"The RT-PCR test being used for
COVID involves a cycling function.
The more you cycle the test material in the lab, the more people test positive for COVID. If you cycle the test material 60 times, every sample tests positive for COVID. If you cycle it 10 times, no one tests positive. If you cycle it 30 times, some test positive and some don't. This means all our corrupt goverments have full control of how many people test positive, depending on how many times they insist the test material be cycled. They've picked this test
purposely so they can
up-regulate or down-regulate the
pandemic at will..."
Jason Christoff
COVID involves a cycling function.
The more you cycle the test material in the lab, the more people test positive for COVID. If you cycle the test material 60 times, every sample tests positive for COVID. If you cycle it 10 times, no one tests positive. If you cycle it 30 times, some test positive and some don't. This means all our corrupt goverments have full control of how many people test positive, depending on how many times they insist the test material be cycled. They've picked this test
purposely so they can
up-regulate or down-regulate the
pandemic at will..."
Jason Christoff
👍75
This Thursday, I will be interviewing David Daleiden, who was exposing Planned Parenthood on felony charges for selling aborted fetal parts. Kamala Harris dismissed the charges against Planned Parenthood and fined David millions of dollars for bringing the truth to the people. Ever ask yourself who’s buying???
Ever wonder why I’m so adamantly against vaccines? Because the abortion industry and the vaccine industry are one and the same.
“Today, more than 23 vaccines are contaminated by the use of aborted fetal cells. There is no law that requires that consumers be informed that some vaccines are made using aborted fetal cells and contain residual aborted fetal DNA. While newer vaccines produced using aborted fetal cells do inform consumers, in their package inserts, that the vaccines contain contaminating DNA from the cell used to produce the vaccines, they do not identify the cells as being derived from electively aborted human fetuses.”
Dr. Theresa Deisher, Ph.D.
Ever wonder why I’m so adamantly against vaccines? Because the abortion industry and the vaccine industry are one and the same.
“Today, more than 23 vaccines are contaminated by the use of aborted fetal cells. There is no law that requires that consumers be informed that some vaccines are made using aborted fetal cells and contain residual aborted fetal DNA. While newer vaccines produced using aborted fetal cells do inform consumers, in their package inserts, that the vaccines contain contaminating DNA from the cell used to produce the vaccines, they do not identify the cells as being derived from electively aborted human fetuses.”
Dr. Theresa Deisher, Ph.D.
👍45
CARMEN WHITE May 4, 2013 at 10:35 pm This is so AWESOME!!!! Thank you for taking the time to put this together. Hopefully with more people like you, we can continue to educate more parents about the harmful effects of vaccines. Reply
sandy fleming May 5, 2013 at 1:53 am I am really curious, how did you find these? I thought I was pretty good at googling, but never came across so much hard science when I did my research, instead I’d come across something on “Natural News” but never able to find these peer reviewed studies. If you don’t mind sharing, can you tell me how you found most of these? Reply
Pingback: my response to a friend who fears vaccination and is unsure what to do. | The Refurbished Rogue's Blog
myautisticmuslimchild June 1, 2013 at 1:24 am Thank you for this post. i will be posting this link on my blog. I researched a lot, bc my son’s problem started after his 13 months vaccine (rather 12 but i was late for 1 month). i always swear by that his autism has something to do with his vaccination since he got so sick after 4 combination shots. We are still struggling, but if I can help other families to make a better decision about vaccination ut will worth all the fight. Reply
the referbished rogue June 1, 2013 at 1:57 am thank you for the kind words. I don’t know how God decides which children will become autistic..but I do know that he chooses strong families who are not broken by this condition and he chooses parents like yourself who search to help others even through their own challenges. Thank you for allowing others to enter into your world and learn from your experiences. Keep fighting the good fight -briana Reply
Sheri Nakken, former RN, MA, Hahnemannian Homeopath November 17, 2013 at 7:03 pm I really don’t think God decides this…………….my God doesn’t cause injury or harm or pain. It is humans who do this.
the referbished rogue November 17, 2013 at 9:09 pm You are right..evil does not come from God but from sinful man. I do, however, believe that God allows bad things to happen at times for a higher purpose. For a purpose that only He knows. He allows bad things to happen only when the outcome from them will do good things. example: a Christian lady has cancer but while she is in the hospital, she witnesses to her roommate and her roommate becomes a follower of Jesus Christ. There could be two endings to this story..both good, one – the lady could receive healing and go on to live a long life. or two – the Lord could take her to spend an eternity with Him.
Sheri Nakken, former RN, MA, Hahnemannian Homeopath November 17, 2013 at 9:13 pm those outcomes could happen, but a perfect loving God could NOT cause these things, or even allow these things (if allowed them, is not the perfect God). I have a different view on this. If God allows or causes, then God is not a perfect loving being. Yes, those outcomse could happen, but not because God uses us in this way.
the referbished rogue November 17, 2013 at 10:06 pm The world that God intented for us to live was perfect..no pain..no sadness. But because God gave us freewill and is not a dictator..man chose to go against God and sin entered this world. From that point on..man has had to toil to eat..women scream out in pain during childbirth. But out of these hardships do you not still see love? Food to fill our bellies and children to love. The ultimate reason that I know that God is love through all the darkness..is that He sent his son Jesus Christ to die for our sins so that we may have life. Nothing that happens to us on this earth matters when you realize that heaven is ours because of what Jesus did on behalf of His Father. Just one example I would like for you look into if you like, is the book of Job. Regardless that we may see some things differently..let us keep our eyes on what really matters. Let us keep our eyes on Jesus. http://www.gotquestions.org/God-allow-Satan-attack.html
sandy fleming May 5, 2013 at 1:53 am I am really curious, how did you find these? I thought I was pretty good at googling, but never came across so much hard science when I did my research, instead I’d come across something on “Natural News” but never able to find these peer reviewed studies. If you don’t mind sharing, can you tell me how you found most of these? Reply
Pingback: my response to a friend who fears vaccination and is unsure what to do. | The Refurbished Rogue's Blog
myautisticmuslimchild June 1, 2013 at 1:24 am Thank you for this post. i will be posting this link on my blog. I researched a lot, bc my son’s problem started after his 13 months vaccine (rather 12 but i was late for 1 month). i always swear by that his autism has something to do with his vaccination since he got so sick after 4 combination shots. We are still struggling, but if I can help other families to make a better decision about vaccination ut will worth all the fight. Reply
the referbished rogue June 1, 2013 at 1:57 am thank you for the kind words. I don’t know how God decides which children will become autistic..but I do know that he chooses strong families who are not broken by this condition and he chooses parents like yourself who search to help others even through their own challenges. Thank you for allowing others to enter into your world and learn from your experiences. Keep fighting the good fight -briana Reply
Sheri Nakken, former RN, MA, Hahnemannian Homeopath November 17, 2013 at 7:03 pm I really don’t think God decides this…………….my God doesn’t cause injury or harm or pain. It is humans who do this.
the referbished rogue November 17, 2013 at 9:09 pm You are right..evil does not come from God but from sinful man. I do, however, believe that God allows bad things to happen at times for a higher purpose. For a purpose that only He knows. He allows bad things to happen only when the outcome from them will do good things. example: a Christian lady has cancer but while she is in the hospital, she witnesses to her roommate and her roommate becomes a follower of Jesus Christ. There could be two endings to this story..both good, one – the lady could receive healing and go on to live a long life. or two – the Lord could take her to spend an eternity with Him.
Sheri Nakken, former RN, MA, Hahnemannian Homeopath November 17, 2013 at 9:13 pm those outcomes could happen, but a perfect loving God could NOT cause these things, or even allow these things (if allowed them, is not the perfect God). I have a different view on this. If God allows or causes, then God is not a perfect loving being. Yes, those outcomse could happen, but not because God uses us in this way.
the referbished rogue November 17, 2013 at 10:06 pm The world that God intented for us to live was perfect..no pain..no sadness. But because God gave us freewill and is not a dictator..man chose to go against God and sin entered this world. From that point on..man has had to toil to eat..women scream out in pain during childbirth. But out of these hardships do you not still see love? Food to fill our bellies and children to love. The ultimate reason that I know that God is love through all the darkness..is that He sent his son Jesus Christ to die for our sins so that we may have life. Nothing that happens to us on this earth matters when you realize that heaven is ours because of what Jesus did on behalf of His Father. Just one example I would like for you look into if you like, is the book of Job. Regardless that we may see some things differently..let us keep our eyes on what really matters. Let us keep our eyes on Jesus. http://www.gotquestions.org/God-allow-Satan-attack.html
PubMed
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders - PubMed
The first conjugate vaccine was approved for use in the US in 1988 to protect infants and young children against the capsular bacteria Haemophilus influenzae type b (Hib). Since its introduction in the US, this vaccine has been approved in most developed…
👍4
the referbished rogue November 17, 2013 at 10:36 pm I just thought about this post..i wrote this over a year ago but this touches on our discussion and this is from my heart. https://therefurbishedrogue.wordpress.com/2012/07/03/on-the-child-i-lost-the-child-who-waits-for-me/
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shanklandfamily September 13, 2013 at 6:11 pm What an amazing list! Thank you SO MUCH for putting this together!! I have been looking for more factual information like this and your list is just what I need to get started in my reading. Your hard work is much appreciated. Reply
the referbished rogue September 15, 2013 at 4:27 am So very glad to hear it. God bless! Reply
Kathleen E W Bailey September 15, 2013 at 4:14 pm Reblogged this on Soul Kitty and commented: Wow, a wealth of info! Reply
Sheri Nakken, former RN, MA, Hahnemannian Homeopath November 17, 2013 at 7:02 pm What an incredible list you have compiled! Wonderful and thank you. Will have to read further and see who you are! Reply
the referbished rogue November 17, 2013 at 9:03 pm thank you and your welcome! ohh Lord..im afraid of what you may find. Laugh, laugh. God bless you! Reply
puameliaclinic November 17, 2013 at 10:43 pm Reblogged this on The Pua Melia Clinic and commented: A page on getting some papers on Jab research Reply
notidlechatter November 18, 2013 at 1:45 pm I love all the titles to your blogs. It seems as if we have been on a similar journey. I also bask in God’s grace and seek to share the truths He teaches me with others. I have a particular interest in health, wellness and avoiding vaccines. I am learning about the technology I need to get the message out more effectively. I’ve started a blog at http://www.journeyboost.com I appreciate all the work you have put in and I wish all my friends and acquaintances who want to convince me that the science supports vaccines would read every article! Thank you. Reply
the referbished rogue November 18, 2013 at 4:58 pm Thank you for the encouragement! Seriously..that meant a lot to me. I can’t wait to.check out your blog 🙂 In Christ’s love and maranatha – briana Reply
Lou January 7, 2014 at 6:45 am Wonderful – many thanks. In my own years of research, it always bugged me why some children / people were effected and others not (I get this question sometimes). There are a few that I recall which explains why: 1. manufacture conditions can vary and ingredients/contamination occurs in “batches”. 2. temperature control 3. varying levels of toxic additives (e.g. mercury – can be more damaging if the vial is not shaken before injection) 4. the state of the immune system 5. autism is higher in boys because of the way mercury reacts with male hormones. Just to name a few….Certain groups are used more for “guinea pig” testing than other groups. Reply
the referbished rogue January 7, 2014 at 9:59 am Very good reasoning! I agree with you. It’s a shame that an industry that affects ( I really hope i used the right one there. . I always question myself ha) isn’t more aware and looking to fix these issues for the sake of the millions of children who, by blind faith, are subjected to these things. God bless you. – briana Reply
David September 2, 2015 at 10:58 am It’s about genetics. Some people have gene combinations that don’t allow them to methylate the toxins in Vaccines (along with other genes that contribute to adverse reactions in other ways). Meaning, their body doesn’t detect the toxins and therefore doesn’t get rid of them, so you have Aluminum, Mercury and other carcinogenics circulating in the system or burying into cells. There are therapies such as Chelation which flush these toxins, so there is hope. The problem is that NO ONE does genetic testing prior to Vaccination to determine if this is a problem. This is why some people have adverse reactions to Vaccines and some do not.
