Guest guest Posted March 8, 2003 Report Share Posted March 8, 2003 Hi Wendi - Number one question: Was Sky having a bad day the day of his testing? Some of the observations you state such as specifically " no pointing or following points " and " no pretend play, not much interactive play " Do you agree with them? Did the psychologist ask for history -or even for video tapes of your child during normal play in his natural environment? What made them come to the conclusion that your child likes sameness? Are there examples you see of this too? You state that four other therapy professionals don't believe two year old Sky is autistic. What did they see that these other professionals didn't? What scores and observations do they have for Sky and what were their feelings on this new diagnosis for Sky? I would recommend also seeing a neurodevelopmental pediatrician or pediatric neurologist for another opinion if that is possible. Perhaps someone from this group in your area can suggest someone they love? And speaking of diagnosis -I know it's hard not to -but don't get upset over diagnosis since it unfortunately still depends on both where you live, what type of professional you see and what their research and studies are in. It even can depend on specifically which one and on what day you see this professional -with the same exact child -what diagnosis you may come home with that day. I like to call it the " what will it be? " game. So if you hear " This child is apraxic " then " It's not apraxia -it's a motor planning disorder " and then " It's not a motor planning disorder -it's a severe expressive language delay " does your child have three diagnosis's or like the new math do we have to figure out based on the facts that apraxia is a motor planning disorder which presents frequently as a severe expressive language delay that your child is most likely " apraxic " even though two out of the three professionals said " not apraxic " ? *Important -it doesn't have to be just one diagnosis either. Also - I'm the rare bird that does not believe that all children with multi faceted communication impairments fall under the autism spectrum. Various Communication impairments can overlap. In addition - communication impairments can overlap with other learning disabilities, disorders, and syndromes. For example based on the quotes from the professionals about Sky -he could have hypothetically the following - global apraxia (severe motor planning problems throughout the body) which could effect his ability to point -ADHD -which could affect his attention span -frustration which could make him either withdraw from trying -or could make him lash out. Explore all possiblities. Since our chidren can't communicate yet -it's up to us to be the voice for them. As I always stress -it takes a skilled neuromedical professional in most cases to differentiate -and even then mistakes can be made. Our main goal as parents and professionals is to know the symptoms and treatments available to our children so that we can provide them with the most appropriate therapies based on what they present with. This is better than just blindly providing a large cluster of children with multi faceted (meaning presenting with more than one symptom) communication impairments with the same label/therapy which may only help one percentage and hurt the rest. We want to provide our children with the best chance possible for a productive and expressive future. CHERAB advisors developmental pediatricians Dr. Agin or Dr. Laveman may have comments too. Let us know how it goes and good luck! ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 9, 2003 Report Share Posted March 9, 2003 Hello, I have a 6 year old who is recovering from Autism- and let me be the first to tell you your little Sky is very sick. I wish someone had told me that 3 and a half years ago- As Skys Mom many deccisions are going to fall on you --but with the right knowledge you will be a strong leader - you can do it- and you know Sky best. I tossed with the diagnosis also and now I know it was a blessing because it moved me to take action- BIG ACTION. Please read and print the paper on line at the Children's Boimedical Center of Utah Inc. called Understanding Autism by Jepson MD . I have not found great support from normal doctors and my suggestion is to see and lead a DAN doctor -a list is at the Autism Research Institute ARI( Read every thing at the ARI). Get organized pick 2 points from the pie chart in the paper Understanding Autism and start testing and learning. If Sky has been on several rounds of antibiotic one right after another she will have a yeast over growth when I got yeast under control with my son it made a big differance. ( don't stay on 1 treatment to long you must decide when to move on ) I would suggest you buy and follow the supplement chart in the book Prescription for Nutritional Healing by Balch and Balch. It is right on. Other favorite site are Dana's View, slaw, Mercury and Autism group( you can ask any ? there) and sign up to get the Schafer Autism Report. My 2 cents Ann --- In , " wendie " <hwendie@h...> wrote: > Hi guys well we got the diagnosis I didn't want to get yesterday. We > met Sky's Ped. Neuro. & his team & they believe Sky falls into the > Autism Spectrum. I was pretty shocked by this, I wasn't expecting to > hear autism. We've talked to 2 S.T. & 2 O.T. who all had observed > Sky & all of them said they didn't feel as if she was autistic. > We're getting some blood work & a EEG lined up to rule out other > things also. Our Dr. wanted to wait until these tests came back > before we really started to proceed w/things. They did suggest S.T. > (which she's been receiving through E.I.), O.T.