Guest guest Posted July 1, 2008 Report Share Posted July 1, 2008 LD--you can get dr bronners at Trader Joes here in sd. LL > From: Joan Wood <joanwood@...> > Subject: Re: Re: Wal-Mart and Ammonia > bird mites > Date: Tuesday, July 1, 2008, 7:55 PM > You can buy them in some health food stores (Vitamin Shoppe > for one) or order from internet. www,drbronner.com/ > Joan > > Re: Wal-Mart and Ammonia > > > Thanks Myrtle, Joan, and others, > > Yes, we are all guinea pigs when it comes to all these > chemicals. > Luckily, my skin and hair are in tact but then again so > are the mites! > I will have to look into Bronner's soaps. Are those > sold in the local > stores? Have a good day! > > LD > > > > > > > > > > > > > > > > Hi Gang, > > > > > > > > > > > > > > For those of us who use > ammonia in the laundry...I went > to > > > Wal- > > > > > Mart > > > > > > > last night and when I went > to the check-out stand with 4 > > > bottles > > > > > of > > > > > > > ammonia the cashier told me > that I was limited to only 2 > > > bottles. > > > > > It > > > > > > > seems that ammonia is used > to make meth-amphetamine and > Wal- > > > mart > > > > > is now > > > > > > > limiting their sales! > Luckily, the person behind me said > he > > > > > would buy > > > > > > > two for me and then I paid > him. Have any of you run into > > > this > > > > > > > problem? > > > > > > > > > > > > > > I also noticed that Epsom > Salt, Hydrogen Peroxide and > Rubbing > > > > > Alcohol > > > > > > > were all grouped together > in one large display in the > center > > > > > aisle. I > > > > > > > think someone else here had > pointed that out as well. > > > > > > > Hmmmmmmmmmmmmmmmmmmm! > > > > > > > > > > > > > > Lady Dee > > > > > > > > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2011 Report Share Posted March 1, 2011 Ivy & group, First, let's review.. Your son was on SPEAK---hypervitaminosis-which seems to explain the reason for his regression. Your son is only 3 yrs. Learning Disorders-dyslexia, dysgraphria, etc. can't be dx until a child is 5-7yrs. Why? One of the reasons is that the areas in the brain that are responsible for these skills do not mature until ~7yrs. Correspondingly, many of the formal specific language tests cannot be given until 5yrs. So, I would not worry about LD yet. He still has time to develop. WHENEVER you go to a new practitioner (dr, SLP, etc) DO take any evals/medical notes from within the past 6 mo-1yr. Medical and therapy history is very important to get an accurate picture of any child. So glad he is back on the NV! 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/ffcentralmaryland#!/pages/Help-Me-Speak-LLC/10462885 2032 Call me with any questions about NutriiVeda! **************************************************************************** ************** The above email is for intended recipient only and may be confidential and is legally privileged. If you are not the intended recipient of this communication, you are hereby notified that any unauthorized review, use, dissemination, distribution, downloading, or copying of this communication is strictly prohibited. If you have received this communication in error, please immediately notify us by reply email, delete the communication and destroy all copies. Unauthorized use or distribution is prohibited and may be unlawful. **************************************************************************** *** From: [mailto: ] On Behalf Of Ivy Sent: Tuesday, March 01, 2011 7:30 AM Subject: Re: [ ] Re: NV update Alyssa who finds these learning disabilities? We have been to many perfessionals..and even considering if worth going to get another neurodevelp eval far from us. Maybe i shouldnt even bring past evals to the next person we see? I have always wondered if " all normal " written on evals is hindering findings...my son has o ly been dx'd with verbal apraxia, sensory dysfunction, oral apraxia and global apraxia, hypotonia in torso. Another advice is appreciated. Thanks! Ivy On Feb 25, 2011, at 7:31 AM, Alyssa <aw_nagy@... <mailto:aw_nagy%40> > wrote: > Ivy, > I have been reading only some of these posts. However I did want to respond to your last question. Many times children with CAS also have co existing learning disabilities. I know in our case that makes the rate of Matts gains much slower than a child with only CAS. For us this is true in all academic areas. Believe me I understand your frustration. > Alyssa > > On Feb 25, 2011, at 7:03 AM, " Ivy " <ivygreene88@... <mailto:ivygreene88%40gmail.com> > wrote: > > > - I certainly will read Sherry's blog, thank you for directing me to it. About the IEP, I know the wrights law and that I can have my district place him appropriately. > > > > No, I do not think my son has a develpmental & nbsp;delay. He & nbsp;has & nbsp;severe verbal apraxia. Ifit is possible to have both..andthat is why he is not making progress, then nobodyhas ever told & nbsp;me that. > > Can & nbsp;a child have both?yetthat wouldnot explainwhy he was doing better with progress a year and halfback and lost it only to revert tobuh buh inhis jargon. He has always jargoned. > > > > Is it possible a child with CAS can go for long periods of time & nbsp;without anyprogress? Maybe that is the question I shouldbe asking..and I should keep working hard with him and rewards will happen??? > > Thanks again! & nbsp; > > Ivy > > -- Sent from my Palm Pre > > On Feb 25, 2011 1:29 AM, kiddietalk & lt;kiddietalk@... <mailto:kiddietalk%40> & gt; wrote: > > > > & nbsp; > > > > Your message is very difficult to read- but think I got the point you can't or don't want to share what the background is due to privacy? The good thing about a grouplist such as this that you can have an email address just for this account with a fake name or a silly name and nobody would