Guest guest Posted May 2, 2006 Report Share Posted May 2, 2006 Hi Dr. Neubrander described shortterm hyperactivity, stimming, mouthing objects and and over-emotional behavior outbursts as all short term positives which should last 4-6 months and then settle down. So hyperactivity is unfortunately one of the side effects of MB 12 that lasts 4-6 months. My son was also really bad. We did find that upping his zinc monomethionine (one of the 2 most aborbable forms) really helped. Also, Dr. Neubrander mentioned at the Long Beach DAN that about 20% of kids can not tolerate folinic and/or TMG while on MB 12, even if they tolerated it before MB 12. Taurine also really helped calm him down. At first our negative MB12 side effects were "good and tolerable" and he started using complex sentences like "I just can't take it any more." ********* The really strange is, that folinic as the exact opposite on most of the kids, it calms them down and maximizes the benefits of MB 12. But then he downward spiraled and we took him off folinic and TMG and added zinc, magnesium sulfate and taurine and everything got better. We tried several times to add back the TMG and folinic, but the regression got really out of control. Folinic made my son completely insane and out of control spacey. Folinic is recommended by virtually all DANs as the way to maximize the benefits of MB12, but some kids just can not tolerate it. He started thriving on MB 12 with taurine, magnesium sulfate, folate and 110 mgs of zinc per day (except we skip the chelation PM dose). We have since reduced the zinc and he is doing fine. But the extra zinc really helped pull us through the rough six months. The key is to only change one thing at a time and give each change two weeks. When things got out of control we stopped almost everything and restarted with just zinc. We then added back MB 12 and one item at a time that was recommended by Dr. Neubrander and also Stan at the Long Beach DAN. They also told us to replace the folinic with folate. Dr. Kartzinel wants us to now try something else (Laucdrin I think) instead of folate, but I have not gotten to it yet and to try adding DMG to replace the TMG. Again, we have not gotten to it yet. VeraChapnalli <chapnalli@...> wrote: Kim, Hyperactivity is very common with MB-12 and Dr. Deth told me if you can stand it to keep going and hyperactivity may be overcome. How long have you been on valtrex and do you have an antifungal. CJ is on nystatin (yes I know we have to switch and will) but I am starting to see either yeast die off or nystatin isn't quite getting it all while on Valtrex. Structured 2to 1 may not be the worst thing, it may be better to give him more and then move him out later when he regains skills. Although I really know how hard it is to take when they go backwards at all. Where are the acutaly regressions. In learning, in behaviors or just ability to get the info out?? Did you possible start giving Calcium or folinic acid at all? ->From: Kim GIll <kim.gill@...>>Date: Tue May 02 11:04:34 CDT 2006>mb12 valtrex >Subject: Re: What if you can't handle the Valtrex?->Thanks : Admittedly, I have not been looking/searching his >body for any rash. I thought that it would just be obvious, but now >i will look a little more. Thanks for the info...this is very >disturbing. Just 2 months ago, our son was almost ready for >mainstream kindergarten. Now, his teachers/therapists thinks he has >regressed so much that he will be in a structured kindergarten with a >2 to 1 ratio. >>The weird thing is...he also started the MB-12 shots, which made him >really really hyper. I wonder if I should stop those?>>Kim>>>>>> >>> > Do you know about the healing regression period. I get excited >> when I see my son 6yr 48lbs getting the viral reactions because it >> means it's working. Every reaction has not lasted long. I think >> though you are on a small dose and you should be splitting it up 3x >> per day. My son is on 750mgtotal with 250mg split 3x. CJ got a >cold >> sore yesterday that is already gone and I cheered for joy. >> > ->> > >> > >From: mermaidawnmom <Mermaidawn@>>> > >Date: Thu Apr 27 07:43:34 CDT 2006>> > >mb12 valtrex >> > >Subject: What if you can't handle the Valtrex?>> > >> > >Hi all,>> > >>> > >My son had tested positive to herpes, CMV and very high EB all >IgG >> > >results. We started valtrex early this week, 500mg once a day >(he >> is >> > >almost 6 and aprox 50lbs) and after the second day he developed >> very >> > >red itchy eyes (I had posted about this earlier). I had never >seen >> this >> > >reaction to anything we have given him before, he really could >not >> keep >> > >them open until after a long hot shower. Our DAN has asked us >to >> hold >> > >the Valtrex and said maybe we would start at a 1/2 a dose again >in >> a >> > >few days. >> > >>> > >If he cannont tolerate the Valtrex, what are the alternatives? >> I'm >> > >sure there are some natural anti-virals but I don't know what >they >> are >> > >and would like to research them before our dr's apt. on Monday.