Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of " Kansas City. " I don't know who you see, but just throwing that out there in case you are looking for a change. I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 Oops,should have finished reading... LOL :-) I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 That is the doctor that wouldn't listen to us. I had tried to talk with him about the new retrovirus and he flat out pretty much yeld at me why would you even want to know there arn't any treatments just forget about it. I just think that if you are treating a certain kind of illness that keeping up on recent events would help. Through him we have established that Luke has cronic inflamation, and that he has yeast infection, clostridia, but the dr. isn't willing to give us diflucan, or try anti-virials. He does go to the DAN confrences but doesn't get info about new treatments. We really are tired of waiting around doing the not so effective treatments give him the real stuff. To: mb12 valtrex Sent: Sat, May 8, 2010 10:08:20 AMSubject: Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of "Kansas City." I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 That is the doctor that wouldn't listen to us. I had tried to talk with him about the new retrovirus and he flat out pretty much yeld at me why would you even want to know there arn't any treatments just forget about it. I just think that if you are treating a certain kind of illness that keeping up on recent events would help. Through him we have established that Luke has cronic inflamation, and that he has yeast infection, clostridia, but the dr. isn't willing to give us diflucan, or try anti-virials. He does go to the DAN confrences but doesn't get info about new treatments. We really are tired of waiting around doing the not so effective treatments give him the real stuff. To: mb12 valtrex Sent: Sat, May 8, 2010 10:08:20 AMSubject: Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of "Kansas City." I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 That is the doctor that wouldn't listen to us. I had tried to talk with him about the new retrovirus and he flat out pretty much yeld at me why would you even want to know there arn't any treatments just forget about it. I just think that if you are treating a certain kind of illness that keeping up on recent events would help. Through him we have established that Luke has cronic inflamation, and that he has yeast infection, clostridia, but the dr. isn't willing to give us diflucan, or try anti-virials. He does go to the DAN confrences but doesn't get info about new treatments. We really are tired of waiting around doing the not so effective treatments give him the real stuff. To: mb12 valtrex Sent: Sat, May 8, 2010 10:08:20 AMSubject: Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of "Kansas City." I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 For some great info about using valtrex with a child with autism you may want to read Stan Kurtz's paper www.talkaboutcuringautism.org/.../comprehensive-anti-viral-autism.htm Subject: ValtrexTo: mb12 valtrex Date: Saturday, May 8, 2010, 11:05 AM I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 Wow, like I said Christel really raves about him. That is too bad. :-( That is the doctor that wouldn't listen to us. I had tried to talk with him about the new retrovirus and he flat out pretty much yeld at me why would you even want to know there arn't any treatments just forget about it. I just think that if you are treating a certain kind of illness that keeping up on recent events would help. Through him we have established that Luke has cronic inflamation, and that he has yeast infection, clostridia, but the dr. isn't willing to give us diflucan, or try anti-virials. He does go to the DAN confrences but doesn't get info about new treatments. We really are tired of waiting around doing the not so effective treatments give him the real stuff. To: mb12 valtrex Sent: Sat, May 8, 2010 10:08:20 AMSubject: Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of " Kansas City. " I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 Wow, like I said Christel really raves about him. That is too bad. :-( That is the doctor that wouldn't listen to us. I had tried to talk with him about the new retrovirus and he flat out pretty much yeld at me why would you even want to know there arn't any treatments just forget about it. I just think that if you are treating a certain kind of illness that keeping up on recent events would help. Through him we have established that Luke has cronic inflamation, and that he has yeast infection, clostridia, but the dr. isn't willing to give us diflucan, or try anti-virials. He does go to the DAN confrences but doesn't get info about new treatments. We really are tired of waiting around doing the not so effective treatments give him the real stuff. To: mb12 valtrex Sent: Sat, May 8, 2010 10:08:20 AMSubject: Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of " Kansas City. " I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 jenny a few things, we see dr baptist and our son recovered with him. there are a few things you are leaving out have you done liver testing and how is his liver doing? if liver is not doing well detoxing it would be unhealthy to put a child on diflucan. also if nystatine is working you wouldn't want to put him on something stronger that is ruffer on the body when the more mild thing is working. valtrex is also not suppose to be done unless you have titers showing herpies issues. baptist ran titers for our son and he had none, therefore it would be foolish to just put him on valtrex for the sake of just putting him on it. what course of action