CDC- Mistakes

CDC- Mistakes


CDC labs close due to cross contamination of anthrax, small pox, and deadly flu strain
http://www.cidrap.umn.edu/news-perspective/2014/07/more-problems-shutter-cdc-labs-prompt-review

CDC says it improperly sent deadly pathogens at least 5 times in the past decade
http://www.washingtonpost.com/national/health-science/cdc-says-it-improperly-sent-dangerous-pathogens-in-five-incidents-in-past-decade/2014/07/11/acd55bfc-0882-11e4-a0dd-f2b22a257353_story.html

According to two Merck scientists who filed a False Claims Act complaint in 2010 vaccine manufacturer Merck knowingly falsified its mumps vaccine test data, spiked blood samples with animal antibodies, sold a vaccine that actually promoted mumps and measles outbreaks, and ripped off governments and consumers who bought the vaccine thinking it was "95% effective."
http://www.courthousenews.com/2012/06/27/47851.htm

Los Angeles Times, Merck & Co., the makers of several vaccines, knew in 1991 that the cumulative amount of mercury in vaccines given to infants by six months of age was about 87 times the level then thought to be safe

CDC's Vaccine Safety Research is Exposed as Flawed and Falsified in Peer-Reviewed Scientific Journalistically
https://www.yahoo.com/finance/news/cdcs-vaccine-safety-research-exposed-115600020.html

Poul Thorsen, the man that conducted the study for the CDC claiming there is no link between vaccines and autism, is on the most wanted fugitive list for the Office of Inspector General for stealing over $1 million in grant money from the CDC. Thorsen submitted fraudulent invoices on CDC letterhead to medical facilities assisting in the research for reimbursement of work allegedly covered by the grants. The invoices were addressed to Aarhaus University and Sahlgrenska University Hospital. The fact that the invoices were on CDC letterhead made it appear that CDC was requesting the money from Aarhaus University and Sahlgrenska University Hospital although the bank account listed on the invoices belonged to Thorsen.
https://oig.hhs.gov/fraud/fugitives/profiles.asp#thorsen

Thorsen's partner Kreesten Madsen recently came under fierce criticism after damning e-mails surfaced showing Madsen in cahoots with CDC officials intent on fraudulently cherry picking facts to prove vaccine safety.
http://www.putchildrenfirst.org/chapter5.html

It was already well known that vaccines have caused the cancer epidemic in today’s society. Both the Small Pox and the Oral Polio Vaccine are made from monkey serum. This serum has helped many monkey viruses to enter the human blood stream. Out of these the only researched virus, SV 40, has been found to be cancerous. As per recent revelations these viruses continue to be in the vaccines. The presence of SV 40 in various human cancers has been demonstrated. Today it is known that the virus is being passed on to future generations as its presence in the mother’s milk and human sperms has been established.


GlaxoSmithKline (GSK) also produces vaccines
A roughly nine-year federal investigation has exposed GSK's rampant abuse of the law by illegally marketing drugs, forging drug safety data, bribing doctors to promote dangerous and expensive drugs, ripping off Medicare and Medicaid, and lying about the effectiveness and safety of drugs
http://www.nytimes.com/2012/07/03/business/glaxosmithkline-agrees-to-pay-3-billion-in-fraud-settlement.html



"Nations that require more vaccines tend to have higher infant mortality rates"
http://het.sagepub.com/content/early/2011/05/04/0960327111407644.full.pdf


"Thorsen's 2003 Danish study reported a 20-fold increase in autism in Denmark after that country banned mercury based preservatives in its vaccines. His study concluded that mercury could therefore not be the culprit behind the autism epidemic.
His study has long been criticized as fraudulent since it failed to disclose that the increase was an artifact of new mandates requiring, for the first time, that autism cases be reported on the national registry. This new law and the opening of a clinic dedicated to autism treatment in Copenhagen accounted for the sudden rise in reported cases rather than, as Thorsen seemed to suggest, the removal of mercury from vaccines."
http://www.huffingtonpost.com/robert-f-kennedy-jr/central-figure-in-cdc-vac_b_494303.html


Conclusions
The present study provides new epidemiologic evidence showing that African American males receiving the MMR vaccine prior to 24 months of age or 36 months of age are more likely to receive an autism diagnosis.
http://web.archive.org/web/20140824230839/http://www.translationalneurodegeneration.com/content/3/1/16/abstract 


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

Abstract
"There is a compelling argument that the occurrence of regressive autism is attributable to genetic and chromosomal abnormalities, arising from the overuse of vaccines, which subsequently affects the stability and function of the autonomic nervous system and physiological systems. That sense perception is linked to the autonomic nervous system and the function of the physiological systems enables us to examine the significance of autistic symptoms from a systemic perspective. Failure of the excretory system influences elimination of heavy metals and facilitates their accumulation and subsequent manifestation as neurotoxins: the long-term consequences of which would lead to neurodegeneration, cognitive and developmental problems. It may also influence regulation of neural hyperthermia. This article explores the issues and concludes that sensory dysfunction and systemic failure, manifested as autism, is the inevitable consequence arising from subtle DNA alteration and consequently from the overuse of vaccines."
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/

