Guest guest Posted March 26, 2011 Report Share Posted March 26, 2011 Marie you so need private evaluations outside the school- and in my opinion unless it's a rare educational psych who has great knowledge about speech impairments and how to appropriately test one with a verbal disability I would stick with neuroMD exams instead for apraxia as apraxia is not a psychological condition and I've seen too many misdiagnosis. I don't care for any school that feels that a test will answer all your questions as I happen to have heard from Dr. a Tallal one of the Cherab advisers that there are currently no 100 percent accurate cognitive or receptive tests for a verbal disabled individual. Here's Dr. Tallal's background http://www.cmbn.rutgers.edu/research/tallal/ I have a hunch based on her research and educational background in working with our population she knows a wee bit more than the people at your town school. My son Tanner when we lived in NJ it was the same type of school -awesome public school for regular students and their program for apraxia was HIGHLY inappropriate and bordered on abusive to what they did to my poor son Tanner. I have story after story in the archives of how they punished him, how when they tried to get him to say " Good morning Mrs. Whiseman " when the child couldn't even have said the first word of that sentence (!) they put him in front of the class and he had his head down and the teacher took his face and forced him to look up and patted his face -not hard enough to be a smack but more like a " come on you can do it " kind of double quick pat and said " Come on Tanner you can do it. Say Good morning Mrs. Whiseman " How do I know about those 2 alone? The first the teacher told me and the second I saw through the double glass observation room when he first started in this class which I didn't announce I was there -because I didn't know I was supposed to as it was all new -and they made it super clear to me that I was never to observe the class without announcing I was there to observe. To put it bluntly how bad they were with my son Tanner -they took a completely sweet child who worked so hard in therapy prior to his few months in this horror and created a child that they pegged and wrote into his IEP was " manipulative " Zimet CCC SLP from this group who's now in Georgia was Tanner's EI therapist in Jersey before we moved so she and Dr. Agin and Ortega can vouch for how Tanner was prior to this placement. So yes I advocated and had enough history to get Tanner placed in out of district placement at the Summit Speech School which is an oral based school for the hearing impaired in NJ and one of the top in the country. And the nightmare was over as that school was incredible in every single way. A bunch of us with apraxia had hearing apraxic children at the school soon after Tanner got in - but from what I know after Kanter the school director passed away and someone else took over they cracked down on not letting kids in that were hearing. Honestly that school saved my son and I don't know where he would be without it. But when Tanner went to transition into kindergarten (at 6 -we kept him at SSS until then and most of the kids at this school don't transition to public school until 6 and the school has an extremely high success rate of mainstream after preschool) he had to be tested by the same public school we left and by the same educational psychologist. To make a long story short the public school as well as my son was doing didn't think he'd " make it " in a mainstream kindergarten class. Oh don't get me started -what a group of idiots they were! And his work in SSS and appropriate testing should have shown that. As it ended up this story gets to much worse as to someone from my NJ district calling the case manager where I moved to in Florida to say that a mistake was being made and he didn't belong in the mainstream that it's almost difficult to believe. And for the educators reading this -I am so aware that so many of you are awesome -but I also know that the edcational psych tests they give verbal disabled children are typically are so unfair and in some cases are a violation of our children's Civil Rights of not being tested on their abilities on their disability. here's are links to the letter to parents I wrote years ago with the update about kindergarten http://www.cherab.org/information/familiesrelate/letter.html or http://www.cherabfoundation.org/2006/a-letter-to-parents-who-have-a-child-that-i\ s-a-late-talker-first-written-7400-and-update-from-1003/ So if you don't have to do the testing just say no -if you do -get second opinions. Actually either way I'd get second opinions because it seems based on just a few comments you heard you are dealing with some professionals that have already pegged your son even prior to testing. Oh and about top academic private schools...after kindergarten - mainstream where Tanner according to his teacher Mrs. was " not just making it but one of the top students in his class " he went to a private school that was for academically advanced students and was a straight A student. So don't say it's not possible -your child sounds very bright to me -why shouldn't he be top in his class? PS...OK did you start the NV yet???? If you didn't please start it -it helps with so much more than speech and motor planning, it's helping with academics too. Here's one example about a 6 year old Professional anecdotal update from kindergarten teacher of a 6 year old apraxic child after less than 2 weeks on Nutriiveda. “I wanted to let you know how things are going with Dominic. I think it’s safe to say that everyone that works with him has noticed a great change in him over the past 1-2 weeks. He is much more outgoing, much more in tune with what it going on in the classroom, and very talkative. I think what I’ve noticed the most is that he is talking much more with his peers during work time and play time. He also seems to be much more self-directed when we do classwork. For example, last Monday when we made the Valentine’s Day card, he did very well with the project and did not need much direction from me to complete it. He did most of the project independently, even the sticky tape (which has always been a challenge for him). I also heard that on Friday, during their speech time with Mrs. Kulig, he came into class, took out his ABC book and without any prompting from anyone, read the entire book for the rest of the kids in the group! This is all great!!†Parents add “his teacher is not aware we have him on NV. We are pretty excited since it has been six years with nothing like this until now.