Guest guest Posted July 24, 2008 Report Share Posted July 24, 2008 We use NACD for two of our boys and have been thrilled with the whole thing. There were many posts by a number of us over the past year about NACD, so perhaps you could search the archives. Janice in particular is the best person to discuss NACD. We started with NACD for my son (6 years old), but it was after he was over the speech part of his dyspraxia. We mostly work on auditory processing, coordination, reading, and math. We are keeping an eye out for dyslexia, which is not uncommon among apraxic/dyspraxic kids. The NACD approach really works on hemispheric dominance issues and going back to the developmental steps you missed and doing them now. The better job WE do on getting the program done, the better he does. The proof is in the pudding, as they say. If you have severe speech issues, you will probably need them to develop an intensive speech program in addition to your basic program, but the basic one should cover all of your key issues in some form. Once you pay the upfront evaluation fee, all you pay is a monthly fee going forward. That includes phone consults, re- evaluations every three months, etc. For us, this is much cheaper than hiring therapists and tutors, and the results are much, much better. I wish I had discovered them years ago. I never would have found NACD if it weren't for Janice 's posts on this group. We recently started doing NACD with our two year old, who is showing all the signs of expressive language delay and some coordination/tone issues. His basic program includes a number of oral motor activities and some to develop receptive and expressive language. Compliance is challenging with him, but we are starting to make progress with him as well. He is having a nice burst of new words this week. Yay! Here are two links you might find helpful: ApraxiaDyspraxiaBiomedSupport/ --This is the group that many of the NACD people are on. It's very open to all discussions, but is theoretically about biomedical interventions. I love this group! Don't be intimidated by the posters who are doing more involved biomed -- just skip over what is too much for you. CM_RDI_with_ND --This is a new group that has sprung out of the above one. It is more focused on ND therapies, including NACD, but also has a lot of discussion about homeschooling and Charlotte Mason and RDI. I don't know anything about that stuff, but I lurk for NACD posts. Anyone interested in more information may email me off the group. Or check out www.nacd.org in NJ > > Hello everyone, > Do any of you do neurodevelopmental therapies with your children? Does > any one have experience with NACD (www.nacd.org) or any of the other > similar ND agencies (Hope and a Future, Little Giant Steps, etc)? I am > researching this option for my DS. Its an expensive option though and I > want to research as much as possible. Thank you for any replies. > Becky > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 25, 2008 Report Share Posted July 25, 2008 Hi , Thanks for all the info on NACD--?? but it would have been bettr to spell out what it stands for to get more people to read since the acronym means NOTHING to so many of us and some may just skip over it and never read further. I do really want to learn more and more about this as it has helped our daughter, who has definite metabolic disturbances along with her apraxia, the most. Speech therapy is a tool, but it doesn't address what's wrong to begin with,--as a friend of mine put it " it was like teaching a dog tricks--but nothing really stuck around to take him to the next learning step, the whole communication process was impaired because nothing was really retained outside therapy " =--- or very little. " For us it was the same until we started the diet/biomed stuff and now the progress is steady and she surprises us everyday, her skin psoriasis is better, her behavior has improved, now we have hope. Thank s again for the info. Elena Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 28, 2008 Report Share Posted July 28, 2008 The original poster referred to it as NACD so I believe that is why ran with it. It stands for: National Association for Child Development It was founded by the son of a physiatrist and cocreatoer of The Listening Program. He was the head of the educational component of the United Cerebral Palsy Foundation for a while. They know education, they know kids, they know nutrition and they know how it all fits to take the kid where they can go ar their personal optimal level. So far this has been the best find for us. Like any tool to help you with your kid you must use it to your advantage. You must talk to them and ask for help on how to implement it with other commitments in your life: be it drs, school, etc. Here is an overview: http://nacd.org/getting_started/index.html Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 28, 2008 Report Share Posted July 28, 2008 I see that Liz already answered the question, but let me add that they have about a dozen locations in the US and abroad. Their main office is in Utah, and their other permanent office is in West Chester, PA. (That's where we go.) Check their website for the specifics of the other spots. Anyone interested in the National Association for Child Development (NACD) can email me offlist. in NJ > > Hi , > Thanks for all the info on NACD--?? but it would have been bettr to spell out what it stands for to get more people to read since the acronym means NOTHING to so many of us and some may just skip over it and never read further. > > I do really want to learn more and more about this as it has helped our daughter, who has definite metabolic disturbances along with her apraxia, the most. Speech therapy is a tool, but it doesn't address what's wrong to begin with,--as a friend of mine put it " it was like teaching a dog tricks--but nothing really stuck around to take him to the next learning step, the whole communication process was impaired because nothing was really retained outside therapy " =--- or very little. " > > For us it was the same until we started the diet/biomed stuff and now the progress is steady and she surprises us everyday, her skin psoriasis is better, her behavior has improved, now we have hope. > Thank s again for the info. > Elena > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 28, 2008 Report Share Posted July 28, 2008 Thanks Liz. I'll look into it. Seems like there's always something more to learn and do... Elena Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2008 Report Share Posted July 29, 2008 Just to chime in here..... NACD literally changed my son's life. He was a special education lifer and after one year on their program, he went to mainstream junior high with no aids or accomodations. Today he is 'almost' neurotypical with many, many friends, pretty good grades and a social life to die for. He is truly a transformed kid and I owe them so so much for helping him. We are coming to the end of our 2nd year with NACD and I don't know that we will need to do an entire 3rd year..... my boy is doing pretty well now. I am a big, big fan of NACD. It is a lot of work but nothing else was helping and nothing else was working for him. This really did! Janice Mother of Mark, 13 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2008 Report Share Posted July 29, 2008 All I can add to this is a resounding AAAAAAMEN! YES-- this is something that I agree with 100% speaking about my 4 yr old who is Globally Dyspraxic. It's a hellish life, and we're just at the beginning stages of it-- but thank GOD we know now so we can work like the dickens to help him as much as we possibly can becky Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2008 Report Share Posted July 29, 2008 Janice thank you for your other good wishes and for chiming about NACD. I will look into it. That's what we all need a champion method/provider to help our children overcome their weaknesses and maximize their strengths. I'm so glad your son is doing so well now. You must be so proud knowing how far you've all come from where he was initially. Thanks again! -Elena Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2008 Report Share Posted July 29, 2008 How old was Mark when you started?!!! And how long did he do the program for?!!! Love, Gabby. :0) http://stemcellforautism.blogspot.com/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2008 Report Share Posted July 29, 2008 Not the answer you were looking for but something to be aware of. Since 2000 NACD has only been brought up by 3 people here other than one or two in the past two years who bring it up lots and still bring it up today. The other one or two who tried it said it was too expensive or too difficult. In general it's best to follow the successful pattern in this group and most stuck with the norm therapy traditional and alternative. It's good to be aware there are other things out there but again you don't have to start with the most expensive ...and obscure. If it was that good more would say good things about it. There's much negative press and not at all on just this group as again the overwhelming majority never heard of it nor tried it. So personally I'd explore a proven to be successful for the majority Montessori or other multisensory school over this method. Just a few links but much more out there. Psychomotor Patterning An Expose of a Cruel Pseudoscience Novella, MD 10/1/1996 The line which sharply demarcates mainstream medicine from alternative medicine is the line of science. It is possible to cross that line, however. Any alternative treatment which is tested in a rigorous scientific manner and found to be safe and effective, will be incorporated into mainstream medicine, it will have crossed the line. A therapy, on the other hand, which begins within the halls of mainstream medicine as a legitimate proposal, and is found, when tested scientifically, to be of no real value, will be discarded. Most such discarded therapies are destined to become forgotten footnotes in the annals of medical research. Some, however, are salvaged by practitioners of alternative medicine. These therapies have crossed the line in the other direction, descending from science into pseudoscience. The method of psychomotor patterning for the treatment of mental deficiencies is one such therapy. It began 30 years ago as a legitimate, if incorrect, scientific concept for a new treatment modality for mental retardation, brain injury, learning disabilities, and other cognitive maladies. The method was subjected to controlled trials and found to be of no value. It was debated in the scientific literature up until the early 1970's, when finally the medical community arrived at the consensus that patterning should be discarded as a false concept with no therapeutic role. Use of the techniques of patterning, however, has not died, as we will see. The concept of patterning was invented by Glenn Doman and C. Delacato in the 1960's, and is therefore often referred to as the Doman- Delacato technique.1 Their theories are primarily an extension of the older concept that ontogeny (the stages through which organisms develop from single cell to maturity) recapitulates phylogeny (the evolutionary history of the species). Therefore, the neurodevelopmental stages of crawling, creeping, crude walking, and mature walking through which normal children develop is directly related to the amphibian, reptilian, and mammalian evolutionary human ancestors. 2 Doman and Delacato's concept of mental retardation is that of failure of the individual to develop through the proper phylogenetic stages. Their treatment modality is therefore designed to stimulate the proper development of these stages, each of which must be mastered before progress can be made to the next stage. This stimulation is achieved through the method known as patterning. The patterning treatment involves the patient moving repeatedly in the manner of the current stage. In the " homolateral crawling " stage, for instance, the patient crawls by turning his head to one side while flexing the arm and leg of that side and extending the arm and leg of the opposite side. For patients who are unable to execute this exercise by themselves, they are passively moved in this manner by 4- 5 adults, alternating back and forth in a smooth manner. This must be repeated for at least 5 minutes 4 times per day. The purpose of this exercise is to impose the proper " pattern " onto the central nervous system. In the full treatment program, the exercises are combined with sensory stimulation, breathing exercises which are designed to increase oxygen flow to the brain, and a program of restriction and facilitation designed to promote hemispheric dominance. 