(she'll be starting > soon through E.I.) & P.T. Has anyone had to request all 3 of these > services through their county & how hard was it to get these > services? The Dr. & his staff suggested a program called the Start > Program-Autism Recovery, has anyone heard of this before? I can't > find any info on it anywhere. > > All day I've been going back & forth on this diagnosis. I guess it > may have something to do w/Sky having such a good day. We don't have > the typed up report, but I'm going to include her scores & their > comments(I took lots of notes). > BTW, Sky turned 2 in January. > Comments from the Neuropsychologist > short attention span, no pointing or following points, likes sameness > Score - 16 month level (sp?) Scale > > Comments from S.T. > Receptive 12-14 months scattered to 18-20 months > Expressive 14-16 months scattered to 18-20 months > no pretend play, not much interactive play > > Comments from O.T. > motor planning issues, fine motor skill issues, sensory integrating > issues, hypotonia(sp?) > scored less than 50 on (sp?) Scale delay around 13 months Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 9, 2003 Report Share Posted March 9, 2003 , thanks for your post! I was hoping you would have some comments because you always have such great info. Sky has seen the Ped. Neuro & his team twice and I did provide them w/a video tape of two S.T. sessions & random shots of her playing around the house alone & w/her twin sister. During the evals I think they got to see her at her worst & best. The first evaluation she didn't want anything to do w/them & cried for an hour. She finally fell asleep & when she woke up she was her usual happy self & they were able to do 2 out of the 4 evals. The 2nd time around started out the same, but she calmed down a lot quicker & we were able to complete the eval. As for the pointing, not following pointing, & no pretend play I do agree w/them. However she's is picking up on the pretend play a little bit. Sometimes I can engage her & she will copy my pretend play for maybe a minute then she stops. As for the interactive play, I've seen a lot of progress when she's playing w/her sister. In the past couple of weeks she's improved a lot in that area. Two of the therapist that have seen Sky were from E.I. Of course they don't diagnose, but they have told me their gut feelings were she didn't have Autism. The other two therapist were from The Spectrum Center(they use the Tomatis Method) & they didn't do a formal eval, just observed her & asked us questions. They also agreed w/E.I. that she wasn't Autistic. They believed she has DSI, APD, motor planning problems & low muscle tone. As I stated before the Dr. that diagnosed Sky is a Ped. Neuro so should we still see a Dev. Ped.? I don't have a problem getting a 2nd opinion, but not right now. She's been through so many evals lately & she just hates it. I agree with what you said about multiple diagnosis too. I've also wondered about global apraxia & infact that's what I was gearing myself up to hear not Autism. I guess another thing I should note is Sky's attention span changes depending on what she's doing. She doesn't have any problem watching a disney movie & sitting still through the whole movie. Infact we've took the girls to the movie theater twice to see Disney movies & they did just fine. Thank you so much for listening & I really cherish all the advise I've been given so far. I'm not so concerned w/the label, but I do want to make sure Sky is getting the right services & therapies she needs. Wendie > Hi Wendi - > > Number one question: > > Was Sky having a bad day the day of his testing? > > Some of the observations you state such as specifically " no pointing > or following points " and " no pretend play, not much interactive > play " Do you agree with them? Did the psychologist ask for > history -or even for video tapes of your child during normal play > in his natural environment? What made them come to the conclusion > that your child likes sameness? Are there examples you see of this > too? > > You state that four other therapy professionals don't believe two > year old Sky is autistic. What did they see that these other > professionals didn't? What scores and observations do they have for > Sky and what were their feelings on this new diagnosis for Sky? > > I would recommend also seeing a neurodevelopmental pediatrician or > pediatric neurologist for another opinion if that is possible. > Perhaps someone from this group in your area can suggest someone > they love? > > And speaking of diagnosis -I know it's hard not to -but don't get > upset over diagnosis since it unfortunately still depends on both > where you live, what type of professional you see and what their > research and studies are in. It even can depend on specifically > which one and on what day you see this professional -with the same > exact child -what diagnosis you may come home with that day. I like > to call it the " what will it be? " game. So if you hear " This child > is apraxic " then " It's not apraxia -it's a motor planning disorder " > and then " It's not a motor planning disorder -it's a severe > expressive language delay " does your child have three diagnosis's or > like the new math do we have to figure out based on the facts that > apraxia is a motor planning disorder which presents frequently as a > severe expressive language delay that your child is most > likely " apraxic " even though two out of the three professionals > said " not apraxic " ? > > *Important -it doesn't have to be just one diagnosis either. Also - > I'm the rare bird that does not believe that all children with multi > faceted communication impairments fall under the autism spectrum. > Various Communication impairments can overlap. In addition - > communication impairments can overlap with other learning > disabilities, disorders, and syndromes. > > For example based on the quotes from the professionals about Sky - he > could