Guest guest Posted January 23, 2012 Report Share Posted January 23, 2012 http://www.virology.ws/ i am so bad at putting up links but found this over at the europe autism yahoo group and thought it looked really interesting...easy to follow channa Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2012 Report Share Posted January 23, 2012 Hey Channa: A little off the topic here, but what are people doing for Lyme and possibly coinfections as a comorbidity with autism spectrum disorder. My husband says we can't afford the 25-35K IV antibiotic treatment for lyme that has been offered to us by the infectious disease doctor . Have to find other options, so I thought I should start asking here. Thanks,Bettina To: mb12valtrex Sent: Monday, January 23, 2012 8:27 PM Subject: blog on viruses http://www.virology.ws/ i am so bad at putting up links but found this over at the europe autism yahoo group and thought it looked really interesting...easy to follow channa Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2012 Report Share Posted January 23, 2012 People might not see this. My suggestion is to send a new post with lyme in the subject. We have lots of lyme-literate parents here. ~ Antiviral Therapy 101~ gryffinstail.wordpress.com ~~ @Gryffins_Tail ~ http://www.virology.ws/ i am so bad at putting up links but found this over at the europe autism yahoo group and thought it looked really interesting...easy to follow channa Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2012 Report Share Posted January 23, 2012 oh bettina nothing is OT on this group:) i dont know specific info on lyme as i never pursued trying to find my sons specific viruses...I do know there is some super smart people over at the LIA yahoo group...you should join they got lot info on files.. dr klinghart has a lyme protocol i think it is in the files over their if not I will look for in my files and send to you... channa To: "mb12valtrex " <mb12valtrex > Sent: Monday, January 23, 2012 8:53 PMSubject: Re: blog on viruses Hey Channa: A little off the topic here, but what are people doing for Lyme and possibly coinfections as a comorbidity with autism spectrum disorder. My husband says we can't afford the 25-35K IV antibiotic treatment for lyme that has been offered to us by the infectious disease doctor . Have to find other options, so I thought I should start asking here. Thanks,Bettina To: mb12valtrex Sent: Monday, January 23, 2012 8:27 PMSubject: blog on viruses http://www.virology.ws/ i am so bad at putting up links but found this over at the europe autism yahoo group and thought it looked really interesting...easy to follow channa Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2012 Report Share Posted January 23, 2012 borrelia multiple infections and autism yahoo group....that is the LIA group i wrote in my other post... To: "mb12valtrex " <mb12valtrex > Sent: Monday, January 23, 2012 8:53 PMSubject: Re: blog on viruses Hey Channa: A little off the topic here, but what are people doing for Lyme and possibly coinfections as a comorbidity with autism spectrum disorder. My husband says we can't afford the 25-35K IV antibiotic treatment for lyme that has been offered to us by the infectious disease doctor . Have to find other options, so I thought I should start asking here. Thanks,Bettina To: mb12valtrex Sent: Monday, January 23, 2012 8:27 PMSubject: blog on viruses http://www.virology.ws/ i am so bad at putting up links but found this over at the europe autism yahoo group and thought it looked really interesting...easy to follow channa Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2012 Report Share Posted January 23, 2012 I like this PDF/slide presentation.http://andreannarainville.com/klinghardt_docs/AutismProtocol09.pdfOn Tue, Jan 24, 2012 at 12:32 AM, Channa Brennon wrote: oh bettina nothing is OT on this group:) i dont know specific info on lyme as i never pursued trying to find my sons specific viruses...I do know there is some super smart people over at the LIA yahoo group...you should join they got lot info on files.. dr klinghart has a lyme protocol i think it is in the files over their if not I will look for in my files and send to you... channa To: " mb12valtrex " <mb12valtrex > Sent: Monday, January 23, 2012 8:53 PMSubject: Re: blog on viruses Hey Channa: A little off the topic here, but what are people doing for Lyme and possibly coinfections as a comorbidity with autism spectrum disorder. My husband says we can't afford the 25-35K IV antibiotic treatment for lyme that has been offered to us by the infectious disease doctor . Have to find other options, so I thought I should start asking here. Thanks,Bettina To: mb12valtrex Sent: Monday, January 23, 2012 8:27 PM Subject: blog on viruses http://www.virology.ws/ i am so bad at putting up links but found this over at the europe autism yahoo group and thought it looked really interesting...easy to follow channa -- --------------------------------------------------------------------------------------------Click to find info about Vitamins and Minerals:http://www.facebook.com/note.php?note_id=10150543521682565 --------------------------------------------------------------------------------------------Click to find links to info about the Low Oxalate Diet :http://www.facebook.com/note.php?note_id=10150543495292565 ------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 January 24, 2012 Report Share Posted January 24, 2012 Bettina, my son has been on oral antibiotics for 4 years and also takes antivirals, etc. You should find a lyme literate practitioner. ID drs usually treat for a month only with IVs. Many families also treat herbally. You should join borreliamultipleinfections andautism group for lyme