Guest guest Posted February 24, 2008 Report Share Posted February 24, 2008 My son 27 months, diagnosed Autistic 3 months back. He use dto have few words, he lost all of them. From last 2 days he is saying eyes. Can anybody suggest me what to do and how to get him talking. Any suggestions are welcome. Thanks for your time. MS Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 24, 2008 Report Share Posted February 24, 2008 Welcome aboard. Many people can give you many places to look. One thing I can tell you is that we had lost words at that age and our deal was metabolic. I only knew where to look and what to do when I reviewed the malabsorption stuff and apraxia labs in the links section of this board. As for the rest of the welcome, I'll leave that to others. Best wishes to you and your child and never, ever give up hope or be fearful of asking a question, you found the right board. > > My son 27 months, diagnosed Autistic 3 months back. He use dto have few > words, he lost all of them. From last 2 days he is saying eyes. > Can anybody suggest me what to do and how to get him talking. > > Any suggestions are welcome. > > Thanks for your time. > > MS > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2008 Report Share Posted February 25, 2008 Hi MS and welcome!! Do you agree with the diagnosis and if so why? Who gave the diagnosis to your child and did you take him for a second opinion? When you say your child is saying " eyes " do you mean the letter " I " or did you mean to say something about eye contact? Loss of words can also be a sign of apraxia or other reasons, not just a sign of autism. If the diagnosis was not from a neuroMD (pediatric neurologist or developmental pediatrician) than for that reason alone he needs to be taken to one. (and again if you did take your child to one nothing wrong with a second opinion from someone that is knowledgeable and respected. You could probably get some names of good MDs from this group) There are those children that have both autism and apraxia. Also in this group we have parents like Jeanne Buesser who is a moderator here and President of the Apraxia Network of Bergen County and mom to one child with ADHD and apraxia and one with autism. There is a distinct difference between autism and apraxia in regards to both diagnosis and therapy even though some aspects of both diagnosis can overlap in regards to for example sensory issues. It's most important at the stage you are in to make sure that the diagnosis is appropriate before anything else. Diagnosis names wouldn't typically matter if the treatment was the same. In this case misdiagnosis does matter so that's why I'm trying to help you find out if your diagnosed-before-2-years-old child really is autistic. And if not -then what and why for the loss of words? If your child is 'not' autistic then some of the therapies (specifically ABA) are not appropriate and may even be detrimental to your child..so you want to know. If a child has both autism and apraxia they would need modified ABA by one who is knowledgeable about apraxia so you don't end up with psychological damage on top of the primary diagnosis. Apraxia is a motor planning disorder where the child knows what he or she wants to say or do -and desperately wants to be able to -but can't. Have you read The Late Talker book because there is a wealth of new to " late talker " info that may point you in the right direction. Below is an archive about a parent who has a child that was given two different diagnosis by the same team and my response to her. ~~~~~~~~~~~~~~~start of archive Hi Patti, The two diagnosis from the same team? " Different treatment, prognosis " is this what they said, or you are not sure? We don't know your child, any of the history or symptoms...or even age -so your guess is better than any of ours at this point what this means. Actually better yet -if you want to know you'll have to ask the professionals (MD? SLP? OT?) that gave these two diagnosis, but I do have a few observations. Since apraxia is one of the diagnosis and insurance is so needed to help cover the years of intensive therapy costs if private therapy is also done -probably whomever you took your child to either didn't read The Late Talker book that I co wrote with neurodevelopmental MD and Medical Director of NYC EI Marilyn Agin MD, or didn't get up to page 87 of the book if they included both of these diagnosis on your child's report. The " developmental " codes which include 315.31, the code used for developmental expressive language disorder, is under the " codes to avoid " in our book The Late Talker -and we state " Use them at your peril, as you may not be reimbursed. " What codes did they use for insurance reasons? " Some speech disorders can overlap, or be misdiagnosed. For example, " Verbal apraxia, a disorder of central nervous system (CNS) processing, and dysarthria, a disorder of output, are commonly confused " , says Dr. , chief of child development at the Chicago College of Medicine. " Experts are able to differentiate between these two disorders by listening carefully to a child's speech and by identifying certain physical clues " , says Dr. , but adds, " These disorders are poorly understood by physicians and by a lot of speech therapists as well. " It is possible for phonological disorders, apraxia and dysarthria to all occur together in the same child. Speech Language Impairments, which is connected to language based learning difficulties may also be present. And the severity of each may vary. " http://www.cherab.org/information/latetalkerhandout.html Yes speech impairments can overlap and coexist together