3 The claim made for the technique by Doman, Delacato and their supporters is that, with this treatment method, mentally retarded and brain injured children can achieve improved, and even normal, development in the areas of visuo-spatial tasks, motor coordination, social skills, and intellect. They have also expanded these claims to include the idea that their techniques can promote superior development in a normal child. 4 The theoretical basis of psychomotor patterning is therefore based on two primary principles, the recapitulationist theory of ontogeny and phylogeny, and the belief that passive movements can influence the development and structure of the brain. Delacato himself writes " Man has evolved phylogenetically in a known pattern. The ontogenetic development of normal humans in general recapitulates that phylogenetic process. We have been able to take children who deviate from normal development (severe brain injured) and through the extrinsic imposition of normal patterns of movement and behavior have been able to neurologically organize them sufficiently so that they can be placed within a human developmental pattern of crawling, creeping, and walking. " 3 Medical treatments are evaluated on two criteria, their theoretical basis and their empirical value. Patterning has been rejected by the scientific community on both accounts. The theory of recapitulation has never been fully accepted, and even by the 1960's had been all but discarded by evolutionary and biological scientists. The essential flaw in the theory of recapitulation is that it is based on an incorrect linear concept of evolution. Evolutionary lines continuously branch and deviate, forming a complex bush of relationships, not a linear ladder of descent. Embryological development does not reflect the mature stages of other distant branches of this evolutionary bush. Studying the embryology of the developing fetus also does not reveal any evidence of successive stages reflecting past evolutionary ancestors. There is also no theoretical basis for the belief that patterns can be impressed upon the developing cortex. Brain development is genetically driven and involves a complex sequence of cell growth, migration, organization, and even programmed cell death. Abnormalities in this process can be caused by genetic flaws, toxic insults, infection, or biochemical abnormalities. There is no model by which any of these disparate causes can be influenced by passive, or even active, movement of the neck and limbs. Thirty years of subsequent neurological, embryological, and medical progress have failed to lend any theoretical support for Doman and Delacato's principles. Their practice of using breathing exercises to promote oxygen delivery to the brain also lacks an accepted theoretical basis. The brain and the cardiovascular system are designed to give highest priority to oxygen flow to the brain cells. Elaborate and powerful feedback mechanisms ensure adequate delivery. It is true that carbon dioxide retention, in this case achieved through breathing techniques, does increase blood flow to the brain. There is absolutely no reason to believe, however, that such increased flow is at all helpful to the developing brain. Despite the fact that patterning is theoretically bankrupt, if empirical evidence existed which demonstrated that patterning improves neurological development, it would be accepted and used. There are many mainstream interventions which are employed in modern medicine that lack a fully understood theoretical basis. Physicians are, at their heart, practical individuals, and if something works, it works. They require proof, however, that an intervention does indeed work and is safe. On this score, patterning has just not delivered. Over a period of approximately ten years in the late 60's and early 70's there were dozens of clinical trials comparing improvement in groups of developmentally delayed children given patterning treatment compared to controls who were given no treatment but similar amounts of attention. 2,5-7 Although most of the studies had significant methodological flaws, some were fairly well designed. None were perfect. More importantly, none confirmed the claims of Doman and Delacato. Some of the studies did show modest improvement in motor skills or visuo-spatial skills over controls. None showed improved intellectual development. The few positive results found were not impressive or reproducible. Eventually, such clinical trials stopped, as the technique was abandoned as a blind alley. This point marked the unequivocal crossing over of patterning from science to pseudoscience. The tragedy of this story does not stem from the fact that patterning is a failed theory. It is regrettable that patterning did not deliver as promised, for any legitimate treatment for brain injured and retarded children would be most welcome. The real tragedy began, however, when Doman and Delacato released their claims for a new dramatic treatment before their theories had been scientifically validated. This behavior, reminiscent of the cold fusion fiasco, is more than just professionally irresponsible. In physics, such behavior is merely bad form; when dealing with the desperate parents of brain injured children, it can be considered cruel. Doman and Delacato were widely criticized for publicizing their unsubstantiated claims, giving false hope to vulnerable parents and their afflicted children. The saga, however, did not end with the scientific death of patterning. Doman, Delacato and their associates began incorporating the patterning technique into their Institutes for the Achievement of Human Potential (IAHP), which was established in Philadelphia in the 1950's. They continued to advertise and use patterning uninterrupted right through the scientific controversy, past the scientific condemnation, and on into the present day. I was also able to locate one other institution, the National Academy of Child Development (NACD), located in Huntsville, Utah, that offers patterning as part of their treatment program. The NACD is run by Doman, the nephew of Glenn Doman, although both institutions are eager to point out that there is currently no association between the two. On August 8, 1996, NBC aired a program titled " Miracle Babies " , hosted by Kathy Lee Gifford. The program included a segment portraying an apparent " miracle cure " of a child suffering from moderate mental retardation. As is all too typical of the lay press, Kathy Lee provided an emotionally appealing yet completely uncritical presentation of the patterning technique, touting its virtues without even a hint of skepticism. There was no evidence that NBC did any investigative reporting into the background and validity of the intervention they were promoting on their program. The segment did bring out, however, even if for the wrong reasons, the desperateness of the parents. They were clearly devastated, as any parents would be, by the need to finally accept that their child was not developing normally. In their desperation, they sought any possible hope, and it was offered to them by the IAHP. The hope that they purchased, however, came at a heavy price, both financial and emotional. Both the IAHP and the NACD rely heavily on the family as the primary deliverers of the patterning treatment method. In order to even reach the stage where their child can be enrolled into the aggressive treatment program, they must first complete a training and evaluation course which begin for both institutions with purchasing and listening to a set of audio tapes. The IAHP states in their literature that only the most dedicated and capable parents will make it to the final stage of treatment. The NACD appears less demanding, but they follow the same principle. The end result is that the parents and other family members of the patient must alter their lives to institute a daily program of patterning exercises, breathing exercises, and programs of sensory stimulation. The mother interviewed by Kathy Lee stated that the program was so demanding that it dominated her life, resulting in emotional and physical exhaustion. The exceptional demands of the patterning method is the primary reason cited in the medical literature for caution in evaluating patterning, for the obvious harm that would ensue if the method were recommended prematurely, without good proof that it is effective. The program also illuminated another important feature of the patterning phenomenon, the difference between anecdotal and scientific evaluation of its effectiveness. One important fact to understand is that most children, even severely mentally retarded children, still grow and develop, although on a slower curve than average. Therefore, any child admitted into any treatment program will make some progress as an inevitable consequence of time and their natural development, even if that treatment program is completely worthless. Without adequate controls, it is therefore impossible to evaluate any such treatment. Of course, Kathy Lee and the parents of the child on the program reported remarkable progress. Whether or not the treatments played any role, however, cannot be known. The viewers, however, were meant to come away with the sense that they had witnessed a miracle cure. The NACD and IAHP literature both caution that individual results will vary. By emphasizing the need for dedicated capable parents, they also create a situation in which, if a patient fails to make significant progress, the parents are the ones to blame. These parents now have the added guilt of feeling inadequate to have helped their injured child. Most practitioners of alternative medicine either practice or are at least accepting of many different forms of alternative cures. This results from the fact that if one has a casual, or even anti, science attitude regarding one alternative modality, then they will likely have a similar attitude towards other modalities. It is not surprising, therefore, that the NACD embraces other scientifically questionable practices. For instance, the NACD advertises on their web site that they also evaluate and treat for food sensitivities. Although there is not the space here to adequately address this complex issue, suffice to say that food sensitivities are controversial at best, and certainly lack scientific acceptance. The excerpt in the box below is quite revealing. 8 I doubt there are many children who do not have three or more of these symptoms, especially since many are vague or qualified enough to apply to anyone. The NACD also offers a consultation with an " orthomolecular physician. " Again, I will not delve into this issue here, but suffice to say such " physicians " are clearly outside of the mainstream. Unproved therapies can be harmful in many ways, not always by direct toxicity or physical harm. The promotion of psychomotor patterning by institutions which make bold unsubstantiated claims about its effectiveness may cause significant financial and emotional damage. Such claims instill false hope in people who are likely already plagued by guilt and depression. By doing so, these desperate parents are being set up for a crushing disappointment or further guilt of inadequacy. In the process they must spend a great deal of their resources of time, energy, emotion, and money. These resources are taken away from their other children and other important facets of their lives, resources they might not be willing to spend if not for the fantastic claims which have lured them to this path. They are also distracted from dealing with the situation in other practical ways and coping psychologically as a family with the reality of having a brain injured or mentally retarded child. They are encouraged, in fact, to remain in a state of denial while they are pursuing a false cure. The Doman-Delacato patterning technique is pseudoscience because it is premised on a bankrupt and discarded theory and, more importantly, has failed to demonstrate any significant effectiveness under controlled conditions, and yet it is being purveyed as an innovative and effective treatment, and even possibly a cure. The IAHP and NACD cannot support the claims that they make, and are therefore guilty of fraud. Current regulations should prevent such abuse, but unfortunately such institutions as the FDA lack the manpower and the teeth to properly enforce such regulations and fulfill their role to protect the public from the snake-oil salesman, dressed up in the modern clothes of alternative medicine, that increasingly prey upon the vulnerable, the sick, and the desperate. References: 1. Doman RJ, Spitz EB, Zucman E, Delacato CH, and Doman G: Children with severe brain injuries, Neurologic organization in terms of mobility. JAMA, 174:257, 1960 2. Cohen HJ, Birch HG, Taft LT: Some considerations for evaluating the Doman-Delacato " Patterning " method. Pediatrics, 45:302-14, 1970 3. Delacato CH: The Diagnosis and Treatment of Speech and Reading Problems. Springfield, Illinois: C , 1963. 