Guest guest Posted January 9, 2006 Report Share Posted January 9, 2006 Hi, Your son sounds just like mine at that age. I would look into early intervention programs in your state. You don't wait to evaluate a child!! That is why it is called EARLY INTERVENTION. He will qualify under expressive language for sure, since he should typically be putting two word sentences together at this point. You could also probably get him in under social/emotional delays by emphasizing the lack of attention and eye contact issues. Playing by himself, etc. These are all valid points. Pediatricians, unfortunately, are the last people to listen to with their " wait it out " line. I would recommend a developmental pediatrician and/or a psyche eval for behavioral observation/input. I don't mean to scare you, I am just saying that there appears to be more going on. He may be just " a boy " as I'm sure you've also heard, but you don't want to put all your eggs in that basket. Besides, if he starts on some therapy now, it will just seem like play. Getting on this list was a good start. Ok, if you want more info/advice, let me know. I don't want to ramble on b/c believe me, I could! Cheryl Butterworth Collin and 's Mama cheryl@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2006 Report Share Posted January 10, 2006 My son has just recieved a dx of verbal apraxia. He too, has no delays in any other areas except expressive. He is at an 11 month level at 2.9 years. He has a vocab of 3 intelligible words to me or strangers. I started him signing at 18 months and he loved it. I would suggest Signing Time DVD's. They are engaging and fun for all ages. It has allowed my older children to learn with him and eased alot of tension. He is now learning to sign his ABC's and can match letters with signs. I ran the DVD's over and over in the house and in the car. The rest of the family never knew what hit them! I can't say enough about these movies. You can get them at Amazon and if you would like to read more go to their website, www. <http://www.signingtime.com> signingtime.com I am a firm believer in teaching some type of two way communication and 1 year later I'm so glad because we are still using it. I stopped a few times when I thought we were making progress then we would go into a slump and I'd start again. My advice is to keep using it so it's there when you need it. I sign every word I know when I'm talking to him even when is not looking. I must look weird to other people but it's a good habit. Good luck. Let me know how it goes. Karin [ ] 19 month old not talking Hi, I am new to this group and hope someone here has some suggestions for me. My son currently 19 months old is not talking. He started babbling at around 6-9 months and actually babbled quite a bit until the last couple of months when that has decreased. He can say mama, and will say it unrelated to me, but not very often (1-2 times a week). He does not use gestures to indicate what he wants or is interested in. As far as following simple commands, it is hit and miss. Sometimes he can follow " get the yellow ball " and other times he completely ignores me. He is an active toddler and i have no issues with his physical and motor skills. He can build blocks together and throughly enjoys playing with his toys ignoring everyone else around him. Getting his attention can sometimes be a struggle and he will not always respond to his name when called. I do talk to him everyday about what is happening and things around him and have been reading to him since birth. He will not sit still to read just one little book, so I usually end up reading to him while he plays with his toys, He will run over and look at a few of the pictures during the book, but does not point at anything and I have no idea what he is understanding from the books. If i let him touch the books then he runs away with it and treats it like any other toy and therefore no other reading gets done. We have been to the peditrician and he wants to wait until he is older. I have referred him to a speech and language center provided by government health care, however they feel he is too young to be assessed. I have spent hours searching the web for things i can do as a parent to facilitate his language production, but have come up with not much. I have recently started signing with him, however getting him to look at me when I make the sign is a task in itself. Please help !! How to promote language in him ? How to read to him properly ? I hope this had made sense to all of you and will appreciate your feedback. Thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2006 Report Share Posted January 10, 2006 Hi, I wanted to respond to your post. I Have a son who is 19mos and your description was very similar to . He is not talking, but does babble. He says Mama but not in trelation to me. He sometimes gestures, points to what he wants. The reading is exactly the same. He will not sit for a book. I usually end up reading it to my husband or myself. I had him evaluated by EI and he now receives services 6x week. I suggest you do the same. He will probably qualify for speech at the least. Diane > > Hi, I am new to this group and hope someone here has some suggestions > for me. My son currently 19 months old is not talking. He started > babbling at around 6-9 months and actually babbled quite a bit until > the last couple of months when that has decreased. He can say mama, > and will say it unrelated to me, but not very often (1-2 times a > week). He does not use gestures to indicate what he wants or is > interested in. As far as