have hypothetically the following > - global apraxia (severe motor planning problems throughout the > body) which could effect his ability to point > -ADHD -which could affect his attention span > -frustration which could make him either withdraw from trying -or > could make him lash out. > Explore all possiblities. Since our chidren can't communicate yet - it's up to us to be the voice for them. > > As I always stress -it takes a skilled neuromedical professional in > most cases to differentiate -and even then mistakes can be made. > Our main goal as parents and professionals is to know the symptoms > and treatments available to our children so that we can provide them > with the most appropriate therapies based on what they present with. > This is better than just blindly providing a large cluster of children with > multi faceted (meaning presenting with more than one symptom) > communication impairments with the same label/therapy which may only > help one percentage and hurt the rest. We want to provide our > children with the best chance possible for a productive and > expressive future. > > CHERAB advisors developmental pediatricians Dr. Agin or Dr. Laveman > may have comments too. > > Let us know how it goes and good luck! > > ===== > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 22, 2005 Report Share Posted July 22, 2005 I find this very interesting in light of the fact that over 700 families of children with autism are marching on Congress this week to argue the possibility of a connection between vaccines/thimerisol and autism. Of course, the AMA, FDA, and CDC all proclaim the safety of such vaccines! If they (vaccines) are so safe, then why have 'they' (powers that be) discontinued the use of thimerisol, which contains mercury, in childhood vaccines? Mercury is one of the most toxic naturally occurring element on the face of the earth! Unused mercury amalgal material in dental offices has to be disposed of as 'hazardous waste', yet they say it is safe placed only inches from one's brain?!?! Thimerisol is supposedly only used in flu shots now! Gee that offers much comfort! IMHO, if 'they' were to warn of the hazards associated with such vaccines, it would create a class-action lawsuit that would dig into the pocketbooks of too many powerful industries! Now, I'll step down from my soapbox! Marcie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 22, 2005 Report Share Posted July 22, 2005 Marcie, I unfortunately could not make it to Washington and the rally, but many of my friends went and said it went well, overall. As far as thimerosal, I can safely say that they are still putting it into vaccines in some form, even if it’s only in the production. I do not trust the pharmaceutical firms to take it out completely. That would cause too much of a quick drop in the rate of autism. As far as the class action law suit, there is in fact one that is on hold in the vaccine courts. Roughly four thousand of us are involved in it; yet I doubt I will ever see any restitution. I got on this group, by accident. There are a bunch of us with autistic children that have begun LDN due to a doctor and her relentless search to help our children. I am also on it for preventative measures. Today was my son’s first day on it and we have had an awesome first day. For myself, I have had a tremendous headache all day and pupils will not dialate; they are just little circles. It is four pm and I am beginning to feel a little better. I am definitely going to take some melatonin tonight to hopefully get some sleep. Thanks for everyone’s help and support. I will let you all know how LDN is working for my son as the weeks progress. - NJ Re: [low dose naltrexone] Re: autism I find this very interesting in light of the fact that over 700 families of children with autism are marching on Congress this week to argue the possibility of a connection between vaccines/thimerisol and autism. Of course, the AMA, FDA, and CDC all proclaim the safety of such vaccines! If they (vaccines) are so safe, then why have 'they' (powers that be) discontinued the use of thimerisol, which contains mercury, in childhood vaccines? Mercury is one of the most toxic naturally occurring element on the face of the earth! Unused mercury amalgal material in dental offices has to be disposed of as 'hazardous waste', yet they say it is safe placed only inches from one's brain?!?! Thimerisol is supposedly only used in flu shots now! Gee that offers much comfort! IMHO, if 'they' were to warn of the hazards associated with such vaccines, it would create a class-action lawsuit that would dig into the pocketbooks of too many powerful industries! Now, I'll step down from my soapbox! Marcie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2005 Report Share Posted July 23, 2005 Hi , Have you heard many success stories regarding other Autistic children taking LDN? Thanks Aletha RE: [low dose naltrexone] Re: autism Marcie, I unfortunately could not make it to Washington and the rally, but many of my friends went and said it went well, overall. As far as thimerosal, I can safely say that they are still putting it into vaccines in some form, even if it’s only in the production. I do not trust the pharmaceutical firms to take it out completely. That would cause too much of a quick drop in the rate of autism. As far as the class action law suit, there is in fact one that is on hold in the vaccine courts. Roughly four thousand of us are involved in it; yet I doubt I will ever see any restitution. I got on this group, by accident. There are a bunch of us with autistic children that have begun LDN due to a doctor and her relentless search to help our children. I am also on it for preventative measures. Today was my son’s first day on it and we have had an awesome first day. For myself, I have had a tremendous headache