Guest guest Posted May 10, 2002 Report Share Posted May 10, 2002 Hi, Our son's former SLP (Janice Shintani) from The Rehab @ Aiea was great. Not sure if she's has that training but I'm sure you can call and ask. Our little boy has had 4 other SLP here in Ca but none compares to Miss Janice's dedication. Goodluck in your search, we're still looking for someone like her here :-( Annie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 10, 2002 Report Share Posted May 10, 2002 My daughter was dx w/ oral and verbal apraxia last week by her dev ped and current SLT (through the state). The insurance approved intensive therapy through a civilian therapist. They sent me a list of providers. How do I know which one to choose? Are there certain questions I should ask when calling around? Or is there a list of SLT's who have training in apraxia or do all SLT's have training? Traci mom to Kennedy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 10, 2002 Report Share Posted May 10, 2002 Hi Annie! Well, what a coincedence! That is our SLT through the state! I'll have to look at the list of providers....I just assumed since we received her through the state that she would not be on the list, but maybe she is! Yes, I agree she is wonderful! After about 6 months w/ Janice I became a little discouraged and felt Kennedy was not making much progress. Janice then showed me just how much progress Kennedy had made. She then told me she suspected Kennedy had apraxia and if she did, then she was doing great! We then comfirmed the dx of oral and verbal apraxia through her dev ped at TAMC (Dr Buckley). Kennedy seems to have come much further in the past 6 months then most kids w/ apraxia. (just by the stories I have read). Traci, mom to Kennedy 2.0 GDD, apraxia, SID/DSI > > Hi, > > Our son's former SLP (Janice Shintani) from The Rehab @ Aiea was great. > Not sure if she's has that training but I'm sure you can call and ask. Our > little > boy has had 4 other SLP here in Ca but none compares to Miss Janice's > dedication. Goodluck in your search, we're still looking for someone like > her > here :-( > > > Annie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 10, 2002 Report Share Posted May 10, 2002 Annie, do you mind emailing me personally or giving me your address. I would like to ask a couple of questions that I didn't want to post on here. Thanks, Traci > > Hi, > > Our son's former SLP (Janice Shintani) from The Rehab @ Aiea was great. > Not sure if she's has that training but I'm sure you can call and ask. Our > little > boy has had 4 other SLP here in Ca but none compares to Miss Janice's > dedication. Goodluck in your search, we're still looking for someone like > her > here :-( > > > Annie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 10, 2002 Report Share Posted May 10, 2002 Hi Traci! I know that Deb lived in Hawaii for awhile and she's the one that put together the " Can We Talk? " website that I used to use so much when Tanner was first diagnosed - I found it so parent friendly with some useful articles http://tayloredmktg.com/dyspraxia/. Debbie is really nice -she (like many of us with websites) got overwhelmed however with keeping up with emails, the website, etc. and has stepped back a bit and hasn't updated the site in awhile. I have her new phone number someplace (she no longer lives in Hawaii as it states on the tayloredmarketing site). Her email is deb@... and it sometimes takes her awhile to get back. On this page http://tayloredmktg.com/dyspraxia/das.html she has a great article written by 2 SLPs, and it would have been good for you if they were from Hawaii -however I know at least one is not. Also, I found these names from the stuttering foundation of America for you. Not that any may be knowledgeable about apraxia -but since current research http://www.mankato.msus.edu/dept/comdis/kuster/research.html suggest a connection between stuttering and (like apraxia) the neurological coordination of the speech mechanism (motor speech?) some of us do believe with future research we may find definite links (or overlaps) between stuttering and apraxia. And the one therapist your child had is mentioned here -So it may be worth at least calling and asking. Dorothy D. Craven, M.A., CCC-SLP 4921 Waa Street Honolulu, HI 96821-1445 (808) 373-9369J Miriam Hellreich, M.A., CCC-SLP Kailua Professional Center 40 Aulike Street, Suite 311 Kailua, HI 96734-2742 (808) 262-9222 Marasovich, M.A., CCC-SLP Oahu Speech Language Therapy 1010 S King St, #B6 Honolulu, HI 96814-1701 (808) 537-4030 (808) 537-4030 fax also mmar@... ine A. Mashima, Ph.D., CCC-SLP Chief of Speech Pathology Speech Pathology Clinic Tripler Army Medical Center Tripler AMC, HI 96859-5000 (808) 433-3193 (808) 433-6488 Janice Shintani, M.S., CCC-SLP 94-201 Mahapili Street Mililani, HI 96789-1805 (808) 623-0115 When you call, you can ask the therapist is he or she has experience and training in working with children with motor speech disorders -or oral motor disorders -not all use the name " apraxia " but you can ask that too. In general -it's good to also ask if they have worked with autistic children as well since I've found some of the best therapists and doctors for Tanner were those sensitive to the various other challenges of autism that are in addition to communication issues (like sensory issues, etc.) You can also ask if they are knowledgeable about oral motor therapy, touch cueing or PROMPT, and the Kaufman techniques. Many good therapists combine these various therapies with others and incorporate them in fun ways with toys, or music etc. and adjust to the individual child. ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2002 Report Share Posted May 11, 2002 Thanks for all the info.!!! Traci --- In @y..., " kiddietalk " <kiddietalk@y...> wrote: > Hi Traci! > > I know that Deb lived in Hawaii for awhile and she's the one > that put together the " Can We Talk? " website that I used to use so > much when Tanner was first diagnosed - I found it so parent friendly > with some useful articles http://tayloredmktg.com/dyspraxia/. Debbie > is really nice -she (like many of us with websites) got overwhelmed > however with keeping up with emails, the website, etc. and has > stepped back a bit and hasn't updated the site in awhile. Quote Link to comment Share on other sites More sharing options...
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