Guest guest Posted December 6, 2006 Report Share Posted December 6, 2006 Please do not punish him this is a typical response to a child who has sensory integration dysfunction. They are either hyper or hypo sensitive to pain. Please make an appointment with an occupational therapist and have him thoroughly assessed for sensory intergration dyfunction. If he is in school the school can do an assessment. Connie Ajay Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 6, 2006 Report Share Posted December 6, 2006 Anyone have a child who is under responsive to pain? Mine is. He's 11, and on no meds. He frequently hurts himself, occassionally compulsively, but doesn't seem to feel it. For example, recently he touched the needles on my cactus, and say " Ouch " , but the " ouch " is almost surly a learned response, because he didn't flinch with it. Additionally, he continued to stick his finger back on it repeatedly, as if trying to determine how much pain he can take. If he is angry with himself, like if he forgets something important, he bangs himself on the head repeatedly with a hardback book, often leaving a knot/bruise. His doc said some meds may help for compulsions, but the best route was to punish him for it. While the logic of punishing undesirable behavior makes complete sense to me, the idea of punishing him for already hurting himself (especially if it's self inflicted punishment for a mistake) just feels counter-productive somehow. I've talked/explained about it being inappropiate to him until I'm blue in the face with no improvement. Anyone have any strategies or suggestions for coping with this type of behavior? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 6, 2006 Report Share Posted December 6, 2006 I always wondered what the connection, if there was one, to a high pain tolerance and AS...but of course, that makes a lot of sense. > > Please do not punish him this is a typical response to a child who has > sensory integration dysfunction. They are either hyper or hypo sensitive to pain. > Please make an appointment with an occupational therapist and have him > thoroughly assessed for sensory intergration dyfunction. If he is in school the > school can do an assessment. > > Connie Ajay > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 7, 2006 Report Share Posted December 7, 2006 Hi, only a moment now. But first thoughts are to redirect him whenever he starts an inappropriate behavior like the banging or touching the cactus repeatedly. Now, what to redirect him " to " I can't think of an example right now, LOL. Or when you redirect with the banging, you might have an " alternative " for him to do instead (and no idea at the moment for that either!). I imagine it will take time to replace/redirect for this strategy to begin working until it becomes routine/habit, etc. Quick thoughts this a.m.! > > Anyone have a child who is under responsive to pain? Mine is. He's 11, > and on no meds. He frequently hurts himself, occassionally > compulsively, but doesn't seem to feel it. For example, recently he > touched the needles on my cactus, and say " Ouch " , but the " ouch " is > almost surly a learned response, because he didn't flinch with it. > Additionally, he continued to stick his finger back on it repeatedly, > as if trying to determine how much pain he can take. If he is angry > with himself, like if he forgets something important, he bangs himself > on the head repeatedly with a hardback book, often leaving a > knot/bruise. His doc said some meds may help for compulsions, but the > best route was to punish him for it. While the logic of punishing > undesirable behavior makes complete sense to me, the idea of punishing > him for already hurting himself (especially if it's self inflicted > punishment for a mistake) just feels counter-productive somehow. I've > talked/explained about it being inappropiate to him until I'm blue in > the face with no improvement. Anyone have any strategies or suggestions > for coping with this type of behavior? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 7, 2006 Report Share Posted December 7, 2006 my boy is turning 4 and we first reported this to his doctor at 18 months- it was an important piece of his Sensory Integration diagnosis. No tips except to say don't punish him because his brain didn't process something! tushanna_m wrote Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 7, 2006 Report Share Posted December 7, 2006 I have read about kids who do this type of thing in the Sensory Processing Disorder group I belong to. Some report that OT that gives deep sensory input (it sounds like your son is a sensory seeker) can diminish the behavior. Then the child/parent is taught how to do deep pressure therapy at home to help too. Good luck. This must be hard as his mother to watch. <@...