Vaccine News – Everything You’ll Need to Know about Vaccines

Pet owner spreading vaccination awareness after senior pet’s death
By Alyssa Goard and Nadine Bonewitz Published: September 29, 2017,
AUSTIN (KXAN) — Joann Saathoff’s 14-year-old Pomeranian, Lexy, died on Sept. 24, and she believes the round of vaccinations Lexy received 12 days earlier led to her death.
Now Saatoff is trying to raise awareness about the options owners of senior pets have when it comes to getting shots for their furry friends.
It all started when Lexy went in for her annual check up. She was evaluated by the vet first, who said Lexy was in good health. Then Lexy received five shots, the same exact group of shots she’d received the year before. Within a few hours, Saathoff said her active dog had grown lethargic.
She took Lexy back to the vet the next day and they said her reaction was common, so they gave her an antibiotic and fluids. But Lexy’s condition continued to decline, the six pound dog threw up everything she ate. When she died, she weighed only three pounds. Saathoff said the cause of Lexy’s death was starvation, but the veterinarian told her that it started with the vaccinations which were “too much for her system.”
Saathooff began researching.
“I found out there’s a lot of senior dogs out there that can’t handle the full regimen of vaccinations,” she said.
She says she doesn’t blame her vet, she just wishes she knew about other options. Now she’s urging other pet owners to ask about what is best for their pets.
“My message to the community is you have options with your senior level dogs,” she said.

23 ‘must-see’ vaccine documentaries
By Britny Murray
In no particular order, here are 23 highly informative, must-see vaccine documentaries that you could share with your firends.
They all have to do with various factors of vaccination – evidence,, efficacy, injuries, health effects and medicinal politics.
They come with a brief description pulled from YouTube. Most of them are free and featured here in-full.

Deadly Immunity – Government Cover-Up Of A Mercury/Autism Scandal
Sep 30, 2017
World Mercury Project note: With the ongoing mainstream media blackout on questions regarding vaccine safety, we want to remind our followers of the publication–and subsequent retraction–of Robert F. Kennedy, Jr.’s 2005 article “Deadly Immunity” in Salon. The history of repression of crucial vaccine safety data runs deep. The article laid out the scientific link between thimerosal and childhood neurological disorders and published explosive excerpts from the transcripts from the CDC’s secretive June 2000 Simpsonwood conference which brought together government public health officials, vaccine manufacturers and professional medical associations. The article was groundbreaking at the time and received lots of media attention for uncovering the cozy relationship between government and industry at the expense of children’s health. Even though a dozen years have passed, the article’s facts have stood the test of time. An important read for people new to the movement and long-time advocates alike.

Transcript – Scientific Review of Vaccine Safety Datalink Information

Everything You’ll Need to Know about Vaccines
With this enormous effort in marketing vaccines and the money spent sponsoring large cohort studies showing that vaccines are always safe and effective, never expressing anything negative, and in some countries enforcing mandatory vaccine schedules wouldn’t any normal sensible person become a little suspicious and ask themselves..ARE THEY TRYING TO HIDE SOMETHING ??. It took the medical mafia 12 years to remove the evidence in Wakefield and Walker smith’s study analysis of 12 children with serious intestinal abnormalities that their parents confirmed had developed after receiving the MMR vaccine. The British media found a scapegoat using British journalist Brian Deer to uncover a potential conflict of interest to ‘blow the smoke away ‘ from the findings of the study. At the time autism was on the rise without explanation 6.2/10,000 births in 1990 to 42.5/10,000 births in 2001..for the most part the vaccine marketing machine ignored any correlation or causality toward their glorious vaccines. Why was Merck allowed to manufacture a Vaccine that included a benign children’s disease when the CDC confirmed there was no need to protect against Mumps, but the MMR vaccine was allowed anyway to be included in CDC’s vaccine schedule.

