Guest guest Posted November 2, 2008 Report Share Posted November 2, 2008 Come to think of it, one could even make a " video " out of the available photos. What to call it, though, to get it findable. My trouble is not so much making a video as using MS Movie Maker and then trying to get it small enough to play on MediaPlayer. Am currently working on that problem. I end up with huge files. I guess I could join YouTube to put a video on (if I had one), but maybe someone here is already a member? Rowena You know, there should be. Anyone know how to go about filming and posting to You Tube? Sorry I am the dunce about this.. bG > > Is there anything up on YouTube about the 6v battery ziller? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 2, 2008 Report Share Posted November 2, 2008 Hi Rowena, maybe call it germ killer Or 6 volt germ killer Take care, V > Come to think of it, one could even make a " video " out of the available > photos. > What to call it, though, to get it findable. > My trouble is not so much making a video as using MS Movie Maker and then > trying to get it small enough to play on MediaPlayer. Am currently working > on that problem. I end up with huge files. > I guess I could join YouTube to put a video on (if I had one), but maybe > someone here is already a member? > Rowena > You know, there should be. Anyone know how to go about filming and > posting to You Tube? Sorry I am the dunce about this.. > bG >> Is there anything up on YouTube about the 6v battery ziller? -- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 15, 2010 Report Share Posted November 15, 2010 I have been reading this group emails for quite some time now. Parents coming up with wonderfull results with NV. But i dont see any online videos, especially on youtube on this subject. Usually, parents with special need kids are quick to share their reviews about therapies, products on youtube with live before/after kind of videos. When i did search on YouTube, i find 0 link on this subject. Can anyone explain this? Thanks. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 15, 2010 Report Share Posted November 15, 2010 Sharon has a video on Youtube but for some reason only the before. She has the after videos here on her blog http://apraxiastory.wordpress.com/before-after-video/ Other parents have videos on their blog as well -Gretchen from this group for example for sure who is a TV news producer (so super cute and well done before and after NV videos- Gretchen the one about the " what is it? " raccoon video!!!) -but don't know if others want to share with everyone on Youtube? Since I don't know if she wants to share here -you can read Gretchen's testimony here http://pursuitofresearch.org/testimonials.html and her son went on video from being unintelligible to an amazing communicator in very short time. Search the archives for gretchie9@... And what is going on with this is typical of what happened with fish oils. Parents are more active when they are worried about their kids -and then they fade off. Again very few stick around to help after they don't 'need' to be here. Understandable and normal. And because things are going so quick with NV -even more understandable there are less videos. So note to new people yet to try NV -do a before and after video I know Sharon isn't faded off even though her son too is doing amazing. She is in the middle of a HUGE move from Ohio across country so her life is a bit hectic -but otherwise I'm sure she'd answer this herself -and I know this is why she only has the one up at Youtube -just has not had a chance to catch up with life yet. Give it a bit of time -there will be some willing to share on Youtube -there always is. Thing is that with NV you have to make sure you videotape prior to starting because the surges in most cases are within one day to three and nobody expects it even though it's reported over and over. Perhaps on the new testimonial page for Pursuit of Research http://pursuitofresearch.org/testimonials.html we can have a section to upload videos? ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 15, 2010 Report Share Posted November 15, 2010 One of the items that I have recommended to all of my clients' parents ( & to parents here on this list)is to video their child before NV and then at least one month afterwards---doing the same things: (which depend on the child's age and skills) saying ABCs, reading the same book, naming common pictures, etc. Some parents may not want their child's video on YouTube since that is an open public forum, but as said there are many that do as you can tell if you search apraxia, including 's son Tanner when he was on Inside Edition and some other TV shows. Warmest wishes, Barbara Barbara A. , M.S., CCC-SLP CEO/ 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! > > Sharon has a video on Youtube but for some reason only the before. She has the after videos here on her blog http://apraxiastory.wordpress.com/before-after-video/ Other parents have videos on their blog as well -Gretchen from