Wednesday 25 May 2011

I am developing an aversion to children...

Not my own you understand, but I've just had a tricky situation in the playground at school.

I'm very fortunate in that I can take my children to school most days. I know there are lots of mums who have to work so miss out on the "school run". Today I was stood chatting to a couple of the other mums, you know how it is: one eye on the conversation, one eye on the clock, one eye on my 6 year old, one eye on Tok. I was enjoying the opportunity of observing Tok in "his natural environment", he was stood with a group of children who ranged in age upto around 6. They seemed to be laughing and joking and generally enjoying themselves. But my Mummy radar was tingling (I should mention that I have special powers when it comes to sniffing out trouble) and decided a little wander to get closer to the group was in order.

I was more than a little annoyed when I heard one of the boys stage-whisper "Say the "s" word" just as another little boy ran past and said "Say pooh bum". *gutted* My little Tok thought this was a wonderful game, he loves people giving him attention and was obviously delighted to have so many children milling around him.

Suffice to say I VERY firmly told each boy "You DO NOT teach the little ones to say rude words" and stalked away. I then approached one of the Mum's to let her know what I had said to her son, and why. Sad to say that I waited with baited breath to see if she would be okay with me dealing with the situation in the way I had (I'm happy for my children to be told off in an appropriate way if they are being naughty but not everyone is) and was relieved when she said it wasn't a problem and that she'd have a word with him after school.

I'm calm.

I realise that early years of school come with their share of "rude" words being heard (as a Mum of 3 I'm hardly a novice). But what's heartbreaking about this situation is the very fine line that is being trod between "children playing with Tok" and "children showing malintent towards Tok".

How do I explain subtle difference between "larking around with friends" and "inappropriate play"? I think I would struggle to explain this to an average 5 year old let alone our little chap....

-- Mum of Tok

Friday 15 April 2011

Problems with water? What? Me? I think not!

The beauty of parenting any child (with or without ASD) is their unwavering ability to prove you wrong. Do they get taken aside at school and given "How to make Mummy/Daddy look like they don't know anything" classes?

We've gone from a screeching child in the pool on Monday, to a little boy merrily splashing around up to his neck - fetching pool toys, laughing, smiling and generally having high jinks - on Friday.

What a difference a week (and some one on one attention) makes.

Not only have we just come back from a truly fun swimming session, he also spent about an hour in the showers afterward (see previous post to understand the full gravity of that statement).

*gobsmacked and delighted*

-- Mum of Tok

Thursday 14 April 2011

Just keep swimming, just keep swimming, just keep swimming

Tok has always had issues with spaces that have poor acoustics - swimming pools, photographer studios, bathrooms and the like - he used to be absolutely TERRIFIED of bath time, it was always an epic battle that involved lots of tears (his and mine).

Over the last couple of years we have persevered and he is now able to cope with bath time (as long as we don't wash his hair) and he'll stay in the bathroom when the shower is turned on (but won't go anywhere near it).

Towards the end of last year we went on holiday and I made it my mission to get Tok into the paddling pool.

Everyday we all traipsed down to the pool, the siblings would merrily launch themselves into the deep end, throw themselves down the slide and generally enjoy themselves.

Tok would stare, tremble a little and keep asking to "go home". Bit by bit (sounds like my SALT training) we got closer and closer to the pool. Lots of comfort, lots of reassurance, sitting on the edge, dipping our toes in, getting used to the "pool" concept. On the last day of our holiday, SUCCESS! We went into the paddling pool, he was somewhat nervous at first but within minutes merrily splashing around and going down the toddler water slide - talk about from zero to hero! That's Tok all over though, it might take him a while but when he "get's it" he is off!

That was last year, this Easter break one of his siblings is having swimming lessons everyday. It's been a few months since that one and only time he's been in a pool and you could have blown me away when, whilst watching us get ready for the lesson, he announced "I want to go splish splash whoosh swimming".