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

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.
“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

"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

“Autoimmunity to the central nervous system (CNS), especially to myelin basic protein (MBP), may play a causal role in autism, a neurodevelopmental disorder. Because many autistic children harbor elevated levels of measles antibodies, we conducted a serological study of measles-mumps-rubella (MMR) and MBP autoantibodies. Using serum samples of 125 autistic children and 92 control children, antibodies were assayed by ELISA or immunoblotting methods. ELISA analysis showed a significant increase in the level of MMR antibodies in autistic children. Immunoblotting analysis revealed the presence of an unusual MMR antibody in 75 of 125 (60%) autistic sera but not in control sera. This antibody specifically detected a protein of 73-75 kD of MMR. This protein band, as analyzed with monoclonal anti bodies, was immunopositive for measles hemagglutinin (HA) protein but not for measles nucleoprotein and rubella or mumps viral proteins. 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

Aluminum is in the following vaccines:
DTaP, Pediarix (DTaP-Hepatitis B-Polio combination), Pentacel (DTaP-HIB-Polio combination), Hepatitis A, Hepatitis B, Haemophilus influenzae B (HIB), Human Papilloma Virus (HPV), and Pneumococcal vaccines

"In adults, aluminum exposure can lead to apparently age-related neurological deficits resembling Alzheimer's and has been linked to this disease and to the Guamanian variant, ALS-PDC. Similar outcomes have been found in animal models. In addition, injection of aluminum adjuvants in an attempt to model Gulf War syndrome and associated neurological deficits leads to an ALS phenotype in young male mice. 
In young children, a highly significant correlation exists between the number of pediatric aluminum-adjuvanted vaccines administered and the rate of autism spectrum disorders. Many of the features of aluminum-induced neurotoxicity may arise, in part, from autoimmune reactions, as part of the ASIA syndrome."
http://www.ncbi.nlm.nih.gov/m/pubmed/23609067/

Abstract 
"Immune challenges during early development, including those vaccine-induced, can lead to permanent detrimental alterations of the brain and immune function. Experimental evidence also shows that simultaneous administration of as little as two to three immune adjuvants can overcome genetic resistance to autoimmunity. In some developed countries, by the time children are 4 to 6 years old, they will have received a total of 126 antigenic compounds along with high amounts of aluminum (Al) adjuvants through routine vaccinations. According to the US Food and Drug Administration, safety assessments for vaccines have often not included appropriate toxicity studies because vaccines have not been viewed as inherently toxic. Taken together, these observations raise plausible concerns about the overall safety of current childhood vaccination programs. When assessing adjuvant toxicity in children, several key points ought to be considered: (i) infants and children should not be viewed as "small adults" with regard to toxicological risk as their unique physiology makes them much more vulnerable to toxic insults; (ii) in adult humans Al vaccine adjuvants have been linked to a variety of serious autoimmune and inflammatory conditions (i.e., "ASIA"), yet children are regularly exposed to much higher amounts of Al from vaccines than adults; (iii) it is often assumed that peripheral immune responses do not affect brain function. However, it is now clearly established that there is a bidirectional neuro-immune cross-talk that plays crucial roles in immunoregulation as well as brain function. In turn, perturbations of the neuro-immune axis have been demonstrated in many autoimmune diseases encompassed in "ASIA" and are thought to be driven by a hyperactive immune response; and (iv) the same components of the neuro-immune axis that play key roles in brain development and immune function are heavily targeted by Al adjuvants. In summary, research evidence shows that increasing concerns about current vaccination practices may indeed be warranted. Because children may be most at risk of vaccine-induced complications, a rigorous evaluation of the vaccine-related adverse health impacts in the pediatric population is urgently needed."
http://www.ncbi.nlm.nih.gov/m/pubmed/22235057/

"Anxiety-like behavior was more pronounced among mice immunized with alum. In conclusion, herein we report that immunization with the HBVv (hepatitis b vaccine) aggravated kidney disease in an animal model of SLE. Immunization with either HBVv or alum affected blood counts, neurocognitive functions and brain gliosis. Our data support the concept that different component of vaccines may be linked with immune and autoimmune mediated adverse events."
http://www.ncbi.nlm.nih.gov/m/pubmed/25042822/

Aluminum hydroxide (which is in vaccines) injections lead to motor deficits and motor neuron degeneration
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2819810/

Aluminum adjuvant linked to Gulf War illness induces motor neuron death in mice.
"Aluminum-treated groups also showed significant motor neuron loss (35%) and increased numbers of astrocytes (350%) in the lumbar spinal cord. The findings suggest a possible role for the aluminum adjuvant in some neurological features associated with GWI and possibly an additional role for the combination of adjuvants."
http://www.ncbi.nlm.nih.gov/pubmed/17114826

