I get so frustrated with individuals and various group leaders posting complete nonsense, along with their lack of simply "UNDERSTANDING LYME". OSPA and Lyme is a reality. OSPA and Bartonella is reality. Two peas in a pod using the same fungal antigen OSPA. I'm quite convinced you can't have one without the other. BARTONELLA and CANCER is a reality. Just do a simple search "Bartonella and cancer pubmed." We know that Dr. Klinghardt just established that a person with the polymicrobial infection known as Lyme Disease is also carrying some form of Bartonella, maybe more than one. http://www.chronicwellnesssummits.com/klinghardt-develops-more-accurate-lyme-disease-test/ If you watch the video @ 7:41 he says out of 120 patients tested they All had some form of Borrelia, some form of Bartonella and some form of Babesia. So for practical purposes if you have "Lyme" you have Bartonella regardless of what your doctors testing says. We also know that Bartonella is a transgenic bacteria that can alter your DNA and when it does this it changes multiple growth factors, shuts down Apoptosis and initiates Infectious Angiogenesis. The result is free cell proliferation of mutated cells resulting in tumors. http://www.pnas.org/content/108/35/14643.abstract “Conjugative DNA transfer into human cells by the VirB/VirD4 type IV secretion system of the bacterial pathogen Bartonella henselae” https://www.ncbi.nlm.nih.gov/pubmed/?term=bartonella+fgf [Infection and angiomatous cutaneous lesions] “these are associated with multifocal tumorous proliferations (of endothelial and fusiform cells) affected by angiogenic growth factors (PDGF, FGF, IL6, alpha TGF, HIV tat, androgens” http://scholarworks.gsu.edu/cgi/viewcontent.cgi?article=1068&context=biology_diss "Bartonella Henselae Inhibits Cellular Apoptotic Regulators to Ensure Survival" Apoptosis is an immune system function designed to kill abnormal mutated cells. https://www.ncbi.nlm.nih.gov/pubmed/14507641"Infectious angiogenesis: Bartonella bacilliformis infection results in endothelial production of angiopoietin-2 and epidermal production of vascular endothelial growth factor. https://www.ncbi.nlm.nih.gov/pubmed/25857345“Reprogramming of myeloid angiogenic cells by Bartonella henselae leads to microenvironmental regulation of pathological angiogenesis.” “Our results demonstrate that manipulation of myeloid cells by pathogenic bacteria can contribute to microenvironmental regulation of pathological tissue growth and suggest parallels underlying both bacterial infections and cancer.” You don’t really need to take a giant leap of understanding to see what is taking place and that is why the NB protocol was designed to treat this cancer condition. Cancer- *The disease caused by an uncontrolled division of abnormal cells in a part of the body. * Malignant growth or tumor resulting from the division of abnormal cells. Lyme disease is an infectious version of Cancer.So please GROUP LEADERS at least lets try and understand the disease before you offer any advice on the matter. People are extremely taxed in every way by the effects of Bartonella and the immune suppression of the OSPA etc, the fungal antigens, that allow any number of latent viruses to proliferate.
In the midst of a local measles outbreak, a recently immunized child was investigated for a new-onset measles-type rash. Nucleic acid testing identified that a vaccine-type measles virus was being shed in the urine. Clinically differentiating measles from a nonmeasles rash is challenging, but can be supported by a thorough medical history evaluation. Rashes are expected to occur after immunization; nucleic acid testing can be used when it is difficult to differentiate between wild and attenuated strains.
In the spring of 2010, several imported cases of measles were reported within the province of Alberta (population of 3.5 million in 2009). Most cases of measles in Alberta, like the rest of Canada and the Americas, are linked to an imported illness or exposure during travel. Given the infrequent occurrence of measles in Alberta, and the high potential for transmission, an advisory was issued notifying all physicians to be on high alert for patients exhibiting symptoms consistent with measles infection. We describe a case of rash illness in a patient whose nasopharyngeal (NP) swab and urine sample tested positive for the measles virus using a nucleic acid amplification test following mumps-measles-rubella (MMR) immunization. The present case illustrates the difficulty in clinically differentiating various causes of childhood exanthemas, and serves as a reminder of the expected effects associated with the administration of the MMR vaccine. It also reinforces the expected limitations that should be placed on laboratory testing for measles.
