Tuesday, May 24, 2011

Apraxia Therapy Materials: Doodle Buddy iPhone / iPad App

Doodle Buddy is another iPhone / iPad app that can be a wonderful way to elicit speech or sound effects from your child. The program is free, but is overrun with really obtrusive ads. You can choose to pay $0.99 to remove the ads from the application.

This program does many things all of which can be used as a therapy activity.

  • It is a drawing program. (Please don't laugh at my lack of artistic skills.) You can draw things for your child to label. Alternately, you can follow their instructions and draw what they tell you to. If they say "car," you do your best to draw one.

  • The program has "stamps". There are tons of little pictures that your child can transfer to the screen just by choosing the one they want and then tapping as many times as they like. Even better, each stamp has a sound effect. So the frog croaks, the crying face cries, the dog barks, and so on. Your child can label the stamp or imitate the sound effect. Even if they are non-verbal and using signs, you can wait until they make the sign for "more" before you let them put more stamps on the page. Here is a sampling of the stamps available. There are many more than would fit on one page.

  • There are backgrounds and themed stamps to go along with them. Some come with the program. Some you have to "buy" with points. If you are willing to install a few free programs on your machine you can get more points for free to get additional themes.

    So you pull up a background. Backgrounds (themes) include dinosaurs, cars, beach, farmyard, lake, princess, space, underwater, winter, spooky house, doghouse in backyard, desert, and more. You make up a story about the picture adding stamps as you go along. You get your child to repeat words that are part of the story. Here are some examples.

    Farm: Mama chicken was at the farm today. (insert chicken, have child say, "chicken"). She had three baby chicks with her. (insert three baby chicks counting, "one, two, three") They were lonely! They wanted to play with some friends. (toss in a couple of sheep and practice saying, "baa") I could continue, but you get the idea.


    Here are examples of the lake and princess themes as well.


  • My kids particularly enjoy the haunted house theme, the cars theme, and the farm theme. I'm sure your kids will have their favorites too. Really, the possibilities for using this program as a therapy tool are only limited by your imagination. (I make up really boring stories when put on the spot, but the kids don't seem to care. I get lots of speech and vocabulary practice in and that is all that really matters.)


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Monday, May 23, 2011

Counterproductive?

We're trying to rebuild our deck and therefore we have a ton of random pieces of cut-off wood lying around. I had a brilliant idea to drill some holes in a piece of wood and let the children play with the block of wood, some wood screws and a couple of screwdrivers.
  1. They loved it.
  2. Michael gets to play with a screwdriver and screws in a sanctioned way.
  3. Hmm... do I really want to give him additional, sanctioned, practice with a screwdriver? (See this and this for reasons that this activity is possibly counterproductive.)

NutriiVeda vs NutriiVeda Achieve Comparison

Our first shipment of NutriiVeda Achieve arrived. As expected the product now comes packaged in a resealable 30-serving foil pouch rather than in two 15-serving canisters. The flavor is now French Vanilla rather than Vanilla. Here is a chart highlighting the main nutritional differences between the old NutriiVeda formula and the new NutriiVeda Achieve formula.


The differences I see as most significant, nutritionally are the reduced sugar, added fiber, and added sodium. Although interesting, the added Omegas are not super significant for me because they come from plant sources rather than fish sources making them less appropriate as a supplement for apraxia. Also the dosage is less than generally recommended as a therapeutic dose.

I tried it myself. I do believe that the new NutriiVeda Achieve formulation results in a creamier "shake" (mixed with skim milk) than the original formula. I also think that the new formulation is a little more subtle than the old one. To be honest, I personally disliked the old one. I'm not in love with the new one, but I dislike it less. I found the old one difficult to mix into milk without ending up with lots of big clumps. The new one has the same problem.

The original NutriiVeda mixed beautifully into yogurt. It almost disappeared in terms of texture. If anything, it seemed to make the yogurt a little bit thinner. The new NutriiVeda Achieve seems to mix into the yogurt and give it a creamier, thicker, fluffier texture a little like a mousse.