†http://pursuitofresearch.com/2010/11/22/is-nutriiveda-creating-a-paradigm-shift-\ in-treatment-of-speech-impairments/ Sorry if I went and this message seemed strong -but you have no idea -I have so much more on this topic. So again -no from me for this exam unless you have to -and if you do -be prepared to double check them. They are not always right -I'll just leave it at that. ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2011 Report Share Posted March 26, 2011 Thank you so much for your reply. It is difficult to go against the well regarded professionals in the area. The other parents know that they don't know all the answers and aren't the best in the country, but the thought is " they're the best we have here. " I'm from CT and NY (I was born in NJ), so my gut tends to still go with northern thoughts (a whole 'nother issue . I have a good friend whose son has apraxia and he's in a mainstream public school in Darien and doing just fine. There are just lots of different thoughts on it. If they were more honest and upfront, I'd be more impressed and trusting. His non-class OT only works there p/t. She is much more progressive and willing to try different therapies and talk about nutrition- she's not in full agreement with everything at the school (she's the one who did the therap. listening and wants to get the school onboard with ILS- let's just say she's frustrasted). She's the one who seems most interested in conferences and being up with the newest research, but I don't think many of them are really experts on apraxia at this school. They know that low tone and sensory comes with it, but that's really about it. They treat it from there. Anyway, thank you for your thoughts. Much appreciated and yes, today was day 1 of NV. It all went down. He has 2 mos. left of school, so we'll see how it goes! Thanks, Marie ________________________________ From: kiddietalk <kiddietalk@...> Sent: Sat, March 26, 2011 4:26:32 PM Subject: [ ] Re: psycho. educ. evaluation Marie you so need private evaluations outside the school- and in my opinion unless it's a rare educational psych who has great knowledge about speech impairments and how to appropriately test one with a verbal disability I would stick with neuroMD exams instead for apraxia as apraxia is not a psychological condition and I've seen too many misdiagnosis. I don't care for any school that feels that a test will answer all your questions as I happen to have heard from Dr. a Tallal one of the Cherab advisers that there are currently no 100 percent accurate cognitive or receptive tests for a verbal disabled individual. Here's Dr. Tallal's background http://www.cmbn.rutgers.edu/research/tallal/ I have a hunch based on her research and educational background in working with our population she knows a wee bit more than the people at your town school. My son Tanner when we lived in NJ it was the same type of school -awesome public school for regular students and their program for apraxia was HIGHLY inappropriate and bordered on abusive to what they did to my poor son Tanner. I have story after story in the archives of how they punished him, how when they tried to get him to say " Good morning Mrs. Whiseman " when the child couldn't even have said the first word of that sentence (!) they put him in front of the class and he had his head down and the teacher took his face and forced him to look up and patted his face -not hard enough to be a smack but more like a " come on you can do it " kind of double quick pat and said " Come on Tanner you can do it. Say Good morning Mrs. Whiseman " How do I know about those 2 alone? The first the teacher told me and the second I saw through the double glass observation room when he first started in this class which I didn't announce I was there -because I didn't know I was supposed to as it was all new -and they made it super clear to me that I was never to observe the class without announcing I was there to observe. To put it bluntly how bad they were with my son Tanner -they took a completely sweet child who worked so hard in therapy prior to his few months in this horror and created a child that they pegged and wrote into his IEP was " manipulative " Zimet CCC SLP from this group who's now in Georgia was Tanner's EI therapist in Jersey before we moved so she and Dr. Agin and Ortega can vouch for how Tanner was prior to this placement. So yes I advocated and had enough history to get Tanner placed in out of district placement at the Summit Speech School which is an oral based school for the hearing impaired in NJ and one of the top in the country. And the nightmare was over as that school was incredible in every single way. A bunch of us with apraxia had hearing apraxic children at the school soon after Tanner got in - but from what I know after Kanter the school director passed away and someone else took over they cracked down on not letting kids in that were hearing. Honestly that school saved my son and I don't know where he would be without it. But when Tanner went to transition into kindergarten (at 6 -we kept him at SSS until then and most of the kids at this school don't transition to public school until 6 and the school has an extremely high success rate of mainstream after preschool) he had to be tested by the same public school we left and by the same educational psychologist. To make a long story short the public school as well as my son was doing didn't think he'd " make it " in a mainstream kindergarten class. Oh don't get me started -what a group of idiots they were! And his work in SSS and appropriate testing should have shown that. As it ended up this story gets to much worse as to someone from my NJ district calling the case manager where I moved to in Florida to say that a mistake was being made and he didn't belong in the mainstream that it's almost difficult to believe. And for the educators reading this -I am so aware that so many of you are awesome -but I also know that the edcational psych tests they give verbal disabled children are typically are so unfair and in some cases are a violation of our children's Civil Rights of not being tested on their abilities on their disability. here's are links to the letter to parents I wrote years ago with the update about kindergarten http://www.cherab.org/information/familiesrelate/letter.html or http://www.cherabfoundation.org/2006/a-letter-to-parents-who-have-a-child-that-i\ s-a-late-talker-first-written-7400-and-update-from-1003/ So if you don't have to do the testing just say no -if you do -get second opinions. Actually either way I'd get second opinions because it seems based on just a few comments you heard you are dealing with some professionals that have already pegged your son even prior to testing. Oh and about top academic private schools...after kindergarten - mainstream where Tanner according to his teacher Mrs. was " not just making it but one of the top students in his class " he went to a private school that was for