Guest guest Posted September 25, 2007 Report Share Posted September 25, 2007 We started with IV’s once a week and then I added the pills daily. The only thing different we saw was increase speech and understanding, etc. Not sure what you should try- good luck. Are you on the autism treatment list? They might know too. On 9/24/07 9:22 PM, " snowhite6503 " <gentsandgems@...> wrote: My son just started taking L-Glutathione 100 mg. yesterday. Has anyone else tried this and if so, did you see any initial side effects? Changes in behavior? Did this stop within a short period of time? His behavior has been VERY aggresive the past 2 days and this is the ONLY thing that has changed! I am with a D.A.N. doctor now but unfortunately I have not had much help from this particular doctor. Any past experience with this that you can share would be greatly appreciated!!! Thank you! Tammy McNair Mommy of 11 Proud mommy of someone with Autism! www.letsbeatautismnow.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2007 Report Share Posted September 25, 2007 Thank you. Could you send me the link to the autism treatment list? I am really concerned. The lutathione and glutamine were the 2 supps that concerned me the most when I started down this path. (I did the DAN protocol for 16 months prior to getting a DAN doctor). I asked my DAN doctor which one I needed and she went to her office and came back and said both. I asked her which one I should start first and she said either. I had to request bloodwork to test the level of vitamins and minerals. She told me I could not get a complete work up done unless I went through a specific lab and that medicaid would not cover it. But I know of others that have had this test run and medicaid covered it. Instead we are waiting on the results of the bloodwork we did get done. She asked me what I wanted tested!!! I told her everything that they would allow. Sorry to rant on. I am just very unhappy with what I am getting from her right now. And I had waited for such a long time to get in with a DAN doctor, ya know? I just thought that she would be telling me what we needed to do.....not me telling her. I guess I expected too much. Thank you again! Tammy McNair Mommy of 11 Proud mommy of someone with Autism! www.letsbeatautismnow.com > > > > > > > > > > > My son just started taking L-Glutathione 100 mg. yesterday. Has anyone > > else tried this and if so, did you see any initial side effects? > > Changes in behavior? Did this stop within a short period of time? > > > > His behavior has been VERY aggresive the past 2 days and this is the > > ONLY thing that has changed! I am with a D.A.N. doctor now but > > unfortunately I have not had much help from this particular doctor. > > > > Any past experience with this that you can share would be greatly > > appreciated!!! > > > > Thank you! > > Tammy McNair > > Mommy of 11 > > Proud mommy of someone with Autism! > > www.letsbeatautismnow.com > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2007 Report Share Posted September 25, 2007 Thank you so much for posting this Dr. Stoller!!! I feel much better! I know that she has the medical training but I think she is just too busy with her regular practice. And I am guilty of knowing much more than what she expected....she herself stated this! I requested a parasite test and she asked why and I explained that he is on potato milk. Potatoes being night shade vegetables, parasites would feed on them. She gave a smirk and wrote out the Rx for the test. I will talk to her some more in depth this week. I waited so long to find a DAN doctor that would take medicaid (after fighting to get it), and I am really hoping that this will eventually work out. I even " considered " going to medical school and every conference in between and then any training so that I could become a DAN doctor! But at the age of 42 and not knowing for sure what my son's future might hold, I think I will leave the medical aspect in the hands of the experts. But also take your advice and go with my heart and intuition. Thank you again so much!!! Tammy McNair Mommy of 11 Proud mommy of someone with Autism! www.letsbeatautismnow.com > > As a " DAN " doc...let me point out that just being a DAN doc is no guarantee of being anything more than someone who took the training offered by the ARI at sometime in the past several years. > > Being up-to-date in treating autistic children means having very current knowledge of what is taking place as interventions change slightly every few months (MONTHS!). For example, only now is m B12 and HBOT getting into the books that are coming out, such as the 3rd ed of Children with Starving Brains, or the new Jepson book. > > When I see a new patient I tell the parents that they are going to be the doc...I am going to be the facilitator. THey get a reading list of four of the latest books (required reading). And we start peeling the layers back and go down the rabbit hole of biomedical intervention. It is a lot of work for me but even more for parents. > > Do not trust doctors trust yourself. Read everything you