educationally normal', I ask you? How is this right?

Limpeh: What about the parents of these children then? How do they cope?

Katie: It depends, every case is different. Depending on their education background, their social class, their cultural background, religion, family experiences, every parent reacts and copes differently with this kind of challenges. Most want the best for their children, of course. But, in some instances, I have struggled with parents who go into denial.
Different parents react differently to these challenges.

Limpeh: Really. How so?

Katie: The classic case is when the parents spend a lot of money on some kind of therapy, so the therapist keeps telling the parents just what great progress the child is making because they don't wanna say, "I know you've paid me a lot of money, but I'm barely able to make any difference. In truth I really can't help your child." No, they want to give the impression that they are good at their jobs and can justify charging a lot of money. So the parents come away with a false impression that their child has made great progress - that's all a pile of lies of course. Complete bullshit. The proof of the pudding is whether or not the child can actually learn in a classroom environment - that's where I can see whether or not progress has been made and if I don't see much progress, I have to be honest with the parents. And that's when they turn around and accuse me of being a bad teacher, because they have effectively paid a therapist to tell them how great their child is. They can't help it - they are irrational because it is human to prefer listening to encouraging good news rather than face the ugly truth. I used to get angry with them - now I just feel sorry for them.

In my experience, society is conditioned to be kind and encouraging to these parents - when you see parents struggling with children like that, what do you do? You say nice things to them, you don't say things to put them down or tell them that there's no hope for their children. But what this kindness does, is that it leads to parents having all kinds of false hope - that their children will 'grow out of it' and somehow the problem will go away by itself or that there's a cure for it. Of course it doesn't work like that - but you have no shortage of kindhearted people offering encouraging advice on no basis other than their willful desire to say something nice. None of this 'encouragement' is based on evidence or medical science of course - yet these nice people mislead these parents with their encouragement. There are days when I struggle to find something nice to say to the parents when they come to me and ask them how their children are doing - I can't be too negative of course, but I never say anything nice for the sake of being nice. I feel that it all becomes fairly meaningless when people are just saying nice things to each other out of social decorum. But to be fair, most parents are pretty good and they understand what I have to go through.
How can we react as a society to such children then?

Limpeh: Thank you very much for sharing your insights with me.

Katie: That's okay. Good luck to your friend Mrs V and Joe.

22 comments:

  1. There could be any number of reasons why he is behind this badly. I wouldn't call him stupid as his mom did even though I am not a proponent of political correctness. His brain is wired differently for sure. Here, he would have been sent off for assessments galore and a label pinned on him. He would receive extra support from special needs staff at school. This support may range from full-time to as-needed basis depending on the extent of his needs.
    Unfortunately, we don't have a system that works perfectly either, but I can say with confidence that a child with special needs gets more support than a child in Singapore would (from the system, that is).
    Joe sounds like he is on the autistic spectrum, just based on his lack of social skills.
    I hope your friend gets all the help she needs to support the child. It's a long road ahead.

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    1. The problem with the British system is that in order to satisfy the criteria for 'special needs', you need to tick certain boxes and if you have a situation that falls outside those boxes, then you get no help. Ouch. That's bad. I didn't want to speculate on Joe's case as I haven't even met the boy before, but I wanted to talk more generally about the issue and explore Katie's experience as a teacher.

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  2. LIFT, thanks for doing a feature on this very important topic of kids not fitting into clear-cut classifications within the education system.
    Singapore is addressing this by opening more pathways, but due to emphasis on achievement, these new categories like IP, IB, PFP, DPP, through train, gifted, sap (options for secondary students) are for high performers.
    For low performing but otherwise "normal" kids, sec sch is a glorified babysitting /child care centre for them to bide time, tide over the stormy teenage years without getting into too much trouble. After that, there is only vocational training at ITE or a private school offering certification by recognised bodies in skills like baking or coaching.

