Guest guest Posted April 26, 2001 Report Share Posted April 26, 2001 Janet, I am interested to read that article on lyme (bb) found in semen, found in urine, seems to make sense, as both come out urethra. pat nj Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 26, 2001 Report Share Posted April 26, 2001 In a message dated 4/26/2001 12:29:34 AM Pacific Daylight Time, writes: > > Just my two cents on this subject but I've had Lyme for 11 yrs. and my hubby > shows NO sign of Lyme whatsoever. We don't use any birth control ... > vasectomy and hysterectomy ... so it seems like if he was going to get it, he > would have by now. > While I am glad your husband has no symptoms, there is an entire body of literature on individuals who are infected by carry the spirochete asymptomatically or in a subclinical state. As I recall, many of these studies were done by European researchers and when you look at who's in the studies -- although it doesn't break down the findings by gender -- you get the feeling that a lot of the people who are asymptomatic but infected are males. Many doctors have noticed that women seem to have more problems in terms of the severity of symptoms and their difficulty clearing the organism. there is very little you can find on the medical literature on this, however. Lynn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 27, 2001 Report Share Posted April 27, 2001 Lynn, > While I am glad your husband has no symptoms, there is an entire body of > literature on individuals who are infected by carry the spirochete > asymptomatically or in a subclinical state. As I recall, many of these > studies were done by European researchers and when you look at who's in the > studies -- although it doesn't break down the findings by gender -- you get > the feeling that a lot of the people who are asymptomatic but infected are > males. I am not saying we know whether Lyme is or is not sexually transmissible but I think I have an explanation as to why the " healthy " carriers in European studies (I know of several French ones) were largely males, the studies were done on ....foresters and hunters because they were interested in people who had obvious exposure to ticks! Hence the high numbers of males. I wonder what they would find if they look at the general population and if they had reliable tests, and if they were truly looking at the problem. > Many doctors have noticed that women seem to have more problems in terms of > the severity of symptoms and their difficulty clearing the organism. This may very well be the case. I am certainly a lot sicker than my husband, but in my situation, I think it's a question of one tickbite too many! I was bitten many, many times whereas my husband was only in contact with ticks once (several ticks, though over a period of a few days). Nelly (in France) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 2, 2001 Report Share Posted May 2, 2001 In a message dated 4/27/2001 10:58:53 AM Eastern Daylight Time, janel@... writes: > I am certainly a lot sicker than my husband, > but in my situation, I think it's a question of one tickbite too many! I was > bitten many, many times whereas my husband was only in contact with ticks > once (several ticks, though over a period of a few days). > > Nelly (in France) > Good point, Nelly. I've had Lyme for at least 13 years now, wasn't diagnosed until 1999. My symptoms kept worsening, but kinda gradually, over the years. Then, when I did very active hiking in the woods, getting probably hundreds of tick bites (unknown to me at the time), I suppose that, like you, I just got one ( or a hundred!!!) bite too many & it pushed me over the edge, making my symptoms 1000% worse & it happened literally overnite. I just don't believe that only one tick bite caused this, and I know I've had years of exposure hiking in the beautiful woods " for my health. " Hugs, a Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 12, 2004 Report Share Posted November 12, 2004 from MO - I'd be happy to discuss w/ you my personal experience with the Pearland ISD school district (suburb of Houston). We have had positive experience's here. You can email me directly at wendywellen@... Our church has also just started a Special Needs ministry that isn't fully up and running but will be with in the next few weeks. If anyone wants info on that as well email me personally. Dana - regarding bike camp - I thought my kid was the only one who would not ride without training wheels. He's 8 and it's the crashing he fears. I am very interested and would be willing to volunteer if I'm able. What do we need to do? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 12, 2004 Report Share Posted November 12, 2004 from MO - I'd be happy to discuss w/ you my personal experience with the Pearland ISD school district (suburb of Houston). We have had positive experience's here. You can email me directly at wendywellen@... Our church has also just started a Special Needs ministry that isn't fully up and running but will be with in the next few weeks. If anyone wants info on that as well email me personally. Dana - regarding bike camp - I thought my kid was the only one who would not ride without training wheels. He's 8 and it's the crashing he fears. I am very interested and would be willing to volunteer if I'm able. What do we need to do? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 12, 2004 Report Share Posted November 12, 2004 I must confess that I don't always scroll through every day and read every single article, but wanted to take the time to send a message today about the series Channel 2 Houston is doing on Autism. If you watched the 4pm news Thursday, you saw my family on the " recovering with DAN " spot. What is important to note is that they did an incredible job of editing that piece to show what is really happening for our family with the DAN protocol, but it doesn't show the dedication, time, patience, and cost involved. That would simply be too much. The reason I feel we have had such good results with the DAN protocol are that we have read EVERYTHING we could get our hands on, we've traveled to meet the doctors and hear the researchers give their case studies (I did a lot of that before I put on methyl b-12 and DMSA chelation), we've been gf/cf for almost 3 years, our entire household is gf/cf, not just our son, and we work together as a team in therapies, homework, communication, household running, etc. It is a tremendous process, but if you saw the piece and saw my son hug me and say, " mommy I love you, " and you want that, too, AND you are willing to do whatever it takes, then do the DAN protocol. Not just pieces of it. ALL of it, and get a GOOD DAN! doctor that believes in the protocol and have patience to allow things time to work. Most importantly, have faith, and put it all in the hands that are big enough to carry the load. My prayer is that other families will have recovery like we have with our son. He was never " severe, " but he just wasn't here with us. His speech was 2.5 year level at age 5, and he had SID's, stimming, etc. He's with us now! We are planning an autism conference with Dr. Volpe to be held at our church, League City United Methodist Church, on April 10th from 1:30-6. There will be no cost for this event, but in January, I'll send out notices so you can call and reserve tickets to hear our family's story, and hear the newest up to date DAN! data from Dr. Volpe. We are also looking for one more person that would be willing to speak. My husband will be doing an overview of the rise of autism with stats, studies, charts, videos and all. I'll be sharing our recovery story of , and Dr. Volpe will be there to answer questions. I'd like to have one more speaker to possibly talk about getting insurance help, different therapies, or something along those lines. If you read this and have a suggestion, please email me at lsantos@... Oh, p.s. If you were one of the people I referred to as " a bunch of kooks and nut eating weirdoes, " before I believed the theories on vaccine damage, thank you for paving the way for us to remove the thimerosol from my son's system. It's parents who began this that we owe the recovery of our son. Thank you from the bottom of a very grateful heart. With love and belief, Fellow kook and nut eating weirdo, P. Santos 281 332 1339 www.marykay.com/lsantos Cadillac Unit December 2004 www.laurasantos.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 12, 2004 Report Share Posted November 12, 2004 I must confess that I don't always scroll through every day and read every single article, but wanted to take the time to send a message today about the series Channel 2 Houston is doing on Autism. If you watched the 4pm news Thursday, you saw my family on the " recovering with DAN " spot. What is important to note is that they did an incredible job of editing that piece to show what is really happening for our family with the DAN protocol, but it doesn't show the dedication, time, patience, and cost involved. That would simply be too much. The reason I feel we have had such good results with the DAN protocol are that we have read EVERYTHING we could get our hands on, we've traveled to meet the doctors and hear the researchers give their case studies (I did a lot of that before I put on methyl b-12 and DMSA chelation), we've been gf/cf for almost 3 years, our entire household is gf/cf, not just our son, and we work together as a team in therapies, homework, communication, household running, etc. It is a tremendous process, but if you saw the piece and saw my son hug me and say, " mommy I love you, " and you want that, too, AND you are willing to do whatever it takes, then do the DAN protocol. Not just pieces of it. ALL of it, and get a GOOD DAN! doctor that believes in the protocol and have patience