Autism Therapy: drawing

definition of drawing: not yet defined.

No Factsheets to Display

Pro-Fono Revista de Atualizacao Cientifica, by Gioconda_de_Lima_e_Menezes, C., and Perissinoto J., published in 2008, summarized Mar 2, 2009

Adults may be able to teach joint attention to children with autism by starting out doing things that the child wants to see or do.

The authors defined shared attention as drawing the attention of the other to achieve something desired. This study was designed to look at when children with autism have trouble pointing out things to others (joint attention). The authors looked at whether or not the children pointed to things, showed things to others, or looked to see what an adult was doing. Children were more likely to respond to adult actions than to start a shared action themselves. The authors found that, although children with autism had less joint attention than other children, they did have some low level of joint attention.


Art Therapy: Journal of the American Art Therapy Association, by Martin, N., published in 2008, summarized Jun 10, 2008

Art therapy may help children with autism to converse and form a relationship with their therapist.

This article looked at portrait drawing as a form of therapy for children with autism. The drawings by the children with autism showed a wide range in drawing style and ability. Children who paid close attention to the task made better drawings. The drawings showed that people with autism spectrum disorder (ASD) can see others and draw their portraits.


Developmental Medicine and Child Neurology, by Sugden, D., published in 2007, summarized Aug 14, 2007

Movement coaches can help focus their different therapies on teaching a child how to move better through space.

Some children with autism are clumsy (development coordination disorder (DCD)). There are not many therapies that have been shown to help children who are clumsy. This review article describes how sensory integration therapy can be one tool. In order for the therapy to work, the child has to be an active part of the therapy. Therapy should focus on tasks that have meaning for the child (e.g., riding a bicycle, drawing, and writing). Parents can also learn how they can help to change the task so that it is easier for the child.


Many parents will use some form of applied behavior analysis (ABA) therapy with their children with autism. ABA has been in use for over 35 years, and is a therapeutic intervention that can be done in a clinic, at school, and/or at home; it works best when it’s used throughout the child’s day. Dr. Nina Pinnock, director of the consultation program at the Fernandes Center for Children & Families at St. Anne’s Hospital in MA, explained, “ABA is a playful way of managing behaviors and also skill-building by working on many different things each day: using building blocks, finishing puzzles and drawing with crayons. It’s all the things you might do with a preschooler, but with a child who is resistant you would find a reinforcer such as praise, a high-five, a tap on the shoulder or an edible — sometimes we just switch on a toy that lights up.”

Read original article: ABA Therapy Helps Autistic Kids Develop Positive Habits


Creative Therapies is a program for kids with autism and other special needs that provides dance and art therapies. Creative Therapies is a joint venture between Pinckneyville Park Community Center and Spectrum in the Norcross Georgia area. Recreation Leader Kim Gerlach believes that the combination of dance and art will lead to better self-esteem and improve social skills. Dance can help with posture and can calm as well as stimulate youngsters. The art therapy will include clay, drawing and painting, and pottery.

Read original article: New Program Uses Art, Dance as Therapy


For the past 12 years, Jerry Sapp, manager at the Publix at 2816 Washington Road (Augusta GA), and employees have provided gifts to special education children at A. Brian Merry Elementary School. Many of the children come from homes that might not be able to provide the toys, crafts, and clothing. One young non-verbal boy in especially loved the toy cars he received, while another youngster planned a drawing with his box of 24 crayons. Publix and the school have been holiday partying together ever since a PE teacher contacted Publix to see if they could provide cake and ice cream for the kids before winter break.

Read original article: Making Things Merry, Bright


Dr. Jeff Kinner, a pediatric dentist in Nevada, sets aside one day a week to treat children with autism. He has adapted the principles of applied behavior analysis (ABA) therapy to ease children's fears, "establishing eye contact, calmly repeating instructions and praising good behavior while not drawing attention to poor behavior." While he does not have special needs children of his own, Dr. Kinner saw the need and sought training from occupational therapists because he could not find dental ABA training. He likes for the parents to participate in the dental process and talk to their children about the office visit in terms their children best understand. One mom "told her son, who loves the movie 'Transformers,' that Dr. Kinner would look for robots in his mouth," and if there were bad robotshe would take them out.