following simple commands, it is hit and > miss. Sometimes he can follow " get the yellow ball " and other times > he completely ignores me. He is an active toddler and i have no issues > with his physical and motor skills. He can build blocks together and > throughly enjoys playing with his toys ignoring everyone else around > him. Getting his attention can sometimes be a struggle and he will not > always respond to his name when called. > I do talk to him everyday about what is happening and things around > him and have been reading to him since birth. He will not sit still to > read just one little book, so I usually end up reading to him while he > plays with his toys, He will run over and look at a few of the > pictures during the book, but does not point at anything and I have no > idea what he is understanding from the books. If i let him touch the > books then he runs away with it and treats it like any other toy and > therefore no other reading gets done. > We have been to the peditrician and he wants to wait until he is > older. I have referred him to a speech and language center provided by > government health care, however they feel he is too young to be assessed. > I have spent hours searching the web for things i can do as a parent > to facilitate his language production, but have come up with not much. > I have recently started signing with him, however getting him to look > at me when I make the sign is a task in itself. > Please help !! > How to promote language in him ? > How to read to him properly ? > I hope this had made sense to all of you and will appreciate your > feedback. > Thanks > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2006 Report Share Posted January 10, 2006 I couldn't agree enough. At first sign language (learned quickly through signing time videos) gave my 2 year old a way to communicate and frustration/tantrums disappeared literally overnight. Now that he is making progress in speech (about 35 understandable words) - he is trying so hard to talk but I often have no idea what he is trying to say. Frustration is again occuring after he repeats himself again and again, but when I ask him if he can sign what he is talking about - he can usually think of at least one sign that gives us a clue. It is so helpful - even on the next evel. - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2006 Report Share Posted January 10, 2006 My son LOVES Signing Time DVD's even though he can't sgin. He's 4 and non verbal. He has poor fine motor control although he has some " Will signs " . Signs he's made up! Sherry <claudiamorris@...> wrote: I couldn't agree enough. At first sign language (learned quickly through signing time videos) gave my 2 year old a way to communicate and frustration/tantrums disappeared literally overnight. Now that he is making progress in speech (about 35 understandable words) - he is trying so hard to talk but I often have no idea what he is trying to say. Frustration is again occuring after he repeats himself again and again, but when I ask him if he can sign what he is talking about - he can usually think of at least one sign that gives us a clue. It is so helpful - even on the next evel. - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2006 Report Share Posted January 10, 2006 Hi, I am new to this group as well, but it seems you don't really know specifically what might be the cause of your son's language delay. I also am on another board called NaturalLateTalkers that includes parents of children with many kinds of speech and language disorders. It is a huge site with a wealth of information. Perhaps you would benefit from joining that group as well. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2006 Report Share Posted January 10, 2006 Hi, I'm sorry that your Pediatrician is not helping. I would definitely suggest that you contact Early Intervention (which is for children Birth-3). They will have therapists come out and evaluate your son to determine if he qualifies for therapy. I'd strongly recommend this. My son has been receiving these services since he was 4 months old. He is 2 1/2 years old and recieves 6-7 therapies per week. It's a lot of therapy but it's so worth it. His speach therapist is working on oral motor strengthening, PROPMT, sign and we are getting an Augmentitive Communication Device. If you have any questions, please ask away. Good Luck! Proud Mommy to > > > > Hi, I am new to this group and hope someone here has some > suggestions > > for me. My son currently 19 months old is not talking. He started > > babbling at around 6-9 months and actually babbled quite a bit > until > > the last couple of months when that has decreased. He can say mama, > > and will say it unrelated to me, but not very often (1-2 times a > > week). He does not use gestures to indicate what he wants or is > > interested in. As far as following simple commands, it is hit and > > miss. Sometimes he can follow " get the yellow ball " and other > times > > he completely ignores me. He is an active toddler and i have no > issues > > with his physical and motor skills. He can build blocks together > and > > throughly enjoys playing with his toys ignoring everyone else > around > > him. Getting his attention can sometimes be a struggle and he will > not > > always respond to his name when called. > > I do talk to him everyday about what is happening and things around > > him and have been reading to him since birth. He will not sit > still to > > read just one little book, so I usually end up reading to him > while he > > plays with his toys, He will run over