In the spring of 2010, there was heightened awareness of measles infection in the physician community as a result of a public health notification related to several imported measles cases in Alberta. During this period, a 15-month-old child presented to his paediatrician’s office with irritability, a fever (38.8°C), a cough and conjunctivitis. The child had a five-day history of illness that began with an elevated temperature and a raised, sandpaper-like rash that originated at the occiput, and eventually spread to and covered the torso. There was mild cervical lymphadenopathy, and no rhinitis or Koplik spots. The child was not immunocompromised and had no significant medical history. Just 12 days before presentation to his paediatrician, the child was immunized with the M-M-R II vaccine (Merck Canada Inc). A thorough investigation by the Division of Population and Public Health, Alberta Health Services, revealed no significant travel history and no contact with any known measles patients in the preceding four weeks. All other members of the household were healthy and previously immunized with an MMR vaccine.
Clinical specimens were collected and submitted for laboratory testing, which included a throat swab for Streptococcus pyogenes (group A streptococcus), a serum sample for measles immunoglobulin (Ig) M and IgG antibodies (Enzygnost Anti-Measles Virus IgM and IgG ELIZA, Siemens Healthcare Diagnostics, Germany), a urine sample and an NP swab for a measles reverse transcription polymerase chain reaction (RT-PCR) test at the Provincial Laboratory for Public Health (ProvLab) in Alberta (1). The child’s serum tested positive for both measles IgM and IgG antibodies. Both the urine sample and the NP swab tested positive for measles by RT-PCR at ProvLab, and the samples were referred to the National Microbiology Laboratory in Winnipeg, Manitoba, for genotyping (2). At the community laboratory, the throat swab tested positive for group A streptococcus, and because the clinical presentation was consistent with scarlet fever, amoxicillin was prescribed. Two weeks after the resolution of symptoms, the National Microbiology Laboratory reported the measles virus in both samples as being genotype A – 100% identical to Genbank entry #FJ2111583 (the Edmonston-Enders vaccine strain).
The MMR vaccine contains live attenuated measles virus. It is estimated that administration of this vaccine is associated with moderate (39.4°C) fever in as many as 5% of recipients, and a rash in approximately 2% of those receiving immunization (3). These events typically occur approximately five to 12 days following immunization and often resolve without medical intervention. These systemic effects are likely caused by replication of the attenuated strains and host immune reaction. It has been shown that following the immunization of healthy children, the measles virus can be detected in urine as early as one day and as late as 14 days (4). Similarly, during acute infection by wild-type measles, the virus could be detected by RT-PCR for up to 14 days in >50% of healthy children (5) and up to one month in >90% of HIV-infected children (6). With the high sensitivity of an RT-PCR assay for measles virus and the lower detection limit at approximately 10 to 100 copies per reaction (7), recently immunized patients could test positive for an attenuated vaccine strain for two weeks or longer. In addition to shedding the vaccine strain for a prolonged period of time, administration of the vaccine to an individual with HIV infection and, in particular, those with AIDS, can rarely result in disseminated illness (8). In the original study by Katz et al (9), the measles virus could not be cultured from throat swabs or blood samples in the postimmunization period in a cohort of 31 children. While the attenuated virus can be detected in clinical specimens following immunization, it is understood that administration of the MMR vaccine to immunocompetent individuals does not carry the risk of secondary transmission to susceptible hosts (10). There is a case report suggesting the transmission of vaccine strain between immunocompetent siblings, but the conclusion was based only on clinical presentation, with no laboratory confirmation of infection (11,12).
In jurisdictions where measles is uncommon, a measles-like rash may be mistaken for other viral agents such as adenovirus, enterovirus or parvovirus B19 (13). The successful genotyping and identification of the measles virus as a vaccine strain in the present child serves to remind clinicians of potential signs and symptoms following the administration of live attenuated viral vaccines (14). In the immediate postimmunization time period, testing patients for the specific viral agents in the attenuated vaccine by molecular assays needs to be accompanied by characterization of the detected virus because it is expected that the serological tests will be positive and not indicative of acute wild-type infection (15). In true wild-type measles infection, measles IgM may be negative during the first few days of the rash and in susceptible individuals with waning immunity – an observation also reported in mumps cases (16,17). Testing for measles should only be considered in specific circumstances for which there is a possible exposure history to wild-type virus. This could include travel to an endemic area and/or exposure to a confirmed case of disease. An exposure history may be complicated by international travel and undetected exposures in airport terminals (18). The detection and characterization of the measles virus is important for Public Health purposes and in environments where such clinical illness is rare but wild-type virus is circulating (18,19). For suspected measles cases, laboratory tests should include measles IgM and IgG serology, as well as an NP swab and a urine sample for the detection of the measles virus. This testing should only be considered if exposure to the wild-type (not vaccine-strain) virus is strongly suspected.