all day and pupils will not dialate; they are just little circles. It is four pm and I am beginning to feel a little better. I am definitely going to take some melatonin tonight to hopefully get some sleep. Thanks for everyone’s help and support. I will let you all know how LDN is working for my son as the weeks progress. - NJ -----Original Message-----From: low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of marciemjm@...Sent: Friday, July 22, 2005 8:41 AMlow dose naltrexone Subject: Re: [low dose naltrexone] Re: autism I find this very interesting in light of the fact that over 700 families of children with autism are marching on Congress this week to argue the possibility of a connection between vaccines/thimerisol and autism. Of course, the AMA, FDA, and CDC all proclaim the safety of such vaccines! If they (vaccines) are so safe, then why have 'they' (powers that be) discontinued the use of thimerisol, which contains mercury, in childhood vaccines? Mercury is one of the most toxic naturally occurring element on the face of the earth! Unused mercury amalgal material in dental offices has to be disposed of as 'hazardous waste', yet they say it is safe placed only inches from one's brain?!?! Thimerisol is supposedly only used in flu shots now! Gee that offers much comfort! IMHO, if 'they' were to warn of the hazards associated with such vaccines, it would create a class-action lawsuit that would dig into the pocketbooks of too many powerful industries! Now, I'll step down from my soapbox! Marcie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2005 Report Share Posted July 23, 2005 Aletha, One of our DAN (Defeat Autism Now) doctor’s ran a three month (approx.) study on the effects of LDN on autistic children. It has gone overall well, that is why many of us are trying it now. We have heard pretty good things. I do know that if the child has an issue with gluten or casein and there are infractions, LDN will aid in the display of the issues with a lot of whining and crying. Some are showing increased appetite. Others are saying that there is better sleep, more “contact” with the world around them, an overall sense of well-being. We have been on it for two days. He is much calmer. We are not on the gluten-free (we are casein free), had been for three years, so for us this was going to be the telling sign if gluten was going to be an issue. Any allergy tests we have done showed he was not allergic to gluten, but as you know, the first step for our kids is to take them off gluten/casein and we did for three years. We have had no issues as was stated in the above, so I guess the tests were accurate! Those are some of the points I remember from other group discussions. There is a group called Autism_LDN that is documenting the reactions of our kids on LDN. Hope this helps some. Take care. Re: [low dose naltrexone] Re: autism Hi , Have you heard many success stories regarding other Autistic children taking LDN? Thanks Aletha Re: [low dose naltrexone] Re: autism I find this very interesting in light of the fact that over 700 families of children with autism are marching on Congress this week to argue the possibility of a connection between vaccines/thimerisol and autism. Of course, the AMA, FDA, and CDC all proclaim the safety of such vaccines! If they (vaccines) are so safe, then why have 'they' (powers that be) discontinued the use of thimerisol, which contains mercury, in childhood vaccines? Mercury is one of the most toxic naturally occurring element on the face of the earth! Unused mercury amalgal material in dental offices has to be disposed of as 'hazardous waste', yet they say it is safe placed only inches from one's brain?!?! Thimerisol is supposedly only used in flu shots now! Gee that offers much comfort! IMHO, if 'they' were to warn of the hazards associated with such vaccines, it would create a class-action lawsuit that would dig into the pocketbooks of too many powerful industries! Now, I'll step down from my soapbox! Marcie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 7, 2006 Report Share Posted April 7, 2006 > > Hi i am brand new. My friend Bob told me about your site and what the drug " N " is doing > for him. He has MS and he told me that some people on the site have written about using > this drug for autism. I met a mother yesterday who mentioned using the drug on her > autistic son (who also suffers from Epstein Barr) and seeing great benefit in terms of his > being able to think more clearly. My son is 10, has brrn diagnosed with mild to moderate > autsim. He processes information slowly and he has some problems using his right arm > (acutally he refuses to use it) and has poor grip when writing with his left hand. > > Right now we are getting ready to experiment with Aricept (used for Alzheimers). Our > doctor is very cautious and is interested in doing lots of testing once we begin. if anyone > reads this and knows of any studies pertaining to autism and Naltrexone or if there are > members using Naltrexone for Autsim, please respond. I would appreciate hearing about it. > Thank you, Debby > ======== The link to the Autism-LDN(Low Dose Naltrexone) group is below. The owner of the group is on the road doing conferences so I'm not sure if she has someone else approving membership to that group for her or not. She is the doctor(Dr. Jaquelyn McCandless) who is using LDN in autistic individuals. Autism_LDN : Autism LDN Autism_LDN/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 7, 2006 Report Share Posted April 7, 2006 Hi Debby, Here you' ll find what you are looking for autism_ldn Hope it helps! > > Hi i am brand new. My friend Bob told me about your site and what the drug " N " is doing > for him. He has MS and he told me that some people on the site have written about using > this drug for autism. I met a mother yesterday