>> > >>> > >Thanks for any advice>> > >>> > >>> > >>> > >>> > >>> > > >> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 2, 2006 Report Share Posted May 2, 2006 Hi Dr. Neubrander described shortterm hyperactivity, stimming, mouthing objects and and over-emotional behavior outbursts as all short term positives which should last 4-6 months and then settle down. So hyperactivity is unfortunately one of the side effects of MB 12 that lasts 4-6 months. My son was also really bad. We did find that upping his zinc monomethionine (one of the 2 most aborbable forms) really helped. Also, Dr. Neubrander mentioned at the Long Beach DAN that about 20% of kids can not tolerate folinic and/or TMG while on MB 12, even if they tolerated it before MB 12. Taurine also really helped calm him down. At first our negative MB12 side effects were "good and tolerable" and he started using complex sentences like "I just can't take it any more." ********* The really strange is, that folinic as the exact opposite on most of the kids, it calms them down and maximizes the benefits of MB 12. But then he downward spiraled and we took him off folinic and TMG and added zinc, magnesium sulfate and taurine and everything got better. We tried several times to add back the TMG and folinic, but the regression got really out of control. Folinic made my son completely insane and out of control spacey. Folinic is recommended by virtually all DANs as the way to maximize the benefits of MB12, but some kids just can not tolerate it. He started thriving on MB 12 with taurine, magnesium sulfate, folate and 110 mgs of zinc per day (except we skip the chelation PM dose). We have since reduced the zinc and he is doing fine. But the extra zinc really helped pull us through the rough six months. The key is to only change one thing at a time and give each change two weeks. When things got out of control we stopped almost everything and restarted with just zinc. We then added back MB 12 and one item at a time that was recommended by Dr. Neubrander and also Stan at the Long Beach DAN. They also told us to replace the folinic with folate. Dr. Kartzinel wants us to now try something else (Laucdrin I think) instead of folate, but I have not gotten to it yet and to try adding DMG to replace the TMG. Again, we have not gotten to it yet. VeraChapnalli <chapnalli@...> wrote: Kim, Hyperactivity is very common with MB-12 and Dr. Deth told me if you can stand it to keep going and hyperactivity may be overcome. How long have you been on valtrex and do you have an antifungal. CJ is on nystatin (yes I know we have to switch and will) but I am starting to see either yeast die off or nystatin isn't quite getting it all while on Valtrex. Structured 2to 1 may not be the worst thing, it may be better to give him more and then move him out later when he regains skills. Although I really know how hard it is to take when they go backwards at all. Where are the acutaly regressions. In learning, in behaviors or just ability to get the info out?? Did you possible start giving Calcium or folinic acid at all? ->From: Kim GIll <kim.gill@...>>Date: Tue May 02 11:04:34 CDT 2006>mb12 valtrex >Subject: Re: What if you can't handle the Valtrex?->Thanks : Admittedly, I have not been looking/searching his >body for any rash. I thought that it would just be obvious, but now >i will look a little more. Thanks for the info...this is very >disturbing. Just 2 months ago, our son was almost ready for >mainstream kindergarten. Now, his teachers/therapists thinks he has >regressed so much that he will be in a structured kindergarten with a >2 to 1 ratio. >>The weird thing is...he also started the MB-12 shots, which made him >really really hyper. I wonder if I should stop those?>>Kim>>>>>> >>> > Do you know about the healing regression period. I get excited >> when I see my son 6yr 48lbs getting the viral reactions because it >> means it's working. Every reaction has not lasted long. I think >> though you are on a small dose and you should be splitting it up 3x >> per day. My son is on 750mgtotal with 250mg split 3x. CJ got a >cold >> sore yesterday that is already gone and I cheered for joy. >> > ->> > >> > >From: mermaidawnmom <Mermaidawn@>>> > >Date: Thu Apr 27 07:43:34 CDT 2006>> > >mb12 valtrex >> > >Subject: What if you can't handle the Valtrex?>> > >> > >Hi all,>> > >>> > >My son had tested positive to herpes, CMV and very high EB all >IgG >> > >results. We started valtrex early this week, 500mg once a day >(he >> is >> > >almost 6 and aprox 50lbs) and after the second day he developed >> very >> > >red itchy eyes (I had posted about this earlier). I had never >seen >> this >> > >reaction to anything we have given him before, he really could >not >> keep >> > >them open until after a long hot shower. Our DAN has asked us >to >> hold >> > >the Valtrex and said maybe we would start at a 1/2 a dose again >in >> a >> > >few days. >> > >>> > >If he cannont tolerate the Valtrex, what are the alternatives? >> I'm >> > >sure there are some natural anti-virals but I don't know what >they >> are >> > >and would like to research them before our dr's apt. on Monday.>> > >>> > >Thanks for any advice>> > >>> > >>> > >>> > >>> > >>> > > >> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2006 Report Share Posted May 3, 2006 -- Hi, I know how disturbing a regression is my daughter is in one. and she in now in second grade. I am desparately trying to figure out the regression. We are wondering if we got a false negative on her last urnine provocative challenge. ALso, we had a case of lice and had to treat for that twice.We tried all of the natural rmedies and none of them worked. I cannot figure out the reason for the regression. My question is does or has anyone used DMpS IV provocative that is what our new Dan is suggesting( we switched as we moved across state) I am a little leary of it but will do it. He thinks that will yuield a us a more accurate response in regards to her metal situraion. ALso, what is TMG? I read that in one of these emails? THanks a ton!! 12valtrex , Vera <sircarlito@...