> wrote: Hi, only a moment now. But first thoughts are to redirect him whenever he starts an inappropriate behavior like the banging or touching the cactus repeatedly. Now, what to redirect him " to " I can't think of an example right now, LOL. Or when you redirect with the banging, you might have an " alternative " for him to do instead (and no idea at the moment for that either!). I imagine it will take time to replace/redirect for this strategy to begin working until it becomes routine/habit, etc. Quick thoughts this a.m.! > > Anyone have a child who is under responsive to pain? Mine is. He's 11, > and on no meds. He frequently hurts himself, occassionally > compulsively, but doesn't seem to feel it. For example, recently he > touched the needles on my cactus, and say " Ouch " , but the " ouch " is > almost surly a learned response, because he didn't flinch with it. > Additionally, he continued to stick his finger back on it repeatedly, > as if trying to determine how much pain he can take. If he is angry > with himself, like if he forgets something important, he bangs himself > on the head repeatedly with a hardback book, often leaving a > knot/bruise. His doc said some meds may help for compulsions, but the > best route was to punish him for it. While the logic of punishing > undesirable behavior makes complete sense to me, the idea of punishing > him for already hurting himself (especially if it's self inflicted > punishment for a mistake) just feels counter-productive somehow. I've > talked/explained about it being inappropiate to him until I'm blue in > the face with no improvement. Anyone have any strategies or suggestions > for coping with this type of behavior? > --------------------------------- Everyone is raving about the all-new beta. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 8, 2006 Report Share Posted December 8, 2006 This got better for us after about a year of biomedical treatment. All the best, Jill " And all things, whatever you ask in prayer, believing, you will receive. " Matt 21:22 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 21, 2006 Report Share Posted December 21, 2006 Just wanted to thank everyone who replied to this for your insight. The psychologist who diagnosed DID recommend SI with an OT, but I had no clue what it was at the time. I also enjoyed this morning's ongoing discussions of SI v/s ABA/VB. Seems we have a bit of an internal family battle on that issue as well, so the pros and cons were very helpful to me, and I suppose I've landed somewhere in the middle. Since the initail AS diag EONov, we've had him evaluated by an OT (because insurance does pay for that), who says the only issues she can find are a few mild handwriting issues with letter formation and speed (news to me since I thought they were severe issues, but his sample for her was close to perfect) and some pretty severe sensory disfunctions. Of course the sensory disfunctions were based entirely on a history she took from me. Never the less, she started SI with him yesterday and she taught me the brushing technique in hopes it would help him. However, she made the mistake of telling me, in front of him, that if it worked, it could permanently lower his pain threshold. He freaked out about this, and doesn't understand why I would make him do something that will make him feel pain more readily. My explainations were just inadequate for him, so now he's resistant to the brushing, though he tolerated it fine for her in the office initially. Another issue is that his Dad and I are divorced with split custody. He's with his Dad for Christmas break until the 27th, and his Dad says there is no way he is going to follow the technique every 2 hrs as recommended. He feels the SI is " voodoo " , and that we'd " have better luck shaking chicken bones at him and dancing around him " . I've sent him many links where parents have found it successful, but suspect he's pretty close minded to it. I plan to do the technique she recommended with him starting on the 27th, and see if we get any improvement before his next OT session on Jan 3. Dad feels that the OT, because it's fun, is a positive behavioral reinforcement to " get him to do what he's supposed to do anyway " . While I can see his point, I don't feel the behaviors like refusing to bath, refusing to get out of the tub, refusing to wash his face, overstuffing his mouth, gagging and vomiting at some smells others don't find offensive, having a public meltdown and ripping his clothes because a tag is scrathing him,etc are things he can control or are behavioral in nature. I can physically see his anxiety, so believe it is very real to him. Yes, I think he can be TAUGHT to behave differently when his senses " lie " to him, but I also am hoping we can use the SI to get them to stop lying to him so frequently. Now the issue is that Dad (who has done no research and attended only 2 meeting at the psychologist) thinks not only will the SI not be effective in the long run, but that the child does not even have AS and need ST/OT at all. (Our son is very mild, almost indistinguishable from peers at school, so his teachers do not want to believe the diagnosis either) Dad has convinced himself that for some reason I WANT something to be wrong with our son, and that I've brainwashed a psychologist, a ST, and an OT that our son has something he does not. Personally, I think the problem is that the more info I get and pass on from the professionals, the more Dad sees himself and does not want to think there is anything " wrong " with himself. But, that's my opinion. Meanwhile, all I can do is continue to work it, and hope that somewhere along the lines we stumble onto the right answers to help our son be more successful in life. Again, thanks to everyone in the group for for advice and shared insight. It really has been enlightening. Tushanna > > Anyone have a child who is under responsive to pain? Mine is. He's 11, > and on no meds. He frequently hurts himself, occassionally > compulsively, but doesn't seem to feel it. For example, recently he > touched the needles on my cactus, and say " Ouch " , but the " ouch " is > almost surly a learned response, because he didn't flinch with it. > Additionally, he continued to stick his finger back on it repeatedly, > as if trying to determine how much pain he can take. If he is angry > with himself, like if he forgets something important, he bangs himself > on the head repeatedly with a hardback book, often leaving a > knot/bruise. His doc said some meds may help for compulsions, but the > best route was to punish him for it. While the logic of punishing > undesirable behavior makes complete sense to me, the idea of punishing > him for already hurting himself (especially if it's self inflicted > punishment for a mistake) just feels counter-productive somehow. I've > talked/explained about it being inappropiate to him until I'm blue in > the face with no improvement. Anyone have any strategies or suggestions > for coping with this type of behavior? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 21, 2006 Report Share Posted December 21, 2006 Thanks. That is my gut feeling as well. I first reported this to the doctor when he was 18 mos too. I was told not to worry about it, that it was behavioral- " premature terrible 2's " and he would " outgrow it " . But then that was before much was known about AS, and " autism " was a " bad word " . Glad we are progressing, and so thankful for those with shared experiences like yourself. > > my boy is turning 4 and we first reported this to his doctor at 18 > months- it was an important piece of his Sensory Integration diagnosis. > No tips except to say don't punish him because his brain didn't process > something! > > > > tushanna_m wrote > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 21, 2006 Report Share Posted December 21, 2006 My AS son was under-responsive to pain until age 4. He would scrape both knees and blood would pour out of them and he did not notice he was hurt. He had ear infections where his drums would rupture & bleed and he wasn't bothered. Then he started school & saw other kids cry when they were hurt. He figured he should be upset when he saw blood on himself too. So now he has the opposite problem........when he barely bumps his arm on the wall or something minor, he FREAKS OUT!!! He cries the most dramatic cry, screams & forces tears out! It is really getting out of hand now, he will be 8 in August. tushanna_m <tushanna_m@...> wrote: Just wanted to thank everyone who replied to this for your insight. The psychologist who diagnosed DID recommend SI with an OT, but I had no clue what it was at the time. I also enjoyed this morning's ongoing discussions of SI v/s ABA/VB. Seems we have a bit of an internal family battle on that issue as well, so the pros and cons were very helpful to me, and I suppose I've landed somewhere in the middle. Since the initail AS diag EONov, we've had him evaluated by an OT (because insurance does pay for that), who says the only issues she can find are a few mild handwriting issues with letter formation and speed (news to me since I thought they were severe issues, but his sample for her was close to perfect) and some pretty severe sensory disfunctions. Of course the sensory disfunctions were based entirely on a history she took from me. Never the less, she started SI with him yesterday and she taught me the brushing technique in hopes it would help him. However, she made the mistake of telling me, in front of him, that if it worked, it could permanently lower his pain threshold. He freaked out about this, and doesn't understand why I would make him do something that will make him feel pain more readily. My explainations were just inadequate for him, so now he's resistant to the brushing, though he tolerated it fine for her in the office initially. Another issue is that his Dad and I are divorced with split custody. He's with his Dad for Christmas break until the 27th, and his Dad says there is no way he is going to follow the technique every 2 hrs as recommended. He feels the SI is " voodoo " , and that we'd " have better luck shaking chicken bones at him and dancing around him " . I've sent him many links where parents have found it successful, but suspect he's pretty close minded to it. I plan to do the technique she recommended with him starting on the 27th, and see if we get any improvement before his next OT session on Jan 3. Dad feels that the OT, because it's fun, is a positive behavioral reinforcement to " get him to do what he's supposed to do anyway " . While I can see his point, I don't feel the behaviors like refusing to bath, refusing to get out of the tub, refusing to wash his face, overstuffing his mouth, gagging and vomiting at some smells others don't find offensive, having a public meltdown and ripping his clothes because a tag is scrathing him,etc are things he can control or are behavioral in nature. I can physically see his anxiety, so believe it is very real to him. Yes, I think he can be TAUGHT to behave differently when his senses " lie " to him, but I also am hoping we can use the SI to get them to stop lying to him so frequently. Now the issue is that Dad (who has done no research and attended only 2 meeting at the psychologist) thinks not only will the SI not be effective in the long run, but that the child does not even have AS and need ST/OT at all. (Our son is very mild, almost indistinguishable from peers at school, so his teachers do not want to believe the diagnosis either) Dad has convinced himself that for some reason I WANT something to be wrong with our son, and that I've brainwashed a psychologist, a ST, and an OT that our son has something he does not. Personally, I think the problem is that the more info I get and pass on from the professionals, the more Dad sees himself and does not want to think there is anything " wrong " with himself. But, that's my opinion. Meanwhile, all I can do is continue to work it, and hope that somewhere along the lines we stumble onto the right answers to help our son be more successful in life. Again, thanks to everyone in the group for for advice and shared insight. It really has been enlightening. Tushanna > > Anyone have a child who is under responsive to pain? Mine is. He's 11, > and on no meds. He frequently hurts himself, occassionally > compulsively, but doesn't seem to feel it. For example, recently he > touched the needles on my cactus, and say " Ouch " , but the " ouch " is > almost surly a learned response, because he didn't flinch with it. > Additionally, he continued to stick his finger back on it repeatedly, > as if trying to determine how much pain he can take. If he is angry > with himself, like if he forgets something important, he bangs himself > on the head repeatedly with a hardback book, often leaving a > knot/bruise. His doc said some meds may help for compulsions, but the > best route was to punish him for it. While the logic of punishing > undesirable behavior makes complete sense to me, the idea of punishing > him for already hurting himself (especially if it's self inflicted > punishment for a mistake) just feels counter-productive somehow. I've > talked/explained about it being inappropiate to him until I'm blue in > the face with no improvement. Anyone have any strategies or suggestions > for coping with this type of behavior? > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 21, 2006 Report Share Posted December 21, 2006 My almost 18 yo is under-responsive to pain. He had the same ear problems - he wouldn't cry until it was ready to burst. I started to learn when he " might " have an ear infection and took him in many times just to check his ears. A few doc's thought I was a nut. But out regular doctor knew why we did it that way. He didn't feel a lot with his hands either. He also would come home with blood dripping down his legs and no idea he was hurt. Just last week, he cut his hand and didn't even flinch. He said it did not hurt at all but it did make a sound when the glass went in his hand. ewwwww. It took forever to stop bleeding. He is more interested in seeing the wound than anything else. Roxanna Re: ( ) Re: Under responsive to pain... My AS son was under-responsive to pain until age 4. He would scrape both knees and blood would pour out of them and he did not notice he was hurt. He had ear infections where his drums would rupture & bleed and he wasn't bothered. Then he started school & saw other kids cry when they were hurt. He figured he should be upset when he saw blood on himself too. So now he has the opposite problem........when he barely bumps his arm on the wall or something minor, he FREAKS OUT!!! He cries the most dramatic cry, screams & forces tears out! It is really getting out of hand now, he will be 8 in August. tushanna_m <tushanna_m@...> wrote: Just wanted to thank everyone who replied to this for your insight. The psychologist who diagnosed DID recommend SI with an OT, but I had no clue what it was at the time. I also enjoyed this morning's ongoing discussions of SI v/s ABA/VB. Seems we have a bit of an internal family battle on that issue as well, so the pros and cons were very helpful to me, and I suppose I've landed somewhere in the middle. Since the initail AS diag EONov, we've had him evaluated by an OT (because insurance does pay for that), who says the only issues she can find are a few mild handwriting issues with letter formation and speed (news to me since I thought they were severe issues, but his sample for her was close to perfect) and some pretty severe sensory disfunctions. Of course the sensory disfunctions were based entirely on a history she took from me. Never the less, she started SI with him yesterday and she taught me the brushing technique in hopes it would help him. However, she made the mistake of telling me, in front of him, that if it worked, it could permanently lower his pain threshold. He freaked out about this, and doesn't understand why I would make him do something that will make him feel pain more readily. My explainations were just inadequate for him, so now he's resistant to the brushing, though he tolerated it fine for her in the office initially. Another issue is that his Dad and I are divorced with split custody. He's with his Dad for Christmas break until the 27th, and his Dad says there is no way he is going to follow the technique every 2 hrs as recommended. He feels the SI is " voodoo " , and that we'd " have better luck shaking chicken bones at him and dancing around him " . I've sent him many links where parents have found it successful, but suspect he's pretty close minded to it. I plan to do the technique she recommended with him starting on the 27th, and see if we get any improvement before his next OT session on Jan 3. Dad feels that the OT, because it's fun, is a positive behavioral reinforcement to " get him to do what he's supposed to do anyway " . While I can see his point, I don't feel the behaviors like refusing to bath, refusing to get out of the tub, refusing to wash his face, overstuffing his mouth, gagging and vomiting at some smells others don't find offensive, having a public meltdown and ripping his clothes because a tag is scrathing him,etc are things he can control or are behavioral in nature. I can physically see his anxiety, so believe it is very real to him. Yes, I think he can be TAUGHT to behave differently when his senses " lie " to him, but I also am