    Mrs V wants to know if her son will be better off if they migrate; Katie says not necessarily, they face other challenges if they uproot.
    I agree they shouldnt make a hasty decision now, BUT I also think the need to eventually migrate is very real.
    She can at least start preparing, eg get her paperwork & documents ready just in case.
    My in-laws' son was in EM3, the "low" stream in primary sch. Because of that, the family migrated to Australia after a long process involving tons of red tape and money.
    There he thrived, even got into an accelerated learning program, & skipped a couple of years, coming out of Year 12 (equivalent of A-levels) at age 17. So it was all worth it!
    Singapore's small size, the stigma of being a weak student, culture of conformity to follow model answers, obsession with exams, zero tolerance for failure -all point to the fact that, if a child cant cope here, s/he will be 100x better off in a more open minded flexible country, with enlightened views toward diverse capabilities.
    Here's wishing Mrs V & her son all the best: may you make the right choice:)

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    1. Thanks for your comment.

      I think Katie's concern is genuine - the worst case scenario is that they move to the UK (Mrs V's husband used to study here and has connections in the UK) and Joe gets stuck in the no-man's land: he is certified as a borderline case. Clearly there are some issues with the kid, but is he messed up enough to qualify for special needs help? Katie can't say for sure and her experience has not be reassuring (ref: very sick kid with MS and epilepsy who is still classed as educationally normal).

      I do warn you though, about encouraging Mrs V like that - okay, so things worked out for your in-law's son, but let's not go down the road of "because things worked out for them, if you follow the same path, things will work out for Joe too!" It doesn't work like that. Every child is unique and faces a unique set of challenges and thus require a different set of solutions.

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    2. There are no right answers. Mrs. V. is right to make inquiries now. What they decide on should depend on countless factors. I feel for them.

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    3. You mentioned Joe may be "certified as a borderline case". This means being borderline is a grouping on its own so the system will have provision for it.
      What bothers me is if borderline means "neither here nor there". Thats when parents try to influence their child's psychological test result, so that the kid can fit into a particular standard either too high or low for the kid, which compounds the kid's misery.
      For example if the boy with MS/ epilepsy was classed as educationally normal based on an isolated IQ test, but his school performance is below par, is it justifiable for his parents to make him fake a poor IQ score so he qualifies for special needs benefits?
      Others try to get their kid into a better bracket, hoping it will encourage the kid. But speaking from experience, it doesnt make much difference ultimately.

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    4. No, I think you've misread the interview CLT (or you can blame me for not having presented it clearly enough) - but either way, allow me to explain.

      The teachers (or the parents) can recommend kids who are struggling in school to be sent for 'testing' to see if they have special needs. If there's no problems, then the kids won't even be sent for that kind of tests. Teachers are of course, hoping for the kids to be certified as 'special needs' because that means one vital thing: MONEY. The government has earmarked money to help kids with special needs adapt to their learning at school - but the authorities are aware that the money is limited, it is not a bottomless pot of money. So they have to make sure they only give that money to the kids who really need it and not just to any kid who is not doing well at school for a variety of reasons: for example, a kid who is neglected at home by the parents may suffer academically because he's just not studying, but that doesn't mean he has 'special needs' - which refers quite specifically a set of medical conditions that affects the learning process. The set of criteria is quite narrow - Katie thinks it is too narrow in fact.

      Whilst there is the phrase 'borderline case' being used in some cases, there is NO provision for people in that group. I repeat, NO MONEY is allocated for those considered 'borderline case'. It's the worst possible group to end up in - because the system recognizes that there is a problem, but it is considered 'not serious enough' to warrant intervention and the best they can do is "we'll keep your case on file and see how you get on, but in the meantime you get NO help, NO money, NOTHING from us." That's when the teacher like Katie goes, "whaaaat? No help?"

      The British government isn't that generous - there is money, but they are quite selective as to how they spend it and whom gets the money. In short, (my words, not Katie's) if you're not fucked up enough, you're not going to get any help. Only those who are well and truly fucked up get the money. If you're only somewhat fucked up ('borderline case'), tough shit - you're on your own. Good luck to your parents and teachers, but the government is not giving you any help.