> wrote: > > Hi > > Dr. Neubrander described shortterm hyperactivity, stimming, mouthing objects and and over-emotional behavior outbursts as all short term positives which should last 4-6 months and then settle down. > > So hyperactivity is unfortunately one of the side effects of MB 12 that lasts 4-6 months. My son was also really bad. We did find that upping his zinc monomethionine (one of the 2 most aborbable forms) really helped. Also, Dr. Neubrander mentioned at the Long Beach DAN that about 20% of kids can not tolerate folinic and/or TMG while on MB 12, even if they tolerated it before MB 12. Taurine also really helped calm him down. At first our negative MB12 side effects were " good and tolerable " and he started using complex sentences like " I just can't take it any more. " ********* The really strange is, that folinic as the exact opposite on most of the kids, it calms them down and maximizes the benefits of MB 12. > > But then he downward spiraled and we took him off folinic and TMG and added zinc, magnesium sulfate and taurine and everything got better. We tried several times to add back the TMG and folinic, but the regression got really out of control. Folinic made my son completely insane and out of control spacey. Folinic is recommended by virtually all DANs as the way to maximize the benefits of MB12, but some kids just can not tolerate it. He started thriving on MB 12 with taurine, magnesium sulfate, folate and 110 mgs of zinc per day (except we skip the chelation PM dose). We have since reduced the zinc and he is doing fine. But the extra zinc really helped pull us through the rough six months. The key is to only change one thing at a time and give each change two weeks. When things got out of control we stopped almost everything and restarted with just zinc. We then added back MB 12 and one item at a time that was recommended by Dr. Neubrander and also Stan at the Long > Beach DAN. They also told us to replace the folinic with folate. Dr. Kartzinel wants us to now try something else (Laucdrin I think) instead of folate, but I have not gotten to it yet and to try adding DMG to replace the TMG. Again, we have not gotten to it yet. > > Vera > Chapnalli <chapnalli@...> wrote: > Kim, > Hyperactivity is very common with MB-12 and Dr. Deth told me if you can stand it to keep going and hyperactivity may be overcome. How long have you been on valtrex and do you have an antifungal. CJ is on nystatin (yes I know we have to switch and will) but I am starting to see either yeast die off or nystatin isn't quite getting it all while on Valtrex. Structured 2to 1 may not be the worst thing, it may be better to give him more and then move him out later when he regains skills. Although I really know how hard it is to take when they go backwards at all. Where are the acutaly regressions. In learning, in behaviors or just ability to get the info out?? Did you possible start giving Calcium or folinic acid at all? - > > >From: Kim GIll <kim.gill@...> > >Date: Tue May 02 11:04:34 CDT 2006 > >mb12 valtrex > >Subject: Re: What if you can't handle the Valtrex?- > > >Thanks : Admittedly, I have not been looking/searching his > >body for any rash. I thought that it would just be obvious, but now > >i will look a little more. Thanks for the info...this is very > >disturbing. Just 2 months ago, our son was almost ready for > >mainstream kindergarten. Now, his teachers/therapists thinks he has > >regressed so much that he will be in a structured kindergarten with a > >2 to 1 ratio. > > > >The weird thing is...he also started the MB-12 shots, which made him > >really really hyper. I wonder if I should stop those? > > > >Kim > > > > > > > > > >> > > >> > Do you know about the healing regression period. I get excited > >> when I see my son 6yr 48lbs getting the viral reactions because it > >> means it's working. Every reaction has not lasted long. I think > >> though you are on a small dose and you should be splitting it up 3x > >> per day. My son is on 750mgtotal with 250mg split 3x. CJ got a > >cold > >> sore yesterday that is already gone and I cheered for joy. > >> > - > >> > > >> > >From: mermaidawnmom <Mermaidawn@> > >> > >Date: Thu Apr 27 07:43:34 CDT 2006 > >> > >mb12 valtrex > >> > >Subject: What if you can't handle the Valtrex? > >> > > >> > >Hi all, > >> > > > >> > >My son had tested positive to herpes, CMV and very high EB all > >IgG > >> > >results. We started valtrex early this week, 500mg once a day > >(he > >> is > >> > >almost 6 and aprox 50lbs) and after the second day he developed > >> very > >> > >red itchy eyes (I had posted about this earlier). I had never > >seen > >> this > >> > >reaction to anything we have given him before, he really could > >not > >> keep > >> > >them open until after a long hot shower. Our DAN has asked us > >to > >> hold > >> > >the Valtrex and said maybe we would start at a 1/2 a dose again > >in > >> a > >> > >few days. > >> > > > >> > >If he cannont tolerate the Valtrex, what are the alternatives? > >> I'm > >> > >sure there are some natural anti-virals but I don't know what > >they > >> are > >> > >and would like to research them before