Guest guest Posted August 27, 2010 Report Share Posted August 27, 2010 Dear Marcia, , Sandy, Tammy, Toni, Judy, , and Amy:Thank yo soooooo much for your answers. Believe it or not, they do help and give me comfort as I know that I am not alone. Though I have to confess that I am a little confused on the under and over methylator issue. I have a lot of reading and researching to do. Thank you for Dr. Kartzinel's presentation, I have analyzed it completely and took out my labs to compare. I think after all my son should not be doing the MB12. In his labs, all his lows and highs in the interpretation part suggest B6 and from what I understand, the B12 and B6 are by no means the same. I hope to God that what were are going through is Die-off and that after a few more days on the dyflican he will feel better. My husband is taking him tomorrow to Ecuador (South America) looking for a miracle. I will stay home with the other 3 as they begin school Monday. There is a doctor out there who apparently is curing autism, alt-zimers(spelling) and other things. My sisters-in-law have insisted so much he goes, so tomorrow he is off. He is only going for an appointment Monday where they will do a cerebral mapping and I'm not worry my husband in not so up on all that we do, as the doctor wants no previous history. Yes one of the therapies he does is HBOT so I am really hesitant after all that has been said but this is my husbands grain of salt and I'm letting him act. There is no therapy until March of next year available and that usually takes 4 weeks so I am not worried for now. We will see what the doctor has to offer as therapy and what he says about my son. I will report back.Getting back to all of you, thank you again. I am praying that this is the yeast leaving his body as Marcia suggests. On the 13th also I am moving to Baltimore for 2 months as my son also doesn't eat and so he was accepted at the 's Hopkins GI Feeding Clinic where they will teach him how to eat. If anyone is interested in the types of therapies they use, when I sit waiting in that hospital lobby for 9 or so hours I can report to whoever is interested so you can try it out........I am hoping this will work........too.I am praying for all of you and your children. Thank you for taking the time to answer back.To: mb12 valtrex From: waggersitter@...Date: Fri, 27 Aug 2010 20:26:55 +0000Subject: Re: Yeast , this was me just a few months ago. We started nystatin and the MB12 shots very close together. Same thing happened to my little boy and I was in a state of panic. His symptoms were so mild before I started trying to "fix" him. I stopped everything immediately, I didn't care about die-off, whatever. He came back around after about a month and I have learned a very valuable lesson--one thing at the time, very slowly. And give what you're doing a minute to work--not the easiest thing for this instant gratification girl to do Hang in there, sweetie. Keep asking these guys for their advice, they help me all the time! Amy B > > I need you opinion. I started my son on MB12 shots (have to admit I have not been constant) and soon after he started with the itchy butt and very yellow poops. I started the diflucan and activated charcoal on Monday. Now he is a child I don't know. He had never had so many autistic symptoms as now. No eye contact, no receptive or expressive language - no connection. Little aggressive which he's never been. Now I understand when I read about symptoms on other kids here. > > Should I give up on the medication or is this what you guys call die-off? > > My heart is breaking, we are moving deeper into autism instead of taking him out. > > Anything will help. > > > Sent via BlackBerry by AT & T > > Yeast > > > > > > > > I have found with my son that we couldn't stop the yeast medications or antiviral meds. He is now recovered but not cured. must remain on these meds for his body to function properly. Until the big cure comes along that corrects the immune system permanently. I think of it like someone who has diabetes who must take insulin for their body to function normally. As long as his blood test continue to be normal, we are okay. Fortunately in all the sixteen years we have been doing NIDS and these medication, there has not been a abnormal blood test. The reason Dr. Goldberg requires so many labs is to make sure problems with medications are caught before they do any damage to our children. > Marcia > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 27, 2010 Report Share Posted August 27, 2010 You're welcome, hope it helps with the puzzle.nancy j a child is diagnosed with asd every 20 secondsSubject: RE: Re: Yeast - thank youTo: mb12 valtrex Date: Friday, August 27, 2010, 7:27 PM Dear Marcia, , Sandy, Tammy, Toni, Judy, , and Amy:Thank yo soooooo much for your answers. Believe it or not, they do help and give me comfort as I know that I am not alone. Though I have to