- I see a boy with a tongue tie who is silent ...but he has Selective Mutism so the tongue tie is irrelevant!
- The NHS website has lots of information but in essence, if it is severe enough to restrict the baby's ability to breast feed then its worth having it snipped but otherwise, there's probably no real point, in most cases. The movement required to successfully breast feed is more than enough to produce the placement necessary for speech sounds.
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Thursday, 16 July 2015
Myths and mis-information:tongue tie
Thursday, 9 July 2015
Our new Speech, Language and Communication Centre is now open!
We are happy to have a new centre, to which families can come to see us from further away. We already have families from West Yorkshire, North Wales, Sussex, Surrey and Buckinghamshire booked in. I've just taken call from someone in France who wants to come too!
We will have an official opening ceremony soon but meantime here's a preview:
Can you spot Ralph, the therapy dog waiting at the door. He's happy to welcome anyone but especially enjoys working with children with ASD and Selective Mutism. There's a safe place for him if you don't like dogs though.
This is the reception area where you can wait with a coffee. There's toys and books for the children and magazines for the adults.
From reception you go through into the therapist's room. Its full of toys but these can be screened off if they're too distracting.
This is the training room below but it's also a multi-purpose room as the tables fold away. We might use this room for very distractible younger ones or for older ones who don't want to be in a play-type room.
We are happy to see people from all over so please get in touch if you think there's anything we can help with.
We will have an official opening ceremony soon but meantime here's a preview:
From reception you go through into the therapist's room. Its full of toys but these can be screened off if they're too distracting.
This is the training room below but it's also a multi-purpose room as the tables fold away. We might use this room for very distractible younger ones or for older ones who don't want to be in a play-type room.
We are happy to see people from all over so please get in touch if you think there's anything we can help with.
Thursday, 11 June 2015
June 2015 SEND Reforms Survey
The Communication Trust is committed to supporting all those working within the reformed SEND system to meet the needs of children and young people with SLCN and their families. As part of this work, they undertook two online surveys in June and November 2014 to find out how practitioners, service providers and commissioners were preparing for and implementing the SEND Reforms. They used the valuable information gained from these surveys to ensure we are able to offer relevant support to those working with children and young people with SLCN in the areas they report needing it most.
They are now running a third survey across June 2015, to find out more about the perceived opportunities and remaining challenges of the reformed SEND system for children and young people with SLCN, almost a whole academic year on from the reforms coming into effect. The survey will take less than 10 minutes to complete and we would be extremely grateful if you would take the time to complete it and pass the link on to your colleagues and networks to help get the broadest response possible.
The survey will be open from 29th May - 29th June 2015 and is available here: www.surveymonkey.com/s/sendreformsforslcn2015.
Thursday, 4 June 2015
Billy: Born Naughty? Channel 4 series 1 episode 4
Billy aged 3 years, along with his Mum and Grandmother came to a children's centre which was local to me but was a good 3 hours drive from their home. I played with him a for a short time and then screened his spoken language skills. I was looking for: his attention level, listening ability, auditory memory, understanding level (information carrying words), vocabulary, verbal reasoning and expressive language. I was also looking for his social communication/pragmatic skills which includes three major communication
skills:
Using language for different purposes, such as
§ greeting (e.g. hello, goodbye)
§ informing (e.g. I'm going home)
§ demanding (e.g. Take me home)
§ promising (e.g. I'm going to take you home)
§ requesting (e.g. I would like to go home, please)
§ informing (e.g. I'm going home)
§ demanding (e.g. Take me home)
§ promising (e.g. I'm going to take you home)
§ requesting (e.g. I would like to go home, please)
Following rules for conversations and storytelling, such as
§ taking turns in conversation
§ introducing topics of conversation
§ staying on topic
§ starting conversations appropriately
§ finishing conversations e.g. not walking away mid-sentence
§ how to use and read verbal and nonverbal signals
§ how close to stand to someone when speaking
§ how to use facial expressions and eye contact
§ introducing topics of conversation
§ staying on topic
§ starting conversations appropriately
§ finishing conversations e.g. not walking away mid-sentence
§ how to use and read verbal and nonverbal signals
§ how close to stand to someone when speaking
§ how to use facial expressions and eye contact
It also includes Modifying language according to the needs of a listener or situation (for older children but Billy is too young for this), such as
§ giving background information to an unfamiliar listener
§ speaking differently in a classroom than on a playground
§ giving background information to an unfamiliar listener
§ speaking differently in a classroom than on a playground
He coped really well with the assessment and scored highly on everything. I'd also put out a variety toys to see what the level of his play was like. His pretend play was amazing: he used lego as soup, made Batman and Robin from square shapes and pretended with imaginary toys too.