who mentioned using the drug on her > autistic son (who also suffers from Epstein Barr) and seeing great benefit in terms of his > being able to think more clearly. My son is 10, has brrn diagnosed with mild to moderate > autsim. He processes information slowly and he has some problems using his right arm > (acutally he refuses to use it) and has poor grip when writing with his left hand. > > Right now we are getting ready to experiment with Aricept (used for Alzheimers). Our > doctor is very cautious and is interested in doing lots of testing once we begin. if anyone > reads this and knows of any studies pertaining to autism and Naltrexone or if there are > members using Naltrexone for Autsim, please respond. I would appreciate hearing about it. > Thank you, Debby > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2006 Report Share Posted April 8, 2006 Thanks for your help- i will check the source out. Debby Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 21, 2006 Report Share Posted August 21, 2006 Some thoughts on this..... I have an Autistic 6-yo. I don't see the " link " in the article. A link, for me, would be research - something scientific and not just another emotionally-laden blinders-on article about mercury ala Kirby and his EOHarm cult. Some of us believe that mercury is secondary - the immune system has become damaged (bacterial, viral, ad nauseum) rendering it incapable of defending the brain/nervous/gut system, all of which are affected in those on the Autism spectrum. In my son's case, his birth-mother had herpes. Research at s-Hopkins is showing that herpes transcends the placenta barrier. In his case, he had a live virus (herpes) in his body - and when infected with the MMR, which was another live virus, the two caused the immune system to respond in an abnormal way, and instead of defending the body, started to destroy the nervous system and gut. On top of that, there are enough environmental factors to add to the toxin-theories, in addition to mercury, as well as birth-mothers who are not toxin-free, etc., to add to the possible theories of Why. IMO, the mercury-done-it is subsiding, with people recognizing it's more complex than " just " that.....HTH... What I can say is, my son has made tremendous strides on an all organic, raw goat milk, grass-fed meat, no processed oils, MamaMakesTheButter diet ala Nourishing Traditions. Sharon On 8/21/06, crayfishfeed <crayfishfeed@...> wrote: > > My friend sent me this article. I thought it was a basic well written > article that links mercury and autism > http://readthehook.com/stories/2005/04/07/coverGenerationHgIsAutismP.ht > ml > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2006 Report Share Posted September 22, 2006 Hi Don, I would suggest cking out Pecanbread.com, and the groupmb12 valtrex, both are great resources.......good luck, Rhonda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2006 Report Share Posted September 22, 2006 Have you read Dr. Megson's article on westonaprice.org? Here's a copy from another site: " IS AUTISM A G-ALPHA PROTEIN DEFECT REVERSIBLE WITH NATURAL VITAMIN A? " http://www.dzieci.bci.pl/strony/autism/witAang.htm ------------------------ Peptizyde: I got this for my daughter who had scary reactions to dairy, food colorings, and some additives. She is a new person now, had been making gradual improvements with the cod liver oil and nutritional supplements, but now she can have dairy again as long as she takes her peptizyde, and her behavior is actually better than when she's not taking it! http://www.autismcoach.com/peptizyde_and_hn-zyme_prime.htm " In a survey of 260 parents over a 7 month period, 90% of parents using Peptizyde and HN-Zyme Prime together reported sustained improvements in behavior and level of ability. " ---------------------------------- Three-lac (probiotic) " ThreeLac is a powder, dissolved on the tongue or mixed in a small amount of liquid and taken orally after a meal. Ingredients are: Bacillus Coagulans (200 million CFU), Bacillus Subtilis (25 million CFU), Group D, nontoxic strain of Enterococcus Faecalis (25 million CFU), Lemon Juice Powder, Refined Yeast Powder (feeds the live bacteria in storage and does not affect yeast sensitive individuals), and Fiber (FOS). " They also had remarkable results in their study, privately funded by a couple. http://www.autism-study.com/ --------------------------------- Wobenzyme - enzyme blend I know a woman whose daughter got autism-type symptoms from lyme and her mother believes wobenzyme is one of the things that reversed this over the course of 9 months or so. It's a good enzyme blend. --------------------------------- Chelation is helpful to many children with autism and often results in decrease in symptoms, but careful not to try it on childen who also have lyme (could have gotten it prenatally) because it can cause a worsening of symptoms. http://www.autismwebsite.com/ARI/treatment/chelationsafety.htm There are also reports of children with autism who have had very good improvements on antiparasitic medications (after travelling abroad and picking something up) that stopped when the antiparasitic meds stopped. Artemisinin is one that mothers of a couple of autistic children (recovering) told me helped minimize their symptoms. It's very safe and effective against protozoal parasites like malaria and babesia, but unless the family has travelled abroad or knows they have lyme, that's probably a long shot. ------------------------------------- It does sound like the issue that causes autism in most children is primarily a combination of toxins, especially heavy metals and mercury, and dysbiosis; I've read studies where nearly all autistic children tested had some form of dysbiosis, much more than children from the general population. A doctor in Europe found that the Measles part of the MMR stays in the GI of some children after vaccination, and even contaminates the GI of their unvaccinated siblings. Could this be the source of the dysbiosis of some children with autism? Sounds likely. He was fired from his job and threatened for publishing the study. http://www.autismcanada.org/News/wakefield_autism4.pdf --- In , " donfree228 " <df228@...