DS (almost 5) has recently been ‘diagnosed’ (I know in terms of disorders etc. it’s not a diagnosis as such but for want of a better term...) with poor proprioception. He has a lot of sensory seeking behaviours and as a result he struggles to focus, play independently and has very clumsy and uncoordinated movement.
I’m reading up on it and getting increasingly concerned as, whilst activities and exercises are classed as ‘treatments’ I can’t see anywhere that says they will fix his receptors.
Is he going to need activities and input like this throughout his whole school life?
In reception it’s fine as they’re learning through play anyway, so adding in a few extra sensory activities is fine. Even through primary I can envision it, although I’m sad that he’s going to be markedly different from his peers and they will start to pick up on that. But secondary...
Will he still need this input when he’s 12/13 and what will school do about it? Is he destined to be labelled as the child who won’t listen and sit still, or is this actually going to help him focus?
For what it’s worth, this ‘diagnosis’ is no surprise to us and we already do many of the suggested activities on a daily basis (and have done since he was 2 years old). They haven’t helped so far.
I’m so worried for him 😭