4. Doman G, Delacato CH: Train Your Baby to be a Genius. McCall's Magazine, p. 65, March 1965 5. Neman R, Roos P, McCann BM, Menolascino FJ, Heal LW: Experimental Evaluation of Sensorimotor Patterning used with Mentally Retarded Children. Am J Mental Deficiency, 79:372-84, 1975 6. Ziegler E, S: On " An Experimental Evaluation of Sensorimotor Patterning " : A Critique. Am J Mental Deficiency, 79:483- 92, 1975 7. Freeman RD: Controversy Over " Patterning " as a Treatment for Brain Damage in Children. JAMA, 202:83-86, 1967 8. NACD website, URL-http://www.nacd.org/articles/food.html http://www.theness.com/articles.asp?id=56 Kathleen Ann Quill 'Teaching children with autism' book: " thousands of families have wasted time and money to follow Doman's methods. " " Professionals have nothing to learn from Doman's pseudoscientific treatments, but they have plenty to learn from his marketing strategy " , which is aimed at parent's " hopes and fantasies " . (if you read from this book sounds like he blames the mom so I'm shocked anyone would support this method!!!) http://books.google.com/books?id=kT8DbfNcU5wC & pg=PA57 & lpg=PA57 & dq=Kathleen+Ann+Q\ uill+doman & source=web & ots=y36f65kn6g & sig=y0Z1Xa1lvutcBW44YrmLNUhx3BQ & hl=en & sa=X & \ oi=book_result & resnum=1 & ct=result A blog about it " Ok...my Sister-in-law has a son who was born with Down Syndrome. Such a gorgeous little guy. My SIL is all business, but when she got pregnant we saw a new side of her come out. Some emotion. Some Mothering. She is a high powered business lady and she was thinking of being a stay at home Mom! Too cool! The babe was born and the babe has DS. A lot of upset in their home and for the family as might be expected when things down go as planned. SIL was then definitely thinking SAHM. Then she decided not to be a AHM and went with daycare (which is provided by multi-billion dollar corporation for which she works). They got involved pretty early with NACD. This has the hairs on the back of my neck rasied. We checked out NACD at the same time we checked out Son-rise. I listened to 16 CD's I think. 12 Lecture, 2 on Autism and 2 on parent reactions. Some of this clicked with me (as I liked the medical model they were posing), but a WHOLE LOT did not. I went to my pediatrician who is very knowledgeable. He has been doing this for 30 years and is very well-respected. In addition, he keeps up with all the latest and he will get on the web and research the heck out of anything you bring to him. I mention NACD and he has not heard of it. He asks me about what they do. As soon as I say, " Neurological disorganization " he stops me and says... " Is this Glenn Doman? Are they based out of PA? " Well...it is a Doman and they have a campus in PA. " He never gets animated about this stuff. Very open to whatever you want to try, but is very protective of us (and all his patients) and usually simply states that the more expensive usually something is wrong. He gets animated about Doman/Delacatto and states unequivocally that they are a scam. Thatthey founded IAHP (The Institute for the Advancement of Human Potential). He says that if you bring up their names at a conference you will be laughed out of the hall and that they have been around for a long time, switching names to stay alive with no external research to back up their treatments. WHOA! I had googled negative stuff on NACD and could not find much. Now I googled Doman. Yeah...there it was. Obviously, we did not go that route (and I apologize to anyone here who is using this successfully. This is simply my experience. SIL is using NACD almost exclusively. She buys the whole enchilada. She say that the Birth to Three therapists are " worthless. " She sticks to a strict program with her babe. The kid is now a year old and not crawling (belly only). With a PT he should be there by now. She is passing on so many theapies and has no tolerance for anything save NACD! She even says that if/when she has another kid even if the kid is NT she is going to put him/her into the NACD program! HOLY MOONIE BATMAN! I can't say anyting can I? I know I can't. It just kills me! The only good thing I see is that it has made her (and hopefully her hubby) more involved with the kid. They have to be with the babe 2hours minimum per day. This is part of the program. That can never hurt...all that 1:1 attention. But the rest...it chaps my a$$. Thanks for reading. Good grief! She definitely sounds brainwashed if she would want to follow a rigorous program for a child without special needs. I have only heard of Doman used on children/people with severe brain injuries, not Down syndrome. No matter what you say, she will not change her mind so like you said there's no point in arguing with her. But who knows, maybe modelling good interaction with your autistic child will eventually rub off on her. Good luck with everything. http://www.autism-pdd.net/testdump/test15578. The Doman-Delacato patterning technique is pseudoscience because it is premised on a bankrupt and discarded theory and, more importantly, has failed to demonstrate any significant effectiveness under controlled conditions, and yet it is being purveyed as an innovative and effective treatment, and even possibly a cure. The IAHP and NACD cannot support the claims that they make, and are therefore guilty of fraud. Current regulations should prevent such abuse, but unfortunately such institutions as the FDA lack the manpower and the teeth to properly enforce such regulations and fulfill their role to protect the public from the snake-oil salesman, dressed up in the modern clothes of alternative medicine, that increasingly prey upon the vulnerable, the sick, and the desperate. http://trusted.md/feed/items/system/2008/03/12/brain_gym_educational_kinesiology\ _not_effective ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2008 Report Share Posted July 29, 2008 This cracks me up. I spent $3000 on useless speech therapy for my boy last year for the most part. The Prompt Therapist was knowledgeable but by the time we got him there her work was done. I only really did it to be sure and based on this type of post here...did not want to go against the grain like I did with the milk. I will spend $2520 this year on NACD and I will know what it did and did not do. So far, from what I can see, it is worth every penny. Part of that $ is for continuous consult in case the program is too difficult. NACD has been around as long as or longer as traditional therapy and is, in fact, traditional therapy done right. The question is not one of who posts about it but rather whether it works. > > Not the answer you were looking for but something to be aware of. > > Since 2000 NACD has only been brought up by 3 people here other than > one or two in the past two years who bring it up lots and still bring > it up today. The other one or two who tried it said it was too > expensive or too difficult. In general it's best to follow the > successful pattern in this group and most stuck with the norm therapy > traditional and alternative. It's good to be aware there are other > things out there but again you don't have to start with the most > expensive ...and obscure. If it was that good more would say good > things about it. There's much negative press and not at all on just > this group as again the overwhelming majority never heard of it nor > tried it. So personally I'd explore a proven to be successful for > the majority Montessori or other multisensory school over this method. > > Just a few links but much more out there. > > Psychomotor Patterning > > An Expose of a Cruel Pseudoscience > > Novella, MD > > > > 10/1/1996 > > > The line which sharply demarcates mainstream medicine from > alternative medicine is the line of science. It is possible to cross > that line, however. Any alternative treatment which is tested in a > rigorous scientific manner and found to be safe and effective, will > be incorporated into mainstream medicine, it will have crossed the > line. A therapy, on the other hand, which begins within the halls of > mainstream medicine as a legitimate proposal, and is found, when > tested scientifically, to be of no real value, will be discarded. > Most such discarded therapies are destined to become forgotten > footnotes in the annals of medical research. Some, however, are > salvaged by practitioners of alternative medicine. These therapies > have crossed the line in the other direction, descending from science > into pseudoscience. > > The method of psychomotor patterning for the treatment of mental > deficiencies is one such therapy. It began 30 years ago as a > legitimate, if incorrect, scientific concept for a new treatment > modality for mental retardation, brain injury, learning disabilities, > and other cognitive maladies. The method was subjected to controlled > trials and found to be of no value. It was debated in the scientific > literature up until the early 1970's, when finally the medical > community arrived at the consensus that patterning should be > discarded as a false concept with no therapeutic role. Use of the > techniques of patterning, however, has not died, as we will see. > > The concept of patterning was invented by Glenn Doman and C. Delacato > in the 1960's, and is therefore often referred to as the Doman- > Delacato technique.1 Their theories are primarily an extension of the > older concept that ontogeny (the stages through which organisms > develop from single cell to maturity) recapitulates phylogeny (the > evolutionary history of the species). Therefore, the > neurodevelopmental stages of crawling, creeping, crude walking, and > mature walking through which normal children develop is directly > related to the amphibian, reptilian, and mammalian evolutionary human > ancestors. 2 > > Doman and Delacato's concept of mental retardation is that of failure > of the individual to develop through the proper phylogenetic stages. > Their treatment modality is therefore designed to stimulate the > proper development of these stages, each of which must be mastered > before progress can be made to the next stage. This stimulation is > achieved through the method known as patterning. > > The patterning treatment involves the patient moving repeatedly in > the manner of the current stage. In the " homolateral crawling " stage, > for instance, the patient crawls by turning his head to one side > while flexing the arm and leg of that side and extending the arm and > leg of the opposite side. For patients who are unable to execute this > exercise by themselves, they are passively moved in this manner by 4- > 5 adults, alternating back and forth in a smooth manner. This must be > repeated for at least 5 minutes 4 times per day. The purpose of this > exercise is to impose the proper " pattern " onto the central nervous > system. In the full treatment program, the exercises are combined > with sensory stimulation, breathing exercises which are designed to > increase oxygen flow to the brain, and a program of restriction and > facilitation designed to promote hemispheric dominance. 3 > > The claim made for the technique by Doman, Delacato and their > supporters is that, with this treatment method, mentally retarded and > brain injured children can achieve improved, and even normal, > development in the areas of visuo-spatial tasks, motor coordination, > social skills, and intellect. They have also expanded these claims to > include the idea that their techniques can promote superior > development in a normal child. 