Soul-destroying

My son had difficulties that were blindingly obvious from a very early age and first flagged up at pre-school. He ticks every box apart from the “eye contact” and “ability to empathise” areas and this, along with our god-awful mistake of raising him to be polite, friendly, well mannered and behaved, has stood in the way of him getting a break his entire life.

One of my closest friends is a clinical psychologist and suspected AS when he was still very young. She couldn’t assess / diagnosis him formally but did carry out “off the record” assessments to see what the results were. She advised me to push for assessments with Educational Psychology and Clinical Psychology etc which were first completed in 2007 but never followed up because “He’s a nice boy really and I think we just need to help him to find coping strategies”

It wasn’t until I personally requested a referral to CAMHS that any further referrals were made. I asked for their input because his mental health bombed and he started pulling out his eyelashes, eyebrows and hair having become totally isolated and without any friends whatsoever.

To make matters worse he was due to transfer to secondary in 2011. His teacher supported my request to have him attend a smaller secondary where he would be less overwhelmed and more supported and helped me prepare for a panel hearing.

To try and speed things up and get the help he needed, the head teacher referred to the Consultant Paediatrician. CAMHS said they thought he might need counselling / confidence building sessions but would need to await the outcome of the Consultant Paed’s assessments.

The OT’s went ballistic when they learned he was first assessed by EP four years earlier but never followed up because there was nothing they could do other than offer advice and suggestions. He scored just below the 2nd percentile on his physical assessments, indicating significant difficulties that unfortunately, can’t now be put right.

The paediatrician was too taken with how polite and friendly my son was to listen to anything I said and couldn’t understand my concerns about the allocated school having over 1600 pupils with routines and schedules that would leave him spinning. Without a formal diagnosis to add weight to his cause and having been subjected to the most farcical hearing imaginable with utterly clueless panel members (“Why doesn’t he take medication? Can’t be that bad if he can manage without”), the appeal was not allowed and my son has been home-schooled ever since.

My options were either risk his mental health and emotional wellbeing by letting him attend a school I know full well would crucify him from the outset - or risk his general development and potentially leave him dependent on care support as an adult. Nice set of options.

He has been unfairly cheated out of any / all support he deserves because he’s a “nice” boy who likes giving people hugs and quite literally wouldn’t harm a fly. He’s missed out on a whole year’s education and emotional development by the tribunal hearing panel and I remain bitterly resentful that he has been denied so many opportunities.

I’ve applied for another appeal hearing for September this year although I’m already bracing myself for the letter that says they’re going to do nothing for him.

It’s soul-destroying beyond belief and I’ve no fight left in me. All I want is for him to go to school and be happy.

God, I’m fed up. Cry

Parents
  • Hi Parly

    I have a 12 yr old son - recently diagnosed with ASD. We ended up on the diagnosis route after my son started secondary school and then refused to go back after the first half-term. We tried a second school, but he hasn't been now since Feb half term. These schools were both smallish independent schools. We're now applying for a statement, although have been refused an assessment and we are going to have to appeal. So, although my story is different to yours, I can certainly understand how soul-destroying it all is for you. All we want for our children is to have an education and a happy life, and yet we have to fight every step of the way, and it is hard for us as parents to keep on going.

    It sounds like we were lucky to at least get the diagnosis. What is happening for you on the diagnosis front? Has somebody done an ADOS assessment with him? 

    When you say your son has eye contact - do you think he uses eye contact in the same way as other children his age? My son has eye contact, but I don't think it is the same as other children. You mentioned empathy too, until recently I'd always thought that my son had empathy. Maybe I just hadn't realised that it was possible for people not to have empathy - but now I can see that he doesn't, and it probably explains why I never used to get anywhere with him when I was trying to get him to empathise with me! Do you think that maybe because your son is nice, kind, polite that this is being confused as him having empathy. Even if he does have empathy, this shouldn't rule out a diagnosis if everything else is glaringly obvious.

    So, is your appeal hearing in September to get him into the school you want? Maybe getting your local county councillor and MP on side would be a good idea, I think this is the sort of case where they would be supportive and may be able to help. I'm assuming this is a mainstream school and that your son doesn't have a statement.

    How is your son getting on with the home schooling? My son just refuses to do anything school-like at home, so I haven't been able to educate him at all since he has been away from school.

    Sharon

Reply
  • Hi Parly

    I have a 12 yr old son - recently diagnosed with ASD. We ended up on the diagnosis route after my son started secondary school and then refused to go back after the first half-term. We tried a second school, but he hasn't been now since Feb half term. These schools were both smallish independent schools. We're now applying for a statement, although have been refused an assessment and we are going to have to appeal. So, although my story is different to yours, I can certainly understand how soul-destroying it all is for you. All we want for our children is to have an education and a happy life, and yet we have to fight every step of the way, and it is hard for us as parents to keep on going.

    It sounds like we were lucky to at least get the diagnosis. What is happening for you on the diagnosis front? Has somebody done an ADOS assessment with him? 

    When you say your son has eye contact - do you think he uses eye contact in the same way as other children his age? My son has eye contact, but I don't think it is the same as other children. You mentioned empathy too, until recently I'd always thought that my son had empathy. Maybe I just hadn't realised that it was possible for people not to have empathy - but now I can see that he doesn't, and it probably explains why I never used to get anywhere with him when I was trying to get him to empathise with me! Do you think that maybe because your son is nice, kind, polite that this is being confused as him having empathy. Even if he does have empathy, this shouldn't rule out a diagnosis if everything else is glaringly obvious.

    So, is your appeal hearing in September to get him into the school you want? Maybe getting your local county councillor and MP on side would be a good idea, I think this is the sort of case where they would be supportive and may be able to help. I'm assuming this is a mainstream school and that your son doesn't have a statement.

    How is your son getting on with the home schooling? My son just refuses to do anything school-like at home, so I haven't been able to educate him at all since he has been away from school.

    Sharon

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