The authors acknowledge Ms Joy Jaipaul, Dr Alberto Severini and Dr Graham Tipples for their invaluable assistance in the investigation of the measles cluster in Alberta and the preparation of this manuscript.
1. Tipples GA, Hiebert J. Detection of measles, mumps and rubella viruses. In: Stephenson JR, Warnes A, eds. Diagnostic Virology Protocols, 2nd edn. New York: Springer Science and Business Media, 2011. Methods Mol Biol. 2011;665:183–93.[PubMed]
2. Tipples GA, Gray M, Garbutt M, Rota PA, Canadian Measles Surveillance Program Genotyping of measles virus in Canada: 1979–2002. J Infect Dis. 2004;189:S171–6. [PubMed]
4. Rota PA, Khan AS, Durigon E, Yuran T, Villamarzo YS, Bellini WJ. Detection of measles virus RNA in urine specimens from vaccine recipients. J Clin Microbiol. 1995;33:2485–8. [PMC free article] [PubMed]
5. Riddell MA, Chibo D, Kelly HA, Catton MG, Birch CJ. Investigation of optimal specimen type and sampling time for detection of measles virus RNA during a measles epidemic. J Clin Microbiol. 2001;39:375–6. [PMC free article] [PubMed]
6. Permar SR, Moss WJ, Ryon JJ, et al. Prolonged measles virus shedding in human immunodeficiency virus-infected children, detected by reverse transcriptase-polymerase chain reaction. J Infect Dis. 2001;183:532–8. [PubMed]
7. Hummel KB, Lowe L, Bellini WJ, Rota PA. Development of quantitative gene-specific real-time RT-PCR assays for the detection of measles virus in clinical specimens. J Virol Methods. 2006;132:166–73. [PubMed]
8. Angel JB, Walpita P, Lerch RA, et al. Vaccine-associated measles pneumonitis in an adult with AIDS. Ann Intern Med. 1998;129:104–6. [PubMed]
9. Katz SL, Kempe CH, Black FL, et al. Studies on an attenuated measles virus vaccine. N Engl J Med. 1960;263:180–4. [PubMed]
10. Katz SL, Enders JF, Holloway A. Studies on an attenuated measles-virus vaccine. II. Clinical, virologic and immunologic effects of vaccine in institutionalized children. N Engl J Med. 1960;263:159–61. [PubMed]
11. Millson D. Brother-to-sister transmission of measles after measles, mumps and rubella immunization. Lancet. 1989;333:271. [PubMed]
12. Campbell AGM. Brother-to-sister transmission of measles after measles, mumps and rubella immunization. Lancet. 1989;333:442. [PubMed]
13. Davidkin I, Valle M, Peltola H, et al. Etiology of measles- and rubella-like illness in measles, mumps and rubella-vaccinated children. J Inf Dis. 1998;178:1567–70.[PubMed]
14. Freeman TR, Stewart MA, Turner L. Illness after measles-mumps-rubella vaccination. CMAJ. 1993;149:1669–74. [PMC free article] [PubMed]
15. Hyde TB, Nandy R, Hickman CJ, et al. Laboratory confirmation of measles in elimination settings: Experience from the Republic of the Marshall Islands, 2003. Bull World Health Organ. 2009;87:93–8. [PMC free article] [PubMed]
16. Akiyoshi K, Suga T, Nukuzuma S, et al. Reevaluation of laboratory methods for diagnosis of measles. Jpn J Infect Dis. 2010;63:225–8. [PubMed]
17. Hatchette T, Davidson R, Clay S, et al. Laboratory diagnosis of mumps in a partially immunized population: The Nova Scotia experience. Can J Infect Dis Med Microbiol. 2009;20:e157–62. [PMC free article] [PubMed]
18. Centers for Disease Control and Prevention (CDC) Measles imported by returning U.S. travelers aged 6–23 months, 2001–2011. MMWR Morb Mortal Wkly Rep. 2011;60:397–400. [PubMed]
Copy and paste of the planned American hell. Posted by Elizabeth Hill in The Ready Room - Takedown of The Global Elite group.
