Guest guest Posted November 28, 2011 Report Share Posted November 28, 2011 Has anyone here tried a glutathione IV? I ask because I seem to remember my DAN practitioner suggesting it for my son a few years ago and now the neurologist that I am researching for my mom's parkinsons is a big fan of glutathione IVs. Does anyone have any first had experience with the glutathione IV? Thanks! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2011 Report Share Posted November 29, 2011 Hi , I have two boys with autism, and my mom has Parkinson's. We have been doing IV glutathione with my youngest son off and on for years. He does fantastic with them, and asks for them all the time. He is non-verbal, but points to the crook of his arm (where the IV goes) and makes the " ssss " sound for shot. We would take him more often, but we pay 100% of the cost out of pocket, and they are 100 bucks each. For a while we were going 2 times a week, and boy does that add up! Your post here reminds me he is overdue to go in, so I will be making an appointment today. I have been wanting my mom to do them for ages, but she lives 100 miles away. She visits for weeks at a time, so I just need to coordinate our schedules so I can get her a new patient appointment with Nicks doctor. Nick has the gene mutation GSTM1 - Null, which means he is naturally very low in glutathine since he is missing that gene that makes one of the glutathione producing enzymes. Since my mom has Parkinsons, it is a pretty good guess that she is GSTM1 - null as well, although she hasn't been tested. If money was no object, I would get glutathione IV's as well, so I could avoid Parkinsons and other health problems in the future. I think glutathione is a major player in our family. Between my two boys with autism, it is Nick, my youngest, who is the most severe. He is the one I gave Tylenol (which depletes glutathione) at each vaccine appointment - I didn't do that with his older brother. So I think it was all that Tylenol on top of his GSTM1 - null status on top of all the toxins in vaccines that caused Nick to be so severely injured. Sylvia > > Has anyone here tried a glutathione IV? I ask because I seem to remember my DAN practitioner suggesting it for my son a few years ago and now the neurologist that I am researching for my mom's parkinsons is a big fan of glutathione IVs. Does anyone have any first had experience with the glutathione IV? Thanks! > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 30, 2011 Report Share Posted November 30, 2011 Regarding a family history of both autism and Parkinson's, I would seriously pursue Lyme disease as e causative. > > > > Has anyone here tried a glutathione IV? I ask because I seem to remember my DAN practitioner suggesting it for my son a few years ago and now the neurologist that I am researching for my mom's parkinsons is a big fan of glutathione IVs. Does anyone have any first had experience with the glutathione IV? Thanks! > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 2, 2011 Report Share Posted December 2, 2011 Sylvia,Can you educate me about GSTM1 testing? Where did you get it done? Is it Yasko? Also, did you get a PIC line placed or do you just insert a new IV each time?BTW, we share the same name--same spelling.Best,Sylvia Hi , I have two boys with autism, and my mom has Parkinson's. We have been doing IV glutathione with my youngest son off and on for years. He does fantastic with them, and asks for them all the time. He is non-verbal, but points to the crook of his arm (where the IV goes) and makes the "ssss" sound for shot. We would take him more often, but we pay 100% of the cost out of pocket, and they are 100 bucks each. For a while we were going 2 times a week, and boy does that add up! Your post here reminds me he is overdue to go in, so I will be making an appointment today. I have been wanting my mom to do them for ages, but she lives 100 miles away. She visits for weeks at a time, so I just need to coordinate our schedules so I can get her a new patient appointment with Nicks doctor. Nick has the gene mutation GSTM1 - Null, which means he is naturally very low in glutathine since he is missing that gene that makes one of the glutathione producing enzymes. Since my mom has Parkinsons, it is a pretty good guess that she is GSTM1 - null as well, although she hasn't been tested. If money was no object, I would get glutathione IV's as well, so I could avoid Parkinsons and other health problems in the future. I think glutathione is a major player in our family. Between my two boys with autism, it is Nick, my youngest, who is the most severe. He is the one I gave Tylenol (which depletes glutathione) at each vaccine appointment - I didn't do that with his older brother. So I think it was all that Tylenol on top of his GSTM1 - null status on top of all the toxins in vaccines that caused Nick to be so severely injured. Sylvia > > Has anyone here tried a glutathione IV? I ask because I seem to remember my DAN practitioner suggesting it for my son a few years ago and now the neurologist that I am researching for my mom's parkinsons is a big fan of glutathione IVs. Does anyone have any first had experience with the glutathione IV? Thanks! > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 2, 2011 Report Share Posted December 2, 2011 Hi Sylvia! (judging by your name, you must be a wonderufl person! The GSTM1 test was on a panel we did years ago from Genova Labs: http://www.gdx.net/product/10038 This made a lot of sense to me when we learned this. My oldest son was showing problems developmemtally (I had no idea about the vaccine link back then), so when Nick was born, I was determined I was going to do everything " by the book " to ensure nothing went wrong. WORST thing I have ever done. Nick got Tylenol before every single vaccine visit, which I never did with my oldsest son because I was never one to give drugs without a good reason. But this was (and still is!) the advice of most all pediatricians, so I did. Nick's reactions to every vaccine was extreme, much worse than his older brothers. Ofcourse the doctors office blew me off each and every time I called, and said all these reactions (screaming for hours, projectile vomiting, fever) were normal and not to worry he would be fine. He was not ever fine. So the son that had more vaccines and hardly any Tylenol is mildly affected with autism, and the son that had copious amounts of Tylenol and less vaccines is severe. If I had known then that he was GSTM1 null, he never would have had Tylenol, EVER. But IV glutathione is helping. He just does regular IV's in the doctors office. The practice is mostly adults, and everyone says he is the best patient ;0) He doesn't even flinch when the needle goes in! Sylvia > > > > > > Has anyone here tried a glutathione IV? I ask because I seem to remember my DAN practitioner suggesting it for my son a few years ago and now the neurologist that I am researching for my mom's parkinsons is a big fan of glutathione IVs. Does anyone have any first had experience with the glutathione IV? Thanks! > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 2, 2011 Report Share Posted December 2, 2011 Thanks Sylvia! (I love writing "my" name to someone else. There aren't many of us).SylviaSent from my iPad Hi Sylvia! (judging by your name, you must be a wonderufl person! The GSTM1 test was on a panel we did years ago from Genova Labs: http://www.gdx.net/product/10038 This made a lot of sense to me when we learned this. My oldest son was showing problems developmemtally (I had no idea about the vaccine link back then), so when Nick was born, I was determined I was going to do everything "by the book" to ensure nothing went wrong. WORST thing I have ever done. Nick got Tylenol before every single vaccine visit, which I never did with my oldsest son because I was never one to give drugs without a good reason. But this was (and still is!) the advice of most all pediatricians, so I did. Nick's reactions to every vaccine was extreme, much worse than his older brothers. Ofcourse the doctors office blew me off each and every time I called, and said all these reactions (screaming for hours, projectile vomiting, fever) were normal and not to worry he would be fine. He was not ever fine. So the son that had more vaccines and hardly any Tylenol is mildly affected with autism, and the son that had copious amounts of Tylenol and less vaccines is severe. If I had known then that he was GSTM1 null, he never would have had Tylenol, EVER. But IV glutathione is helping. He just does regular IV's in the doctors office. The practice is mostly adults, and everyone says he is the best patient ;0) He doesn't even flinch when the needle goes in! Sylvia > > > > > > Has anyone here tried a glutathione IV? I ask because I seem to remember my DAN practitioner suggesting it for my son a few years ago and now the neurologist that I am researching for my mom's parkinsons is a big fan of glutathione IVs. Does anyone have any first had experience with the glutathione IV? Thanks! > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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