Appology to Polly Tommy
Gross misconduct from the Australian Government

Hammond vaccine terror #vaxxed #vaxxedperiscope

Donations to help our case and cause
My name is Tanya and on the 26th of September 2012, James my son was born 8 weeks premature weighing in at just 2.4oz.
We live in a remote mining community in southern WA called Kalgoorlie and Ben, my beautiful husband, worked in the mines and because our son was born prem, he had to have a dTap vaccination and that’s just what you do. So just to be safe, as our entire family was protected and as good parents we believed we were, we always did the right thing.
James ended up and is doing fine but Ben, a healthy 34-year-old loving father and beautiful husband, sadly and totally unknowingly suffered the worst fate possible.
Both reported and recorded by the CDC (Centre for Disease Control) on their website, Ben had developed post vaccination ADEM (Acute Disseminated Encephalomyelitis) – our lives were shattered!
By October the 11th, 2012, Ben was classified a quadriplegic and since then, his health mentally, emotionally and physically has deteriorated so bad, that our lives will never be the same again.
Our vows in sickness and in health, no longer see any of the later and I’m now a full-time carer for Ben, no different than he would have done for me because our love for each other was so strong, but this curveball of life has put us to the test.
We’ve lost so much and are on the brink of extinction. We’re in surmounting debt, unable to work because we have 5 children and can’t afford childcare to work and bring home anything because the growing costs to care for Ben are not met with any government support.

Girl, 8, left with no skin after horrific allergic reaction to childhood vaccination meant it fell off when mum touched her
By Erin Elizabeth – September 26, 2017
At 18 months old, Isabel Olesen of Melbourne, Australia was taken to her pediatrician’s office for routine vaccinations (the kind that almost never cause a reaction and yet, our website is FULL of children who have suffered or died from very “rare” vaccine reactions) that ended up leaving her partially blind and covered with painful blisters all over her body, just 48 hours later.
Part of the problem with the one size fits all vaccine schedule is that you can’t tell when a child has Stevens-Johnson Syndrome (SJS) – a rare but life-threatening allergic reaction to medication or an infection. And Isabel had the worst form of SJS that doctors had ever seen. In fact, when Mom Edwina would touch her daughter, her skin would fall off. 1
It took three months of fighting for her life in the hospital, but even though Isabel lost the majority of her sight (SJS can break down the membranes around the eyes and cause them to become extremely dry) and needed to learn to walk, eat, and talk all over again- she’s now a healthy second grader who loves to ride her bike and run triathlons.

Real News with David Knight – EXPOSED: Secretive Vax Court
Wayne Rohde, author of “The Vaccine Court”, exposing the origins of the little known court that is the only recourse to those who have been harmed by vaccines. Wayne also explains what happened with the Somali population in Minnesota and why they refused vaccines.


Big Pharma Executive Blows Whistle on Vaccines: ‘Vaccinations are Deadly’ Pfizer Vice

President Dr. Peter Rost exposes dangers of Gardsil inoculation By: Jay Greenberg |@NeonNettle on 23rd September 2017
The former vice president of the world’s largest pharmaceutical company has blown the whistle to expose the true dangers of mandatory vaccinations. Dr. Peter Rost lifted the lid on vaccines and revealed that the Gardasil inoculation, in particular, is in fact, “deadly”. In a shocking exposé from one of the highest-ranking whistleblowers to date, Rost has also claimed that Big Pharma is purposely keeping the public unhealthy so they can make a fortune from continual treatments of illnesses rather than curing them. Dr. Rost made the revelations during an interview for the “One More Girl” documentary in which he candidly discussed how the main objective for vaccines and pharmaceutical drugs is to keep the public in a constant state of dis-ease. Rost also likened mandatory vaccinations to “child abuse” saying; “I would never vaccinate my children”