When I gave it to the kids (occasionally I feed the mix to both kids - it's just simpler that way) Michael immediately noticed the change. He said, "This is a new yogurt. It tastes different. It tastes salty." Now, yes, the new NutriiVeda Achieve does have sodium while the old one did not, but you're also taking the word of a 3 1/2 year old that it tastes salty. I'm not sure he uses the term accurately. That might just be the only word he knows to describe a change in taste. On the other hand, they added sodium and removed over half the sugar content. It may actually taste saltier to him.

He continued to comment on the change as he consumed the bowl. He ate it, but I'm not sure he liked it. Ava ate hers and did not comment on the difference. We've only had one serving so far. I'll let you know if the difference in taste (or texture?) becomes a problem.

Bottom Line The new NutriiVeda Achieve is significantly different in taste and texture from the old NutriiVeda formula. I like the concept of increased fiber and reduced sugar, but I also need Ava to eat it. We'll see if she continues to eat the new formula. I'm not super fond of the increase in sodium. My opinion of the added Omega 3 and Omega 6 from plant sources is neutral.

Sunday, May 22, 2011

Free Themed Preschool and Toddler Activities

I stumbled upon a website with a great set of free activities. The authors have created themed sets of learning activities for toddlers and preschoolers. The reproducibles are downloadable in .pdf form. I downloaded all of them because I'm a collector and I'm like that.

I decided to start with the Transportation Theme Pack because transportation is popular with both my children. I did not print out every activity included with the pack because I didn't feel like my two and three year olds were ready for the letter tracing and writing activities just yet. I did print out the matching transportation picture/word cards, the shadow matching activity, the tracing lines activities, the 3-piece puzzle cards, the bus size sequencing activity, the counting cards, the left and right sorting cards, and the beginning-sound word cards. I printed most of them on cardstock and I may even laminate them. Here is a picture of some of the pages right after I printed them and a picture of the materials once I cut them out.



We have already tried the shadow matching activity and the number cards. The kids enjoyed them. They identified the vehicles and their colors. They practiced counting and matching. Michael worked on number recognition and Ava worked on her speech a little ("on top"). We had fun and there are several more activities left. You could easily play with the materials for a week, put them away for a while and pull them back out again in a couple of months and do it all again.

The Preschool Packs currently available are:

The Tot Packs currently available are:


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Saturday, May 21, 2011

Reality Check

When we started all of this Ava had too little speech to give her any kind of formal articulation assessment. You can't ask an essentially nonverbal child to label pictures in a book so that you can score how well they did making sounds. Now that Ava has so many words her early intervention therapist and I decided to give her an articulation test to see where she is.

The Goldman-Fristoe Test of Articulation 2 is very simple in concept. It is a book of pictures. Your child labels the pictures and the Speech-Language Pathologist transcribes how your child pronounces each word exactly as your child says it. The test is designed so that after all of the pictures have been pronounced your child has attempted to pronounce every consonant sound (and some blends) in every position (beginning, middle, end) of words in which they appear in the English language.

We gave the test to Ava. It took us two sessions. There are a lot of words on the test and it is hard to get a two year old to focus. She did better than I expected. She got sounds on the test that she doesn't usually get in regular conversation. I was feeling pretty good about the whole thing.

Then I scored the test. She got a standard score of 72. That's equivalent to the 7th percentile. That means that 93% of children her age perform better than her on this test. Wow! Seeing that number was a huge reality check for me.

I've been so focused on all the improvements. She's made amazing progress since we started getting her help. She had no words. Now she had more than I can count. She went from one-word utterances to two and three-word phrases. Now we are frequently hearing four and five-word sentences. She was a pretty silent toddler who wasn't even trying to talk any more - a toddler who had to resort to gestures and pulling me around to ask for what she wanted. Now she talks all the time. She communicates with her parents, grandparents, brother, teachers, and friends. She even talks to herself. She tries to sing and hum. I was proud. I was excited.

Now, with this new number (7th percentile!) I am sad and discouraged again. I know that this new information takes nothing away from all of her accomplishments. I do know that. I know that this new information is a valuable reality check. It gives me information I can use to go forward and plan our next steps. As a speech-pathologist the test results are interesting, valuable, and even a little exciting. As Ava's Mama, those test results make me sad. They are a reminder of her struggle and the long road that is still ahead of us. Reality really stinks sometimes.

Friday, May 20, 2011

How did he do it?