confess that I am a little confused on the under and over methylator issue. I have a lot of reading and researching to do. Thank you for Dr. Kartzinel's presentation, I have analyzed it completely and took out my labs to compare. I think after all my son should not be doing the MB12. In his labs, all his lows and highs in the interpretation part suggest B6 and from what I understand, the B12 and B6 are by no means the same. I hope to God that what were are going through is Die-off and that after a few more days on the dyflican he will feel better. My husband is taking him tomorrow to Ecuador (South America) looking for a miracle. I will stay home with the other 3 as they begin school Monday. There is a doctor out there who apparently is curing autism, alt-zimers(spelling) and other things. My sisters-in-law have insisted so much he goes, so tomorrow he is off. He is only going for an appointment Monday where they will do a cerebral mapping and I'm not worry my husband in not so up on all that we do, as the doctor wants no previous history. Yes one of the therapies he does is HBOT so I am really hesitant after all that has been said but this is my husbands grain of salt and I'm letting him act. There is no therapy until March of next year available and that usually takes 4 weeks so I am not worried for now. We will see what the doctor has to offer as therapy and what he says about my son. I will report back.Getting back to all of you, thank you again. I am praying that this is the yeast leaving his body as Marcia suggests. On the 13th also I am moving to Baltimore for 2 months as my son also doesn't eat and so he was accepted at the 's Hopkins GI Feeding Clinic where they will teach him how to eat. If anyone is interested in the types of therapies they use, when I sit waiting in that hospital lobby for 9 or so hours I can report to whoever is interested so you can try it out........I am hoping this will work........too.I am praying for all of you and your children. Thank you for taking the time to answer back.To: mb12 valtrex From: waggersitter@...Date: Fri, 27 Aug 2010 20:26:55 +0000Subject: Re: Yeast , this was me just a few months ago. We started nystatin and the MB12 shots very close together. Same thing happened to my little boy and I was in a state of panic. His symptoms were so mild before I started trying to "fix" him. I stopped everything immediately, I didn't care about die-off, whatever. He came back around after about a month and I have learned a very valuable lesson--one thing at the time, very slowly. And give what you're doing a minute to work--not the easiest thing for this instant gratification girl to do Hang in there, sweetie. Keep asking these guys for their advice, they help me all the time! Amy B > > I need you opinion. I started my son on MB12 shots (have to admit I have not been constant) and soon after he started with the itchy butt and very yellow poops. I started the diflucan and activated charcoal on Monday. Now he is a child I don't know. He had never had so many autistic symptoms as now. No eye contact, no receptive or expressive language - no connection. Little aggressive which he's never been. Now I understand when I read about symptoms on other kids here. > > Should I give up on the medication or is this what you guys call die-off? > > My heart is breaking, we are moving deeper into autism instead of taking him out. > > Anything will help. > > > Sent via BlackBerry by AT & T > > Yeast > > > > > > > > I have found with my son that we couldn't stop the yeast medications or antiviral meds. He is now recovered but not cured. must remain on these meds for his body to function properly. Until the big cure comes along that corrects the immune system permanently. I think of it like someone who has diabetes who must take insulin for their body to function normally. As long as his blood test continue to be normal, we are okay. Fortunately in all the sixteen years we have been doing NIDS and these medication, there has not been a abnormal blood test. The reason Dr. Goldberg requires so many labs is to make sure problems with medications are caught before they do any damage to our children. > Marcia > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 28, 2010 Report Share Posted August 28, 2010 Hi everybody, I am a Bulgarian mother and I am new to the group. My son is three years old and was diagnosed with autism a couple of months ago. You all know how it feels but add to that the fact that my country is far behind in what treating autism is concerned - we don't have any DAN! doctor here, no occupational therapists in the sense you know them. It is very very difficult for me and my husband to fight trying to cure our baby. I got in touch with an Italian DAN! doctor who is helping us from a distance but it is not the same. I am very interested in Dr. Goldberg's work but I can't reach him - I sent two mails to the address in