If you want to live in this hell, just keep sitting on your butt watching the TV propaganda. That's what they're counting on:
Wherever you stand, please take the time to read this; it ought to scare the bejeebies out of you!
We know Dick Lamm as Governor of Colorado. In that context his thoughts are particularly poignant. Last week there was an immigration overpopulation conference in Washington D.C., filled to capacity by many of America's finest minds and leaders. A brilliant college professor [and farmer] by the name of Victor Davis Hanson talked about his latest book, Mexifornia, explaining how immigration - both legal and illegal - was destroying the entire state of California. He said it would march across the country until it destroyed all vestiges of The American Dream.
Moments later, former Colorado Governor Richard D. Lamm stood up and gave a stunning speech on how to destroy America.
The audience sat spellbound as he described eight methods for the destruction of the United States. He said, "If you believe that America is too smug, too self-satisfied, too rich, then let's destroy America. It is not that hard to do. No nation in history has survived the ravages of time Arnold Toynbee observed that all great civilizations rise and fall and that 'An autopsy of history would show that all great nations commit suicide.'
"Here is how they do it," Lamm said:
"First, to destroy America, turn America into a bilingual or multi-lingual and bi-cultural country. History shows that no nation can survive the tension, conflict, and antagonism of two or more competing languages and cultures It is a blessing for an individual to be bilingual; however, it is a curse for a society to be bilingual. The historical scholar, Seymour Lipset, put it this way: 'The histories of bilingual and bi-cultural societies that do not assimilate are histories of turmoil, tension, and tragedy.' Canada, Belgium, Malaysia, and Lebanon all face crises of national existence in which minorities press for autonomy, if not independence. Pakistan and Cyprus have divided. Nigeria suppressed an ethnic rebellion France faces difficulties with Basques, Bretons, Corsicans and Muslims.'
Lamm went on:
"Second, to destroy America, invent 'multiculturalism' and encourage immigrants to maintain their culture. Make it an article of belief that all cultures are equal; that there are no cultural differences. Make it an article of faith that the Black and Hispanic dropout rates are due solely to prejudice and discrimination by the majority. Every other explanation is out of bounds.
"Third, we could make the United States an 'Hispanic Quebec' without much effort. The key is to celebrate diversity rather than unity. As Benjamin Schwarz said in the Atlantic Monthly recently: 'The apparent success of our own multi-ethnic and multicultural experiment might have been achieved not by tolerance but by hegemony. Without the dominance that once dictated ethnocentricacy and what it meant to be an American, we are left with only tolerance and pluralism to hold us together.'
Lamm said, "I would encourage all immigrants to keep their own language and culture. I would replace the melting pot metaphor with the salad bowl metaphor. It is important to ensure that we have various cultural subgroups living in America enforcing their differences rather than as Americans, emphasizing their similarities.
"Fourth, I would make our fastest growing demographic group the least educated. I would add a second underclass, un-assimilated, under-educated, and antagonistic to our population. I would have this second underclass have a 50% dropout rate from high school.
"My fifth point for destroying America would be to get big foundations and business to give these efforts lots of money. I would invest in ethnic identity, and I would establish the cult of 'Victimology.' I would get all minorities to think that their lack of success was the fault of the majority. I would start a grievance industry blaming all minority failure on the majority.
"My sixth plan for America's downfall would include dual citizenship, and promote divided loyalties. I would celebrate diversity over unity. I would stress differences rather than similarities. Diverse people worldwide are mostly engaged in hating each other - that is, when they are not killing each other. A diverse, peaceful, or stable society is against most historical precept. People undervalue the unity it takes to keep a nation together.