our dr's apt. on Monday. > >> > > > >> > >Thanks for any advice > >> > > > >> > > > >> > > > >> > > > >> > > > >> > > > >> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2006 Report Share Posted May 3, 2006 -- Hi, I know how disturbing a regression is my daughter is in one. and she in now in second grade. I am desparately trying to figure out the regression. We are wondering if we got a false negative on her last urnine provocative challenge. ALso, we had a case of lice and had to treat for that twice.We tried all of the natural rmedies and none of them worked. I cannot figure out the reason for the regression. My question is does or has anyone used DMpS IV provocative that is what our new Dan is suggesting( we switched as we moved across state) I am a little leary of it but will do it. He thinks that will yuield a us a more accurate response in regards to her metal situraion. ALso, what is TMG? I read that in one of these emails? THanks a ton!! 12valtrex , Vera <sircarlito@...> wrote: > > Hi > > Dr. Neubrander described shortterm hyperactivity, stimming, mouthing objects and and over-emotional behavior outbursts as all short term positives which should last 4-6 months and then settle down. > > So hyperactivity is unfortunately one of the side effects of MB 12 that lasts 4-6 months. My son was also really bad. We did find that upping his zinc monomethionine (one of the 2 most aborbable forms) really helped. Also, Dr. Neubrander mentioned at the Long Beach DAN that about 20% of kids can not tolerate folinic and/or TMG while on MB 12, even if they tolerated it before MB 12. Taurine also really helped calm him down. At first our negative MB12 side effects were " good and tolerable " and he started using complex sentences like " I just can't take it any more. " ********* The really strange is, that folinic as the exact opposite on most of the kids, it calms them down and maximizes the benefits of MB 12. > > But then he downward spiraled and we took him off folinic and TMG and added zinc, magnesium sulfate and taurine and everything got better. We tried several times to add back the TMG and folinic, but the regression got really out of control. Folinic made my son completely insane and out of control spacey. Folinic is recommended by virtually all DANs as the way to maximize the benefits of MB12, but some kids just can not tolerate it. He started thriving on MB 12 with taurine, magnesium sulfate, folate and 110 mgs of zinc per day (except we skip the chelation PM dose). We have since reduced the zinc and he is doing fine. But the extra zinc really helped pull us through the rough six months. The key is to only change one thing at a time and give each change two weeks. When things got out of control we stopped almost everything and restarted with just zinc. We then added back MB 12 and one item at a time that was recommended by Dr. Neubrander and also Stan at the Long > Beach DAN. They also told us to replace the folinic with folate. Dr. Kartzinel wants us to now try something else (Laucdrin I think) instead of folate, but I have not gotten to it yet and to try adding DMG to replace the TMG. Again, we have not gotten to it yet. > > Vera > Chapnalli <chapnalli@...> wrote: > Kim, > Hyperactivity is very common with MB-12 and Dr. Deth told me if you can stand it to keep going and hyperactivity may be overcome. How long have you been on valtrex and do you have an antifungal. CJ is on nystatin (yes I know we have to switch and will) but I am starting to see either yeast die off or nystatin isn't quite getting it all while on Valtrex. Structured 2to 1 may not be the worst thing, it may be better to give him more and then move him out later when he regains skills. Although I really know how hard it is to take when they go backwards at all. Where are the acutaly regressions. In learning, in behaviors or just ability to get the info out?? Did you possible start giving Calcium or folinic acid at all? - > > >From: Kim GIll <kim.gill@...> > >Date: Tue May 02 11:04:34 CDT 2006 > >mb12 valtrex > >Subject: Re: What if you can't handle the Valtrex?- > > >Thanks : Admittedly, I have not been looking/searching his > >body for any rash. I thought that it would just be obvious, but now > >i will look a little more. Thanks for the info...this is very > >disturbing. Just 2 months ago, our son was almost ready for > >mainstream kindergarten. Now, his teachers/therapists thinks he has > >regressed so much that he will be in a structured kindergarten with a > >2 to 1 ratio. > > > >The weird thing is...he also started the MB-12 shots, which made him > >really really hyper. I wonder if I should stop those? > > > >Kim > > > > > > > > > >> > > >> > Do you know about the healing regression period. I get excited > >> when I see my son 6yr 48lbs getting the viral reactions because it > >> means it's working. Every reaction has not lasted long. I think > >> though you are on a small dose and you should be splitting it up 3x > >> per day. My son is on 750mgtotal with 250mg split 3x. CJ got a > >cold > >> sore yesterday that is already gone and I cheered for joy. > >> > - > >> > > >> > >From: mermaidawnmom <Mermaidawn@> > >> > >Date: Thu Apr 27 07:43:34 CDT 2006 > >> > >mb12 valtrex > >> > >Subject: What if you can't handle the Valtrex? > >> > > >> > >Hi all, > >> > > > >> > >My son had tested positive to herpes, CMV and very high EB all > >IgG > >> > >results. We started valtrex