this group for example for sure who is a TV news producer (so super cute and well done before and after NV videos- Gretchen the one about the " what is it? " raccoon video!!!) -but don't know if others want to share with everyone on Youtube? Since I don't know if she wants to share here -you can read Gretchen's testimony here http://pursuitofresearch.org/testimonials.html and her son went on video from being unintelligible to an amazing communicator in very short time. Search the archives for gretchie9@... And what is going on with this is typical of what happened with fish oils. Parents are more active when they are worried about their kids -and then they fade off. Again very few stick around to help after they don't 'need' to be here. Understandable and normal. And because things are going so quick with NV -even more understandable there are less videos. So note to new people yet to try NV -do a before and after video > > I know Sharon isn't faded off even though her son too is doing amazing. She is in the middle of a HUGE move from Ohio across country so her life is a bit hectic -but otherwise I'm sure she'd answer this herself -and I know this is why she only has the one up at Youtube -just has not had a chance to catch up with life yet. Give it a bit of time -there will be some willing to share on Youtube -there always is. Thing is that with NV you have to make sure you videotape prior to starting because the surges in most cases are within one day to three and nobody expects it even though it's reported over and over. Perhaps on the new testimonial page for Pursuit of Research http://pursuitofresearch.org/testimonials.html we can have a section to upload videos? > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 15, 2010 Report Share Posted November 15, 2010 Hello all - Sharon here. is right - we're in crazy hectic mode trying to get settled in CO before the onslaught of the holidays. I've only got the one youtube video up as mentioned, but plan on getting the rest up - most likely not until the new year. And...I'll also make an effort to get more video footage of 's progress since it's been a month or so. The best way to see before and after is the link included in the note below - that's our personal apraxia blog. Proud to say, is thriving even more. He has letters/sounds we've been working on for over a year that are just coming out more and more. All of this with a move, a new home, a new speech therapist, new school and totally different climate/weather - none has affected him negatively from an apraxia perspective, which is not always the case with that many transition factors happening all at once. AND...I've finally been able to reduce his fish oil intake from 2 tsp of NN 3,6,9 to 1 tsp with no regression. YEA! What's more, he's getting sick of the way I mix his NV shake, and has started refusing it. I'm working on crafty new ways to get it in him, but all this to say that even with several skipped doses of NV he's had no regressions. This further makes me feel that NV has HEALED something within him. Whether metabolic or neurological - there's a marked difference. He's still having stomach problems, after all the homeopathic efforts we've made, so we're finally taking him to a GI doc next month to see if something more is wrong. We saw great improvements here too with NV, digestive enzymes and probiotics, but there's still a daily stomach ache so we have to dig deeper here. Overall, I'm too busy to stay completely active in this group for the moment, but I'm still a-lurkin' and will be present again soon. If you want to speak about the video, feel free to email me svraciu@.... Things are looking good and we couldn't be happier with 's progress! Sharon > > Sharon has a video on Youtube but for some reason only the before. She has the after videos here on her blog http://apraxiastory.wordpress.com/before-after-video/ Other parents have videos on their blog as well -Gretchen from this group for example for sure who is a TV news producer (so super cute and well done before and after NV videos- Gretchen the one about the " what is it? " raccoon video!!!) -but don't know if others want to share with everyone on Youtube? Since I don't know if she wants to share here -you can read Gretchen's testimony here http://pursuitofresearch.org/testimonials.html and her son went on video from being unintelligible to an amazing communicator in very short time. Search the archives for gretchie9@... And what is going on with this is typical of what happened with fish oils. Parents are more active when they are worried about their kids -and then they fade off. Again very few stick around to help after they don't 'need' to be here. Understandable and normal. And because things are going so quick with NV -even more understandable there are less videos. So note to new people yet to try NV -do a before and after video > > I know Sharon isn't faded off even though her son too is doing amazing. She is in the middle of a HUGE move from Ohio across country so her life is a bit hectic -but otherwise I'm sure she'd answer this herself -and I know this is why she only has the one up at Youtube -just has not had a chance to catch up with life yet. Give it a bit of time -there will be some willing to share on Youtube -there always is. Thing is that with NV you have to make sure you videotape prior to starting because the surges in most cases are within one day to three and nobody expects it even though it's reported over and over. Perhaps on the new testimonial page for Pursuit of Research http://pursuitofresearch.org/testimonials.html we can have a section to upload videos? > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 15, 2010 Report Share Posted November 15, 2010 Here's our video trail....starting with before was diagnosed, all the way up to improvements from fish oil and Nutriiveda. The video that makes me teary every time I watch....as grunts for cookies (he was barely 3 here). This was before the apraxia diagnoses and I hate myself for trying to get him to say cookies over and over. Sigh. after starting fish oil and working with an awesome SLP 4 days a week (6 months after diagnoses). He was still 3 here. 6 months later and after 1 month on 1 scoop of Nutriiveda...(age 4) Major improvements in eye contact, focus and conversation skills! Even more improvements...scoop and a half of Nutriiveda 3 months later (age 4) This video showing an alarming visual stemming behavior started doing while he was 4 years old. It has been eliminated since we upped his Nutriiveda dosage to 2 scoops. http://www.youtube.com/watch?v=3ogvdO1rsuQ & feature=related This video was taken just over a month ago (Coop just turned 5). Hold on to your hats. He's come a lllooonnnnnggg way :) Nutriiveda, fish oil and intensive speech therapy have all been the things that have helped most. He was diagnosed as severely apraxic at age 3. He is now 5 and I just had his pre-K parent-teacher conference today. His teacher told me that 's biggest problem is that he is often too busy socializing to complete all his work. She probably thought I was nuts when I smiled at that. I was just always worried that he would have a hard time making friends because of speech issues...like the other kids might not be able to understand him? 's made so much progress, it looks like I'll be battling to keep speech services through the district next year. It's a battle I'm happy to fight because I know he still has a ways to go, but the improvements are happening every day with the right tools Overall, the biggest improvements we saw from Nutriiveda are related to focus and conversation skills. Coop tested above average in vocabulary at school and I swear we have NV to thank for that too! Gretchen Walsh (Columbus, OH) ________________________________ From: kiddietalk <kiddietalk@...> Sent: Mon, November 15, 2010 2:16:26 PM Subject: [ ] Re: Youtube? Sharon has a video on Youtube but for some reason only the before. She has the after videos here on her blog http://apraxiastory.wordpress.com/before-after-video/ Other parents have videos on their blog as well -Gretchen from this group for example for sure who is a TV news producer (so super cute and well done before and after NV videos- Gretchen the one about the " what is it? " raccoon video!!!) -but don't know if others want to share with everyone on Youtube? Since I don't know if she wants to share here -you can read Gretchen's testimony here http://pursuitofresearch.org/testimonials.html and her son went on video from being unintelligible to an amazing communicator in very short time. Search the archives for gretchie9@... And what is going on with this is typical of what happened with fish oils. Parents are more active when they are worried about their kids -and then they fade off. Again very few stick around to help after they don't 'need' to be here. Understandable and normal. And because things are going so quick with NV -even more understandable there are less videos. So note to new people yet to try NV -do a before and after video I know Sharon isn't faded off even though her son too is doing amazing. She is in the middle of a HUGE move from Ohio across country so her life is a bit hectic -but otherwise I'm sure she'd answer this herself -and I know this is why she only has the one up at Youtube -just has not had a chance to catch up with life yet. Give it a bit of time -there will be some willing to share on Youtube -there always is. Thing is that with NV you have to make sure you videotape prior to starting because the surges in most cases are within one day to three and nobody expects it even though it's reported over and over. Perhaps on the new testimonial page for Pursuit of Research http://pursuitofresearch.org/testimonials.html we can have a section to upload videos? ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 15, 2010 Report Share Posted November 15, 2010 Gretchen these are amazing!! You know how I always notice stuff that sometimes others don't? In the original video of Coop prior to fish oils, NV and even therapy -he has those same droop eyes that Tanner suddenly had after he had the high fevers and regression in babble at 11 months. Like in Tanner's case anyway - the tone just disappeared from his face. But that wasn't permanent for Tanner either. Like Tanner in 's later videos just months after the fish oils and NV wide eyed - " normal " no more droop on the side of the eyes. I sometimes wonder if I never put Tanner on the fish oils and now NV what he would look...and not just look like -but be like today...but like you I am just beyond thrilled that in addition to awesome therapists who became part of the family -we were given the gift of the easy button.....(and some people thought that was just a fake easy button on the Staples commercial!!!) There was a video about 3 months prior to NV where was saying he wanted to watch a Charlie Brown special -and if you didn't translate for him I wouldn't have known what he was saying. I know you were going to see if you found anything even closer- but do you have that one- because I remember showing my husband that one and then some of your afters and he was blown away!! Your kids are adorable, the surges are obvious and you get the gold star at being (other than Sharon???) the only one that documented NV progress!!! Any tips for those that want to document that haven't started yet? (since you are a professional in this area- I mean who better than a producer for CBS news?!! Here's your one month update you shared here! One Month Update - Nutriiveda What a Winter it has been! We've been super buried with snow here in Columbus, Ohio since February began. I'm talking 25 inches of snow. I've been reading all the emails from the group, but because of the snow (and now a major roof problem) I've been working a lot of hours, so I haven't had much of a chance to respond. Here's how is doing.... He started Nutriiveda back in January, and has now been on it for one month. We've increased his dosage from one scoop to almost 2 a day. I was able to do so because I've found so many ways to include it in his diet. We're still mostly mixing it with milk, but I've also been making him a milkshake every day before he goes to his afternoon preschool class. It's a typical chocolate milkshake with ice cream, milk, a small amount of chocolate syrup and one scoop of powder. He LOVES it and I must say, it tastes pretty darn good. The gains. Oh the gains. I'm really happy with the amazing progress. 's progress has been HUGE across the board. His main SLP is not aware that we have been trying Nutriiveda. When I took to speech 2 weeks ago, she happily told me that she is seeing " fewer signs of classic apraxia. " She now says his issues more resemble a phonological processing disorder - which is apparently a lot less severe than apraxia. She has always described as having classic apraxia - since she first started treating him when he was barely 3-years-old. Of course, I love that Coop's articulation is improving, but the difference I'm most excited about is 's new word usage. The things that are popping out of his mouth without him even thinking about... Tonight, for instance, and I were having a conversation about recycling. His Dad walked by and jokingly said " I think we should recycle all the little boys in this house. " And without missing a beat, replied " No Daddy. That would hurt! I can't go in the garbage truck! " That's just one of dozens of examples of sentences that have flowed from his mouth without him thinking about it so much. He just seems to be thinking quicker on his feet. Other areas of improvement have been fine motor, which was the area where we saw the fastest improvement once we started Nutriiveda. has also grown! I'm not sure how that plays into all this...but I did have a Dad who follows DAN protocol for his child tell me that sometimes when things get straightened out metabolically, you'll see a growth spurt. And has shot up about a half and inch. All good things! We are so excited! Gretchen (up at http://pursuitofresearch.org/testimonials.html ) I just can't believe how amazing is doing at just turned 5 years old -just incredible Gretchen!! WOW -it really was and is a Happy Birthday for !! ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 16, 2010 Report Share Posted November 16, 2010 My only documentation secret is my Flip Cam. It's always with me and I love getting quick/easy videos of the boys. My parents live out of town so I send a lot of the clips to them and sometimes, when I go back and watch them I realize what progress is making. http://www.theflip.com/en-us/ As for the droopy eyes, you couldn't be more right on! I think about that every time I look at a picture of when he was a toddler. I have no idea when that started or what caused it. Maybe it was always there? He's not a kid who had language and then lost it. It was never there. My first real sign that there was a problem was when 's " babbling " didn't progress. He babbled away from 18 months all the way to 3 years of age. But there were never any real words said. Sure