Read original article.



Please comment on this autism topic.

longterm vaccine damage: CNS

Aug 4, 2009 by Anonymous

Hi:  has anyone out there heard of treating live viruses (residual from those vaccines given at 12 months) by drawing them out of the CNS?  Our kindergarten kiddo has just been diagnosed with live viruses way up behind his ears, right up in that major nerve, in a place that has selective access to the CNS /spinal cord.  So the first step is to treat the inflammation of the CNS and then draw out the viruses so that the immune system can attack these guys.  Has any one ever gone this route?  Once the viruses are out~about 5 months~ then that's that.


vaccines/neurosensory therapy

Aug 4, 2009 by Anonymous

Hi:  has anyone out there heard of treating live viruses (residual from those vaccines given at 12 months) by drawing them out of the CNS?  Our kindergarten kiddo has just been diagnosed with live viruses way up behind his ears, right up in that major nerve, in a place that has selective access to the CNS /spinal cord.  So the first step is to treat the inflammation of the CNS and then draw out the viruses so that the immune system can attack these guys.  Has any one ever gone this route?  Once the viruses are out~about 5 months~ then that's that. 

Please reply if you have had experience in this arena. OK, thank you.


Cabin fever in June...

Jun 15, 2009 by Anonymous

Summer vacation has begun and I’m already being driven nuts by these children. These small, charming Gifts from God are making me wonder if we should move to a district that has a twelve-month school year. What’s really going on here is that Thomas and Hayley are driving each other nuts and that, in turn, is making me crazy. The root of the problem is that the weather has been so crummy (for mid-June) that we haven’t been able to do anything. If it’s warm enough to swim, it’s raining. If it’s sunny outside, it’s too cool to go swimming and all the slides at the park have big pools at the bottom. We’re still waiting and waiting for the weather to improve.
Today was actually pretty nice, but I made a grooming appointment for the dog that we had to work around. We left the groomer’s straight for Uncle Tom’s Pool and stayed there until the groomer called us to come pick up Sophie. Frantic pool and swimming activity usually works wonders on kids who have cabin-fever (in June, for crying-out-loud!) but my kids are not like other people’s kids.
We did have a few playdates a few weeks ago with the family I mentioned in my last blog. Thomas was actually really good with his buddy. I explained before they came over that he couldn’t just sit alone and play when we had “company” (what’s “company,” Mommy?) but he had to play with his friend. So, since he couldn’t play PSP, Thomas and his friend played MarioKart on the Wii. Whatever. They had fun. Hayley and her friend played Barbies and the littlest wee one just bounced back and forth, watching. Hopefully we’ll see them again soon and maybe meet at the park or something.
Graduation went fine, but of ALL DAYS for me to forget to give Thomas his Strattera, the graduation ceremony day was probably the worst. He had to sit quietly for semi-extended periods of time which didn’t work out too well for him. The video is funny because he kept waving me away, telling me to turn the camera off and go sit down. But he got an extra-special hug from Mrs. H., who I could tell was genuinely sad to have to say good-bye for the summer.
After the graduation ceremony, Thomas had just one more day of school that happened to be on Tuesday, my help-out day. So I got to be there for the last day, helping take everything off the walls and put things away for the summer. It was kind of sad. I’ve been there every Tuesday all year and have apparently built up a sentimental interest in the Kindergarten classroom and the routine. I really appreciated how much emotional investment the teachers must have in their kids by the end of the year and how hard it is for them to have to let them go. During the graduation ceremony, Mrs. H. gave a short speech about how once the kids go through her classroom for a year, they’ll always be “hers” and can come back and see her anytime. She got choked up as usual and it was very sweet. The kids all wore caps and gowns and Thomas kept pulling his up to reveal the decidedly un-formal t-shirt and shorts I put him in that day. No point making him doubly-uncomfortable in fancy pants AND mortar boards, I though. Nobody gave me any funny looks, though.
