Although not the official school sports day, Little A was chosen to participate in the sports event called The Trevictus Games. This sports event held at our school is mainly for children with minor to severe learning disabilities not just in our school but also from other local Cornish schools. It shows how inclusive sports can be no matter your physical or mental health. Little A had a wonderful day and I feel that this shot of him jumping into the sand pit was my favourite.
Showing posts with label special needs. Show all posts
Showing posts with label special needs. Show all posts
Our Paediatric Appointment and the Start of Our Journey
The day before our appointment to see a paediatrician I wrote this post about hoping to be taken seriously and in general just hoping to get some answers.
I wasn't nervous at all about this appointment which was a good sign. I really didn't know what to expect and ever since I knew we were going to visit our paediatrician I tried to research what may happen. Everyone visits these professionals for different reasons but just to find a personal account of what a parent could expect as a rough guide would've been really comforting to me. As an anxious person, I really like to know what I'm facing so I can feel more in control! I'm writing this partly as a memory for my blog, partly as an insight into what may happen when other parents are meeting their paediatrician for the first time and it will also become part of a page that I'm setting up now we know that Little A most likely has Sensory Processing Disorder.
The Meeting:
I received my letter for appointment 3 months after my meeting at nursery with a member of staff from the Special Educational Needs (S.E.N) department. I phoned to confirm Little A's appointment at my local outpatient health clinic and waited for Thursday morning to roll around. If your child is old enough to understand i'd recommend talking to them about this appointment before you go (if you think this would be helpful) Little A didn't really understand but I told him we were seeing a special doctor.
When we entered the room, which was a basic GP surgery room with the usual equipment, bed and what not, Little A sat nearest the desk where he would soon be able to do some puzzles and drawing for the paediatrician. I was asked to clarify how old A was (very nearly 4) we spoke about a few points that were in the report from the nursery and the S.E.N department, just confirming the points and discussing how he has been getting on. At this point I mentioned the list I had brought with me (please do this parents and carers!) after a few more minutes of talking she suggested she look over this list I had put together (2 sides of A4 detailing any behaviours I could think of) immediately she asked if I heard of sensory processing. I said that I had recently come across it on line and found a processing disorder which I felt was so like my son and wanted to mention in the session today. I was given very little detail and was told they wouldn't diagnose it per-say because of his age (lots of children dislike their hair being brushed and teeth cleaned etc so it's difficult but based on other details I had written it was a case of 'this is what is most likely going on with your son.')
Little A was quite keen to interact with his doctor and after a short while his height and weight were taken (all normal) and we spoke about his eating which she confirmed was common behaviour in S.P.D, only liking very certain foods, not having a very broad range of likable foods or disliking the foods touching for example) she got A to jump and hop and balance which was all normal for his age and development. Then she spoke to Little A about the pictures he had drawn ( a spider and Olaf) with some input from myself. She spoke about his speech and I said that I'm happy to continue with speech therapy because he has come such a long way. She agreed and felt developmentally wise physically he is doing great, it is just his speech and communication that is behind.
Then Little A did some colour matching. He performed this very well, only getting 3 colours mixed up. He couldn't tell her the names of any colours but that was expected. He then did 2 simple puzzles perfectly. Seems he's achieved the goals that were set after our first meeting at nursery now I re read it! Excellent! Anyway, these were the only activities A had to participate in. We spoke about his sleep as this is a big problem for us. The only thing we can really conclude is that he has trouble when transitioning from periods of light and deep sleep. There isn't a cure, just some things we can try. I'll have to accept this as a long term problem with A and hope that one day soon he can grow out of it, could be a while!
To conclude the meeting, the paediatrician felt there were no other behavioural problems to deal with and I admitted that I felt the same but felt sure there was 'something' and Sensory Processing Disorder fits very well and means I can work with A better. We are getting A referred to an Occupational Therapist which is a common process as I understand with S.P.D in both children and adults. Hopefully we can learn what A can stand and what he really dislikes, although we are already discovering some main causes of distress.
The whole appointment for us lasted 45 minutes and was a friendly and relaxed appointment. I left feeling helped and hopeful. A was very restless by the end of it and very bored so it ended at the right time! I'm going to be doing more writing about S.P.D. I've found some blogs I want to share and to write about our own journey with A as it's all so very different; one thing I have learnt already!