to allow things time to work. Most importantly, have faith, and put it all in the hands that are big enough to carry the load. My prayer is that other families will have recovery like we have with our son. He was never " severe, " but he just wasn't here with us. His speech was 2.5 year level at age 5, and he had SID's, stimming, etc. He's with us now! We are planning an autism conference with Dr. Volpe to be held at our church, League City United Methodist Church, on April 10th from 1:30-6. There will be no cost for this event, but in January, I'll send out notices so you can call and reserve tickets to hear our family's story, and hear the newest up to date DAN! data from Dr. Volpe. We are also looking for one more person that would be willing to speak. My husband will be doing an overview of the rise of autism with stats, studies, charts, videos and all. I'll be sharing our recovery story of , and Dr. Volpe will be there to answer questions. I'd like to have one more speaker to possibly talk about getting insurance help, different therapies, or something along those lines. If you read this and have a suggestion, please email me at lsantos@... Oh, p.s. If you were one of the people I referred to as " a bunch of kooks and nut eating weirdoes, " before I believed the theories on vaccine damage, thank you for paving the way for us to remove the thimerosol from my son's system. It's parents who began this that we owe the recovery of our son. Thank you from the bottom of a very grateful heart. With love and belief, Fellow kook and nut eating weirdo, P. Santos 281 332 1339 www.marykay.com/lsantos Cadillac Unit December 2004 www.laurasantos.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 12, 2004 Report Share Posted November 12, 2004 Dear , I am very happy that your daughter is doing much better following the DAN protocol. Please keep in mind that every child may be affected differently, there is not one answer for everyone. We have done GFCF for 2 years, SCD, B12 shots, DMSA, ABA, TTFD, probiotiocs, EFAs, DMG, enzymes, BIOSET, ST, OT, 6+ DAN doctors, Gazillion supplements and vitamins, and a host of other things and still have not seen any progress. Others have simply put their kids in a PPCD program or took out milk from their diet and their kids have made significant progress. I don't want to discourage anyone but at the same time, it is unrealistic to simplify the plight of others who have not found their magic pill yet. Re: Digest Number 1780 > > I must confess that I don't always scroll through every day and read every > single article, but wanted to take the time to send a message today about > the series Channel 2 Houston is doing on Autism. If you watched the 4pm > news Thursday, you saw my family on the " recovering with DAN " spot. What is > important to note is that they did an incredible job of editing that piece > to show what is really happening for our family with the DAN protocol, but > it doesn't show the dedication, time, patience, and cost involved. That > would simply be too much. > > The reason I feel we have had such good results with the DAN protocol are > that we have read EVERYTHING we could get our hands on, we've traveled to > meet the doctors and hear the researchers give their case studies (I did a > lot of that before I put on methyl b-12 and DMSA chelation), we've > been gf/cf for almost 3 years, our entire household is gf/cf, not just our > son, and we work together as a team in therapies, homework, communication, > household running, etc. > > It is a tremendous process, but if you saw the piece and saw my son hug me > and say, " mommy I love you, " and you want that, too, AND you are willing to > do whatever it takes, then do the DAN protocol. Not just pieces of it. > ALL of it, and get a GOOD DAN! doctor that believes in the protocol and have > patience to allow things time to work. Most importantly, have faith, and > put it all in the hands that are big enough to carry the load. > > My prayer is that other families will have recovery like we have with our > son. He was never " severe, " but he just wasn't here with us. His speech > was 2.5 year level at age 5, and he had SID's, stimming, etc. He's with us > now! > > We are planning an autism conference with Dr. Volpe to be held at our > church, League City United Methodist Church, on April 10th from 1:30-6. > There will be no cost for this event, but in January, I'll send out notices > so you can call and reserve tickets to hear our family's story, and hear the > newest up to date DAN! data from Dr. Volpe. We are also looking for one > more person that would be willing to speak. > > My husband will be doing an overview of the rise of autism with stats, > studies, charts, videos and all. I'll be sharing our recovery story of > , and Dr. Volpe will be there to answer questions. I'd like to have > one more speaker to possibly talk about getting insurance