academically advanced students and was a straight A student. So don't say it's not possible -your child sounds very bright to me -why shouldn't he be top in his class? PS...OK did you start the NV yet???? If you didn't please start it -it helps with so much more than speech and motor planning, it's helping with academics too. Here's one example about a 6 year old Professional anecdotal update from kindergarten teacher of a 6 year old apraxic child after less than 2 weeks on Nutriiveda. “I wanted to let you know how things are going with Dominic. I think it’s safe to say that everyone that works with him has noticed a great change in him over the past 1-2 weeks. He is much more outgoing, much more in tune with what it going on in the classroom, and very talkative. I think what I’ve noticed the most is that he is talking much more with his peers during work time and play time. He also seems to be much more self-directed when we do classwork. For example, last Monday when we made the Valentine’s Day card, he did very well with the project and did not need much direction from me to complete it. He did most of the project independently, even the sticky tape (which has always been a challenge for him). I also heard that on Friday, during their speech time with Mrs. Kulig, he came into class, took out his ABC book and without any prompting from anyone, read the entire book for the rest of the kids in the group! This is all great!!†Parents add “his teacher is not aware we have him on NV. We are pretty excited since it has been six years with nothing like this until now.†http://pursuitofresearch.com/2010/11/22/is-nutriiveda-creating-a-paradigm-shift-\ in-treatment-of-speech-impairments/ Sorry if I went and this message seemed strong -but you have no idea -I have so much more on this topic. So again -no from me for this exam unless you have to -and if you do -be prepared to double check them. They are not always right -I'll just leave it at that. ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2011 Report Share Posted March 27, 2011 Is there a way for me to set up a meeting/call with Dr. Tallah or would she know of anyone else I could meet with to discuss this? My aunt, a psychologist in Baltimore, has been telling me for months to seek out a professional at s Hopkins. I just want to talk to someone who is really in the know for a 2nd opinion- especially re: testing before we move on. I have family in Baltimore, northern NJ, NY and CT and am willing to travel if needed to talk to someone I can trust and who is very knowledgeable. Thanks, Marie ________________________________ From: kiddietalk <kiddietalk@...> Sent: Sat, March 26, 2011 4:26:32 PM Subject: [ ] Re: psycho. educ. evaluation Marie you so need private evaluations outside the school- and in my opinion unless it's a rare educational psych who has great knowledge about speech impairments and how to appropriately test one with a verbal disability I would stick with neuroMD exams instead for apraxia as apraxia is not a psychological condition and I've seen too many misdiagnosis. I don't care for any school that feels that a test will answer all your questions as I happen to have heard from Dr. a Tallal one of the Cherab advisers that there are currently no 100 percent accurate cognitive or receptive tests for a verbal disabled individual. Here's Dr. Tallal's background http://www.cmbn.rutgers.edu/research/tallal/ I have a hunch based on her research and educational background in working with our population she knows a wee bit more than the people at your town school. My son Tanner when we lived in NJ it was the same type of school -awesome public school for regular students and their program for apraxia was HIGHLY inappropriate and bordered on abusive to what they did to my poor son Tanner. I have story after story in the archives of how they punished him, how when they tried to get him to say " Good morning Mrs. Whiseman " when the child couldn't even have said the first word of that sentence (!) they put him in front of the class and he had his head down and the teacher took his face and forced him to look up and patted his face -not hard enough to be a smack but more like a " come on you can do it " kind of double quick pat and said " Come on Tanner you can do it. Say Good morning Mrs. Whiseman " How do I know about those 2 alone? The first the teacher told me and the second I saw through the double glass observation room when he first started in this class which I didn't announce I was there -because I didn't know I was supposed to as it was all new -and they made it super clear to me that I was never to observe the class without announcing I was there to observe. To put it bluntly how bad they were with my son Tanner -they took a completely sweet child who worked so hard in therapy prior to his few months in this horror and created a child that they pegged and wrote into his IEP was " manipulative " Zimet CCC SLP from this group who's now in Georgia was Tanner's EI therapist in Jersey before we moved so she and Dr. Agin and Ortega can vouch for how Tanner was prior to this placement. So yes I advocated and had enough history to get Tanner placed in out of district placement at the Summit Speech School which is an oral based school for the hearing impaired in NJ and one of the top in the country. And the nightmare was over as that school was incredible in every single way. A bunch of us with apraxia had hearing apraxic children at the school soon after Tanner got in - but from what I know after Kanter the school director passed away and someone else took over they cracked down on not letting kids in that were hearing. Honestly that school saved my son and I don't know where he would be without it. But when Tanner went to transition into kindergarten (at 6 -we kept him at SSS until then and most of the kids at this school don't transition to public school until 6 and the school has an extremely high success rate of mainstream after preschool) he had to be tested by the same public school we left and by the same educational psychologist. To make a long story short the public school as well as my son was doing didn't think he'd " make it " in a mainstream kindergarten class. Oh don't get me started -what a group of idiots they were! And his work in SSS and appropriate testing should have shown that. As it ended up this story gets to much worse as to someone from my NJ district calling the case manager where I moved to in Florida to say that a mistake was being made and he didn't belong in the mainstream that it's almost difficult to believe. And for the educators reading this -I am so aware that so many of you are awesome -but I also know that the edcational psych tests they give verbal disabled children are typically are so unfair and in some cases are a violation