Pingback: Vaccine Research » My Autistic Muslim Child
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shanklandfamily September 13, 2013 at 6:11 pm What an amazing list! Thank you SO MUCH for putting this together!! I have been looking for more factual information like this and your list is just what I need to get started in my reading. Your hard work is much appreciated. Reply
the referbished rogue September 15, 2013 at 4:27 am So very glad to hear it. God bless! Reply
Kathleen E W Bailey September 15, 2013 at 4:14 pm Reblogged this on Soul Kitty and commented: Wow, a wealth of info! Reply
Sheri Nakken, former RN, MA, Hahnemannian Homeopath November 17, 2013 at 7:02 pm What an incredible list you have compiled! Wonderful and thank you. Will have to read further and see who you are! Reply
the referbished rogue November 17, 2013 at 9:03 pm thank you and your welcome! ohh Lord..im afraid of what you may find. Laugh, laugh. God bless you! Reply
puameliaclinic November 17, 2013 at 10:43 pm Reblogged this on The Pua Melia Clinic and commented: A page on getting some papers on Jab research Reply
notidlechatter November 18, 2013 at 1:45 pm I love all the titles to your blogs. It seems as if we have been on a similar journey. I also bask in God’s grace and seek to share the truths He teaches me with others. I have a particular interest in health, wellness and avoiding vaccines. I am learning about the technology I need to get the message out more effectively. I’ve started a blog at http://www.journeyboost.com I appreciate all the work you have put in and I wish all my friends and acquaintances who want to convince me that the science supports vaccines would read every article! Thank you. Reply
the referbished rogue November 18, 2013 at 4:58 pm Thank you for the encouragement! Seriously..that meant a lot to me. I can’t wait to.check out your blog 🙂 In Christ’s love and maranatha – briana Reply
Lou January 7, 2014 at 6:45 am Wonderful – many thanks. In my own years of research, it always bugged me why some children / people were effected and others not (I get this question sometimes). There are a few that I recall which explains why: 1. manufacture conditions can vary and ingredients/contamination occurs in “batches”. 2. temperature control 3. varying levels of toxic additives (e.g. mercury – can be more damaging if the vial is not shaken before injection) 4. the state of the immune system 5. autism is higher in boys because of the way mercury reacts with male hormones. Just to name a few….Certain groups are used more for “guinea pig” testing than other groups. Reply
the referbished rogue January 7, 2014 at 9:59 am Very good reasoning! I agree with you. It’s a shame that an industry that affects ( I really hope i used the right one there. . I always question myself ha) isn’t more aware and looking to fix these issues for the sake of the millions of children who, by blind faith, are subjected to these things. God bless you. – briana Reply
David September 2, 2015 at 10:58 am It’s about genetics. Some people have gene combinations that don’t allow them to methylate the toxins in Vaccines (along with other genes that contribute to adverse reactions in other ways). Meaning, their body doesn’t detect the toxins and therefore doesn’t get rid of them, so you have Aluminum, Mercury and other carcinogenics circulating in the system or burying into cells. There are therapies such as Chelation which flush these toxins, so there is hope. The problem is that NO ONE does genetic testing prior to Vaccination to determine if this is a problem. This is why some people have adverse reactions to Vaccines and some do not.
PubMed
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders - PubMed
The first conjugate vaccine was approved for use in the US in 1988 to protect infants and young children against the capsular bacteria Haemophilus influenzae type b (Hib). Since its introduction in the US, this vaccine has been approved in most developed…
👍4
This is a hard science, called Epigenetics. Reply
Judy March 12, 2014 at 6:55 pm So many Newspapers are pushing provax messages – these journalists have not done any research. It is important to add to the comments whenever you can – not only do you educate the journalists but you may help inform the public and give another view. Love your Blog – great information, thank you so much. Reply
the referbished rogue March 15, 2014 at 1:56 am Your welcome so much, Judy 🙂 it makes me happy when I get a notification that this post has been viewed by someone referred to it from a comment on a pro vax, propaganda article. God bless 🙂 Reply
Chris March 14, 2014 at 2:28 am Keep up the good work!! The world is waking up. .. Reply
Gabriel March 19, 2014 at 8:15 pm Thanks for doing all this work. I do have one question. How do you know that the articles are “peer reviewed”? Thanks! Reply
the referbished rogue March 30, 2014 at 6:31 pm Your welcome Gabriel.. And thank you. All the links are to articles that have been published in journals that have a panel of medical / science professionals which must approve the data and the integrity of the article before it is allowed to be published. Reply
David Fenton December 20, 2015 at 6:13 pm Hi, I’m developing a web site called real-morality and would like to use you list of peer reviewed articles as is, with a credit to you and link. In time I might organise them into some logical groups. My website is still in parking mode. Thanks and appreciation
the referbished rogue January 16, 2016 at 9:20 pm Sure, that sounds fine. Thank you for wanting to include it. God bless, briana
David September 2, 2015 at 11:00 am Most of these are from NIH. I’ve found these myself as well. You can’t get more peer-reviewed than a government health and technology agency. Reply
Chris Robison March 30, 2014 at 6:04 pm bless you for doing this!! but I thought all anti-vaxxers are “anti-science”.. that’s what the science magazines all tell us.. 🙂 Reply
Tina "I" April 2, 2014 at 6:48 am Wow! This is wonderful! Thanks so much for the time you have put into this, and especially for “sharing”. Everyone needs to keep getting the word out, so those that blindly follow, might eventually get their wake-up call… Hopefully, before it’s too late. Thank you! Thank you! Thank you! So nice to have it all in one place, as a reference. Reply
the referbished rogue April 2, 2014 at 10:47 am Your welcome.. And thank you for commenting (every girl likes to feel special sometimes..ha) God bless! Reply
Merideth April 19, 2014 at 8:34 pm Can you add a Pinterest link, so I can pin it, and keep it forever! Thanks Reply
the referbished rogue April 21, 2014 at 6:06 pm Yes :)… Once I figure it out and am at my desktop..I will add it. Reply
Shane Thepeopleschemist Ellison April 28, 2014 at 6:49 pm Good parent! Reply
Lee June 14, 2014 at 5:21 pm Awesome job!!!!! Thanks Reply
Kim July 14, 2014 at 8:37 pm Thank you SO VERY MUCH for doing this! I have been helping members of my family research this issue (some of them for the very first time); this will help tremendously. Reply
Melinda Blondeaux July 27, 2014 at 12:09 pm You will probably want to add this one too: Abstract: “Background: The Shaken Baby Syndrome conceived by Guthkeltch to explain bruises, fractures, retinal and cerebral haemorrhage and encephalopathy in children, called the “triad”, can be explained by an autoimmune reaction to antigens in a genetically susceptible child. Method: Children diagnosed as suffering from Non-accidental injuries were investigated for evidence of immune response reactions following mandated vaccination and childhood illnesses.
