Guest guest Posted February 20, 2010 Report Share Posted February 20, 2010 Hi all, I am an SLP in private practice, Help Me Speak, LLC, in Marriottsville, MD. I have several clients with either apraxia & /or autism who have started using NV. Here are some changes we have noted: 1. Client-M.; 6-6 yrs; male; global apraxia & HI w/fine motor, sensory challenges too; picky eater (huge gains here prior to NV); he has only been taking 1 scoop/day in choc pudding BUT as his mom and I discussed today, we are seeing subtle changes!! Fine motor-he was interested (not before!) in writing his name by connecting the dots---never done that before per his mom; more willing to try school work (before did not want to practice much); multitasking-today during play, he showed a sense of humor while using his words; many more attempts to imitate words in isolation and in combination 2. Client-M; 9yrs; male; dyspraxia and ASD; speech-language: before he needed cues and reminders to use full sentences; now, he is putting many more words together spontaneously!!; many more comments than before too 3. Client-J; ASD; dyspraxia; mostly nonverbal; only on it for 2 wks w/many more attempts at sentences than previously!! 4. Client-E.; 3yrs; many more attempts at a variety of sounds than he had previously; at first, had difficulty focusing, but that has resolved after a few days and now is attending during sessions w/o difficulty; new sounds--/n, k, g/ which means that his tongue is elevating more at the front and back of his mouth, also means that he is dissociating (separating) his tongue from his jaw; WOW! Even if your child " seems " to make small changes---behavior, a few new sounds, etc., the underlying skills required to make those changes are many more than you would think! 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 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 20, 2010 Report Share Posted February 20, 2010 Barbara Thanks for sharing . My son Adam is 5 1/2 yrs ASD i posted earlier in week we had him on 1 1/2 scoop we upped to 2 scoops over the past few days. We have sen progress in that prior o this he had approx 10 words (partial words) we are getting lots of babbling mama dada (not in contex) and he is rolling his tongue around his mouth and making sounds ih his while doing this.. However he has gone so hyper and pinching laughing have you seen this reaction .. tHANKS FOR ANY IMPUT cAROLINE Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 20, 2010 Report Share Posted February 20, 2010 Sorry I didn't post more details about ea client but I don't have the files in front of me. They're @ my office. The reason that client #1 is only taking one scoop/day is because he's a picky eater. He doesn't like milk, so no NV in shake form, nor yogurt. Any other ideas to put the NV in to increase his amt/day? He doesn't like a lot of pureed foods so options are decreased. The other clients are all on full doses for their ages. Warmest wishes, Barbara A , M.S., CCC-SLP Executive Director, Help Me Speak, LLC 410-442-9791 [ ] client updates Hi all, I am an SLP in private practice, Help Me Speak, LLC, in Marriottsville, MD. I have several clients with either apraxia & /or autism who have started using NV. Here are some changes we have noted: 1. Client-M.; 6-6 yrs; male; global apraxia & HI w/fine motor, sensory challenges too; picky eater (huge gains here prior to NV); he has only been taking 1 scoop/day in choc pudding BUT as his mom and I discussed today, we are seeing subtle changes!! Fine motor-he was interested (not before!) in writing his name by connecting the dots---never done that before per his mom; more willing to try school work (before did not want to practice much); multitasking-today during play, he showed a sense of humor while using his words; many more attempts to imitate words in isolation and in combination 2. Client-M; 9yrs; male; dyspraxia and ASD; speech-language: before he needed cues and reminders to use full sentences; now, he is putting many more words together spontaneously!!; many more comments than before too 3. Client-J; ASD; dyspraxia; mostly nonverbal; only on it for 2 wks w/many more attempts at sentences than previously!! 4. Client-E.; 3yrs; many more attempts at a variety of sounds than he had previously; at first, had difficulty focusing, but that has resolved after a few days and now is attending during sessions w/o difficulty; new sounds--/n, k, g/ which means that his tongue is elevating more at the front and back of his mouth, also means that he is dissociating (separating) his tongue from his jaw; WOW! Even if your child " seems " to make small changes---behavior, a few new sounds, etc., the underlying skills required to make those changes are many more than you would think! 