early this week, 500mg once a day > >(he > >> is > >> > >almost 6 and aprox 50lbs) and after the second day he developed > >> very > >> > >red itchy eyes (I had posted about this earlier). I had never > >seen > >> this > >> > >reaction to anything we have given him before, he really could > >not > >> keep > >> > >them open until after a long hot shower. Our DAN has asked us > >to > >> hold > >> > >the Valtrex and said maybe we would start at a 1/2 a dose again > >in > >> a > >> > >few days. > >> > > > >> > >If he cannont tolerate the Valtrex, what are the alternatives? > >> I'm > >> > >sure there are some natural anti-virals but I don't know what > >they > >> are > >> > >and would like to research them before our dr's apt. on Monday. > >> > > > >> > >Thanks for any advice > >> > > > >> > > > >> > > > >> > > > >> > > > >> > > > >> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2006 Report Share Posted May 3, 2006 , Please research very carefully before doing the IV your DAN is recommending. That stuff scares the daylights out of me based on what I have read on the autism list. There are other ways to assess metal issues that are non-invasive and run no risks. Anne > > >> > > > >> > Do you know about the healing regression period. I get excited > > >> when I see my son 6yr 48lbs getting the viral reactions because it > > >> means it's working. Every reaction has not lasted long. I think > > >> though you are on a small dose and you should be splitting it up 3x > > >> per day. My son is on 750mgtotal with 250mg split 3x. CJ got a > > >cold > > >> sore yesterday that is already gone and I cheered for joy. > > >> > - > > >> > > > >> > >From: mermaidawnmom <Mermaidawn@> > > >> > >Date: Thu Apr 27 07:43:34 CDT 2006 > > >> > >mb12 valtrex > > >> > >Subject: What if you can't handle the Valtrex? > > >> > > > >> > >Hi all, > > >> > > > > >> > >My son had tested positive to herpes, CMV and very high EB all > > >IgG > > >> > >results. We started valtrex early this week, 500mg once a day > > >(he > > >> is > > >> > >almost 6 and aprox 50lbs) and after the second day he developed > > >> very > > >> > >red itchy eyes (I had posted about this earlier). I had never > > >seen > > >> this > > >> > >reaction to anything we have given him before, he really could > > >not > > >> keep > > >> > >them open until after a long hot shower. Our DAN has asked us > > >to > > >> hold > > >> > >the Valtrex and said maybe we would start at a 1/2 a dose again > > >in > > >> a > > >> > >few days. > > >> > > > > >> > >If he cannont tolerate the Valtrex, what are the alternatives? > > >> I'm > > >> > >sure there are some natural anti-virals but I don't know what > > >they > > >> are > > >> > >and would like to research them before our dr's apt. on Monday. > > >> > > > > >> > >Thanks for any advice > > >> > > > > >> > > > > >> > > > > >> > > > > >> > > > > >> > > > > >> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2006 Report Share Posted May 3, 2006 , Please research very carefully before doing the IV your DAN is recommending. That stuff scares the daylights out of me based on what I have read on the autism list. There are other ways to assess metal issues that are non-invasive and run no risks. Anne > > >> > > > >> > Do you know about the healing regression period. I get excited > > >> when I see my son 6yr 48lbs getting the viral reactions because it > > >> means it's working. Every reaction has not lasted long. I think > > >> though you are on a small dose and you should be splitting it up 3x > > >> per day. My son is on 750mgtotal with 250mg split 3x. CJ got a > > >cold > > >> sore yesterday that is already gone and I cheered for joy. > > >> > - > > >> > > > >> > >From: mermaidawnmom <Mermaidawn@> > > >> > >Date: Thu Apr 27 07:43:34 CDT 2006 > > >> > >mb12 valtrex > > >> > >Subject: What if you can't handle the Valtrex? > > >> > > > >> > >Hi all, > > >> > > > > >> > >My son had tested positive to herpes, CMV and very high EB all > > >IgG > > >> > >results. We started valtrex early this week, 500mg once a day > > >(he > > >> is > > >> > >almost 6 and aprox 50lbs) and after the second day he developed > > >> very > > >> > >red itchy eyes (I had posted about this earlier). I had never > > >seen > > >> this > > >> > >reaction to anything we have given him before, he really could > > >not > > >> keep > > >> > >them open until after a long hot shower. Our DAN has asked us > > >to > > >> hold > > >> > >the Valtrex and said maybe we would start at a 1/2 a dose again > > >in > > >> a > > >> > >few days. > > >> > > > > >> > >If he cannont tolerate the Valtrex, what are the alternatives? > > >> I'm > > >> > >sure there are some natural anti-virals but I don't know what > > >they > > >> are > > >> > >and would like to research them before our dr's apt. on Monday. > > >> > > > > >> > >Thanks for any advice > > >> > > > > >> > > > > >> > > > > >> > > > > >> > > > > >> > > > > >> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2006 Report Share Posted May 3, 2006 I was scared to death of the IV DMPS also. However, after 16 mos. of TDDMPS and minimal gains, we did our first IV DMPS 3 wks ago and the pulls were phenomenal. All except 3 metals (berillium, thorium and platinum) were high green to almost yellow (including mercury and lead) and tin and bismuth were high yellow. This is far beyond his pulls of all of his previous urine tests on chelation. We are going to have his 2nd