Judy March 12, 2014 at 6:55 pm So many Newspapers are pushing provax messages – these journalists have not done any research. It is important to add to the comments whenever you can – not only do you educate the journalists but you may help inform the public and give another view. Love your Blog – great information, thank you so much. Reply
the referbished rogue March 15, 2014 at 1:56 am Your welcome so much, Judy 🙂 it makes me happy when I get a notification that this post has been viewed by someone referred to it from a comment on a pro vax, propaganda article. God bless 🙂 Reply
Chris March 14, 2014 at 2:28 am Keep up the good work!! The world is waking up. .. Reply
Gabriel March 19, 2014 at 8:15 pm Thanks for doing all this work. I do have one question. How do you know that the articles are “peer reviewed”? Thanks! Reply
the referbished rogue March 30, 2014 at 6:31 pm Your welcome Gabriel.. And thank you. All the links are to articles that have been published in journals that have a panel of medical / science professionals which must approve the data and the integrity of the article before it is allowed to be published. Reply
David Fenton December 20, 2015 at 6:13 pm Hi, I’m developing a web site called real-morality and would like to use you list of peer reviewed articles as is, with a credit to you and link. In time I might organise them into some logical groups. My website is still in parking mode. Thanks and appreciation
the referbished rogue January 16, 2016 at 9:20 pm Sure, that sounds fine. Thank you for wanting to include it. God bless, briana
David September 2, 2015 at 11:00 am Most of these are from NIH. I’ve found these myself as well. You can’t get more peer-reviewed than a government health and technology agency. Reply
Chris Robison March 30, 2014 at 6:04 pm bless you for doing this!! but I thought all anti-vaxxers are “anti-science”.. that’s what the science magazines all tell us.. 🙂 Reply
Tina "I" April 2, 2014 at 6:48 am Wow! This is wonderful! Thanks so much for the time you have put into this, and especially for “sharing”. Everyone needs to keep getting the word out, so those that blindly follow, might eventually get their wake-up call… Hopefully, before it’s too late. Thank you! Thank you! Thank you! So nice to have it all in one place, as a reference. Reply
the referbished rogue April 2, 2014 at 10:47 am Your welcome.. And thank you for commenting (every girl likes to feel special sometimes..ha) God bless! Reply
Merideth April 19, 2014 at 8:34 pm Can you add a Pinterest link, so I can pin it, and keep it forever! Thanks Reply
the referbished rogue April 21, 2014 at 6:06 pm Yes :)… Once I figure it out and am at my desktop..I will add it. Reply
Shane Thepeopleschemist Ellison April 28, 2014 at 6:49 pm Good parent! Reply
Lee June 14, 2014 at 5:21 pm Awesome job!!!!! Thanks Reply
Kim July 14, 2014 at 8:37 pm Thank you SO VERY MUCH for doing this! I have been helping members of my family research this issue (some of them for the very first time); this will help tremendously. Reply
Melinda Blondeaux July 27, 2014 at 12:09 pm You will probably want to add this one too: Abstract: “Background: The Shaken Baby Syndrome conceived by Guthkeltch to explain bruises, fractures, retinal and cerebral haemorrhage and encephalopathy in children, called the “triad”, can be explained by an autoimmune reaction to antigens in a genetically susceptible child. Method: Children diagnosed as suffering from Non-accidental injuries were investigated for evidence of immune response reactions following mandated vaccination and childhood illnesses.
PubMed
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders - PubMed
The first conjugate vaccine was approved for use in the US in 1988 to protect infants and young children against the capsular bacteria Haemophilus influenzae type b (Hib). Since its introduction in the US, this vaccine has been approved in most developed…
Results: It was found in all the cases reported here the response to antigenic stimulation damaged the Beta cells in the Pancreas causing Hypoinsulinaemia which inhibited the cellular uptake of Vitamin C resulting in liver dysfunction, failure of carboxylation of the Vitamin K dependent proteins resulting in haemorrhages and fractures associated with the “triad”. Conclusion: Fractures, retinal and subdural haemorrhages and encephalopathy in children – is an autoimmune response to antigenic stimulation in a genetically susceptible individual. Common antigens are the mandated vaccines, viral bacterial and parasitic infections. ” Interpretation “In all four cases shown here there is evidence that hyperglycaemia followed vaccination and hyperglycaemia implies hypoinsulinism, an autoimmune disorder resulting from the destruction of the Beta cells of the pancreas. Since insulin is required for the transfer of vitamin C into the cells the intracellular vitamin C is reduced[12]. The resulting “tissue scurvy” compromises the function of the Liver by inhibiting carboxylation of the clotting and bone forming factors and is manifested as the signs and symptoms of the “triad”. Both Dr Kalokerinos and Professor Clemetson recommended giving the infant Vitamin C before vaccination but it would seem more appropriate to do an intradermal skin test to test for sensitivity in every case. Both were firmly of the view that a metabolic abnormality of Vitamin C was the essential cause of the signs and symptoms of the alleged “Non-accidental injuries”. ” Michael D Innis. Autoimmunity and Non-Accidental Injury in Children. Clinical Medicine Research. Vol. 2, No. 3, 2013, pp. 40-44. doi: 10.11648/j.cmr.20130203.15 Click to access 10.11648.j.cmr.20130203.15.pdf Reply
the referbished rogue August 28, 2014 at 9:43 pm Thank you 🙂 I will add this along with some others. Reply
Megan @LivingWhole.org September 6, 2014 at 8:37 pm Wow! You really did your research! I am very impressed and am glad I came across your blog. Keep it up. 🙂 Reply
the referbished rogue September 7, 2014 at 11:01 am If this is Megan from the living whole that recently published the article about God not liking vaccines.. wow!! I am honored!! Your website is awesome. Reply
Marcella Piper-Terry February 2, 2015 at 11:22 am Thank-you so much for this amazing resource! I would love to share it as a guest blog on VaxTruth.org. Reply
the referbished rogue February 2, 2015 at 5:27 pm Oh wow! Thank you thank you! Of course you may! I am tickled right now 🙂 and honored for you to have read my blog!!! I love TTMR! Reply
the referbished rogue February 2, 2015 at 5:31 pm I love vax truth as well.. I was so excited I don’t know what I wrote! God bless!!
punyahannawilbur February 3, 2015 at 4:55 am Reblogged this on Hanna Wilbur's. Reply
Lou July 22, 2015 at 11:08 pm Praise God for this site! Reply
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the referbished rogue August 28, 2014 at 9:43 pm Thank you 🙂 I will add this along with some others. Reply
Megan @LivingWhole.org September 6, 2014 at 8:37 pm Wow! You really did your research! I am very impressed and am glad I came across your blog. Keep it up. 🙂 Reply
the referbished rogue September 7, 2014 at 11:01 am If this is Megan from the living whole that recently published the article about God not liking vaccines.. wow!! I am honored!! Your website is awesome. Reply
Marcella Piper-Terry February 2, 2015 at 11:22 am Thank-you so much for this amazing resource! I would love to share it as a guest blog on VaxTruth.org. Reply
the referbished rogue February 2, 2015 at 5:27 pm Oh wow! Thank you thank you! Of course you may! I am tickled right now 🙂 and honored for you to have read my blog!!! I love TTMR! Reply
the referbished rogue February 2, 2015 at 5:31 pm I love vax truth as well.. I was so excited I don’t know what I wrote! God bless!!
punyahannawilbur February 3, 2015 at 4:55 am Reblogged this on Hanna Wilbur's. Reply
Lou July 22, 2015 at 11:08 pm Praise God for this site! Reply
Leave a Reply
Your email address will not be published. Required fields are marked *
Comment *
Name *
Email *
Website
Notify me of new comments via email.
Notify me of new posts via email.
RECENT POSTS
Abortion is forever
Why we should welcome homosexuals into our churches – the thoughts of an evangelical, pentecostal Christian
(no title)
On Peace and the Little Girl Who Altered My Heart
“Vaccines Saved Us” – Intellectual Dishonesty At Its Most Naked
MOST VIEWED RECENT POSTS
my list of peer reviewed vaccine research
On Peace and the Little Girl Who Altered My Heart
Biblical reasons to oppose vaccination
Read the back of your toothpaste - fluoride IS poison. if there's doubt - GET IT OUT!
WHAT WOULD YOU LIKE TO READ ABOUT?
what would you like to read about?
Select Category
Finding God
Fluoride is bad for you
God is Love
homeschool stuff
my take on proverbs
my testimony
my thoughts on true christianity
on when God grew skin
redemption
spiritual warfare
The bible is smart
the praying parent
thinking free
To Train Up A Child
Uncategorized
vaccination
PubMed
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders - PubMed
The first conjugate vaccine was approved for use in the US in 1988 to protect infants and young children against the capsular bacteria Haemophilus influenzae type b (Hib). Since its introduction in the US, this vaccine has been approved in most developed…
👍2
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REFURBISHED ROGUE – FACEBOOK STYLE
I WILL SPEAK FOR THOSE WHO CANNOT. ABOLISH HUMAN ABORTION.
May 2013
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PubMed
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders - PubMed
The first conjugate vaccine was approved for use in the US in 1988 to protect infants and young children against the capsular bacteria Haemophilus influenzae type b (Hib). Since its introduction in the US, this vaccine has been approved in most developed…
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The Refurbished Rogue's Blog
the random scribbles and unrestrained convictions of a wayward fool liberated by grace
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May 3, 2013
my list of peer reviewed vaccine research
• 57 Comments
This list is just a thrown together list and is pretty helter skelter..but, there are a lot of links to lead you down the research path if you are searching. There are are so many, many, many more out there that haven’t made it to this list. They sit and wait for me to find them..i better get to looking.. May our truth digging be successful!
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders.
the potential effects of conjugate vaccines on neural development merit close examination. Conjugate vaccines fundamentally change the manner in which the immune systems of infants and young children function by deviating their immune responses to the targeted carbohydrate antigens from a state of hypo-responsiveness to a robust B2 B cell mediated response. This period of hypo-responsiveness to carbohydrate antigens coincides with the intense myelination process in infants and young children, and conjugate vaccines may have disrupted evolutionary forces that favored early brain development over the need to protect infants and young children from capsular bacteria.
http://www.ncbi.nlm.nih.gov/pubmed/21993250
Serological association of measles virus and human herpesvirus-6 with brain autoantibodies in autism.