is he wanting you to do first. it would not be wise body wise to start in with antivirals that would create MORE yeast till you get yeast levels down. and you don't want to just take antivials unless you KNOW those are his issues. meaning you have to SHOW you have herpies issues to benifit from valtrex. and I think that is the big part of what you are missing. you are asking him to perscribe something you have no evidence you have need for. which would be both foolish and jeperdize his liscience. just because valtrex helps a bunch of kids doesn't mean it will help your child unless your child has THOSE issues it addresses....make sence? this IS his speciality, he is an immunologist and allergist! what is your childs diet like? carbs and sugar and fruit wise? is he wanting you to address those things first? is your child on regular insurence? that may also be one of the problems. he has to justify to insurence on WHY he is doing those things. we paid out of pocket so we had more freedom. our son has been perscirbed diflucan SEVERAL times through dr Bapist over the years with no problem. but our son is also nystatin resistant and for him it IS the best choice for him. we also work on yeast through diet and do things like milk thistel and do regular liver testing ot make sure he is handleing it well. .. Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of "Kansas City." I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 jenny a few things, we see dr baptist and our son recovered with him. there are a few things you are leaving out have you done liver testing and how is his liver doing? if liver is not doing well detoxing it would be unhealthy to put a child on diflucan. also if nystatine is working you wouldn't want to put him on something stronger that is ruffer on the body when the more mild thing is working. valtrex is also not suppose to be done unless you have titers showing herpies issues. baptist ran titers for our son and he had none, therefore it would be foolish to just put him on valtrex for the sake of just putting him on it. what course of action is he wanting you to do first. it would not be wise body wise to start in with antivirals that would create MORE yeast till you get yeast levels down. and you don't want to just take antivials unless you KNOW those are his issues. meaning you have to SHOW you have herpies issues to benifit from valtrex. and I think that is the big part of what you are missing. you are asking him to perscribe something you have no evidence you have need for. which would be both foolish and jeperdize his liscience. just because valtrex helps a bunch of kids doesn't mean it will help your child unless your child has THOSE issues it addresses....make sence? this IS his speciality, he is an immunologist and allergist! what is your childs diet like? carbs and sugar and fruit wise? is he wanting you to address those things first? is your child on regular insurence? that may also be one of the problems. he has to justify to insurence on WHY he is doing those things. we paid out of pocket so we had more freedom. our son has been perscirbed diflucan SEVERAL times through dr Bapist over the years with no problem. but our son is also nystatin resistant and for him it IS the best choice for him. we also work on yeast through diet and do things like milk thistel and do regular liver testing ot make sure he is handleing it well. .. Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of "Kansas City." I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 jenny a few things, we see dr baptist and our son recovered with him. there are a few things you are leaving out have you done liver testing and how is his liver doing? if liver is not doing well detoxing it would be unhealthy to put a child on diflucan. also if nystatine is working you wouldn't want to put him on something stronger that is ruffer on the body when the more mild thing is working. valtrex is also not suppose to be done unless you have titers showing herpies issues. baptist ran titers for our son and he had none, therefore it would be foolish to just put him on valtrex for the sake of just putting him on it. what course of action is he wanting you to do first. it would not be wise body wise to start in with antivirals that would create MORE yeast till you get yeast levels down. and you don't want to just take antivials unless you KNOW those are his issues. meaning you have to SHOW you have herpies issues to benifit from valtrex. and I think that is the big part of what you are missing. you are asking him to perscribe something you have no evidence you have need for. which would be both foolish and jeperdize his liscience. just because valtrex helps a bunch of kids doesn't mean it will help your child unless your child has THOSE issues it addresses....make sence? this IS his speciality, he is an immunologist and allergist! what is your childs diet like? carbs and sugar and fruit wise? is he wanting you to address those things first? is your child on regular insurence? that may also be one of the problems. he has to justify to insurence on WHY he is doing those things. we paid out of pocket so we had more freedom. our son has been perscirbed diflucan SEVERAL times through dr Bapist over the years with no problem. but our son is also nystatin resistant and for him it IS the best choice for him. we also work on yeast through diet and do things like milk thistel and do regular liver testing ot make sure he is handleing it well. .. Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of "Kansas City." I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010  he is doing biofilm, what all are you wanting him to do that he is not doing other then valtrex that you don't have need for with out titers showing you have issues there? he is even up on some yasko stuff and has an HBOT in his office Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of "Kansas City." I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010  he is doing biofilm, what all are you wanting him to do that he is not doing other then valtrex that you don't have need for with out titers showing you have issues there? he is even up on some yasko stuff and has an HBOT in his office Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of "Kansas City." I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010  he is doing biofilm, what all are you wanting him to do that he is not doing other then valtrex that you don't have need for with out titers showing you have issues there? he is even up on some yasko stuff and has an HBOT in his office Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of "Kansas City." I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 he I believe in on the missiouri side of kansas if we are talking about the same person Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of "Kansas City." I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chem> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 he I believe in on the missiouri side of kansas if we are talking about the same person Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of "Kansas City." I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chem> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 ~ I am not a dr. but mom to mom~ ok? our DAN! started my 4 yr. old out on Valtrex at 500 mg. per day and he said if no improvement by day 14 to up to 1000 mg. (this is the proto i believe,1,000, but because my son is so young he wanted to start at 500 mg) Anyway, i have a different kid now....we also are GF/CF/Sf of course, MB12 and culterelle, etc...multi vitamin.....on day 12 or so of this Valtrex my son was walking and talking in circles (rain man stuff) i was so terrified and came close to calling our DAN! but he was "specific" about if nothing occurs by 14 days..I've NEVER doubted our DAN! he has been one for 14 yrs with son on spectrum as well....so i waited and day 14 my son was looking at me and asking questions like a typical kid....i had an emotional breakdown of joy that day and have been on Valtrex everyday since. We've missed days here and there...but strict for 2 months.We had not done any sort of testing before hand just the occasional OAT~ I've not ever chelated (yet) either so??? I'm learning still but this is our Valtrex story.....it works well for us.....along with MB12 every 3 days.Traci~Jack & Scarlett's momTo: mb12 valtrex Sent: Sat, May 8, 2010 8:09:28 AMSubject: Re: Valtrex Oops,should have finished reading... LOL :-)On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 ~ I am not a dr. but mom to mom~ ok? our DAN! started my 4 yr. old out on Valtrex at 500 mg. per day and he said if no improvement by day 14 to up to 1000 mg. (this is the proto i believe,1,000, but because my son is so young he wanted to start at 500 mg) Anyway, i have a different kid now....we also are GF/CF/Sf of course, MB12 and culterelle, etc...multi vitamin.....on day 12 or so of this Valtrex my son was walking and talking in circles (rain man stuff) i was so terrified and came close to calling our DAN! but he was "specific" about if nothing occurs by 14 days..I've NEVER doubted our DAN! he has been one for 14 yrs with son on spectrum as well....so i waited and day 14 my son was looking at me and asking questions like a typical kid....i had an emotional breakdown of joy that day and have been on Valtrex everyday since. We've missed days here and there...but strict for 2 months.We had not done any sort of testing before hand just the occasional OAT~ I've not ever chelated (yet) either so??? I'm learning still but this is our Valtrex story.....it works well for us.....along with MB12 every 3 days.Traci~Jack & Scarlett's momTo: mb12 valtrex Sent: Sat, May 8, 2010 8:09:28 AMSubject: Re: Valtrex Oops,should have finished reading... LOL :-)On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 ~ I am not a dr. but mom to mom~ ok? our DAN! started my 4 yr. old out on Valtrex at 500 mg. per day and he said if no improvement by day 14 to up to 1000 mg. (this is the proto i believe,1,000, but because my son is so young he wanted to start at 500 mg) Anyway, i have a different kid now....we also are GF/CF/Sf of course, MB12 and culterelle, etc...multi vitamin.....on day 12 or so of this Valtrex my son was walking and talking in circles (rain man stuff) i was so terrified and came close to calling our DAN! but he was "specific" about if nothing occurs by 14 days..I've NEVER doubted our DAN! he has been one for 14 yrs with son on spectrum as well....so i waited and day 14 my son was looking at me and asking questions like a typical kid....i had an emotional breakdown of joy that day and have been on Valtrex everyday since. We've missed days here and there...but strict for 2 months.We had not done any sort of testing before hand just the occasional OAT~ I've not ever chelated (yet) either so??? I'm learning still but this is our Valtrex story.....it works well for us.....along with MB12 every 3 days.Traci~Jack & Scarlett's momTo: mb12 valtrex Sent: Sat, May 8, 2010 8:09:28 AMSubject: Re: Valtrex Oops,should have finished reading... LOL :-)On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 Oh sorry, LOL I must have my geography wrong??? Hmmm. Can't be two Dr. Baptist who are DAN lol he I believe in on the missiouri side of kansas if we are talking about the same person Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of " Kansas City. " I don't know who you see, but just throwing that out there in case you