His family were concerned that he might have Autism as his uncle has a diagnosis of ASD. They were worried that his behaviour was due to this. However, if we look at the older way of looking at ASD: i.e. the triad of impairment of language ability, social communication and flexibility, Billy scores so highly as to void any suggestion of ASD, this, together with Ravi's observations, meant I did not therefore do any formal ASD assessment. His mum is to be congratulated on a fantastic job done!
We needed to look for an different explanation of the behaviour and called in the wonderful Deb Sugden, sleep expert.
Monday, 1 June 2015
Impaired Perspective Taking: as seen on Born Naughty? Channel 4 28th May 2015
The best person to tell you more about this is Michelle Garcia Winner, the founder of Social Thinking:
Small Talk Speech & Language Therapy use Social Thinking as part of their daily work
Thursday, 28 May 2015
I lay on the floor and carried on talking....he didn't notice!: Thomas from Born Naughty episode 3
Most people have an idea of what a person with Autism might be like. This will depend on their previous experience or what they've watched for instance when Rain Man with Dustin Hoffman was shown, people assumed all children with ASD were like that with extra abilities in one area. Many teachers tell me they've worked with children with autism before when I'm discussing a potential new one, as if that makes them experts. The real truth is that the spectrum is so wide and each individual so different, that its very hard to be an expert in all aspects of ASD: 'when you've met one person with autism, you've met one person with autism' is by far the best quote I've come across. We must be aware of the aspects of ASD and potential strategies to help but each will require their own individual programme.
Diagnosing ASD can be very straight forwards with some children because the red flags are so numerous while others can be very difficult because they have become skilled at coping and the right questions must be asked in the right situations. Dr Ravi from 'Born Naughty' says that for some children, its like appraising fine art' so just like some of us may look at a Picasso and think that's definitely NOT art, others would be able to admire the subtle messages portrayed within.
When you first met Thomas, you don't see any red flags initially: non verbal communication, language skills and even pragmatic skills can look to be within normal limits to the un-trained eye. I saw him in a clinic situation at first, we chatted, played a little and did some formal and informal language assessments. He coped well with the filming and having to do things again for the camera angle. We'd dedicated the entire afternoon to the initial part of the assessment so we had a tea-break in the middle.
At this point, I hadn't spoken to his mother very much as my plan was to see her after Thomas so he could get something to eat and so we weren't talking in front of him. While we were in the kitchen area, she showed me her phone with a video of Thomas having a temper tantrum. It wasn't a major one, in fact as a mother of a child the same age, I would say it was 5/10, BUT my son would be absolutely mortified if he thought I'd told anyone let alone, videoed and shown it. Was Thomas bothered? No way, he didn't see that I would think anything.... he has impaired perspective taking, he couldn't put himself in others shoes (no theory of mind) and I needed to explore that route.
I saw him at his special sports club with his instructors: he didn't follow any instructions yet told everyone else what to do. The other children all attended special, schools but he didn't notice their differences.
I spent some time at home before doing the first session of social thinking (Garcia-Winner) which is about being a social detective. I introduce the session and then lie on the floor while I'm still talking...... did he look shocked, look to see where I'd gone, say anything about an adult lying on a classroom floor? NO, he carried on talking!! I got out the ASD assessment!
Sure enough he scored a profile which together with the parental interviews and Ravi's observations, would suggest mild to moderate ASD.
With the programme, you get a snapshot of the assessment, which actually took several days over a month. Thomas was seen at home, in a school setting, sports group setting and in a clinic by me and at home by the Paediatrician. I interviewed parents on three separate occasions too. ASD diagnosis needs to be thorough to be sure.