First there was the redecoration of the room. Then there was the disassembly of the dollhouse. Then, following today's adventures in not-napping, we discover this:


Notice the new gold knob on the lower drawer. So, where exactly did he acquire the new knob?


And where did he put the old knob?


But here's the thing. How did he do it this time? There was no screwdriver in the room!

We obviously need to get this boy some kind of outlet! We're thinking erector set maybe?

The Weekly Review: Week Ten

Funny Blog Post I completely agree with:

Kristen at Motherhood Uncensored wrote a hilarious post about her philosophy of motherhood. Check it out first for the humor and second for the nuggets of wisdom hidden within.

Blog Post that made me want to give the author a big hug

Mona at kirida dot com recently wrote a post about her pediatrician recommending that she have her son evaluated for autism. It was a touching post. I thought she did an amazing job of expressing the awfulness of having to wait to be evaluated for a diagnosis.

In August 2010, Mona wrote a post about her son's speech and her feelings of protectiveness that really resonated with me. I think I found it so meaningful because I was already ignoring so many red flags about Ava. This post perfectly expresses so many of my own feelings about Ava. Then, and now, it helps me feel less alone.

Website Resource of the Week:

Therapy Fun Zone is a website full of great OT and PT activities. Even if your child doesn't need PT or OT help, the activities are still a lot of fun. I'm going to start with this one as soon as I get to the store for gumdrops and toothpicks. Fair warning though: the website is incredibly slow and each page takes several seconds to load. I feel like I'm on a modem. Second, the pages are poorly designed and an email signup form shows up at the top of each page so you have to scroll down to see the actual article. The activity ideas (complete with pictures) are worth putting up with the technical issues though.

Sibling Moment of the Week:

The children have large stuffed armchairs. Their game of the week (intended to give me a heart attack) is to tip an armchair on its side, climb on top together, and then slowly shift their balance so the whole thing tips over tumbling them onto the floor in a heap. Laughter from the two of them fills the air and they work together to tip the armchair back over again so they can start over.


Quote of the Week from Michael:

Michael has coined the phrase, "Visitor Day" for the day of the week that we usually have friends come over to play. He'll say, "Is tomorrow visitor day Mama?"

Ava's Quote of the Week:

"Come sit with me, Mama!"

Project of the Week:

I was happy to get my three part series on Apraxia Therapy Principles finished and posted.

Thursday, May 19, 2011

Another Perspective (On NutriiVeda) Is Always Valuable

We've been trying NutriiVeda with Ava. I'm frustrated by the lack of anything other than anecdotal evidence of improvements, but given that lots of parents are seeing improvements with their children I had to try it. Tentatively, I feel like we've seen an increase in the amount of speech from Ava, and in the length of her sentences since we started using NutriiVeda about six weeks ago.

However, NutriiVeda is expensive and there is no scientific evidence. I came across a well written post on the blog of another mother with a daughter who has Childhood Apraxia of Speech. She tried NutriiVeda with her daughter for three months and did not feel like she saw significant improvements. She saw no regression when she stopped using the product. Check out her post on NutriiVeda. If you're thinking about trying NutriiVeda, you should read the opinions of people who tried it and didn't like it in addition to the posts of all the parents who love it.

While on the topic of the Apraxia Adventures blog, I really identified with her post on her son learning to kiss as well. I am way too familiar with that bittersweet feeling of being happy and sad (jealous!) at the same time.

Since both of my children have oral apraxia, I feel it when I see another woman's baby look at me and smile - so easily and naturally. I enjoy the smile. I enjoy the sweetness of it. And then I wish I had been able to experience that with my children. I wish it had been natural and easy. Or recently, I watched a video of a toddler Ava's age being interviewed by her mother about things like her favorite toy, food, game, etc. The video was adorable as was the toddler. Her speech was so clear. The sentences were so long. I want that ease for Ava. Will I always see other children through the lens of what I want for Ava?

Bah! Enough of this self-pity and sadness. Overall things are good. Improvements abound. I refuse to dwell overly long on depressing thoughts. I'll just share them briefly and then move on.

Wednesday, May 18, 2011

Six!!!