4 > > The theoretical basis of psychomotor patterning is therefore based on > two primary principles, the recapitulationist theory of ontogeny and > phylogeny, and the belief that passive movements can influence the > development and structure of the brain. Delacato himself writes " Man > has evolved phylogenetically in a known pattern. The ontogenetic > development of normal humans in general recapitulates that > phylogenetic process. We have been able to take children who deviate > from normal development (severe brain injured) and through the > extrinsic imposition of normal patterns of movement and behavior have > been able to neurologically organize them sufficiently so that they > can be placed within a human developmental pattern of crawling, > creeping, and walking. " 3 > > Medical treatments are evaluated on two criteria, their theoretical > basis and their empirical value. Patterning has been rejected by the > scientific community on both accounts. The theory of recapitulation > has never been fully accepted, and even by the 1960's had been all > but discarded by evolutionary and biological scientists. > > The essential flaw in the theory of recapitulation is that it is > based on an incorrect linear concept of evolution. Evolutionary lines > continuously branch and deviate, forming a complex bush of > relationships, not a linear ladder of descent. Embryological > development does not reflect the mature stages of other distant > branches of this evolutionary bush. Studying the embryology of the > developing fetus also does not reveal any evidence of successive > stages reflecting past evolutionary ancestors. > > There is also no theoretical basis for the belief that patterns can > be impressed upon the developing cortex. Brain development is > genetically driven and involves a complex sequence of cell growth, > migration, organization, and even programmed cell death. > Abnormalities in this process can be caused by genetic flaws, toxic > insults, infection, or biochemical abnormalities. There is no model > by which any of these disparate causes can be influenced by passive, > or even active, movement of the neck and limbs. Thirty years of > subsequent neurological, embryological, and medical progress have > failed to lend any theoretical support for Doman and Delacato's > principles. > > Their practice of using breathing exercises to promote oxygen > delivery to the brain also lacks an accepted theoretical basis. The > brain and the cardiovascular system are designed to give highest > priority to oxygen flow to the brain cells. Elaborate and powerful > feedback mechanisms ensure adequate delivery. It is true that carbon > dioxide retention, in this case achieved through breathing > techniques, does increase blood flow to the brain. There is > absolutely no reason to believe, however, that such increased flow is > at all helpful to the developing brain. > > Despite the fact that patterning is theoretically bankrupt, if > empirical evidence existed which demonstrated that patterning > improves neurological development, it would be accepted and used. > There are many mainstream interventions which are employed in modern > medicine that lack a fully understood theoretical basis. Physicians > are, at their heart, practical individuals, and if something works, > it works. They require proof, however, that an intervention does > indeed work and is safe. > > On this score, patterning has just not delivered. Over a period of > approximately ten years in the late 60's and early 70's there were > dozens of clinical trials comparing improvement in groups of > developmentally delayed children given patterning treatment compared > to controls who were given no treatment but similar amounts of > attention. 2,5-7 Although most of the studies had significant > methodological flaws, some were fairly well designed. None were > perfect. More importantly, none confirmed the claims of Doman and > Delacato. > > Some of the studies did show modest improvement in motor skills or > visuo-spatial skills over controls. None showed improved intellectual > development. The few positive results found were not impressive or > reproducible. Eventually, such clinical trials stopped, as the > technique was abandoned as a blind alley. This point marked the > unequivocal crossing over of patterning from science to pseudoscience. > > The tragedy of this story does not stem from the fact that patterning > is a failed theory. It is regrettable that patterning did not deliver > as promised, for any legitimate treatment for brain injured and > retarded children would be most welcome. The real tragedy began, > however, when Doman and Delacato released their claims for a new > dramatic treatment before their theories had been scientifically > validated. > > This behavior, reminiscent of the cold fusion fiasco, is more than > just professionally irresponsible. In physics, such behavior is > merely bad form; when dealing with the desperate parents of brain > injured children, it can be considered cruel. Doman and Delacato were > widely criticized for publicizing their unsubstantiated claims, > giving false hope to vulnerable parents and their afflicted children. > > The saga, however, did not end with the scientific death of > patterning. Doman, Delacato and their associates began incorporating > the patterning technique into their Institutes for the Achievement of > Human Potential (IAHP), which was established in Philadelphia in the > 1950's. They continued to advertise and use patterning uninterrupted > right through the scientific controversy, past the scientific > condemnation, and on into the present day. > > I was also able to locate one other institution, the National Academy > of Child Development (NACD), located in Huntsville, Utah, that offers > patterning as part of their treatment program. The NACD is run by > Doman, the nephew of Glenn Doman, although both institutions > are eager to point out that there is currently no association between > the two. > > On August 8, 1996, NBC aired a program titled " Miracle Babies " , > hosted by Kathy Lee Gifford. The program included a segment > portraying an apparent " miracle cure " of a child suffering from > moderate mental retardation. As is all too typical of the lay press, > Kathy Lee provided an emotionally appealing yet completely uncritical > presentation of the patterning technique, touting its virtues without > even a hint of skepticism. There was no evidence that NBC did any > investigative reporting into the background and validity of the > intervention they were promoting on their program. > > The segment did bring out, however, even if for the wrong reasons, > the desperateness of the parents. They were clearly devastated, as > any parents would be, by the need to finally accept that their child > was not developing normally. In their desperation, they sought any > possible hope, and it was offered to them by the IAHP. The hope that > they purchased, however, came at a heavy price, both financial and > emotional. > > Both the IAHP and the NACD rely heavily on the family as the primary > deliverers of the patterning treatment method. In order to even reach > the stage where their child can be enrolled into the aggressive > treatment program, they must first complete a training and evaluation > course which begin for both institutions with purchasing and > listening to a set of audio tapes. The IAHP states in their > literature that only the most dedicated and capable parents will make > it to the final stage of treatment. The NACD appears less demanding, > but they follow the same principle. > > The end result is that the parents and other family members of the > patient must alter their lives to institute a daily program of > patterning exercises, breathing exercises, and programs of sensory > stimulation. The mother interviewed by Kathy Lee stated that the > program was so demanding that it dominated her life, resulting in > emotional and physical exhaustion. The exceptional demands of the > patterning method is the primary reason cited in the medical > literature for caution in evaluating patterning, for the obvious harm > that would ensue if the method were recommended prematurely, without > good proof that it is effective. > > The program also illuminated another important feature of the > patterning phenomenon, the difference between anecdotal and > scientific evaluation of its effectiveness. One important fact to > understand is that most children, even severely mentally retarded > children, still grow and develop, although on a slower curve than > average. Therefore, any child admitted into any treatment program > will make some progress as an inevitable consequence of time and > their natural development, even if that treatment program is > completely worthless. Without adequate controls, it is therefore > impossible to evaluate any such treatment. Of course, Kathy Lee and > the parents of the child on the program reported remarkable progress. > Whether or not the treatments played any role, however, cannot be > known. The viewers, however, were meant to come away with the sense > that they had witnessed a miracle cure. > > The NACD and IAHP literature both caution that individual results > will vary. By emphasizing the need for dedicated capable parents, > they also create a situation in which, if a patient fails to make > significant progress, the parents are the ones to blame. These > parents now have the added guilt of feeling inadequate to have helped > their injured child. > > Most practitioners of alternative medicine either practice or are at > least accepting of many different forms of alternative cures. This > results from the fact that if one has a casual, or even anti, science > attitude regarding one alternative modality, then they will likely > have a similar attitude towards other modalities. It is not > surprising, therefore, that the NACD embraces other scientifically > questionable practices. > > For instance, the NACD advertises on their web site that they also > evaluate and treat for food sensitivities. Although there is not the > space here to adequately address this complex issue, suffice to say > that food sensitivities are controversial at best, and certainly lack > scientific acceptance. The excerpt in the box below is quite > revealing. 