Look at the ancient Greeks. The Greeks believed that they belonged to the same race; they possessed a common language and literature; and they worshipped the same gods. All Greece took part in the Olympic games. A common enemy, Persia, threatened their liberty. Yet all these bonds were not strong enough to overcome two factors: local patriotism and geographical conditions that nurtured political divisions. Greece fell.
'E. Pluribus Unum' -- From many, one. In that historical reality, if we put the emphasis on the 'pluribus' instead of the 'Unum,' we will 'Balkanize' America as surely as Kosovo.
"Next to last, I would place all subjects off limits. Make it taboo to talk about anything against the cult of 'diversity.' I would find a word similar to 'heretic' in the 16th century - that stopped discussion and paralyzed thinking. Words like 'racist' or 'xenophobe' halt discussion and debate. Having made America a bilingual/bi-cultural country, having established multi-culturalism, having the large foundations fund the doctrine of 'Victimology,' I would next make it impossible to enforce our immigration laws. I would develop a mantra: That because immigration has been good for America , it must always be good. I would make every individual immigrant symmetric and ignore the cumulative impact of millions of them."
In the last minute of his speech, Governor Lamm wiped his brow. Profound silence followed. Finally he said, "Last, I would censor Victor Davis Hanson's book Mexifornia. His book is dangerous. It exposes the plan to destroy America. Unless you feel America deserves to be destroyed, don't read that book."
There was no applause. A chilling fear quietly rose like an ominous cloud above every attendee at the conference. Every American in that room knew that everything Lamm enumerated was proceeding methodically, quietly, darkly, yet pervasively across the United States today. Discussion is being suppressed. Over 100 languages are ripping the foundation of our educational system and national cohesiveness. Even barbaric cultures that practice female genital mutilation are growing as we celebrate "diversity."
American jobs are vanishing into the Third World as corporations create a Third World in America - take note of California and other states To date, ten million illegal aliens and growing fast. It is reminiscent of George Orwell's book, 1984. In that story, three slogans are engraved in the Ministry of Truth building: "War is peace," "Freedom is slavery," and "Ignorance is strength."
Governor Lamm walked back to his seat. It dawned on everyone at the conference that our nation and the future of this great democracy is deeply in trouble and worsening fast. If we don't get this immigration monster stopped within three years, it will rage like a California wildfire and destroy everything in its path, especially The American Dream.
If you care for and love our country as I do, take the time to pass this on just as I did for you.
NOTHING to counteract this is going to happen if you don't!
The Disease is the Cryme: "Saying OspA was a vaccine when it, as a fungal endotoxin, caused the permanent AIDS-like disease, where the opportunistic herpes viruses cause all the trouble."
Or: "OspA causes the DISEASE, and they said it was a vaccine (the opposite, which is CRYME)."
The Cryme is the Disease- Saying OspA prevented the disease, when it actually caused it. ===================
You wont hear about this from any "MD" since they are not actually trained in science or pharma. You wont hear about this from ILADS or the LDA because none of them is a scientist. And it has now been 20 years. LYMErix came out in the Spring of 1999....
In 20 years, you have *NEVER* seen an MD even *ASK* what OspA was, even though they are all supposed to be trained in basic chemistry *nomenclature,* where STRUCTURE predicts FUNCTION/ACTIVITY (the very reason chemists/bio scientists actually *speak* in structures) !!!...
20 years of discussion and debate, but you've never seen an MD say "OspA was a triacyl lipoprotein (fungal)" and there has never been a vaccine for spirochetal fungal disease (syphilis) or Tuberculosis....
There is no vaccine against MRSA (also bears fungal antigens), the biggest killer a hospital can deploy. Kills 10s of thousands of people every year. Go ahead and google that...
You cant make a vaccine out of a triacyl (fatty acids; it floats on water or is insoluble in blood) lipoprotein because such an antigen is a toxin worse than the classic endotoxin since the tolerance is not reversible and it also spreads (the tolerance) to other antigen types.
THE VERY BIGGEST CONCERNS IN MEDICINE... Hospital acquired MRSA... no one comes out and explains what the issue are. Why MRSA is such a disaster is the same reason Lyme is such a disaster. You cant make a vaccine out of a fungal antigen. They are the complete opposite of vaccines - they DESTROY immunity, rather than cause it.
Remember who the real experts are. Not "MDs." You have never seen an MD explain this. It has never been on TV. .