IV next week. Ty 3.9 yrs > > > >> > > > > >> > Do you know about the healing regression period. I get > excited > > > >> when I see my son 6yr 48lbs getting the viral reactions > because it > > > >> means it's working. Every reaction has not lasted long. I > think > > > >> though you are on a small dose and you should be splitting it > up 3x > > > >> per day. My son is on 750mgtotal with 250mg split 3x. CJ > got a > > > >cold > > > >> sore yesterday that is already gone and I cheered for joy. > > > >> > - > > > >> > > > > >> > >From: mermaidawnmom <Mermaidawn@> > > > >> > >Date: Thu Apr 27 07:43:34 CDT 2006 > > > >> > >mb12 valtrex > > > >> > >Subject: What if you can't handle the > Valtrex? > > > >> > > > > >> > >Hi all, > > > >> > > > > > >> > >My son had tested positive to herpes, CMV and very high EB > all > > > >IgG > > > >> > >results. We started valtrex early this week, 500mg once a > day > > > >(he > > > >> is > > > >> > >almost 6 and aprox 50lbs) and after the second day he > developed > > > >> very > > > >> > >red itchy eyes (I had posted about this earlier). I had > never > > > >seen > > > >> this > > > >> > >reaction to anything we have given him before, he really > could > > > >not > > > >> keep > > > >> > >them open until after a long hot shower. Our DAN has > asked us > > > >to > > > >> hold > > > >> > >the Valtrex and said maybe we would start at a 1/2 a dose > again > > > >in > > > >> a > > > >> > >few days. > > > >> > > > > > >> > >If he cannont tolerate the Valtrex, what are the > alternatives? > > > >> I'm > > > >> > >sure there are some natural anti-virals but I don't know > what > > > >they > > > >> are > > > >> > >and would like to research them before our dr's apt. on > Monday. > > > >> > > > > > >> > >Thanks for any advice > > > >> > > > > > >> > > > > > >> > > > > > >> > > > > > >> > > > > > >> > > > > > >> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2006 Report Share Posted May 3, 2006 I was scared to death of the IV DMPS also. However, after 16 mos. of TDDMPS and minimal gains, we did our first IV DMPS 3 wks ago and the pulls were phenomenal. All except 3 metals (berillium, thorium and platinum) were high green to almost yellow (including mercury and lead) and tin and bismuth were high yellow. This is far beyond his pulls of all of his previous urine tests on chelation. We are going to have his 2nd IV next week. Ty 3.9 yrs > > > >> > > > > >> > Do you know about the healing regression period. I get > excited > > > >> when I see my son 6yr 48lbs getting the viral reactions > because it > > > >> means it's working. Every reaction has not lasted long. I > think > > > >> though you are on a small dose and you should be splitting it > up 3x > > > >> per day. My son is on 750mgtotal with 250mg split 3x. CJ > got a > > > >cold > > > >> sore yesterday that is already gone and I cheered for joy. > > > >> > - > > > >> > > > > >> > >From: mermaidawnmom <Mermaidawn@> > > > >> > >Date: Thu Apr 27 07:43:34 CDT 2006 > > > >> > >mb12 valtrex > > > >> > >Subject: What if you can't handle the > Valtrex? > > > >> > > > > >> > >Hi all, > > > >> > > > > > >> > >My son had tested positive to herpes, CMV and very high EB > all > > > >IgG > > > >> > >results. We started valtrex early this week, 500mg once a > day > > > >(he > > > >> is > > > >> > >almost 6 and aprox 50lbs) and after the second day he > developed > > > >> very > > > >> > >red itchy eyes (I had posted about this earlier). I had > never > > > >seen > > > >> this > > > >> > >reaction to anything we have given him before, he really > could > > > >not > > > >> keep > > > >> > >them open until after a long hot shower. Our DAN has > asked us > > > >to > > > >> hold > > > >> > >the Valtrex and said maybe we would start at a 1/2 a dose > again > > > >in > > > >> a > > > >> > >few days. > > > >> > > > > > >> > >If he cannont tolerate the Valtrex, what are the > alternatives? > > > >> I'm > > > >> > >sure there are some natural anti-virals but I don't know > what > > > >they > > > >> are > > > >> > >and would like to research them before our dr's apt. on > Monday. > > > >> > > > > > >> > >Thanks for any advice > > > >> > > > > > >> > > > > > >> > > > > > >> > > > > > >> > > > > > >> > > > > > >> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 4, 2006 Report Share Posted May 4, 2006 My question is does or has anyone used DMpS IV provocative that is , My family doctor has done this for 20 years and I did it once but once i visited the DMPS backfire I just couldn't bring my self to try it again. With that said, I do know some kids it has helped some. such controversy with this http://www.dmpsbackfire.com/default.shtml http://home.earthlink.net/~aprokofiew/We live in a world in which we need to share responsibility. It's easy to say "It's not my child, not my community, not my world, not my problem." Then there are those who see the need and respond. I consider those people my heroes. -- Fred " Mr." , Children's TV Show Star 12valtrex , Vera <sircarlito@...