Suffice to say, he only lasted 45 seconds with the instructor and I had to take him out as he was disrupting the class somewhat, but the next day he went back and lasted around 3 minutes - he walked the entire width of the junior pool (the instructor got him to run to mummy *cunning*). Yesterday I went in the pool with him and for half an hour we had a fabulous time throwing toys around, and I slowly tempted him deeper and deeper (bit by bit again) into the pool and made it all the way to his belly button. Can't wait to see what we will achieve today!

It's challenging at times, but there is no greater prize than your efforts being rewarded with your child adding to their repertoire of abilities, language, knowledge and social skills.

-- Mum of Tok

Monday 7 March 2011

Back away from the professionals Mum...

Mum has been running herself ragged the past few weeks, getting really rather irate about the fact that no-one seems to be setting any targets or working towards my IEP (Individual Education Plan).

She's got a busy week with me this week, we are off to a special hearing clinic - we tried the traditional methods of testing my hearing but I can hardly be expected to understand the "Raise your hand when you hear the beep" instructions. Not just because of my autism but also because I am only 4! So we have a fun few hours locked in a room with a very nice lady who specialises in working with kids like me.

We also have a follow up appointment at a CDAC (Communication Disorder Assessment Clinic), hence the reason Mum has been hassling the education and health professionals even more than she normally does!

Imagine her embarrassment when she got a call from my school, essentially asking her to "Chillax", there was never any intention of me having an IEP or any targets in place until after Easter. These first few weeks are all about getting me settled before the real work begins.

I think Mum would have appreciated someone letting her know before now....

-- Tok (via Mum of Tok)

Sunday 16 January 2011

Give me a reason

We are now in week 2 of a 10 week Hanen Centre programme (more details here) which provides parents of children with Autism Spectrum Disorder (ASD) and related social communication difficulties, practical tools to help their children communicate.

I have to say it has been VERY informative but of all the things we have discussed so far, the piece of information I have passed on to everyone that deals with our boy is "give him a reason to talk". Put obstacles in his way to encourage him to speak in order to get what he wants.

So: Don't give him a drink just because you 'know' he is thirsty. Stop leaving the computer turned on so he can access it whenever he wants. Put his favorite book on the top shelf. Move the yogurts to the top shelf of the fridge.

Leverage is the key to communication, make him ASK.

Obvious when you think about it, but often the very greatest ideas are the simple ones...

-- Mum of Tok

Tuesday 11 January 2011

School Daze

[I am delighted to introduce a new writer to the blog - Tok's Mum! -Ed]

So, after weeks of preparation, the "big day" finally arrived. Our littlest chap started his first day at school. All the checks had been done:
  • His new school had received the all important handover file from Nursery before Christmas, this included his Individual Education Plan, progress to date, an "all about me" summary sheet - everything you could possibly want to know about him.
  • We'd been looking at pictures of the new school and using these to ensure he understood he wouldn't be going to nursery anymore.
  • We'd been practicing saying "Good Morning Mrs (new teachers name)"
  • His uniform had been purchased and clearly named.
  • Everyone had been speaking positively about his move to "big school".
What could possibly go wrong?

Ummm, how about the fact that his new teacher was actually one of two (a job share) and that neither of them had received his file. I kid you not.

Luckily for our little chap, if there is one good thing that has come out of the last few months it's the fact that Mummy has learnt to take NOTHING for granted. A very dear friend advised us to "be a nuisance" as it was one of the only ways to get things done and this has become kind of ingrained in any dealings with the authorities.

His first day consisted of two hours in the afternoon so I "popped" into the office in the morning to ask if I could have a chat with the classroom teacher or the head teacher, just a quick catch up before his first session.... Which is when I found out that his file hadn't been passed over - it was still in the envelope I had hand delivered it in.

You can imagine how mightily unimpressed I was with this news.

When presented challenges you have to face them head on and figure out how best to deal with the situation. So, I took the file up to his new classroom and sat down for half an hour with his (Monday to Wednesday) teacher. In fairness, she asked some good questions and as time was short I encouraged her to read the "all about me" overview as this would be the best tool for her to use in the early days of her time with him.