are looking for a change. I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 i had the very same experience with doc baptist, im looking for a new DAN doc in our area too! if you find one let me know. I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 i had the very same experience with doc baptist, im looking for a new DAN doc in our area too! if you find one let me know. I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 Liver looked good. He didn't run titters on the herpies viruses. Luke is on gf/cf and since he is allergic to pretty much everything under the sun he is on pretty much a caveman diet. No sugar, juices, he sticks to the rotational diet. We were treating yeast; however the nystatin stopped working after 2-3 months. We stopped seeing yeast in his B/M's all together and Luke started reacting to the nystatin. I never asked him to perscribed them, I would like the titters to be ran, he pretty much stopped the conversation as we brought it up. Dr. Baptist got him on supplements, and we are stilll giving him all 50 supplements. Yes our insurance covers the treatments. Honestly I would like the "standard" testing done to actually see what we are up against. Taking over a year to get supplements ajusted and readjusted just seems like such a waste of time. When I talked with the good dr. about his issues with nystatin how we stopped seeing yeast and that Lukes behavior was getting really horrible, he told us to cut down the dose, but we didn't see any improvement when we did. We tried the nystatin again after a few weeks and he had the bad reaction again. We told the good dr. and still he wouldn't switch him. Maybe it is b/c of insurance. When I went to the DAN confrence I talked with other DAN doctors and I will never forget what McCarthys dr said to me, if you have an infection why wouldn't you want to get the problem taken care of as soon as possible. I am glad to hear that you son has recovered, we hope the same for ours. J To: mb12 valtrex Sent: Sat, May 8, 2010 1:07:04 PMSubject: Re: Valtrex jenny a few things, we see dr baptist and our son recovered with him. there are a few things you are leaving out have you done liver testing and how is his liver doing? if liver is not doing well detoxing it would be unhealthy to put a child on diflucan. also if nystatine is working you wouldn't want to put him on something stronger that is ruffer on the body when the more mild thing is working. valtrex is also not suppose to be done unless you have titers showing herpies issues. baptist ran titers for our son and he had none, therefore it would be foolish to just put him on valtrex for the sake of just putting him on it. what course of action is he wanting you to do first. it would not be wise body wise to start in with antivirals that would create MORE yeast till you get yeast levels down. and you don't want to just take antivials unless you KNOW those are his issues. meaning you have to SHOW you have herpies issues to benifit from valtrex. and I think that is the big part of what you are missing. you are asking him to perscribe something you have no evidence you have need for. which would be both foolish and jeperdize his liscience. just because valtrex helps a bunch of kids doesn't mean it will help your child unless your child has THOSE issues it addresses... .make sence? this IS his speciality, he is an immunologist and allergist! what is your childs diet like? carbs and sugar and fruit wise? is he wanting you to address those things first? is your child on regular insurence? that may also be one of the problems. he has to justify to insurence on WHY he is doing those things. we paid out of pocket so we had more freedom. our son has been perscirbed diflucan SEVERAL times through dr Bapist over the years with no problem. but our son is also nystatin resistant and for him it IS the best choice for him. we also work on yeast through diet and do things like milk thistel and do regular liver testing ot make sure he is handleing it well. .. Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of "Kansas City." I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. 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Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 Liver looked good. He didn't run titters on the herpies viruses. Luke is on gf/cf and since he is allergic to pretty much everything under the sun he is on pretty much a caveman diet. No sugar, juices, he sticks to the rotational diet. We were treating yeast; however the nystatin stopped working after 2-3 months. We stopped seeing yeast in his B/M's all together and Luke started reacting to the nystatin. I never asked him to perscribed them, I would like the titters to be ran, he pretty much stopped the conversation as we brought it up. Dr. Baptist got him on supplements, and we are stilll giving him all 50 supplements. Yes our insurance covers the treatments. Honestly I would like the "standard" testing done to actually see what we are up against. Taking over a year to get supplements ajusted and readjusted just seems like such a waste of time. When I talked with the good dr. about his issues with nystatin how we stopped seeing yeast and that Lukes behavior was getting really horrible, he told us to cut down the dose, but we didn't see any improvement when we did. We tried the nystatin again after a few weeks and he had the bad reaction again. We told the good dr. and still he wouldn't switch him. Maybe it is b/c of insurance. When I went to the DAN confrence I talked with other DAN doctors and I will never forget what McCarthys dr said to me, if you have an infection why wouldn't you want to get the problem taken care of as soon as possible. I am glad to hear that you son has recovered, we