of our children's Civil Rights of not being tested on their abilities on their disability. here's are links to the letter to parents I wrote years ago with the update about kindergarten http://www.cherab.org/information/familiesrelate/letter.html or http://www.cherabfoundation.org/2006/a-letter-to-parents-who-have-a-child-that-i\ s-a-late-talker-first-written-7400-and-update-from-1003/ So if you don't have to do the testing just say no -if you do -get second opinions. Actually either way I'd get second opinions because it seems based on just a few comments you heard you are dealing with some professionals that have already pegged your son even prior to testing. Oh and about top academic private schools...after kindergarten - mainstream where Tanner according to his teacher Mrs. was " not just making it but one of the top students in his class " he went to a private school that was for academically advanced students and was a straight A student. So don't say it's not possible -your child sounds very bright to me -why shouldn't he be top in his class? PS...OK did you start the NV yet???? If you didn't please start it -it helps with so much more than speech and motor planning, it's helping with academics too. Here's one example about a 6 year old Professional anecdotal update from kindergarten teacher of a 6 year old apraxic child after less than 2 weeks on Nutriiveda. “I wanted to let you know how things are going with Dominic. I think it’s safe to say that everyone that works with him has noticed a great change in him over the past 1-2 weeks. He is much more outgoing, much more in tune with what it going on in the classroom, and very talkative. I think what I’ve noticed the most is that he is talking much more with his peers during work time and play time. He also seems to be much more self-directed when we do classwork. For example, last Monday when we made the Valentine’s Day card, he did very well with the project and did not need much direction from me to complete it. He did most of the project independently, even the sticky tape (which has always been a challenge for him). I also heard that on Friday, during their speech time with Mrs. Kulig, he came into class, took out his ABC book and without any prompting from anyone, read the entire book for the rest of the kids in the group! This is all great!!†Parents add “his teacher is not aware we have him on NV. We are pretty excited since it has been six years with nothing like this until now.†http://pursuitofresearch.com/2010/11/22/is-nutriiveda-creating-a-paradigm-shift-\ in-treatment-of-speech-impairments/ Sorry if I went and this message seemed strong -but you have no idea -I have so much more on this topic. So again -no from me for this exam unless you have to -and if you do -be prepared to double check them. They are not always right -I'll just leave it at that. ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2011 Report Share Posted March 27, 2011 We live in NY, an hour outside NYC. We have never been able to say, No, to the Psych evaluations that go along with PT OT and Speech. Shes in 4th grade now, but we have reports from days of EI from Psych all thru the years. So even in EI, if you want your child evaluated for OT or PT, you must agree to the Psych or they wont do the others. They're not all bad reports and I get a lot of very useful information for her annual meetings. Just anohter perspective. I've thought of the outside Neuropsych evaluation, but I'm putting off that $2500 price tag as long as I can!!The school psychologist, from our VERY highly repspected district, has done a great job with her over the years! Maureen > > Thank you so much for your reply. It is difficult to go against the well > regarded professionals in the area. The other parents know that they don't know > all the answers and aren't the best in the country, but the thought is " they're > the best we have here. " I'm from CT and NY (I was born in NJ), so my gut tends > to still go with northern thoughts (a whole 'nother issue . I have a good > friend whose son has apraxia and he's in a mainstream public school in Darien > and doing just fine. There are just lots of different thoughts on it. If they > were more honest and upfront, I'd be more impressed and trusting. His non-class > OT only works there p/t. She is much more progressive and willing to try > different therapies and talk about nutrition- she's not in full agreement with > everything at the school (she's the one who did the therap. listening and wants > to get the school onboard with ILS- let's just say she's frustrasted). She's the > one who seems most interested in conferences and being up with the newest > research, but I don't think many of them are really experts on apraxia at this > school. They know that low tone and sensory comes with it, but that's really > about it. They treat it from there. > > > > Anyway, thank you for your thoughts. Much appreciated and yes, today was day 1 > of NV. It all went down. He has 2 mos. left of school, so we'll see how it > goes! > > > Thanks, Marie > > > > > ________________________________ > From: kiddietalk <kiddietalk@...> > > Sent: Sat, March 26, 2011 4:26:32 PM > Subject: [ ] Re: psycho. educ. evaluation > > > Marie you so need private evaluations outside the school- and in my opinion > unless it's a rare educational psych who has great knowledge about speech > impairments and how to appropriately test one with a verbal disability I would > stick with neuroMD exams instead for apraxia as apraxia is not a psychological > condition and I've seen too many misdiagnosis. > > > I don't care for any school that feels that a test will answer all your > questions as I happen to have heard from Dr. a Tallal one of the Cherab > advisers that there are currently no 100 percent accurate cognitive or receptive > tests for a verbal disabled individual. Here's Dr. Tallal's background > http://www.cmbn.rutgers.edu/research/tallal/ I have a hunch based on her > research and educational background in working with our population she knows a > wee bit more than the people at your town school. > > My son Tanner when we lived in NJ it was the same type of school -awesome public > school for regular students and their program for apraxia was HIGHLY > inappropriate and bordered on abusive to what they did to my poor son Tanner. I > have story after story in the archives of how they punished him, how when they > tried to get him to say " Good morning Mrs. Whiseman " when the child couldn't > even have said the first word of that sentence (!) they put him in front of the > class and he had his head down and the teacher took his face and forced him to > look up and patted his face -not hard enough to be a smack but more like a " come > on you can do it " kind of double quick pat and said " Come on Tanner you can do > it. Say Good morning Mrs. Whiseman " How do I know about those 2 alone? The > first the teacher told me and the second I saw through the double glass > observation room when he first started in this class which I didn't announce I > was there -because I didn't know I was supposed to as it was all new -and they > made it super clear to me that I was never to observe the class without > announcing I was there to observe. To put it bluntly how bad they were with my > son Tanner -they took a completely sweet child who worked so hard in therapy > prior to his few months in this horror and created a child that they pegged and > wrote into his IEP was " manipulative " Zimet CCC SLP from this group > who's now in Georgia was Tanner's EI therapist in Jersey before we moved so she > and Dr. Agin and Ortega can vouch for how Tanner was prior to this > placement. > > So yes I advocated and had enough history to get Tanner placed in out of > district placement at the Summit Speech School which is an oral based school for > the hearing impaired in NJ and one of the top in the country. And the nightmare > was over as that school was incredible in every single way. A bunch of us with > apraxia had hearing apraxic children at the school soon after Tanner got in - > but from what I know after Kanter the school director passed away and > someone else took over they cracked down on not letting kids in that were > hearing. Honestly that school saved my son and I don't know where he would be > without it. > > But when Tanner went to transition into kindergarten (at 6 -we kept him at SSS > until then and most of the kids at this school don't transition to public school > until 6 and the school has an extremely high success rate of mainstream after > preschool) he had to be tested by the same public school we left and by the same > educational psychologist. To make a long story short the public school as well > as my son was doing didn't think he'd " make it " in a mainstream kindergarten > class. Oh don't get me started -what a group of idiots they were! And his work > in SSS and appropriate testing should have shown that. As it ended up this > story gets to much worse as to someone from my NJ district calling the case > manager where I moved to in Florida to say that a mistake was being made and he > didn't belong in the mainstream that it's almost difficult to believe. And for > the educators reading this -I am so aware that so many of you are awesome -but I > also know that the edcational psych tests they give verbal disabled children are > typically are so unfair and in some cases are a violation of our children's > Civil Rights of not being tested on their abilities on their disability. > > here's are links to the letter to parents I wrote years ago with the update > about kindergarten > http://www.cherab.org/information/familiesrelate/letter.html or > > http://www.cherabfoundation.org/2006/a-letter-to-parents-who-have-a-child-that-i\ s-a-late-talker-first-written-7400-and-update-from-1003/ > > > So if you don't have to do the testing just say no -if you do -get second > opinions. Actually either way I'd get second opinions because it seems based on > just a few comments you heard you are dealing with some professionals that have > already pegged your son even prior to testing. > > Oh and about top academic private schools...after kindergarten - mainstream > where Tanner according to his teacher Mrs. was " not just making it but one > of the top students in his class " he went to a private school that was for > academically advanced students and was a straight A student. So don't say it's > not possible -your child sounds very bright to me -why shouldn't he be top in > his class? > > PS...OK did you start the NV yet???? If you didn't please start it -it helps > with so much more than speech and motor planning, it's helping with academics > too. > > > Here's one example about a 6 year old > > Professional anecdotal update from kindergarten teacher of a 6 year old apraxic > child after less than 2 weeks on Nutriiveda. > > “I wanted to let you know how things are going with Dominic. I think it’s safe > to say that everyone that works with him has noticed a great change in him over > the past 1-2 weeks. He is much more outgoing, much more in tune with what it > going on in the classroom, and very talkative. > > I think what I’ve noticed the most is that he is talking much more with his > peers during work time and play time. He also seems to be much more > self-directed when we do classwork. For example, last Monday when we made the > Valentine’s Day card, he did very well with the project and did not need much > direction from me to complete it. He did most of the project independently, even > the sticky tape (which has always been a challenge for him). I also heard that > on Friday, during their speech time with Mrs. Kulig, he came into class, took > out his ABC book and without any prompting from anyone, read the entire book for > the rest of the kids in the group! This is all great!!†> > Parents add “his teacher is not aware we have him on NV. We are pretty excited > since it has been six years with nothing like this until now.†> http://pursuitofresearch.com/2010/11/22/is-nutriiveda-creating-a-paradigm-shift-\ in-treatment-of-speech-impairments/ > > > Sorry if I went and this message seemed strong -but you have no idea -I have so > much more on this topic. So again -no from me for this exam unless you have to > -and if you do -be prepared to double check them. They are not always right > -I'll just leave it at that. > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2011 Report Share Posted March 27, 2011 Thanks for your thoughts. what disturbs us is that his classroom teachers (an ST, OT and a special ed. teacher) give us such vague answers and insist that this test will tell us all we need to know. we wonder what we're paying over $20,000 for if his own teachers (therapists) can't tell us. It just seems odd that specialists in the classroom can't tell us much, but a test that is geared toward kids that are more verbal and is just a quick peak at these kids- can tell us more. These kids are so different. A friend of mine with an apraxic kid bucked the system and put her child in an accelerated private school in the area (she teaches there, so had strings to get him in there- i used to teach there- one of the top private schools in the area) in kindergarten. He struggled a little that year, but was reading 4th grade level by 1st grade and is doing well today. a chess player, more on the geeky side vs. athletic, but happy. The therapists disagreed with her going down this route. Another friend (in CT) has her child in public school in Darien (he has apraxia)- he's doing well. When you pay big taxes, you get better schools (and services)- all I'll say. We have to pay out of pocket $3000 for this psych. ed. test, so $2500 would actually be a savings. i just think it's worth a 2nd opinion and to talk to someone more in the know about apraxia- not just all speech/language issues lumped together. Thanks! ________________________________ From: mosense <mosense@...