with other disorders -however children are typically diagnosed as having a developmental expressive language disorder when they rule out motor deficits (apraxia is a motor planning disorder), sensory deficits (most children with apraxia also have mild sensory deficits) and the other multifaceted impairment of communication that most children with apraxia have. Sign of developmental expressive language disorder from the American Psychiatric Association, 1994, pp. 60-61 " If Mental Retardation, a speech-motor or sensory deficit, or environmental deprivation is present, the language difficulties are in excess of those usually associated with these problems. " If your child is preschool age and has symptoms of apraxia then I understand the diagnosis of suspected apraxia. With oral apraxia http://www.cherab.org/information/speechlanguage/oralapraxia.html the diagnosis can made as young as 18 months. Apraxia therapy won't hurt and can help stimulate language in any late talker. What I don't get is since most children with developmental expressive language disorder don't have motor or sensory deficits - if your child is nonverbal or essentially nonverbal, how did they know your child has both diagnosis -or is your child talking? Most of the children with apraxia also have mild (subtle) soft signs of neurological damage even though some children can have more severe symptoms -not as typical of this group http://www.cherab.org/information/speechlanguage/parentfriendlysoftsigns.html such as mild low tone, mild motor planning issues in other areas of the body, mild sensory issues, (and can I add to this stuff nobody talks about yet like -problems blowing their nose on command, late potty training and then once they finally do -constipation?!) And Una -since apraxia is multifaceted, most children that have it typically have other symptoms. Put that together with the fact that most are still clueless about what apraxia is and the fact this " rare " disorder is on the rise (and out of control in NJ and some other states) and the diagnosis your apraxic child could get from someone that isn't knowledgeable about all the multifaceted communication disorders out there could just be any one of the symptoms alone (thus the " your child has an expressive language delay " or " your child has sensory integration dysfunction " which isn't exactly an incorrect diagnosis...but won't help to get your child the appropriate and intensive early intervention that would so greatly benefit him or her in all areas. And...since autism is so well known - your child may receive a diagnosis of " PDD NOS " since in theory that diagnosis could probably fit just about anyone in the world. Only problem with it is that in most cases the therapy recommended for PDD NOS is ABA therapy, which if the child does not have autism or another disorder that requires ABA - is not appropriate for apraxia, and may be detrimental. Children with apraxia, a motor planning disorder, want desperately to talk -and need to be taught how to. There is a big difference between a child who only has severe apraxia and one who has severe autism -there isn't as much of a difference between PDD and severe apraxia in some ways -but for those of us in areas where there are lots of children with both -or for parents who have more than one child who has one of each, the difference is not hard to spot. (PDD NOS -Una just curious -do you live in California?) While most children with less severe disorders of speech can get away with just speech therapy -most of us with apraxic children have our children in speech and occupational therapy -as well as other multisensory therapies to help. While the therapy for apraxia won't hurt and most likely will benefit a child who even has just a mild delay of speech -therapy for a child with a developmental expressive language disorder will not be appropriate for a child with apraxia for multiple reasons. Even though almost all of us with apraxic children thought our children were " just " late talkers when they are two or three -as they grow older (and in hindsight) the symptoms are there and just overlooked, or excused away. Like our calling Tanner " the serious baby " because he had almost no facial expressions -ever. This is the reason to see a neurodevelopmental MD if apraxia is suspected so early intervention can begin. Since this came up recently I just want to add that it's not uncommon for any child with communication frustrations to either withdraw or lash out. You can tell the difference of these behaviors from frustration rather than from another underlying cause including autism by providing your child with alternative ways to communicate and observing to see if and when the behaviors fade or become worse. I know for my son Tanner he was social in one on one situations and withdrew in groups which is why during preschool years we didn't enroll him in a " normal " preschool. Tanner even though " deprived " of normal preschool is now hugely social with no self esteem damage which the frustration can lead to in cases. As parents at times with communication impairments it's important for us to explain and/or videotape our children when not in clinical settings where they may be stressed and " not themselves " to share with the professionals. My questions are: Does your child have any soft signs? How old is your child and how is he or she talking/communicating now? Does your child have any social deficits? Play appropriate with others, toys etc. ~~~~~~~~~~~~~~~end of archive ===== Quote Link to comment Share on other sites More sharing options...
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