support. > > > > Hey Channa: A little off the topic here, but what are people doing for Lyme and possibly coinfections as a comorbidity with autism spectrum disorder. My husband says we can't afford the 25-35K IV antibiotic treatment for lyme that has been offered to us by the infectious disease doctor . Have to find other options, so I thought I should start asking here. Thanks,Bettina > > ________________________________ > > To: mb12valtrex > Sent: Monday, January 23, 2012 8:27 PM > Subject: blog on viruses > > >  > http://www.virology.ws/ i am so bad at putting up links but found this over at the europe autism yahoo group and thought it looked really interesting...easy to follow > channa > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2012 Report Share Posted January 24, 2012 I've done both, joined the group and have taken him to the Jemsek clinic. I just don't have 25-35- K for the IV antibiotic therapy. My husband does not agree with the abx protocol Dr. J is using. He thinks it is overkill. Blue Cross Blue Shield has us under review for going to the ER three times since Sept. MOst likely won't pay for any of this. I really want to so the herbal, rife and homeopathy. ONe month will not take care of an infection that has possibly been there from birth. I need to get tested too. Just chasing my tail right now. To: mb12valtrex Sent: Tuesday, January 24, 2012 7:38 AM Subject: Re: blog on viruses Bettina, my son has been on oral antibiotics for 4 years and also takes antivirals, etc. You should find a lyme literate practitioner. ID drs usually treat for a month only with IVs. Many families also treat herbally. You should join borreliamultipleinfections andautism group for lyme support. > > > > Hey Channa: A little off the topic here, but what are people doing for Lyme and possibly coinfections as a comorbidity with autism spectrum disorder. My husband says we can't afford the 25-35K IV antibiotic treatment for lyme that has been offered to us by the infectious disease doctor . Have to find other options, so I thought I should start asking here. Thanks,Bettina > > ________________________________ > > To: mb12valtrex > Sent: Monday, January 23, 2012 8:27 PM > Subject: blog on viruses > > >  > http://www.virology.ws/ i am so bad at putting up links but found this over at the europe autism yahoo group and thought it looked really interesting...easy to follow > channa > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2012 Report Share Posted January 24, 2012 I have seen his protocol. What does OT mean? Thanks,Bettina To: mb12valtrex Sent: Tuesday, January 24, 2012 12:50 AM Subject: Re: blog on viruses I like this PDF/slide presentation.http://andreannarainville.com/klinghardt_docs/AutismProtocol09.pdfOn Tue, Jan 24, 2012 at 12:32 AM, Channa Brennon wrote: oh bettina nothing is OT on this group:) i dont know specific info on lyme as i never pursued trying to find my sons specific viruses...I do know there is some super smart people over at the LIA yahoo group...you should join they got lot info on files.. dr klinghart has a lyme protocol i think it is in the files over their if not I will look for in my files and send to you... channa To: "mb12valtrex " <mb12valtrex > Sent: Monday, January 23, 2012 8:53 PMSubject: Re: blog on viruses Hey Channa: A little off the topic here, but what are people doing for Lyme and possibly coinfections as a comorbidity with autism spectrum disorder. My husband says we can't afford the 25-35K IV antibiotic treatment for lyme that has been offered to us by the infectious disease doctor . Have to find other options, so I thought I should start asking here. Thanks,Bettina To: mb12valtrex Sent: Monday, January 23, 2012 8:27 PM Subject: blog on viruses http://www.virology.ws/ i am so bad at putting up links but found this over at the europe autism yahoo group and thought it looked really interesting...easy to follow channa -- --------------------------------------------------------------------------------------------Click to find info about Vitamins and Minerals:http://www.facebook.com/note.php?note_id=10150543521682565 --------------------------------------------------------------------------------------------Click to find links to info about the Low Oxalate Diet :http://www.facebook.com/note.php?note_id=10150543495292565 ------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 January 24, 2012 Report Share Posted January 24, 2012 Oh yeah, off topic... To: "mb12valtrex " <mb12valtrex > Sent: Tuesday, January 24, 2012 12:32 AM Subject: Re: blog on viruses oh bettina nothing is OT on this group:) i dont know specific info on lyme as i never pursued trying to find my sons specific viruses...I do know there is some super smart people over at the LIA yahoo group...you should join they got lot info on files.. dr klinghart has a lyme protocol i think it is in the files over their if not I will look for in my files and send to you... channa To: "mb12valtrex " <mb12valtrex > Sent: Monday, January 23, 2012 8:53 PMSubject: Re: blog on viruses Hey Channa: A little off the topic here, but what are people doing for Lyme and possibly coinfections as a comorbidity with autism spectrum disorder. My husband says we can't afford the 25-35K IV antibiotic treatment for lyme that has been offered to us by the infectious disease doctor . Have to find other options, so I thought I should start asking here. Thanks,Bettina To: mb12valtrex Sent: Monday, January 23, 2012 8:27 PMSubject: blog on viruses http://www.virology.ws/ i am so bad at putting up links but found this over at the europe autism yahoo group and thought it looked really interesting...easy to follow channa Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2012 Report