Ava loves cucumber and dip. She ate all the cucumber on her own plate (about 1/4 of a rather large cucumber). Then she eyed Michael's plate and asked if she could have his cucumber. He had already decided that he wasn't going to eat his, so he gave his cucumber to Ava. That quickly disappeared too. At this point, the girl had consumed half a cucumber.

She looked down rather pitifully at her plate and said, "No more on Ava's blue plate!" Six!! That's a six word sentence from the same little girl who had only three words in her entire vocabulary four and a half months ago. I'm practically speechless myself in awe and gratitude. (Standard disclaimer: No, that sentence was not pronounced "correctly" with every sound present, but all the words were there and I could understand them.)

Childhood Apraxia of Speech Therapy Fundamentals: Part 3 - Methods and Content

Childhood Apraxia of Speech (CAS) is neurological speech disorder that causes children to have difficulty with the motor planning, sequencing, and programming necessary to produce volitional speech. Therapy needs to address the core problem of motor planning for speech in the most effective way possible. Every child is different, so therapy must be customized. Therapy for a young child who is nonverbal will be different from therapy for an older child who is using multi-word sentences, but the speech is hard to understand. However, the basic underlying fundamentals of therapy for apraxia are going to be similar. These underlying fundamentals are based on current research and professional consensus.

What methods are used during therapy for Childhood Apraxia of Speech?

When reviewing the most effective methods for treatment of children with Childhood Apraxia of Speech there seems to be a unifying theme and that is neurology. CAS is a neurological disorder. The areas and pathways in the brain that are typically responsible for the motor planning of speech are not functioning properly. The purpose of therapy is to retrain those areas to be more efficient at their job and to recruit other areas and pathways in the brain to help when possible. The best way to enlist other areas of the brain to help out is to take a multisensory approach to therapy.

Multisensory Stimulation Techniques

Typically speech involves listening to a speech stimulus and responding appropriately. This uses specific areas in the brain that are separate from the areas that listen to and enjoy music. The speech listening pathways are different from the areas involved in watching and interpreting visual signals. The speech listening pathways are different from the sensory receptors that feel touch on the skin.

What does all of that mean for therapy? It means that when you use multiple sensory pathways when trying to stimulate speech, you recruit other areas of the brain to help out the speech areas that are struggling. So, the speech therapist may use music to try to elicit speech productions to enlist the help of the part of the brain that listens to and enjoys music. The speech therapist may use tapping (tapping, clapping, or snapping with each syllable) to enlist the part of the brain that involves rhythm and basic math. Tapping draws the attention to each separate syllable in a way that simply saying them separately does not. You can use tapping to engage multiple pathways by gently tapping the child's hand or leg along with the syllables which also engages the part of the brain that senses touch. The speech therapist may use visual hand signals paired with specific speech sounds to enlist the part of the brain that interprets visual signals. The speech therapist may use touch on the child's face to cue certain speech sounds or movements.

For children who are nonverbal, often big body motions like swinging on a swing or bouncing on an exercise ball paired with music can help elicit some first sounds. The therapist will try to engage different senses to find one type of stimulation that helps or a combination of stimulation methods that help elicit speech.

Manipulate rate

Sometimes slowing down speech can help. Doing things more slowly allows more time for motor planning. Your therapist may incorporate practice with slowing down speech production to try to help your child be successful at producing speech targets.

What does a speech language pathologist teach children with Childhood Apraxia of Speech?

This is an incredibly complex topic. I'm just going to try to give you a basic overview of the type of things your therapist will think about when choosing goals for your child.

Your therapist will choose targets for your child based upon their professional expertise, their assessment of your child's current skill level, their knowledge of which targets would be age-appropriate, what the child is stimulable for, and their assessment of your child's most pressing needs. (Your child may be missing 10 age-appropriate sounds, but one particular missing sound makes him or her really hard to understand. That would be the sound to work on first.)

When working with children with Childhood Apraxia of Speech therapists are usually following a therapy principle called a series of successive approximations. Essentially, the therapist starts with what your child can do and treats that as correct. Then they try to get that a little closer to "correct" and treat that new level as correct. Once that is well established, they make it a little harder and call that new level correct. For example, your child might be saying "ba" for "bottle," but not very often. First your therapist will treat that as correct, and just get your child to do it more often. Then the therapist will make the task a little harder and try to get your child to say "baba." Now "ba" is considered to be incorrect and "baba is considered to be correct. Once "baba" is well established the difficulty would be increased again to "bata." And so on.