Vaccine News – Study – Gender-selective toxicity of thimerosal – Mar.2009
A recent report shows a correlation of the historical use of thimerosal in therapeutic immunizations with the subsequent development of autism; however, this association remains controversial. Autism occurs approximately four times more frequently in males compared to females; thus, studies of thimerosal toxicity should take into consideration gender-selective effects. The present study was originally undertaken to determine the maximum tolerated dose (MTD) of thimersosal in male and female CD1 mice. However, during the limited MTD studies, it became apparent that thimerosal has a differential MTD that depends on whether the mouse is male or female. At doses of 38.4-76.8mg/kg using 10% DMSO as diluent, seven of seven male mice compared to zero of seven female mice tested succumbed to thimerosal. Although the thimerosal levels used were very high, as we were originally only trying to determine MTD, it was completely unexpected to observe a difference of the MTD between male and female mice. Thus, our studies, although not directly addressing the controversy surrounding thimerosal and autism, and still preliminary due to small numbers of mice examined, provide, nevertheless, the first report of gender-selective toxicity of thimerosal and indicate that any future studies of thimerosal toxicity should take into consideration gender-specific differences. – 15.Mar.2010
Mercury (Hg) exposure from dental amalgam fillings and thimerosal in vaccines is not a major health hazard, but adverse health effects cannot be ruled out in a small and more susceptible part of the exposed population. Individual differences in toxicokinetics may explain susceptibility to mercury. Inbred, H-2-congenic A.SW and B10.S mice and their F1- and F2-hybrids were given HgCl2 with 2.0 mg Hg/L drinking water and traces of (203)Hg. Whole-body retention (WBR) was monitored until steady state after 5 weeks, when the organ Hg content was assessed. Despite similar Hg intake, A.SW males attained a 20-30% significantly higher WBR and 2- to 5-fold higher total renal Hg retention/concentration than A.SW females and B10.S mice. A selective renal Hg accumulation but of lower magnitude was seen also in B10.S males compared with females. Differences in WBR and organ Hg accumulation are therefore regulated by non-H-2 genes and gender. Lymph nodes lacked the strain- and gender-dependent Hg accumulation profile of kidney, liver and spleen. After 15 days without Hg A.SW mice showed a 4-fold higher WBR and liver Hg concentration, but 11-fold higher renal Hg concentration, showing the key role for the kidneys in explaining the slower Hg elimination in A.SW mice. The trait causing higher mercury accumulation was not dominantly inherited in the F1 hybrids. F2 mice showed a large inter-individual variation in Hg accumulation, showing that multiple genetic factors influence the Hg toxicokinetics in the mouse. The genetically heterogeneous human population may therefore show a large variation in mercury toxicokinetics.
US National Library of Medicine – National Institutes of Health – Feb.2015
Developmental Domain: ASD Diagnostic Criteria
Social Communication/Social Interaction
Deficits in social communication and social interaction are core factors in the diagnostic criteria of ASD. Impairments in social communication may present as abnormalities in eye contact, poor integration of verbal and nonverbal behaviors, and difficulties understanding the nonverbal communication of others (American Psychiatric Association, 2013). In some cases, persons with ASD may not participate in conversation or struggle with pragmatic language (American Psychiatric Association, 2013). Impairments in social interaction include difficulties with social-emotional reciprocity, failure to develop peer relationships, and reduced empathetic understanding and/or response (American Psychiatric Association, 2013).
There were 21 articles reviewed on social communication and social interaction in persons with ASD published between 1993 and 2013: 13 case-control studies, 7 cross-sectional studies, and 1 surveillance study. Nine studies were conducted in the United States and 12 studies were conducted at outside of the US. Of these 21 articles, 14 address social communication or other language abilities. In samples of children with varying cognitive abilities, some studies showed no significant differences in communication, conversational deficits, and language levels between males and females with ASD (Andersson et al., 2013; Dawson et al., 2007; Nicholas et al., 2008; Pilowsky et al., 1998; Park et al., 2012a, 2012b; Mayes and Calhoun, 2011; Mandy et al., 2012; Sipes et al., 2011; Solomon et al., 2012; Amr et al., 2011). One study found that males with ASD had greater expressive and receptive language skills than females with ASD (Carter et al., 2007) and another study found that females with ASD had more impaired social communication skills than males with ASD (Hartley and Sikora, 2009). Conversely, Park et al. (2012b) found that females with ASD had stronger non-verbal communication abilities than males with ASD. The majority of the literature reviewed on social communication found no difference between males and females with ASD, but there is some inconsistency.