> Sent: Sun, March 27, 2011 8:40:25 AM Subject: [ ] Re: psycho. educ. evaluation We live in NY, an hour outside NYC. We have never been able to say, No, to the Psych evaluations that go along with PT OT and Speech. Shes in 4th grade now, but we have reports from days of EI from Psych all thru the years. So even in EI, if you want your child evaluated for OT or PT, you must agree to the Psych or they wont do the others. They're not all bad reports and I get a lot of very useful information for her annual meetings. Just anohter perspective. I've thought of the outside Neuropsych evaluation, but I'm putting off that $2500 price tag as long as I can!!The school psychologist, from our VERY highly repspected district, has done a great job with her over the years! Maureen > > Thank you so much for your reply. It is difficult to go against the well > regarded professionals in the area. The other parents know that they don't know > > all the answers and aren't the best in the country, but the thought is " they're > > the best we have here. " I'm from CT and NY (I was born in NJ), so my gut tends > > to still go with northern thoughts (a whole 'nother issue . I have a good > friend whose son has apraxia and he's in a mainstream public school in Darien > and doing just fine. There are just lots of different thoughts on it. If they > were more honest and upfront, I'd be more impressed and trusting. His non-class > > OT only works there p/t. She is much more progressive and willing to try > different therapies and talk about nutrition- she's not in full agreement with > everything at the school (she's the one who did the therap. listening and wants > > to get the school onboard with ILS- let's just say she's frustrasted). She's >the > > one who seems most interested in conferences and being up with the newest > research, but I don't think many of them are really experts on apraxia at this > school. They know that low tone and sensory comes with it, but that's really > about it. They treat it from there. > > > > Anyway, thank you for your thoughts. Much appreciated and yes, today was day 1 > of NV. It all went down. He has 2 mos. left of school, so we'll see how it > goes! > > > Thanks, Marie > > > > > ________________________________ > From: kiddietalk <kiddietalk@...> > > Sent: Sat, March 26, 2011 4:26:32 PM > Subject: [ ] Re: psycho. educ. evaluation > > > Marie you so need private evaluations outside the school- and in my opinion > unless it's a rare educational psych who has great knowledge about speech > impairments and how to appropriately test one with a verbal disability I would > stick with neuroMD exams instead for apraxia as apraxia is not a psychological > condition and I've seen too many misdiagnosis. > > > I don't care for any school that feels that a test will answer all your > questions as I happen to have heard from Dr. a Tallal one of the Cherab > advisers that there are currently no 100 percent accurate cognitive or >receptive > > tests for a verbal disabled individual. Here's Dr. Tallal's background > http://www.cmbn.rutgers.edu/research/tallal/ I have a hunch based on her > research and educational background in working with our population she knows a > wee bit more than the people at your town school. > > My son Tanner when we lived in NJ it was the same type of school -awesome >public > > school for regular students and their program for apraxia was HIGHLY > inappropriate and bordered on abusive to what they did to my poor son Tanner. >I > > have story after story in the archives of how they punished him, how when they > tried to get him to say " Good morning Mrs. Whiseman " when the child couldn't > even have said the first word of that sentence (!) they put him in front of the > > class and he had his head down and the teacher took his face and forced him to > look up and patted his face -not hard enough to be a smack but more like a > " come > > on you can do it " kind of double quick pat and said " Come on Tanner you can do > it. Say Good morning Mrs. Whiseman " How do I know about those 2 alone? The > first the teacher told me and the second I saw through the double glass > observation room when he first started in this class which I didn't announce I > was there -because I didn't know I was supposed to as it was all new -and they > made it super clear to me that I was never to observe the class without > announcing I was there to observe. To put it bluntly how bad they were with my > > son Tanner -they took a completely sweet child who worked so hard in therapy > prior to his few months in this horror and created a child that they pegged and > > wrote into his IEP was " manipulative " Zimet CCC SLP from this group > who's now in Georgia was Tanner's EI therapist in Jersey before we moved so she > > and Dr. Agin and Ortega can vouch for how Tanner was prior to this > placement. > > So yes I advocated and had enough history to get Tanner placed in out of > district placement at the Summit Speech School which is an oral based school >for > > the hearing impaired in NJ and one of the top in the country. And the >nightmare > > was over as that school was incredible in every single way. A bunch of us with > > apraxia had hearing apraxic children at the school soon after Tanner got in - > but from what I know after Kanter the school director passed away and > someone else took over they cracked down on not letting kids in that were > hearing. Honestly that school saved my son and I don't know where he would be > without it. > > But when Tanner went to transition into kindergarten (at 6 -we kept him at SSS > until then and most of the kids at this school don't transition to public >school > > until 6 and the school has an extremely high success rate of mainstream after > preschool) he had to be tested by the same public school we left and by the >same > > educational psychologist. To make a long story short the public school as well > > as my son was doing didn't think he'd " make it " in a mainstream kindergarten > class. Oh don't get me started -what a group of idiots they were! And his >work > > in SSS and appropriate testing should have shown that. As it ended up this > story gets to much worse as to someone from my NJ district calling the case > manager where I moved to in Florida to say that a mistake was being made and he > > didn't belong in the mainstream that it's almost difficult to believe. And for > > the educators reading this -I am