Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 I think so...My son has processing issues and has Apraxia (well now Dyspraxia because he talks). I'm trying out the Listening Therapy for my son to address his auditory processing problems staring Feb. 15th. Look up Alfred Tomatis studies....it's really interesting! Can anyone tell me (or give me an opinion) -- When a child has apraxia, and is diagnosed as " processing more slowly " than normal -- are the two related? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 In a message dated 2/4/2008 5:28:04 P.M. Eastern Standard Time, kiddietalk@... writes: Even to the general public the words " This is why I brought up partial paralysis as an example. Again you can't judge one's ability on their disability. So yes an apraxic child may tie his shoe slower, but that doesn't mean he cognitively doesn't understand what he 'needs' to do -he has trouble executing the motor skills needed to perform the task as quickly as he wants. So an apraxic has slow processing on actions -not slow processing on thoughts. There is a difference. I agree with this statement, but just wanted to point out that there are so many different things that people may be referring to when they use the term " slow processing " in reference to our kids. I don't think that most people MEAN to offend with this term, but rather lack ANOTHER term to use that might describe the thought behind what they are referring to. I know that I sometimes think of Asa as having " slow processing " even while the child is literally a genius and I KNOW he has no problem with processing the THOUGHTS of things, but of course, since it's a motor planning problem, I know he has the problem of EXECUTION to those tasks-- so it can actually be, depending on how a person is using the term-- can be, in fact, slow processing. (even though we know it's not the processing on the thoughts or brain) I dunno if I'm saying this to make sense, because I AGREE with what you've said above, because my son has Global Apraxia/Developmental Dyspraxia, so I've seen those looks people give when they assume he's " not all there " and that he's " slow " , and there's nothing further from the truth! But I think they just lack the FULL UNDERSTANDING of the condition, so the terms can sometimes be misused or used in an incorrect situation. Becky **************Biggest Grammy Award surprises of all time on AOL Music. (http://music.aol.com/grammys/pictures/never-won-a-grammy?NCID=aolcmp00300000002\ 5 48) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 Apraxia does not go hand in hand with slow processing!!! Yes there could be children in this group who have other diagnosis co existing with the apraxia. As parents of children that are verbal disabled -if you give up and believe your child to have " slow processing " then who is there to advocate for him or her? And perhaps some have to look outside of the verbal disabled box into one most have more understanding of. If a child has partial paralysis and takes more time to follow a task due to that partial paralysis...does that mean he has " slow processing " or that he needs a bit more time to overcome his disability? You have to test processing on ability -not on disability -or that is a violation of that individual's civil rights! Our children with apraxia have to overcome a motor planning disorder of speech which takes them longer to motor plan. (try doing anything while looking in a mirror and you'll understand better what they deal with every minute of their life) They have so much discrimination to fight against in the world being there is so little awareness of apraxia - as is one would suspect based upon more recent autism awareness that autism and apraxia are one in the same. They are not. Autism is not just a lack of speech -apraxia could be. But many with apraxia have low tone, sensory issues to deal with too. I've been saying for years to not pile up diagnosis on diagnosis unless you know for sure that it's needed to help that child. What good would the diagnosis of slow processing do to a child and their future? Or should we say " what bad " which is more like it. Give the children without a voice the benefit of the doubt like I did -and let them prove everyone wrong like my son Tanner did. In almost all cases they will -check the archives. Here's my son Tanner story http://www.cherab.org/information/familiesrelate/letter.html Here's an archive on " diagnosis du jour " start of archive from 2004~~~~~~~~~~~~~~~~~~~ I know this was not one of your questions...but at what age - considering how well your daughter is doing especially -do they stop using the diagnosis " developmental language disorder " ?... Why not just " language disorder? " Speaking of which -you want to be sure that what your daughter has truly is a language or receptive disorder and not just an expressive disorder, or a combination of both receptive and expressive. Too many communication impaired children are assumed to have receptive disorders that do not. Typically a child with " just " a language disorder does not have other neurological " soft signs " like DSI (sensory integration dysfunction) so you may want to make sure the language disorder diagnosis is correct. A great person to speak to about this is Dr. a Tallal who is an advisor to the CHERAB Foundation. http://www.cherab.org/information/speechlanguage/advisoryboard.html " SLI is a developmental language disorder in the absence of frank neurological, sensori-motor, non-verbal cognitive or social emotional deficits (see Watkins, 1994). " http://web.gc.cuny.edu/Speechandhearing/labs/dnl/sli.htm As Dr. Tallal and I discussed one day -unfortunately a late talker - may be diagnosed or misdiagnosed as apraxic, PDD, speech language impaired -or just plain old speech delayed depending upon where you live in the country or the world and who you see on a particular day. And speaking of early signs of a language disorder from another CHERAB advisor - Kaufman: http://www.kidspeech.com/signs_recept.html Until there is genetic, blood, or other testing to know for sure, speech and language impairment diagnosis are up to the whim of the professional diagnosing them. It's not clear cut like a broken arm...or a cut, and due to the varied diagnosis and assumptions of the child's capabilities, the therapies and treatments vary, some being more appropriate than others for the specific child, some even being inappropriate. This is why it's so important to seek out the most accurate diagnosis so you can seek the most appropriate therapies to best help your child get up to speed prior to kindergarten if possible. Due to the epileptic pattern in the left temporal lobe, what does the neurodevelopmental doctor have to say? What grade is your child in and what type of placement? Is she mainstreamed in kindergarten or first grade for example. Does she have friends, or have trouble making friends? How does she communicate and how often do others understand her? I'm sure all is OK since you say it seems like now she is on the right track -just wanted to post all of the above just in case. ~~~~~~~~~~~~~~~~~end of archive from 2004 ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 Apraxia is a neurological motor planning disorder - the message to/from the brain to the affected areas of the body (verbal, oral, limb, etc.) is not getting through in a clear, consistent, and efficient manner. So, yes, apraxia is equated with " slow processing. " Also, from my understanding, apraxia is the absence of something - thus the absence of the neurological messages in, for our kids, speech production. Dyspraxia is the inconsistency in the messages. So, you are really correct in saying that because your ds now is speaking, it probably should be referred to as dyspraxia (although most of us here still call it apraxia - we all still have a pretty darn good idea what we all mean!). Sherry and Josh myra.bauza@... wrote: I think so...My son has processing issues and has Apraxia (well now Dyspraxia because he talks). I'm trying out the Listening Therapy for my son to address his auditory processing problems staring Feb. 15th. Look up Alfred Tomatis studies....it's really interesting! Can anyone tell me (or give me an opinion) -- When a child has apraxia, and is diagnosed as " processing more slowly " than normal -- are the two related? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 Isn't the processing issue related to neuropathy? > > Apraxia does not go hand in hand with slow processing!!! > > Yes there could be children in this group who have other diagnosis co > existing with the apraxia. As parents of children that are verbal > disabled -if you give up and believe your child to have " slow > processing " then who is there to advocate for him or her? And > perhaps some have to look outside of the verbal disabled box into one > most have more understanding of. > > If a child has partial paralysis and takes more time to follow a task > due to that partial paralysis...does that mean he has " slow > processing " or that he needs a bit more time to overcome his > disability? > > You have to test processing on ability -not on disability -or that is a > violation of that individual's civil rights! > > Our children with apraxia have to overcome a motor planning disorder > of speech which takes them longer to motor plan. (try doing anything while looking > in a mirror and you'll understand better what they deal with every > minute of their life) They have so much discrimination to fight > against in the world being there is so little awareness of apraxia - > as is one would suspect based upon more recent autism awareness that > autism and apraxia are one in the same. They are not. Autism is not > just a lack of speech -apraxia could be. > > But many with apraxia have low tone, sensory issues to deal with too. > > I've been saying for years to not pile up diagnosis on diagnosis > unless you know for sure that it's needed to help that child. What > good would the diagnosis of slow processing do to a child and their > future? Or should we say " what bad " which is more like it. Give the > children without a voice the benefit of the doubt like I did -and let > them prove everyone wrong like my son Tanner did. In > almost all cases they will -check the archives. > > Here's my son Tanner story > http://www.cherab.org/information/familiesrelate/letter.html > > Here's an archive on " diagnosis du jour " > > start of archive from 2004~~~~~~~~~~~~~~~~~~~ > > I know this was not one of your questions...but at what age - > considering how well your daughter is doing especially -do they stop > using the diagnosis " developmental language disorder " ?... Why not > just " language disorder? " > > Speaking of which -you want to be sure that what your daughter has > truly is a language or receptive disorder and not just an expressive > disorder, or a combination of both receptive and expressive. Too > many communication impaired children are assumed to have receptive > disorders that do not. > > Typically a child with " just " a language disorder does not have > other neurological " soft signs " like DSI (sensory integration > dysfunction) so you may want to make sure the language disorder > diagnosis is correct. A great person to speak to about this is Dr. > a Tallal who is an advisor to the CHERAB Foundation. > http://www.cherab.org/information/speechlanguage/advisoryboard.html > " SLI is a developmental language disorder in the absence of frank > neurological, sensori-motor, non-verbal cognitive or social > emotional deficits (see Watkins, 1994). " > http://web.gc.cuny.edu/Speechandhearing/labs/dnl/sli.htm > > As Dr. Tallal and I discussed one day -unfortunately a late talker - > may > be diagnosed or misdiagnosed as apraxic, PDD, speech language > impaired -or just plain old speech delayed depending upon where you > live in the country or the world and who you see on a particular day. > > And speaking of early signs of a language disorder from another > CHERAB advisor - Kaufman: > http://www.kidspeech.com/signs_recept.html > > Until there is genetic, blood, or other testing to know for sure, > speech and language impairment diagnosis are up to the whim of the > professional diagnosing them. It's not clear cut like a broken > arm...or a cut, and due to the varied diagnosis and assumptions of > the child's capabilities, the therapies and treatments vary, some > being more appropriate than others for the specific child, some even > being inappropriate. This is why it's so important to seek out the > most accurate diagnosis so you can seek the most appropriate > therapies to best help your child get up to speed prior to > kindergarten if possible. > > Due to the epileptic pattern in the left temporal lobe, what does > the neurodevelopmental doctor have to say? > > What grade is your child in and what type of placement? Is she > mainstreamed in kindergarten or first grade for example. Does she > have friends, or have trouble making friends? How does she > communicate and how often do others understand her? I'm sure all is > OK since you say it seems like now she is on the right track -just > wanted to post all of the above just in case. > ~~~~~~~~~~~~~~~~~end of archive from 2004 > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 I think the two are separate issues, but they are frequently co-morbid conditions. I just watched the NACD dvd on Learning and Attention Problems (very good!), and I learned some very interesting things about auditory processing. There are many frequencies of sound from 20Hz to 20,000, but hearing tests only test 6-8! You can pass a hearing testing and still have significant hearing issues. The brain learns to process specific frequencies of sound in the first two years of life, but this process can be interrupted any time there is fluid in the middle ear (not just ear infection). This problem is almost never identified. (It can be easily detected by a tympanagram, but pediatricians do not usually do this test.) Bob Doman thinks that dairy products are a large part of the problem. When this development doesn't happen, the ear can't process tones, language development is delayed and, since it affects the vestibular system, motor development can be delayed as well. The Listening Program re-educates the brain to process sound (tonal processing). According to Bob Doman, about 1 in 1,000 kids who have auditory problems have a problem with processing tones fast enough. Since they are slow to process the first tone of a word, they can't move on to the next sound, etc. FastForward is a program that works on that type of problem. And then there is auditory sequential processing, which is improved by practicing digit spans. Also, there is auditory dominance, which affects long memory (storage) of information. The NACD likes kids to have their dominant ear, eye, hand, and foot all be on the same side, and they give activities to make this happen. I think many SLPs and other experts tend to misuse one term for the other. A good audiologist can probably tell you which type of problem your child has, but they usually don't want to evaluate them until they are 6-8 years old. In the meantime, you have lost valuable time. That's why I love the NACD approach. They can give you stuff to improve today. in NJ > > Can anyone tell me (or give me an opinion) -- When a child has apraxia, and is diagnosed as > " processing more slowly " than normal -- are the two related? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 Right after I posted my message I thought about the fact that apraxia 'is' a motor planning disorder so thanks for bringing this up Sherry! Yes you are correct that apraxia is a motor planning disorder and at times they will take longer to do things based on their motor planning disorder -but that doesn't exactly mean that our children have " slow processing " in regards to a cognitive/receptive angle/separate diagnosis which is the direction I based the emails when auditory processing as a diagnosis was brought up. Even to the general public the words " This is why I brought up partial paralysis as an example. Again you can't judge one's ability on their disability. So yes an apraxic child may tie his shoe slower, but that doesn't mean he cognitively doesn't understand what he 'needs' to do -he has trouble executing the motor skills needed to perform the task as quickly as he wants. So an apraxic has slow processing on actions -not slow processing on thoughts. There is a difference. As you know as a mom -our children desperately at times know what they want to say or do -but can't. I just as always want to make sure that those with apraxia are not underestimated -so I will always be the one (at times lone) voice that believes in the untapped ability of that verbal disabled child. " Never underestimate the power of dreams and the influence of the human spirit. We are all the same in this notion: The potential for greatness lives within each of us. " Wilma Rudolph quotes (First American woman Runner to win three gold medals at a single Olympics. 