we could decipher a few....mama was " nana. " Chocolate milk was " nano. " He was my first born and I just thought kids learned to talk by babbling. I started getting worried once I saw how my friends' children were progressing compared to . I'm not the kind of mom who likes to compare kids, but the language difference between and his peers was like black and white. That seems like ages ago now. still has miles to tavel. But it's wonderful seeing his regular progress and , I thank you from the bottom of my heart for advocating for our children the way you do. I don't know where would be without this group - which is where I first discovered fish oil, PROMPT therapy and NV :) Gretchen Walsh (Columbus, OH) ________________________________ From: kiddietalk <kiddietalk@...> Sent: Mon, November 15, 2010 10:19:30 PM Subject: [ ] Re: Youtube? Gretchen these are amazing!! You know how I always notice stuff that sometimes others don't? In the original video of Coop prior to fish oils, NV and even therapy -he has those same droop eyes that Tanner suddenly had after he had the high fevers and regression in babble at 11 months. Like in Tanner's case anyway - the tone just disappeared from his face. But that wasn't permanent for Tanner either. Like Tanner in 's later videos just months after the fish oils and NV wide eyed - " normal " no more droop on the side of the eyes. I sometimes wonder if I never put Tanner on the fish oils and now NV what he would look...and not just look like -but be like today...but like you I am just beyond thrilled that in addition to awesome therapists who became part of the family -we were given the gift of the easy button.....(and some people thought that was just a fake easy button on the Staples commercial!!!) There was a video about 3 months prior to NV where was saying he wanted to watch a Charlie Brown special -and if you didn't translate for him I wouldn't have known what he was saying. I know you were going to see if you found anything even closer- but do you have that one- because I remember showing my husband that one and then some of your afters and he was blown away!! Your kids are adorable, the surges are obvious and you get the gold star at being (other than Sharon???) the only one that documented NV progress!!! Any tips for those that want to document that haven't started yet? (since you are a professional in this area- I mean who better than a producer for CBS news?!! Here's your one month update you shared here! One Month Update - Nutriiveda What a Winter it has been! We've been super buried with snow here in Columbus, Ohio since February began. I'm talking 25 inches of snow. I've been reading all the emails from the group, but because of the snow (and now a major roof problem) I've been working a lot of hours, so I haven't had much of a chance to respond. Here's how is doing.... He started Nutriiveda back in January, and has now been on it for one month. We've increased his dosage from one scoop to almost 2 a day. I was able to do so because I've found so many ways to include it in his diet. We're still mostly mixing it with milk, but I've also been making him a milkshake every day before he goes to his afternoon preschool class. It's a typical chocolate milkshake with ice cream, milk, a small amount of chocolate syrup and one scoop of powder. He LOVES it and I must say, it tastes pretty darn good. The gains. Oh the gains. I'm really happy with the amazing progress. 's progress has been HUGE across the board. His main SLP is not aware that we have been trying Nutriiveda. When I took to speech 2 weeks ago, she happily told me that she is seeing " fewer signs of classic apraxia. " She now says his issues more resemble a phonological processing disorder - which is apparently a lot less severe than apraxia. She has always described as having classic apraxia - since she first started treating him when he was barely 3-years-old. Of course, I love that Coop's articulation is improving, but the difference I'm most excited about is 's new word usage. The things that are popping out of his mouth without him even thinking about... Tonight, for instance, and I were having a conversation about recycling. His Dad walked by and jokingly said " I think we should recycle all the little boys in this house. " And without missing a beat, replied " No Daddy. That would hurt! I can't go in the garbage truck! " That's just one of dozens of examples of sentences that have flowed from his mouth without him thinking about it so much. He just seems to be thinking quicker on his feet. Other areas of improvement have been fine motor, which was the area where we saw the fastest improvement once we started Nutriiveda. has also grown! I'm not sure how that plays into all this...but I did have a Dad who follows DAN protocol for his child tell me that sometimes when things get straightened out metabolically, you'll see a growth spurt. And has shot up about a half and inch. All good things! We are so excited! Gretchen (up at http://pursuitofresearch.org/testimonials.html ) I just can't believe how amazing is doing at just turned 5 years old -just incredible Gretchen!! WOW -it really was and is a Happy Birthday for !! ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 17, 2010 Report Share Posted November 17, 2010 My son still has a bit of that droop on the outer sides of his eyes even though in pictures it doesn't seem as obvious since therapy and fish oils. I was watching these videos and would you say the NV helped the most with this? I noticed it but never brought it up to anyone and no professional or family member ever brought it up either. Is this part of apraxia? Also congratulations, I pray my son speaks this well one day. And spelling his name like he does?! You must be so proud! Kate > > My only documentation secret is my Flip Cam. It's always with me and I love > getting quick/easy videos of the boys. My parents live out of town so I send a > lot of the clips to them and sometimes, when I go back and watch them I realize > what progress is making. > > > http://www.theflip.com/en-us/ > > As for the droopy eyes, you couldn't be more right on! I think about that every > time I look at a picture of when he was a toddler. I have no idea when > that started or what caused it. Maybe it was always there? He's not a kid who > had language and then lost it. It was never there. My first real sign that > there was a problem was when 's " babbling " didn't progress. He babbled > away from 18 months all the way to 3 years of age. But there were never any > real words said. Sure we could decipher a few....mama was " nana. " Chocolate > milk was " nano. " He was my first born and I just thought kids learned to talk > by babbling. I started getting worried once I saw how my friends' children were > progressing compared to . I'm not the kind of mom who likes to compare > kids, but the language difference between and his peers was like black > and white. That seems like ages ago now. still has miles to tavel. > But it's wonderful seeing his regular progress and , I thank you from the > bottom of my heart for advocating for our children the way you do. I don't know > where would be without this group - which is where I first discovered > fish oil, PROMPT therapy and NV :) > > Gretchen Walsh > (Columbus, OH) > > > > ________________________________ > From: kiddietalk <kiddietalk@...> > > Sent: Mon, November 15, 2010 10:19:30 PM > Subject: [ ] Re: Youtube? > > Gretchen these are amazing!! You know how I always notice stuff that sometimes > others don't? In the original video of Coop prior to fish oils, NV and even > therapy -he has those same droop eyes that Tanner suddenly had after he had the > high fevers and regression in babble at 11 months. Like in Tanner's case anyway > - the tone just disappeared from his face. But that wasn't permanent for Tanner > either. Like Tanner in 's later videos just months after the fish oils > and NV wide eyed - " normal " no more droop on the side of the eyes. > > > I sometimes wonder if I never put Tanner on the fish oils and now NV what he > would look...and not just look like -but be like today...but like you I am just > beyond thrilled that in addition to awesome therapists who became part of the > family -we were given the gift of the easy button.....(and some people thought > that was just a fake easy button on the Staples commercial!!!) > > > There was a video about 3 months prior to NV where was saying he wanted > to watch a Charlie Brown special -and if you didn't translate for him I wouldn't > have known what he was saying. I know you were going to see if you found > anything even closer- but do you have that one- because I remember showing my > husband that one and then some of your afters and he was blown away!! Your kids > are adorable, the surges are obvious and you get the gold star at being (other > than Sharon???) the only one that documented NV progress!!! > > > Any tips for those that want to document that haven't started yet? (since you > are a professional in this area- I mean who better than a producer for CBS > news?!! > > Here's your one month update you shared here! > > One Month Update - Nutriiveda > > What a Winter it has been! > We've been super buried with snow here in Columbus, Ohio since February began. > I'm talking 25 inches of snow. > I've been reading all the emails from the group, but because of the snow (and > now a major roof problem) I've been working a lot of hours, so I haven't had > much of a chance to respond. > > Here's how is doing.... > > He started Nutriiveda back in January, and has now been on it for one month. > > We've increased his dosage from one scoop to almost 2 a day. I was able to do so > because I've found so many ways to include it in his diet. We're still mostly > mixing it with milk, but I've also been making him a milkshake every day before > he goes to his afternoon preschool class. It's a typical chocolate > milkshake with ice cream, milk, a small amount of chocolate syrup and one scoop > of powder. He LOVES it and I must say, it tastes pretty