Specific therapy targets will vary widely from child to child. The targets may include specific consonant or vowel sounds, eliminating a speech habit (like leaving off consonants at the ends of words), increasing the number of words in your child's vocabulary, increasing the types of syllables your child can use, and increasing your child's utterance length (from no words to one-word utterances, from one-word utterances to two-word phrases, from two-word phrases to three-word phrases, etc.).

Summary

Your therapist will carefully choose individualized targets for your child based upon their assessment of your child and their professional expertise. They will slow down their rate of speech and your child's rate of speech to allow for extra processing time. They will use multisensory therapy techniques in order to engage as many areas of the brain as possible to improve speech production. They will start with what your child can do and gradually increase their expectations over time as your child improves.

You just finished Part 3 of a three part series on Childhood Apraxia of Speech Therapy Fundamentals.
Read the other two parts of the series:

You might also be interested in the following articles:

Tuesday, May 17, 2011

Apraxia Therapy Materials: Talking Carl iPhone / iPad App

If you have access to an iPhone or iPad there are a lot of apps that can be used to elicit speech from your little one. One in particular that can work well with a child at any stage is Talking Carl. (Note: There are other "talking" apps as well. Most are free or 99 cents. Just be sure to try a couple and choose the one you like best before you try it with your child. Some of them are not appropriate for children.)

Talking Carl is an interactive little monster with big eyes and a big mouth. He will giggle when tickled, and complain when poked. Children almost always crack up laughing themselves when they tickle or poke Carl. If you have a nonverbal child, just being able to get a giggle or an "ouch" in sympathy is good speech practice.


The other key thing Carl does is listen to what your child says when they talk into your phone and then repeat their words back to them. So if your child says, "Hi!" Carl will repeat, "Hi!" Carl will repeat anything the child says. If you are looking for a fun way to get your child to talk, this might do the trick for you. Check it out.

Here is a short YouTube video that demonstrates most of the things Talking Carl does (except the giggling). I chose this one because it was short, but did a nice demonstration of the speech repetition (not in English, but still a good demonstration).



You might also be interested in the following articles:

Childhood Apraxia of Speech Therapy Fundamentals: Part 2 - Types and Variability of Practice

Childhood Apraxia of Speech (CAS) is neurological speech disorder that causes children to have difficulty with the motor planning, sequencing, and programming necessary to produce volitional speech. Therapy needs to address the core problem of motor planning for speech in the most effective way possible. Every child is different, so therapy must be customized. Therapy for a young child who is nonverbal will be different from therapy for an older child who is using multi-word sentences, but the speech is hard to understand. However, the basic underlying fundamentals of therapy for apraxia are going to be similar. These underlying fundamentals are based on current research and professional consensus.

How is therapy for Childhood Apraxia of Speech structured?

We've already discussed the fact that therapy for a motor planning problem needs to involve lots and lots of practice. The next question is how to structure that practice in order to get the best results.

Blocked versus Random practice

Blocked practice is practicing one target at a time, over and over again. This is where the therapist starts when trying to teach something entirely new. If you have a child who can't make a /b/ sound and you are trying to teach it, you are going to practice /b/ over and over again in blocks until the child experiences some success. A blocked practice structure is great at establishing a new skill, but doesn't carry over well outside of the therapy session. When the child begins to perform well in a blocked structure the therapist will move to a random practice structure.

Random practice is when several targets are practiced during a single activity. Now the therapist will practice that same /b/ sound, but will also throw in one or two other sounds the child can make too. The therapist will switch between the two or three sounds randomly. This increases the motor planning demands of the task because the child has to switch between different targets. It also makes the task a little more like real world speech demands when you are not saying the same sound over and over and over again.

Variability of practice

Therapy practice needs to vary in speech context, social context, and environmental context. Targets need to be practiced in multiple speech contexts. That /b/ needs to be practiced at the beginning, middle and ends of words. It needs to be practiced in multiple syllable structures. It needs to be practiced in phrases, sentences, and in conversation.