his site but I received a message that they weren't delivered. Can somebody help me with this - alternative email address maybe? Thank you in advance, Dani To: mb12 valtrex Sent: Sat, August 28, 2010 8:36:29 AMSubject: RE: Re: Yeast - thank you You're welcome, hope it helps with the puzzle.nancy ja child is diagnosed with asd every 20 seconds Subject: RE: Re: Yeast - thank youTo: mb12 valtrex Date: Friday, August 27, 2010, 7:27 PM Dear Marcia, , Sandy, Tammy, Toni, Judy, , and Amy:Thank yo soooooo much for your answers. Believe it or not, they do help and give me comfort as I know that I am not alone. Though I have to confess that I am a little confused on the under and over methylator issue. I have a lot of reading and researching to do. Thank you for Dr. Kartzinel's presentation, I have analyzed it completely and took out my labs to compare. I think after all my son should not be doing the MB12. In his labs, all his lows and highs in the interpretation part suggest B6 and from what I understand, the B12 and B6 are by no means the same. I hope to God that what were are going through is Die-off and that after a few more days on the dyflican he will feel better. My husband is taking him tomorrow to Ecuador (South America) looking for a miracle. I will stay home with the other 3 as they begin school Monday. There is a doctor out there who apparently is curing autism, alt-zimers(spelling) and other things. My sisters-in-law have insisted so much he goes, so tomorrow he is off. He is only going for an appointment Monday where they will do a cerebral mapping and I'm not worry my husband in not so up on all that we do, as the doctor wants no previous history. Yes one of the therapies he does is HBOT so I am really hesitant after all that has been said but this is my husbands grain of salt and I'm letting him act. There is no therapy until March of next year available and that usually takes 4 weeks so I am not worried for now. We will see what the doctor has to offer as therapy and what he says about my son. I will report back.Getting back to all of you, thank you again. I am praying that this is the yeast leaving his body as Marcia suggests. On the 13th also I am moving to Baltimore for 2 months as my son also doesn't eat and so he was accepted at the 's Hopkins GI Feeding Clinic where they will teach him how to eat. If anyone is interested in the types of therapies they use, when I sit waiting in that hospital lobby for 9 or so hours I can report to whoever is interested so you can try it out........I am hoping this will work........too.I am praying for all of you and your children. Thank you for taking the time to answer back. To: mb12 valtrex From: waggersitter@...Date: Fri, 27 Aug 2010 20:26:55 +0000Subject: Re: Yeast ,this was me just a few months ago. We started nystatin and the MB12 shots very close together. Same thing happened to my little boy and I was in a state of panic. His symptoms were so mild before I started trying to "fix" him. I stopped everything immediately, I didn't care about die-off, whatever. He came back around after about a month and I have learned a very valuable lesson--one thing at the time, very slowly. And give what you're doing a minute to work--not the easiest thing for this instant gratification girl to do Hang in there, sweetie. Keep asking these guys for their advice, they help me all the time! Amy B>> I need you opinion. I started my son on MB12 shots (have to admit I have not been constant) and soon after he started with the itchy butt and very yellow poops. I started the diflucan and activated charcoal on Monday. Now he is a child I don't know. He had never had so many autistic symptoms as now. No eye contact, no receptive or expressive language - no connection. Little aggressive which he's never been. Now I understand when I read about symptoms on other kids here. > > Should I give up on the medication or is this what you guys call die-off? > > My heart is breaking, we are moving deeper into autism instead of taking him out. > > Anything will help. > > > Sent via BlackBerry by AT & T> > Yeast> > > > > > > > I have found with my son that we couldn't stop the yeast medications or antiviral meds. He is now recovered but not cured. must remain on these meds for his body to function properly. Until the big cure comes along that corrects the immune system permanently. I think of it like someone who has diabetes who must take insulin for their body to function normally. As long as his blood test continue to be normal, we are okay. Fortunately in all the sixteen years we have been doing NIDS and these medication, there has not been a abnormal blood test. The reason Dr. Goldberg requires so many labs is to make sure problems with medications are caught before they do any damage to our children. > Marcia> Quote Link to comment Share on other sites More sharing options...
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