The literature on sex differences in social interaction among persons with ASD (13 of 21 articles reviewed) is also inconsistent but generally suggests no significant sex differences in social interaction skills (Andersson et al., 2013; Dawson et al., 2007; Nicholas et al., 2008; Pilowsky et al., 1998; Mayes and Calhoun, 2011; Park et al. 2012b; Mandy et al., 2012; Sipes et al., 2011; Solomon et al., 2012). In population-level surveillance of eight-year olds, 80 % of children with ASD had poor social-emotional reciprocity with no significant difference between males and females (Nicholas et al., 2008). Szatmari et al. (2012) also found no sex differences in social-emotional reciprocity for children with varying cognitive abilities in a study from the Autism Genome Project. Oppositely, in an age and IQ matched case–control study, female adults with ASD were found to have fewer socio-communication difficulties during interpersonal interaction than male adults with ASD (Lai et al., 2013). Lastly, no sex differences have been noted in emotional reactiveness or being withdrawn (Hartley and Sikora, 2009) and in empathetic understanding and responses (Auyeung et al., 2009).
Cognitive functioning is likely to play a role in these social processes. Lower intellectual abilities are often linked with greater social impairment regardless of sex (Dawson et al., 2007). Among children with high functioning autism (IQ≥70), social skills have been found to be more impaired in female children than male children (Holtmann et al., 2007) and more severe as children aged (McLennan et al., 1993). In contrast, other studies found adult females with high functioning autism to have less socio-communication issues compared to males (Lai et al., 2011) or there were no sex differences in socio-communication skills in older children and adolescents (Holtmann et al., 2007; Kopp and Gillberg, 2011).
Overall, the 21 articles reviewed suggest no difference in social interaction between males and females with ASD and inconsistent differences in social communication between males and females with ASD, although both social interaction and social communication may be influenced by intellectual ability and age.
Restricted, Repetitive Patterns of Behavior, Interests, or Activities
There were 18 articles reviewed on restricted and repetitive patterns of behaviors and interests (RRBI) published between 1993 and 2013: nine cross-sectional studies, seven case–control studies, one cohort study, and one surveillance study. Eleven studies were conducted in the United States and seven studies were conducted in other countries. Based on this review, the literature suggests that males with ASD have more RRBI than females with ASD (Hattier et al., 2011; Carter et al., 2007). When assessing individual facets of RRBI, restricted interests are seen more often in males with ASD than females with ASD independent of cognitive ability (Kohane et al., 2012; May et al., 2012; Mandy et al., 2012; Szatmari et al., 2012). Males with ASD are also more likely to have more routines, rituals, and fascination with parts of objects than females with ASD (Nicholas et al., 2008; Park, et al., 2012b; Beuker et al., 2013). The literature on repetitive motor movements is less consistent: adult males with high functioning autism or Asperger’s syndrome had more repetitive motor movements than adult females with high functioning autism or Asperger’s syndrome in one case-control study (May et al., 2012), but there were no sex differences in repetitive motor movements among persons with autism in two other case-control studies (McLennan et al., 1993; Worley and Matson, 2011), one cross-sectional study (Auyeung et al., 2009), and one population-based cross-sectional study (Nicholas et al., 2008).
Age may influence the presentation of RRBI in males and females with ASD. One study found no sex difference among RRBI in toddlers (Sipes et al., 2011), whereas a different study found significantly more RRBI among adult males with ASD compared to females with ASD (Hattier et al., 2011). In summation, most studies reviewed suggested that males with ASD are likely to have more RRBI than females with ASD across levels of cognitive ability, although RRBI may be influenced by age.