hoping we can use the SI to get them to stop lying to him so frequently. Now the issue is that Dad (who has done no research and attended only 2 meeting at the psychologist) thinks not only will the SI not be effective in the long run, but that the child does not even have AS and need ST/OT at all. (Our son is very mild, almost indistinguishable from peers at school, so his teachers do not want to believe the diagnosis either) Dad has convinced himself that for some reason I WANT something to be wrong with our son, and that I've brainwashed a psychologist, a ST, and an OT that our son has something he does not. Personally, I think the problem is that the more info I get and pass on from the professionals, the more Dad sees himself and does not want to think there is anything " wrong " with himself. But, that's my opinion. Meanwhile, all I can do is continue to work it, and hope that somewhere along the lines we stumble onto the right answers to help our son be more successful in life. Again, thanks to everyone in the group for for advice and shared insight. It really has been enlightening. Tushanna > > Anyone have a child who is under responsive to pain? Mine is. He's 11, > and on no meds. He frequently hurts himself, occassionally > compulsively, but doesn't seem to feel it. For example, recently he > touched the needles on my cactus, and say " Ouch " , but the " ouch " is > almost surly a learned response, because he didn't flinch with it. > Additionally, he continued to stick his finger back on it repeatedly, > as if trying to determine how much pain he can take. If he is angry > with himself, like if he forgets something important, he bangs himself > on the head repeatedly with a hardback book, often leaving a > knot/bruise. His doc said some meds may help for compulsions, but the > best route was to punish him for it. While the logic of punishing > undesirable behavior makes complete sense to me, the idea of punishing > him for already hurting himself (especially if it's self inflicted > punishment for a mistake) just feels counter-productive somehow. I've > talked/explained about it being inappropiate to him until I'm blue in > the face with no improvement. Anyone have any strategies or suggestions > for coping with this type of behavior? > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 21, 2006 Report Share Posted December 21, 2006 Roxanna, Was he also under-responsive when potty training? My 10yo aspie is hyposensitive to pain and was a major problem potty training - just flat out didn't notice being wet. Leah Roxanna wrote: > > My almost 18 yo is under-responsive to pain. He had the same ear > problems - he wouldn't cry until it was ready to burst. I started to > learn when he " might " have an ear infection and took him in many times > just to check his ears. A few doc's thought I was a nut. But out > regular doctor knew why we did it that way. He didn't feel a lot with > his hands either. He also would come home with blood dripping down his > legs and no idea he was hurt. Just last week, he cut his hand and > didn't even flinch. He said it did not hurt at all but it did make a > sound when the glass went in his hand. ewwwww. It took forever to stop > bleeding. He is more interested in seeing the wound than anything else. > > Roxanna > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2006 Report Share Posted December 22, 2006 I know he didn't notice being wet but we just got those extra thick cotton training pants and he learned a lot faster that way. He Still was probably 4 1/2 before he was trained. And then he was trained like magic - one day he just got it and was never wet again after that. Veeerrrry strange kid. lol. Roxanna Re: ( ) Re: Under responsive to pain... Roxanna, Was he also under-responsive when potty training? My 10yo aspie is hyposensitive to pain and was a major problem potty training - just flat out didn't notice being wet. Leah Roxanna wrote: > > My almost 18 yo is under-responsive to pain. He had the same ear > problems - he wouldn't cry until it was ready to burst. I started to > learn when he " might " have an ear infection and took him in many times > just to check his ears. A few doc's thought I was a nut. But out > regular doctor knew why we did it that way. He didn't feel a lot with > his hands either. He also would come home with blood dripping down his > legs and no idea he was hurt. Just last week, he cut his hand and > didn't even flinch. He said it did not hurt at all but it did make a > sound when the glass went in his hand. ewwwww. It took forever to stop > bleeding. He is more interested in seeing the wound than anything else. > > Roxanna > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2006 Report Share Posted December 23, 2006 has anyone asked their OT about " brushing therapy " Roxanna <madideas@...> wrote: My almost 18 yo is under-responsive to pain. He had the same ear problems - he wouldn't cry until it was ready to burst. I started to learn when he " might " have an ear infection and took him in many times just to check his ears. A few doc's thought I was a nut. But out regular doctor knew why we did it that way. He didn't feel a lot with his hands either. He also would come home with blood dripping down his legs and no idea he was hurt. Just last week, he cut his hand and didn't even flinch. He said it did not hurt at all but it did make a sound when the glass went in his hand. ewwwww. It took forever to stop bleeding. He is more interested in seeing the wound than anything else. Roxanna Re: ( ) Re: Under responsive to pain... My AS son was under-responsive to pain until age 4. He would scrape both knees and blood would pour out of them and he did not notice he was hurt. He had ear infections where his drums would rupture & bleed and he wasn't bothered. Then he started school & saw other kids cry when they were hurt. He figured he should be upset when he saw blood on himself too. So now he has the opposite problem........when he barely bumps his arm on the wall or something minor, he FREAKS OUT!!! He cries the most dramatic cry, screams & forces tears out! It is really getting out of hand now, he will be 8 in August. tushanna_m <tushanna_m@...