so aware that so many of you are awesome -but >I > > also know that the edcational psych tests they give verbal disabled children >are > > typically are so unfair and in some cases are a violation of our children's > Civil Rights of not being tested on their abilities on their disability. > > here's are links to the letter to parents I wrote years ago with the update > about kindergarten > http://www.cherab.org/information/familiesrelate/letter.html or > >http://www.cherabfoundation.org/2006/a-letter-to-parents-who-have-a-child-that-\ is-a-late-talker-first-written-7400-and-update-from-1003/ >/ > > > So if you don't have to do the testing just say no -if you do -get second > opinions. Actually either way I'd get second opinions because it seems based >on > > just a few comments you heard you are dealing with some professionals that have > > already pegged your son even prior to testing. > > Oh and about top academic private schools...after kindergarten - mainstream > where Tanner according to his teacher Mrs. was " not just making it but >one > > of the top students in his class " he went to a private school that was for > academically advanced students and was a straight A student. So don't say it's > > not possible -your child sounds very bright to me -why shouldn't he be top in > his class? > > PS...OK did you start the NV yet???? If you didn't please start it -it helps > with so much more than speech and motor planning, it's helping with academics > too. > > > Here's one example about a 6 year old > > Professional anecdotal update from kindergarten teacher of a 6 year old apraxic > > child after less than 2 weeks on Nutriiveda. > > “I wanted to let you know how things are going with Dominic. I think it’s safe > to say that everyone that works with him has noticed a great change in him over > > the past 1-2 weeks. He is much more outgoing, much more in tune with what it > going on in the classroom, and very talkative. > > I think what I’ve noticed the most is that he is talking much more with his > peers during work time and play time. He also seems to be much more > self-directed when we do classwork. For example, last Monday when we made the > Valentine’s Day card, he did very well with the project and did not need much > direction from me to complete it. He did most of the project independently, >even > > the sticky tape (which has always been a challenge for him). I also heard that > on Friday, during their speech time with Mrs. Kulig, he came into class, took > out his ABC book and without any prompting from anyone, read the entire book >for > > the rest of the kids in the group! This is all great!!†> > Parents add “his teacher is not aware we have him on NV. We are pretty excited > > since it has been six years with nothing like this until now.†>http://pursuitofresearch.com/2010/11/22/is-nutriiveda-creating-a-paradigm-shift\ -in-treatment-of-speech-impairments/ >/ > > > Sorry if I went and this message seemed strong -but you have no idea -I have so > > much more on this topic. So again -no from me for this exam unless you have to > > -and if you do -be prepared to double check them. They are not always right > -I'll just leave it at that. > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2011 Report Share Posted March 27, 2011 That is why I said you should be able to say no -or at least choose who evaluates if you are paying. You aren't in a public school as they don't charge. Why isn't your son in the public school system? And if they say he wouldn't make it -I say " says who?! " Save yourself money and grief as they sound clueless anyway and try public for next year. ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 27, 2011 Report Share Posted March 27, 2011 The $2500 is the estimate!! from one of the ONLY Pediatric Neuropsychologists in NYC. One of my very good friends is an Adult/Couples/Family Neuropsychologist who practices in NYC. I asked him for some names of colleagues who treat children. The name he gave me is the only one he told me that is strictly pediatric. His office said its a 5-6hour evaluation, at the least but would be very thorough and more information than the school psych testing. > > > > Thank you so much for your reply. It is difficult to go against the well > > regarded professionals in the area. The other parents know that they don't know > > > > all the answers and aren't the best in the country, but the thought is " they're > > > > the best we have here. " I'm from CT and NY (I was born in NJ), so my gut tends > > > > to still go with northern thoughts (a whole 'nother issue . I have a good > > friend whose son has apraxia and he's in a mainstream public school in Darien > > and doing just fine. There are just lots of different thoughts on it. If they > > > were more honest and upfront, I'd be more impressed and trusting. His non-class > > > > OT only works there p/t. She is much more progressive and willing to try > > different therapies and talk about nutrition- she's not in full agreement with > > > everything at the school (she's the one who did the therap. listening and wants > > > > to get the school onboard with ILS- let's just say she's frustrasted). She's > >the > > > > one who seems most interested in conferences and being up with the newest > > research, but I don't think many of them are really experts on apraxia at this > > > school. They know that low tone and sensory comes with it, but that's really > > about it. They treat it from there. > > > > > > > > Anyway, thank you for your thoughts. Much appreciated and yes, today was day 1 > > > of NV. It all went down. He has 2 mos. left of school, so we'll see how it > > goes! > > > > > > Thanks, Marie > > > > > > > > > > ________________________________ > > From: kiddietalk <kiddietalk@> > > > > Sent: Sat, March 26, 2011 4:26:32 PM > > Subject: [ ] Re: psycho. educ. evaluation > > > > > > Marie you so need private evaluations outside the school- and in my opinion > > unless it's a rare educational psych who has great knowledge about speech > > impairments and how to appropriately test one with a verbal disability I would > > > stick with neuroMD exams instead for apraxia as apraxia is not a psychological > > > condition and I've seen too many misdiagnosis. > > > > > > I don't care for any school that feels that a test will answer all your > > questions as I happen to have heard from Dr. a Tallal one of the Cherab > > advisers that there are currently no 100 percent accurate cognitive or > >receptive > > > > tests for a verbal disabled individual. Here's Dr. Tallal's background > > http://www.cmbn.rutgers.edu/research/tallal/ I have a hunch based on her > > research and educational background in working with our population she knows a > > > wee bit more than the people at your town school. > > > > My son Tanner