> wrote: > > Hi > > I have a friend with Autism. > > Does anyone know of any research on healing mild cases of Autism in > young kids. It is related to Leaky gut. > > I know Donna Gates has some information on Autism but I don't like > the marketing aspect of her approach. > > I have been a member of this group for 9 months and have learned so > much about healing foods. > > Do I suggest to this family just start making cultured vegetables and > fermented foods for their autistic child? > > Any ideas or links on autism would be appreicated. > Thanks > Don > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2006 Report Share Posted September 22, 2006 I don't have personal experience but some cases seem to respond to NAET. I think the site is NAET.com Irene At 10:12 AM 9/22/06, you wrote: >Hi > >I have a friend with Autism. > >Does anyone know of any research on healing mild cases of Autism in >young kids. It is related to Leaky gut. > >I know Donna Gates has some information on Autism but I don't like >the marketing aspect of her approach. > >I have been a member of this group for 9 months and have learned so >much about healing foods. > >Do I suggest to this family just start making cultured vegetables and >fermented foods for their autistic child? > >Any ideas or links on autism would be appreicated. >Thanks >Don > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2006 Report Share Posted September 24, 2006 On 9/24/06, Emma Davies <emma@...> wrote: > Probably because they are all in some way incompletely treating the > same metabolic problem. I personally regard GFCF as the least useful > based on the anecdotal failure rates. Here's the argument why: > > http://www.mercola.com/2004/jun/26/autism_malnutrition.htm This thoroughly unreferenced and speculative article strikes me as rather dogmatic: >Science cannot support the presumption that a casein-free diet reduces autistic >symptoms. All the literature on casein restriction indicates this only causes a >developmental delay. If an improvement is seen on a casein-free diet, it is only >because of the removal of free lactose, and the removal of constipating foods. Suze has a book containing a chapter by Shaw that supplies 17 references for the elevated levels of undigested gluten-derived and casein-derived peptides in the urine of children with autism (and adults with schizophrenia). The highly speculative conclusion that lactose is the sole component of milk contributing to autism cannot account for the observation of undigested *peptides* in the urine of autistic children, and she doesn't attempt to explain that fact. Nowhere in the article does she so much as mention gluteomorphin (or gliadorphin) or caseomorphin, the undigested opioids derived from gluten and casein, that are elevated in autistic children and her observation that " casein restriction " leads to " developmental delay " is entirely vague, unreferenced, and has no clear relevance to the actual discussion. The highly speculative and unsupported assertion that raw milk is quite fine becuase it doesn't have dead heat-treated bacteria in it contradicts the experiences of broad numbers of people who have discovered that they can NOT tolerate raw milk. And the idea that because lactose might play a role that casein cannot is unnecessarily and counterproductively myopic. Chris -- The Truth About Cholesterol Find Out What Your Doctor Isn't Telling You: http://www.cholesterol-and-health.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2006 Report Share Posted September 24, 2006 > --- " donfree228 " <df228@> wrote: > > > I have a friend with Autism. > > > > Does anyone know of any research on healing mild cases of Autism > > in young kids. It is related to Leaky gut. > --- " Emma Davies " <emma@...> wrote: > Yoghurt and quickly cultured (12 h) kefir should be okay, but of > course these contain casein! I've read that milk from Jersey cows has a form of casein that most people can tolerate - especially if it is not pastuerized. It may, however, be difficult to find a dairy with all Jersey cows. Most use Holsteins because of much greater milk production (quantity wins over quality as usual). In Texas, the Strykly dairy is all Jersey and offers raw milk and cream (local pickup) and cheeses (mail order): http://www.texascheese.com/ I wish there were more dairies like this one! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2006 Report Share Posted September 24, 2006 , > I've read that milk from Jersey cows has a form of casein that most > people can tolerate - especially if it is not pastuerized. Jersey doesn't matter. It is A1 versus A2 milk. You are more likely to get more A2 beta-casein (a good thing) with Jersey cows than with Holstein cows, but the cow being Jersey does not gurantee straight A2 milk. Genetic testing is needed for this. Straight A2 milk may not yield significant quantities of a particular beta-casein-derived opioid, BCM-7: ============== http://www.a2corporation.com/index.php/pi_pageid/40 Beta casein A1 has been shown to yield the protein fragment, or peptide, termed 'beta casomorphin 7' (BCM-7). First reported in 1979 [6] as a casein derived opioid, BCM-7 can subsequently be metabolised to beta casomorphin 5 (BCM-5). These peptides have the 3rd highest and highest affinity, or binding, to opiate receptors of those reviewed [1]. BCM-7 has been shown to be significantly more resilient to metabolic processing [7] than other studied food derived exomorphins . Thus, by removing