Hopefully the weather will turn better so we can walk to the park more often and maybe go to the zoo. All I know is that if we’re all cooped up in this house together for much longer, I’m going to start frantic home-improvement projects like re-painting or something. Hayley’s fifth birthday is coming up; her party is this weekend and Jonathan is apparently going to be up at 4 a.m., slow-cooking pork butts on the grill. It’s the only way, I guess. What I really want to do is get pictures of this madness. We’re going to turn the pork butts into pulled pork sandwiches made with Jonathan’s homemade BBQ sauce. He’s such a gourmand. I’m in charge of potato salad and coleslaw. And I’ll be buying beer too, I think.
We’re going to a wedding in Peoria June 26-28 and leaving the kids with Grandma Jackson. The dog’s going to my brother-in-law and sister-in-law’s house, God bless them. That’s the main reason I just had her at the vet and the groomer. Nothing says, “Gee, we sure do appreciate this” like dumping a shaggy, smelly and potentially unhealthy dog off with relatives. Jonathan and I certainly could use a break. We keep talking about taking a “date night” for ourselves, but there is just no time! This Friday, we’re going to be getting ready for Hayley’s party which is on Saturday, and I have to work on Sunday. We should be able to have some quality alone time in Peoria, if you can have quality alone time with twenty aunts and uncles, thirty cousins and their dates or spouses, your mom, dad and sisters all staying in hotel rooms nearby. We’ll have to take whatever we can get, I think. We’re going to be driving down with my sister and her husband, whose company we genuinely enjoy, so that will be fun too. Plus, I get to dress up! Yee-haw!
A couple weeks ago, Jonathan only had a half-day at work so we took the kids to see “Up” at the theater. We had never, ever taken both kids to the show before! Like so many things we’ve been doing recently, it was to be a litmus test for Thomas’ performance during stage and theater presentations at Disney. He was GREAT! Outstanding, even! He was, in fact, better behaved than Hayley. He sat in his seat and wore the 3-D glasses (yes, we sprung for the 3-D effect, but don’t think it added too much to the show. The previews were more impressive in 3-D than the movie was, so FYI, you can probably skip the 3-D showing and do the less expensive non-3-D show) and watched the WHOLE THING without complaint. The only problem was that he talked a lot during the show, asking a lot of questions, but he wasn’t too loud asking the questions and didn’t disturb others. There were plenty of children at this showing in particular that were allowed to run wild all over the place and I’m so glad to say that mine were not among them.
I’m trying to keep up with helping the kid’s reading and writing so that their brains don’t turn to mush over the summer but Thomas is totally on to me. He says, “I’m not in school anymore! I don’t have homework!” And then he finds something else to do. Hmpf. Hayley is still really interested in writing and will write words, asking how to spell them and drawing really cute pictures of people who look like potatoes with toothpicks sticking out for arms and legs. They’re really cute.
Well, there goes the random quiet moment I was able to enjoy today. Thomas is stealing noodles out of the colander and making Jonathan crazy and Hayley has fallen asleep next to me in a position that cannot possibly be comfortable. Ho-hum.


Still on my plate

Sep 30, 2007 by Anonymous

            We’ve been so busy that I just haven’t had the energy to write lately.  At night, I just want to hang out in front of the TV or escape into the world of Harry Potter for a while.