I asked her to set up a home-school diary, she readily agreed to do this stating that it wouldn't be written in everyday, just if there was an incident to report... I'm happy to say that once I clarified that due to his main issue being one of COMMUNICATION I was looking for them to log things which I could then use as tools to facilitate communication at home and encourage him to recount his day i.e. a book they have read, an activity they did, a song they sang etc.

So, whilst not at all happy with the situation, I was at least confident that our boy would walk into an understanding environment.

As it happens, this wasn't the case, but luckily for them a fabulous little girl from his nursery (who has been somewhat motherly towards him since they first met) also joined and she very firmly took him by the hand and forcefully led him into their first session. I will be forever grateful to her.

My next course of action was thus:
  • booked an appointment with the School SENCO
  • called the SALT to explain the situation and ask her to be mindful of the fact there are two teachers involved in his case
  • called the area special needs teacher requesting she get into the school PDQ
  • booked an appointment to see the Thursday-Friday teacher
I'm pleased to report that since initially flagging the rather obvious issue that no-one was ready to receive this wonderful - albeit a little ''challenged' - child into the class, the school seem to have raised their game. He and his classmates have had a few short sessions with their first "full" day coming up soon. I have to say he seems to be happy, so far, so good...

But I'll still be keeping my appointments at the school, and will most likely be making a lot more inquiries than I would had this situation not arisen, the school has a duty of care to every child it teaches and I will be giving them a LOT of support and encouragement when it comes to mine.

One of my friends said "He's lucky to have you fighting his corner", I don't look at it as a fight, I think it's more like a journey. He's a tourist and I'm the tour guide responsible for showing him the sights, sounds and customs of this foreign culture he's found himself living in.

--Mum of Tok

Sunday 14 November 2010

Horses for Courses

I think I need to write more frequent, smaller posts. So much of the cool stuff that's happened hasn't got told because I always ending up writing an essay.

Today we took Little M for a horse riding lesson, his first for ages and asked Tokoroth if he wanted to watch his brother on a horse. He was super keen (for someone who rarely expresses a keen interest in anything other than food or going to Grandma's) and we've often been told about the connection that ASD kids make with horses.



From the moment we got there and Little M had saddled up the Tokoroth was squealing "Iwantogoonahorse Iwantogoonahorse Iwantogoonahorse Iwantogoonahorse" on permanent loop. He was so distressed he wasn't actually on a horse I couldn't let him watch his brother. The staff were pretty cool and told us that a few autistic kids ride at the school and that they get them involved with grooming, etc.

While Little M finished up his lesson, Tokoroth and I hung out in the stables meeting the horses and a smile lit up his face. The great big smile we rarely get to see. He loved the horses. Sadly this meant that when we left without him still having been on a horse and this led to a fairly predictable mini-meltdown.

 Technically a success though as the hunch about him bonding with horses paid off. Talking of paid...as thrilled as I am to see that smile I have no idea how we're going to afford lessons for both of them!

Wednesday 1 September 2010

(AS)D for Diagnosis!

The CDAC was today - the end of the line or the start of the journey depending on how you perceive it. The CDAC/CDC = Communication Disorder (Assessment) Clinic is the last of a year long series of tests, observations and interviews at home, at the hospital and at his Montessori nursery.

Tokoroth's case was passed up to the consultant paediatrician, after the earlier assessment by Dr N who thought that a more senior colleague should make the final diagnosis (because it was felt that Tokoroth was only-just or not-at-all meeting the criteria for an ASD).

I stopped blogging about all of the stages we have been going through because, as I have explained, I had grown more fearful of the Fragile X diagnosis and just stuck my head in the sand a bit and left it to Tok's mum to coordinate the battery of recent tests and interviews.