" By applying Hill's criteria for establishing causality between exposure and outcome we investigated whether exposure to Al (aluminum) from vaccines could be contributing to the rise in ASD (autism spectrum disorders) prevalence in the Western world. Our results show that: (i) children from countries with the highest ASD prevalence appear to have the highest exposure to Al from vaccines; (ii) the increase in exposure to Al adjuvants significantly correlates with the increase in ASD prevalence in the United States observed over the last two decades"
http://www.ncbi.nlm.nih.gov/pubmed/22099159

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.”
http://link.springer.com/article/10.1007%2Fs10565-013-9239-0

"Repeated immunization with antigen causes systemic autoimmunity in mice otherwise not prone to spontaneous autoimmune diseases. Overstimulation of CD4 + T cells by repeated immunization with antigen led to the development of a fully-matured autoantibody-inducing CD4 + T (aiCD4 + T) cell which had undergone T cell receptor (TCR) revision and was capable of inducing autoantibodies. The aiCD4 + T cell was induced by de novo TCR revision but not by cross-reaction to immunizing antigen, and subsequently overstimulated CD8 + T cells, driving them to become MHC class I-restricted, antigen-specific cytotoxic T lymphocytes (CTL). These CTLs could be further matured by antigen cross-presentation, after which they caused autoimmune tissue injury akin to systemic lupus erythematosus (SLE). Autoimmune tissue injury did not appear in CD8 + T cell-deficient mice. Further, inhibition of antigen-cross presentation by treating with chloroquine abrogated the generation of CTL and autoimmune tissue injury."
Conclusion: 
"Systemic autoimmunity appears to be the inevitable consequence of over-stimulating the host’s immune ‘system’ by repeated immunization with antigen, to the levels that surpass system’s self-organized criticality."
http://www.jimmunol.org/cgi/content/meeting_abstract/184/1_MeetingAbstracts/93.39

Autoimmunity and non-accidental injury in children 
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. 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 
http://article.sciencepublishinggroup.com/pdf/10.11648.j.cmr.20130203.15.pdf

Encephalitis
"Encephalitis is inflammation of the brain that occurs when a virus directly infects the brain or when a virus, vaccine, or something else triggers inflammation. The spinal cord may also be involved, resulting in a disorder called encephalomyelitis."
" Encephalitis can occur in the following ways:
A virus directly infects the brain. A virus that caused an infection in the past becomes reactivated and directly damages the brain. A virus or vaccine triggers a reaction that makes the immune system attack brain tissue (an autoimmune reaction)."
" Autoimmune encephalitis: After certain viral infections or vaccines, the body's immune system sometimes attacks the layers of tissue that wrap around nerve fibers (called the myelin sheath) in the brain and spinal cord The attack occurs because proteins in myelin resemble those in the virus. As a result, nerve transmission becomes very slow. The resulting disorder, called acute disseminated encephalomyelitis, resembles multiple sclerosis except that symptoms do not come and go as they do in multiple sclerosis. The viruses most often involved include enteroviruses, Epstein-Barr virus, hepatitis A or B virus, human immunodeficiency virus (HIV), and influenza viruses."
http://www.merckmanuals.com/home/brain_spinal_cord_and_nerve_disorders/brain_infections/encephalitis.html

The common immunogenic etiology of chronic fatigue syndrome: from infections to vaccines via adjuvants to the ASIA syndrome. 
Abstract:
Chronic fatigue syndrome (CFS) is characterized by unexplained fatigue that lasts for at least 6 months with a constellation of other symptoms. Most cases start suddenly, and are usually accompanied by a flu-like illness. It is a symptom-based diagnosis of exclusion, the pathogenesis of which is unknown. Studies have examined and hypothesized about the possible biomedical and epidemiologic characteristics of the disease, including genetic predisposition, infections, endocrine abnormalities, and immune dysfunction and psychological and psychosocial factors. Recently, the AISA (autoimmune/inflammatory syndrome induced by adjuvants) syndrome was recognized, indicating the possible contribution of adjuvants and vaccines to the development of autoimmunity.
http://www.ncbi.nlm.nih.gov/pubmed/22054760

Review of Vaccine Induced Immune Overload and the Resulting Epidemics of Type 1 Diabetes and Metabolic Syndrome, Emphasis on Explaining the Recent Accelerations in the Risk of Prediabetes and other Immune Mediated Diseases
Abstract 
"There has been an epidemic of inflammatory diseases that has paralleled the epidemic on iatrogenic immune stimulation with vaccines. Extensive evidence links vaccine induced immune over load with the epidemic of type 1 diabetes. More recent data indicates that obesity, type 2 diabetes and other components of metabolic syndrome are highly associated with immunization and may be manifestations of the negative feedback loop of the immune system reacting to the immune overload. The epidemic of diabetes/prediabetes appears to be accelerating at a time when the prevalence of obesity has stabilized, indicating that the negative feedback system of the immune system has been over whelmed. The theory of vaccine induced immune overload can explain the key observations that have confounded many competing hypothesis. The current paper reviews the evidence that vaccine induced immune overload explains the disconnect between the increase in prediabetes and nonalcoholic fatty liver at a time when the obesity epidemic is waning in children."
http://www.omicsonline.com/open-access/vaccine-induced-immune-overload-and-the-resulting-epidemics-of-type-diabetes-and-metabolic-syndrome-1747-0862.S1-025.php?aid=24058