Sensory issues are prevalent among persons with ASD (Nicholas et al., 2008) and are included as a RRBI in the DSM 5 (American Psychiatric Association, 2013). Common issues are oversensitivity to touch, sound, smell, taste, and attraction to certain tactile stimuli (American Psychiatric Association, 2013; Baranek et al., 2006; Rogers et al., 2003). Abnormal sensory reactions have been reported to occur in up to 47 % of persons with ASD, which is a rate ten times higher than reported in the general population (Nicholas et al., 2008). Additionally, there is a significant correlation between sensory issues in each of the individual senses (Kern et al., 2007); therefore, impairment is compounded for persons with ASD and sensory abnormalities.
Cross-sectional studies found no observed differences between males and females in sensitivity to sound (Mandy et al., 2012) or sensory sensitivity in general (Louisa et al., 2012; Mayes and Calhoun, 2011; Baranek et al., 2006). Mandy et al. (2012) examined RRBI in children and adolescents 3 to 18 years of age and found that age did not influence the presentation of RRBI. However, Lai et al. (2011) found that adult females with high functioning autism had more lifetime sensory issues than males with ASD. Overall, the majority of articles reviewed that addressed sensory issues in ASD do not suggest a sex difference, although aging may be a factor and should be further explored.
Developmental Domain: other Developmental Endophenotypes
Attention Deficit Hyperactivity Disorder
Attention deficit hyperactivity disorder (ADHD) and corresponding symptoms are common in children with ASD (Bradley and Isaacs, 2006; Nicholas et al., 2008). Previous studies show that 50 % to 83 % of children and teenagers with ASD had hyperactivity and attention problems (Nicholas et al., 2008; Bradley and Isaacs, 2006). There were seven articles that met search criteria and addressed ADHD. These seven articles were published between 2008 and 2012 with five cross-sectional studies and two cohort studies. Two studies were conducted in the United States and five were conducted in other countries.
A study of 7 to 12 year-olds with varying cognitive abilities found that males with ASD had higher levels of hyperactivity and impulsivity than females with ASD and this difference was more pronounced at younger ages (May et al., 2012). Males with high functioning autism from middle childhood to adolescence had higher levels of hyper-activity and inattention in teacher reports as compared to female peers, but there was no difference in parental reports (Mandy et al., 2012). A study of children and young adults aged 5 to 20 with high functioning autism found females had more attention problems (Bryson et al., 2008). A majority of studies found no difference in ADHD co-occurrence between males and females with ASD (Simonoff et al., 2008; Sinzig et al., 2009; Mayes and Calhoun, 2011; Horovitz et al., 2011). In summary, the current literature leans toward no sex differences in the co-occurrence of ADHD and ASD, but there is still inconsistency in the literature and thus, the sex difference is largely inconclusive
Challenging Behavior (Aggressiveness/Temper Tantrums/Oppositional Tendencies)
Challenging behavior is a common associated feature of ASD and includes aggression expressed toward other people, temper tantrums, and oppositional and defiant tendencies. Aggression expressed toward other people and temper tantrums are found in 50 % and 54 % of children with ASD compared to only 28 % and 23 % of children without ASD (Nicholas et al., 2008). The 12 articles in this review that met search criteria and addressed challenging behaviors were published between 2005 and 2012 and included six cross-sectional studies, four case–control studies, one clinical trial, and one surveillance study. Six studies were conducted in the United States and six were conducted in other countries. In general, there were no differences in aggression, temper tantrums, or anger between child sexes, regardless of age or cognitive ability (Kozlowski et al., 2012; Worley and Matson, 2011; Carter et al., 2007; Murphy et al., 2009; Mandy et al., 2012; Quek et al., 2012; Mayes and Calhoun, 2011; Horovitz et al., 2011). One study found that females with ASD had more “challenging behaviors” than males with ASD, although challenging behaviors were not explicitly defined (Dworzynski et al., 2012). Delinquent behavior (Park et al., 2012b) and oppositional defiance (Gadow et al., 2005) were more prevalent in males than in females with ASD in two studies reviewed.