1940-1994) ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 Maybe it is me but I am less hung up on labels. I also have the benefit of a young child who has yet to be scarred by labels but here is my take on the whole processing thing. My child is slow in processing in three areas. Auditory processing: be it a B12 deficiency, yeast or toxins, something has prevented him from hearing things correctly and he therefore can't articulate well. Whether that continues now or whether his current articulation is from simply hearing things wrong for so long I do not know. It is likely a combo and I am intent on finding the cause and the solution. His second delayed processing area is visual. He just got glasses so whether he has true phonemic awareness issues or whether he is just now seeing things right and we have to play catch up I do not know. What I do know is that he was holding an " O " from a game and saying " It's an O " when he was on E which I had to take him off of to address a bleeding issue. It will be nice if I can get that back. Lastly, he has an issue with his hands. The OT said he crossed the midline but something is up with his hands. My guess is he did not cross it properly and that he has peripheral neuropathy that interferes with this intermittently. It is the best it has ever been but we must investigate MB12 issues and general toxicity among other things to see what is behind this. > > Right after I posted my message I thought about the fact that > apraxia 'is' a motor planning disorder so thanks for bringing this up > Sherry! Yes you are correct that apraxia is a motor planning > disorder and at times they will take longer to do things based on > their motor planning disorder -but that doesn't exactly mean that our > children have " slow processing " in regards to a cognitive/receptive > angle/separate diagnosis which is the direction I based the emails > when auditory processing as a diagnosis was brought up. Even to the > general public the words " This is why I brought up partial paralysis > as an example. Again you can't judge one's ability on their > disability. So yes an apraxic child may tie his shoe slower, but > that doesn't mean he cognitively doesn't understand what he 'needs' > to do -he has trouble executing the motor skills needed to perform > the task as quickly as he wants. So an apraxic has slow processing > on actions -not slow processing on thoughts. There is a difference. > As you know as a mom -our children desperately at times know what > they want to say or do -but can't. I just as always want to make > sure that those with apraxia are not underestimated -so I will always > be the one (at times lone) voice that believes in the untapped > ability of that verbal disabled child. > > " Never underestimate the power of dreams and the influence of the > human spirit. We are all the same in this notion: The potential for > greatness lives within each of us. " > Wilma Rudolph quotes (First American woman Runner to win three gold > medals at a single Olympics. 1940-1994) > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 This is where mainstream medicine served us well. We had that test and my son has that issue and it is resolving. He had fluid, it was never infected, but would not leave. That, for him, was milk. Doris Rapp says that children requiring tubes typically need to be off milk and that that allergy causes the problems requiring the tubes. Similar to what my ENT said about our son...after the darn surgery! Doris Rapp also says that despite the belief that children grow out of milk allergies typically 75% of them do not but they allergic reaction that occurs is different and leads to other issues. That explains the bald and gut impaired members of my family who think they grew out of it. Asthma is another milk allergic indicator according to Rapp or Bock (can;t say as I am reading both at the same time). , this is a big help. At least I understand why we have had such a great response to TLP. Also makes me think catching the milk thing early (though not early enough for my eternal mommy guilt) saved us from a much worse condition. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 Absolutely, - I've been around this board for quite some time and you know I would never underestimate what our kiddoes are capable of accomplishing! Yikes, when you figure that evil doc originally saying Josh had MR, would never walk unassisted, would never speak intelligibly - and look what he's accomplished over the years! I never meant to imply that our kiddoes have some cognitive issues or muscle tone issues or sensory issues affecting their ability to process - unless, of course, that has been a proper diagnosis in addition to the apraxia (which, in Josh's case, it has). So, as I wrote, apraxia is a motor planning disorder which, in and of itself, does affect the processing of the neurological messages. Sherry and Josh (who, notwithstanding what the evil doc said years ago, was a gold medal winner in Special Olympic basketball skills and will be going to the State competition next month! HAH! to that doc!!!) kiddietalk <kiddietalk@...> wrote: Right after I posted my message I thought about the fact that apraxia 'is' a motor planning disorder so thanks for bringing this up Sherry! Yes you are correct that apraxia is a motor planning disorder and at times they will take longer to do things based on their motor planning disorder -but that doesn't exactly mean that our children have " slow processing " in regards to a cognitive/receptive angle/separate diagnosis which is the direction I based the emails when auditory processing as a diagnosis was brought up. Even to the general public the words " This is why I brought up partial paralysis as an example. Again you can't judge one's ability on their disability. So yes an apraxic child may tie his shoe slower, but that doesn't mean he cognitively doesn't understand what he 'needs' to do -he has trouble executing the motor skills needed to perform the task as quickly as he wants. So an apraxic has slow processing on actions -not slow processing on thoughts. There is a difference. As you know as a mom -our children desperately at times know what they want to say or do -but can't. I just as always want to make sure that those with apraxia are not underestimated -so I will always be the one (at times lone) voice that believes in the untapped ability of that verbal disabled child. " Never underestimate the power of dreams and the influence of the human spirit. We are all the same in this notion: The potential for greatness lives within each of us. " Wilma Rudolph quotes (First American woman Runner to win three gold medals at a single Olympics. 1940-1994) ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 I think this is where autism and apraxia have crossed paths. We all know that there is something going on neurologically with unparallel development. Addressing the issues through therapy and biomedically is what apraxia and autism have in common. Autism to me is just a wider spectrum of disorders and include apraxia. The old autism model (classic Kraner model) does not really apply as much as Autism Spectrum Disorder does in today's times. As for as disorders involving autism, some kids have a few, and some kids have more. What I have learned though that all of these kids are actually very smart in different ways, Unfortunately when you start to fine tune the diagnosis, sometimes you are denied services for disorders that are not quite defined. I actually was denied some support because the doctor diagnosed my kids with Autism Spectrum Disorder and not Autism. UGG! Its the same thing. On the other hand I was given more services than I would have if the dx would have been just apraxia. This is where labeling gets in the way. I wish the dx could just be " something's not right, and some things are very right " and just help my child where there are shortfalls. I am happy to report though that after 9 months of diet and biomedical interventions, the autism and apraxia have resolved for one of my twins and the other is doing quite well. All fine and large motor skills are there and we now have beautiful articulation. His receptive language is near age appropriate, but his expressive language is a little to selective to be normal. No real therapies done. A few weeks ago we started OT and PT and ST. We were on a 9 month waiting list. The therapists are all scratching their heads wondering why we are there.(except for the ST and OT for the one twin that still has some minor issues) So I will have to jump on board with Liz. More concerned with what has prevented my child from developing normally and reversing it. Along this path comes the necessary rehabilitation (therapy). I am sure some kids have fully recovered from using one or the other but I am just covering my bases. Nickerson [ ] Re: Apraxia and Slow Processing > Maybe it is me but I am less hung up on labels. I also have the > benefit of a young child who has yet to be scarred by labels but here > is my take on the whole processing thing. My child is slow in > processing in three areas. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 Liz there is much in the archives and in research about self- fulfilling prophecies and the research of Dr. Rosenthal. Please don't assume that it's OK because your child is younger to say your child is " slow " in three areas! There is a huge problem with many here assuming that apraxia and processing disorders co exist or that children with apraxia have slow receptive/cognitive processing skills which is also a sign of mental retardation. And the fact so many today are accepting this is very sad. Perhaps unlike the children here from over the years like my son Tanner -the children in the group today won't be mainstreamed. Is that the belief? Because belief becomes reality and you get to choose now. Your child's future depends in some part on your belief. Isn't it a mother and father's instinct to raise our child up? And to answer the question about therapy for another diagnosis working. Many here with autistic children found some of the methods used for apraxia to work as well. The Kaufman Kit can be used by any late talker- even one that isn't apraxic. We tried various therapies for Tanner that are used for deaf children including learning sign -that doesn't mean Tanner is deaf. Just because a therapy helps doesn't mean a child has the diagnosis that therapy was originally designed for. Please do some homework on the awesome Dr. Rosenthal and the work he has done. You will also find much about him in the archives. Sadly if you believe your child to be slow..in three areas no less -you 'are' probably going to find out you are right. When nobody else believed in Tanner Glenn and I did and guess who proved everyone but us wrong -not us -but Tanner did! I loved sharing the whole story with Dr. Rosenthal because he is brilliant and he is the one that inspired me. And I saw it work. They could have been right and Tanner would have been in special ed today. http://www.cherab.org/information/familiesrelate/letter.html I know some of you don't understand this -but again don't assume the worst and don't underestimate those that can't verbally prove you wrong...yet. Sometimes it's best to be wrong and if you believe apraxia and slow processing of receptive or cognitive skills go hand in hand -then you 'are' wrong. Apraxia is not a cognitive disorder. And even if in your child's case you were right and for example one's child has co existing mental retardation with the apraxia -you are still best to believe in your child and give the benefit of the doubt. Look at Robin's daughter -it's a hard pill to swallow to be wrong -or assume others are right with bogus diagnosis about your child - years down the road. http://www.cherab.org/news/.html And while for ethical reasons Dr. Rosenthal's research was done in the positive -in speaking with him he agrees that it works both ways. If that's the case why think anything but the positive? http://www.facultydirectory.ucr.edu/cgi-bin/pub/public_individual.pl?faculty=534 http://www.pineforge.com/newman4study/resources/rosenthal1.htm http://www.psichi.org/pubs/articles/article_121.asp http://www.accel-team.com/pygmalion/prophecy_01.html http://www.musicedmagic.com/class-management/classroom-vision-and-the-self-fulfi\ lling-prophecy.html http://www.motivation-tools.com/workplace/social_prejudice.htm tons more -just google it or search the archives here ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 I gotta tell ya..... We corrected auditory tonal processing via The Listening Program We brought Marks auditory digit spans up to a solid 8 (high functioning adult) from a 5 (five year old child); We changed his auditory dominance from left to right by plugging his ear. We eliminated milk products & other stuff to address allergens (remains a continuous work in process as we discover more items). We ensure that the ear stays clear and functional. TA DAAAAAAAA! The result is a brand new kid.... I swear, the difference to function with these steps is from really disfunctional child to highly functional child and the benefits are simpley too numerous to list. They effect every single area of life just as dyspraxia affects every single area of life...... For those of you who have not yet investigated this path, I highly recommend it. Many of our children have severe auditory processing issues! (which go undetected by many professionals) Janice Mother of Mark, 13 [sPAM][ ] Re: Apraxia and Slow Processing I think the two are separate issues, but they are frequently co-morbid conditions. I just watched the NACD dvd on Learning and Attention Problems (very good!), and I learned some very interesting things about auditory processing. There are many frequencies of sound from 20Hz to 20,000, but hearing tests only test 6-8! You can pass a hearing testing and still have significant hearing issues. The brain learns to process specific frequencies of sound in the first two years of life, but this process can be interrupted any time there is fluid in the middle ear (not just ear infection). This problem is almost never identified. (It can be easily detected by a tympanagram, but pediatricians do not usually do this test.) Bob Doman thinks that dairy products are a large part of the problem. When this development doesn't happen, the ear can't process tones, language development is delayed and, since it affects the vestibular system, motor development can be delayed as well. The Listening Program re-educates the brain to process sound (tonal processing). According to Bob Doman, about 1 in 1,000 kids who have auditory problems have a problem with processing tones fast enough. Since they are slow to process the first tone of a word, they can't move on to the next sound, etc. FastForward is a program that works on that type of problem. And then there is auditory sequential processing, which is improved by practicing digit spans. Also, there is auditory dominance, which affects long memory (storage) of information. The NACD likes kids to have their dominant ear, eye, hand, and foot all be on the same side, and they give activities to make this happen. I think many SLPs and other experts tend to misuse one term for the other. A good audiologist can probably tell you which type of problem your child has, but they usually don't want to evaluate them until they are 6-8 years old. In the meantime, you have lost valuable time. That's why I love the NACD approach. They can give you stuff to improve today. in NJ > > Can anyone tell me (or give me an opinion) -- When a child has apraxia, and is diagnosed as > " processing more slowly " than normal -- are the two related? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 Go Josh! You must inform that doc. > Right after I posted my message I thought about the fact that > apraxia 'is' a motor planning disorder so thanks for bringing this up > Sherry! Yes you are correct that apraxia is a motor planning > disorder and at times they will take longer to do things based on > their motor planning disorder -but that doesn't exactly mean that our > children have " slow processing " in regards to a cognitive/receptive > angle/separate diagnosis which is the direction I based the emails > when auditory processing as a diagnosis was brought up. Even to the > general public the words " This is why I brought up partial paralysis > as an example. Again you can't judge one's ability on their > disability. So yes an apraxic child may tie his shoe slower, but > that doesn't mean he cognitively doesn't understand what he 'needs' > to do -he has trouble executing the motor skills needed to perform > the task as quickly as he wants. So an apraxic has slow processing > on actions -not slow processing on thoughts. There is a difference. > As you know as a mom -our children desperately at times know what > they want to say or do -but can't. I just as always want to make > sure that those with apraxia are not underestimated -so I will always > be the one (at times lone) voice that believes in the untapped > ability of that verbal disabled child. > > " Never underestimate the power of dreams and the influence of the > human spirit. We are all the same in this notion: The potential for > greatness lives within each of us. " > Wilma Rudolph quotes (First American woman Runner to win three gold > medals at a single Olympics. 1940-1994) > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 LOL Crazy women! My hubby loved that! [sPAM]Re: [ ] Re: Apraxia and Slow Processing > > > Absolutely, - I've been around this board for quite some time and > you know I would never underestimate what our kiddoes are capable of > accomplishing! Yikes, when you figure that evil doc originally saying Josh > had MR, would never walk unassisted, would never speak intelligibly - and > look what he's accomplished over the years! I never meant to imply that > our kiddoes have some cognitive issues or muscle tone issues or sensory > issues affecting their ability to process - unless, of course, that has > been > a proper diagnosis in addition to the apraxia (which, in Josh's case, it > has). So, as I wrote, apraxia is a motor planning disorder which, in and > of itself, does affect the processing of the neurological messages. > > Sherry and Josh (who, notwithstanding what the evil doc said years ago, > was a gold medal winner in Special Olympic basketball skills and will be > going to the State competition next month! HAH! to that doc!!!) > > kiddietalk <kiddietalk@...