and look at a few of the > > pictures during the book, but does not point at anything and I > have no > > idea what he is understanding from the books. If i let him touch > the > > books then he runs away with it and treats it like any other toy > and > > therefore no other reading gets done. > > We have been to the peditrician and he wants to wait until he is > > older. I have referred him to a speech and language center > provided by > > government health care, however they feel he is too young to be > assessed. > > I have spent hours searching the web for things i can do as a > parent > > to facilitate his language production, but have come up with not > much. > > I have recently started signing with him, however getting him to > look > > at me when I make the sign is a task in itself. > > Please help !! > > How to promote language in him ? > > How to read to him properly ? > > I hope this had made sense to all of you and will appreciate your > > feedback. > > Thanks > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2006 Report Share Posted January 10, 2006 Hi all! Just want to jump in and remind everyone that even with the rise in children with speech impairments, 75% of late talkers are just that - children that talk late. And that's with or without therapy. Thing is that speech therapy is benign even if not needed, and may in fact provide stimulation to encourage the speech to come in sooner even with a simple delay. I'm also posting because there is a large group here of parents and professionals who were faced with children that they 'thought' was just a late talker, or 'just' ____. What we all want isn't the assurance from friends, relatives and even our spouse...we need to know from a professional who is skilled at knowing the difference between all the various reasons why your child may not talk yet at all or as much as you'd like. Below is an archive which clearly lets everyone know that I too thought Tanner was " just " a late talker, and then thought he " just " had apraxia. OK -so he had a few other things going on. Today Tanner is a cool little 9 year old boy who continues to amaze not just me -but those that work with him. Again I had two " late talkers " both my boys, Dakota and Tanner. For those say " just give him time " that are right most of the time - since 75% of the children are just late talkers -they would have been wrong with 50% of my children (Tanner) We all heard about late talkers with simple delays....just like We all know about colds with sniffles.... We all know about scrapes that need a band aid. We don't join a grouplist to learn about colds and scrapes. This group isn't just for apraxia -but apraxia is a condition we need to talk about more since there's no information just about anywhere else and it appears to be on the rise. At least know the warning signs and if needed, learn how to help. Knowledge is power, and in this case, comforting. (there is so much hope no matter what!) Below is an archive on more: From: " kiddietalk " <kiddietalk@...> Date: Mon Jul 26, 2004 10:08 pm Subject: Re: question on receptive communication delays/pure apraxia? Hi Gail and welcome! Based on what you wrote it would be hard to say if your daughter has apraxia. What are the 5 to 10 words she can say? Believe me, as one who has been there and done that I look back now at what I considered " words " when Tanner was three. " Ma ma mommy " was a three word sentence to me of " Where is Mommy? " And when Tanner " learned " my sister 's name, Aunt , we were all excited to hear him call her " Doo doo " (we all laugh at that one today -even Tanner) You guys that read The Late Talker have my Tanner dictionary that I gave to the school in there, so you know what I mean! So, how clear and how complex are the words? Does she say them consistently the same way each time? How quick did she learn the word? Did she ever say a word and then 'lose' it, where she couldn't say it again? Can she imitate various sounds? Different from needing encouragement -apraxic children want to be able to repeat -they just can't -it's part of the disorder in that at times the more they want to say it the more it eludes them. This is why some will say words while you are playing chase, or while you are pushing them on a swing -while they are not thinking about it. Apraxia creates of problem of doing the activity 'on demand' Once a word like " ma " is in an apraxic child's 'motor memory' they tend to say it the same each time. It's how they learned those words, and how complex they are. You did give one sign of apraxia. The child's receptive ability being ahead of the expressive ability is just one of the signs of apraxia. Apraxia is simply a motor planning disorder. In itself apraxia is not a cognitive or psychological behavior, even though it can co exist with many disorders. Can a gymnast have apraxia? Sure. Depending on what type of apraxia a child has, it may or may not affect the child's motor abilities in movement of the body outside of speech at all. It's wonderful that your daughter is excelling at gymnastics because it brings her something to take pride in that doesn't demand verbal abilities. Other children with apraxia may enjoy karate, swimming, dance, cooking, art, etc. I too thought Tanner was 'just' a late talker as you will read below. We, like most, didn't notice his warning signs that were there long before the neuroMDs and therapists spotted them. After all, Tanner passed all his developmental milestones on time or early. Because most apraxic children have normal receptive ability - they are aware of what is