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/

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 FluMist influenza vaccine strains replicate in the nasopharynx and can be recovered and cultured from respiratory secretions of vaccinated individuals (shed). The pattern and duration of shedding is important to understand because with prolonged shedding at high titer there is a theoretical risk of loss of attenuated phenotype, reassortment with wild-type influenza virus during influenza season, and transmission of vaccine virus to unvaccinated people, some of whom may be immunocompromised and/or at risk for complications of live viral infections."
"In each age group, among subjects who shed, shedding was most often observed on days 2-3 post vaccination. Among the population for whom FluMist is currently approved for use, i.e., individuals 2-49 years of age (n = 443), vaccine virus titers did not exceed 1.5 log10 TCID50/mL after day 11, though some individuals shed vaccine strain virus as late as day 28 post-vaccination. "
http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM259175.pdf

Clustering of cases of insulin dependent diabetes (IDDM) occurring three years after hemophilus influenza B (HiB) immunization support causal relationship between immunization and IDDM.
http://www.ncbi.nlm.nih.gov/pubmed/12911277

CONCLUSION: 
"We documented here the evidence of the potential of the HPV vaccine to trigger a life-disabling autoimmune condition. The increasing number of similar reports of post HPV vaccine-linked autoimmunity and the uncertainty of long-term clinical benefits of HPV vaccination are a matter of public health that warrants further rigorous inquiry."
http://www.ncbi.nlm.nih.gov/m/pubmed/23902317/

Conclusions: 
"These findings are consistent with the hypothesis that immunization with the recombinant hepatitis B vaccine is associated with an increased risk of MS, and challenge the idea that the relation between hepatitis B vaccination and risk of MS is well understood."
http://www.neurology.org/content/63/5/838.abstract

Conclusions:
"Hepatitis B vaccination does not generally increase the risk of CNS inflammatory demyelination in childhood. However, the Engerix B vaccine appears to increase this risk, particularly for confirmed multiple sclerosis, in the longer term. Our results require confirmation in future studies."
http://www.ncbi.nlm.nih.gov/pubmed/18843097

" A majority of the ophthalmological complications seen following hepatitis B vaccination consist of vision loss, optic neuritis, papillary edema, uveitis, acute placoid pigment epitheliopathy and central vein occlusion. We present a 9-year-old girl who was referred to our hospital with decrease in vision and pain in the left eye a week after hepatitis B vaccination. A diagnosis of vaccine-induced optic neuritis was made."
http://www.ncbi.nlm.nih.gov/pubmed/19948437

Conclusions:
Children vaccinated in infancy are at increased risk of hepatitis B virus infection in the late teens
http://www.bmj.com/content/325/7364/569


"Acquired autoimmunity syndromes occur after viral vaccinations. Molecular mimicry is involved in these phenomena as is the necessity for the presence of two chemically complimentary antigens and an immunologic adjuvant. The HLA pattern of the host is also an important factor. The example used to explain these phenomena is demyelinating disease that follows hepatitis B vaccination. The somatic antigen of the hepatitis B virus in the vaccine has chemical complimentarity with the Epstein-Barr virus antigen in the vaccine recipient. The Epstein-Barr virus shows molecular mimicry with human myelin. The immunologic adjuvant is either present in the vaccine or muramyl peptides in the individual who is vaccinated. Why more than one type of autoimmune disease occurs is explained by the fact that specific autoimmune T-cells have been shown to develop clones that attack multiple human tissues."
http://www.ncbi.nlm.nih.gov/pubmed/17630224

Fall Baby Shower

The Little pumpkin themed baby shower.  These are the gift tags I made. 

Below are the tags for food

Handmade Little Pumpkin banner

Front door sign for the shower

Gift table sign

I love the rolled up flatware

The favor gift tags in use.

Each Vaccine and what they are for.

Should you get or give this vaccine to your child?

By waiting until between 2 and 3 years old, you can significantly reduce the amount of vaccines your child receives because they don’t need boosters (because their immune systems functions on its own, and more importantly the blood/brain barrier (BBB) will be developed. Teething produces histamines, which are a neurotransmitter that causes consistent BBB opening, giving vaccine neurotoxins direct access to baby’s brain. Most babies are done teething by the age of 3.