> wrote: > Right after I posted my message I thought about the fact that > apraxia 'is' a motor planning disorder so thanks for bringing this up > Sherry! Yes you are correct that apraxia is a motor planning > disorder and at times they will take longer to do things based on > their motor planning disorder -but that doesn't exactly mean that our > children have " slow processing " in regards to a cognitive/receptive > angle/separate diagnosis which is the direction I based the emails > when auditory processing as a diagnosis was brought up. Even to the > general public the words " This is why I brought up partial paralysis > as an example. Again you can't judge one's ability on their > disability. So yes an apraxic child may tie his shoe slower, but > that doesn't mean he cognitively doesn't understand what he 'needs' > to do -he has trouble executing the motor skills needed to perform > the task as quickly as he wants. So an apraxic has slow processing > on actions -not slow processing on thoughts. There is a difference. > As you know as a mom -our children desperately at times know what > they want to say or do -but can't. I just as always want to make > sure that those with apraxia are not underestimated -so I will always > be the one (at times lone) voice that believes in the untapped > ability of that verbal disabled child. > > " Never underestimate the power of dreams and the influence of the > human spirit. We are all the same in this notion: The potential for > greatness lives within each of us. " > Wilma Rudolph quotes (First American woman Runner to win three gold > medals at a single Olympics. 1940-1994) > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 My friends..... I have to agree.... with both of you(!).... that word 'processing' is awefully vague and doesn't really tell us a whole lot. Every thing in our bodies is a 'process' of some sort. Our intellect is comprised of so many variables that to simply say a child has slow 'processing' is really a cop-out. My digestive system is also a 'process' and has nothing to do with my knowledge base or intellect. The key is to locate 'which' process (es) is not functioning up to speed and to remediate it. This is the key and it can be done extremely successfully with the 'right' professional or therapeutic approach. If we don't have a therapy to fix something, then it simply means that we haven't developed it yet, not that our child lacks the ability to overcome and heal whatever ailment he/she may have. Our children are not limited by their label but have unlimited potential. Thus 'slow' processing is a demeaning term orchastrated by a person who is obviously ill-qualified to professionally assess a child with any proficiency! It is a polite way of saying MR! (and not too polite at that!) While my child 'HAD' (past tense as this is remedied now) poor auditory processing, his visual processing was off the charts and he was years and years ahead of his age group (7 years ahead of his age-group to be exact!) Yet.... to a casual observer, he too seemed 'slow'. But, he was actually extremely gifted and uniquely intelligent. Our children quite often 'hide' their gifts but usually they are in there.... just waiting to be discovered and displayed to the world! So.... please do not believe this person if they want to pigeon hole your child as being 'slow'. Our kids are a lot more complex and more interesting than this professional realizes. Stick around for a while and hear about our kids and what we are learning about them. Here and there you will find gems that completely apply to your child. Do not get overwhelmed by discussions of chemical toxicity, special diets, etc. Take it slow and read the posts without giving up on us 'crazy' women too soon. Together we are forging a path to unlock the various secrets of our children...... They are all wonderful children and so full of promise! Janice Mother of Mark, 13 [sPAM]Re: [ ] Re: Apraxia and Slow Processing Absolutely, - I've been around this board for quite some time and you know I would never underestimate what our kiddoes are capable of accomplishing! Yikes, when you figure that evil doc originally saying Josh had MR, would never walk unassisted, would never speak intelligibly - and look what he's accomplished over the years! I never meant to imply that our kiddoes have some cognitive issues or muscle tone issues or sensory issues affecting their ability to process - unless, of course, that has been a proper diagnosis in addition to the apraxia (which, in Josh's case, it has). So, as I wrote, apraxia is a motor planning disorder which, in and of itself, does affect the processing of the neurological messages. Sherry and Josh (who, notwithstanding what the evil doc said years ago, was a gold medal winner in Special Olympic basketball skills and will be going to the State competition next month! HAH! to that doc!!!) kiddietalk <kiddietalk@...> wrote: Right after I posted my message I thought about the fact that apraxia 'is' a motor planning disorder so thanks for bringing this up Sherry! Yes you are correct that apraxia is a motor planning disorder and at times they will take longer to do things based on their motor planning disorder -but that doesn't exactly mean that our children have " slow processing " in regards to a cognitive/receptive angle/separate diagnosis which is the direction I based the emails when auditory processing as a diagnosis was brought up. Even to the general public the words " This is why I brought up partial paralysis as an example. Again you can't judge one's ability on their disability. So yes an apraxic child may tie his shoe slower, but that doesn't mean he cognitively doesn't understand what he 'needs' to do -he has trouble executing the motor skills needed to perform the task as quickly as he wants. So an apraxic has slow processing on actions -not slow processing on thoughts. There is a difference. As you know as a mom -our children desperately at times know what they want to say or do -but can't. I just as always want to make sure that those with apraxia are not underestimated -so I will always be the one (at times lone) voice that believes in the untapped ability of that verbal disabled child. " Never underestimate the power of dreams and the influence of the human spirit. We are all the same in this notion: The potential for greatness lives within each of us. " Wilma Rudolph quotes (First American woman Runner to win three gold medals at a single Olympics. 1940-1994) ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 , Because we have older children and have experienced the 'stupidity' of the 'system', we have a better understanding of the word 'slow' and the insidious nature to which many of the professionals out there use it..... It is a one way ticket to special education..... and 'opportunities' class.... I say... Run Forest, RUN! Yes, I do jokingly call my boy Forest Gump.... but I have to run myself for he gives me a chase & a threat at my joke. (yes, he does get it!) In the educational system, SLOW processing is not used in a nice way.... Usually people use the word 'slow' to mean mental retardation of some sort. In actuality, Marks original IQ tests in grade 2, described him as being borderline mentally handicapped with regards to non-verbal persuits. I have it in black and white.... Unbelievable! Now, once they state this about your child at the tender age of 8, it is assumed to be never-changing and a testament to that childs abilities.... FOREVER!!! That is your child's life-promise as per the educational system. This is a BAAAAAAD thing for it forever limits your child within the system. This is sooooo wrong! I listened to these people who encouraged me to do 'nothing' for my child and so my child did not improve. As soon as I researched and found help for my child, everything turned around and he got better. His IQ has definately changed and someday (when I have extra $$$), I shall have him retested to prove it! So.... Liz and all of you with little ones..... if you wonder why , myself and others 'react' so reflexively to the word slow as though we have been back-handed across the face.... this is the reason. We have had such aweful experiences with the system and with others (usually complete idiots) who assume that our kids are stupid. They only see what is in front of them and perform the 'easy' diagnosis. They do not look beneath the surface to the diamond that sparkles and glows beneath the rough exterior.... our children are truly.... diamonds in the rough! Janice Mother of Mark, 13 [sPAM][ ] Re: Apraxia and Slow Processing Liz there is much in the archives and in research about self- fulfilling prophecies and the research of Dr. Rosenthal. Please don't assume that it's OK because your child is younger to say your child is " slow " in three areas! There is a huge problem with many here assuming that apraxia and processing disorders co exist or that children with apraxia have slow receptive/cognitive processing skills which is also a sign of mental retardation. And the fact so many today are accepting this is very sad. Perhaps unlike the children here from over the years like my son Tanner -the children in the group today won't be mainstreamed. Is that the belief? Because