beta casein A1 from milk and thereby eliminating the yield of BCM-7 the risk presented by opioid peptide yield from milk may be significantly reduced. ============== However, this is not the only dietary opioid that can be derived from milk protein: ============= http://www.a2corporation.com/index.php/pi_pageid/40 A review published in 2000 [5] describes in detail a range of peptides with opioid function that derive from all the casein subgroups; a-casein, b-casein, k-casein, as well as from whey fraction proteins a-lactalbumin, b-lactoglobulin and serum albumin. Thus noted, eliminating beta casein from milk would not remove the total theoretical risk of opioid peptide yield. ============== Nevertheless, there is some evidence that drinking A2 milk reduces opioid-related symptoms and BCM-7 has the third highest affinity for opiate receptors and can metabolically yield BCM-5 which has the highest, so it may be much more physiologically significant than the others. This leads the A2 Corporation, who has a financial stake in the matter, to believe: ============== http://www.a2corporation.com/index.php/pi_pageid/40 These reports, coupled with published research, lead A2 Corporation to believe that the exclusion of beta casein A1 from milk products may render exomorphin yields physiologically insignificant. =============== Chris -- The Truth About Cholesterol Find Out What Your Doctor Isn't Telling You: http://www.cholesterol-and-health.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2006 Report Share Posted September 24, 2006 Emma, > Perhaps I'm not using a fair sample, but I'm signed up to a lot of > autism groups, and most of them are coming from a post-GFCF > perspective, having tried it and moved on, it having helped for some, > but not fixed things. But the fact that it is insufficient does not make it unnecessary. Chris -- The Truth About Cholesterol Find Out What Your Doctor Isn't Telling You: http://www.cholesterol-and-health.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2006 Report Share Posted September 24, 2006 Emma, > > But the fact that it is insufficient does not make it unnecessary. > Sorry, didn't mean to suggest that. Probably the fastest dietary > approach is a combination of all of the diets, i.e. pretty much > nothing but meat and eggs... uh, actually, eggs contain lutein, so... > just meat... You didn't say it, but the author of that ridiculously dogmatic article stated it pretty clearly, and advocated drinking raw milk with free abandon. I'm sure drinking lactose-free raw yogurt or something would be far better than fresh pasteurized milk, and maybe some of the opioid precursors are even broken down, but if some of them are not, and the opioid theory has any merit (which it appears to), then the suggestion could be harmful. And whether or not properly fermented raw yogurt has opioid potential is something that needs to be answered by additional research, not dogmatic assumptions. I haven't researched the various diets myself so I don't know if they have equal merit, but the ones with clear merit should be combined. Chris -- The Truth About Cholesterol Find Out What Your Doctor Isn't Telling You: http://www.cholesterol-and-health.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 21, 2006 Report Share Posted October 21, 2006 For stories on the Eli Lily Bandit go to: http://www.tompaine.com/Archive/scontent/6932.html Eventually, Dick Armey, ret. Congressman from TX admitted that he did it after being asked by the Whitehouse. The WHitehouse denied it. The " inserted " 2 paragraphs were almost the same exact language that Frist used in a similar bill earlier that year. He denied any connection. They finally succeded in Dec 05 - they secretly added the same thing into the Defense Appropiations Bill. Vaccine makers and makers of the vaccine toxic componets can no longer be held accountable. There are many peer-reviewed research papers concerning mercury & neurodevelopmental disorders. Comparison of Blood and Brain Mercury Levels in Infant Monkeys Exposed to Methylmercury or Vaccines Containing Thimerosal, M. Burbacher, Danny D. Shen, Noelle Liberato, S. Grant, Elsa Cernichiari, and son, April 2005 Environmental mercury release, special education rates, and autism disorder: an ecological study of Texas F. Palmer, Blanchard, Zachary Stein, Mandell, , Health & Place, March 2005 Thimerosal and autism? A plausible hypothesis that should not be dismissed Blaxill, Redwood, Bernard, Medical Hypothesis, May 2004 A Case-Control Study of Mercury Burden in Children with Autistic Spectrum Disorders, Bradstreet, Geier, Kartzinel, , Geier - Journal of American Physicians and Surgeons, Volume 8, Number 3, Summer 2003 We found out the hard way. After years of unknowingly exposing our son to mold thru our SUV, then a vaccine with mercury & aluminum. He started with the fatigue, bone pain & sinus infections for 2 yrs or so. Docs said it was growing pains, fatigue was also from growing. Then a hep b shot. Wham - the spiral downhill was unstoppable. At 10 yrs old, within weeks he started showing symptoms that were autistic-like. Hand-flapping, rocking, perserveration, toe walking, touch aversion, etc. These were all actions to relieve pain - he was in total pain from head to toe all day long for months. As we made dietary changes, started IVIG and other nutrient additions, he got somewhat better. But only when we found the mold source and got him away from it, did he get well enough to go off of the weekly IVIG. He's 18 now, and extremely sensitive to mold/mycotoxins. Unfortunately, a 15-20 minute encounter can set him back for months. It's scarey not knowing when you'll walk into something like that. At least you can see the mack truck barreling down. The toxic soup that's in our children's environments is really scarey. Hard to figure how they can survive all of these toxins. SW In , " npzjewel6 " <npzjewel6@...