      It boils down to money Mr Toh. It's all about money.

      As for the boy with MS and epilepsy, I understand that he has had some tests over a period and he showed normal IQ and so that's why he was classed as 'educationally normal'. Like I said, there could be a whole range of issues to affect one's performance at school, in this case, it's mostly the side-effects of his medication.

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    5. Hello, I just want to drop a comment here. 1st: To give my professional opinion, many of the Ministry of Education school psychologists are over-worked, underpaid, and generally not as experienced as you want them to be (read between my lines). 2nd: Many "psychologists" in Singapore do not have the appropriate training and expertise in atypical child development (again, read between my lines).

      Consider the boy with MS and epilepsy. Having normal IQ does not mean that he can be classed as "educationally normal". If his psychologists said that, I will dispute (and rip) that statement immediately, as it shows a fundamental lack of understanding regarding the relationship between IQ and educational functioning. Also, given the type and amount of medications needed by the child, it is ludicrous if the psychologists did not consider how these will impact on his education and learning.

      If the child has seen a better-trained (and more thoughtful) psychologist, he will NOT be assessed as "borderline" and "no special needs". It is ridiculous if he, as well as the school teacher, is not given access to support/money because of a crappy psychologist.

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    6. Dave, you do realize that Katie is British and I was asking her about the situation in the UK. The case of the boy with MS & epilepsy is in a school in London, where Katie teaches.

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    7. Oh my, I must have gotten too riled up and missed that detail. Clearly, I was referring to Singapore when I made those comments. My apologies.

      I had a young teenager (schooling in the UK) who was born with a genetic condition (i.e., hearing-impaired since young, and she needs a hearing implant). The school is not able to provide educational interventions, because the child was deemed "academically competent". Her IQ scores were relatively high (above average), so the logic is that she must be normal (even if severely hearing-impaired); hence, no funding. She probably can be classified by many as a "borderline case".

      Fortunately, the family often comes to Singapore. I did the assessment and wrote a strongly worded report, which the parents used to obtain intervention services from the NHS and the school. In this case, the child needs special education support, because it is clear that she is not able to cope - even with her best efforts - with the academic rigor of the British education system (note: If Singaporean parents think that the UK education system is more slack or more relaxed, there are really misinformed).

      It is, perhaps, a necessary evil to "pay more" to see the health professionals in private practice (which costs a lot more). This is true in the UK and in Singapore. It is all about taking a piece of the "funding pie" for children with needs. And there are ways to go about it: One way is to pay the high fees and see a health professional in private practice.

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  3. It seems to me that Joe might be a case of dyslexia. Has Mrs.V approached the dyslexia association in Singapore? I have a friend who is a teacher within the association. AFAIK, the teachers tackle dyslexia by attempting to discover what the students’ optimal learning methodology is and trains the student on applying that methodology on their normal studies.

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    1. Oh you're wrong. You're so so wrong. Joe is 5 years old and is not at a stage in his life where reading is a part of his everyday life. You need to struggle with reading in order to be diagnosed with dyslexia but you're pinning your diagnosis on dyslexia? Are you perhaps even confusing it with autism? Cos it does sound like there is an element of autism to his behaviour (inability to interact with others, inability to follow instructions). The kid is in kindergarten and it is mostly just playing around in there, the kid hasn't even started primary one yet.

      If he has dyslexia - then that's ON TOP OF everything else that's already causing the problems he has (which has led Mrs V to confess that he has the mental age of a 3 year old at best). Now that's not dyslexia - dyslexia doesn't cause a child to be unable to control his/her urine - you're going to draw a link between dyslexia and Joe not being toilet trained at the age of 5? The vast majority of children are already capable of using the toilet independently at that age.

      I'm only going by what Mrs V has told me (and she's seen a lot of specialists) - and yes, autism has been mentioned. A lot. Oh a lot. Which is probably why she came to me as she knows I've blogged on the issue.

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    2. Oops, I am sorry that I missed out on reading the part on wetting himself.