Perspective taking and high level ASD is fascinating and we'll look at that more another time.
Tuesday, 19 May 2015
A story about Autism by Luke ....and my brother is called Tomas
Author and illustrator Egle Gelaziute-Petrauskiene has written a lovely book about her son Tomas who has ASD. I thought you'd like to hear the story behind the book............
It was October 2006 when we
moved to the Midlands - Tomas and Lukas were
two and four – Lukas started at nursery – me and Tomas started visiting play
groups, started making friends. Tomas learned some English words, few names and
also to sing happy birthday‘
We visited places, and then
winter came with viruses and ears infections, temperatures and medicines ...
lots of crying and sleepless nights. –
In spring we noticed that Tomas made no
progress in any areas. It was June we were asking him repeatedly ,what colour
are your socks?‘- which was red‘and it took twenty repetitions to get any answer
from him. He did not want to answer. Just ignored . He did not wanted to look
at what we showed. To say his name – he wanted to play with sharp knifes and
empty bottles. Kept walking around repeating same phrases 'tom tom put bottle'
. And then all the questions we asked ourselves – why he is so cry baby in
public places, why he does not ask questions, why he is happy just be left
alone, why he is so clingy, why he does not want to play on slides and climbing
frames any more, why he is scared to death of shower and bath and stairs, why
he does not like listening to story books, why he does not play with toys just
building towers from everything?
It takes time to realise that
you need to look for help, especially when you think you have an ordinary child
– that disorder is so difficult to spot, to believe to and understand – your
autistic child looks quite normal one day, then tomorrow you think, no,
something is not right‘ – and next day he does something bright again, it is
not visible, it is not even clear at the start – it took us till Christmas to
phone the health visitor to share concerns... Tomas lost most of his
previously-had speech when he was three and half. And got the diagnosis
'working diagnosis of autistic spectrum disorders‘ next spring. He was most
severe one from that small group of kids who went for assessment together – he
could not even put any simple puzzle together nor sit still for a minute. Constantly
on the move with no purpose. Autism is a
vast spectrum and Tomas is somewhat near the bad end, but it takes years to
accept it. It takes lots of energy to swallow it and try to find ways to help, as no proper help is
readily available. We new only very little about autism at all, almost nothing,
so had to read and find out what to do.
We had to rule out all treatments advertised on line – dolphin therapies
and food therapies, food supplements made from see weeds and so on. And it is
everyday life to cope with tantrums and eating nothing, door banging, no sleep,
poor sleep. It took few years to accept that most likely he will be like that.
That's how he is. And we love him even more.
This book I wrote when Tomas
was about seven, Lukas friends used to come round or play in garden and stay
for tea, we had to meet other kids in school summer fairs, outings, parks – I
realised it is not clear for kids, not
even for adults, as if it would have been to me before Tomas why is that – why
he is screaming and shouting, why he is eating so strangely and why he is
allowed to do that, why we cant accept invite to party in swimming pool, why
mum looks too tired – all that.
Autism is invisible
disability. You have to explain a lot.
Why why why? When he will talk ? Will he
grow up and will be normal? In the book i tried to explain things through Lukas
point of view – using simple words and lots of illustrations. About everyday life. That's it- we live with
Tomas and life is a bit different because of that. We do not know what future
holds for him and us, but no one knows. So I just hope that this book will be
helpful and will give more understanding about families affected by autism.
We also rise money from this book for NAS Stafford branch and, as this
playgroup was the place were we could turn for advice- they try to find whats
around and having opportunity to meet other families in same situation is
priceless. No judging looks at your child there too.
And yes, if you see a child in
the park running quickly to you to fetch your bottle of drink paying no
attention to any protests (and mum running after him) that might be someone
just like Tomas. Be patient, be aware
that autistic kids and they families exist, and they go to parks too..and they
try their best to behave! Do not tell them off.
Tomas mum, Egle
Gelaziute-Petrauskiene
This book will be available from our new website when it launches next week www.speechtherapyactivties.co.uk
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