Considering an autoimmunity and autism connection, brain autoantibodies to myelin basic protein (anti-MBP) and neuron-axon filament protein (anti-NAFP) have been found in autistic children. In this current study, we examined associations between virus serology and autoantibody by simultaneous analysis of measles virus antibody (measles-IgG), human herpesvirus-6 antibody (HHV-6-IgG), anti-MBP, and anti-NAFP. We found that measles-IgG and HHV-6-IgG titers were moderately higher in autistic children but they did not significantly differ from normal controls. Moreover, we found that a vast majority of virus serology-positive autistic sera was also positive for brain autoantibody: (i) 90% of measles-IgG-positive autistic sera was also positive for anti-MBP; (ii) 73% of measles-IgG-positive autistic sera was also positive for anti-NAFP; (iii) 84% of HHV-6-IgG-positive autistic sera was also positive for anti-MBP; and (iv) 72% of HHV-6-IgG-positive autistic sera was also positive for anti-NAFP. This study is the first to report an association between virus serology and brain autoantibody in autism; it supports the hypothesis that a virus-induced autoimmune response may play a causal role in autism.
http://www.ncbi.nlm.nih.gov/pubmed/9756729
Effectiveness of pertussis vaccines for adolescents and adults: case-control study
The adjusted estimate of effectiveness of Tdap vaccination against pertussis was 53.0.
http://www.bmj.com/content/347/bmj.f4249
Neurologic Adverse Events Following Vaccination (Progress in Health Sciences Vol. 2(1) 2012•pp 129-141.)
“Conclusions: Despite the assurances of the necessity and safety of vaccinations, there are more and more questions and doubts, which both physicians and parents are waiting to be clarified… It seems that it would be worthwhile to apply the precautionary principle – the ethical principle (from 1988) according to which if there is a probable, although poorly known, risk of adverse effects of new technology, it is better not to implement it rather than risk uncertain but potentially very harmful consequences.”
http://progress.umb.edu.pl/sites/progress.umb.edu.pl/files/129-141.pdf
Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism.
the random scribbles and unrestrained convictions of a wayward fool liberated by grace
Main menu
Skip to content
Finding God
vaccination
my thoughts on true christianity
my list of peer reviewed vaccine research
what’s wrong with this world!
forgiveness
thinking free
About
redemption
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my testimony
Fluoride is bad for you
homeschool stuff
SEARCH
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May 3, 2013
my list of peer reviewed vaccine research
• 57 Comments
This list is just a thrown together list and is pretty helter skelter..but, there are a lot of links to lead you down the research path if you are searching. There are are so many, many, many more out there that haven’t made it to this list. They sit and wait for me to find them..i better get to looking.. May our truth digging be successful!
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders.
the potential effects of conjugate vaccines on neural development merit close examination. Conjugate vaccines fundamentally change the manner in which the immune systems of infants and young children function by deviating their immune responses to the targeted carbohydrate antigens from a state of hypo-responsiveness to a robust B2 B cell mediated response. This period of hypo-responsiveness to carbohydrate antigens coincides with the intense myelination process in infants and young children, and conjugate vaccines may have disrupted evolutionary forces that favored early brain development over the need to protect infants and young children from capsular bacteria.
http://www.ncbi.nlm.nih.gov/pubmed/21993250
Serological association of measles virus and human herpesvirus-6 with brain autoantibodies in autism.
Considering an autoimmunity and autism connection, brain autoantibodies to myelin basic protein (anti-MBP) and neuron-axon filament protein (anti-NAFP) have been found in autistic children. In this current study, we examined associations between virus serology and autoantibody by simultaneous analysis of measles virus antibody (measles-IgG), human herpesvirus-6 antibody (HHV-6-IgG), anti-MBP, and anti-NAFP. We found that measles-IgG and HHV-6-IgG titers were moderately higher in autistic children but they did not significantly differ from normal controls. Moreover, we found that a vast majority of virus serology-positive autistic sera was also positive for brain autoantibody: (i) 90% of measles-IgG-positive autistic sera was also positive for anti-MBP; (ii) 73% of measles-IgG-positive autistic sera was also positive for anti-NAFP; (iii) 84% of HHV-6-IgG-positive autistic sera was also positive for anti-MBP; and (iv) 72% of HHV-6-IgG-positive autistic sera was also positive for anti-NAFP. This study is the first to report an association between virus serology and brain autoantibody in autism; it supports the hypothesis that a virus-induced autoimmune response may play a causal role in autism.
http://www.ncbi.nlm.nih.gov/pubmed/9756729
Effectiveness of pertussis vaccines for adolescents and adults: case-control study
The adjusted estimate of effectiveness of Tdap vaccination against pertussis was 53.0.
http://www.bmj.com/content/347/bmj.f4249
Neurologic Adverse Events Following Vaccination (Progress in Health Sciences Vol. 2(1) 2012•pp 129-141.)
“Conclusions: Despite the assurances of the necessity and safety of vaccinations, there are more and more questions and doubts, which both physicians and parents are waiting to be clarified… It seems that it would be worthwhile to apply the precautionary principle – the ethical principle (from 1988) according to which if there is a probable, although poorly known, risk of adverse effects of new technology, it is better not to implement it rather than risk uncertain but potentially very harmful consequences.”
http://progress.umb.edu.pl/sites/progress.umb.edu.pl/files/129-141.pdf
Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism.
PubMed
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders - PubMed
The first conjugate vaccine was approved for use in the US in 1988 to protect infants and young children against the capsular bacteria Haemophilus influenzae type b (Hib). Since its introduction in the US, this vaccine has been approved in most developed…
“Thus the MMR antibody in autistic sera detected measles HA protein, which is unique to the measles subunit of the vaccine. Furthermore, over 90% of MMR antibody-positive autistic sera were also positive for MBP autoantibodies, suggesting a strong association between MMR and CNS autoimmunity in autism. Stemming from this evidence, we suggest that an inappropriate antibody response to MMR, specifically the measles component thereof, might be related to pathogenesis of autism.”
http://www.ncbi.nlm.nih.gov/pubmed/12145534
Influenza: marketing vaccine by marketing disease
Closer examination of influenza vaccine policies shows that although proponents employ the rhetoric of science, the studies underlying the policy are often of low quality, and do not substantiate officials’ claims. The vaccine might be less beneficial and less safe than has been claimed, and the threat of influenza appears overstated.
http://www.bmj.com/content/346/bmj.f3037
An unmasking phenomenon in an observational post-licensure safety study of adolescent girls and young women.
Our recent experience in a post-licensure safety study of autoimmune conditions following the quadrivalent human papillomavirus vaccine in 189,629 girls and young women ages 9-26 years led us to question the adequacy of the exclusion of Day 0 events to prevent the erroneous association of prevalent conditions with vaccination. Of the 18 confirmed cases of Graves’ disease diagnosed in days 1-60 following vaccination, only 6 cases appeared to be truly new onset. Among the remaining 12 cases, 2 cases had abnormal thyroid stimulating hormone or thyroxine labs drawn prior to or on Day 0 but had no documented pre-existing symptoms. The other 10 cases had mention of symptoms of hyperthyroidism referencing a period prior to first HPV-4 dose. This ‘unmasking’ phenomenon, due to health care visits that include vaccination and new workups of preexisting symptoms, may not be adequately controlled through the exclusion of Day 0 events.
http://www.ncbi.nlm.nih.gov/m/pubmed/22580356/
How aluminum, an intracellular ROS generator promotes hepatic and neurological diseases: the metabolic tale
Metal pollutants are a global health risk due to their ability to contribute to a variety of diseases. Aluminum (Al), a ubiquitous environmental contaminant is implicated in anemia, osteomalacia, hepatic disorder, and neurological disorder. In this review, we outline how this intracellular generator of reactive oxygen species (ROS) triggers a metabolic shift towards lipogenesis in astrocytes and hepatocytes. This Al-evoked phenomenon is coupled to diminished mitochondrial activity, anerobiosis, and the channeling of α-ketoacids towards anti-oxidant defense. The resulting metabolic reconfiguration leads to fat accumulation and a reduction in ATP synthesis, characteristics that are common to numerous medical disorders. Hence, the ability of Al toxicity to create an oxidative environment promotes dysfunctional metabolic processes in astrocytes and hepatocytes. These molecular events triggered by Al-induced ROS production are the potential mediators of brain and liver disorders.”
Advertisement
The Role of Spiritual Enlightenment a...
An Analogy with Butterfly Metamorphosis Today’s discourse touches upon the in...
http://link.springer.com/article/10.1007%2Fs10565-013-9239-0
Waning of Maternal Antibodies Against Measles, Mumps, Rubella, and Varicella in Communities With Contrasting Vaccination Coverage
Conclusions: Children of mothers vaccinated against measles and, possibly, rubella have lower concentrations of maternal antibodies and lose protection by maternal antibodies at an earlier age than children of mothers in communities that oppose vaccination. This increases the risk of disease transmission in highly vaccinated populations.
http://jid.oxfordjournals.org/content/early/2013/04/29/infdis.jit143.full
“vaccine injury is so rare..don’t worry about it!” who has heard this?
http://www.ncbi.nlm.nih.gov/pubmed/12145534
Influenza: marketing vaccine by marketing disease
Closer examination of influenza vaccine policies shows that although proponents employ the rhetoric of science, the studies underlying the policy are often of low quality, and do not substantiate officials’ claims. The vaccine might be less beneficial and less safe than has been claimed, and the threat of influenza appears overstated.
http://www.bmj.com/content/346/bmj.f3037
An unmasking phenomenon in an observational post-licensure safety study of adolescent girls and young women.
Our recent experience in a post-licensure safety study of autoimmune conditions following the quadrivalent human papillomavirus vaccine in 189,629 girls and young women ages 9-26 years led us to question the adequacy of the exclusion of Day 0 events to prevent the erroneous association of prevalent conditions with vaccination. Of the 18 confirmed cases of Graves’ disease diagnosed in days 1-60 following vaccination, only 6 cases appeared to be truly new onset. Among the remaining 12 cases, 2 cases had abnormal thyroid stimulating hormone or thyroxine labs drawn prior to or on Day 0 but had no documented pre-existing symptoms. The other 10 cases had mention of symptoms of hyperthyroidism referencing a period prior to first HPV-4 dose. This ‘unmasking’ phenomenon, due to health care visits that include vaccination and new workups of preexisting symptoms, may not be adequately controlled through the exclusion of Day 0 events.
http://www.ncbi.nlm.nih.gov/m/pubmed/22580356/
How aluminum, an intracellular ROS generator promotes hepatic and neurological diseases: the metabolic tale
Metal pollutants are a global health risk due to their ability to contribute to a variety of diseases. Aluminum (Al), a ubiquitous environmental contaminant is implicated in anemia, osteomalacia, hepatic disorder, and neurological disorder. In this review, we outline how this intracellular generator of reactive oxygen species (ROS) triggers a metabolic shift towards lipogenesis in astrocytes and hepatocytes. This Al-evoked phenomenon is coupled to diminished mitochondrial activity, anerobiosis, and the channeling of α-ketoacids towards anti-oxidant defense. The resulting metabolic reconfiguration leads to fat accumulation and a reduction in ATP synthesis, characteristics that are common to numerous medical disorders. Hence, the ability of Al toxicity to create an oxidative environment promotes dysfunctional metabolic processes in astrocytes and hepatocytes. These molecular events triggered by Al-induced ROS production are the potential mediators of brain and liver disorders.”
