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DS2 - Opinions/advice please

(8 Posts)

DS2 was born 5 weeks early, but was ok after an initial 3 days in SCBU.

He is now nearly 8, and things have niggled about him for a while.

He was slower to talk and has speech therapy, but was discharged from that by the time he was 4. He walked at 15 months so not really late. He cannot seem to walk anywhere, and has to be running/skipping jumping, hopping all the time.

He is bright and interested in everything, can tell you all about cars and computer games and remembers facts about football, even friends registration plates. He remembers events that happened to him from years ago. confused

He thinks everyone is interested in whatever he has to say, and will interrupt conversation to tell people things totally unrelated to what they are talking about, despite being told it's not appropriate, and will often continue with what he is saying, as if he has to get the words out or burst. Often the only way to get him to stop is to drag him away. blush
He struggles to make his sentences concise when talking, and its sometimes as though he struggles to get the words he has in his head out, so there are sometimes gaps in his speech as he thinks about what he wants to say next. He usually starts by saying "do you know", and then has to think about the response when the other persons says "no, tell me".

He is accident prone, and seems a bit uncoordinated, though his child minder does not think he is worse than a lot of others she has seen. PE is not his strong point, though his is very flexible. He is possibly slightly Hypermobile, but nowhere near as much as my DD. He is mostly left handed for writing, though is fairly ambidextrous, and depending on task will switch hands comfortably.

He is doing OK at school, but his handwriting is shockingly bad. The teachers have said his handwriting and inability to be concise are holding him back, as is the speed of his work. They are frustrated because they see so much potential in him. They say his vocabulary and understanding are very good for his age. He got a 2b for writing, 2A for reading, 2A for maths and a 3 for science in his year 2 SATS. His teacher told me that if he had better handwriting and pace he would have been a 3 across the board. School however are rubbish and because he is doing ok they wont investigate or do anything else with him, other than try to give him more writing practice.

Socially he has plenty of friends, but he gets upset very easily if someone doesn't share or says something "mean" to him. He cries to the point of hysterics when this happens, but calms down quickly and once calm seems to move on from the incident very quickly. He has a lovely sense of humour and is very tactile and affectionate, of the 3 kids he is the one who can drive me made but also reduce me to tears of laughter.

I'm at a bit of a loss, because each thing on its own is not a concern, but together the put a picture in my head that niggles. I have two other DC, and I just have an itch that something isn't quite "right".

Where do I go from here? School will be useless, judging by friends experiences, though they have recently changed SENCO. But I am not sure a doctors appointment is the way to go.

Sorry it's so long, but it's taken me ages to actually put what I am thinking on paper, and reading it has actually made me realize that there is probably something going on. I'm thinking Dyspraxia/Aspergers?

kyz1981 Fri 30-Aug-13 09:37:11

Not sure but some of it sounds like you could really benefit from seeing a good OT, They would look at some of the issues in much more detail then GP's or peads especially with the movement need and the handwriting, I would ask the GP if he can refer you or tell you the process to get seen by children's OT. Hope that helps

Thank you, I appreciate the reply, I will make an appointment with the GP asap then - the only thing is would I need to take DS with me? I'm not sure picking apart the issues in front of him would be a good idea, but I am not sure if the GP would see me about him without him being there? confused

twainiac Fri 30-Aug-13 10:40:03

Hiya,
This is my first post here too!

So, not too much I can advise I'm afraid. Except to say that your DS sounds a lot like mine (although mine does not have many friends :-( )
We are in the process of diagnosis at the mo - I started with the GP, I went for an appointment without DS. The GP agreed to refer him based on what I said, however she did want to see him too. We made another appointment and told him that it was a new doctor who wanted to meet us all. Doctor had a quick chat with him and then he waited outside for a minute. The doctor said she couldn't see any problems but still referred him based on my testimony.

As for the rest of the process, well, it's been over a year now and a complete mess! But that's another story......

Good luck x

2boysnamedR Fri 30-Aug-13 11:25:55

I agree with the ot. She was key is really getting to route of my ds's issues and noticed things I hadn't. Not sure if your son needs to go the doctors with you, just write out all the points above. Except for checking hypermobilty I can't see why he needs to be there

Thanks smile I will book into the doctor when they are back at school. smile

PolterGoose Fri 30-Aug-13 11:45:22

Keep a diary, make notes of what you observe and anything you read that seems relevant, video any behaviours you think are odd or relevant in some way, eg things he only does at home. Make an appointment to see GP and take all your 'evidence'. I think he needs referring to a developmental paed, an OT and physio, based on my experience with my ds (he's 10 and has dx of Aspergers, Sensory Processing Disorder and hypermobility).

Good luck and keep posting flowers

PeteTrantersSister Fri 30-Aug-13 12:02:07

Your child sounds exactly the same as mine, (even the same SATS results!) and after problems at school last year took him to GP with a list of my concerns.
She wasn't helpful but I begged for a referral so eventually saw a paediatrician who then referred us to an OT.
Anyway, finally he has been diagnosed with hypermobility and Sensory processing disorder.
Sadly there is no help in our area for that, but I have read a lot about it and all the little issues make sense.
Maybe you could google SPD and see if it fits?

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