help, different > therapies, or something along those lines. If you read this and have a > suggestion, please email me at lsantos@... > > Oh, p.s. If you were one of the people I referred to as " a bunch of kooks > and nut eating weirdoes, " before I believed the theories on vaccine damage, > thank you for paving the way for us to remove the thimerosol from my son's > system. It's parents who began this that we owe the recovery of our son. > Thank you from the bottom of a very grateful heart. > > With love and belief, > Fellow kook and nut eating weirdo, > > P. Santos > 281 332 1339 > www.marykay.com/lsantos > Cadillac Unit December 2004 > www.laurasantos.com > > > > > Texas Autism Advocacy > > > Unlocking Autism > www.UnlockingAutism.org > > Autism-Awareness-Action > Worldwide internet group for parents who have a > child with AUTISM. > > SeekingJoyinDisability - Prayer support for those touched by Disability: > SeekingJoyinDisability/ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 12, 2004 Report Share Posted November 12, 2004 Dear , I am very happy that your daughter is doing much better following the DAN protocol. Please keep in mind that every child may be affected differently, there is not one answer for everyone. We have done GFCF for 2 years, SCD, B12 shots, DMSA, ABA, TTFD, probiotiocs, EFAs, DMG, enzymes, BIOSET, ST, OT, 6+ DAN doctors, Gazillion supplements and vitamins, and a host of other things and still have not seen any progress. Others have simply put their kids in a PPCD program or took out milk from their diet and their kids have made significant progress. I don't want to discourage anyone but at the same time, it is unrealistic to simplify the plight of others who have not found their magic pill yet. Re: Digest Number 1780 > > I must confess that I don't always scroll through every day and read every > single article, but wanted to take the time to send a message today about > the series Channel 2 Houston is doing on Autism. If you watched the 4pm > news Thursday, you saw my family on the " recovering with DAN " spot. What is > important to note is that they did an incredible job of editing that piece > to show what is really happening for our family with the DAN protocol, but > it doesn't show the dedication, time, patience, and cost involved. That > would simply be too much. > > The reason I feel we have had such good results with the DAN protocol are > that we have read EVERYTHING we could get our hands on, we've traveled to > meet the doctors and hear the researchers give their case studies (I did a > lot of that before I put on methyl b-12 and DMSA chelation), we've > been gf/cf for almost 3 years, our entire household is gf/cf, not just our > son, and we work together as a team in therapies, homework, communication, > household running, etc. > > It is a tremendous process, but if you saw the piece and saw my son hug me > and say, " mommy I love you, " and you want that, too, AND you are willing to > do whatever it takes, then do the DAN protocol. Not just pieces of it. > ALL of it, and get a GOOD DAN! doctor that believes in the protocol and have > patience to allow things time to work. Most importantly, have faith, and > put it all in the hands that are big enough to carry the load. > > My prayer is that other families will have recovery like we have with our > son. He was never " severe, " but he just wasn't here with us. His speech > was 2.5 year level at age 5, and he had SID's, stimming, etc. He's with us > now! > > We are planning an autism conference with Dr. Volpe to be held at our > church, League City United Methodist Church, on April 10th from 1:30-6. > There will be no cost for this event, but in January, I'll send out notices > so you can call and reserve tickets to hear our family's story, and hear the > newest up to date DAN! data from Dr. Volpe. We are also looking for one > more person that would be willing to speak. > > My husband will be doing an overview of the rise of autism with stats, > studies, charts, videos and all. I'll be sharing our recovery story of > , and Dr. Volpe will be there to answer questions. I'd like to have > one more speaker to possibly talk about getting insurance help, different > therapies, or something along those lines. If you read this and have a > suggestion, please email me at lsantos@... > > Oh, p.s. If you were one of the people I referred to as " a bunch of kooks > and nut eating weirdoes, " before I believed the theories on vaccine damage, > thank you for paving the way for us to remove the thimerosol from my son's > system. It's parents who began this that we owe the recovery of our son. > Thank you from the bottom of a very grateful heart. > > With love and belief, > Fellow kook and nut eating weirdo, > > P. Santos > 281 332 1339 > www.marykay.com/lsantos > Cadillac Unit December 2004 > www.laurasantos.com > > > > > Texas Autism Advocacy > > > Unlocking