Therapy practice needs to vary in social context as well. Practicing a /b/ with the speech therapist is different than practicing it with Mama or Grandpa. Practicing a /b/ in a speech therapy session or during a practice session at home is different than practicing every /b/ word that comes up when reading a bedtime story with Daddy.

Finally, variability can also include environmental variation. The child should be working to improve their production of speech targets in therapy, at home, at the grandparent's house, in the car, at the grocery store, at school or daycare, etc.

The greater the three kinds of practice variability the better the child will internalize the new target and be able to use it spontaneously in a variety of contexts. This is why the participation of the parent is so important. The speech therapist cannot achieve social and environmental variability by him or herself. The practice the parents do at home and out and about during their daily life is an essential part of the therapy picture.

Summary

Therapy sessions for Childhood Apraxia of Speech need to involve lots and lots of speech productions. When learning something new, the therapist will used a blocked practice structure and only target that new skill. Once your child learns the new skill, the therapist will switch to a random practice structure and randomly switch between the newly learned skill and some old ones in order to improve performance when the demands of the task are harder. The speech skills also need to be practiced in different speech contexts, social contexts, and environmental contexts. Home practice is essential for this variability in practice.

You just finished Part 2 of a three part series on Childhood Apraxia of Speech Therapy Fundamentals.
Read the other two parts of the series:

You might also be interested in the following articles:

Monday, May 16, 2011

A Little Bit of Innocence Lost

A while back, I got Ava a box of assorted hair accessories hoping that three kinds of hair bands, two kinds of hair clips, and two kinds of barrettes all in 6 colors each would fascinate her enough to persuade her to let me put a barrette in her hair.


Instead she calls them all her treasures, the box they came in her "treasure box", uses the hair bands as bracelets, and thinks it's hilarious to put the hair clips on all her fingers at once. Well, at least it was entertaining.

A couple of months ago, when I was trying to persuade Ava yet again that these things were HAIR accessories by putting them in my hair, Michael decided that it was great fun and wanted me to put them in his hair. It was adorable. We all had fun. Ava though Michael looked great while still completely resisting participating herself.

Today I got the box back out for yet another try. My mom was over and snuck a hair clip into Michael's hair from behind. After asking her to take it back out he said, "I'm not a girl. I don't want those in my hair." I was actually completely surprised. I've never said anything like that around the house. He must have gotten that from school. It isn't that I want him to wear pink hair clips forever. I'm just sad that a little bit of innocence has been lost. He thought it was fun before and it was fun. Now he won't participate in that fun any more because someone at school told him hair accessories are only for girls. He's growing up so fast.

Childhood Apraxia of Speech Therapy Fundamentals: Part 1 - How Much and How Often?

Childhood Apraxia of Speech (CAS) is neurological speech disorder that causes children to have difficulty with the motor planning, sequencing, and programming necessary to produce volitional speech. Therapy needs to address the core problem of motor planning for speech in the most effective way possible. Every child is different, so therapy must be customized. Therapy for a young child who is nonverbal will be different from therapy for an older child who is using multi-word sentences, but the speech is hard to understand. However, the basic underlying fundamentals of therapy for apraxia are going to be similar. These underlying fundamentals are based on current research and professional consensus.

How much therapy is usually necessary to treat Childhood Apraxia of Speech?

Intensity of Speech Therapy

It is essential that a child with Childhood Apraxia of Speech get as many opportunities as possible to actually produce speech. You cannot improve motor planning skills if no speech production is happening. Therapy for CAS needs to focus on getting as many speech productions as possible from the child during each session. A child is not improving their motor planning skills when they are just listening or watching the therapist or other children. For this reason, it is usually recommended that speech therapy sessions be individual (one-on-one) rather than group (one therapist with several children). It is also recommended that the therapist stay very focused on having the child practice rather than on having the child listen and watch while the therapist "teaches". Therapy for Childhood Apraxia of Speech needs to be very intense.

Frequency and Duration of Speech Therapy

Children with Childhood Apraxia of Speech typically need a lot of therapy to show improvement. One study (Campbell, 1999) showed that "the children with apraxia of speech required 81% more individual treatment sessions than the children with severe phonological disorders in order to achieve a similar functional outcome."