      On another hand, inability to control urination or display apprehension might also be symptoms of a neurological problem. Have Joe been examined by neurologists? Just to remove that possibility.

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    3. Hmm I certainly will not think of dyslexia. My best friend's daughter and my nephew are both dyslexic. While they show up in different ways, there is a common theme, namely an inability to read and spell, especially for English. My friend's daughter has no trouble with Chinese characters at all. Socially, both of the kids are perfectly normal and in fact, I will say the clue to their dyslexia was that their intelligence was not congruent with their poor English spelling and reading skills. Otherwise, both kids are able to speak and understand instructions and learn normally.

      I think that this is more likely to be a case of a poorly functional condition on the autistic spectrum than dyslexia. The diagnosis is not easy as it takes several sessions of interactions with the psychologist and the paediatrician. I am not sure of the case in UK but in Singapore, children can be considered to have special education needs if they meet guidelines requirement (http://www.apsn.org.sg/wp-content/uploads/2011/07/Guidelines-for-schools_new.pdf). Based on my very lay understanding, it looks pretty tight and if Joe falls into the borderline category, then it will be very challenging.

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    4. Yeah, whilst kids at 5 are already reading and playing with other boys and girls, Joe is unable to even control his urination and hasn't even developed the skills to play with others. At best, his 'playtime' involves his mother reading to him, indulging him with some toys and it's all very much led by his mum - he is very passive and shows little initiative. When left on his own, he doesn't do much. For example, he likes watching TV. He could stare at the TV for a long time, but when Mrs V then tries to asks him, "what was that cartoon about?" He doesn't have the vocabulary to describe what he has seen. So one wonders how much is actually going in when he watches a cartoon, like he is clearly entertained by the cartoon, but how engaged is his brain in the story? That's more what you'll expect of a 3 year old, not a 5 (about to turn 6) year old.

      Just to reassure you - Mrs V has brought Joe to practically all the best doctors in S'pore. She's hoping for a solution - a cure. Nobody has offered her one. The most blunt doctor told her to accept the fact that her kid has below average IQ and prepare for a difficult process of bringing up an educationally subnormal child. He was even blunt enough to tell her, "at least you and your husband are rich, you own your flat, your son never has to worry about a roof over his head as he will inherit your flat and you have enough money to support him forever."

      But that's not what she wants to hear. She still hopes for a 'cure'.

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    5. Ah I get it now. My typical male "fix the problem" mindset thought that Mrs V was searching for options to help Joe manage. It sounds like she is still hoping for a way to turn him into a normal IQ boy which I think is not realistic. I guess the acceptance phase is still not quite there.

      In Singapore, there is some governmental help in special schools for children with subnormal IQ. Unfortunately, similar to UK, the criteria is rather tight. Even in such schools, what will happen is that children are thought to cope with the basic challenges of daily life. It is not a cure to boost their intelligence but it will guide them to be at least functional on a basic level, including perhaps learning to not wet himself when the bladder is full.

      Unfortunately, it may be as you said, not something which is acceptable at this stage.

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    6. Allow me to explain it like this Shane - I think Mrs V feels that as a mother, she cannot give up hope on Joe. So in her mind, acceptance that some things cannot be changed/improved = giving up hope. But one does wonder at what stage you draw the line, because hope should be based on evidence - when you place hope on an unlikely outcome (such a a cure for Joe that turns him into a high IQ, high functioning child), then one wonders why she is setting herself up for disappointment like that. So often, we talk about the disabled child, but we never really discuss the mindset of the parent(s) in this case. I can talk about this because I have observed my sister in close quarters and her thinking has surprised me at times.

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  4. If Joe is on the autistic spectrum, he has the option of attending special (private)schools in the UK or in Sibgapore such as Pathlight - she should perhaps investigate. But first she needs to get a firm diagnosis.

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  5. While she works out her long term plan, i suggest she also think about short term arrangements. He child most prob need to register for primary 1 this year and this is compulsory.

