A Model of stillness, calm and focus!

June 7, 2012 by in SPD with 5 Comments

Focus is defined as the ability to concentrate; to focus ones thoughts. Calm is defined as being free from excitement or passion; tranquil. Still is remaining in place or at rest; motionless; stationary. Our son Harry is defined as a ‘sensory seeker’ meaning he needs to manage and calm his nervous system through seeking out sensory stimuli, he also has proprioceptive dysfunction. This means his under responsiveness to sensory stimulus (sensory seeking need) is teamed with overwhelming needs for crashing around, stomping, chewing and general loudness and fidgeting. In society’s eyes Harry is the unruly child due to bad parenting, though let’s face it society is dissolusioned a great deal! So, I guess your wondering why all the definitions? The answer is simple Harry’s school defined him as a ‘model of stillness, calm and focus!’.  You can probably imagine our frustrations from this point forth.

This week my husband and I had simply grown exhausted from Harry’s constant meltdowns both before and immediately following school. We decided that we should write to school and ‘get them onboard’. Currently we are waiting for Harry’s OT report and so, we figured until it arrives maybe school would implement some recommendations such as weighted activities, a daily diary (for our purposes) and allowing Harry to bring his sensory ‘tools’ into school. Sadly, Harry’s school met us with opposition – Harry is a ‘model of stillness, calm and focus’! Apparently, ‘we’ are singling Harry out and ‘making’ him different. NO! Harry IS different. Yes! We accept and recognise this fact, it is imperative for Harrys wellbeing that we do. As I’m sure you can imagine I left Harry’s school feeling angry, anxious, distraught and to be perfectly honest a total emotional wreck!

Questions began to stream through my mind – have we got it wrong? Are we making him different? Why is Harry such a model pupil in school and a crazy lunatic at home? Are we going mad? Have we made it all up? No! No! No! This is absurd! If we have ‘made it all up’ why does my gut tell me otherwise? What makes the OT convinced Harry has SPD? No! We are not mad and Harry’s school should be better informed! In fact, they should be ashamed! This self doubt and tooing and throwing haunted me all day at work. Everytime someone asked ‘are you ok’? it took all the strength I had to push back the tears until I was in solitude. But, it was this mind battle that got me really, truly thinking.

Our cry for help from school was because we were trying to establish what was placing Harry into sensory overload before and after school. Although school have failed and downright refused to help us – they have helped! Let me remind you that my son is a ‘sensory seeker’, let me also remind you that Harry is defined as a ‘model of stillness, calm and focus’. Let’s evaluate this scenario – my son who needs to fidget, chew, crash, bang, stomp around and touch everything is – come on everyone –  all together now – ‘a model of stillness, calm and focus’ . On top of this his school says he is provided a FULL sensory diet, not a specific, targeted sensory diet! Alas, I wonder who needs to educate who! I mean no wonder my son is breaking down before and after school, he is  putting all he has got to conform as perfectly as possible during school.

So, as one would imagine we contacted Harry’s OT who was rather unimpressed and has insisted on a visit in school to discuss the needs of Harry in full detail. We are also due back to meet with the peaditrician and discuss where we go from here. Indeed, after my initial emotional wreckage from being dismissed and ignored I now sit here a ‘model of stillness, calm and focus’ and I send out this message to my fellow sensory families – don’t doubt, dig deeper! As for Harry’s school, watch out! A mother scorned is a dangerously determined mother indeed :D

Related Posts Plugin for WordPress, Blogger...
Be Sociable, Share!

Tags: , , , , ,
Be Sociable, Share!

About mysensorybaby

I am a mum of four beautiful children, 3 boys and 1 girl. I'm a trained secondary school teacher but currently work as a one-one support worker in a key stage 2 primary school UK. I have a sensory seeking 5yr old and I love him to pieces as I do my other 3 children. My husband and I live in SE England where the NHS is free but getting the right help is a long haul! We have had to do a whole lot of research and everytime found ourselves back at the SPD checklists! It is thanks to amazing sites like these that our son is beginning to cope with life because 'we' have learned how to support him without making things worse.

    Comments

  • MaryJane


    Hello, I think your blog is terrific.I can relate because I also have 2 sons who are diagnosed with SPD’s, along with Asperger’s and ADHD.
    I experienced the same issues with the IEP team that you’re experiencing now. I don’t know the laws in the UK, but this book helped me tremendously: “How To Compromise With Your School District Without Compromising Your Child by Gary Meyeron, Esq. It will explain a LOT of the behaviors of the school teachers, therapist and Administrators and how to get the IEP that your child deserves.
    Good Luck!!

    • Mysensorybaby


      Thanks so much we will make sure we get a copy and have a good read. Xx

  • Mary


    I don’t know if this will help you any, but my 9yo has SPD. She does not have Autism. She probably has ADHD but the school says she doesn’t. :(

    Her IEP for preschool (she wasn’t diagnosed yet then, wonderful school system not to tell me she had SPD) disappeared after preschool without my knowledge or consent.

    The school says she is a perfect angel. But like your situation with your son, I am totally exhausted by the time I get her to school. When I pick her up, her first words are “I hate you”–if she is using actual words that day, that is, and not grunts.

    What our OTs have told us is that we need to ask for a 504 instead of an IEP. I haven’t done this because I have so far been able to work with the teachers one-on-one to get her what she needs and the OT through the school system is reportedly a joke. But we have recently gone gluten-free so I will need to get paperwork started this summer on the 504. We could do without it, but I want it on record for everyone’s protection.

    The OTs have said my daughter wouldn’t qualify for an IEP and that’s why they recommended the 504 plan.

    I hope something in this helps. I’m having an ADD kind of day. :) I don’t know more about the 504 because I haven’t gotten into it yet.

  • Kaylee


    Your kid behaves himself at school. School is required to provide him with a FAPE (vs best education possible on planet earth, despite how lovely that would be) and whatever accommodations are necessary to ensure he receives it. It sure sounds like he is current receiving a FAPE without any accommodations.

    It sure looks like the school is fulfilling its legal requirements to your son right now. Should he develop a need for accommodations at school at a later date, you can revisit the issue.

  • Jenny from the Block


    I can so relate to your story! Both of my kids have elements of Harry. Hang in there!

    Leave a Comment

    Your email is never shared.
    Required fields are marked *