            Last week was very busy for our family.  Thomas had that video EEG on Wednesday and Thursday so he missed school those days.  He was actually very good for the test part which consisted mainly of just hanging out.  The hook-up and un-hook was very traumatic for us and Thomas especially.  Jonathan had to hold him down while the EEG technician super-glued twenty-four leads to Thomas’ head; each lead taking approximately one and a half minutes from start to finish.  It was awful.  Thomas was freaking out, and the nurse who was putting these things on Thomas seemed extremely frustrated with him.  He kept screaming “Ow!  It hurts!  Mommy, help me!”  He certainly knows how to play his mom!  The “Mommy, help me!” thing went on for quite a while.  I cried intermittently.  But the nurse, despite Thomas screaming about how much it hurt, kept telling Thomas that it didn’t hurt, there was no “ouch,” no boo-boo, etc.  I was getting mad!  How does she know how that super-glue and air-gun combo feels to Thomas?  No, there weren’t sharp needles and certainly nothing that would hurt an average person, but to Thomas, that air-gun thing and the acrid smell of the glue might have been torture. 

            During the testing part, especially after hook-up on Wednesday, Thomas was really good.  Because it was a video EEG, Thomas was on camera the whole time.  A nurse/technician was in the room with us from beginning to end making sure that the camera was pointing at Thomas every second (except in the bathroom).  He stayed on his bed most of the day and was very well-behaved.  Nice volunteers kept coming in to bring toys and movies for Thomas and he was very pleased to learn that this whole test thing included all the chocolate ice cream he could eat.  And he ate plenty.  Whenever he seemed to be getting restless or antsy, we’d run to the freezer and get a little ice cream cup.  It worked really well.  He had ice cream with every meal and for every snack.

            During the night on Wednesday was the really important time for the test since it is Thomas’ sleep problems that brought us to this point initially.  We were not allowed to give Thomas his sleep medication, so he was up until 11:30 p.m.  He got up a couple of times in the night.  He tried to crawl into my recliner at 4 a.m. but it was too small for both of us, so I got into his hospital bed with him.  We stayed there until he awoke at 6:30 a.m.  That was when his breakfast came!  Is it just me, or is 6:30 in the morning way too early for food service employees to be bringing clattering trays of lukewarm food into children’s hospital rooms?  Anyway, that’s what woke Thomas up. 

            In addition to keeping the camera trained on Thomas, the attending technician also kept a log of Thomas’ activity every few minutes or so.  When we woke up on Thursday morning, I looked at the log and noticed that the computer recorded two “events” during the night.  One was at 12:30 a.m. and the other was about two hours later.  These are obviously neurological events, so I’ll be eager to hear what the doctor has to say about them.  We have to wait two weeks for the doctor to review the test and call us back.

            While Thomas was being really good on Wednesday, Jonathan’s mom came to see him.  Thomas sat in his bed and talked for nearly two hours, nonstop.  It was exhausting for us to listen to, but it was so funny too!  Jonathan finally realized what was going on with Thomas; since he was tethered to a machine and unable to go very far, he was getting rid of all his energy through his mouth.  He would not stop, I tell you!  It was really funny and interesting.  I knew Jonathan was right…I couldn’t believe that Thomas was being as still and well-behaved as he was, yet his body had to find some way to expend the pent-up energy.  Thank goodness he decided to talk it out.

            The frustrated nurse came back again on Thursday to take the leads off Thomas’ head, and this experience was almost as horrible as putting them on.  They put mineral oil or some kind of spirits on his head to dissolve the glue (non-acetone nail polish remover, I think) and Thomas was not having any of that.  He freaked out again, but at the end of it the leads were off instead of on.  We rinsed his head and Jonathan took him to the play room down the hall while I waited (and waited and waited…why are hospitals so slow to discharge patients?) for the nurse to give me discharge instructions.  Every time I have been in the hospital, I seriously consider just walking out after the doctor gives me permission to go home.  What were we waiting for?  Thomas was not sick, not post-operative and had no wounds or dressings or fevers that needed care …why do we have to wait forever to be officially discharged? 