belief becomes reality and you get to choose now. Your child's future depends in some part on your belief. Isn't it a mother and father's instinct to raise our child up? And to answer the question about therapy for another diagnosis working. Many here with autistic children found some of the methods used for apraxia to work as well. The Kaufman Kit can be used by any late talker- even one that isn't apraxic. We tried various therapies for Tanner that are used for deaf children including learning sign -that doesn't mean Tanner is deaf. Just because a therapy helps doesn't mean a child has the diagnosis that therapy was originally designed for. Please do some homework on the awesome Dr. Rosenthal and the work he has done. You will also find much about him in the archives. Sadly if you believe your child to be slow..in three areas no less -you 'are' probably going to find out you are right. When nobody else believed in Tanner Glenn and I did and guess who proved everyone but us wrong -not us -but Tanner did! I loved sharing the whole story with Dr. Rosenthal because he is brilliant and he is the one that inspired me. And I saw it work. They could have been right and Tanner would have been in special ed today. http://www.cherab.org/information/familiesrelate/letter.html I know some of you don't understand this -but again don't assume the worst and don't underestimate those that can't verbally prove you wrong...yet. Sometimes it's best to be wrong and if you believe apraxia and slow processing of receptive or cognitive skills go hand in hand -then you 'are' wrong. Apraxia is not a cognitive disorder. And even if in your child's case you were right and for example one's child has co existing mental retardation with the apraxia -you are still best to believe in your child and give the benefit of the doubt. Look at Robin's daughter -it's a hard pill to swallow to be wrong -or assume others are right with bogus diagnosis about your child - years down the road. http://www.cherab.org/news/.html And while for ethical reasons Dr. Rosenthal's research was done in the positive -in speaking with him he agrees that it works both ways. If that's the case why think anything but the positive? http://www.facultydirectory.ucr.edu/cgi-bin/pub/public_individual.pl?faculty=534 http://www.pineforge.com/newman4study/resources/rosenthal1.htm http://www.psichi.org/pubs/articles/article_121.asp http://www.accel-team.com/pygmalion/prophecy_01.html http://www.musicedmagic.com/class-management/classroom-vision-and-the-self-fulfi\ lling-prophecy.html http://www.motivation-tools.com/workplace/social_prejudice.htm tons more -just google it or search the archives here ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 I do believe my and my childrens digestive processing, impaired as it was, dis affect and in fact compromise the full expression of their intellect and knoeledge base. Turns out I have a kid with good visual processing and bad auditory and the reverse in the other kid. As for overwhelming posts, try these books...much more succinct: Is this Your Child The A's by Dr. Bock Feast without yeast Sincerely, A crazy mom > Right after I posted my message I thought about the fact that > apraxia 'is' a motor planning disorder so thanks for bringing this up > Sherry! Yes you are correct that apraxia is a motor planning > disorder and at times they will take longer to do things based on > their motor planning disorder -but that doesn't exactly mean that our > children have " slow processing " in regards to a cognitive/receptive > angle/separate diagnosis which is the direction I based the emails > when auditory processing as a diagnosis was brought up. Even to the > general public the words " This is why I brought up partial paralysis > as an example. Again you can't judge one's ability on their > disability. So yes an apraxic child may tie his shoe slower, but > that doesn't mean he cognitively doesn't understand what he 'needs' > to do -he has trouble executing the motor skills needed to perform > the task as quickly as he wants. So an apraxic has slow processing > on actions -not slow processing on thoughts. There is a difference. > As you know as a mom -our children desperately at times know what > they want to say or do -but can't. I just as always want to make > sure that those with apraxia are not underestimated -so I will always > be the one (at times lone) voice that believes in the untapped > ability of that verbal disabled child. > > " Never underestimate the power of dreams and the influence of the > human spirit. We are all the same in this notion: The potential for > greatness lives within each of us. " > Wilma Rudolph quotes (First American woman Runner to win three gold > medals at a single Olympics. 1940-1994) > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 Oh no, I get it. It is thanks to parents like you and who fought for proper treatment of our children that moms like me with little ones have an easier time of it and a better path for our children. Many thanks to you, , and all the moms and caregivers who blaxed that trail making it far easier for us newbies. > > , > > Because we have older children and have experienced the 'stupidity' of the 'system', we have a better understanding of the word 'slow' and the insidious nature to which many of the professionals out there use it..... It is a one way ticket to special education..... and 'opportunities' class.... > > I say... Run Forest, RUN! Yes, I do jokingly call my boy Forest Gump.... but I have to run myself for he gives me a chase & a threat at my joke. (yes, he does get it!) > > In the educational system, SLOW processing is not used in a nice way.... Usually people use the word 'slow' to mean mental retardation of some sort. In actuality, Marks original IQ tests in grade 2, described him as being borderline mentally handicapped with regards to non-verbal persuits. I have it in black and white.... Unbelievable! > > Now, once they state this about your child at the tender age of 8, it is assumed to be never-changing and a testament to that childs abilities.... FOREVER!!! That is your child's life-promise as per the educational system. This is a BAAAAAAD thing for it forever limits your child within the system. > > This is sooooo wrong! > > I listened to these people who encouraged me to do 'nothing' for my child and so my child did not improve. As soon as I researched and found help for my child, everything turned around and he got better. His IQ has definately changed and someday (when I have extra $$$), I shall have him retested to prove it! > > So.... Liz and all of you with little ones..... if you wonder why , myself and others 'react' so reflexively to the word slow as though we have been back-handed across the face.... this is the reason. We have had such aweful experiences with the system and with others (usually complete idiots) who assume that our kids are stupid. They only see what is in front of them and perform the 'easy' diagnosis. They do not look beneath the surface to the diamond that sparkles and glows beneath the rough exterior.... our children are truly.... diamonds in the rough! > > Janice > Mother of Mark, 13 > > > > [sPAM][ ] Re: Apraxia and Slow Processing > > > Liz there is much in the archives and in research about self- > fulfilling prophecies and the research of Dr. Rosenthal. Please > don't assume that it's OK because your child is younger to say your > child is " slow " in three areas! There is a huge problem with many > here assuming that apraxia and processing disorders co exist or that > children with apraxia have slow receptive/cognitive processing skills > which is also a sign of mental retardation. And the fact so many > today are accepting this is very sad. Perhaps unlike the children > here from over the years like my son Tanner -the children in the > group today won't be mainstreamed. Is that the belief? Because > belief becomes reality and you get to choose now. Your child's > future depends in some part on your belief. Isn't it a mother and > father's instinct to raise our child up? > > And to answer the question about therapy for another diagnosis > working. Many here with autistic children found some of the methods > used for apraxia to work as well. The Kaufman Kit can be used by any > late talker- even one that isn't apraxic. > > We tried various therapies for Tanner that are used for deaf children > including learning sign -that doesn't mean Tanner is deaf. Just > because a therapy helps doesn't mean a child has the diagnosis that > therapy was originally designed for. > > Please do some homework on the awesome Dr. Rosenthal and the > work he has done. You will also find much about him in the > archives. Sadly if you believe your child to be slow..in three areas > no less -you 'are' probably going to find out you are right. When > nobody else believed in Tanner Glenn and I did and guess who proved > everyone but us wrong -not us -but Tanner did! I loved sharing the whole > story with Dr. Rosenthal because he is brilliant and he is the one > that inspired me. And I saw it work. They could have been right and > Tanner would have been in special ed today. > http://www.cherab.org/information/familiesrelate/letter.html > > I know some of you don't understand this -but again don't assume the > worst and don't underestimate those that can't verbally prove you > wrong...yet. Sometimes it's best to be wrong and if you believe > apraxia and slow processing of receptive or cognitive skills go hand > in hand -then you 'are' wrong. Apraxia is not a cognitive disorder. > > And even if in your child's case you were right and for example one's > child has co existing mental retardation with the apraxia -you are > still best to believe in your child and give the benefit of the > doubt. Look at Robin's daughter -it's a hard pill to swallow > to be wrong -or assume others are right with bogus diagnosis about > your child - years down the road. > http://www.cherab.org/news/.html > > And while for ethical reasons Dr. Rosenthal's research was done in > the positive -in speaking with him he agrees that it works both > ways. If that's the case why think anything but the positive? > > http://www.facultydirectory.ucr.edu/cgi- bin/pub/public_individual.pl?faculty=534 > http://www.pineforge.com/newman4study/resources/rosenthal1.htm > http://www.psichi.org/pubs/articles/article_121.asp > http://www.accel-team.com/pygmalion/prophecy_01.html > http://www.musicedmagic.com/class-management/classroom-vision-and- the-self-fulfilling-prophecy.html > http://www.motivation-tools.com/workplace/social_prejudice.htm > > tons more -just google it or search the archives here > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 I want to go further with my praise for the moms of older kids and moms of kids in school. Make no mistake, I could never, ever do what you do. If I had to sit through meetings with people who were labeling my kid without a grasp of who he is or what he can do...his true potential, well, let me describe what the scene of 's IEP would be like: " Picture a 41 year old redhead in an orange jumpsuit with duct tape on her mouth sitting between to her long-suffering and patient husband and the police officer the school brought in to keep the peace. This is one of the many reasons I am homeschooling. Joke of it is I was, back in the day, a very obedient and quiet student and remained that way as an adult...until this. My voice comes out in writing I suppose. My passion comes out whem the subject is near and dear to me, as my family is. > > , > > Because we have older children and have experienced the 'stupidity' of the 'system', we have a better understanding of the word 'slow' and the insidious nature to which many of the professionals out there use it..... It is a one way ticket to special education..... and 'opportunities' class.... > > I say... Run Forest, RUN! Yes, I do jokingly call my boy Forest Gump.... but I have to run myself for he gives me a chase & a threat at my joke. (yes, he does get it!) > > In the educational system, SLOW processing is not used in a nice way.... Usually people use the word 'slow' to mean mental retardation of some sort. In actuality, Marks original IQ tests in grade 2, described him as being borderline mentally handicapped with regards to non-verbal persuits. I have it in black and white.... Unbelievable! > > Now, once they state this about your child at the tender age of 8, it is assumed to be never-changing and a testament to that childs abilities.... FOREVER!!! That is your child's life-promise as per the educational system. This is a BAAAAAAD thing for it forever limits your child within the system. > > This is sooooo wrong! > > I listened to these people who encouraged me to do 'nothing' for my child and so my child did not improve. As soon as I researched and found help for my child, everything turned around and he got better. His IQ has definately changed and someday (when I have extra $$$), I shall have him retested to prove it! > > So.... Liz and all of you with little ones..... if you wonder why , myself and others 'react' so reflexively to the word slow as though we have been back-handed across the face.... this is the reason. We have had such aweful experiences with the system and with others (usually complete idiots) who assume that our kids are stupid. They only see what is in front of them and perform the 'easy' diagnosis. They do not look beneath the surface to the diamond that sparkles and glows beneath the rough exterior.... our children are truly.... diamonds in the rough! > > Janice > Mother of Mark, 13 > > > > [sPAM][ ] Re: Apraxia and Slow Processing > > > Liz there is much in the archives and in research about self- > fulfilling prophecies and the research of Dr. Rosenthal. Please > don't assume that it's OK because your child is younger to say your > child is " slow " in three areas! There is a huge problem with many > here assuming that apraxia and processing disorders co exist or that > children with apraxia have slow receptive/cognitive processing skills > which is also a sign of mental retardation. And the fact so many > today are accepting this is very sad. Perhaps unlike the children > here from over the years like my son Tanner -the children in the > group today won't be mainstreamed. Is that the belief? Because > belief becomes reality and you get to choose now. Your child's > future depends in some part on your belief. Isn't it a mother and > father's instinct to raise our child up? > > And to answer the question about therapy for another diagnosis > working. Many here with autistic children found some of the methods > used for apraxia to work as well. The Kaufman Kit can be used by any > late talker- even one that isn't apraxic. > > We tried various therapies for Tanner that are used for deaf children > including learning sign -that doesn't mean Tanner is deaf. Just > because a therapy helps doesn't mean a child has the diagnosis that > therapy was originally designed for. > > Please do some homework on the awesome Dr. Rosenthal and the > work he has done. You will also find much about him in the > archives. Sadly if you believe your child to be slow..in three areas > no less -you 'are' probably going to find out you are right. When > nobody else believed in Tanner Glenn and I did and guess who proved > everyone but us wrong -not us -but Tanner did! I loved sharing the whole > story with Dr. Rosenthal because he is brilliant and he is the one > that inspired me. And I saw it work. They could have been right and > Tanner would have been in special ed today. > http://www.cherab.org/information/familiesrelate/letter.html > > I know some of you don't understand this -but again don't assume the > worst and don't underestimate those that can't verbally prove you > wrong...yet. Sometimes it's best to be wrong and if you believe > apraxia and slow processing of receptive or cognitive skills go hand > in hand -then you 'are' wrong. Apraxia is not a cognitive disorder. > > And even if in your child's case you were right and for example one's > child has co existing mental retardation with the apraxia -you are > still best to believe in your child and give the benefit of the > doubt. Look at Robin's daughter -it's a hard pill to swallow > to be wrong -or assume others are right with bogus diagnosis about > your child - years down the road. > http://www.cherab.org/news/.html > > And while for ethical reasons Dr. Rosenthal's research was done in > the positive -in speaking with him he agrees that it works both > ways. If that's the case why think anything but the positive? > > http://www.facultydirectory.ucr.edu/cgi- bin/pub/public_individual.pl?faculty=534 > http://www.pineforge.com/newman4study/resources/rosenthal1.htm > http://www.psichi.org/pubs/articles/article_121.asp > http://www.accel-team.com/pygmalion/prophecy_01.html > http://www.musicedmagic.com/class-management/classroom-vision-and- the-self-fulfilling-prophecy.html > http://www.motivation-tools.com/workplace/social_prejudice.htm > > tons more -just google it or search the archives here > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 Well said Janice! Thanks for being there as another " old timer " !! And you are right - Forrest Gump as a movie is a great example of a mother's belief in her child. " Run Forrest Run! " My " old timer " favorite of course is Helen Keller -and her story is a testimony to teachers as well. " Helen's key achievement the one she craved most of all was learning how to speak " Learn how she did and learn how she says (oh this is so profound isn't it) " I am not dumb now " http://www.youtube.com/watch?v=0uBlIDp9CWY ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2008 Report Share Posted February 4, 2008 , I have been meaning to write you back about getting the boys in touch with one another. I broached the subject to Mark the other day and he seemed curious to talk to another dyspraxic kid even though he