> wrote:>> Hi> > Dr. Neubrander described shortterm hyperactivity, stimming,mouthing objects and and over-emotional behavior outbursts as allshort term positives which should last 4-6 months and then settle down. > > So hyperactivity is unfortunately one of the side effects of MB 12that lasts 4-6 months. My son was also really bad. We did find thatupping his zinc monomethionine (one of the 2 most aborbable forms)really helped. Also, Dr. Neubrander mentioned at the Long Beach DANthat about 20% of kids can not tolerate folinic and/or TMG while on MB12, even if they tolerated it before MB 12. Taurine also reallyhelped calm him down. At first our negative MB12 side effects were"good and tolerable" and he started using complex sentences like "Ijust can't take it any more." ********* The really strange is, thatfolinic as the exact opposite on most of the kids, it calms them downand maximizes the benefits of MB 12.> > But then he downward spiraled and we took him off folinic and TMGand added zinc, magnesium sulfate and taurine and everything gotbetter. We tried several times to add back the TMG and folinic, butthe regression got really out of control. Folinic made my soncompletely insane and out of control spacey. Folinic is recommendedby virtually all DANs as the way to maximize the benefits of MB12, butsome kids just can not tolerate it. He started thriving on MB 12 withtaurine, magnesium sulfate, folate and 110 mgs of zinc per day (exceptwe skip the chelation PM dose). We have since reduced the zinc and heis doing fine. But the extra zinc really helped pull us through therough six months. The key is to only change one thing at a time andgive each change two weeks. When things got out of control we stoppedalmost everything and restarted with just zinc. We then added back MB12 and one item at a time that was recommended by Dr. Neubrander andalso Stan at the Long> Beach DAN. They also told us to replace the folinic with folate. Dr. Kartzinel wants us to now try something else (Laucdrin I think)instead of folate, but I have not gotten to it yet and to try addingDMG to replace the TMG. Again, we have not gotten to it yet.> > Vera> Chapnalli <chapnalli@...> wrote:> Kim,> Hyperactivity is very common with MB-12 and Dr. Dethtold me if you can stand it to keep going and hyperactivity may beovercome. How long have you been on valtrex and do you have anantifungal. CJ is on nystatin (yes I know we have to switch and will)but I am starting to see either yeast die off or nystatin isn't quitegetting it all while on Valtrex. Structured 2to 1 may not be theworst thing, it may be better to give him more and then move him outlater when he regains skills. Although I really know how hard it isto take when they go backwards at all. Where are the acutalyregressions. In learning, in behaviors or just ability to get theinfo out?? Did you possible start giving Calcium or folinic acid atall? -> > >From: Kim GIll <kim.gill@...>> >Date: Tue May 02 11:04:34 CDT 2006> >mb12 valtrex > >Subject: Re: What if you can't handle theValtrex?-> > >Thanks : Admittedly, I have not been looking/searching his > >body for any rash. I thought that it would just be obvious, but now > >i will look a little more. Thanks for the info...this is very > >disturbing. Just 2 months ago, our son was almost ready for > >mainstream kindergarten. Now, his teachers/therapists thinks he has > >regressed so much that he will be in a structured kindergarten with a > >2 to 1 ratio. > >> >The weird thing is...he also started the MB-12 shots, which made him > >really really hyper. I wonder if I should stop those?> >> >Kim> >> >> >> >> >> >> >> > Do you know about the healing regression period. I get excited > >> when I see my son 6yr 48lbs getting the viral reactions because it > >> means it's working. Every reaction has not lasted long. I think > >> though you are on a small dose and you should be splitting it up 3x > >> per day. My son is on 750mgtotal with 250mg split 3x. CJ got a > >cold > >> sore yesterday that is already gone and I cheered for joy. > >> > -> >> > > >> > >From: mermaidawnmom <Mermaidawn@>> >> > >Date: Thu Apr 27 07:43:34 CDT 2006> >> > >mb12 valtrex > >> > >Subject: What if you can't handle the Valtrex?> >> > > >> > >Hi all,> >> > >> >> > >My son had tested positive to herpes, CMV and very high EB all > >IgG > >> > >results. We started valtrex early this week, 500mg once a day > >(he > >> is > >> > >almost 6 and aprox 50lbs) and after the second day he developed > >> very > >> > >red itchy eyes (I had posted about this earlier). I had never > >seen > >> this > >> > >reaction to anything we have given him before, he really could > >not > >> keep > >> > >them open until after a long hot shower. Our DAN has asked us > >to > >> hold > >> > >the Valtrex and said maybe we would start at a 1/2 a dose again > >in > >> a > >> > >few days. > >> > >> >> > >If he cannont tolerate the Valtrex, what are the alternatives? > >> I'm > >> > >sure there are some natural anti-virals but I don't know what > >they > >> are > >> > >and would like to research them before our dr's apt. on Monday.> >> > >> >> > >Thanks for any advice> >> > >> >> > >> >> > >> >> > >> >> > >> >> > > > >> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 4, 2006 Report Share Posted May 4, 2006 My question is does or has anyone used DMpS IV provocative that is , My family doctor has done this for 20 years and I did it once but once i visited the DMPS backfire I just couldn't bring my self to try it again. With that said, I do know some kids it has helped some. such controversy with this http://www.dmpsbackfire.com/default.shtml http://home.earthlink.net/~aprokofiew/We live in a world in which we need to share responsibility. It's easy to say "It's not my child, not my community, not my world, not my problem." Then there are those who see the need and respond. I consider those people my heroes. -- Fred " Mr." , Children's TV Show Star 12valtrex , Vera <sircarlito@...