darn good. > > The gains. Oh the gains. > I'm really happy with the amazing progress. > > 's progress has been HUGE across the board. > > His main SLP is not aware that we have been trying Nutriiveda. When I took > to speech 2 weeks ago, she happily told me that she is seeing " fewer > signs of classic apraxia. " She now says his issues more resemble a phonological > processing disorder - which is apparently a lot less severe than apraxia. She > has always described as having classic apraxia - since she first started > treating him when he was barely 3-years-old. > > Of course, I love that Coop's articulation is improving, but the difference I'm > most excited about is 's new word usage. The things that are popping out > of his mouth without him even thinking about... > > Tonight, for instance, and I were having a conversation about recycling. > His Dad walked by and jokingly said " I think we should recycle all the little > boys in this house. " And without missing a beat, replied " No Daddy. That > would hurt! I can't go in the garbage truck! " > > That's just one of dozens of examples of sentences that have flowed from his > mouth without him thinking about it so much. He just seems to be thinking > quicker on his feet. > > Other areas of improvement have been fine motor, which was the area where we saw > the fastest improvement once we started Nutriiveda. > > has also grown! I'm not sure how that plays into all this...but I did > have a Dad who follows DAN protocol for his child tell me that sometimes when > things get straightened out metabolically, you'll see a growth spurt. And > has shot up about a half and inch. > > All good things! > We are so excited! > > Gretchen > (up at http://pursuitofresearch.org/testimonials.html ) > > > I just can't believe how amazing is doing at just turned 5 years old > -just incredible Gretchen!! WOW -it really was and is a Happy Birthday for > !! > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 2, 2010 Report Share Posted December 2, 2010 Hi there- I am one of those people who do not have any videos on you tube.... WHY? Because I have no idea how to do it.... and I have not taken the time to try to figure out how to do it! LOL... days are so busy.... I'm often up very late simply paying bills online! I recently purchased a new lap top.... and I am even having some issues trying to figure out all the differences that I have noticed with windows 7! I do know that some people have issues with placing videos of their kids on you Tube due to privacy concerns. I would be ok with placing a video of my son on it.... just have no clue how to do it.... and have not had the time to try to figure it out! Geez- I've even suddenly had trouble with simply, e-mailing pictures to friends with this new computer! (I loved Windows XP Media Edition... this windows 7 drives me nuts).... my hubby is completely clueless with computers... so he is no help to me! LOL- one of these days I will get to adding a video to You Tube! K [ ] Re: Youtube? Sharon has a video on Youtube but for some reason only the before. She has the after videos here on her blog http://apraxiastory.wordpress.com/before-after-video/ Other parents have videos on their blog as well -Gretchen from this group for example for sure who is a TV news producer (so super cute and well done before and after NV videos- Gretchen the one about the " what is it? " raccoon video!!!) -but don't know if others want to share with everyone on Youtube? Since I don't know if she wants to share here -you can read Gretchen's testimony here http://pursuitofresearch.org/testimonials.html and her son went on video from being unintelligible to an amazing communicator in very short time. Search the archives for gretchie9@... And what is going on with this is typical of what happened with fish oils. Parents are more active when they are worried about their kids -and then they fade off. Again very few stick around to help after they don't 'need' to be here. Understandable and normal. And because things are going so quick with NV -even more understandable there are less videos. So note to new people yet to try NV -do a before and after video I know Sharon isn't faded off even though her son too is doing amazing. She is in the middle of a HUGE move from Ohio across country so her life is a bit hectic -but otherwise I'm sure she'd answer this herself -and I know this is why she only has the one up at Youtube -just has not had a chance to catch up with life yet. Give it a bit of time -there will be some willing to share on Youtube -there always is. Thing is that with NV you have to make sure you videotape prior to starting because the surges in most cases are within one day to three and nobody expects it even though it's reported over and over. Perhaps on the new testimonial page for Pursuit of Research http://pursuitofresearch.org/testimonials.html we can have a section to upload videos? ===== Quote Link to comment Share on other sites More sharing options...
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