Guest guest Posted February 26, 2008 Report Share Posted February 26, 2008 Has anyone been to Children's Hospital of Pittsburgh to see the apraxia specialist (an slp), Hammer? Another parent just emailed me about how much he helped her child. Any feeback is welcomed. Thanks, Carolyn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2008 Report Share Posted March 4, 2008 Hi, I have not had my child seen him but I have heard good things about him. I would have posted earlier except I wanted to wait until after I attended his workshop this past Friday. I would like to share some of the information I gleaned. This workshop was geared towards SLPs but parents were welcomed. In talking to the SLPS he presented a powerpoint slide where he talked about the SLPs gathering information before determining if the child has apraxia. What does my CAS assessment include? *for most young children, most is informal * formal test resources available * get in-depth parent information *investigate other apraxic features (i.e. limb apraxia) * look at nonspeech oral skills * concern for misdiagnosing 1. nonverbal child 2. Dysarthric child 3. severe phonologically disordered child 4. confounding diagnosis child (he explained this as a child that has other needs or multiple issues that require a formal diagnosis that can only be made someone else other than the SLP. The examples he used were autism, etc. The next slide was a statement that said " Unfortunately, pure apraxia of speech is rare! " He said that apraxia is usually mixed with something else such as sensory issues, down's syndrome, and so forth. He talked a bit about how a lot of apraxic kids become non-risk takers, but some kids think everyone understands them and take lots of risk. I felt that this applied to my daughter who becomes a non-risk taker when it comes to doing things that require her to use her mouth such as speech and blowing musical horns etc. He also shared a 3 columned-chart that compares the differences between childhood apraxia of speech, dysarthria and severe phonological disorder (again this chart geared for SLPs but I found this very useful). Very useful info was that he stated how CAS therapy differs from Articulation/Phonological therapies ***Motor learning theory should drive our treatment of children with CAS (11/6/07 ASHA LEADER). Most importantly, he states that " no single program works for all children with apraxia. Therapists must individualize, and be flexible and look for serendipous learning opportunities. " He showed lots of video clips of his clients, all kids ranging from ages 2 to 12, and their successful progress over several years. He seems to be a warm and personable guy. If you can get your child in to see him for speech therapy, I say go for it!!! I hope this information was helpful and useful to this group. Lori > > Has anyone been to Children's Hospital of Pittsburgh to see the apraxia > specialist (an slp), Hammer? Another parent just emailed me about > how much he helped her child. Any feeback is welcomed. Thanks, Carolyn > Quote Link to comment Share on other sites More sharing options...
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