To learn more about the blood brain barrier. https://vaccinesbytheoutliers.wordpress.com/2015/10/08/injecting-vaccines-before-a-childs-blood-brain-barrier-is-fully-developed/

 it is pointless to administer drugs intended to stimulate antibody production to babies who are too young to produce antibodies. Infants in their first year mostly depend on generalized, non-specific immunity, including (hopefully) immunoglobulins from breast milk, to protect their young bodies from infection. They do not produce antibodies of their own until about age one. Despite this basic fact, the medical establishment insists administering a total of 19 shots, containing 24 vaccines, to infants on the 2, 4 and 6 month pediatric visits(Source: cdc.gov). Somehow, the basic facts of human physiology and development do not apply to vaccines.

Hep B - No baby needs this.

Hepatitis B is spread when blood, semen, or other body fluid infected with the Hepatitis B virus enters the body of a person who is not infected.

Hepatitis B is not a killer disease for most people.

Symptoms of Hepatitis B infection include nausea, vomiting, fatigue, low grade fever, pain and swelling in joints, headache and cough that may occur one to two weeks before the onset of jaundice (yellowing of the skin) and enlargement and tenderness of the liver, which can last for three to four weeks

People can become infected with the virus during activities such as:

•Birth (spread from an infected mother to her baby during birth)

•Sex with an infected partner

•Sharing needles, syringes, or other drug-injection equipment

•Sharing items such as razors or toothbrushes with an infected person

•Direct contact with the blood or open sores of an infected person

•Exposure to blood from needles or other sharp instruments

Hepatitis B vaccination-induced protective antibodies can last for up to 15 years, but appears to fall off over time when they are more likely to be at risk. In one study, in just 5 years, efficacy of the vaccine fell to 67%.

Duration of Immunity - at least 20 years- So all the years your kid will probably not need to be protected from this it will have an immunity for it.

CDC states booster doses not routinely recommended. So once you get to the age of doing drugs and sex they don't think you need to worry about getting a vaccine for it even though the vaccine has worn off.

-"These findings are consistent with the hypothesis that immunization with the recombinant hepatitis B vaccine is associated with an increased risk of MS, and challenge the idea that the relation between hepatitis B vaccination and risk of MS is well understood."

http://www.neurology.org/content/63/5/838.abstract

Babies and young children should not be vaccinated against a sexually transmitted disease at birth, with a vaccine that contains up to 125 times the “safe” limit of aluminum (according to the EPA regulations),

-"Hepatitis B vaccine might be followed by various rheumatic conditions and might trigger the onset of underlying inflammatory or autoimmune rheumatic diseases. "

​http://www.ncbi.nlm.nih.gov/pubmed/10534549

No, there is no medicine that can cure hepatitis. But in most cases, hepatitis B goes away by itself within 4 to 8 weeks. More than 9 out of 10 adults with HBV recover completely. - See more at: http://www.plannedparenthood.org/health-info/stds-hiv-safer-sex/hepatitis-b#sthash.XDD5bwrF.dpuf

HPV

Out of 130 different types of HPV, vaccine is for 4 types. The 3 series shot given to 12 year old girls to prevent HPV (an STD) which “MIGHT” but has never been confirmed, contribute to cervical cancer.

The manufacturer is only claiming 5 years of efficacy. The problem with this is 2 fold. 1. The average age of cervical cancer is 50. 2. The shot is administered to 12 year old girls.

So we have a system pushing multiple shots (boosters) with a supposed 5 year efficacy timeline onto pre-teen girls, that was never tested on them, for a disease that has an average age of 50. You give it a 12 year old and by the time she’s 17 the effects are worn off and then you claim you can prevent cervical cancer as they get older.

Your daughter could be one less?

If your daughter receives an HPV vaccine at the recommended age of 11, protection will have waned by age 16.The data collected from the above agency confirms approximately 0.0% deaths from cervical cancer under age 20. What is "one less" then 0%?

According to published data (2010 Discovery Medicine Journal), HPV vaccine efficacy must last at least 15 years to contribute to the prevention of cervical cancers. At the current time, protection against is at best 5-8 years

HPV infection is common, occuring in 1 out of 5 women. 90% of HPV cases will resolve within 1-3 year without any intervention, less than 8% of HPV cases will screen positive for cervical dysplasia

-"We documented here the evidence of the potential of the HPV vaccine to trigger a life-disabling autoimmune condition. The increasing number of similar reports of post HPV vaccine-linked autoimmunity and the uncertainty of long-term clinical benefits of HPV vaccination are a matter of public health that warrants further rigorous inquiry."

http://www.ncbi.nlm.nih.gov/m/pubmed/23902317/

Is it Worth the Risk?

"Your daughter could be one more"

You may find yourself asking if it is even appropriate to risk any adverse effects to a preadolescent girl for a vaccine that is (1) only theoretically proven to prevent a disease that (2) she only has a 0.66% risk of developing over her lifetime – WHEN THE SAME CAN BE PREVENTED WITH REGULAR PAP SCREENING

- VAERS

Another point worth addressing regarding safety is the adverse events reported after vaccination to various governments worldwide.

