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- Marilyn
- Rankin
- No
- 305 W Broadway Ave
Fort Worth
Texas
76104
United States - Carter Therapy
Fort Worth
Texas
76104
United States
I have been working with patients who have CAS for roughly 20 years, based on the DTTC strategies taught by the guru Edythe Strand. Over the years I have honed my skills, and continued my own educational journey related to CAS. When I start working with a new patient, I begin primarily by building trust. Kids oftentimes come to me after trying other therapy, without much success. Sometimes they have avoidance behaviors and significant frustration with failed communicative attempts. I demonstrate that I will ask them to do things that may be challenging, but it will be worthwhile; and we will be a wonderful team. You can almost see the moment when kids let down their armor and “give in” to the new process and therapeutic relationship.
Based on a thorough evaluation, we start treatment with sounds and word forms that are within the patient’s ability, with some level of support. We build up those words until they can be produced consistently and independently. As those words are being developed and practiced with high frequency, I am always looking for new words that are important in the child's life and that they may be stimulable for, to bring new sounds and words into the repertoire. This is not necessarily based on the typical progression of speech sound development. In any given session, I target about 7-10 words with many repetitions.
After many years of treating children with CAS, I feel like the treatment techniques have become something of an art-form. I adjust my level of support for each production the child makes. I adjust timing, pitch, and loudness to find the best way for the child to match the movements from one phoneme to the next. I generally do not focus on one phoneme at a time, rather the movement from sound to sound. I pay particular attention to the vowels and diphthongs, as these highly impact intelligibility. I do not teach approximations; I encourage accurate production on every trial. Other cues that I use, as needed, are tactile and visual prompts, for example manually helping the child squeeze his/her lips together, or using a pointing finger to highlight my lip movement for “b”. As word forms develop, these are built into longer, multisyllabic utterances - phrases, and sentences. I incorporate another CAS treatment strategy called REST and some phonological strategies when they become appropriate and necessary. Throughout treatment, I am regularly observing and addressing language (especially morphological development), phonological awareness/pre-reading skills, and pragmatic skills, as I find that these are critical areas which are often challenging for children with severely delayed speech due to CAS. In addition, signs, picture symbols and assistive technology are utilized to help the children successfully express themselves and continue building their language and social skills, while we are working towards more intelligible speech.
Parents are invited to watch or be in the therapy sessions, though it is their choice as to how much specific involvement they wish to have. Some kids work better with parents outside the treatment room. Parents are educated about the levels of cueing that are used (ex. slow- simultaneous, tactile cues...) I encourage parents to try the techniques within the sessions so feedback can be given and adjustments made. I don’t suggest a great deal of “homework” in general. I do NOT provide word lists for intensive drill at home. I do, however, suggest that as kids show significant progress with some of their words, the family begins to create opportunities to use those words in more natural contexts. Parents can hold the kids accountable for using their new words with accuracy across environments. Overall, I encourage families to keep things positive with the overall message that kids’ ideas, opinions, and needs are important to us, and we really want to hear them. All sessions end with a period to discuss successes and road blocks, and for parents to share their insights and concerns.
Many of my younger patients with Apraxia come with a highly restricted sound repertoire and therefore have unsuccessful communication attempts. Many are either "shutting down" avoiding communication or are having behavioral issues due to frustration. At times, I implement sign language to increase successful communication attempts and get over the initial transitional time. As I have become more experienced, I am more commonly recommending a robust communication system early in the treatment process. Children tend to be quite savvy in learning the systems and can develop phrases, sentence structure and use of verb conjugations… on these systems, before their speech will support such skills. AAC use stimulates the language areas of the brain, to alleviate some of the subsequent language deficits that are quite typical of children with CAS.
I have used both low tech (ex. PECS, Go Talk) and high tech (ex. LAMP WFL, and Dynavox). I have had significant training in using these resources. I am quite fluent in LAMP-WFL, which is also based on motor principles. I work to increase one's ability to express needs, wants, and thoughts via AAC, and spend time training the family how to interact using a device. This allows language to flourish without jeopardizing speech accuracy. I do, continue to work on speech accuracy while using AAC.