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Help why do they think Im the cause?
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<blockquote data-quote="Matty's Mummy" data-source="post: 240174" data-attributes="member: 5222"><p>With have a child with Down syndrome, our house has pitchers of animals object . and sign language pics and font, to go with them all. So Im buggered if they think Im pushing Matthew lol No just kidding its all aimed at As level not Matts </p><p></p><p>yes ok good point</p><p>It was the Pead who said possibly Obsessive Compulsive Disorder (OCD), but the Pead Occupational Therapist (OT) has put just about all of it down to Sensory disorder. </p><p>What I need from mental health (M/H) is for them to look at all the quirks (as the Pead called them, with the possibility of some being Obsessive Compulsive Disorder (OCD))but they need to figure this out, what is what. I had hoped going to them they would have more of a team, that could possibly work this out. </p><p> </p><p>Instead they freaked me out with Its learned behaviour oh and another thing I forgot to mention is, they want me to take Matt to their Psychiatrist, who specialises in Kids. So that is great, only I did make it clear I wont be putting him on medication. I did also say (as I did to the Pead when she mentioned medications) was that I would only go down the medication path if he went back to how he was, when he had all that anxiety but only if it didnt go, Id give him time to work through it first </p><p> </p><p></p><p> </p><p><span style="font-size: 10px">Im taking notes thanks and will remember this for if we ever get a diagnosis. </span></p><p><span style="font-size: 10px">Sounds like youve been through it all, which is helpful to me but Geesh its a lot to deal with. </span></p><p> <span style="font-size: 10px"></span></p><p><span style="font-size: 10px">With Matts hair pulling once we told him and showed him the spot, it wasnt long and he stopped which was good. </span></p><p><span style="font-size: 10px">Once the Occupational Therapist (OT) sends me her report we should be able to get a clearer pitcher of what is sensory and whats not. </span></p><p> <span style="font-size: 10px"></span></p><p><span style="font-size: 10px">So far the school has been wonderful, I really wanted a diagnosis or something to give them but it wasnt needed. It was good they put so much in place by what the special school had sent over, which wasnt much. </span></p><p> <span style="font-size: 10px"></span></p><p><span style="font-size: 10px">We have noticed a huge change in Matthews behaviour, since cutting out some foods mainly fruit. </span></p><p><span style="font-size: 10px">I did mention this to them but didnt really get a response. </span></p><p><span style="font-size: 10px">Is it worth perusing this food stuff with them or do that on my own separately? Its just I know the Pead was and doctors see m to have once response alternative even vitamins for my child with Ds the Pead said they arent needed and are alternative then she doesnt discus it further. </span></p><p> <span style="font-size: 10px"></span></p><p><span style="font-size: 10px">any thougths on this ?</span></p><p><span style="font-size: 10px"></span></p></blockquote><p></p>
[QUOTE="Matty's Mummy, post: 240174, member: 5222"] With have a child with Down syndrome, our house has pitchers of animals object . and sign language pics and font, to go with them all. So Im buggered if they think Im pushing Matthew lol No just kidding its all aimed at As level not Matts yes ok good point It was the Pead who said possibly Obsessive Compulsive Disorder (OCD), but the Pead Occupational Therapist (OT) has put just about all of it down to Sensory disorder. What I need from mental health (M/H) is for them to look at all the quirks (as the Pead called them, with the possibility of some being Obsessive Compulsive Disorder (OCD))but they need to figure this out, what is what. I had hoped going to them they would have more of a team, that could possibly work this out. Instead they freaked me out with Its learned behaviour oh and another thing I forgot to mention is, they want me to take Matt to their Psychiatrist, who specialises in Kids. So that is great, only I did make it clear I wont be putting him on medication. I did also say (as I did to the Pead when she mentioned medications) was that I would only go down the medication path if he went back to how he was, when he had all that anxiety but only if it didnt go, Id give him time to work through it first [SIZE=2]Im taking notes thanks and will remember this for if we ever get a diagnosis. Sounds like youve been through it all, which is helpful to me but Geesh its a lot to deal with. With Matts hair pulling once we told him and showed him the spot, it wasnt long and he stopped which was good. Once the Occupational Therapist (OT) sends me her report we should be able to get a clearer pitcher of what is sensory and whats not. So far the school has been wonderful, I really wanted a diagnosis or something to give them but it wasnt needed. It was good they put so much in place by what the special school had sent over, which wasnt much. We have noticed a huge change in Matthews behaviour, since cutting out some foods mainly fruit. I did mention this to them but didnt really get a response. Is it worth perusing this food stuff with them or do that on my own separately? Its just I know the Pead was and doctors see m to have once response alternative even vitamins for my child with Ds the Pead said they arent needed and are alternative then she doesnt discus it further. any thougths on this ? [/SIZE] [/QUOTE]
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