hope the same for ours. J To: mb12 valtrex Sent: Sat, May 8, 2010 1:07:04 PMSubject: Re: Valtrex jenny a few things, we see dr baptist and our son recovered with him. there are a few things you are leaving out have you done liver testing and how is his liver doing? if liver is not doing well detoxing it would be unhealthy to put a child on diflucan. also if nystatine is working you wouldn't want to put him on something stronger that is ruffer on the body when the more mild thing is working. valtrex is also not suppose to be done unless you have titers showing herpies issues. baptist ran titers for our son and he had none, therefore it would be foolish to just put him on valtrex for the sake of just putting him on it. what course of action is he wanting you to do first. it would not be wise body wise to start in with antivirals that would create MORE yeast till you get yeast levels down. and you don't want to just take antivials unless you KNOW those are his issues. meaning you have to SHOW you have herpies issues to benifit from valtrex. and I think that is the big part of what you are missing. you are asking him to perscribe something you have no evidence you have need for. which would be both foolish and jeperdize his liscience. just because valtrex helps a bunch of kids doesn't mean it will help your child unless your child has THOSE issues it addresses... .make sence? this IS his speciality, he is an immunologist and allergist! what is your childs diet like? carbs and sugar and fruit wise? is he wanting you to address those things first? is your child on regular insurence? that may also be one of the problems. he has to justify to insurence on WHY he is doing those things. we paid out of pocket so we had more freedom. our son has been perscirbed diflucan SEVERAL times through dr Bapist over the years with no problem. but our son is also nystatin resistant and for him it IS the best choice for him. we also work on yeast through diet and do things like milk thistel and do regular liver testing ot make sure he is handleing it well. .. Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of "Kansas City." I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. 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Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 What do you mean he is doing biofilm? Is he perscribing EDTA now with anti-fungals? If so I am amazed!!!!! I brought him back the simanar notes from the DAN confrence and asked for his help on getting Luke on that treatment. To: mb12 valtrex Sent: Sat, May 8, 2010 1:19:50 PMSubject: Re: Valtrex  he is doing biofilm, what all are you wanting him to do that he is not doing other then valtrex that you don't have need for with out titers showing you have issues there? he is even up on some yasko stuff and has an HBOT in his office Re: Valtrex Hey ,I am not much help but I know Christel sees Dr. Baptist and raves about him. He's on the Kansas side of "Kansas City." I don't know who you see, but just throwing that out there in case you are looking for a change. On Sat, May 8, 2010 at 11:05 AM, jennifer smiglewski <jjs7a7chemyahoo (DOT) com> wrote: I am in Kansas City and was wondering if anyone has done the valtrex treatment with their child? I haven't been too impressed with the DAN doctor in our area. He doesn't listen to what we have to say; doesn't really try to problem solve. Everyone gets the same course of treatment. We actually found a wonderful Ped. who is willing to do bio-medical treatments, however the dr and I do not know where to begin. The things that I notice about my son is that his fingernail are horrible looking, which we got him on all the supplements the DAN dr recommended and we saw great improvement. When we went to treat his clostrdia and yeast the dr put our son on herbals and nystatin. The nystatin worked for about 2 months where we saw lots of yeast coming out and then it just stopped and his behavior got horrible. We continued on the nystatin for 5 weeks more and we saw no more yeast. We talked with the dr about switching to Diflucan, he wanted us to stay on the nystatin, so we tried it again and our baby was miserable again for the 2 weeks we put him back on it. Talked with the dr again and he still would not switch. The most frustrating thing in the world is when a dr doesn't listen to you. After that we lost faith in him. He wasn't willing to try new things. I asked about Valtrex, and he said that that was way down the road. We decided to go a different route and find a dr that would listen to us and not ignore the systems that we see in Luke. By the way Luke has been on gf/cf and a version of the sc diet for over a year. Finally to the question: Has anyone tried a Valtrex treatment with their son? Could you get me started on the right course, so I can get the testing done by Luke's Ped? Is there titter testing involved? What should we titter test for? What kind of dosing should we be looking at? How long do is the general treatment plan? What should signs should I be looking for in Luke? We are going to do combination treatment and also put him on Diflucan. I really believe that combination treatment is the best course b/c all the infections relay upon one another to survive if you do one at a time you arn't really taking it out from all directions. I think that is why Nystatin stopped working the infections changed his body and I believe they played a role in making him become allergic to the Nystatin plus the yeast becaome tolerent of its toxin, nystatin. By the way happy mothers day everone!!!!! -- Toni------Mind like a steel trap...Rusty and illegal in 37 states. Quote Link to comment Share on other sites More sharing options...
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