> wrote: Just wanted to thank everyone who replied to this for your insight. The psychologist who diagnosed DID recommend SI with an OT, but I had no clue what it was at the time. I also enjoyed this morning's ongoing discussions of SI v/s ABA/VB. Seems we have a bit of an internal family battle on that issue as well, so the pros and cons were very helpful to me, and I suppose I've landed somewhere in the middle. Since the initail AS diag EONov, we've had him evaluated by an OT (because insurance does pay for that), who says the only issues she can find are a few mild handwriting issues with letter formation and speed (news to me since I thought they were severe issues, but his sample for her was close to perfect) and some pretty severe sensory disfunctions. Of course the sensory disfunctions were based entirely on a history she took from me. Never the less, she started SI with him yesterday and she taught me the brushing technique in hopes it would help him. However, she made the mistake of telling me, in front of him, that if it worked, it could permanently lower his pain threshold. He freaked out about this, and doesn't understand why I would make him do something that will make him feel pain more readily. My explainations were just inadequate for him, so now he's resistant to the brushing, though he tolerated it fine for her in the office initially. Another issue is that his Dad and I are divorced with split custody. He's with his Dad for Christmas break until the 27th, and his Dad says there is no way he is going to follow the technique every 2 hrs as recommended. He feels the SI is " voodoo " , and that we'd " have better luck shaking chicken bones at him and dancing around him " . I've sent him many links where parents have found it successful, but suspect he's pretty close minded to it. I plan to do the technique she recommended with him starting on the 27th, and see if we get any improvement before his next OT session on Jan 3. Dad feels that the OT, because it's fun, is a positive behavioral reinforcement to " get him to do what he's supposed to do anyway " . While I can see his point, I don't feel the behaviors like refusing to bath, refusing to get out of the tub, refusing to wash his face, overstuffing his mouth, gagging and vomiting at some smells others don't find offensive, having a public meltdown and ripping his clothes because a tag is scrathing him,etc are things he can control or are behavioral in nature. I can physically see his anxiety, so believe it is very real to him. Yes, I think he can be TAUGHT to behave differently when his senses " lie " to him, but I also am hoping we can use the SI to get them to stop lying to him so frequently. Now the issue is that Dad (who has done no research and attended only 2 meeting at the psychologist) thinks not only will the SI not be effective in the long run, but that the child does not even have AS and need ST/OT at all. (Our son is very mild, almost indistinguishable from peers at school, so his teachers do not want to believe the diagnosis either) Dad has convinced himself that for some reason I WANT something to be wrong with our son, and that I've brainwashed a psychologist, a ST, and an OT that our son has something he does not. Personally, I think the problem is that the more info I get and pass on from the professionals, the more Dad sees himself and does not want to think there is anything " wrong " with himself. But, that's my opinion. Meanwhile, all I can do is continue to work it, and hope that somewhere along the lines we stumble onto the right answers to help our son be more successful in life. Again, thanks to everyone in the group for for advice and shared insight. It really has been enlightening. Tushanna > > Anyone have a child who is under responsive to pain? Mine is. He's 11, > and on no meds. He frequently hurts himself, occassionally > compulsively, but doesn't seem to feel it. For example, recently he > touched the needles on my cactus, and say " Ouch " , but the " ouch " is > almost surly a learned response, because he didn't flinch with it. > Additionally, he continued to stick his finger back on it repeatedly, > as if trying to determine how much pain he can take. If he is angry > with himself, like if he forgets something important, he bangs himself > on the head repeatedly with a hardback book, often leaving a > knot/bruise. His doc said some meds may help for compulsions, but the > best route was to punish him for it. While the logic of punishing > undesirable behavior makes complete sense to me, the idea of punishing > him for already hurting himself (especially if it's self inflicted > punishment for a mistake) just feels counter-productive somehow. I've > talked/explained about it being inappropiate to him until I'm blue in > the face with no improvement. Anyone have any strategies or suggestions > for coping with this type of behavior? > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.