expected of them and will push themselves to keep up. This is why most that don't receive early intervention will have " other symptoms " that pop up down the road when more is expected of the child and they can't keep up. http://www.cherab.org/information/speechlanguage/parentfriendlysoftsigns.html Most children with apraxia today present with a delay in speech, normal to above average receptive ability, and one or more neurological " soft signs " such as hypotonia (low tone -weakness of the muscle for speech or body), sensory integration dysfunction, and/or mild motor planning deficits in the body. Some can be so mild that they are not obvious to most until the child reaches school age and more is expected of them. This is the reason for a thorough neurodevelopmental exam, so that if any signs are present you can begin early interventions...early. If there are soft signs present they should also be viewed as warning signs of a possible speech impairment like apraxia. This is because most of the children today with " multifaceted " impairments of speech like apraxia do not have " pure " apraxia. Pure apraxia is possible, just not probable. What is pure apraxia? Archive (of an archive?) answer! ~~~~~~~~~~~~~~~~~~~~~ From: " kiddietalk " <kiddietalk@...> Date: Wed Mar 17, 2004 4:06 pm Subject: Re: PURE APRAXIA Hi AC, Pure apraxia is possible but rare. More common would be misdiagnosis of apraxia (the child really is/was " just " a late talker with a simple delay in speech) Below is an archive on this subject -and yes it's always been a popular topic and one with many opinions, even from the experts. From: " kiddietalk " <kiddietalk@...> Date: Mon Jan 26, 2004 2:21 pm Subject: Re: any pure apraxia children? In response to some of the many posts on this -this group is a mixture of all types of late talkers ranging from mild " just " late talkers with simple delays in speech, to those with more complex and severe impairments that overlap with other conditions. The majority here do not post and lurk instead, and this includes the majority of those with " just " late talkers. Some have told me they don't want to post because they don't believe their child's problems will be taken seriously in comparison to what others are going through. I just want to once again say -all are welcome here and all is taken seriously. Out of the few that do post, there are a handful that post to reach out to help others (thank you for all that do this!) and share updates and we get to know them. Most post when they have a question or when they are upset about something, but a few come here to share joys that only we can understand (like being excited about a 4 year old that says " hi " for the first time) Pure apraxia is a question that comes up often, and as long ago as when Tanner was first diagnosed. In fact below are two of my first ever messages on this where first I question what " pure apraxia " is a day or so after Tanner was diagnosed -and then another where I sign next to Tanner's name " pure apraxia " (and yes -I too was wrong) Interestingly enough in my first messages I describe Tanner's signs of oral apraxia and sensory problems and hypotonia which -but since nobody including Tanner's pediatrician knew they were warning signs - none were addressed until after these " soft signs " were diagnosed by the neurodevelopmental MDs. I'll put my post below, here is just one of the more recent archives and then some other comments below that on your direct question: " From what I've seen personally and in this group, apraxia, like autism, is multifaceted in most cases...meaning it's not " just " an impairment of speech. Bilker is one of the only children I know who has " pure " apraxia of speech and nothing else. http://www.debtsmart.com/talk/brandon.html (even though most of us in the early stages also believe it's " only " a speech delay as you will even read in my first posts 4 years ago.) " Most children with apraxia do not have PDD, however it's not uncommon for children with PDD to have apraxia. Most children with apraxia do have mild low tone (weakness) and/or mild motor planning problems in other areas of the body. It's also not uncommon for a 'typical' apraxic child to have sensory integration dysfunction, even if it's mild. Through anecdotal reports apraxic children are also late to potty train and may be prone to constipation. (and if asked to blow their nose into a tissue they will breath in instead of blow out!) Children with apraxia or any communication disorder are known through studies to be at risk for learning disabilities. the issue of using verbal based cognitive or receptive testing on verbal disabled children? http://www.cherab.org/news/verbaldisabledtest.html Just like in the story behind the movie " Stand and Deliver " -I love the quote " students will rise to the level of expectations " http://www.kcbx.net/~jbunin/files/reviews/teachers.html which is most likely based in proof by the research of Dr. Rosenthal. http://www.pineforge.com/newman4study/resources/rosenthal1.htm I've spoken to Dr. Rosenthal about the current testing problem our society and school systems are placing on verbal disabled children, how this is discriminatory - and the damaging impact of using this type of testing based on what his research proves. Dr. Rosenthal is shocked to say the least -and agrees with my views on this -he believes this should be studied as well. Please contact me if you are interested in learning more about this too. We as the ones that care for these children have to believe that this is not necessarily true -my son Tanner