The Waiting
This morning though as we sat waiting for the team to call us in I made a list of his current strengths/deficits against the core triad of impairments. Some days he is more autistic than others, something I refer to jokingly as the 'autistic pendulum'. Although he has made a lot of progress with his IEP (Individual Education Plan) crafted by the SALT and local SENCO and implemented by the nursery with support from us I still felt he was ticking a lot of boxes. Enough, in my layperson's opinion, to warrant a diagnosis but with that diagnosis being applied according to the ICD the best I could envisage was PDD-unspecified which isn't quite as encompassing (or useful as it happens) as the (U.S.) DSM-IV-TR equivalent of PDD-Not Otherwise Specified.

Again, it's not the label that's important, it's the help and services a diagnosis unlocks as well as paving the way for a choice between mainstream school or an 'MLD' school (for children with moderate learning disorders).

I listed the characteristics he still exhibited under the social/communication/repetitive behaviour headings and wondered if I'd get a chance to present them to the consultant.

Waiting for the CDC to begin...

The Interview
The morning started with Tokoroth going off with a SALT and his special needs health visitor who, without parents present, ran him through a series of tests (possibly DISCO, I forgot to ask) and the consultant interviewed Tok's Mum and I (possibly the ADI, again I forgot to ask and was also trying not to 'flag' myself).

The interview went well and the consultant pre-empted a lot of of my concerns by evidently drawing the same conclusions from the years reports and assessments. I hardly needed to have worried that she would miss any of this stuff. She made the point about the diagnosis being made according to ICD criteria and again I kept quiet. The interview progressed and I made some gentle points about his imperative/declarative pointing and his echolalia and just like the previous paediatrician she actually welcomed these comments so I just went ahead and talked through my list and unburdened myself about the Fragile X fears. This is where everything started going really well.

The Chat
The consultant said that she felt he warranted an autism diagnosis but still had to go through the processes with her colleagues. She said that she would immediately organise a series of blood tests to rule out Fragile X, any form of thyroid problem as well as a creatine kinase test to rule out any form of muscular dystrophy. The last two tests are simply because he is small for his age but mostly just to give me something else to worry about, I'm sure.

The Waiting Revisited
Eventually we were sent out while the consultant and the rest of the team deliberated, cogitated and digested the morning's sessions. A little over an hour and some anxious coffees later we were called back in.

The Diagnosis
The jury had considered and was about to deliver its verdict. And there it was, written on a piece of paper. Right there, in black and white (and slightly pale yellow due to crappy phone camera).
The Diagnosis

I could hardly believe it. Straight up plain and simple ASD. Just as I called it a year ago before I knew my ASD from my elbow. This piece of paper was in a blue folder which, as Tok's mum put it so perfectly 'unlocks the keys to the city'.

"Wow," I said to the consultant, "he's one A short of an ASDA!" (for the Americans that's the Walmart equivalent of 'four quarters short of a dollar' and I apologise for my awful sense of humour!).

The Help
With immediate effect Tok is under the supervision of the Early Years team who mentor him through pre-school up to age 5. In addition we have regular scheduled speech and language therapy (rather than observation) and access to sign language classes, picture exchange systems and a whole set of interventions I have been coveting for the last year.

Finally, finally, some big, BIG help.

But there was still one more question to be asked: "WHAT'S IN IT FOR ME?!" and as it turns out there are some little extras like a little card that gets you priority access to toilets, let's you jump the queue at theme parks, all the, you know, REALLY useful stuff!

The Parking Permit
Top of that list of 'stuff' for me though is the revelation that we might be entitled to a blue disabled parking permit. I can't tell you how amazing these things are for parking in central London! So for another month I still have the blood tests to worry about, Fragile X could still be the cause of his ASD and a co-morbid condition. Also the bloods could reveal issues relating to his growth and development. But, in the following few weeks while I worry about that, I am under strict instructions to stop hugging him affectionately while referring to him as 'my little blue badge'!

Wednesday 14 July 2010

The CDAC! The CDAC! The CDAC is here!

You might be forgiven for thinking there had been a moratorium on this blog and that I hadn't been writing. You'd be right, kinda. I have been starting posts, just never finishing them. We had an almost successful trip to the cinema, yes the CINEMA, where I actually got him inside (with out too much force) and he watched (some of) the film. I wrote a lot about that but just couldn't get to the end.