when we lived in NJ it was the same type of school -awesome > >public > > > > school for regular students and their program for apraxia was HIGHLY > > inappropriate and bordered on abusive to what they did to my poor son Tanner. > >I > > > > have story after story in the archives of how they punished him, how when they > > > tried to get him to say " Good morning Mrs. Whiseman " when the child couldn't > > even have said the first word of that sentence (!) they put him in front of the > > > > class and he had his head down and the teacher took his face and forced him to > > > look up and patted his face -not hard enough to be a smack but more like a > > " come > > > > on you can do it " kind of double quick pat and said " Come on Tanner you can do > > > it. Say Good morning Mrs. Whiseman " How do I know about those 2 alone? The > > first the teacher told me and the second I saw through the double glass > > observation room when he first started in this class which I didn't announce I > > > was there -because I didn't know I was supposed to as it was all new -and they > > > made it super clear to me that I was never to observe the class without > > announcing I was there to observe. To put it bluntly how bad they were with my > > > > son Tanner -they took a completely sweet child who worked so hard in therapy > > prior to his few months in this horror and created a child that they pegged and > > > > wrote into his IEP was " manipulative " Zimet CCC SLP from this group > > who's now in Georgia was Tanner's EI therapist in Jersey before we moved so she > > > > and Dr. Agin and Ortega can vouch for how Tanner was prior to this > > placement. > > > > So yes I advocated and had enough history to get Tanner placed in out of > > district placement at the Summit Speech School which is an oral based school > >for > > > > the hearing impaired in NJ and one of the top in the country. And the > >nightmare > > > > was over as that school was incredible in every single way. A bunch of us with > > > > apraxia had hearing apraxic children at the school soon after Tanner got in - > > but from what I know after Kanter the school director passed away and > > someone else took over they cracked down on not letting kids in that were > > hearing. Honestly that school saved my son and I don't know where he would be > > > without it. > > > > But when Tanner went to transition into kindergarten (at 6 -we kept him at SSS > > > until then and most of the kids at this school don't transition to public > >school > > > > until 6 and the school has an extremely high success rate of mainstream after > > preschool) he had to be tested by the same public school we left and by the > >same > > > > educational psychologist. To make a long story short the public school as well > > > > as my son was doing didn't think he'd " make it " in a mainstream kindergarten > > class. Oh don't get me started -what a group of idiots they were! And his > >work > > > > in SSS and appropriate testing should have shown that. As it ended up this > > story gets to much worse as to someone from my NJ district calling the case > > manager where I moved to in Florida to say that a mistake was being made and he > > > > didn't belong in the mainstream that it's almost difficult to believe. And for > > > > the educators reading this -I am so aware that so many of you are awesome -but > >I > > > > also know that the edcational psych tests they give verbal disabled children > >are > > > > typically are so unfair and in some cases are a violation of our children's > > Civil Rights of not being tested on their abilities on their disability. > > > > here's are links to the letter to parents I wrote years ago with the update > > about kindergarten > > http://www.cherab.org/information/familiesrelate/letter.html or > > > >http://www.cherabfoundation.org/2006/a-letter-to-parents-who-have-a-child-that-\ is-a-late-talker-first-written-7400-and-update-from-1003/ > >/ > > > > > > So if you don't have to do the testing just say no -if you do -get second > > opinions. Actually either way I'd get second opinions because it seems based > >on > > > > just a few comments you heard you are dealing with some professionals that have > > > > already pegged your son even prior to testing. > > > > Oh and about top academic private schools...after kindergarten - mainstream > > where Tanner according to his teacher Mrs. was " not just making it but > >one > > > > of the top students in his class " he went to a private school that was for > > academically advanced students and was a straight A student. So don't say it's > > > > not possible -your child sounds very bright to me -why shouldn't he be top in > > his class? > > > > PS...OK did you start the NV yet???? If you didn't please start it -it helps > > with so much more than speech and motor planning, it's helping with academics > > too. > > > > > > Here's one example about a 6 year old > > > > Professional anecdotal update from kindergarten teacher of a 6 year old apraxic > > > > child after less than 2 weeks on Nutriiveda. > > > > “I wanted to let you know how things are going with Dominic. I think it’s safe > > > to say that everyone that works with him has noticed a great change in him over > > > > the past 1-2 weeks. He is much more outgoing, much more in tune with what it > > going on in the classroom, and very talkative. > > > > I think what I’ve noticed the most is that he is talking much more with his > > peers during work time and play time. He also seems to be much more > > self-directed when we do classwork. For example, last Monday when we made the > > Valentine’s Day card, he did very well with the project and did not need much > > direction from me to complete it. He did most of the project independently, > >even > > > > the sticky tape (which has always been a challenge for him). I also heard that > > > on Friday, during their speech time with Mrs. Kulig, he came into class, took > > out his ABC book and without any prompting from anyone, read the entire book > >for > > > > the rest of the kids in the group! This is all great!!†> > > > Parents add “his teacher is not aware we have him on NV. We are pretty excited > > > > since it has been six years with nothing like this until now.†> >http://pursuitofresearch.com/2010/11/22/is-nutriiveda-creating-a-paradigm-shift\ -in-treatment-of-speech-impairments/ > >/ > > > > > > Sorry if I went and this message seemed strong -but you have no idea -I have so > > > > much more on this topic. So again -no from me for this exam unless you have to > > > > -and if you do -be prepared to double check them. They are not always right > > -I'll just leave it at that. > > > > ===== > > Quote Link to comment Share on other sites More sharing options...
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