know (or care) In addition this is a private group -in the ten years I've run it that I know of even when people give out their home numbers as many have done we have had no issues ever. Not saying you can't keep your guard up -but just saying the question I asked was about your child's history which can be done without ever mentioning his name or even what country you live in. > > > > You do have a very perplexing situation, but the fact your child doesn't have an IEP, and one of the neurologists said he is " fine " I'm just wondering what you are dealing with- if anything. I'm honestly perplexed and as it seems you have been to so many SLPs, MDs, biomedical experts and are still coming up blank- I don't honestly know what else can be said. And I don't get why not an IEP if he is impaired even in just speech?? You say enclosed classroom but if the placement isn't appropriate you can advocate for out of district placement for preschool. My son Tanner's out of district placement was at the Summit Speech School in New Providence NJ and LOVED it!! We all loved it that had our kids go to that school -they worked miracles with apraxic children as well as with the hearing impaired population -and as that school is one of the top oral based schools for the hearing impaired -it was amazing that many of the children that were hearing impaired with cochlear implants spoke better than the hearing apraxic ones! > > > > But back to your son...is it possible you need to step back a bit? even for a month? > > > > Thought...and just throwing this out there....is it possible that you can just for a short time assume that perhaps it may just be developmental and not apraxia? One parent in NJ Cheryl reported that her child was put on so many biomedical things she had a meltdown (she's now doing well on NV as she posted recently) > > > > Is developmental delay ruled out??? Maybe he just needs a regular preschool, a healthy diet, things like fish oils and NV are providing essential nutrients which are needed by anyone but perhaps you don't need to do so much of the other? I can't explain the regression at around (before?) 2 and the regression again at around 3 but from what you are writing it sounds like it's mainly in speech? Most with apraxia present multifacted and have hypotonia, sensory and or motor planning issues in the body. I know you may have shared all this in all the other emails but honestly can't recall. > > > > Again if you want to start another account with a different email nobody would know...Do whatever is comfortable to you. And by the way we have quite a few lawyers in this group who do write here with their names...in fact Sherry Silvern is one of our all time favorite lawyers of this group who has been a member that has reached out to share not just her own son's story but to help others as well. And not only does Sherry share here -but wrote a blog to update all about her son Josh's experience on NV http://budsnvblog.blogspot.com/ (amazing journey like many of the NV blogs out there) -and we certainly could never fit all Sherry wrote up on our testimony page!!! http://pursuitofresearch.org/products/nutriiveda/nutriiveda-testimonials/ If anything I believe Sherry's journal blog which she did a great job of keeping for so long will be a great source of information for those that want to study NV in the next year or so to see why it's working > > > > ===== > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2011 Report Share Posted March 1, 2011 Ivy I do agree with Barbara. I didn't realize how young your baby is. However that being said when he is a bit older you can have him evaluated by a Neuro psychologist to do an educational eval. Best of luck Alyssa On Mar 1, 2011, at 10:51 AM, " Barbara " <helpmespeak@...> wrote: > Ivy & group, > > First, let's review.. > > Your son was on SPEAK---hypervitaminosis-which seems to explain the reason > for his regression. > > Your son is only 3 yrs. Learning Disorders-dyslexia, dysgraphria, etc. > can't be dx until a child is 5-7yrs. Why? One of the reasons is that the > areas in the brain that are responsible for these skills do not mature until > ~7yrs. Correspondingly, many of the formal specific language tests cannot > be given until 5yrs. > > So, I would not worry about LD yet. He still has time to develop. > > WHENEVER you go to a new practitioner (dr, SLP, etc) DO take any > evals/medical notes from within the past 6 mo-1yr. Medical and therapy > history is very important to get an accurate picture of any child. > > So glad he is back on the NV! > > 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/ffcentralmaryland#!/pages/Help-Me-Speak-LLC/10462885 > 2032 > > Call me with any questions about NutriiVeda! > > **************************************************************************** > ************** > > The above email is for intended recipient only and may be confidential and > is legally privileged. If you are not the intended recipient of this > communication, you are hereby notified that any unauthorized review, use, > dissemination, distribution, downloading, or copying of this communication > is strictly prohibited. If you have received this communication in error, > please immediately notify us by reply email, delete the communication and > destroy all copies. Unauthorized use or distribution is prohibited and may > be unlawful. > > **************************************************************************** > *** > > From: > [mailto: ] On Behalf Of Ivy > Sent: Tuesday, March 01, 2011 7:30 AM > > Subject: Re: [ ] Re: NV update > > Alyssa who finds these learning disabilities? We have been to many > perfessionals..and even considering if worth going to get another > neurodevelp eval far from us. Maybe i shouldnt even bring past evals to the > next person we