doesn't do well with the telephone. He thought it might be easier if it were speakerphone? I have been so absolutely ill this past week that I just have been 'getting through' but we haven't forgotten this idea.... let me recover and we will give it a shot? Question: Does Tanner sweat? This is one of the next things up on our agenda with the environmental doctor.... getting Mark to start sweating. He rarely breaks a sweat even after running 4 or 5 kms in a cross country run! I understood it when he was younger but he should be sweating by now. The most he gets is a little clammy behind his neck. So to sweat is to detox..... we must get him to sweat! Hence.... an infared sauna is the next item on the 'big' ticket list. My doctor is so funny. We sit in his office, we first discuss how Mark is doing, how he is faring, and look at any health protocols that we should be changing. Then he will slap his hand on a chess timer, and will say..... are you ready for your environmental lesson dear? And then we start..... and I learn all about excitotoxins, mold, water, dishware, Pabain (bad stuff, in the lotions, sunscreen & creams), and electromagnectic energy and why my son cannot handle these things and how to reduce his exposure while he is detoxing. It is actually a very 'cool' experience. One of the things that I learned is that smelling is worse than inhalation with regards to chemical sensitivity. When you smell a toxic substance in through your nose, it crosses the blood/brain barrier which is why we will often get a headache to noxious fumes. When you inhale a toxic substance, the bodies natural filtration system kicks in and you are not as adversely affected; the blood brain barrier is not crossed. This is why the 'smell' of household cleaners and such is often very hard on our children. It goes straight to their head! Janice Mother of Mark, 13 [sPAM]Re:[ ] Re: Apraxia and Slow Processing Well said Janice! Thanks for being there as another " old timer " !! And you are right - Forrest Gump as a movie is a great example of a mother's belief in her child. " Run Forrest Run! " My " old timer " favorite of course is Helen Keller -and her story is a testimony to teachers as well. " Helen's key achievement the one she craved most of all was learning how to speak " Learn how she did and learn how she says (oh this is so profound isn't it) " I am not dumb now " http://www.youtube.com/watch?v=0uBlIDp9CWY ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 5, 2008 Report Share Posted February 5, 2008 In a message dated 2/5/2008 9:40:30 A.M. Eastern Standard Time, lizlaw@... writes: I had a similar reaction when a friend at lunch the other week said " is almost normal now, right? " This is a woman, a scientist, who is pregnant and recently overreacted to a prematurely done ultrasound and almost aborted her child because there was a suggestion of shortened femur. Oh my!!! I can't even go there with this sort of mom who thinks this ways let alone makes that sort of comment to another mom of a special needs child!!!! Good thing she said it to YOU and not ME, because I'm not so sure I would have been as patient as you were with that comment. for the record-- according to my last U/S about 3wks ago, the baby's femur was measuring shorter in length than they wanted. They spent an INORDINANT amount of time looking at every single detail of the baby's heart, and the U/S was well over an hour and half almost! I was just slightly annoyed, because I feel they over react with this sort of thing, and that the femur length is NOT a marker for down's syndrome but is simply something they " look for " . Of course I have to go back next week so they can measure the length again, but seriously-- they just worry moms so unnecessarily so! And the thought of going in for yet ANOTHER Ultra Sound, REALLY bothers me greatly. I do NOT buy the whole " they're perfectly safe " thing-- I just don't agree and I can't stand that they are putting the baby at MORE risk, I feel, to continue having all these ultrasounds. <sigh> bek **************Biggest Grammy Award surprises of all time on AOL Music. (http://music.aol.com/grammys/pictures/never-won-a-grammy?NCID=aolcmp00300000002\ 5 48) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 5, 2008 Report Share Posted February 5, 2008 Interesting . Again you are the youtube finder of great things. My son started Prompt Therapy (sort of a hybrid therapy with prompt mixed in as he is talking unprompted). Since I am new to this I may get this wrong but when watching this it dawned on me that Helen learning to speak occurred from sort of a reverse Prompt Therapy kind of intervention. Very cool. > > Well said Janice! Thanks for being there as another " old timer " !! > And you are right - Forrest Gump as a movie is a great example of a > mother's belief in her child. " Run Forrest Run! " > > My " old timer " favorite of course is Helen Keller -and her story is a > testimony to teachers as well. > " Helen's key achievement the one she craved most of all was learning > how to speak " Learn how she did and learn how she says > (oh this is so profound isn't it) > " I am not dumb now " > http://www.youtube.com/watch?v=0uBlIDp9CWY > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 5, 2008 Report Share Posted February 5, 2008 I had a similar reaction when a friend at lunch the other week said " is almost normal now, right? " This is a woman, a scientist, who is pregnant and recently overreacted to a prematurely done ultrasound and almost aborted her child because there was a suggestion of shortened femur. Not trying to stir up the abortion debate here at all and was not trying to stir it up with her. Instead I spent the weeks between her early ultrasound and the gentic testing results (that came out fine and the femur is now the correct size) encouraging her to recalculate dates, look at the promise and hope of NACD kids, etc. I also asked her to get a water filter (shameless I know but she is doing it because she grew up in fluoridated Canada and lives in a particularly toxic part of NJ and works in a pharmaceutical plant where all the goodies are manufactured) and I pointed her to more expansive research on the femur issue that was encouraging. She told another friend that I supported her in ways she thought not possible. I am not saying that to pat myself on the back (it was my job as a friend) but rather to express that despite how annoying I can be she received the info well. (I also gave it to her piecemeal after assessing if it was appropriate...there was no master plan to bombard her, it was about support). So, she was not the first person I was expecting to drudge up the whole " normal " comment. Still, I think it was her way of saying " He's doing well isn't he? " I won't lie though, it still hurt. > > > In a message dated 2/4/2008 5:28:04 P.M. Eastern Standard Time, > kiddietalk@... writes: > > Even to the > general public the words " This is why I brought up partial paralysis > as an example. Again you can't judge one's ability on their > disability. So yes an apraxic child may tie his shoe slower, but > that doesn't mean he cognitively doesn't understand what he 'needs' > to do -he has trouble executing the motor skills needed to perform > the task as quickly as he wants. So an apraxic has slow processing > on actions -not slow processing on thoughts. There is a difference. > > > > > > > I agree with this statement, but just wanted to point out that there are so > many different things that people may be referring to when they use the term > " slow processing " in reference to our kids. > I don't think that most people MEAN to offend with this term, but rather > lack ANOTHER term to use that might describe the thought behind what they are > referring to. > > I know that I sometimes think of Asa as having " slow processing " even while > the child is literally a genius and I KNOW he has no problem with processing > the THOUGHTS of things, but of course, since it's a motor planning problem, I > know he has the problem of EXECUTION to those tasks-- so it can actually be, > depending on how a person is using the term-- can be, in fact, slow > processing. (even though we know it's not the processing on the thoughts or brain) > I dunno if I'm saying this to make sense, because I AGREE with what you've > said above, because my son has Global Apraxia/Developmental Dyspraxia, so I've > seen those looks people give when they assume he's " not all there " and that > he's " slow " , and there's nothing further from the truth! But I think they > just lack the FULL UNDERSTANDING of the condition, so the terms can sometimes be > misused or used in an incorrect situation. > > > Becky > > > > **************Biggest Grammy Award surprises of all time on AOL Music. > (http://music.aol.com/grammys/pictures/never-won-a-grammy? NCID=aolcmp003000000025 > 48) > > > Quote Link to comment Share on other sites More sharing options...
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