Share Posted January 24, 2012 did you see the recent post rita put over their about viruses and tx? it was really really very good....mostly natural stuff but from what i understand powerful stuff.... also i accidently stumbled apon red algae and it was quite impressive to me the research on the particular algae with viruses....you could look into that too.....let me know if you cant find post in borellia group by rita it was under the post title "Valtrex" im into all cheaper and natural stuff.... not that any thing in biomed is ever cheap.... channa To: "mb12valtrex " <mb12valtrex > Sent: Tuesday, January 24, 2012 8:12 AMSubject: Re: Re: blog on viruses I've done both, joined the group and have taken him to the Jemsek clinic. I just don't have 25-35- K for the IV antibiotic therapy. My husband does not agree with the abx protocol Dr. J is using. He thinks it is overkill. Blue Cross Blue Shield has us under review for going to the ER three times since Sept. MOst likely won't pay for any of this. I really want to so the herbal, rife and homeopathy. ONe month will not take care of an infection that has possibly been there from birth. I need to get tested too. Just chasing my tail right now. To: mb12valtrex Sent: Tuesday, January 24, 2012 7:38 AMSubject: Re: blog on viruses Bettina, my son has been on oral antibiotics for 4 years and also takes antivirals, etc. You should find a lyme literate practitioner. ID drs usually treat for a month only with IVs. Many families also treat herbally. You should join borreliamultipleinfections andautism group for lyme support.>> > > Hey Channa: A little off the topic here, but what are people doing for Lyme and possibly coinfections as a comorbidity with autism spectrum disorder. My husband says we can't afford the 25-35K IV antibiotic treatment for lyme that has been offered to us by the infectious disease doctor . Have to find other options, so I thought I should start asking here. Thanks,Bettina > > ________________________________> > To: mb12valtrex > Sent: Monday, January 23, 2012 8:27 PM> Subject: blog on viruses> > >  > http://www.virology.ws/ i am so bad at putting up links but found this over at the europe autism yahoo group and thought it looked really interesting...easy to follow > channa> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2012 Report Share Posted January 24, 2012 > Unfortunately, the amount of people who go broke from treating Lyme is grand. So, just saying that treating for Lyme can take a long time and cost a lot. Samento is the cheapest way that I know of. Keep in mind that it's not really considered a cure, but reportedly can help some people lose most of their symptoms. I have seen docs say that about half of their patients can go back to work on Samento alone, but the rest need lots more stuff. Samento is known to cause huge die-off at first - just one drop a day. I have heard of many who test positive for Lyme say that they have very little symptoms and didn't feel ill. So, it's complicated and depends upon the person's immune system and toxin load. Just saying that treating Lyme is very similar to recovering from autism in those with chronic Lyme. The good news is that I have seen several reports of autism recovery from treating for Lyme and other tickborne infections. Love and prayers, Heidi N > Hey Channa: A little off the topic here, but what are people doing for Lyme and possibly coinfections as a comorbidity with autism spectrum disorder. My husband says we can't afford the 25-35K IV antibiotic treatment for lyme that has been offered to us by the infectious disease doctor . Have to find other options, so I thought I should start asking here. Thanks,Bettina Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2012 Report Share Posted January 24, 2012 Doctor J and husband should conversed and agreed to do oral abx Mon, Wed,Frid. Do you think it would be reasonable to do Cowans protocol with the oral abx? I also went to teh Rife Lyme yahoo group and they introduced me to MMS and have been doing Rife machine. Just don't know if anything the doctors are doing are working. Getting afraid to try for waste of time and money. Can't do nothing though.Thanks,Bettina To: mb12valtrex Sent: Tuesday, January 24, 2012 12:11 PM Subject: Re: blog on viruses > Unfortunately, the amount of people who go broke from treating Lyme is grand. So, just saying that treating for Lyme can take a long time and cost a lot. Samento is the cheapest way that I know of. Keep in mind that it's not really considered a cure, but reportedly can help some people lose most of their symptoms. I have seen docs say that about half of their patients can go back to work on Samento alone, but the rest need lots more stuff. Samento is known to cause huge die-off at first - just one drop a day. I have heard of many who test positive for Lyme say that they have very little symptoms and didn't feel ill. So, it's complicated and depends upon the person's immune system and toxin load. Just saying that treating Lyme is very similar to recovering from autism in those with chronic Lyme. The good news is that I have seen several reports of autism recovery from treating for Lyme and other tickborne infections. Love and prayers, Heidi N > Hey Channa: A little off the topic here, but what are people doing for Lyme and possibly coinfections as a comorbidity with autism spectrum disorder. My husband says we can't afford the 25-35K IV antibiotic treatment for lyme that has been offered to us by the infectious disease doctor . Have to find other options, so I thought I should start asking here. Thanks,Bettina Quote Link to comment Share on other sites More sharing options...
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