> wrote:>> Hi> > Dr. Neubrander described shortterm hyperactivity, stimming,mouthing objects and and over-emotional behavior outbursts as allshort term positives which should last 4-6 months and then settle down. > > So hyperactivity is unfortunately one of the side effects of MB 12that lasts 4-6 months. My son was also really bad. We did find thatupping his zinc monomethionine (one of the 2 most aborbable forms)really helped. Also, Dr. Neubrander mentioned at the Long Beach DANthat about 20% of kids can not tolerate folinic and/or TMG while on MB12, even if they tolerated it before MB 12. Taurine also reallyhelped calm him down. At first our negative MB12 side effects were"good and tolerable" and he started using complex sentences like "Ijust can't take it any more." ********* The really strange is, thatfolinic as the exact opposite on most of the kids, it calms them downand maximizes the benefits of MB 12.> > But then he downward spiraled and we took him off folinic and TMGand added zinc, magnesium sulfate and taurine and everything gotbetter. We tried several times to add back the TMG and folinic, butthe regression got really out of control. Folinic made my soncompletely insane and out of control spacey. Folinic is recommendedby virtually all DANs as the way to maximize the benefits of MB12, butsome kids just can not tolerate it. He started thriving on MB 12 withtaurine, magnesium sulfate, folate and 110 mgs of zinc per day (exceptwe skip the chelation PM dose). We have since reduced the zinc and heis doing fine. But the extra zinc really helped pull us through therough six months. The key is to only change one thing at a time andgive each change two weeks. When things got out of control we stoppedalmost everything and restarted with just zinc. We then added back MB12 and one item at a time that was recommended by Dr. Neubrander andalso Stan at the Long> Beach DAN. They also told us to replace the folinic with folate. Dr. Kartzinel wants us to now try something else (Laucdrin I think)instead of folate, but I have not gotten to it yet and to try addingDMG to replace the TMG. Again, we have not gotten to it yet.> > Vera> Chapnalli <chapnalli@...> wrote:> Kim,> Hyperactivity is very common with MB-12 and Dr. Dethtold me if you can stand it to keep going and hyperactivity may beovercome. How long have you been on valtrex and do you have anantifungal. CJ is on nystatin (yes I know we have to switch and will)but I am starting to see either yeast die off or nystatin isn't quitegetting it all while on Valtrex. Structured 2to 1 may not be theworst thing, it may be better to give him more and then move him outlater when he regains skills. Although I really know how hard it isto take when they go backwards at all. Where are the acutalyregressions. In learning, in behaviors or just ability to get theinfo out?? Did you possible start giving Calcium or folinic acid atall? -> > >From: Kim GIll <kim.gill@...>> >Date: Tue May 02 11:04:34 CDT 2006> >mb12 valtrex > >Subject: Re: What if you can't handle theValtrex?-> > >Thanks : Admittedly, I have not been looking/searching his > >body for any rash. I thought that it would just be obvious, but now > >i will look a little more. Thanks for the info...this is very > >disturbing. Just 2 months ago, our son was almost ready for > >mainstream kindergarten. Now, his teachers/therapists thinks he has > >regressed so much that he will be in a structured kindergarten with a > >2 to 1 ratio. > >> >The weird thing is...he also started the MB-12 shots, which made him > >really really hyper. I wonder if I should stop those?> >> >Kim> >> >> >> >> >> >> >> > Do you know about the healing regression period. I get excited > >> when I see my son 6yr 48lbs getting the viral reactions because it > >> means it's working. Every reaction has not lasted long. I think > >> though you are on a small dose and you should be splitting it up 3x > >> per day. My son is on 750mgtotal with 250mg split 3x. CJ got a > >cold > >> sore yesterday that is already gone and I cheered for joy. > >> > -> >> > > >> > >From: mermaidawnmom <Mermaidawn@>> >> > >Date: Thu Apr 27 07:43:34 CDT 2006> >> > >mb12 valtrex > >> > >Subject: What if you can't handle the Valtrex?> >> > > >> > >Hi all,> >> > >> >> > >My son had tested positive to herpes, CMV and very high EB all > >IgG > >> > >results. We started valtrex early this week, 500mg once a day > >(he > >> is > >> > >almost 6 and aprox 50lbs) and after the second day he developed > >> very > >> > >red itchy eyes (I had posted about this earlier). I had never > >seen > >> this > >> > >reaction to anything we have given him before, he really could > >not > >> keep > >> > >them open until after a long hot shower. Our DAN has asked us > >to > >> hold > >> > >the Valtrex and said maybe we would start at a 1/2 a dose again > >in > >> a > >> > >few days. > >> > >> >> > >If he cannont tolerate the Valtrex, what are the alternatives? > >> I'm > >> > >sure there are some natural anti-virals but I don't know what > >they > >> are > >> > >and would like to research them before our dr's apt. on Monday.> >> > >> >> > >Thanks for any advice> >> > >> >> > >> >> > >> >> > >> >> > >> >> > > > >> > > Quote Link to comment Share on other sites More sharing options...
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