8 I doubt there are many children who do not have three or > more of these symptoms, especially since many are vague or qualified > enough to apply to anyone. The NACD also offers a consultation with > an " orthomolecular physician. " Again, I will not delve into this > issue here, but suffice to say such " physicians " are clearly outside > of the mainstream. > > Unproved therapies can be harmful in many ways, not always by direct > toxicity or physical harm. The promotion of psychomotor patterning by > institutions which make bold unsubstantiated claims about its > effectiveness may cause significant financial and emotional damage. > Such claims instill false hope in people who are likely already > plagued by guilt and depression. By doing so, these desperate parents > are being set up for a crushing disappointment or further guilt of > inadequacy. In the process they must spend a great deal of their > resources of time, energy, emotion, and money. These resources are > taken away from their other children and other important facets of > their lives, resources they might not be willing to spend if not for > the fantastic claims which have lured them to this path. They are > also distracted from dealing with the situation in other practical > ways and coping psychologically as a family with the reality of > having a brain injured or mentally retarded child. They are > encouraged, in fact, to remain in a state of denial while they are > pursuing a false cure. > > The Doman-Delacato patterning technique is pseudoscience because it > is premised on a bankrupt and discarded theory and, more importantly, > has failed to demonstrate any significant effectiveness under > controlled conditions, and yet it is being purveyed as an innovative > and effective treatment, and even possibly a cure. The IAHP and NACD > cannot support the claims that they make, and are therefore guilty of > fraud. Current regulations should prevent such abuse, but > unfortunately such institutions as the FDA lack the manpower and the > teeth to properly enforce such regulations and fulfill their role to > protect the public from the snake-oil salesman, dressed up in the > modern clothes of alternative medicine, that increasingly prey upon > the vulnerable, the sick, and the desperate. > > References: > > 1. Doman RJ, Spitz EB, Zucman E, Delacato CH, and Doman G: Children > with severe brain injuries, Neurologic organization in terms of > mobility. JAMA, 174:257, 1960 > 2. Cohen HJ, Birch HG, Taft LT: Some considerations for evaluating > the Doman-Delacato " Patterning " method. Pediatrics, 45:302-14, 1970 > 3. Delacato CH: The Diagnosis and Treatment of Speech and Reading > Problems. Springfield, Illinois: C , 1963. > 4. Doman G, Delacato CH: Train Your Baby to be a Genius. McCall's > Magazine, p. 65, March 1965 > 5. Neman R, Roos P, McCann BM, Menolascino FJ, Heal LW: Experimental > Evaluation of Sensorimotor Patterning used with Mentally Retarded > Children. Am J Mental Deficiency, 79:372-84, 1975 > 6. Ziegler E, S: On " An Experimental Evaluation of > Sensorimotor Patterning " : A Critique. Am J Mental Deficiency, 79:483- > 92, 1975 > 7. Freeman RD: Controversy Over " Patterning " as a Treatment for Brain > Damage in Children. JAMA, 202:83-86, 1967 > 8. NACD website, URL-http://www.nacd.org/articles/food.html > http://www.theness.com/articles.asp?id=56 > > Kathleen Ann Quill 'Teaching children with autism' book: " thousands > of families have wasted time and money to follow Doman's > methods. " " Professionals have nothing to learn from Doman's > pseudoscientific treatments, but they have plenty to learn from his > marketing strategy " , which is aimed at parent's " hopes and fantasies " . > > (if you read from this book sounds like he blames the mom so I'm > shocked anyone would support this method!!!) > http://books.google.com/books?id=kT8DbfNcU5wC & pg=PA57 & lpg=PA57 & dq=Kathleen+Ann+Q\ uill+doman & source=web & ots=y36f65kn6g & sig=y0Z1Xa1lvutcBW44YrmLNUhx3BQ & hl=en & sa=X & \ oi=book_result & resnum=1 & ct=result > > A blog about it > > " Ok...my Sister-in-law has a son who was born with Down Syndrome. > Such a gorgeous little guy. > My SIL is all business, but when she got pregnant we saw a new side > of her come out. Some emotion. Some Mothering. She is a high > powered business lady and she was thinking of being a stay at home > Mom! Too cool! The babe was born and the babe has DS. A lot of > upset in their home and for the family as might be expected when > things down go as planned. SIL was then definitely thinking SAHM. > Then she decided not to be a AHM and went with daycare (which is > provided by multi-billion dollar corporation for which she works). > They got involved pretty early with NACD. This has the hairs on the > back of my neck rasied. We checked out NACD at the same time we > checked out Son-rise. I listened to 16 CD's I think. 12 Lecture, 2 > on Autism and 2 on parent reactions. Some of this clicked with me > (as I liked the medical model they were posing), but a WHOLE LOT did > not. > I went to my pediatrician who is very knowledgeable. He has been > doing this for 30 years and is very well-respected. In addition, he > keeps up with all the latest and he will get on the web and research > the heck out of anything you bring to him. I mention NACD and he has > not heard of it. He asks me about what they do. As soon as I > say, " Neurological disorganization " he stops me and says... " Is this > Glenn Doman? Are they based out of PA? " Well...it is a Doman and > they have a campus in PA. " He never gets animated about this stuff. > Very open to whatever you want to try, but is very protective of us > (and all his patients) and usually simply states that the more > expensive usually something is wrong. He gets animated about > Doman/Delacatto and states unequivocally that they are a scam. > Thatthey founded IAHP (The Institute for the Advancement of Human > Potential). He says that if you bring up their names at a conference > you will be laughed out of the hall and that they have been around > for a long time, switching names to stay alive with no external > research to back up their treatments. > WHOA! > I had googled negative stuff on NACD and could not find much. Now I > googled Doman. Yeah...there it was. Obviously, we did not go that > route (and I apologize to anyone here who is using this > successfully. This is simply my experience. > SIL is using NACD almost exclusively. She buys the whole enchilada. > She say that the Birth to Three therapists are " worthless. " She > sticks to a strict program with her babe. The kid is now a year old > and not crawling (belly only). With a PT he should be there by now. > She is passing on so many theapies and has no tolerance for anything > save NACD! She even says that if/when she has another kid even if > the kid is NT she is going to put him/her into the NACD program! > HOLY MOONIE BATMAN! > I can't say anyting can I? I know I can't. It just kills me! > The only good thing I see is that it has made her (and hopefully her > hubby) more involved with the kid. They have to be with the babe > 2hours minimum per day. This is part of the program. That can never > hurt...all that 1:1 attention. > But the rest...it chaps my a$$. > Thanks for reading. > Good grief! She definitely sounds brainwashed if she would want to > follow a rigorous program for a child without special needs. I have > only heard of Doman used on children/people with severe brain > injuries, not Down syndrome. > No matter what you say, she will not change her mind so like you said > there's no point in arguing with her. But who knows, maybe modelling > good interaction with your autistic child will eventually rub off on > her. > Good luck with everything. > http://www.autism-pdd.net/testdump/test15578. > > The Doman-Delacato patterning technique is pseudoscience because it > is premised on a bankrupt and discarded theory and, more importantly, > has failed to demonstrate any significant effectiveness under > controlled conditions, and yet it is being purveyed as an innovative > and effective treatment, and even possibly a cure. The IAHP and NACD > cannot support the claims that they make, and are therefore guilty of > fraud. Current regulations should prevent such abuse, but > unfortunately such institutions as the FDA lack the manpower and the > teeth to properly enforce such regulations and fulfill their role to > protect the public from the snake-oil salesman, dressed up in the > modern clothes of alternative medicine, that increasingly prey upon > the vulnerable, the sick, and the desperate. > http://trusted.md/feed/items/system/2008/03/12/brain_gym_educational_kinesiology\ _not_effective > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2008 Report Share Posted July 29, 2008 Re: 1196 article Patterning, the type talked about there, was not what NACD did and they no longer do full patterning at all from what I am told. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2008 Report Share Posted July 29, 2008 , Considering I pay $142 a month for NACD.... I hardly think that's too expensive! I know that new clients pay more now-a-days but not much more and that is exactly what I pay..... I can email my invoices if you wish. It is NON-PROFIT!! I believe that the first evaluation is $950. Believe me.... the airfair I pay is more than the cost of our program. But considering the numerous therapies that my son needed at the cost of $150 to $200 an hour..... NACD was the place for me! In addition, there are plenty out there doing NACD very successfully and perhaps they don't have time to write on the boards. As a matter of fact, I went to their Rendez-vous and met two others that are on this list who do not post anymore. Perhaps they got scared off. At NACD, I have gotten OT, PT, vision therapy, Auditory processing therapy, etc. etc. The price is right but the work is hard since I am the therapist. THAT is the downside of NACD..... it is a lot of work and takes committment. People talk about it because it is working for their child. I don't understand why you 'trash' things that you have no personal knowledge of? Does not make sense. In the 9.5 years my son has spent in therapy.... Not MUCH was achieved! 2 years of NACD and right now my boy has 3 friends over.... he just whipped the A student's butt in Scrabble and they are all in the back right now playing football. I hate to tell you what he 'used' to be like before NACD...... a special education 'Lifer'. A kid with zero future and few friends..... He just got back from a 10 day Adventure Camp in California where my dyspraxic 13 year old paddled around the Channel Islands, climbed mountains, body surfed, and went riding for a few days. He flew there and back on his own, lugged around an enormous duffle bag stuffed full of gear on his own, had a great time and wants to do it again next year. His camp counselor actually contacted me to tell me what a nice kid he was and how funny and popular he was with the other boys. He was one of the youngest kids at the camp since the ages were from 13-17. None of this would have been possible without the daily work that NACD had me do with him.... none of it! But... it certainly was WORK!!! Now-a-days, his program is MUCH easier and is really 'fine-tuning' his skills and is dedicated towards academic advancement and becoming an accellerated student. I would love that.... from being classified as 'severe' special education kid to 'accellerated child'.... that one would be fun! But we do have a ways to go before that happens but last year he received mostly B's with a couple of A's and a C. He had no special accommodations and I am amazed at how well he did. He has some problems with personal organization that need to be worked on. If you have a child with global dyspraxia..... not apraxia of speech..... but global dyspraxia.... you have a 'mountain' of work ahead of you and believe me.... if your child is not training like a marathon runner to build muscle tone..... he is going to have trouble with many, many things. For instance.... hand writing requires good core body strength and stability. Tying shoe laces requires good visual spatial ability. Our kids don't have this. Our kids fall down the stairs and off out of their desks at school, their bodies are so weak. My son couldn't tie his shoes until he was 10.... and that is about average for the dyspraxic kid who doesn't get DRASTIC intervention. If you can't tie your shoes at 10 years of age.... just think of the countless other things that you cannot do! The list gets bigger and bigger as the child ages.... We have been wheedling that list down now and I am trying to think of a thing that he cannot do that others can. It is wonderously amazing! And.... I will scream to the world... to all of those little dyspraxic babies out there.... you CAN get better.... you really, really CAN! (but it is darn hard work!) My son JUST achieved right hand dominance..... this is supposed to come in at the age of 6-7... he has been ambi-dexterous all of these years and I had been certain that he would never get this developmental milestone and that it was too late for him. BUT.... he got it and it is so important for him because this is a Hallmark of dyspraxia.... being unable to cross the midline. So, it really is never too late but you need the right help for the right condition. I don't advocate NACD for those guys with just late talking issues or apraxia of speech but for kids with ASD, Downs Syndrome (they really do well with DS kids), CP and serious neurodevelopmental disorders, it is a wonderful place! The price is right and the 'knowledge' base is there. .... with all my respect but how familiar are you 'really' with global dyspraxia? Do you have any idea how tough life is for these kids? Think about that one for a while.... .... the bullying, the teasing, the taunting, the loss of self-esteem not to mention the loss of your personal identity. If anyone thinks that global dyspraxia can be conquored with 1 hour stints of therapy a couple of times a week.... then they don't fully understand this condition. It is an insidious monster that requires daily work to overcome. The