Autism > www.UnlockingAutism.org > > Autism-Awareness-Action > Worldwide internet group for parents who have a > child with AUTISM. > > SeekingJoyinDisability - Prayer support for those touched by Disability: > SeekingJoyinDisability/ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 14, 2004 Report Share Posted November 14, 2004 Hi -- I'm just curious, when you say your son has recovered, do you mean that a psychologist has scored him below a 20 on the CARS test? Or that he is talking an participating in life with you? Thanks, Re: Digest Number 1780 I must confess that I don't always scroll through every day and read every single article, but wanted to take the time to send a message today about the series Channel 2 Houston is doing on Autism. If you watched the 4pm news Thursday, you saw my family on the " recovering with DAN " spot. What is important to note is that they did an incredible job of editing that piece to show what is really happening for our family with the DAN protocol, but it doesn't show the dedication, time, patience, and cost involved. That would simply be too much. The reason I feel we have had such good results with the DAN protocol are that we have read EVERYTHING we could get our hands on, we've traveled to meet the doctors and hear the researchers give their case studies (I did a lot of that before I put on methyl b-12 and DMSA chelation), we've been gf/cf for almost 3 years, our entire household is gf/cf, not just our son, and we work together as a team in therapies, homework, communication, household running, etc. It is a tremendous process, but if you saw the piece and saw my son hug me and say, " mommy I love you, " and you want that, too, AND you are willing to do whatever it takes, then do the DAN protocol. Not just pieces of it. ALL of it, and get a GOOD DAN! doctor that believes in the protocol and have patience to allow things time to work. Most importantly, have faith, and put it all in the hands that are big enough to carry the load. My prayer is that other families will have recovery like we have with our son. He was never " severe, " but he just wasn't here with us. His speech was 2.5 year level at age 5, and he had SID's, stimming, etc. He's with us now! We are planning an autism conference with Dr. Volpe to be held at our church, League City United Methodist Church, on April 10th from 1:30-6. There will be no cost for this event, but in January, I'll send out notices so you can call and reserve tickets to hear our family's story, and hear the newest up to date DAN! data from Dr. Volpe. We are also looking for one more person that would be willing to speak. My husband will be doing an overview of the rise of autism with stats, studies, charts, videos and all. I'll be sharing our recovery story of , and Dr. Volpe will be there to answer questions. I'd like to have one more speaker to possibly talk about getting insurance help, different therapies, or something along those lines. If you read this and have a suggestion, please email me at lsantos@... Oh, p.s. If you were one of the people I referred to as " a bunch of kooks and nut eating weirdoes, " before I believed the theories on vaccine damage, thank you for paving the way for us to remove the thimerosol from my son's system. It's parents who began this that we owe the recovery of our son. Thank you from the bottom of a very grateful heart. With love and belief, Fellow kook and nut eating weirdo, P. Santos 281 332 1339 www.marykay.com/lsantos Cadillac Unit December 2004 www.laurasantos.com Texas Autism Advocacy Unlocking Autism www.UnlockingAutism.org Autism-Awareness-Action Worldwide internet group for parents who have a child with AUTISM. SeekingJoyinDisability - Prayer support for those touched by Disability: SeekingJoyinDisability/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 14, 2004 Report Share Posted November 14, 2004 , our son is below 20 on the CARS, but I don't consider him recovered. He has made tremendous progress in the last 5 years, but still has a long ways to go. Tonya ------------------------------------ Texas Federation of Families Tonya Hettler Trainer thettler@... Route 2 Box 181 Idalou, TX 79329 mobile: (806) 544-0347 http://www.txffcmh.org w-i-n/ ------------------------------------ Re: Digest Number 1780 I must confess that I don't always scroll through every day and read every single article, but wanted to take the time to send a message today about the series Channel 2 Houston is doing on Autism. If you watched the 4pm news Thursday, you saw my family on the " recovering with DAN " spot. What is important to note is that they did an incredible job of editing that piece to show what is really happening for our family with the DAN protocol, but it doesn't show the dedication, time, patience, and cost involved. That would simply be too much. The reason I feel we have had such good results with the DAN protocol are that