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mr.ediebee

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About mr.ediebee

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    Salisbury Hill
  1. Thanks everyone for all your advice. We've reached the point now, where he won't even put the tablet in his mouth!! Have tried all your suggestions, but to no avail. With the meds being a slow release, I don't think that there'll be a liquid form. More of a worry is that he's back at school on monday after the Easter break and I feel that they'll be expecting marked improvement in his behaviour (but not their own towards us or him, that goes without saying!!!) Ediebee is dreading it, I'm dreading it, and so it goes................................................................ Mr.Ediebee
  2. Hi Everyone That is exactly what the Educational Psychologist said to us, and it is very true!! Mr.Ediebee
  3. Hi Trance We have a son with ADHD/ASD (Aspergers) and it has taken approx. 3 years to get that written down on paper. He's statemented but it isn't mentioned yet, but will be!!! We, me and Ediebee, have known what our son's difficulties are for such a long time but you can go around in circles with 'professionals' with their 'we don't want to label him' stance. We did have a wonderful Behavourial Support Worker -early years, who would speak normally to us once our son moved out of her remit. (reception) Labels are good! And don't let anyone tell you otherwise! They open doors, create contacts, help networking (Sh*t, I sound like a management seminar, sorry). I'mcertain that they don't want to give you a 'label' because that would involve 'funding' and in a world of budgets / targets / criteria, we and our children do not fit, the neuro typical 'local councillors' do not want to pay because there is always something more important, such as, digging up your perfectly good flagging and tarmac in your village centre, and replacing it block paving, herringbone style. Mr.Ediebee
  4. Me and Ediebee have agreed to go down the medication route with TS after trying all other avenues, such as diet and strageries. TS has been prescribed concerta xl, the slow release one. We're on day 4 but have hit the brick wall of TS unable to swallow the damn thing. What kind of doctor thinks that a seven year old can swallow f**king tablets?!?! I'm 37 and I have to break up paraceutamol to swallow them!!! We've tried sticking them in yoghout, pasta and ice cream. As Ediebee tries one last time (we've now up to the second hour of trying, persistence is our middle name), I've come to the conclusion that I haven't got clue anymore. I thought I was fairly well up on TS's difficulties (ADHD/ASD (aspergers)) but it would appear that I'm (and Ediebee) are just floundering in a sea of sh*t, with not a rock of sanity in sight!!! We respect the psycharatrist, we think he is a decent man, but I think this is going to unravel the fabric of our family life, I'm crying, Ediebee is crying and JM (our little man who is neuro typical and four) is crying. What do you do? Do you continue in the hope that TS will be able to swallow the tablets or do you say ###### to it and give up? The medication is 'to prevent disaffection at school and reduce the chance of exclusion', so we feel that we're getting pressure from all sides and feel that we've been backed into a corner with no chance of an exit. Family members have said that we should trust the pschartrist. #The one person I want to talk to it about, my brother, I can't because his wife is like a harpy and thinks that we are cr*p parents and that TS is spoilt and in need of a good crack. So what do you do? Please, I'm begging you, help us, we need it!!!!
  5. There's a point in the film called 'French Kiss' with Meg Ryan where she's crying in a phone box with her fist in the air, saying 'I will triumph!' That's how me and Ediebee feel.
  6. Well Phasmid I was very impressed with your advice re exclusions. TS has been 'informally' excluded twice now, but after I rather forcefully put it to the Head, that it was a training need for his staff and that he should address it, it hasn't happen since. The mid day assistants are now getting an ASD Awareness Course run by TS's EP, so bit of a result! Should really be the Head, but, you can't have everything, mustn't be greedy! Mr Ediebee
  7. When posting a reply from phasmid regarding the excellent advice given re exclusions. I was asked for the history of my boy, TS. So here goes........ TS was born in 1998, no complications, just a normal delivery. Everything hunky dory! Very good sleeper but would wake up laughing and chuckling from about 3 months, we just thought it was cute, everyone thought it was cute. No experience of children, TS, being number one son! At four months, TS, decided that sitting up would be fun, at six months crawling, at seven months cruising and on a stroke of being nine months old, walking independently. Me and Ediebee just thought that this was normal, bit advanced for his age but hey ho! Just get on with it! At ten months you could hold a conversation with him, and would have just fifteen minutes kip in the day if we were lucky, but sleep through the night and we thought, we'd rather have evenings together than him being up at all hours! Had learnt the alphabet by 14 months and by eighteen months had progressed through shapes to hexagons. They say that September 11th changed the world but none more so in this little bit of Englands green and pleasant land! While the world watched the enfolding horror, me and Ediebee were sat