can, attend conferences or download the lectures which is possible for both DAN and USAAA meetings. > > It is a lot to ask a parent to get up to speed on biochemistry, but this is what must be done for now. > > > > > > > KP Stoller, MD > President, International Hyperbaric Medical Assoc > Medical Director, Hyperbaric Medical Center of New Mexico > www.hbotnm.com > > Please note: message attached > > > _____________________________________________________________ > Garage overflowing? Click for steel buildings that are durable and easy to install. > http://3rdpartyoffers.netzero.net/TGL2221/fc/Ioyw6i4uigf5UU9EUXlvIGex4 gbEeoploO30EX2uG8eyWBleoNkW6Q/ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2007 Report Share Posted September 25, 2007 > > As a " DAN " doc...let me point out that just being a DAN doc is no guarantee of being anything more than someone who took the training offered by the ARI at sometime in the past several years. > I have to agree with Dr. Stoller on this. Any doctor can become a DAN! doctor. You can find the full spectrum of quality: great ones and not so good ones. Parents still must do their " due diligence " , ask around, google, get referrals, etc. This is why local biomedical parent support lists are so important. There are over 2800 listing on alone that have something to do with autism. Many of those are local support groups that have sprung up over the last five years or so. You should be able to find a support list not too far away geographically from where ever you live in the US. Not all parents, however, are at high education levels and simply cannot do the " required reading " and get self-taught in medical science to be one of Dr. Stoller's patients. The children of less educated parents deserve a chance at recovery, too. We have not only children from less educated, economically disadvantaged families, but also untold number of abandoned autistic foster children who have no loving parents to advocate for them. Are they less any deserving at a chance for recovery? This is in no way a criticism of who Dr. Stoller choses to serve as his patient base, but only to say that families, like the children, come in a spectrum of need. The solutions go beyond what one or a dozen heroic doctors like Stoller can do. We must have political solutions to help children and families across the board of needs and abilities. Lenny Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2007 Report Share Posted September 25, 2007 And that my dear friend Lenny, is the crux of the problem. The children without advocates will continue without advocates, without treatment, without voices, without help, until the message, the methodology, and the treatments and recovery are mainstream. Until it is recognized in the mainstream that our children are damaged and not born defective and hence it is completely or partially reversible, nothing will change. That is our mission. It is what thousands of us have been screaming for years and years, nearly unheard, and what McCarthy is voicing to the world for us, since no one found our voices valid or important. I am filled with so much hope these days, that we are finally taking the tiny steps to recognition, legitimacy, and hence action. I do admit though I still have my fingers crossed behind my back. Kendra > > > > As a " DAN " doc...let me point out that just being a DAN doc is no > guarantee of being anything more than someone who took the training > offered by the ARI at sometime in the past several years. > > > > I have to agree with Dr. Stoller on this. Any doctor can become a > DAN! doctor. You can find the full spectrum of quality: great ones > and not so good ones. Parents still must do their " due diligence " , > ask around, google, get referrals, etc. > > This is why local biomedical parent support lists are so important. > There are over 2800 listing on alone that have something > to do with autism. Many of those are local support groups that have > sprung up over the last five years or so. You should be able to find > a support list not too far away geographically from where ever you > live in the US. > > Not all parents, however, are at high education levels and simply > cannot do the " required reading " and get self-taught in medical > science to be one of Dr. Stoller's patients. The children of less > educated parents deserve a chance at recovery, too. We have not only > children from less educated, economically disadvantaged families, but > also untold number of abandoned autistic foster children who have no > loving parents to advocate for them. Are they less any deserving at a > chance for recovery? > > This is in no way a criticism of who Dr. Stoller choses to serve as > his patient base, but only to say that families, like the children, > come in a spectrum of need. The solutions go beyond what one or a > dozen heroic doctors like Stoller can do. > > We must have political solutions to help children and families across > the board of needs and abilities. > > Lenny > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2007 Report Share Posted September 25, 2007 WITH INSURANCE COVERAGE so parents don't have to choose between putting food on the table and treating their child. > > Amen, Kendra. You got me thinking. > > > > Imagine if just ONE typical biomed approach to treating autism could > become mainstream right now. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2007 Report Share Posted September 25, 2007 I think the chelatingkids 2 group might be helpful too: chelatingkids2/ We also do the IV glutathione for our 8 year old daugher with some noticable increases in understanding language and she is following directions wonderfully now. I have not done oral glutathione because I am afraid it will increase her yeast (this happened when we tried nebulized glutathione so now I try to avoid the gut as much as possible with things that are known to raise yeast levels.) Tina > > > > > > > > > > > My son just started taking L-Glutathione 100 mg. yesterday. Has anyone > > else tried this and if so, did you see any initial side effects? > > Changes in behavior? Did this stop within a short period of time? > > > > His behavior has been VERY aggresive the past 2 days and this is the > > ONLY thing that has changed! I am with a D.A.N. doctor now but > > unfortunately I have not had much help from this particular doctor. > > > > Any past experience with this that you can share would be greatly > > appreciated!!! > > > > Thank you! > > Tammy McNair > > Mommy of 11 > > Proud mommy of someone with Autism! > > www.letsbeatautismnow.com > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2007 Report Share Posted September 25, 2007 Here-here Dr Stoller! I am always second guessing the doc's and looking things up myself. Sometimes I tell them what I want to do and see if they agree. I do trust the doctor that does our daughters chelation but I still challenge somethings and I finally for the first time feel that I AM IN CHARGE! I will never see eye to eye with my pediatrician though--I only see him now for the yearly physical and if ANYONE EVER come near my kid again with a syringe I WILL RUN FOR THE HILLS (after kicking his ass first!)!!!!!! Thank you Dr Stoller for you insight, Tina > > Is is a good thing to have a doc you can trust. > > Having said that....doctors have lost the right to be trusted. > > > KP Stoller, MD > President, International Hyperbaric Medical Assoc > Medical Director, Hyperbaric Medical Center of New Mexico > www.hbotnm.com > > > > _____________________________________________________________ > Garage overflowing? Click for steel buildings that are durable and easy to install. > http://3rdpartyoffers.netzero.net/TGL2221/fc/Ioyw6i4uiggy6ZSNt8Z20XvV KHVHtu1NCouEaNreYK4cQYof4utC5W/ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2007 Report Share Posted September 25, 2007 Your child could have a sulfur issue. Some kids cannot handle Glutathione, or not every day. You may want to do this once a week. But talk to your DR about this. My son cannot handle lots of Glutathione, lots of kids cannot. And not all kids can handle the Methly B-12 shots at first. You may have to start out using Hydroxy B-12 or Cyno B-12 In EOHarm , " snowhite6503 " <gentsandgems@...> wrote: > > My son just started taking L-Glutathione 100 mg. yesterday. Has anyone > else tried this and if so, did you see any initial side effects? > Changes in behavior? Did this stop within a short period of time? > > His behavior has been VERY aggresive the past 2 days and this is the > ONLY thing that has changed! I am with a D.A.N. doctor now but > unfortunately I have not had much help from this particular doctor. > > Any past experience with this that you can share would be greatly > appreciated!!! > > > Thank you! > Tammy McNair > Mommy of 11 > Proud mommy of someone with Autism! > www.letsbeatautismnow.com > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2007 Report Share Posted September 25, 2007 Yes I was told by our DAN we were seeing then that it can stir up yeast and boy did it! We had to go back on Diflucan for 3 weeks because of it. But not with IV form as it bypasses the gut. Tina > > > > > > > > > > > > > > > > > My son just started taking L-Glutathione 100 mg. yesterday. Has > anyone > > > else tried this and if so, did you see any initial side effects? > > > Changes in behavior? Did this stop within a short period of time? > > > > > > His behavior has been VERY aggresive the past 2 days and this is > the > > > ONLY thing that has changed! I am with a D.A.N. doctor now but > > > unfortunately I have not had much help from this particular > doctor. > > > > > > Any past experience with this that you can share would be greatly > > > appreciated!!! > > > > > > Thank you! > > > Tammy McNair > > > Mommy of 11 > > > Proud mommy of someone with Autism! > > > www.letsbeatautismnow.com > > > > > > > > > > > > > > > > > > --------------------------------- > Be a better Globetrotter. Get better travel answers from someone who knows. > Answers - Check it out. > Quote Link to comment Share on other sites More sharing options...
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