Guest guest Posted March 3, 2010 Report Share Posted March 3, 2010 Call and ask for a rectification of the diagnosis according to the SLps diagnosis as he agreed when you left his office. He must have just forgotten by the time he wrote up the report and the dysphasia is a more neurological term--but does not explain his speech needs. If he says this will do---explain that he has severe speech deficits and it is the apraxia diagnosis made by the SLP--and to which he agreed that will get this child the much needed 1:1 3-5 sessions of speech with motor planning expert as recommended BY ASHA. Like I said--he probably just made a mistake--but it is pretty scary for a parent I know--when so much hinges on a workable diagnosis---one that insurance will cover and the right treatments will be done. I would actually go further than thsi since you plan to have him as your doc for the letter of medical necessity. Send him the ASHA document and show him the recommended treatment as well as the neurological definition----and HAVE HIM write BOTH--as in the ASHA document--he can cut and paste---in his letter of medical necessity. Have the SLP do the same--cut and paste from ASHA documents definition and recommendations--in the speech eval report. All doctors should do this for their patients--you regular pediatrician can too--but if the neurologist does it it can carry more weight. Since he goofed up he shoudl make up for it with this letter. if he doesn't---well you know not to go to him ever again and tell all the parents you ever speak to about him----That's about all we can do---but he really should if he's half decent--even if in my experience--most pediatric neurologists know about apraxia in kids about as much as they know about croquet---but that's' another story---he owes you one and let's hope he'll come through.. All the best, Elena ________________________________ From: <maryfmchugh@...> Sent: Wed, March 3, 2010 7:35:36 PM Subject: [ ] Developmental dysphasia diagnosis??? Hi, My now 26 month old son saw a pediatric neurologist back in December to confirm our our Early Intervention DI therapist's unofficial diagnosis of apraxia. After evaluating our son, the pediatric neurologist confirmed he had apraxia. He even recommended The Late Talker book, mentioned there was a website (how I indirectly found this group), and when I asked about fish oils, he recommended the Nordic Naturals. We finally got a copy of his evaluation this evening (10 weeks after our appointment!), and his evaluation indicates that my son has evidence of Developmental Dysphasia, plus mild hypotonia. Developmental Dyspahsia??? What is this??? My husband and I have done some searching, but we can't find much information on this in the Internet. Additionally, I'm more than a little concerned about the " developmental " description, particularly since we already expect a battle with Horizon BC/BS to get coverage for speech therapy. Anyone have any experience with this diagnosis? What should be my next steps, beyond calling and asking for a clarification? Thanks! - ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 21, 2010 Report Share Posted July 21, 2010 Catching up on some posts---- What is the status with this neuro? Did you request clarification? Dysphasia is the same as aphasia---resulting from a brain trauma; could happen at birth, during delivery; Dys= difficulty with A= absence of That is why you will see dyspraxia (difficulty with motor planning for speech sounds) vs. apraxia (absence of speech sounds, more severe difficulty) In reality, the insurance is only interested in the ICD9 (diagnosis) code, which is the same for a-vs. dys--- conditions. Warmest wishes, Barbara Barbara A. , M.S., CCC-SLP Executive Director/ Help Me Speak, LLC <http://www.helpmespeak.com/> http://www.helpmespeak.com (o) 410-442-9791 (f) 410-442-9783 2500 Wallington Way; Suite 103 Marriottsville, MD 21104 follow us on FaceBook: http://www.facebook.com/pages/Marriottsville-MD/Help-Me-Speak-LLC/1046288520 32 Call me with any questions about NutriiVeda! www.hms.myzrii.com From: [mailto: ] On Behalf Of Sent: Wednesday, March 03, 2010 10:36 PM Subject: [ ] Developmental dysphasia diagnosis??? Hi, My now 26 month old son saw a pediatric neurologist back in December to confirm our our Early Intervention DI therapist's unofficial diagnosis of apraxia. After evaluating our son, the pediatric neurologist confirmed he had apraxia. He even recommended The Late Talker book, mentioned there was a website (how I indirectly found this group), and when I asked about fish oils, he recommended the Nordic Naturals. We finally got a copy of his evaluation this evening (10 weeks after our appointment!), and his evaluation indicates that my son has evidence of Developmental Dysphasia, plus mild hypotonia. Developmental Dyspahsia??? What is this??? My husband and I have done some searching, but we can't find much information on this in the Internet. Additionally, I'm more than a little concerned about the " developmental " description, particularly since we already expect a battle with Horizon BC/BS to get coverage for speech therapy. Anyone have any experience with this diagnosis? What should be my next steps, beyond calling and asking for a clarification? Thanks! - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2010 Report Share Posted July 23, 2010 Barbara, Thank you for the details! I think I'm starting to understand why our PT mentioned my son has suspected " motor " dyspraxia versus just saying dyspraxia. As for the neuro, yep, I requested clarification. After several calls, I was finally told that the developmental dysphasia was the same thing as apraxia. I eventually got the doctor's report updated to reflect that - just in case I needed it. I won't go into details, but our first neuro's office staff was such a disaster, I was glad we had not cancelled an appointment with a second neuro (who also agreed with the verbal apraxia diagnosis). Since then, we've also had a speech eval (diagnosis verbal apraxia) and much to my surprise got smooth and quick approval from Horizon BC/BS for speech twice a week (1/2 hour). More to come in other posts... Kind regards, - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2010 Report Share Posted July 23, 2010 Apparently, that neuro's office is clueless because devel dysphasia is NOT the same as apraxia. See my earlier post. Warmest wishes, Barbara A , M.S.,CCC-SLP Executive Director, Help Me Speak, LLC www.helpmespeak.com 2500 Wallington Way Suite 103 Marriottsville, MD 21104 Ask me about NutriiVeda! On Jul 23, 2010, at 11:38 AM, " " <maryfmchugh@...> wrote: > Barbara, > > Thank you for the details! I think I'm starting to understand why our PT mentioned my son has suspected " motor " dyspraxia versus just saying dyspraxia. > > As for the neuro, yep, I requested clarification. After several calls, I was finally told that the developmental dysphasia was the same thing as apraxia. I eventually got the doctor's report updated to reflect that - just in case I needed it. I won't go into details, but our first neuro's office staff was such a disaster, I was glad we had not cancelled an appointment with a second neuro (who also agreed with the verbal apraxia diagnosis). > > Since then, we've also had a speech eval (diagnosis verbal apraxia) and much to my surprise got smooth and quick approval from Horizon BC/BS for speech twice a week (1/2 hour). More to come in other posts... > > Kind regards, > > - > > Quote Link to comment Share on other sites More sharing options...
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