Advertisement
The Role of Spiritual Enlightenment a...
An Analogy with Butterfly Metamorphosis Today’s discourse touches upon the in...
http://link.springer.com/article/10.1007%2Fs10565-013-9239-0
Waning of Maternal Antibodies Against Measles, Mumps, Rubella, and Varicella in Communities With Contrasting Vaccination Coverage
Conclusions: Children of mothers vaccinated against measles and, possibly, rubella have lower concentrations of maternal antibodies and lose protection by maternal antibodies at an earlier age than children of mothers in communities that oppose vaccination. This increases the risk of disease transmission in highly vaccinated populations.
http://jid.oxfordjournals.org/content/early/2013/04/29/infdis.jit143.full
“vaccine injury is so rare..don’t worry about it!” who has heard this?
PubMed
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders - PubMed
The first conjugate vaccine was approved for use in the US in 1988 to protect infants and young children against the capsular bacteria Haemophilus influenzae type b (Hib). Since its introduction in the US, this vaccine has been approved in most developed…
“The Health Resources and Services Administration (HRSA) is publishing this notice of petitions received under the National Vaccine Injury Compensation Program.. A pet…ition may be filed with respect to injuries, disabilities, illnesses, conditions, and deaths resulting from vaccines described in the Vaccine Injury Table… Set forth below is a list of petitions received by HRSA on * March 13, 2013, through April 30, 2013.*”
[take note of #7 and #17..]
1. Tory J. and Sarah E. Moody on behalf of Victorya E. Moody, Bedford, Indiana, Court of Federal Claims No: 13-0190V.
2. Pamela Jean Peguess, Memphis, Tennessee, Court of Federal Claims No: 13-0191V.
3. Eileen Goeschel, Sarasota, Florida, Court of Federal Claims No: 13-0199V.
4. Kearsten Demczuk, Park Ridge, Illinois, Court of Federal Claims No: 13-0205V. 5. Howard Reddy and Hanan Tarabay on behalf of Andrew Howard Reddy, Pensacola, Florida, Court of Federal Claims No: 13-0208V.
6. Mona Marie Troup, Everett, Washington, Court of Federal Claims No: 13-0209V.
7. Angel Blackstone on behalf of S.B., Deceased, Trenton, New Jersey, Court of Federal Claims No: 13-0213V.
8. Isidra Durwin, Sarasota, Florida, Court of Federal Claims No: 13-0214V.
9. Nancy and Sandro Giannetta on behalf of A.M.G., Sarasota, Florida, Court of Federal Claims No: 13-0215V.
10. Kimberly Pedersen, West Allis, Wisconsin, Court of Federal Claims No: 13-0216V.
11. Charles and Jeannie Maikish on behalf of S.M., Nyack, New York,Court of Federal Claims No: 13-0217V.
12. Ina Scanlon, Muncie, Indiana, Court of Federal Claims No: 13-0219V.
13. David Stachlewitz on behalf of H.G.S., Glendale, Arizona, Court of Federal Claims No: 13-0220V.
14. Mary E. Thompson, Brookport, Illinois, Court of Federal Claims No: 13-0222V.
15. Matthew Gorski, Wynnewood, Pennsylvania, Court of Federal Claims No: 13-0224V.
16. Woodrow Coffey, Jr., Irvine, California, Court of Federal Claims No: 13-0225V. 17. Stephen Warren on behalf of Taylor Warren, Deceased, New York, New York, Court of Federal Claims No: 13-0226V.
18. Robert Wiggins, Nashville, North Carolina, Court of Federal Claims No: 13-0228V.
19. Peggy Kalmeyer, Depew, New York, Court of Federal Claims No: 13-0230V.
20. Rosemary and Wayne Trezza on behalf of P.T., West Orange, New Jersey, Court of Federal Claims No: 13-0231V.
21. Jane Tomassetti, Woodbury, Minnesota, Court of Federal Claims No: 13-0234V.
22. Everett Johnson, Sr., Ashland, Kentucky, Court of Federal Claims No: 13-0235V.
23. Edwin W. Fockler, Sarasota, Florida, Court of Federal Claims No: 13-0237V. 24. James Cox, Las Cruces, New Mexico, Court of Federal Claims No: 13-0238V. 25. Chanel and Paul A. Monroe on behalf of Angelina Monroe, Las Vegas, Nevada, Court of Federal Claims No: 13-0239V.
26. Noteel Koss, Houston, Texas, Court of Federal Claims No: 13-0240V.
27. Tamika M. Kratzer on behalf of Ian M. Kratzer, Sacramento, California, Court of Federal Claims No: 13-0243V.
28. Rosalie Peck, Boston, Massachusetts, Court of Federal Claims No: 13-0249V. 29. Shannon Keller, Sacramento, California, Court of Federal Claims No: 13-0250V.
30. Edwina Bradshaw, North Myrtle Beach, North Carolina, Court of Federal Claims No: 13-0252V.
31. William and Brenda Lehann Rodriguez on behalf of C.R., Clayton, Georgia, Court of Federal Claims No: 13-0253V.
32. Corrine K. Ibana, Kamuela, Hawaii, Court of Federal Claims No: 13-0257V. 33. Lorel Cubano, San Juan, Puerto Rico, Court of Federal Claims No: 13-0259V. 34. Brittany and Davey Lambert on behalf of Noah Lambert, Memphis, Tennessee, Court of Federal Claims No: 13-0265V.
35. Scott and Caroline VanScoy on behalf of Alyssa VanScoy, Simi Valley, California, Court of Federal Claims No: 13-0266V.
36. Jane Sprecher, Reading, Pennsylvania, Court of Federal Claims No: 13-0271V.
37. Georgia Murdock, Silver Spring, Maryland, Court of Federal Claims No: 13-0273V.
38. Willie Andre Simmons, Augusta, Georgia, Court of Federal Claims No: 13-0274V.
39. Jung Park, M.D., New York, New York, Court of Federal Claims No: 13-0275V. 40.
[take note of #7 and #17..]
1. Tory J. and Sarah E. Moody on behalf of Victorya E. Moody, Bedford, Indiana, Court of Federal Claims No: 13-0190V.
2. Pamela Jean Peguess, Memphis, Tennessee, Court of Federal Claims No: 13-0191V.
3. Eileen Goeschel, Sarasota, Florida, Court of Federal Claims No: 13-0199V.
4. Kearsten Demczuk, Park Ridge, Illinois, Court of Federal Claims No: 13-0205V. 5. Howard Reddy and Hanan Tarabay on behalf of Andrew Howard Reddy, Pensacola, Florida, Court of Federal Claims No: 13-0208V.
6. Mona Marie Troup, Everett, Washington, Court of Federal Claims No: 13-0209V.
7. Angel Blackstone on behalf of S.B., Deceased, Trenton, New Jersey, Court of Federal Claims No: 13-0213V.
8. Isidra Durwin, Sarasota, Florida, Court of Federal Claims No: 13-0214V.
9. Nancy and Sandro Giannetta on behalf of A.M.G., Sarasota, Florida, Court of Federal Claims No: 13-0215V.
10. Kimberly Pedersen, West Allis, Wisconsin, Court of Federal Claims No: 13-0216V.
11. Charles and Jeannie Maikish on behalf of S.M., Nyack, New York,Court of Federal Claims No: 13-0217V.
12. Ina Scanlon, Muncie, Indiana, Court of Federal Claims No: 13-0219V.
13. David Stachlewitz on behalf of H.G.S., Glendale, Arizona, Court of Federal Claims No: 13-0220V.
14. Mary E. Thompson, Brookport, Illinois, Court of Federal Claims No: 13-0222V.
15. Matthew Gorski, Wynnewood, Pennsylvania, Court of Federal Claims No: 13-0224V.
16. Woodrow Coffey, Jr., Irvine, California, Court of Federal Claims No: 13-0225V. 17. Stephen Warren on behalf of Taylor Warren, Deceased, New York, New York, Court of Federal Claims No: 13-0226V.
18. Robert Wiggins, Nashville, North Carolina, Court of Federal Claims No: 13-0228V.
19. Peggy Kalmeyer, Depew, New York, Court of Federal Claims No: 13-0230V.
20. Rosemary and Wayne Trezza on behalf of P.T., West Orange, New Jersey, Court of Federal Claims No: 13-0231V.
21. Jane Tomassetti, Woodbury, Minnesota, Court of Federal Claims No: 13-0234V.
22. Everett Johnson, Sr., Ashland, Kentucky, Court of Federal Claims No: 13-0235V.
23. Edwin W. Fockler, Sarasota, Florida, Court of Federal Claims No: 13-0237V. 24. James Cox, Las Cruces, New Mexico, Court of Federal Claims No: 13-0238V. 25. Chanel and Paul A. Monroe on behalf of Angelina Monroe, Las Vegas, Nevada, Court of Federal Claims No: 13-0239V.
26. Noteel Koss, Houston, Texas, Court of Federal Claims No: 13-0240V.
27. Tamika M. Kratzer on behalf of Ian M. Kratzer, Sacramento, California, Court of Federal Claims No: 13-0243V.
28. Rosalie Peck, Boston, Massachusetts, Court of Federal Claims No: 13-0249V. 29. Shannon Keller, Sacramento, California, Court of Federal Claims No: 13-0250V.