trick of it is.... it doesn't start out as being so bad. Your kid isn't too much different then other kids. By grade one, he begins to be noticibly 'different' by grade 3..... he is extremely 'odd'. By grade 4.... demands of regular school are way too much. It just gets worse and worse and worse over time. By the time it actually 'dawns' on you how much different your child is and how behind he is..... it is way toooooo late! You are now years and years and years behind. It takes a real committment to get those years back. I speak of my experience with NACD because it worked when nothing else did. But I know that there are many other places to go to that offer neurodevelopmental therapy such as Handle and INPP as well as ICAN. I am sure that these other centres are just as good but I can offer no 'personal' experience tales since I didn't do their program. Again, no offense here but sometimes I think we are talking about Apples and Oranges. There are some kids on this board who require a great deal of intervention and there are others that do not. It is important not to discriminate against those doing interventions that are more involved. Some of the conditions we are treating are global in nature and affect the entire function of a person. These conditions require more.... not less. I believe that it is important that parent of global conditions know that they need to work with their kids doing home therapy.... in whatever fashion they can.... every single day. Again.... OT once or twice a week is a 'drop' in the bucket. It is a mere band-aid by the system and our kids need reams of therapy. The only way can be accomplished is at the home. I squeeze little therapy items into my sons' day.... all day long. I don't even notice it anymore, I'm so used to it! But, that has been the key to his recovery. You will note that most of the people doing NACD don't write about it here but do on ApraxiaDyspraxiaBiomedSupport . Again, I respect your knowledge of speech therapy and of apraxia of speech but I just don't think you 'get' the complexities of global dyspraxia. However, you are a great person and it is GOOD to have constructive debate..... I will, however, continue to defend NACD to the end.... they absolutely RESCUED my boy! Janice Mother of Mark, 13 global dyspraxia, 'almost' recovered (got some gut stuff left!) [sPAM][ ] Re: Neurodevelopmental therapies? Not the answer you were looking for but something to be aware of. Since 2000 NACD has only been brought up by 3 people here other than one or two in the past two years who bring it up lots and still bring it up today. The other one or two who tried it said it was too expensive or too difficult. In general it's best to follow the successful pattern in this group and most stuck with the norm therapy traditional and alternative. It's good to be aware there are other things out there but again you don't have to start with the most expensive ...and obscure. If it was that good more would say good things about it. There's much negative press and not at all on just this group as again the overwhelming majority never heard of it nor tried it. So personally I'd explore a proven to be successful for the majority Montessori or other multisensory school over this method. Just a few links but much more out there. Psychomotor Patterning An Expose of a Cruel Pseudoscience Novella, MD 10/1/1996 The line which sharply demarcates mainstream medicine from alternative medicine is the line of science. It is possible to cross that line, however. Any alternative treatment which is tested in a rigorous scientific manner and found to be safe and effective, will be incorporated into mainstream medicine, it will have crossed the line. A therapy, on the other hand, which begins within the halls of mainstream medicine as a legitimate proposal, and is found, when tested scientifically, to be of no real value, will be discarded. Most such discarded therapies are destined to become forgotten footnotes in the annals of medical research. Some, however, are salvaged by practitioners of alternative medicine. These therapies have crossed the line in the other direction, descending from science into pseudoscience. The method of psychomotor patterning for the treatment of mental deficiencies is one such therapy. It began 30 years ago as a legitimate, if incorrect, scientific concept for a new treatment modality for mental retardation, brain injury, learning disabilities, and other cognitive maladies. The method was subjected to controlled trials and found to be of no value. It was debated in the scientific literature up until the early 1970's, when finally the medical community arrived at the consensus that patterning should be discarded as a false concept with no therapeutic role. Use of the techniques of patterning, however, has not died, as we will see. The concept of patterning was invented by Glenn Doman and C. Delacato in the 1960's, and is therefore often referred to as the Doman- Delacato technique.1 Their theories are primarily an extension of the older concept that ontogeny (the stages through which organisms develop from single cell to maturity) recapitulates phylogeny (the evolutionary history of the species). Therefore, the neurodevelopmental stages of crawling, creeping, crude walking, and mature walking through which normal children develop is directly related to the amphibian, reptilian, and mammalian evolutionary human ancestors. 2 Doman and Delacato's concept of mental retardation is that of failure of the individual to develop through the proper phylogenetic stages. Their treatment modality is therefore designed to stimulate the proper development of these stages, each of which must be mastered before progress can be made to the next stage. This stimulation is achieved through the method known as patterning. The patterning treatment involves the patient moving repeatedly in the manner of the current stage. In the " homolateral crawling " stage, for instance, the patient crawls by turning his head to one side while flexing the arm and leg of that side and extending the arm and leg of the opposite side. For patients who are unable to execute this exercise by themselves, they are passively moved in this manner by 4- 5 adults, alternating back and forth in a smooth manner. This must be repeated for at least 5 minutes 4 times per day. The purpose of this exercise is to impose the proper " pattern " onto the central nervous system. In the full treatment program, the exercises are combined with sensory stimulation, breathing exercises which are designed to increase oxygen flow to the brain, and a program of restriction and facilitation designed to promote hemispheric dominance. 3 The claim made for the technique by Doman, Delacato and their supporters is that, with this treatment method, mentally retarded and brain injured children can achieve improved, and even normal, development in the areas of visuo-spatial tasks, motor coordination, social skills, and intellect. They have also expanded these claims to include the idea that their techniques can promote superior development in a normal child. 4 The theoretical basis of psychomotor patterning is therefore based on two primary principles, the recapitulationist theory of ontogeny and phylogeny, and the belief that passive movements can influence the development and structure of the brain. Delacato himself writes " Man has evolved phylogenetically in a known pattern. The ontogenetic development of normal humans in general recapitulates that phylogenetic process. We have been able to take children who deviate from normal development (severe brain injured) and through the extrinsic imposition of normal patterns of movement and behavior have been able to neurologically organize them sufficiently so that they can be placed within a human developmental pattern of crawling, creeping, and walking. " 3 Medical treatments are evaluated on two criteria, their theoretical basis and their empirical value. Patterning has been rejected by the scientific community on both accounts. The theory of recapitulation has never been fully accepted, and even by the 1960's had been all but discarded by evolutionary and biological scientists. The essential flaw in the theory of recapitulation is that it is based on an incorrect linear concept of evolution. Evolutionary lines continuously branch and deviate, forming a complex bush of relationships, not a linear ladder of descent. Embryological development does not reflect the mature stages of other distant branches of this evolutionary bush. Studying the embryology of the developing fetus also does not reveal any evidence of successive stages reflecting past evolutionary ancestors. There is also no theoretical basis for the belief that patterns can be impressed upon the developing cortex. Brain development is genetically driven and involves a complex sequence of cell growth, migration, organization, and even programmed cell death. Abnormalities in this process can be caused by genetic flaws, toxic insults, infection, or biochemical abnormalities. There is no model by which any of these disparate causes can be influenced by passive, or even active, movement of the neck and limbs. Thirty years of subsequent neurological, embryological, and medical progress have failed to lend any theoretical support for Doman and Delacato's principles. Their practice of using breathing exercises to promote oxygen delivery to the brain also lacks an accepted theoretical basis. The brain and the cardiovascular system are designed to give highest priority to oxygen flow to the brain cells. Elaborate and powerful feedback mechanisms ensure adequate delivery. It is true that carbon dioxide retention, in this case achieved through breathing techniques, does increase blood flow to the brain. There is absolutely no reason to believe, however, that such increased flow is at all helpful to the developing brain. Despite the fact that patterning is theoretically bankrupt, if empirical evidence existed which demonstrated that patterning improves neurological development, it would be accepted and used. There are many mainstream interventions which are employed in modern medicine that lack a fully understood theoretical basis. Physicians are, at their heart, practical individuals, and if something works, it works. They require proof, however, that an intervention does indeed work and is safe. On this score, patterning has just not delivered. Over a period of approximately ten years in the late 60's and early 70's there were dozens of clinical trials comparing improvement in groups of developmentally delayed children given patterning treatment compared to controls who were given no treatment but similar amounts of attention. 