see? I have always wondered if " all normal " written on evals > is hindering findings...my son has o ly been dx'd with verbal apraxia, > sensory dysfunction, oral apraxia and global apraxia, hypotonia in torso. > > Another advice is appreciated. > Thanks! > Ivy > > On Feb 25, 2011, at 7:31 AM, Alyssa <aw_nagy@... > <mailto:aw_nagy%40> > wrote: > > > Ivy, > > I have been reading only some of these posts. However I did want to > respond to your last question. Many times children with CAS also have co > existing learning disabilities. I know in our case that makes the rate of > Matts gains much slower than a child with only CAS. For us this is true in > all academic areas. Believe me I understand your frustration. > > Alyssa > > > > On Feb 25, 2011, at 7:03 AM, " Ivy " <ivygreene88@... > <mailto:ivygreene88%40gmail.com> > wrote: > > > > > - I certainly will read Sherry's blog, thank you for directing me to > it. About the IEP, I know the wrights law and that I can have my district > place him appropriately. > > > > > > No, I do not think my son has a develpmental & nbsp;delay. He & nbsp;has > & nbsp;severe verbal apraxia. Ifit is possible to have both..andthat is why > he is not making progress, then nobodyhas ever told & nbsp;me that. > > > Can & nbsp;a child have both?yetthat wouldnot explainwhy he was doing > better with progress a year and halfback and lost it only to revert tobuh > buh inhis jargon. He has always jargoned. > > > > > > Is it possible a child with CAS can go for long periods of time > & nbsp;without anyprogress? Maybe that is the question I shouldbe asking..and > I should keep working hard with him and rewards will happen??? > > > Thanks again! & nbsp; > > > Ivy > > > -- Sent from my Palm Pre > > > On Feb 25, 2011 1:29 AM, kiddietalk & lt;kiddietalk@... > <mailto:kiddietalk%40> & gt; wrote: > > > > > > & nbsp; > > > > > > Your message is very difficult to read- but think I got the point you > can't or don't want to share what the background is due to privacy? The good > thing about a grouplist such as this that you can have an email > address just for this account with a fake name or a silly name and nobody > would know (or care) In addition this is a private group -in the ten years > I've run it that I know of even when people give out their home numbers as > many have done we have had no issues ever. Not saying you can't keep your > guard up -but just saying the question I asked was about your child's > history which can be done without ever mentioning his name or even what > country you live in. > > > > > > You do have a very perplexing situation, but the fact your child doesn't > have an IEP, and one of the neurologists said he is " fine " I'm just > wondering what you are dealing with- if anything. I'm honestly perplexed and > as it seems you have been to so many SLPs, MDs, biomedical experts and are > still coming up blank- I don't honestly know what else can be said. And I > don't get why not an IEP if he is impaired even in just speech?? You say > enclosed classroom but if the placement isn't appropriate you can advocate > for out of district placement for preschool. My son Tanner's out of district > placement was at the Summit Speech School in New Providence NJ and LOVED > it!! We all loved it that had our kids go to that school -they worked > miracles with apraxic children as well as with the hearing impaired > population -and as that school is one of the top oral based schools for the > hearing impaired -it was amazing that many of the children that were hearing > impaired with cochlear implants spoke better than the hearing apraxic ones! > > > > > > But back to your son...is it possible you need to step back a bit? even > for a month? > > > > > > Thought...and just throwing this out there....is it possible that you > can just for a short time assume that perhaps it may just be developmental > and not apraxia? One parent in NJ Cheryl reported that her child was put on > so many biomedical things she had a meltdown (she's now doing well on NV as > she posted recently) > > > > > > Is developmental delay ruled out??? Maybe he just needs a regular > preschool, a healthy diet, things like fish oils and NV are providing > essential nutrients which are needed by anyone but perhaps you don't need to > do so much of the other? I can't explain the regression at around (before?) > 2 and the regression again at around 3 but from what you are writing it > sounds like it's mainly in speech? Most with apraxia present multifacted and > have hypotonia, sensory and or motor planning issues in the body. I know you > may have shared all this in all the other emails but honestly can't recall. > > > > > > Again if you want to start another account with a different email nobody > would know...Do whatever is comfortable to you. And by the way we have quite > a few lawyers in this group who do write here with their names...in fact > Sherry Silvern is one of our all time favorite lawyers of this group who has > been a member that has reached out to share not just her own son's story but > to help others as well. And not only does Sherry share here -but wrote a > blog to update all about her son Josh's experience on NV > http://budsnvblog.blogspot.com/ (amazing journey like many of the NV blogs > out there) -and we certainly could never fit all Sherry wrote up on our > testimony page!!! > http://pursuitofresearch.org/products/nutriiveda/nutriiveda-testimonials/ If > anything I believe Sherry's journal blog which she did a great job of > keeping for so long will be a great source of information for those that > want to study NV in the next year or so to see why it's working > > > > > > ===== > > > > > > Quote Link to comment Share on other sites More sharing options...
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