30. Edwina Bradshaw, North Myrtle Beach, North Carolina, Court of Federal Claims No: 13-0252V.
31. William and Brenda Lehann Rodriguez on behalf of C.R., Clayton, Georgia, Court of Federal Claims No: 13-0253V.
32. Corrine K. Ibana, Kamuela, Hawaii, Court of Federal Claims No: 13-0257V. 33. Lorel Cubano, San Juan, Puerto Rico, Court of Federal Claims No: 13-0259V. 34. Brittany and Davey Lambert on behalf of Noah Lambert, Memphis, Tennessee, Court of Federal Claims No: 13-0265V.
35. Scott and Caroline VanScoy on behalf of Alyssa VanScoy, Simi Valley, California, Court of Federal Claims No: 13-0266V.
36. Jane Sprecher, Reading, Pennsylvania, Court of Federal Claims No: 13-0271V.
37. Georgia Murdock, Silver Spring, Maryland, Court of Federal Claims No: 13-0273V.
38. Willie Andre Simmons, Augusta, Georgia, Court of Federal Claims No: 13-0274V.
39. Jung Park, M.D., New York, New York, Court of Federal Claims No: 13-0275V. 40.
PubMed
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders - PubMed
The first conjugate vaccine was approved for use in the US in 1988 to protect infants and young children against the capsular bacteria Haemophilus influenzae type b (Hib). Since its introduction in the US, this vaccine has been approved in most developed…
Allison and Steven Council on behalf of Adam Council, Plainfield, Illinois, Court of Federal Claims No: 13-0276V.
41. Maryann Giordano, Lindenhurst, New York, Court of Federal Claims No: 13-0277V.
42. Laura A. Jones, Greensboro, North Carolina, Court of Federal Claims No: 13-0279V.
43. David D. Griffin, Afghanistan, Court of Federal Claims No: 13-0280V.
44. James Demoski, Endicott, New York, Court of Federal Claims No: 13-0286V. 45. Christina N. Steinat, Seattle, Washington, Court of Federal Claims No: 13-0287V.
46. Jessica L. Stone, Baraboo, Wisconsin, Court of Federal Claims No: 13-0289V. 47. Holly Rhew, Wichita, Kansas, Court of Federal Claims No: 13-0293V.
48. Janet DeYear, Dallas, Texas, Court of Federal Claims No: 13-0299V.
49. Cynthia Adkins, Sarasota, Florida, Court of Federal Claims No: 13-0295V.
50. Saurabh V. and Archana Amin on behalf of Sheaa Amin, Linwood, New Jersey, Court of Federal Claims No: 13-0300V.
51. Juliet and Mohamed Edoo on behalf of Justin Edoo, Miami, Florida, Court of Federal Claims No: 13-0302V.
52. James Boyer, Boston, Massachusetts, Court of Federal Claims No: 13-0303V.
*these are from March 13, 2013 – April 30, 2013. 48 days. what is the true number that these 52 petitions represent? how many don’t file claims? think about it..its scary. I wish we could see more about these petitions..more about the injury caused.It is impossible for a parent to make a solid risk/benefit analysis when it comes to vaccinations.. I don’t care what anyone may say.. vaccine injury is downplayed and pushed aside, disease rates and risks are over exaggerated and blasted throughout the media via mass scare campaigns (remember those 8 measly cases of the measles in Wales during the month of march 2013?) ..and natural and safe preventative measures and treatments are suppressed. How are we supposed to make an informed medical decision when it comes to our children being injected with almost 50 doses of 16 vaccines before the age of 6?
https://www.federalregister.gov/articles/2013/05/24/2013-12347/national-vaccine-injury-compensation-program-list-of-petitions-received?utm_content=next&utm_medium=PrevNext&utm_source=Article
“In 1990, infants received a total of 15 vaccine doses prior to their first year of life: 3 DPT injections (9 vaccine doses), 3 polio, and 3 Hib vaccines—5 vaccine doses at 2, 4, and 6 months of age. By 2007, the CDC recommended 26 vaccine doses for infants: 3 DTaP, 3 polio, 3 Hib, 3 hepatitis B, 3 pneumococcal, 3 rotavirus, and 2 influenza vaccines. While each childhood vaccine has individually undergone clinical trials to assess safety, studies have not been conducted to determine the safety (or efficacy) of combining vaccines during a single physician visit as recommended by CDC guidelines. For example, 2-, 4-, and 6-month-old infants are expected to receive vaccines for polio, hepatitis B, diphtheria, tetanus, pertussis, rotavirus, Haemophilus influenzae type B, and pneumococcal, all during a single well-baby visit—even though this combination of 8 vaccine doses was never tested in clinical trials.
An article written by Guess, representing a vaccine manufacturer, claimed that it is “impractical to conduct preapproval studies of all combinations [of vaccines] in clinical practice.”1 However, a recent study by Miller and Goldman found that among the developed nations, infant mortality increased with an increase in the number of vaccine doses.2 Similar associations have also been found with respect to other serious adverse outcomes. Delong reported that the higher the proportion of children receiving recommended vaccinations, the higher the prevalence of autism or speech and language impairment.3 A CDC report on mixed exposures to chemical substances and other stressors, including prescribed pharmaceuticals, found that they may produce “increased or unexpected deleterious health effects.” In addition, “exposures to mixed stressors can produce health consequences that are additive, synergistic, antagonistic, or can potentiate the response expected from individual component exposures.
41. Maryann Giordano, Lindenhurst, New York, Court of Federal Claims No: 13-0277V.
42. Laura A. Jones, Greensboro, North Carolina, Court of Federal Claims No: 13-0279V.
43. David D. Griffin, Afghanistan, Court of Federal Claims No: 13-0280V.
44. James Demoski, Endicott, New York, Court of Federal Claims No: 13-0286V. 45. Christina N. Steinat, Seattle, Washington, Court of Federal Claims No: 13-0287V.
46. Jessica L. Stone, Baraboo, Wisconsin, Court of Federal Claims No: 13-0289V. 47. Holly Rhew, Wichita, Kansas, Court of Federal Claims No: 13-0293V.
48. Janet DeYear, Dallas, Texas, Court of Federal Claims No: 13-0299V.
49. Cynthia Adkins, Sarasota, Florida, Court of Federal Claims No: 13-0295V.
50. Saurabh V. and Archana Amin on behalf of Sheaa Amin, Linwood, New Jersey, Court of Federal Claims No: 13-0300V.
51. Juliet and Mohamed Edoo on behalf of Justin Edoo, Miami, Florida, Court of Federal Claims No: 13-0302V.
52. James Boyer, Boston, Massachusetts, Court of Federal Claims No: 13-0303V.
*these are from March 13, 2013 – April 30, 2013. 48 days. what is the true number that these 52 petitions represent? how many don’t file claims? think about it..its scary. I wish we could see more about these petitions..more about the injury caused.It is impossible for a parent to make a solid risk/benefit analysis when it comes to vaccinations.. I don’t care what anyone may say.. vaccine injury is downplayed and pushed aside, disease rates and risks are over exaggerated and blasted throughout the media via mass scare campaigns (remember those 8 measly cases of the measles in Wales during the month of march 2013?) ..and natural and safe preventative measures and treatments are suppressed. How are we supposed to make an informed medical decision when it comes to our children being injected with almost 50 doses of 16 vaccines before the age of 6?
https://www.federalregister.gov/articles/2013/05/24/2013-12347/national-vaccine-injury-compensation-program-list-of-petitions-received?utm_content=next&utm_medium=PrevNext&utm_source=Article
“In 1990, infants received a total of 15 vaccine doses prior to their first year of life: 3 DPT injections (9 vaccine doses), 3 polio, and 3 Hib vaccines—5 vaccine doses at 2, 4, and 6 months of age. By 2007, the CDC recommended 26 vaccine doses for infants: 3 DTaP, 3 polio, 3 Hib, 3 hepatitis B, 3 pneumococcal, 3 rotavirus, and 2 influenza vaccines. While each childhood vaccine has individually undergone clinical trials to assess safety, studies have not been conducted to determine the safety (or efficacy) of combining vaccines during a single physician visit as recommended by CDC guidelines. For example, 2-, 4-, and 6-month-old infants are expected to receive vaccines for polio, hepatitis B, diphtheria, tetanus, pertussis, rotavirus, Haemophilus influenzae type B, and pneumococcal, all during a single well-baby visit—even though this combination of 8 vaccine doses was never tested in clinical trials.
An article written by Guess, representing a vaccine manufacturer, claimed that it is “impractical to conduct preapproval studies of all combinations [of vaccines] in clinical practice.”1 However, a recent study by Miller and Goldman found that among the developed nations, infant mortality increased with an increase in the number of vaccine doses.2 Similar associations have also been found with respect to other serious adverse outcomes. Delong reported that the higher the proportion of children receiving recommended vaccinations, the higher the prevalence of autism or speech and language impairment.3 A CDC report on mixed exposures to chemical substances and other stressors, including prescribed pharmaceuticals, found that they may produce “increased or unexpected deleterious health effects.” In addition, “exposures to mixed stressors can produce health consequences that are additive, synergistic, antagonistic, or can potentiate the response expected from individual component exposures.
PubMed
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders - PubMed
The first conjugate vaccine was approved for use in the US in 1988 to protect infants and young children against the capsular bacteria Haemophilus influenzae type b (Hib). Since its introduction in the US, this vaccine has been approved in most developed…
”4 Administering six, seven, or eight vaccine doses to an infant during a single physician visit may certainly be more convenient for parents—rather than making additional trips to the doctor’s office—but evidence of a positive association between infant adverse reactions and the number of vaccine doses administered confirms that vaccine safety must remain the highest priority”
http://het.sagepub.com/content/31/10/1012.full
“Maternal transfer of mercury to the developing embryo/fetus: is there a safe level?”