Since 2006, nearly 65% of all deaths and life-threatening reactions reported to VAERS from Gardasil or Cervarix alone. A total of 30,020 reports have been received by US VAERS including 2,574 hospitalizations, 9,114 ER visits 93 deaths.

82% of cases resulting in permanent disability in females under 30 years of age was attributed to HPV vaccines. To date, there is no data confirming HPV vaccines preventing or treating any cervical cancers. The large majority of HPV infection (and a great proportion of Cervical dysplasia) clear spontaneously without medical intervention

Polio- Up to 95% of all polio infections are completely asymptomatic. Approximately 5% of polio infections consist of a minor, nonspecific illness consisting of an upper respiratory tract infection (sore throat and fever) and gastrointestinal disturbances (nausea, vomiting, abdominal pain, and diarrhea). This influenza-like illness, clinically indistinguishable from the myriad of other viral illnesses, is characterized by complete recovery in less than a week with resultant life time immunity. Less than 1% of all polio infections result in paralysis. Most importantly, the vast majority of individuals who contract paralytic poliomyelitis recover with complete—or near complete—return of muscle function. Any weakness that is still present 12 months after onset of paralysis is usually considered permanent.“
Polio was already massively decreasing prior to any vaccine ever introduced. 
 I would also like to add that the highest incidence came at a time our country was in despair (poor sanitation, hygiene, nutrition) during the depression.

Polio was already on the way out prior to any introduction of vaccines.

It was a time where sanitation was poor, hygiene was poor, and nutrition was poor. These are the reasons that third world countries have problems with communicable diseases, not lack of vaccines. As the Great Depression was clearing up, people were living cleaner and healthier and there was also the introduction of a drug class called antibiotics that was given for any sniffle, cough, or fever.

The last natural case of polio in the US was 1979, yet we still give kids 4 rounds of this vaccine at 2, 4, 6-12 months, and 4-6 years. But the fear tactics continue of, “it can come back or you don’t know about the destruction it caused.” I’m not being ignorant to history. I’m being reasonable about the present.

What about Typhoid and Scarlet Fever? They had just as much devastation and with no vaccine, they are not a problem. Nature took its course and with the advent of better sanitation, hygiene, and nutrition, they wiped themselves out.

POLIO-

The polio vaccine of the 1950’s and 60’s was contaminated by the SV40 virus which is now confirmed to have caused cancer in many people who had received the vaccine. New viruses are being discovered all the time, so it’s a matter of Russian roulette on when such a virus will sneak into another vaccine (http://www.sv40foundation.org/CPV-link.html) Both the Small Pox and the Oral Polio Vaccine are made from monkey serum. This serum has helped many monkey viruses to enter the human blood stream. Out of these the only researched virus, SV 40, has been found to be cancerous. As per recent revelations these viruses continue to be in the vaccines. The presence of SV 40 in various human cancers has been demonstrated. Today it is known that the virus is being passed on to future generations as its presence in the mother’s milk and human sperms has been established.

CDC reported that 87% of the cases of polio in the us between 1973-1983 were caused by the vaccine. Jonas Salk, inventor of polio vax testified before a Senate subcommittee that nearly all polio outbreaks since 1961 were caused by the oral polio vacccine.

6 states reported increase in polio one year after the vaccine was introduced, ranging from more than doubling in Vermont to Massachusetts' astounding increase of 642%. Utah actually halted vaccination due to the increased incidence and death rate.

Measles
 But even vaccinating 100% of the population wouldn’t be enough, say scientists at the Mayo Clinic’s Vaccine Research Group, because the measles vaccine is a dud with some people, offering no protection at all, and its effectiveness wanes with others, even if they get boosters. According to Tetyana Obukhanych of Stanford University’s School of Medicine, the measles vaccine works as planned with only 25% of the population, leaving the majority of adults who have been vaccinated as children with little or no protection. Up to half of today’s cases involve adults.  So we have measles, which is associated with a red, itchy, rash, a runny nose, and a cough, lasting up to 2 weeks, that gives lifetime immunity, protection against more serious diseases as adults, and allows a mother to pass these antibodies to her baby for protection during their first year of life.  Severe measles is more likely among poorly nourished young children, especially those with insufficient vitamin A, or whose immune systems have been weakened by HIV/AIDS or other diseases.  Potentially fatal? Technically true, but herein lies the lie. It's been publicized as "the deadliest of all childhood fever/rash illness with a high rate of complications." Deadly? Not in the U.S., or any other developed country with a well-nourished population. The risk of fatality here isn't zero, but it's as close to zero as you can get without actually being zero. It's 1 in many thousands. Will someone pass away in the U.S. from measles one of these years? Tragically yes. That will likely happen to one person. It hasn't happened here in at least ten years (or more - I don't even know how many years we have to go back to find one). When that happens, it will be extremely tragic.
But measles can cause blindness…so can the MMR vaccine. 
But measles can cause encephalitis…so can the MMR vaccine 
But measles can cause pneumonia…so can the MMR vaccine.
But if I don’t get vaccinated, I could get measles…If you do get vaccinated you can get measles, both from the vaccine, and later in life when immunity has disappeared. 