we have read EVERYTHING we could get our hands on, we've traveled to meet the doctors and hear the researchers give their case studies (I did a lot of that before I put on methyl b-12 and DMSA chelation), we've been gf/cf for almost 3 years, our entire household is gf/cf, not just our son, and we work together as a team in therapies, homework, communication, household running, etc. It is a tremendous process, but if you saw the piece and saw my son hug me and say, " mommy I love you, " and you want that, too, AND you are willing to do whatever it takes, then do the DAN protocol. Not just pieces of it. ALL of it, and get a GOOD DAN! doctor that believes in the protocol and have patience to allow things time to work. Most importantly, have faith, and put it all in the hands that are big enough to carry the load. My prayer is that other families will have recovery like we have with our son. He was never " severe, " but he just wasn't here with us. His speech was 2.5 year level at age 5, and he had SID's, stimming, etc. He's with us now! We are planning an autism conference with Dr. Volpe to be held at our church, League City United Methodist Church, on April 10th from 1:30-6. There will be no cost for this event, but in January, I'll send out notices so you can call and reserve tickets to hear our family's story, and hear the newest up to date DAN! data from Dr. Volpe. We are also looking for one more person that would be willing to speak. My husband will be doing an overview of the rise of autism with stats, studies, charts, videos and all. I'll be sharing our recovery story of , and Dr. Volpe will be there to answer questions. I'd like to have one more speaker to possibly talk about getting insurance help, different therapies, or something along those lines. If you read this and have a suggestion, please email me at lsantos@... Oh, p.s. If you were one of the people I referred to as " a bunch of kooks and nut eating weirdoes, " before I believed the theories on vaccine damage, thank you for paving the way for us to remove the thimerosol from my son's system. It's parents who began this that we owe the recovery of our son. Thank you from the bottom of a very grateful heart. With love and belief, Fellow kook and nut eating weirdo, P. Santos 281 332 1339 www.marykay.com/lsantos Cadillac Unit December 2004 www.laurasantos.com Texas Autism Advocacy Unlocking Autism www.UnlockingAutism.org Autism-Awareness-Action Worldwide internet group for parents who have a child with AUTISM. SeekingJoyinDisability - Prayer support for those touched by Disability: SeekingJoyinDisability/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 15, 2004 Report Share Posted November 15, 2004 Singleton <cmtssingleton@...> wrote:Hi -- I'm just curious, when you say your son has recovered, do you mean that a psychologist has scored him below a 20 on the CARS test? Or that he is talking an participating in life with you? Thanks, Re: Digest Number 1780 I must confess that I don't always scroll through every day and read every single article, but wanted to take the time to send a message today about the series Channel 2 Houston is doing on Autism. If you watched the 4pm news Thursday, you saw my family on the " recovering with DAN " spot. What is important to note is that they did an incredible job of editing that piece to show what is really happening for our family with the DAN protocol, but it doesn't show the dedication, time, patience, and cost involved. That would simply be too much. The reason I feel we have had such good results with the DAN protocol are that we have read EVERYTHING we could get our hands on, we've traveled to meet the doctors and hear the researchers give their case studies (I did a lot of that before I put on methyl b-12 and DMSA chelation), we've been gf/cf for almost 3 years, our entire household is gf/cf, not just our son, and we work together as a team in therapies, homework, communication, household running, etc. It is a tremendous process, but if you saw the piece and saw my son hug me and say, " mommy I love you, " and you want that, too, AND you are willing to do whatever it takes, then do the DAN protocol. Not just pieces of it. ALL of it, and get a GOOD DAN! doctor that believes in the protocol and have patience to allow things time to work. Most importantly, have faith, and put it all in the hands that are big enough to carry the load. My prayer is that other families will have recovery like we have with our son. He was never " severe, " but he just wasn't here with us. His speech was 2.5 year level at age 5, and he had SID's, stimming, etc. He's with us now! We are planning an autism conference with Dr. Volpe to be held at our church, League City United Methodist Church, on April 10th from 1:30-6. There will be no cost for this event, but in January, I'll send out notices so you can call and reserve tickets to hear our family's story, and