“This study focused on standardized embryonic and fetal Hg exposures via primary exposure to the pregnant mother of two common Hg sources (dietary fish and parenteral vaccines). Data demonstrated that Hg exposures, particularly during the first trimester of pregnancy, at well-established dose/weight ratios produced severe damage to humans including death. . In light of research suggestive of a mercuric risk factor for childhood conditions such as tic disorders, cerebral palsy, and autism, it is essential that Hg advisories account for secondary prenatal human exposures.”
http://www.tandfonline.com/doi/full/10.1080/02772248.2012.724574
Empirical Data Confirm Autism Symptoms Related to Aluminum and Acetaminophen Exposure
“Autism is a condition characterized by impaired cognitive and social skills, associated with compromised immune function. The incidence is alarmingly on the rise, and environmental factors are increasingly suspected to play a role. This paper investigates word frequency patterns in the U.S. CDC Vaccine Adverse Events Reporting System (VAERS) database. Our results provide strong evidence supporting a link between autism and the aluminum in vaccines. A literature review showing toxicity of aluminum in human physiology offers further support. Mentions of autism in VAERS increased steadily at the end of the last century, during a period when mercury was being phased out, while aluminum adjuvant burden was being increased. Using standard log-likelihood ratio techniques, we identify several signs and symptoms that are significantly more prevalent in vaccine reports after 2000, including cellulitis, seizure, depression, fatigue, pain and death, which are also significantly associated with aluminum-containing vaccines. We propose that children with the autism diagnosis are especially vulnerable to toxic metals such as aluminum and mercury due to insufficient serum sulfate and glutathione. A strong correlation between autism and the MMR (Measles, Mumps, Rubella) vaccine is also observed, which may be partially explained via an increased sensitivity to acetaminophen administered to control fever.”
http://www.mdpi.com/1099-4300/14/11/2227
full text: http://groups.csail.mit.edu/sls/publications/2012/entropy-14-02227.pdf
Acetaminophen use after measles-mumps-rubella vaccination was SIGNIFICANTLY associated with autistic disorder when considering children 5 years of age or less, after limiting cases to children with regression in development and when considering only children who had post-vaccination sequelae adjusting for age, gender, mother’s ethnicity, and the presence of illness concurrent with measles-mumps-rubella vaccination. Ibuprofen use after measles-mumps-rubella vaccination was not associated with autistic disorder. This preliminary study found that acetaminophen use after measles-mumps-rubella vaccination was associated with autistic disorder.
http://www.ncbi.nlm.nih.gov/pubmed/18445737
A 1% increase in vaccination was associated with an additional 680 children having AUT or SLI. Neither parental behavior nor access to care affected the results, since vaccination proportions were not significantly related (statistically) to any other disability or to the number of pediatricians in a U.S. state. The results suggest that although mercury has been removed from many vaccines, other culprits may link vaccines to autism. Further study into the relationship between vaccines and autism is warranted”
http://www.ncbi.nlm.nih.gov/pubmed/21623535
http://het.sagepub.com/content/31/10/1012.full
“Maternal transfer of mercury to the developing embryo/fetus: is there a safe level?”
“This study focused on standardized embryonic and fetal Hg exposures via primary exposure to the pregnant mother of two common Hg sources (dietary fish and parenteral vaccines). Data demonstrated that Hg exposures, particularly during the first trimester of pregnancy, at well-established dose/weight ratios produced severe damage to humans including death. . In light of research suggestive of a mercuric risk factor for childhood conditions such as tic disorders, cerebral palsy, and autism, it is essential that Hg advisories account for secondary prenatal human exposures.”
http://www.tandfonline.com/doi/full/10.1080/02772248.2012.724574
Empirical Data Confirm Autism Symptoms Related to Aluminum and Acetaminophen Exposure
“Autism is a condition characterized by impaired cognitive and social skills, associated with compromised immune function. The incidence is alarmingly on the rise, and environmental factors are increasingly suspected to play a role. This paper investigates word frequency patterns in the U.S. CDC Vaccine Adverse Events Reporting System (VAERS) database. Our results provide strong evidence supporting a link between autism and the aluminum in vaccines. A literature review showing toxicity of aluminum in human physiology offers further support. Mentions of autism in VAERS increased steadily at the end of the last century, during a period when mercury was being phased out, while aluminum adjuvant burden was being increased. Using standard log-likelihood ratio techniques, we identify several signs and symptoms that are significantly more prevalent in vaccine reports after 2000, including cellulitis, seizure, depression, fatigue, pain and death, which are also significantly associated with aluminum-containing vaccines. We propose that children with the autism diagnosis are especially vulnerable to toxic metals such as aluminum and mercury due to insufficient serum sulfate and glutathione. A strong correlation between autism and the MMR (Measles, Mumps, Rubella) vaccine is also observed, which may be partially explained via an increased sensitivity to acetaminophen administered to control fever.”
http://www.mdpi.com/1099-4300/14/11/2227
full text: http://groups.csail.mit.edu/sls/publications/2012/entropy-14-02227.pdf
Acetaminophen use after measles-mumps-rubella vaccination was SIGNIFICANTLY associated with autistic disorder when considering children 5 years of age or less, after limiting cases to children with regression in development and when considering only children who had post-vaccination sequelae adjusting for age, gender, mother’s ethnicity, and the presence of illness concurrent with measles-mumps-rubella vaccination. Ibuprofen use after measles-mumps-rubella vaccination was not associated with autistic disorder. This preliminary study found that acetaminophen use after measles-mumps-rubella vaccination was associated with autistic disorder.
http://www.ncbi.nlm.nih.gov/pubmed/18445737
A 1% increase in vaccination was associated with an additional 680 children having AUT or SLI. Neither parental behavior nor access to care affected the results, since vaccination proportions were not significantly related (statistically) to any other disability or to the number of pediatricians in a U.S. state. The results suggest that although mercury has been removed from many vaccines, other culprits may link vaccines to autism. Further study into the relationship between vaccines and autism is warranted”
http://www.ncbi.nlm.nih.gov/pubmed/21623535
PubMed
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders - PubMed
The first conjugate vaccine was approved for use in the US in 1988 to protect infants and young children against the capsular bacteria Haemophilus influenzae type b (Hib). Since its introduction in the US, this vaccine has been approved in most developed…
“Furthermore, while India has been polio-free for a year, there has been a huge increase in non-polio acute flaccid paralysis (NPAFP). In 2011, there were an extra 47,500 new cases of NPAFP. Clinically indistinguishable from polio paralysis but twice as deadly, the incidence of NPAFP was directly proportional to doses of oral polio received. Though this data was collected within the polio surveillance system, it was not investigated.”
http://www.ncbi.nlm.nih.gov/pubmed/22591873
Detection of fecal shedding of rotavirus vaccine in infants following their first dose of pentavalent rotavirus vaccine. (and how they blame everything on kids that are not vaccinated is beyond me! These vaccines are helping to keep diseases in circulation..)
Studies on rotavirus vaccine shedding and its potential transmission within households including immunocompromised individuals are needed to better define the potential risks and benefits of vaccination. We examined fecal shedding of pentavalent rotavirus vaccine (RV5) for 9 days following the first dose of vaccine in infants between 6 and 12 weeks of age. Rotavirus antigen was detected by enzyme immunoassay (EIA), and vaccine-type rotavirus was identified by nucleotide sequencing based on genetic relatedness to the RV5 VP6 gene. Stool from 22 (21.4%) of 103 children contained rotavirus antigen-positive specimens on ≥ 1 post-vaccination days. Rotavirus antigen was detected as early as post-vaccination day 3 and as late as day 9, with peak numbers of shedding on post-vaccination days 6 through 8. Vaccine-type rotavirus was detected in all 50 antigen-positive specimens and 8 of 8 antigen-negative specimens. Nine (75%) of 12 EIA-positive and 1 EIA-negative samples tested culture-positive for vaccine-type rotavirus. Fecal shedding of rotavirus vaccine virus after the first dose of RV5 occurred over a wide range of post-vaccination days not previously studied. These findings will help better define the potential for horizontal transmission of vaccine virus among immunocompromised household contacts of vaccinated infants for future studies
http://www.ncbi.nlm.nih.gov/pubmed/21477676
“Effectiveness of trivalent inactivated influenza vaccine in influenza-related hospitalization in children: a case-control study.”
“Using the Cochran-Mantel-Haenszel test for asthma status stratification, there was a significant association between hospitalization in asthmatic subjects and TIV (p = 0.001). TIV did not provide any protection against hospitalization in pediatric subjects, especially children with asthma. On the contrary, we found a threefold increased risk of hospitalization in subjects who did get the TIV vaccine. This may be a reflection not only of vaccine effectiveness but also the population of children who are more likely to get the vaccine.”
http://www.ncbi.nlm.nih.gov/pubmed/22525386
The odds of having a history of asthma was twice as great among vaccinated subjects than among unvaccinated subjects (adjusted odds ratio, 2.00; 95% confidence interval, 0.59 to 6.74). The odds of having had any allergy-related respiratory symptom in the past 12 months was 63% greater among vaccinated subjects than unvaccinated subjects (adjusted odds ratio, 1.63; 95% confidence interval, 1.05 to 2.54). The associations between vaccination and subsequent allergies and symptoms were greatest among children aged 5 through 10 years.
DTP or tetanus vaccination appears to increase the risk of allergies and related respiratory symptoms in children and adolescents. Although it is unlikely that these results are entirely because of any sources of bias, the small number of unvaccinated subjects and the study design limit our ability to make firm causal inferences about the true magnitude of effect.
http://www.ncbi.nlm.nih.gov/pubmed/10714532
Four to 12 days post 12 month vaccination, children had a 1.33 (1.29–1.38) increased relative incidence of the combined endpoint compared to the control period, or at least one event during the risk interval for every 168 children vaccinated.
http://www.ncbi.nlm.nih.gov/pubmed/22591873
Detection of fecal shedding of rotavirus vaccine in infants following their first dose of pentavalent rotavirus vaccine. (and how they blame everything on kids that are not vaccinated is beyond me! These vaccines are helping to keep diseases in circulation..)
