Guest guest Posted January 2, 2006 Report Share Posted January 2, 2006 In a message dated 1/2/2006 11:08:27 A.M. Eastern Standard Time, dsaware@... writes: We would like to know if anyone has tried to begin an ABA program on an older child and if so, how was it implemented. Our school district does not have any ABA trained teachers/therapist on staff so we don't know if it will be possible to get this added to her IEP. Trisha is 13, DS/Autism and we just started an ABA program with her this school year. It is working wonderfully! I wished we had tried it years earlier. Carol Trishasmom She isn't typical, She's Trisha! If you always do what you always did, you'll always get what you've always gotten. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2006 Report Share Posted January 2, 2006 No actually, Trisha is going to an autism school at the district's expense. Carol Trishasmom She isn't typical, She's Trisha! If you always do what you always did, you'll always get what you've always gotten. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2006 Report Share Posted January 2, 2006 Hi, welcome aboard. At any age is a good start for ABA. I'm a high fan of ABA. My son started at an older age with ABA and its one of the best intervention for him. In order for school to implement it into the classroom, you would like a CERTIFIED ABA therapist who contracts with the school district to do an eval and work with your child with a plan to work with the staff too. Please do have the Neuro-psychologist write up a recommendation letter and it must include an eval and treatment, well worded to an educational level for the school district. If impossible in the classroom, then something worked around the school hours at an ABA center even its just for 1 hour a day. The school district my son attends will provide transportation for it which hopefully something could be worked around something like this. If the ABA center is willing to work with the school district or vice versa with the school district contracting with a certified ABA Therapist or at an ABA center with private sessions which includes parent and teacher involvement. If great results are shown teacher and staff see tremendous progress, this would be the beginning of implementing it into the classroom. My son does not have ABA done at school, he receives it privately and I do remove him early from school for it with no problem. I have had friends kids receiving the combo of ABA with RDI and this too I have seen great results. Irma,17,DS/ASD > > I'm new to the listserv and am looking forward to learning from others > who share our journey. We have a wonderful 8 1/2 year old daughter > with DS who was recently diagnosed as also having PDD. We are having > her MFE (multi-factorial evaluation) done a little early to determine > if additional goals (mostly behavioral) need to be added to her IEP. > Her Neuro-psychologists has recommended that we have an ABA consult to > determine if it will be of benefit. She also has recommended the > Relationship Development Intervention (RDI) program. We would like to > know if anyone has tried to begin an ABA program on an older child and > if so, how was it implemented. Our school district does not have any > ABA trained teachers/therapist on staff so we don't know if it will be > possible to get this added to her IEP. There are a few programs in our > community that offer the ABA-based curriculum that are not part of the > school systems but most are for younger children. We want to do what > is best for our daughter and are trying to weigh the risk/benefit of an > ABA-based program vs. keeping her in her current environment (multi- > handicapped special ed classroom) with some additional IEP goals to > address the behaviors that interfere with learning. The RDI program > also looks promising but is somewhat costly and time-consuming. We > look forward to your responses on any of these issues. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2006 Report Share Posted January 2, 2006 Thanks Carol- Can you tell me if Trisha is getting her ABA program through her public school? If possible, we would love to keep our daughter in our neighborhood school. --- In , Csvillars@a... wrote: > > > > In a message dated 1/2/2006 11:08:27 A.M. Eastern Standard Time, > dsaware@y... writes: > > We would like to > know if anyone has tried to begin an ABA program on an older child and > if so, how was it implemented. Our school district does not have any > ABA trained teachers/therapist on staff so we don't know if it will be > possible to get this added to her IEP. > > > Trisha is 13, DS/Autism and we just started an ABA program with her this > school year. It is working wonderfully! I wished we had tried it years > earlier. > > Carol > Trishasmom > She isn't typical, She's Trisha! > If you always do what you always did, you'll always get what you've always > gotten. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2006 Report Share Posted January 8, 2006 , First of all, Welcome! You will find this group to be very helpful and also that while we all share a common bond we also have differing needs and styles. That is what makes this list so great. As far as the label, (now remember this is just my own opinion) but I would not worry about how many labels my child has or doesn't have as long as she is getting the services she needs, if you don't need the label to get services that's great, if you do need it to get services then go for it. Think of it this way a label is nothing more than a name which we all have at least 1 and some even more. The label/name doesn't change who we are it just identifies either who we are or things about us that are important. Trisha has a string of labels of which unless it's medically necessary we don't even list because it takes just too much energy to go around listing every thing she has, lol. But when we need a label for a specific service then she has it. I guess I am kinda the odd ball here because getting a label never bothered me or scared me, not even that first day when the doctor came in to tell me he suspected DS. Maybe it's the secretary in me or maybe it's my background in mental health, I don't know. However, believe me there are other things I freak over big time. Things do get better as you go along and sometimes the journey has some very large potholes in the road that we just have to either go around or mend. But it does get better or at least for us it has. As far as knick-knacks, at one time I couldn't have anything on Trisha's level, now I can put out most anything except for candles (which I can only do if I am sitting right there on top of them or wait until she is asleep or at school) she just loves them too much and she doesn't get they can burn her, besides she wants to blow them out as fast as I can light them. lol I also understand about taking them outside, when Trisha was smaller, you had to be on top of her every moment and I even got a child's leash so that she could roam without endangering herself. Oh and the comments that brought on were horrible. But we lived right on the road at that time and her safety was my biggest concern. Now she is pretty good about staying in the yard but if we go near a road I still have to watch her like a hawk because she still doesn't get that those cars could hurt her. (but then how many times do we see so called normal people defying those cars when they walk in the middle of street or dart out in front of an on-coming car?) Carol Trishasmom She isn't typical, She's Trisha! If you always do what you always did, you'll always get what you've always gotten. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2006 Report Share Posted January 8, 2006 In a message dated 1/8/2006 12:00:21 P.M. Eastern Standard Time, cabevizzo@... writes: The only reason I have been shooing off the diagnosis of autism and others have as well is that is very affectionate Again, just my opinion and I'm not a professional so take it with a grain of salt. But in my opinion being affectionate and being social is two different skills. Trisha is very loving on me and sometimes her brother or someone she really cares a lot for, but then it's on her terms most of the time. However, she does not socialize with her peers, she doesn't know how to make a friend, she doesn't know how to start a conversation, she doesn't know how to play games with her peers. She doesn't ask about any of her class mates unless she sees a picture of them and then she just names them when she can. She also doesn't know when enough is enough. For instance she likes me to give her a kiss and then she says yuck and I say no yuck and she will do this over and over even when I say finish. I have to actually walk away before she realizes that we aren't playing any more, that is one of many, many samples. :-) Carol Trishasmom She isn't typical, She's Trisha! If you always do what you always did, you'll always get what you've always gotten. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2006 Report Share Posted January 8, 2006 I can't get this off of my mind this morning and I have a question maybe you could answer, or rather a theory I'd appreciate input on. The only reason I have been shooing off the diagnosis of autism and others have as well is that is very affectionate. He is. I'm thinking, though, that affection is different from social/emotional. On one hand he is very affectionate. On the other he doesn't socialize well with other kids. This is iffy, as this could be developmental as well. BUT...if you yell at him or scare him he has little reaction whereas a typically developing kid would cry or have some kind of large emotional reaction. Does this make sense? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 13, 2006 Report Share Posted January 13, 2006 Jeanne: Our Tori, who will be 6 next month, has DS/PDD-NOS/OCD/NLD. Right now we are trying to minimize her aggressive behaviors. After chatting with drs. who have been treating Autism, I have come to understand that the main umbrella is Pervasive Development Disorder and under that falls: Autism Asperger's PDD-Not otherwise specified Childhood Degenerative Disorder Rhett's Syndrome Most of our kids with a PDD dx. are labeled PDD-NOS because their skills are so splintered. Liz -- Original Message ----- To: < > Sent: Friday, January 13, 2006 7:02 PM Subject: new member > Hi everyone! > I have been enjoying reading what each of you have been sharing > regarding your children. I am Ben's mom 14 yo with DS-ADD/ADHD Speech > Apraxia, Explosive Anger Disorder, etc, etc. Recently our biggest > issue has been with the behavior issues...we have not officially been > diagnosed with ASD but after reading this listserv I am prone to think > that diagnosis would encompass a multitude of our previous diagnoses. > I am hesitant to add another diagnosis officially on the record...our > behavior therapist says that as close as any dr will come to that is > PDD-NOS. One reason it might be advantageous is the funding (as > always, someone wants to take money away from you) and mere mortals > can't afford to pay for all of the therapies required for a kid with > multiple diagnosis. Any words of wisdom? > > Thanks! > > Jeanne > Ben's Mom (14/DS,etc) > > > > > > -------------------------------------------------- > Checkout our homepage for information, bookmarks, and photos > of our kids. Share favorite bookmarks, ideas, and other information by > including them. Don't forget, messages are a permanent record of the > archives for our list. http://groups.yahoo.com/group/ > -------------------------------------------- > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 13, 2006 Report Share Posted January 13, 2006 Hi Jill, my name is Gigi, Mom to Jake, 5. Jake also does not chew. He will eat almost everything as long as it is a texture he can swallow on a spoon. I have a small food processor (like the " magic bullet " ) into which every thing goes. If enough water, milk, pediasure, juice is added it results in food he can tolerate. His breakfast consists of an egg, fruit, a waffle or some oatmeal, lubricated with 1/2 & 1/2 and butter for taste and calories. I also grind up a multivitamin and throw it in. I noticed if he doesn't eat some protein he is more distractable. I have gotten peanut butter into him this way too. PB is a great food. I noticed he eats food more readily if it is spiced with garlic or garlic powder. I grind up the solid contents of soup sometimes and add butter, crackers, etc. If your son will use utensils at school and not at home you should go and observe him eating at school and see what is different. My son has a lot of difficulty just sitting at the table with the family while we eat. I just managed to get him to start eating this year without watching TV. I bought him a stokke kinderzeat for a mere $200 which I hope will make him feel more secure sitting at table. I am trying to find a local place that offers muscle based oral motor therapy for him that accepts health insurance. I found a likely place, but they don't bill. I think he needs more desensitization and exercises to stimulate all the muscles of the mouth and jaw, both at the same time. He will chew on inanimate objects but if its food he won't. That is the problem. When I figure it out I will let you know how it goes. I have to turn on the shower for Jake to pee in the pot. I bought him a play-a-sound book, " Elmo can use the potty " which I use for reinforcement at the end. He likes to wash his hands with soap that smells good and has little granules in it. Also, I read somewhere that kids sometimes won't go if their feet aren't supported so try a stool. Maybe your seat is cold and he doesn't like to sit on it. I know I have difficulty doing this myself on cold winter mornings! If he likes to flush, don't let him do it unless he pees. Make sure he drinks a lot, at least 24 oz a day minimum. As an aside, does anybody have any experiences they can relate about auditory intregration training? Thanks and good luck Gigi Jake's Mom New Member I am a new member to the list serve. My son is 6 years old and has been diagnosed with DS-ASD. He will not chew food of any kind. He eats primarily smashed bananas, smashed pasta with red sauce and oatmeal. He will use utensils at school but not at home. Does any one have any suggestions? Also does anyone have any suggestions on toilet training? He is totally dry in the morningbut he goes into full vetical extension if I try to sit him on the toilet. If I am able to get him on it, he will not go. However, he is fascinated with repeatedly flushing it. -------------------------------------------------- Checkout our homepage for information, bookmarks, and photos of our kids. Share favorite bookmarks, ideas, and other information by including them. Don't forget, messages are a permanent record of the archives for our list. http://groups.yahoo.com/group/ -------------------------------------------- Quote Link to comment Share on other sites More sharing options...
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