            Of course we didn’t just walk out.  We waited around for the very important instructions that told us that Thomas is on a “normal” and unrestricted diet (knew that) and can resume normal activity (knew that, too).  Thomas was very glad to be home and just this weekend got rid of the rest of the glue in his hair.  I’ll make sure to let everyone know about the results when we receive them.

            Thomas and Hayley had a fun weekend!  It started on Friday night when the Cubs clinched the National League Central division title!  Woo-hoo!  My sister and her fiancé came over to watch the game and we had a great time.  Saturday, my mother-in-law picked the kids up and took them to her friends’ ten-acre property for the big Hayride and Bonfire Party that they have each year for everyone’s grandkids.  Thomas and Hayley went with their cousin and Jonathan’s cousin’s son.  That meant that Jonathan and I had some time to ourselves to remember what it was like before we had kids.  We didn’t do much.  We bought a movie at Target and brought it home to watch.  We baked an apple pie and I did a lot of painting (we’re re-painting most of the rooms in our house).  Very exciting, I know.  But it was so quiet!  It was so peaceful!  Then the kids came home this afternoon just as the Bears were officially losing the game against Detroit and thus ended both the quiet and the peaceful.  Especially for Jonathan.  I never realized that a football game, either won or lost, could so greatly affect the general atmosphere in our home.  So alas!  Another week of grumbling and head-shaking.  Thanks for nothing, Bears!

            Thomas’ teacher called us yesterday.  She mentioned that Thomas is the highest functioning child in her class as far as language is concerned so she wondered if it would be okay if he spent some time in another classroom with kids who can help him learn some of the nuances of social language.  Apparently, there’s not a lot of talking amongst the kids in Thomas’ class and his teacher (and the principal, with whom this was discussed) wants to challenge him a bit more and help him really progress this year.  I was very happy to hear that from her since I’ve been a little disappointed in Thomas’ curriculum so far.  The first week was all about colors.  Great, but Thomas already knows his colors.  The next three weeks are about shapes.  I’m a little more on-board with that, since Thomas could use practice drawing shapes.  But still, he knows a lot of shapes.  I don’t really want this year to be a review for Thomas; it has to be a little more challenging so that we can really prepare him for kindergarten.  I never really understood the reasoning behind Thomas’ class-placement this year anyway.  There are no other autistic children in his class, but there are at least two kids with Down Syndrome and other varying disabilities.  I’m not sure what this means.  I know that Thomas is one of the oldest in his class, but I don’t really understand anything about why this class was chosen for Thomas.  Duh…maybe I should ask!

            So Thomas will go to spend play time in another teacher’s class just a couple of times a week at first.  Depending on his response, they may take him there more often.  I’m very interested to see how that goes and if it helps Thomas with social language skills.  His teacher said that the “demographic” in the other classroom is mostly kids with slight to moderate language delays.  I’ll make sure to let everyone know how Thomas responds to this new routine.

            I was really dreading the video EEG thing, but now that it’s over I feel like things are calming down a bit.  The first half of the week is usually a little hectic for us with Hayley’s dance class and Kid Rock.  We’ve been doing okay with the dance class so far; Jonathan has been home by 4 p.m. the last two Tuesdays in a row so my sister Tina didn’t have to come and take care of Thomas for us.  We’re having our windows replaced sometime in the next three weeks and I really want to get the air vents and ducts cleaned before winter hits, and the bedroom carpeting…I always feel like I can only have a few tasks on my mind at a time and no more than that or something will have to give.  The EEG is off my plate, but depending on the results, there’s a good chance that I’ll have to take Thomas in to see the doctor soon.  I can’t really file all of that away until I have the results, if any.  If any medical professional says the word “inconclusive” in reference to that EEG, I’ll scream.  You’ll probably be able to hear me from there.



Please comment on drawing or other autism therapy topics.

  • Factsheet
  • Research
  • News
  • Comments.
  • Share |