Studies on rotavirus vaccine shedding and its potential transmission within households including immunocompromised individuals are needed to better define the potential risks and benefits of vaccination. We examined fecal shedding of pentavalent rotavirus vaccine (RV5) for 9 days following the first dose of vaccine in infants between 6 and 12 weeks of age. Rotavirus antigen was detected by enzyme immunoassay (EIA), and vaccine-type rotavirus was identified by nucleotide sequencing based on genetic relatedness to the RV5 VP6 gene. Stool from 22 (21.4%) of 103 children contained rotavirus antigen-positive specimens on ≥ 1 post-vaccination days. Rotavirus antigen was detected as early as post-vaccination day 3 and as late as day 9, with peak numbers of shedding on post-vaccination days 6 through 8. Vaccine-type rotavirus was detected in all 50 antigen-positive specimens and 8 of 8 antigen-negative specimens. Nine (75%) of 12 EIA-positive and 1 EIA-negative samples tested culture-positive for vaccine-type rotavirus. Fecal shedding of rotavirus vaccine virus after the first dose of RV5 occurred over a wide range of post-vaccination days not previously studied. These findings will help better define the potential for horizontal transmission of vaccine virus among immunocompromised household contacts of vaccinated infants for future studies
http://www.ncbi.nlm.nih.gov/pubmed/21477676
“Effectiveness of trivalent inactivated influenza vaccine in influenza-related hospitalization in children: a case-control study.”
“Using the Cochran-Mantel-Haenszel test for asthma status stratification, there was a significant association between hospitalization in asthmatic subjects and TIV (p = 0.001). TIV did not provide any protection against hospitalization in pediatric subjects, especially children with asthma. On the contrary, we found a threefold increased risk of hospitalization in subjects who did get the TIV vaccine. This may be a reflection not only of vaccine effectiveness but also the population of children who are more likely to get the vaccine.”
http://www.ncbi.nlm.nih.gov/pubmed/22525386
The odds of having a history of asthma was twice as great among vaccinated subjects than among unvaccinated subjects (adjusted odds ratio, 2.00; 95% confidence interval, 0.59 to 6.74). The odds of having had any allergy-related respiratory symptom in the past 12 months was 63% greater among vaccinated subjects than unvaccinated subjects (adjusted odds ratio, 1.63; 95% confidence interval, 1.05 to 2.54). The associations between vaccination and subsequent allergies and symptoms were greatest among children aged 5 through 10 years.
DTP or tetanus vaccination appears to increase the risk of allergies and related respiratory symptoms in children and adolescents. Although it is unlikely that these results are entirely because of any sources of bias, the small number of unvaccinated subjects and the study design limit our ability to make firm causal inferences about the true magnitude of effect.
http://www.ncbi.nlm.nih.gov/pubmed/10714532
Four to 12 days post 12 month vaccination, children had a 1.33 (1.29–1.38) increased relative incidence of the combined endpoint compared to the control period, or at least one event during the risk interval for every 168 children vaccinated.
PubMed
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders - PubMed
The first conjugate vaccine was approved for use in the US in 1988 to protect infants and young children against the capsular bacteria Haemophilus influenzae type b (Hib). Since its introduction in the US, this vaccine has been approved in most developed…
Ten to 12 days post 18 month vaccination, the relative incidence was 1.25 (95%, 1.17–1.33) which represented at least one excess event for every 730 children vaccinated. The primary reason for increased events was statistically significant elevations in emergency room visits following all vaccinations. There were non-significant increases in hospital admissions. There were an additional 20 febrile seizures for every 100,000 vaccinated at 12 months.
Conclusions
There are significantly elevated risks of primarily emergency room visits approximately one to two weeks following 12 and 18 month vaccination. Future studies should examine whether these events could be predicted or prevented
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3236196/
“Administration of thimerosal to infant rats increases overflow of glutamate and aspartate in the prefrontal cortex: protective role of dehydroepiandrosterone sulfate. “
In summary, the present study documents that exposure of infant rats to THIM perturbs the balance between excitatory and inhibitory amino acids in the brain, shifting it toward excessive neuroexcitation. Despite of intrinsic limitations, present findings have important clinical implications, as they provide a plausible mechanism, whereby THIM exerts neurotoxic effects in the brain. It is likely that this mercurial—still present in pediatric vaccines in many countries—causes a similar disturbance of excitatory and inhibitory neurotransmitters in the brains of human infants, leading to neurotoxicity, encephalopaties, and in consequence to neurodevelopmental disorders, including autism..*On the whole, the current study provides further empirical evidence that exposure to THIM leads to neurotoxic changes in the developing brain, arguing for urgent and permanent removal of this preservative from all vaccines for children (and adults) since effective, less toxic and less costly alternatives are available. The stubborn insistence of some vaccine manufacturers and health agencies on continuation of use of this proven neurotoxin in vaccines is testimony of their disregard for both the health of young generations and for the environment.*
http://www.ncbi.nlm.nih.gov/pubmed/22015977
“Thus vaccination DOES NOT account for the impressive declines in mortality seen in the first half of the century”
http://pediatrics.aappublications.org/content/106/6/1307.abstract
Thimerosal, an organomercurial added as a preservative to some vaccines, is a suspected iatrogenic factor, possibly contributing to paediatric neurodevelopmental disorders including autism. We examined the effects of early postnatal administration of thimerosal (four i.m. injections, 12 or 240 μg THIM-Hg/kg, on postnatal days 7, 9, 11 and 15) on brain pathology in Wistar rats. Numerous neuropathological changes were observed in young adult rats which were treated postnatally with thimerosal. They included: ischaemic degeneration of neurons and “dark” neurons in the prefrontal and temporal cortex, the hippocampus and the cerebellum, pathological changes of the blood vessels in the temporal cortex, diminished synaptophysin reaction in the hippocampus, atrophy of astroglia in the hippocampus and cerebellum, and positive caspase-3 reaction in Bergmann astroglia. These findings document neurotoxic effects of thimerosal, at doses equivalent to those used in infant vaccines or higher, in developing rat brain, suggesting likely involvement of this mercurial in neurodevelopmental disorders.
http://www.ncbi.nlm.nih.gov/pubmed/21225508
and it’s the unvaccinated that are spreading pertussis?
“Despite widespread vaccination, whooping cough incidence is on the rise worldwide, making it the only vaccine-preventable disease associated with increasing deaths in the United States. Although this disease is most often attributed to Bordetella pertussis infection, it is also caused by the closely related pathogen, B. parapertussis. However, B. pertussis has remained the center of attention, whereas B. parapertussis has been greatly overlooked in the development of whooping cough vaccines.
Conclusions
There are significantly elevated risks of primarily emergency room visits approximately one to two weeks following 12 and 18 month vaccination. Future studies should examine whether these events could be predicted or prevented
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3236196/
“Administration of thimerosal to infant rats increases overflow of glutamate and aspartate in the prefrontal cortex: protective role of dehydroepiandrosterone sulfate. “
In summary, the present study documents that exposure of infant rats to THIM perturbs the balance between excitatory and inhibitory amino acids in the brain, shifting it toward excessive neuroexcitation. Despite of intrinsic limitations, present findings have important clinical implications, as they provide a plausible mechanism, whereby THIM exerts neurotoxic effects in the brain. It is likely that this mercurial—still present in pediatric vaccines in many countries—causes a similar disturbance of excitatory and inhibitory neurotransmitters in the brains of human infants, leading to neurotoxicity, encephalopaties, and in consequence to neurodevelopmental disorders, including autism..*On the whole, the current study provides further empirical evidence that exposure to THIM leads to neurotoxic changes in the developing brain, arguing for urgent and permanent removal of this preservative from all vaccines for children (and adults) since effective, less toxic and less costly alternatives are available. The stubborn insistence of some vaccine manufacturers and health agencies on continuation of use of this proven neurotoxin in vaccines is testimony of their disregard for both the health of young generations and for the environment.*
http://www.ncbi.nlm.nih.gov/pubmed/22015977
“Thus vaccination DOES NOT account for the impressive declines in mortality seen in the first half of the century”
http://pediatrics.aappublications.org/content/106/6/1307.abstract
Thimerosal, an organomercurial added as a preservative to some vaccines, is a suspected iatrogenic factor, possibly contributing to paediatric neurodevelopmental disorders including autism. We examined the effects of early postnatal administration of thimerosal (four i.m. injections, 12 or 240 μg THIM-Hg/kg, on postnatal days 7, 9, 11 and 15) on brain pathology in Wistar rats. Numerous neuropathological changes were observed in young adult rats which were treated postnatally with thimerosal. They included: ischaemic degeneration of neurons and “dark” neurons in the prefrontal and temporal cortex, the hippocampus and the cerebellum, pathological changes of the blood vessels in the temporal cortex, diminished synaptophysin reaction in the hippocampus, atrophy of astroglia in the hippocampus and cerebellum, and positive caspase-3 reaction in Bergmann astroglia. These findings document neurotoxic effects of thimerosal, at doses equivalent to those used in infant vaccines or higher, in developing rat brain, suggesting likely involvement of this mercurial in neurodevelopmental disorders.
http://www.ncbi.nlm.nih.gov/pubmed/21225508
and it’s the unvaccinated that are spreading pertussis?
“Despite widespread vaccination, whooping cough incidence is on the rise worldwide, making it the only vaccine-preventable disease associated with increasing deaths in the United States. Although this disease is most often attributed to Bordetella pertussis infection, it is also caused by the closely related pathogen, B. parapertussis. However, B. pertussis has remained the center of attention, whereas B. parapertussis has been greatly overlooked in the development of whooping cough vaccines.
PubMed
Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders - PubMed
The first conjugate vaccine was approved for use in the US in 1988 to protect infants and young children against the capsular bacteria Haemophilus influenzae type b (Hib). Since its introduction in the US, this vaccine has been approved in most developed…