Helpful Pointers For Your First Paediatric Appointment
* If you feel it's helpful, talk to your child about the upcoming appointment and what may happen if they're old enough to understand.
* If it helps your child, try to arrive a little earlier than needed (more to get used to the environment than anything else)
* Avoid anything stressful beforehand. I had to leave very early and do a nice activity with A before our appointment just so we could go slow. If A felt rushed he would've been in a foul mood and our meeting would've been very different!
* Do take a list with you. Try to be as specific as possible and don't worry about looking silly, you won't be the first nor the last person to take one of these lists with you!
* Re read any forms and reports you have prior to your meeting and even take them with you just in case. Your paediatrician will probably have the same reports as you so it's good to re read them, I tend to put them in my file and not re read for a while!
* Ask for notes. During our meeting several products and a website were mentioned which the paediatrician wrote down for me so I could look into them. I would've never remembered them as well as all the information!
* Sometimes if your child is under 5 your Red Book can be useful. It wasn't in our case but I know some clinics ask for them so it's worth checking.
* Your first appointment can vary from 30 minutes to an hour, it all depends on what you're being seen for. I'd make sure you prepare for that and also a small wait just in case. Taking some bits for your child if they're young or you know they are likely to get bored in this time (like some juice, a snack for before or after or something they find comforting) could help you.
Good luck with your appointments and if I've missed anything please let me know and I'll add them above!
Cupcake Mumma
Do I Have An Extra Special Little Man?
I want to apologise if that title is patronising to anyone firstly, but it's just how I feel, in that 'Mummy' way. That my children are so super special anyway because they are mine and they are unique and wonderful to me but over the years something has been ticking, I have been struggling and as a family we have been struggling and tomorrow I hope to see if there are any underlying reasons why our family have been finding things so difficult with Little A.
Since he was one and a half, Little A has had rather spectacular tantrums, naturally put down throughout the years as him being a very strong willed infant and toddler. He started head banging floors, walls and doors and also his bed which we had to get padded out. He then head butted his rails but he was too young to sleep without them. Doctors, health visitors and even some family members assured me he would grow out of this upsetting behaviour. I was to keep him as safe as possible and 'ride it out.'
Since he was one and a half, Little A has had rather spectacular tantrums, naturally put down throughout the years as him being a very strong willed infant and toddler. He started head banging floors, walls and doors and also his bed which we had to get padded out. He then head butted his rails but he was too young to sleep without them. Doctors, health visitors and even some family members assured me he would grow out of this upsetting behaviour. I was to keep him as safe as possible and 'ride it out.'
I can ride it out no longer. Thanks to speech therapy his communication has come on very well. He still has this at nursery. After an incident at nursery shortly after he started and which I wrote about here because it upset me so much, we shared some insights into Little A's behaviour, his likes and dislikes and sometimes very particular ones with the the staff there and this set the wheels in motion. We shortly met with a special educational needs lady who works with the council and works with schools in cornwall and she observed Little A. She spotted many things that we considered just something he did and probably every child did but which were actually behaviours on top of other behaviours that she wasn't sure about. Little A's sleep was a her biggest concern with repetitive night terrors, waking every night, being aggressive and head banging, and appearing to be asleep or at least half asleep. I agree it is a lot of work and is breaking me. I can't remember the last time my husband was beside me in bed because I am the only one able to console our son and almost always only being held very tightly in my bed calms him down.
Tomorrow morning I will be nervous but I will be armed with my forms and my own sheet of A4 paper which has both sides filled in of all the things I could think of that might be relevant to our meeting. I will blog our meeting so anyone in our situation can read what to expect from their first paediatric appointments, it's something I have struggled to find online (from a personal point) but luckily several friends have reassured me a little.
I've had many labels for my son over the last few months: Overtired, under stimulated, badly behaved, spoiled, attention seeking you name it but in my heart, deep down, I know there is something else to my boy. I believe he has trouble with sensory processing but you know, I can't say for sure, I'm not a professional after all..The way I see tomorrow, and this only a very personal way of viewing the whole thing and nothing to do with anybody else or their child, tomorrow will tell me, or hopefully soon tell me, that either there is something about my Little A's world I need to accept and learn from or I am failing him as a parent.
I'll be sure to clear my mind further after tomorrow that's for sure.
Cupcake Mumma
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