hear the newest up to date DAN! data from Dr. Volpe. We are also looking for one more person that would be willing to speak. My husband will be doing an overview of the rise of autism with stats, studies, charts, videos and all. I'll be sharing our recovery story of , and Dr. Volpe will be there to answer questions. I'd like to have one more speaker to possibly talk about getting insurance help, different therapies, or something along those lines. If you read this and have a suggestion, please email me at lsantos@... Oh, p.s. If you were one of the people I referred to as " a bunch of kooks and nut eating weirdoes, " before I believed the theories on vaccine damage, thank you for paving the way for us to remove the thimerosol from my son's system. It's parents who began this that we owe the recovery of our son. Thank you from the bottom of a very grateful heart. With love and belief, Fellow kook and nut eating weirdo, P. Santos 281 332 1339 www.marykay.com/lsantos Cadillac Unit December 2004 www.laurasantos.com Texas Autism Advocacy Unlocking Autism www.UnlockingAutism.org Autism-Awareness-Action Worldwide internet group for parents who have a child with AUTISM. SeekingJoyinDisability - Prayer support for those touched by Disability: SeekingJoyinDisability/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 15, 2004 Report Share Posted November 15, 2004 Singleton <cmtssingleton@...> wrote:Hi -- I'm just curious, when you say your son has recovered, do you mean that a psychologist has scored him below a 20 on the CARS test? Or that he is talking an participating in life with you? Thanks, Re: Digest Number 1780 I must confess that I don't always scroll through every day and read every single article, but wanted to take the time to send a message today about the series Channel 2 Houston is doing on Autism. If you watched the 4pm news Thursday, you saw my family on the " recovering with DAN " spot. What is important to note is that they did an incredible job of editing that piece to show what is really happening for our family with the DAN protocol, but it doesn't show the dedication, time, patience, and cost involved. That would simply be too much. The reason I feel we have had such good results with the DAN protocol are that we have read EVERYTHING we could get our hands on, we've traveled to meet the doctors and hear the researchers give their case studies (I did a lot of that before I put on methyl b-12 and DMSA chelation), we've been gf/cf for almost 3 years, our entire household is gf/cf, not just our son, and we work together as a team in therapies, homework, communication, household running, etc. It is a tremendous process, but if you saw the piece and saw my son hug me and say, " mommy I love you, " and you want that, too, AND you are willing to do whatever it takes, then do the DAN protocol. Not just pieces of it. ALL of it, and get a GOOD DAN! doctor that believes in the protocol and have patience to allow things time to work. Most importantly, have faith, and put it all in the hands that are big enough to carry the load. My prayer is that other families will have recovery like we have with our son. He was never " severe, " but he just wasn't here with us. His speech was 2.5 year level at age 5, and he had SID's, stimming, etc. He's with us now! We are planning an autism conference with Dr. Volpe to be held at our church, League City United Methodist Church, on April 10th from 1:30-6. There will be no cost for this event, but in January, I'll send out notices so you can call and reserve tickets to hear our family's story, and hear the newest up to date DAN! data from Dr. Volpe. We are also looking for one more person that would be willing to speak. My husband will be doing an overview of the rise of autism with stats, studies, charts, videos and all. I'll be sharing our recovery story of , and Dr. Volpe will be there to answer questions. I'd like to have one more speaker to possibly talk about getting insurance help, different therapies, or something along those lines. If you read this and have a suggestion, please email me at lsantos@... Oh, p.s. If you were one of the people I referred to as " a bunch of kooks and nut eating weirdoes, " before I believed the theories on vaccine damage, thank you for paving the way for us to remove the thimerosol from my son's system. It's parents who began this that we owe the recovery of our son. Thank you from the bottom of a very grateful heart. With love and belief, Fellow kook and nut eating weirdo, P. Santos 281 332 1339 www.marykay.com/lsantos Cadillac Unit December 2004 www.laurasantos.com Texas Autism Advocacy Unlocking Autism www.UnlockingAutism.org Autism-Awareness-Action Worldwide internet group for parents who have a child with AUTISM. SeekingJoyinDisability - Prayer support for those touched by Disability: SeekingJoyinDisability/ Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.