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 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 20, 2010 Report Share Posted February 20, 2010 You may have missed this but the hyper is one of the side effects of the nutriiveda -or possible side effects. It's very similar to what we see in fish oils when they first start to work -it just means that something is starting to happen so that's a good thing. Typically this hyper behavior will last a few days to around a week but as you reported it comes with increased babble or speech. Sowmya was the first to report it and she stopped the nutriiveda and the hyper stopped -but so did the babble. She put him back on a reduced dosage and has since raised him up even higher than before. What she can probably share more about is that upon further reflection it wasn't so much hyper as all of a sudden aware of surroundings and wanting to see everything -notice of things that he didn't notice prior. Your choice is to go back down the 1/2 scoop to where you were before...or to decrease 1/4 scoop...or just increase the water and wait it out with the quicker increase in babble and mouth movements. Also check with the professionals that work with him. While Sowmya initially saw her son as hyper -the teacher (who didn't know he was on the nutriiveda) reported that he was focused in class for the days he was on it. Like with the fish oils -what we consider a " bad " sign could be a good one. Some of the children in our group never go through the " terrible twos " so days after starting fish oils or nutriiveda when the kid starts going through this normal hyper, defiant stage which is a developmental stage that one should go through -the parent sees it as a bad sign. It's not. Not only is it most probably a stage your child never went through or went through fully -at least you know something is happening. The worst sign would be zero change. Here is the normal stage most kids go through and as the doctor says " it's not terrible " Learn why: http://www.5min.com/Video/How-to-Deal-with-the-Terrible-Twos-9698 ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 20, 2010 Report Share Posted February 20, 2010 My 24mth boy is an exteremely bad eater - also won't take milk or yoghurt. I have now tried several things including icing (which is something he normally eats - but somehow he knew the NV was in it so wouldn't have a part of it). The only way I can get in into him is in chocolate mousse. He would't take it in choc icecream or yogo (not sure if you have that in the states, its like a chocolate custard type stuff). I've managed to get full dosage into him for the last two days now, and he is out of control hyper. Prior to NV he was already an extremely active and inquisitive little boy, who most definitely had a defiant side too. He had a good sense of humour - this also has become much greater in the past 2 days, with him spending all day laughing and playing 'tricks' on me. I've not really noticed any positive change as far as babbling, or attempt at new sounds - he in fact seems to be going backwards here. He started the fish oil not long ago which saw improvements in this area, but that appears to be lost now. I'll keep with the NV for a few more weeks and see what happens. I was wondering, if in fact my boy doesn't have dyspraxia (due to non verbal at this point it is suspected but not officially diagnosed), and he turns out to be just delayed (which both myself and his 2 sp don't feel to be the case), could the NV possibly hinder his progress? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 21, 2010 Report Share Posted February 21, 2010 Yay Ruby!!! I'm so happy you didn't give up after that one 1/2 scoop! No there is nothing in the nutriiveda that I have read, heard about from any doctor or nutritional expert that could be anything but healthy -unless one is allergic to one of the food elements in it. 2 days may be a bit too soon to know yet...but -look at it this way. The fact that you are seeing a sign that is reported as a negative early sign of nutriiveda is a good thing. If it wasn't doing anything you wouldn't see anything! What you can do is cut back a teeny bit to control the hyper- others who have children that went through this stage can comment more on this. I'd say if you can get him to eat it in the mousse -then stick with that for now. Let him get a bit back on a schedule again because it's clear he's not liking that you are trying to get him to eat something he doesn't want to -so that creates stress. With apraxia/dyspraxia speech regresses when they are sick, tired or stressed. Try to keep it fun -and what's not fun about chocolate mousse??? Hey even try reverse psychology " if you aren't good you won't get any chocolate mousse for dessert tonight " I just answered your other message about looking for info for the doctors- I did put a bunch of links here that I put up about a month ago http://www.facebook.com/topic.php?uid=115029735601 & topic=13047 as I just posted however yes we'll put something together that is a bit more formal -and get that survey up (???) I'm happy that you are sticking it out and giving it a chance to work. We've pretty much across the board have seen surges. If nothing else -you know you got your fish oils...I don't know -to me the fact that they " worked " makes it seem like there was more going on than a simple delay in speech -but it's possible of course. ===== Quote Link to comment Share on other sites More sharing options...
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