2,5-7 Although most of the studies had significant methodological flaws, some were fairly well designed. None were perfect. More importantly, none confirmed the claims of Doman and Delacato. Some of the studies did show modest improvement in motor skills or visuo-spatial skills over controls. None showed improved intellectual development. The few positive results found were not impressive or reproducible. Eventually, such clinical trials stopped, as the technique was abandoned as a blind alley. This point marked the unequivocal crossing over of patterning from science to pseudoscience. The tragedy of this story does not stem from the fact that patterning is a failed theory. It is regrettable that patterning did not deliver as promised, for any legitimate treatment for brain injured and retarded children would be most welcome. The real tragedy began, however, when Doman and Delacato released their claims for a new dramatic treatment before their theories had been scientifically validated. This behavior, reminiscent of the cold fusion fiasco, is more than just professionally irresponsible. In physics, such behavior is merely bad form; when dealing with the desperate parents of brain injured children, it can be considered cruel. Doman and Delacato were widely criticized for publicizing their unsubstantiated claims, giving false hope to vulnerable parents and their afflicted children. The saga, however, did not end with the scientific death of patterning. Doman, Delacato and their associates began incorporating the patterning technique into their Institutes for the Achievement of Human Potential (IAHP), which was established in Philadelphia in the 1950's. They continued to advertise and use patterning uninterrupted right through the scientific controversy, past the scientific condemnation, and on into the present day. I was also able to locate one other institution, the National Academy of Child Development (NACD), located in Huntsville, Utah, that offers patterning as part of their treatment program. The NACD is run by Doman, the nephew of Glenn Doman, although both institutions are eager to point out that there is currently no association between the two. On August 8, 1996, NBC aired a program titled " Miracle Babies " , hosted by Kathy Lee Gifford. The program included a segment portraying an apparent " miracle cure " of a child suffering from moderate mental retardation. As is all too typical of the lay press, Kathy Lee provided an emotionally appealing yet completely uncritical presentation of the patterning technique, touting its virtues without even a hint of skepticism. There was no evidence that NBC did any investigative reporting into the background and validity of the intervention they were promoting on their program. The segment did bring out, however, even if for the wrong reasons, the desperateness of the parents. They were clearly devastated, as any parents would be, by the need to finally accept that their child was not developing normally. In their desperation, they sought any possible hope, and it was offered to them by the IAHP. The hope that they purchased, however, came at a heavy price, both financial and emotional. Both the IAHP and the NACD rely heavily on the family as the primary deliverers of the patterning treatment method. In order to even reach the stage where their child can be enrolled into the aggressive treatment program, they must first complete a training and evaluation course which begin for both institutions with purchasing and listening to a set of audio tapes. The IAHP states in their literature that only the most dedicated and capable parents will make it to the final stage of treatment. The NACD appears less demanding, but they follow the same principle. The end result is that the parents and other family members of the patient must alter their lives to institute a daily program of patterning exercises, breathing exercises, and programs of sensory stimulation. The mother interviewed by Kathy Lee stated that the program was so demanding that it dominated her life, resulting in emotional and physical exhaustion. The exceptional demands of the patterning method is the primary reason cited in the medical literature for caution in evaluating patterning, for the obvious harm that would ensue if the method were recommended prematurely, without good proof that it is effective. The program also illuminated another important feature of the patterning phenomenon, the difference between anecdotal and scientific evaluation of its effectiveness. One important fact to understand is that most children, even severely mentally retarded children, still grow and develop, although on a slower curve than average. Therefore, any child admitted into any treatment program will make some progress as an inevitable consequence of time and their natural development, even if that treatment program is completely worthless. Without adequate controls, it is therefore impossible to evaluate any such treatment. Of course, Kathy Lee and the parents of the child on the program reported remarkable progress. Whether or not the treatments played any role, however, cannot be known. The viewers, however, were meant to come away with the sense that they had witnessed a miracle cure. The NACD and IAHP literature both caution that individual results will vary. By emphasizing the need for dedicated capable parents, they also create a situation in which, if a patient fails to make significant progress, the parents are the ones to blame. These parents now have the added guilt of feeling inadequate to have helped their injured child. Most practitioners of alternative medicine either practice or are at least accepting of many different forms of alternative cures. This results from the fact that if one has a casual, or even anti, science attitude regarding one alternative modality, then they will likely have a similar attitude towards other modalities. It is not surprising, therefore, that the NACD embraces other scientifically questionable practices. For instance, the NACD advertises on their web site that they also evaluate and treat for food sensitivities. Although there is not the space here to adequately address this complex issue, suffice to say that food sensitivities are controversial at best, and certainly lack scientific acceptance. The excerpt in the box below is quite revealing. 8 I doubt there are many children who do not have three or more of these symptoms, especially since many are vague or qualified enough to apply to anyone. The NACD also offers a consultation with an " orthomolecular physician. " Again, I will not delve into this issue here, but suffice to say such " physicians " are clearly outside of the mainstream. Unproved therapies can be harmful in many ways, not always by direct toxicity or physical harm. The promotion of psychomotor patterning by institutions which make bold unsubstantiated claims about its effectiveness may cause significant financial and emotional damage. Such claims instill false hope in people who are likely already plagued by guilt and depression. By doing so, these desperate parents are being set up for a crushing disappointment or further guilt of inadequacy. In the process they must spend a great deal of their resources of time, energy, emotion, and money. These resources are taken away from their other children and other important facets of their lives, resources they might not be willing to spend if not for the fantastic claims which have lured them to this path. They are also distracted from dealing with the situation in other practical ways and coping psychologically as a family with the reality of having a brain injured or mentally retarded child. They are encouraged, in fact, to remain in a state of denial while they are pursuing a false cure. The Doman-Delacato patterning technique is pseudoscience because it is premised on a bankrupt and discarded theory and, more importantly, has failed to demonstrate any significant effectiveness under controlled conditions, and yet it is being purveyed as an innovative and effective treatment, and even possibly a cure. The IAHP and NACD cannot support the claims that they make, and are therefore guilty of fraud. Current regulations should prevent such abuse, but unfortunately such institutions as the FDA lack the manpower and the teeth to properly enforce such regulations and fulfill their role to protect the public from the snake-oil salesman, dressed up in the modern clothes of alternative medicine, that increasingly prey upon the vulnerable, the sick, and the desperate. References: 1. Doman RJ, Spitz EB, Zucman E, Delacato CH, and Doman G: Children with severe brain injuries, Neurologic organization in terms of mobility. JAMA, 174:257, 1960 2. Cohen HJ, Birch HG, Taft LT: Some considerations for evaluating the Doman-Delacato " Patterning " method. Pediatrics, 45:302-14, 1970 3. Delacato CH: The Diagnosis and Treatment of Speech and Reading Problems. Springfield, Illinois: C , 1963. 4. Doman G, Delacato CH: Train Your Baby to be a Genius. McCall's Magazine, p. 65, March 1965 5. Neman R, Roos P, McCann BM, Menolascino FJ, Heal LW: Experimental Evaluation of Sensorimotor Patterning used with Mentally Retarded Children. Am J Mental Deficiency, 79:372-84, 1975 6. Ziegler E, S: On " An Experimental Evaluation of Sensorimotor Patterning " : A Critique. Am J Mental Deficiency, 79:483- 92, 1975 7. Freeman RD: Controversy Over " Patterning " as a Treatment for Brain Damage in Children. JAMA, 202:83-86, 1967 8. NACD website, URL-http://www.nacd.org/articles/food.html http://www.theness.com/articles.asp?id=56 Kathleen Ann Quill 'Teaching children with autism' book: " thousands of families have wasted time and money to follow Doman's methods. " " Professionals have nothing to learn from Doman's pseudoscientific treatments, but they have plenty to learn from his marketing strategy " , which is aimed at parent's " hopes and fantasies " . (if you read from this book sounds like he blames the mom so I'm shocked anyone would support this method!!!) http://books.google.com/books?id=kT8DbfNcU5wC & pg=PA57 & lpg=PA57 & dq=Kathleen+Ann+Q\ uill+doman & source=web & ots=y36f65kn6g & sig=y0Z1Xa1lvutcBW44YrmLNUhx3BQ & hl=en & sa=X & \ oi=book_result & resnum=1 & ct=result A blog about it " Ok...my Sister-in-law has a son who was born with Down Syndrome. Such a gorgeous little guy. My SIL is all business, but when she got pregnant we saw a new side of her come out. Some emotion. Some Mothering. She is a high powered business lady and she was thinking of being a stay at home Mom! Too cool! The babe was born and the babe has DS. A lot of upset in their home and for the family as might be expected when things down go as planned. SIL was then definitely thinking SAHM. Then she decided not to be a AHM and went with daycare (which is provided by multi-billion dollar corporation for which she works). They got involved pretty early with NACD. This has the hairs on the back of my neck rasied. We checked out NACD at the same time we checked out Son-rise. I listened to 16 CD's I think. 12 Lecture, 2 on Autism and 2 on parent reactions. Some of this clicked with me (as I liked the medical model they were posing), but a WHOLE LOT did not. I went to my pediatrician who is very knowledgeable. He has been doing this for 30 years and is very well-respected. In addition, he keeps up with all the latest and he will get on the web and research the heck out of anything you bring to him. I mention NACD and he has not heard of it. He asks me about what they do. As soon as I say, " Neurological disorganization " he stops me and says... " Is this Glenn Doman? Are they based out of PA? " Well...it is a Doman and they have a campus in PA. " He never gets animated about this stuff. Very open to whatever you want to try, but is very protective of us (and all his patients) and usually simply states that the more expensive usually something is wrong. He gets animated about Doman/Delacatto and states unequivocally that they are a scam. Thatthey founded IAHP (The Institute for the Advancement of Human Potential). He says that if you bring up their names at a conference you will be laughed out of the hall and that they have been around for a long time, switching names to stay alive with no external research to back up their treatments. WHOA! I had googled negative stuff on NACD and could not find much. Now I googled Doman. Yeah...there it was. Obviously, we did not go that route (and I apologize to anyone here who is using this successfully. This is simply my experience. SIL is using NACD almost exclusively. She buys the whole enchilada. She say that the Birth to Three therapists are " worthless. " She sticks to a strict program with her babe. The kid is now a year old and not crawling (belly only). With a PT he should be there by now. She is passing on so many theapies and has no tolerance for anything save NACD! She even says that if/when she has another kid even if the kid is NT she is going to put him/her into the NACD program! HOLY MOONIE BATMAN! I can't say anyting can I? I know I can't. It just kills me! The only good thing I see is that it has made her (and hopefully her hubby) more involved with the kid. They have to be with the babe 2hours minimum per day. This is part of the program. That can never hurt...all that 1:1 attention. But the rest...it chaps my a$$. Thanks for reading. Good grief! She definitely sounds brainwashed if she would want to follow a rigorous program for a child without special needs. I have only heard of Doman used on children/people with severe brain injuries, not Down syndrome. No matter what you say, she will not change her mind so like you said there's no point in arguing with her. But who knows, maybe modelling good interaction with your autistic child will eventually rub off on her. Good luck with everything. http://www.autism-pdd.net/testdump/test15578. The Doman-Delacato patterning technique is pseudoscience because it is premised on a bankrupt and discarded theory and, more importantly, has failed to demonstrate any significant effectiveness under controlled conditions, and yet it is being purveyed as an innovative and effective treatment, and even possibly a cure. The IAHP and NACD cannot support the claims that they make, and are therefore guilty of fraud. Current regulations should prevent such abuse, but unfortunately such institutions as the FDA lack the manpower and the teeth to properly enforce such regulations and fulfill their role to protect the public from the snake-oil salesman, dressed up in the modern clothes of alternative medicine, that increasingly prey upon the vulnerable, the sick, and the desperate. http://trusted.md/feed/items/system/2008/03/12/brain_gym_educational_kinesiology\ _not_effective ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2008 Report Share Posted July 29, 2008 The other issue is that what worked for the majority in the past is not the cure-all, especially for the new crop of vaccinaated kids who are getting more and different vaccines than the old crowd. Regular therapy and mainstream medicine has not caught up to the reality seen in our homes. The transition to aluminum brought a new crop of delays and an explosion in PDD Nos I bet Just my opinion) because nobody knew what was going on. The crow d of kids with the old vaccines, the secondary crowd with the hybrid as the thimerosol was allegedly being phased out, and the aluminum crowd, will likely need personally tailored interventions and the people who get the ball rolling are parents. Viva la Mommy! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2008 Report Share Posted July 29, 2008 Mark was 11.5 when we started in September, 2006. We still do program each day.... well, most days. The gang of boys is now 'sleeping' over. I've just fed them a low carb dinner with plenty of meat and struggling to come up with ideas for 'treats'. I have some GFCF cookie mix but " jeepers " , I so want to keep him off of sugars and carbs. Maybe they won't notice the lack of 'treats' in this house? Yeah, right.... they're 13.... Do you think some GFCF chocolate chip baked cookies will spoil my yeast free diet aspirations? (offers of fruit do not seem to be doing the trick.....) I'm liking that he is enjoying a normal life and don't want to spoil it too much. Of course, we're chelating right now and I'll have to 'slip' him the DMSA discreetly. Oh.... what a life we lead!!! Janice > > How old was Mark when you started?!!! > And how long did he do the program for?!!! > > > Love, Gabby. :0) > http://stemcellforautism.blogspot.com/ > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2008 Report Share Posted July 29, 2008 Liz I know you've said this before but why not add your kids and others that say their kids are apraxic to the Talking Page? Are you really sure about that somehow today's kids with parents with more knowledge and less vaccines have more vaccines?!!! What shots do kids get today that they didn't get then? Back in 1996 when Tanner was born they still had thimerosal in all the pediatric shots and people didn't do shots separate and there was no known link that I knew of for anything other than a simple reaction as a risk for vaccinating Tanner or Dakota- and it's well documented more recently especially in the last 2-3 years for those in this group with 2-3 year olds that many parents are opting out of shots all together thimerosal or not. It was just front page news in our Sunday paper here how many children are not vaccinated at schools today using the religious exception which is up like 5 times the amount from when Tanner was born. http://www.tcpalm.com/news/2008/jul/27/30gtparents-tell-us-what-you-think/ Also -most of our kids were not talking anywhere close to normal near the age of 3 -so to me it appears that our kids were more severe and yet overcame and most were not even first diagnosed until the age of 3 or older. Therapy and fish oils worked for the majority -still does. I do believe that Tanner was affected in some way by vaccines -but it's also clear that there are dangers from not vaccinating. http://www.popularmechanics.com/science/health_medicine/4273262.html Could be me but it seems that even when the kids are normal today parents are still looking to do stuff. As soon as I could put Tanner in the mainstream both school and activities - that's where I put him - and that's where he has been from kindergarten and has stayed. Only thing he gets that's not " normal " is fish oil every day. It's a handful here that do all this other stuff -as Jeannie just said who has a child with autism and a child with apraxia and still runs an in person support group nonprofit in NJ -most find the basics work and find the other stuff to be a waste of time and money. If it works and you need it that's great -but don't assume that today's autism or apraxia is worse - because based on your child if mine was talking normal by 3 years old last place I'd be is posting and trying to learn more in this group - I'd be out having fun with my family and friends. (I'd probably be at a Disney blog!) ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2008 Report Share Posted July 30, 2008 If you give me the talking page info I'll check with hubby on putting him on as I am bad at anything beyond email and boards. There are far more shots now, at least in NJ. It is the boosters. So many boosters. The required flu shots that used to be optional. Going into preK just 2 years after my daughter did today's kids here have a lot more required shots. Earlier and more often seems to be the rule today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2008 Report Share Posted July 30, 2008 I am not saying it was easier for kids in past nor now. Not at all, just different and different preservatives may warrant different or adjusted intervention. There is still thimerosol in vaccines. 2% rule allows that. There are more required vaccines and exemptions are not available everywhere and there are other obstacles. Sadly, not every parent gets all the info. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2008 Report Share Posted July 30, 2008 If fish oil and therapy worked for most then why try the E? Could it be because it worked better? I am not saying my way is the best way or the only way. I am not even saying my kid is apraxic for just like the kids who have excelled on the formula he no longer presents that way and I remain on a waiting list. I am not on a Disney board because I only take time away from my life for serious matters, like my kids health. From all accounts, including yours, this is, at best, a treatable condition. When I listen to the talk page some kids decline in speech with age though if I am correct they are therapy only kids. With our family's autoimmune history fish oil and E won't cut it. I stay on this board because while diet and therapy are helping, my son may rebel and I need to keep up on other options and innovations as he grows. The waste of money argument does not hold water. You realy should not knock what you have not tried, particularly when the one teen who has tried NACD has improved greatly from that alone even before other measures were taken. There was a previous divide on this board about what to do with older kids and why are we talking about just the young ones. We are all mothers trying to help our kids. There should be no division and I do wish it does not resurface. I do not generally post on milk and would not have posted on NACD were it not posted as a question to someone I was informed (incorrectly) had left the board. I was trying to help. To help and be helped...that is why I post. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2008 Report Share Posted July 30, 2008 EDUCATE BEFORE YOU VACCINATE!!!! www.vacinfo.org Love, Gabby. :0) http://stemcellforautism.blogspot.com/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 31, 2008 Report Share Posted July 31, 2008 What brands of vitamin e have you all been using? I have tried the two to one ratio with the pro efa and pre epa, is seems that my son responds better to just the pro efa speech wise. However, I only tried it a month, he seemed much more quiet when I added the pro epa?? Any ideas. Jen **************Get fantasy football with free live scoring. Sign up for FanHouse Fantasy Football today. (http://www.fanhouse.com/fantasyaffair?ncid=aolspr00050000000020) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 31, 2008 Report Share Posted July 31, 2008 Maybe he has enough omega 6 in diet already? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2008 Report Share Posted August 4, 2008 Hi Jancie, What is your son's diagnosis? Does your son have global apraxia and sensory processing?I am very interested an I live about 15 minutes fro West Chester Pa. Â Do they give recommendations for educational placements? I will contact them directly but in the meantime I was curious.Thanks LYnch Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 6, 2008 Report Share Posted August 6, 2008 Hi janice, I do not post much - my child not being apraxic, but we are on bio-medical intervention, so this group really helps us. We have been NACD for 1years and bio-med for 1. The two work so beautifully together - and work so well for my son and us as a family I just had to chime in. My first evaluator said: we teach to the strengths and remediate the weakness. He is an almost complete visual learner. His whole world is pictures - while this may make him a fantastic engineer or architect in the future, it is a really self limiting way to think. We teach him almost exclusively visually - using flash cards, pictures and objects. We remediate his auditory - TLP (the listening program), digit spans and word spans. One year ago, my 6 year old could not read, write or do maths. He could not hold a conversation, call me mummy, ask or answer questions. he has always had an exceptional vocabulary - he could name everything in picture dictionaries, any object pointed out, he was unable to create original phrases - he had a stock of about 10 learned phrases. It felt to me that he was learning english as a second language without having a first. Today - he reads and comprehends simple stories, will answer questions about the story without using a picture to prompt. A year ago he could not read or write his name. He can do simple maths. He has a love of numbers and this was easy, once NACD taught us to teach him in a way he could get it. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 7, 2008 Report Share Posted August 7, 2008 , My son has global dyspraxia and we love our program. It addresses every area, fine motor, gross motor, vision, processing, academics and social issues. Unbeknownst to me, my son had a lot of auditory processing issues and NACD identified this immediately. Remediating it resulted in some truly profound differences to all of his abilities and his function in life. Despite having been seen by a multitude of experts in the past, NACD was the first to determine this need/deficiency for my son. I am from Canada so educational placement has not been an issue but I can tell you that in one year of doing an individualized home program in my son resulted in leaving special education and attending mainstream with no aides or issues. My son did pretty well last year in school and has adjusted superbly. Prior to NACD he was considered a Special Education 'lifer'. I was told to not expect him ever to leave special programming. We certainly changed 'that' prognosis! But it was a tremendous amount of work and takes a lot of committment. However, my once bullied silly son now has a lot of friends in mainstream education and he is doing very well. I am very happy with NACD. The price is right and the program worked for my boy when nothing else did. Hope this helps you. Janice Mother of Mark, global dyspraxia/apraxia of speech [sPAM]Re: [ ] Re: Neurodevelopmental therapies? Hi Jancie, What is your son's diagnosis? Does your son have global apraxia and sensory processing?I am very interested an I live about 15 minutes fro West Chester Pa. Do they give recommendations for educational placements? I will contact them directly but in the meantime I was curious.Thanks LYnch Quote Link to comment Share on other sites More sharing options...
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