The professional organization of speech language pathologists, the American Speech Language Hearing Association (ASHA) reports that, "There is emerging research support for the need to provide three to five individual sessions per week for children with apraxia as compared to the traditional, less intensive, one to two sessions per week (Hall et al., 1993; Skinder-Meredith, 2001; Strand & Skinder, 1999)." ASHA's technical report also states that, "In view of the Committee's information indicating that children are being enrolled for treatment of CAS at increasingly younger ages, careful consideration should be given to the length of the therapy session. If repetitive practice of speech-motor patterns is targeted in a therapy session, many children in the younger age ranges can remain engaged for only a maximum of 30 minutes per session."

Given a choice, therapy for Childhood Apraxia of Speech should be broken into many shorter sessions per week rather than one or two long sessions per week. This makes sense from a motor planning perspective. You will learn a new motor task (just like riding a bike) faster if you practice a little almost every day rather than practicing for several hours only once a week.

Summary

Ideally, therapy for Childhood Apraxia of Speech should be individual sessions 3-5 days a week. Those sessions should be focused on getting as many productions from the child as possible. Sessions should be no longer in length than the amount of time the child can focus on intense practice. These guidelines are most important when the Childhood Apraxia of Speech is judged to be severe.


You just finished Part 1 of a three part series on Childhood Apraxia of Speech Therapy Fundamentals.
Read the other two parts of the series:

You might also be interested in the following articles:

Sunday, May 15, 2011

Eloquence via the Written Word

Sometimes I feel something and I can hardly figure out how to explain it to myself much less figure out how to explain it to others. And then, being able to express yourself well in writing is taking it to a whole different level. Michelle at earlymama.com has written an amazing post in the form of a letter to her young son Noah about the importance of being happy. I agree with her wholeheartedly. You should read this. It's beautifully written and so true.

Saturday, May 14, 2011

Oral Apraxia - Mealtime Consequences?

I have a question for those of you with children who also have oral apraxia. Oral apraxia is problems with the motor planning of non-speech movements like sticking out the tongue or blowing kisses or bubbles. Both of my children have oral apraxia. Ava has both oral apraxia and childhood apraxia of speech. Michael just has oral apraxia.

I have noticed that both children often seem to bite themselves while eating. Several times a week someone will end up in tears during mealtime because they've bitten their tongue, inside of the mouth, or lip. I was wondering if this is pretty typical for toddlers and preschoolers or if you have noticed the same thing happening with your children with apraxia. Any thoughts?

The Weekly Review: Week Nine

Well, I completely forgot to post my weekly review yesterday, so here it is one day late.

Blog Post I Thoroughly Enjoyed:

Linda at All & Sundry shared a quote by an author that I am completely unfamiliar with from a book that I've never heard of. Nevertheless I thought the quote was a very accurate description of early motherhood. Check it out here.

Sibling Moment of the Week:

I loved watching Ava sit on the sidelines cheering Michael on as he went down the makeshift water slide we created using the hose and the slide on our playset. Even though she didn't want to slide herself, she loved watching Michael go down and clapped and cheered every time he hit bottom.

Quote of the Week from Michael:

Michael says to me "I love you the mostest of everyone."

Ava's Quote of the Week:

"More on back Dada!" when asking her Daddy for yet another piggyback ride.

Incomplete Project of the Week:

Remember when I shared my idea for an alphabet border with you about six weeks ago? At the time I had finished A, B, and C. Well, so far I have only completed two additional letters: D and F. Yes, I have only done two more in six weeks. And even then I skipped E because I haven't figured out how to make an eagle yet. But my D and F are beautiful and I will eventually finish the project. Really!

Friday, May 13, 2011

Disassembly

You might remember my post about Michael's redecoration of his room and my regret at overreacting to what was actually a pretty creative effort on his part. Well, I did slightly better this time when I discovered his efforts at disassembly.

I walked into the basement playroom and was astounded to discover our beautiful wooden dollhouse in pieces. I couldn't even figure out what I was looking at at first. The garage had been completely taken apart. The roof had been removed and disassembled. The screws holding the floors in place had been removed on one side so that they had fallen making it look like the dollhouse had been the victim of an earthquake.