> wrote: > > among other " real " possible causes of autism,(not TV)- I have heard > that immunizations have been in question. > Just wondered- what ever happened with the story of the " Mercury > Bandit " . Does anyone know if they found out who?? > Came across this story again while people on this board were > discussing the flu vaccine. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 29, 2006 Report Share Posted October 29, 2006 Old post, I know, but the autism/mercury debate has always fascinated me because my oldest is on the autistic spectrum (Asperger's) but he had no vaccinations until he was six when he got tetanus for a dog bite...yet he's had problems since he was 2 days old. So I always wonder if maybe he would've been worse had we done the full immunization route...and maybe not doing so helped him avoid full autism...? Cathe [] autism among other " real " possible causes of autism,(not TV)- I have heard that immunizations have been in question. Just wondered- what ever happened with the story of the " Mercury Bandit " . Does anyone know if they found out who?? Came across this story again while people on this board were discussing the flu vaccine. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 29, 2006 Report Share Posted October 29, 2006 Hi, I too wonder, my son also on the spectrum (Aspergers) and S.I. issues. My thinking is this, I would much rather have him with Autism than another medical issue like Mumps or worse. Those are just my thoughts on the subject. [] autism among other " real " possible causes of autism,(not TV)- I have heard that immunizations have been in question. Just wondered- what ever happened with the story of the " Mercury Bandit " . Does anyone know if they found out who?? Came across this story again while people on this board were discussing the flu vaccine. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2006 Report Share Posted October 30, 2006 Mumps- childhood illness with fever and swollen glands that lasts for 2 weeks - Autism can last a lifetime. Mumps is a walk in the park compared to Autism. I sure every parent of a full blown autistic child would trade mumps for autism any day of the week. I've had mumps as have millions of people. You stayed home from school for 2 weeks, big deal! In very RARE instances complications can set in, usually with children already immune compromised. Example of CDC scare tactics about common childhood diseases. Chickenpox. After they developed a vaccine they needed a market for it. All of a sudden it was a horrible disease. Kills 100 per year, so they said. Checking the MMW (Morbidity Mortality Weekly, the CDC's own publication) of the 100 that got chickenpox each year, 40 were children with the vast majority being immune compromised already. They other 60 were elderly. Now, the adverse reactions to the vaccine, 2001-2005, 25,218 injured - 62 dead. That's only the ones reported, according to the CDC's Dr. Kessler 6/2/93, those numbers are under reported by about 99%. Something to be said for natural immunity. SW P.S. Now they're marketing the shingles vaccine - so many getting shingles from the virus shedding of the chickenpox vaccine. (a live virus vaccine like the chickenpox vaccine will shed the virus for up to three weeks after vaccination.) Nothing like keeping people scared! In , " renee " <rzornrn@...> wrote: > > Hi, > I too wonder, my son also on the spectrum (Aspergers) and S.I. issues. My thinking is this, I would much rather have him with Autism than another medical issue like Mumps or worse. Those are just my thoughts on the subject. > > [] autism > > among other " real " possible causes of autism,(not TV)- I have heard > that immunizations have been in question. > Just wondered- what ever happened with the story of the " Mercury > Bandit " . Does anyone know if they found out who?? > Came across this story again while people on this board were > discussing the flu vaccine. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2006 Report Share Posted October 30, 2006 Ok than what a Polio another immunization. Hello Lifetime disease. I would much rather have my autisc child than full blown Polio. Naural immunity for colds Yes. So what now we don't immunize? Come on you think the CDC is out kill all of us. Give me a break... [] autism > > among other " real " possible causes of autism,(not TV)- I have heard > that immunizations have been in question. > Just wondered- what ever happened with the story of the " Mercury > Bandit " . Does anyone know if they found out who?? > Came across this story again while people on this board were > discussing the flu vaccine. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2006 Report Share Posted October 30, 2006 No but I think they might be filled with ex pharmacy people and goal is to get business for their friends in the pharmacy business. I do not think they are impartial. They may even be getting a salary or other monetary rewards from them: <http://www.wtop.com/index.php?nid=104 & sid=945193> I do believe the pharmacy industry have become like drug cartels, pushers and I think some of them are white color criminals. I think the polio vaccine is important but if it has mercury in it I would not take it. I have personal experience because my older sister had polio at age five and one leg is not functional. However she has had full life, did fantastic in college, got an high paying executive job, got married, had two beautiful and smart kids, has beautiful home, she and her husband are quite wealthy now, vacations in nicest of place. Hardly the life any autistic kid would ever have. -- renee <rzornrn@...> wrote: > Ok than what a Polio another immunization. > Hello Lifetime disease. I would much rather > have Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.