Hi all,
I'll try and pack in as much info as possible without waffling!
My DS is 10 ( yr 5). He was diagnosed with a brain tumour aged 5 and had chemotherapy aged 6-8. He's been stable ever since.
Last year he had some assessments done through a hospital psychologist. The report has just become available and his processing speeds are extremely poor as is his executive function. All apparently expected due to the damage the tumour has caused and the treatment.
He's also visually impaired due to the tumour.
Academically he's doing ok, lower end of average in maths, upper end in English. His primary school are fantastic and he has great support from them. They are however unable to apply for an EHCP as he's not performing below average. I know I shouldn't, but I feel really upset about this on DS's behalf. I feel every child should be given the opportunity to achieve their best potential, yet even though school are sure with more support DS would be a achieving higher grades, he'll not manage that without the EHCP
.
School have also recommended that we have DS referred for a potential dyspraxia assessment, however have said this won't mean anything towards the EHCP.
I'm so scared about secondary school. He's a quiet, anxious child, who struggles to ask for help and would rather just try and sort stuff out for himself. I just don't know how he's going to cope.
I just don't know what to do or think.