The words that escaped my mouth in a tone of shocked horror were, "Who did that to our dollhouse?!?" Michael's instant response was, "I don't know!" At this point I was saved from another overreaction by the fact that I was still trying to figure out what on earth had happened exactly. I thought perhaps someone had fallen into the dollhouse and broken it? I was silent for several moments while I just tried to mentally process the scene.

Michael apparently interpreted my silence as evidence that I wasn't too upset about it and volunteered something to the effect of, "I used Daddy's screwdriver." At that point my brain went, "Ohhh....I get it now." (Inside my head a voice was still babbling, "Oh no, look. Look! Look what he did to the dollhouse. When? When did this happen? Wow!")

I took a deep breath and said, "First of all, wow Michael. That was a lot of really impressive screwdriver work. You have to be really, really good with a screwdriver to take all of that apart. But.... Well, some toys are take-apart toys. Toys like your crane truck, or your airplane, or your toolbench - those are take-apart toys. And some toys are stay-together toys. Some toys mommy and daddy work really hard to assemble and they are supposed to stay together and not ever be taken apart. Our dollhouse is a stay-together toy. From now on, we should only use screwdrivers to work on take-apart toys. You and Daddy are going to need to make a special project of reassembling this dollhouse later."

I felt pretty good about how I handled the situation. Michael is obviously really good with a screwdriver. I wonder if you can buy some sort of woodworking sets that involve assembling things (a simple dollhouse or birdhouse or car....) with wood and screws that we could get him that it would be all right for him to assemble and disassemble himself. I should look into it.

Wednesday, May 11, 2011

The True Problem with being Sick

It is true, I suppose, that you can adjust to just about anything. I've been sick so often this winter that I've adjusted to the actual symptoms of being sick. They just don't bother me as much as they did at first. So I go another few days with sinus congestion or a cough or a sore throat. Post nasal drip, body aches, runny nose, and sneezing all get to be old hat. I'm certainly not saying I enjoy it. I'd much rather be healthy. I'm just saying that it's hard to get all worked up and self-pitying about it after the 15th time.

The thing that bothers me about being sick it the effect it has on my parenting. My children are actually at a pretty great age these days. When I am healthy, I sleep well and wake up energized. I look forward to spending the day with my children. The time flies by and we do all of our regular activities and some bonus ones too just because we are all enjoying our time together. There's a positive feedback loop. The kids are in a good mood because I'm in a good mood and I am in a good mood because they are in a good mood. When small conflicts crop up, they stay small because no one (mama) over-reacts and blows things out of proportion.

All of that seems to disappear when I'm sick. I am tired and cranky. Waking up and facing the day with the children seems more like a chore than a pleasure and privilege. The hours creep by. I pass the time by letting them watch television more than I'd like. They are cranky because I am cranky. I get even more cranky because they are cranky. We do hardly any fun activities and just get through the day as best as we can. That's what I regret most about all the time I've spent sick this winter. I feel like the illnesses are stealing some of my quality time with my children. That is the true problem with being sick.

Here's hoping for a healthy spring and summer.

Tuesday, May 10, 2011

NutriiVeda Achieve - Reformulation of NutriiVeda

NutriiVeda has been reformulated. The claim is that it is richer and smoother with better flavor. They are now calling the flavors French Vanilla and Dutch Chocolate instead of Vanilla and Chocolate. They have also changed the packaging. Now it will come in a single 30-serving resealable pouch rather than the two 15-serving canisters.

I cannot find much information on the specifics of the reformulation. So far the company has not released the new nutrition panel. The website looks exactly the same to me except that they have changed the pictures to show the new packaging rather than the old packaging. I should get my first shipment of the new formula by the end of next week. I'll let you know more then.

We have been using the original NutriiVeda for about 5 weeks now. Originally Ava was getting about one scoop a day. We're now using closer to one and a half to two scoops per day. I continue to see improvement in Ava's speech. She is continuing to talk more frequently. She's using longer sentences and trying to string several sentences together to tell a single story. All of that is new. It is possible that she would be making these same improvements without the NutriiVeda, there is no way to tell. It certainly isn't hurting though. As always, I also take comfort in the nutritional boost that the NutriiVeda provides for my picky eater too.
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