DIPHTHERIA

The symptoms that warrant 4 shots of this vaccine before the age of 15 months are: sore throat with a low grade fever with an adherent membrane at the back of the throat. The weird thing is that in order for the toxins to be released, a specific strain of bacteria has to be infected with a specific virus called a B phage. In other words, a certain bacteria has to make out with a certain virus. In any case, it's nothing a simple antibiotic can't clear up, no need for a vaccine. If doctors suspect diphtheria, the infected child or adult receives an antitoxin. The antitoxin, injected into a vein or muscle, neutralizes the diphtheria toxin already circulating in the body.

Pertussis. 
In 2013, the FDA discovered that while the whooping cough vaccine may reduce symptoms in those who are vaccinated, the pertussis vaccine does not prevent infection and transmission of the disease.


In fact, you can get a series of pertussis shots and still become an asymptomatic carrier who is contagious and can spread the disease to others without even knowing it. That study effectively shattered the long-held illusion of vaccine-induced herd immunity.

In an animal study, while acellular-pertussis-vaccinated baby baboons did not develop serious clinical disease symptoms — such as loss of appetite and cough — when they were exposed to the B. pertussis bacteria, they still colonized B. pertussis in their throats and were capable of transmitting the infection to other baboons.

In that same study, the baby baboons that received whole cell DPT vaccine also were able to transmit pertussis infection to other baboons without showing typical pertussis symptoms, but were infectious for a shorter period of time that those which had received acellular pertussis vaccine.

The study's lead author Tod Merkel also explained that when exposed to B. pertussis after recently getting vaccinated, you could be an asymptomatic carrier and infect others, saying: "When you're newly vaccinated, you are an asymptomatic carrier, which is good for you, but not for the population."


The Tdap shot is also recommended for pregnant women, even though there is a lack of credible scientific evidence to demonstrate safety and effectiveness.
http://articles.mercola.com/sites/articles/archive/2016/01/26/whooping-cough-vaccine-ineffective.aspx

 But is the shot safe? According the research of the last 50 years, the vaccine is safe. But what test showed it was safe?

It's called the Mouse Weight Gain Test. "Researchers" would vaccinate mice at their stomachs. If the mice continue to gain weight and don't die right away, it's considered safe. I wish I could make this stuff up.

And if you haven't heard, adults should the shot because it will protect the young. In 2012, Australia stopped this adult vaccine program all together because there was no proof that it was protecting the young.

-Adults getting the shot to make sure babies don't get it?

PARENTS across Australia will no longer receive free whooping cough vaccinations because it is not effective in protecting newborns from the potentially deadly illness, a parliamentary committee has heard.

http://www.news.com.au/breaking-news/states-ending-free-parent-whooping-vaccine/story-e6frfku0-1226350174856#ixzz2ZU7huhZD

An acellular whooping cough vaccine actually enhances the colonization of Bordetella parapertussis in mice; pointing towards a rise in B. parapertussis incidence resulting from acellular vaccination, which may have contributed to the observed increase in whooping cough over the last decade. Pertussis is generally treated with Vitamin C

http://www.ncbi.nlm.nih.gov/pubmed/20200027

TETANUS

The odds of getting tetanus in the U.S. in 1947 when the vaccine was introduced were 1/300,000.  That is not deaths.  Just incidence

One thing I would like to point out is the ridiculousness of giving a tetanus shot AFTER you have a puncture wound. Why get a puncture wound that definitely contains tetanus after a puncture wound that might not contain tetanus? It's sketchy enough to say you're immune from tetanus from the regular vaccine schedule but to say there are curative powers by getting the vaccine AFTER the puncture wound is pretty ballsy, yet many line up to get injected after they think they might have tetanus.

Wounds that bleed will never result in tetanus because the tetanus bacillus is anaerobic.

Many of the reported cases of tetanus were in "fully vaccinated" people.

The document discusses 124 cases of tetanus reported between 1995 and 1997. Here is what was reported:

Nearly twenty -- five percent (24.8%) of those who contracted acute tetanus had at least one dose of the vaccine and more than twelve percent (12.4%) of the patients were fully vaccinated, with three or more doses of tetanus. Of the 66 (53.7%) people who had an "unknown vaccination status," it could reasonably be assumed that a portion of those had had one or more tetanus shots at some point in their lives. Therefore, statement made by the CDC that "the disease continues to occur almost exclusively among persons who are unvaccinated, inadequately vaccinated or whose vaccination histories are unknown or uncertain" is simply not true.

Antibiotic regimens are available for the treatment of both tetanus and diphtheria infections. Until the last few years, government statistics admitted that 40 percent of the child population of the U.S. was not immunized. For all those decades, where were the tetanus cases from all those rusty nails?