    One way is to gather all the professional assessments she has and write to MOE for deferment of registration to primary 1 for her son, since he is physically and mentally not ready to move to pri 1. One of my colleague has successfully applied that for her child and try to get him more mentally and emotionally ready before going into pri 1. This will at least buy some time while she eork out her options.

    I am unsure if she has been referred to the Early intervention programme for infants and children (EIPIC). She will need to show she has some plan in mind to support the child in their development and education to go back to main stream school. This will help her child get moving while she can consider applying to MOE for her child to be enrolled into international school locally which has a more forgiving system than the local sch system.

    Collectively, hope these will buy enough time for her to find options overseas and get the paperwork done to move elsewhere.

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    1. As I have not lived in Singapore since the 90s, I don't know the system in S'pore but I am sure Mrs V knows it very well - I think she was merely exploring whether or not a child like Joe would be better off in the British system. And Katie's answer is "probably not".

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  6. My heart goes out to Mrs V. My mother had a similar experience when she had me. I couldn't communicate or interact or do anything else kids my age could do, and I was diagnosed with autism at age 3. Both the Paediatrician and the kindergarten teachers told her to put me in a special needs school since I was beyond help. My mum didn't know what to do, but didn't want to give up on me so soon, so she kept looking for help.

    Fortunately for us both, she did meet an old friend who advised her to bring me to a Psychiatrist, who in turn diagnosed me with having mild cerebral palsy, and recommended me to Dover Court Preparatory School (Centre
    for Special Education) for the Early Intervention Programme. I underwent Speech, Occupational (with Sensory Intergration), Physio and Reading Therapy when I was 4 years old (can't remember in which order). The therapists there told my parents that they'll try to help but they needed to be prepared for the possibility that I won't respond to the sessions. The therapy sessions stimulated my brain and my condition improved after some months. I could finally communicate and participate in school activities, and my kindergarten teachers and everyone else were shocked and happy. I should however stress that even though I could pass off as normal and was able to integrate into a normal school, I was never "fully cured". I had weak muscles and was slow enough to qualify for extra time during exams, had poor memory, and tip toed instead of walk, among other things. All these were a constant reminder that I was different, and I definitely felt like an outsider, but I suppose that's minor and I should be thankful that I can support myself now despite all that.

    I know I was extremely lucky that my condition was mild, and that I responded well to the therapy sessions. Every case is different, and there's no guarantee that Joe or any other child would have the same outcome as me. Part of me is hesitant to share this story since it could ultimately be false hope for Mrs V, but I can't help but think what I'd be like today if my mum didn't get the advice that sent us to Dover Court. That was in the 1980s, by the way, so I don't know what that school is like now. I know that more special needs schools have appeared since, but I can't comment on their effectiveness since I never went through those nor know anyone who had. Mrs V could try getting Joe assessed by the therapists at Dover Court to see if therapy is an option, but she needs to be prepared for the possibility that it might not work for Joe.

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    1. Hi SN. Thanks for sharing your story. Like you said, every case is unique, every case is different and I am not a doctor - I've not even met Joe since I don't live in Singapore and allow me to assure you at least that Mrs V has gone out of her way to seek help for Joe (but no one therapist/doctor has been able to make any significance difference).

      I guess the frustrating thing for Mrs V is to be told that the therapies she has spent money on has made a difference - the argument they use is that without the help that Joe has received thus far, he would be sitting around all day, staring into space, not communicating, pooing/peeing himself.

      I guess it's a bit like me when I was fighting hairloss and spent a lot of money on therapies - they didn't bloody work, I still lost my hair and when I went back and argued that they didn't work, I was told that if I had not undergone those treatments, I would be as bald as a hen's egg today - that the treatments had made my hairloss less aggressive, that I still have some hair today is evidence of the treatments having worked to some degree. It's a catch-22 situation. I guess Mrs V was hoping for a cure - the same way I was hoping for a full head of hair. I have long accepted that I am a bald man and I shave my head regularly - I don't know if it is helpful for us to tell Mrs V that 'acceptance' can bring some peace, I don't think it is for me to tell my friend what to think.

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