is just one example of a child that could have still been in a special needs class and viewed as low average abilities due to verbal based testing -but instead is a straight A student in all subjects in an accelerated academics first grade class. Many if not all of our children benefit from multisensory therapy as well as multisensory education. For example when Tanner's school taught the children about the circulatory system -each child had a chance to " be " a white blood cell or red blood cell or platelet while walking through the halls of the school. Tanner came home and explained the circulatory system to us and it was amazing. I am also a strong believer that as a group in general most of the children with multifaceted communication impairments (those who don't just have verbal apraxia) will benefit from starting kindergarten at six vs. at five so that they have that extra year to work on the intensive therapy, and give that extra year for development. I don't know anyone that regretted " holding back " their child for a year -but I personally know quite a few that regret starting their child at five, especially if the child is a young five. Here is an archive on how our children, and adults like them that are verbal disabled, have been viewed by the majority: " Now if you want to know the negative view our children will face if we don't change it as a group-then read this link ( http://www.courierpress.com/ecp/gleaner_news/article/0,1626,ECP_4476_2470843,00.\ html ) for the good and the bad: " These children are going to plateau at a certain level -- that is the nature of a disability, " said Harper, who teaches students with autism, learning disabilities, mental retardation, Tourette's syndrome, vision and hearing deficiencies and brain injuries. " These kids are not going to grow out of it, not going to grow up and be OK. It's sad, but that is the way it is. " " In Nashville, Tenn., schools director Pedro called it " ludicrous, to give a (special ed) student a test that they cannot read or understand, much less know the answer. " And this quote opens a can of worms to me: " There is no way some of these kids can meet the testing standards, " she said. " If they could, they wouldn't be with us in the first place. " I'd love to ask this person " And if they were not with you in the first place...could they instead be a straight A student in the mainstream? " and then tell her about my son Tanner who is one of many who would be in these classes due to verbal based IQ and receptive ability tests...but instead is a straight A student in all subjects in the mainstream http://www.cherab.org/news/verbaldisabledtest.html But just like I like to leave out the bad parts most of the time and focus on the good (like saying that even though most children diagnosed with leukemia will be cured...I don't like to talk about what happens to almost all of those few that are not cured. Because there is always hope -and you don't want to ever give that up.) Here is someone to cheer from the same article! " There have been low expectations for some of these children all along, " he said. " And that's not because of mental abilities, but because of poor instruction received in the early grades. We need to challenge schools that these children can achieve. Sure, they will need an intensive program, but they can be brought up to grade level. " ~ Tomalis, acting assistant secretary for elementary and secondary education Hurray for ' Tomalis!! " Subject: Thanks for the talking kids page! Date: Wed, 10 Mar 1999 11:03:00 -0500 From: & Glenn <shop-in-service@...> To: pressone@... Hi , Our 2 3/4 year old son Tanner was diagnosed yesterday with apraxia. However, as I'm sure you are well aware, we have been dealing with his non speech for much longer. (You may have read my e-mail about Tanner.) Tanner looks like a cherub-strangers say that all the time. So we call him " the cherub boy " . It was wonderful to hear your adorable sons, and the other children speak. It really does help. At this point our son sounds the most like when the father says " 1, 2, 3, a, b, c, " . Without much prompting he is non verbal. Also, most of the time, when my husband and I try to ask Tanner questions where he would have to try to answer, my older son, who is four, talks for him. Like your son, Tanner looks and acts normal. Actually outside of expressive speech, Tanner tests on every other area above average. This was unfortunately the reason our pediatrician was never concerned. We had to push to get his hearing and speech evaluation. If you could tell us some background on your son it would be appreciated. When did he first get diagnosed? How many days of therapy a week does he receive? When did you see the greatest improvement? Like Tanner, was there a time he didn't really talk? What is " pure apraxia " ? Even though he is a perfect weight now, I have been concerned with the way he sometimes shoves large amounts of food in his mouth. Is apraxia a rare condition? I've spent the morning trying to find a local support group where I could receive the answers to some of these questions. Even Tanner's speech therapist said there is not much known about it because it is pretty rare. I did find a world wide support group for apraxia in Greenbay Wisconsin called MUMS with 20 to 40 members. Well again, thanks for putting the talking kids page together. Let me know what you need, and my husband and I can send you a tape and picture of Tanner. Best, Quote Link to comment Share on other sites More sharing options...
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