ROTOVIRUS

Rotovirus is responsible for diarrhea. It's estimated that 55,000 children are hospitalized each year in the US. There's an estimated 527,000 deaths worldwide due to rotovirus.

How many die in the US? The only stat I could find was from 1996 Journal of Infectious Disease where less than 40 kids died of rotovirus. Again, any death from anything for a child is devastating. But let's compare rotovirus to lighting strike deaths. Lighting strikes kill about 60 people each year. You have a greater chance of dying from lightning than you do rotovirus.

Not to mention the rotovirus shots are administered at ages 2, 4, and 6 months, a time where a baby cannot develop antibodies against the antigen.

All those worldwide deaths? Those are coming from the same reasons we had a polio epidemic, poor sanitation, poor hygiene, poor nutrition.

MUMPS 

In 2004, there were 350 deaths due to mumps. 312 were from Egypt. 2 were from the US, leaving you with a 0.00000065% chance of dying from mumps.

Mumps never posed a threat to the health and vitality of the American public. In regards to the incidence of mumps, even the CDC states, "before vaccination, mumps was a common illness in children, infants, and adults." Why create a vaccine? There's big money in vaccines. The vaccine industry has 4,000,000 potential new clients every year that will be repeat buyers until the age of 18.

VARICELLA

From 1990-1994, there was about 100 deaths each year due to chicken pox split between kids and adults. Your chance of death by chicken pox is 0.000032%. Between March 1995 and July 1998, the federal Vaccine Adverse Events Reporting System (VAERS) received 6,574 reports of health problems after chickenpox vaccination. Four percent of reported adverse events (about 1 in 33,000 doses) involved serious health problems such as shock, encephalitis (brain inflammation), and thrombocytopenia (a blood disorder), and 14 of the 6,574 chickenpox vaccine adverse event reports ended in death. That was just 3 yrs I don't know what that number is up to now. But I do know that the death rate of chicken pox (which I have had) is zero. While the CDC estimates the vaccine to be 86 percent effective in children, a 2001 CDC study showed that that effectiveness might actually be as low as 40 percent. But authorities at Maryland's Takoma Park Elementary School might quarrel even with that. There, reportedly, 12 of the 16 cases of a recent chickenpox outbreak involved children who had already been vaccinated. http://articles.mercola.com/.../23/chickenpox-vaccine.aspx

Hepatitis A

Eat food that someone else pooped in that is infected with Hepatitis A. There are no statistical reports of deaths from Hep A, just a 0.0098% chance of contracting it. The solution is good sanitation and hygiene.

HiB

This series of 4 shots are given at 2, 4, 6, and 12-15 months. Again, if a baby cannot develop antibodies until after 6 months, what's the point of giving a child any shot this early? HiB is a common cause of bacterial meningitis. If it's bacterial than a simple antibiotic should do the trick. There's no need to add more shots that contain heavy metals into a child's ecosystem. ."Hib immunization contributed to an increased risk for H. influenzae type a meningitis through selection of circulating H. influenzae type a clones." " the incidence for H. influenzae type a meningitis increased 8-fold"

http://jid.oxfordjournals.org/content/187/1/109.full.pdf+html

Meningococcal
First; understand how it spreads. For example, you cannot catch Neisseria meningococcal simply by standing next to someone who has it. In order to catch it and spread it, you have to have an intimate exchange of saliva, such as kissing, or sharing toothbrushes or cups. You won't catch it from someone coughing in an elevator.
Meningococcal is only associated with about 1,400 to 3,000 cases [of meningitis] per year in the United States, out of 308 million Americans. There are five strains (serotypes): A, B, C, Y, and W135. A third to half of the cases of Neisseria meningococcal disease is caused by strain B. And that strain is NOT in the vaccine."
This disease in the last nine years killed an average of 16 children per year under age 12 months in this country.
Vaccine Adverse Events Reporting System (VAERS), which includes only a small fraction of the health problems that occur after vaccination in the U.S., had recorded more than 2,300 serious health problems, hospitalizations and injuries following meningococcal shots, including 39 deaths with about 40% of the deaths occurring in children under age six.  
According to their package inserts, Menactra and Menveo produce "serious adverse events" in 1 percent of recipients. Menomune, with its hefty mercury load, sickens 1.3 percent of those receiving it. According to the CDC Pink Book, 0.3 percent of those with "serious adverse events" from meningitis vaccines will die. So here is the math calculation that thoughtful student governments in Colorado must consider: Example of the mandatory college enter meningitis vaccine law in Colorado.  If you inoculate Colorado's 400,000 college students with the older vaccines, you can expect 4,000 serious adverse events and 12 dead. We do not yet know the effects of widespread vaccination of the hastily-expedited B vaccines, but according to their package inserts, about 2 percent of students who receive the B vaccine will be sickened or hospitalized with a serious adverse event. This could translate into an additional 8,000 sick students and 24 deaths, for a total of 12,000 sick and 36 dead in the attempt to possibly avert three meningitis cases.

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