head in hands, not by what was on the television, but by what his first nursery had told us, 'he's simply wild and we are going to arrange an assessment for him'. Not knowing much about much at this point, we agreed. Then thinking about it, we both came to the conclusion that it couldn't be correct and phoned Early Years Ofsted who were most helpful. The manner and style of the language used was contrary to Ofsted, black mark number one, the 'we are going to get him assessed' was not a joint decision, black mark number two. Needless to say TS didn't stay at that nursery long, luckily Ediebee was pregnant with number two son and was about to go on mat leave. Problem solved, or so we thought!! Next nursery was much the same for TS but this time he had been joined by JM, his little brother. I can't praise this nursery enough! The offer in charge was brilliant with us and the staff, keeping us all onside with regards to TS. JM still goes but will leave this July for school in September. Now to TS at School! His reception teacher was excellent, however he had only been at school for just under two weeks when they lost him! He ended up on a school bus more than two miles away from home. (Jamie Lavis anyone? Child murdered by Bus driver in Manchester?) Within three weeks we had the Behavioural Support Team in (if your LEA provides such a team, befriend them, they are worth their weight in gold or at least the two Ladies who were to deal with us and TS) Had the obligatory home visit to see if we were cr*p parents, good news, it turned out that we weren't! Every cloud!!?? Eh?!? IEP put in place, failed at every turn, did poor TS. Year one teacher was the school SENCO, one thought. good, maybe they will be able to help him. But talking to other parents that we know at the school, they were scathing with regards to the teacher, oh ###### we thought! Year one was a trauma as we had to prepare to the holy cow of the 'statement'. But probably not at traumatic as it was for TS. The last term, the teacher washed their hands of him (it is a Catholic School, bit Pontus Pilot) and he was placed in another class. This helped, the teacher was a wiley old soul, been there, done that and got the t-shirt with a classroom assistant who had obviously read up on the difficulties that TS was having and pit in to practise all the advice we gave to the school. As an aside, who knows your child the best? Who can give the best advice and help to other about your child that will help others help themselves and your child? The worst thing about the situation is no matter what you say to the school, explaining behaviours and triggers and flash points before they happen, do they actually listen to you? They certainly hear you, but do they actually listen and understand. The Head is worst! Clearly just a head for the management role alone! My school, my staff and my concerns, etc etc etc!!!! We have given up all hope that the Head will ever understand! LEA declined to issue a statement initally but as we pointed out, they didn't have all the information and report, missing were the SALT and EP reports. Once they were in, they generously gave TS 7.5 hrs. We appealed giving detailed reasons regarding health and safety and were given 20 hrs. The only advice I can give is to be calm when talking about your childs and their needs to anyone at a LEA, be angry at the situation but don't lose it with the person on the other end of the phone, they are just following the guidelines set down by the nincompoops in your local town hall. THank them for their time and patience, especially if you have been a bit sharp. The Parent Partnership Officers are sent from heaven to help. Use them, take them to meetings at school, like we did, Head surprising quiet! Now TS has a wonderful LSA and his year two teacher is very much onside, now pushing an increase in his hours to 25, fingers crossed?!? TS is under the care of an excellent Psychiatrist who has a rather refreshing approach. He told us the tale of a girl who could play the piano, self taught, to near concert standard, and her school were concerned about her Geography, his answer? Why ? TS is ASD/ADHD with the ASD being Aspergers, like me, like my big brother. The Force is strong within our family. I'm thirty seven and my brother is fifty one and we're okay Mr Ediebee
  8. mr.ediebee

    The Ombudsman

    Bothered I do wonder why they are called the Local Education Authority sometimes! Local? Not on your nelly, most live outside the area paying council tax to another borough or council Education? If they cannot understand the tribunal findings, then they cannot have had an education!! Authority? This is what they specialise in! They are worlds greatest authority on making your life and ruining your child life. LEA stands for Local Egregious A***holes!!! In my opinion, and you know what they say about opinions, they are like bottoms, not always polite to give them an airing in public. Anyway, shoulders down like a front row forward and ruck and maul like Jason Leonard and Brian Moore and John Willie Mcbride and Mick Galwey rolled into one and beat them.
  9. The above-mentioned beautiful lady's husband here! Once again this morning at 10.10am at work I got 'the phone call' to collect the 'boy' from school!! Wish to God that I'd read the above before going to get him. I knew that it was not quite right that the School has asked us to collect on two occasion, but I didn't know how blatantly they have been flouting the law! Not having a good day!! Mr.Ediebee
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