I wrote a post about the SALT (speech therapist) visits to The Montessori. One about the meeting with the SENCO (special educational needs co-ordinator). I wrote a lot about that but just couldn't get to the end. Same story when the Early Years Action Group got involved and when everything finally came together under MAPS (multi-something something service, I have acronym overload right now and I'm too tired to Google it).

The reason I can't get to the end is because at the end of each post I have to acknowledge something. Something I don't want to acknowledge. I don't think Tokoroth is autistic. The pediatrician didn't think he was autisitic. The whatever-the-hell-the-acronym of the last person to assess him at home last week (I blogged about too, nearly) doesn't think he's autistic. Autistic traits, sure. Buckets of those. But not, they say, we think, Autistic.

You may remember I worried about this before.  I know he doesn't have Aspergers. I know he doesn't have full hell-for-leather 'Classic' autism because you don't have to be particularly well read in the subject to make an informal diagnosis for either of those. I was hoping for whatever the ICD equivalent of PDD-NOS is which, to the layperson, is, simply put, an Autism Spectrum Disorder. I'd live with that. No, actually, I'd cheer for that, because it means it isn't the thing I fear. The thing I worry about.

I've just been hiding my head in the sand, refusing to engage and generally being a bit of a twat if I'm being honest. I went out with him on his own the other weekend and we had an amazing time.


Tokoroth out with me eating falafels and houmous in N16

His, and our, quality of life is high, different and challenging, but high. He's my son and I love him and he is also a great footstool and pillow but, as a parent, knowing what is wrong is a very important part of the psychological jig-saw. If it is *that* I will cope. Just for now I'm hiding from it. But not for much longer.

Did I mention, the CDAC is here? This is THE multi-disciplinary assessment where the SALT, the SENCO, MAPS, and any other TLAs that wish to attend, along with the pediatrician and the consultant pediatrician compare notes and perform (more) comprehensive assessments and the eventual outcome of which is THE LABEL. Technically this is referred to as 'The Diagnosis' but it might just as well be called The Label and it might yet be dependent on further tests to rule in (or out) the worrying thing.

The CDAC is here. Well, it's not far away and I'm exceptionally nervous. Did I ever mention that I was a worrier?

Tuesday 13 April 2010

The unfairness of Special

It's not fair! Nothing is fair when you are young. Adults seemingly dictating all the rules, usually while contradicting them with their own behaviour. When a special needs child has siblings there is an extra twist to this.

If Tokoroth's brothers go to the fridge and take out the juice without asking they get told off. If Tokoroth does the same he gets congratulated for making himself a drink.

If Little M asks for something and get's refused and throws a tantrum he gets punished. If Tokoroth gets refused and throws a tantrum he's quite likely to get what he asked for. I'd never give into a tantrum of his brother's but meltdowns from children with specialness are, well, special. They are likely to end with him biting himself or banging his head on the table (and we never have plasters and our kitchen worktops cost a lot of money).

Joking aside, for the sibling of Tokoroth, it's just not fair. What they get told off for, he gets congratulated for, and throwing a tantrum is likely to get them nothing, but him something.

There is however another side to this unfairness. Blame culture. Today I noticed damage, well, ok, very minor damage, to our kitchen cupboards. It was very new and very annoying. We saved for years for those cupboards so I duly lined up the suspects (having eliminated the cat from my enquiries).

Me: Did you do it?
Child 1: Nuh-uh.

Me: Did you do it?
Child 2: Nope.

Me: Did you do it?
Child 3: I want pizza!

(you might be able to guess which one was Tokoroth)

Me: So....WHO did do it?

All eyes turn to the child who can't defend himself. What the siblings have figured out is that Tokoroth can't answer the charge put to him, he can't even look shifty and awkward, he simply doesn't understand the question. Instant get out clause. Tokoroth did it. Every time. And I still don't know who damaged the kitchen cabinet.

It's just not fair!