Cognitive Skills and Intellectual Disability
In a review from 1966 to 2001, Fombonne (2003) found that the median prevalence of intellectual impairment in persons with ASD was 70 % in the studies evaluated. More recent population-based studies have found lower rates of ID in persons with ASD, with a range from 18 % to 55 % (Charman et al., 2011). The National Health Interview Study found 0.71 % of all children aged 3 to 17 from 1998 to 2007 had an ID (Boyle et al., 2011). Our review found 12 articles that met the search criteria and addressed ID or specific cognitive skills. These 12 articles were published between 1983 and 2011, and included seven cross-sectional studies, four case–control studies, and one-surveillance study. Four studies were conducted in the United States and eight were conducted in other countries.
The 12 articles reviewed support a relationship between child sex and co-occurring ID in children with ASD. The sex ratio between males and females without ID is greater than the sex ratio for all levels of cognitive ability combined (Nicholas et al., 2008; Hartley and Sikora, 2009). Consequently, the male to female ratio is lower when there is co-occurring ID compared to when there is no co-occurring ID (Hartley and Sikora, 2009; Nicholas et al., 2008; Yeargin-Allsopp et al., 2003). The ratio of males to females with ASD and co-occurring ID has been seen to range from 1.3:1 (Tsai and Beisler, 1983) to 2.8:1 (Bryson et al., 2008) with a trend toward fewer sex differences as ID becomes more severe (Yeargin-Allsopp et al., 2003). This differential sex difference in ID results in females with ASD, on average, having lower intelligence test scores than males with ASD (Banach et al., 2009; Volkmar et al., 1993).
Specific cognitive skills posited to vary between males and females with ASD include cognitive flexibility, response inhibition, working memory, and attention to detail (Geurts et al., 2004). Female adolescents with high functioning autism were seen to have superior information processing, multiple conceptual tracking, divided attention, and cognitive flexibility compared to male adolescents with high functioning autism (Bolte et al., 2011). In contrast, studies show males with ASD have superior attention to detail, visuo-spatial skills (Auyeung et al., 2009), and inhibitory control (Lemon et al., 2011) compared to females with ASD. There were no sex differences between adults with ASD in the “eyes test” which measures ability to infer mental states through the eyes (Lai et al., 2011). In summary, the 12 journal articles reviewed in this section suggest that females with ASD generally have lower intelligence test scores than males with ASD and that specific cognitive skills may vary by sex.
Developmental Regression
Parents of some children with ASD report a period of typical development followed by a loss in language, social, motor, self-help, imaginative play, or other skills. This developmental regression is usually reported to occur between 15 and 24 months of age (Meilleur and Fombonne, 2009). Our review found six articles that met search criteria and addressed developmental regression. These six articles were published between 2007 and 2013 and comprised two cohort studies, three cross-sectional studies, and one surveillance study. In a population-based surveillance study of children with ASD, 17 % of children had documented developmental regression and that percentage rose if the child had a previous ASD diagnosis (Wiggins et al., 2009). Males had significantly more regression than females and were more likely to regress at a younger age (Wiggins et al., 2009). This higher risk of regression in males was also seen in smaller, non-population based studies (n=4, 8, and 17 female children) (Bernabei et al., 2007; Ekinci et al., 2012; Zhang et al., 2012). In contrast, a cross-sectional study found that females aged 18 months to 15 years had significantly higher occurrence of regression as compared to males (30 % vs. 19 %) (Ben-Itzchak et al., 2013). No difference in the presence of developmental regression between males and females with ASD was observed in a small clinical sample of 20 females (Meilleur and Fombonne, 2009). In sum, the review of sex differences of developmental regression is contradictory and thus inconclusive.
Excess/Absence of Fear
Excess or absence of fear is more common in children with ASD than other children (Evans et al. 2005; Nicholas et al., 2008). In a population-based surveillance of eight-year olds, Nicholas et al. (2008) found that 32 % of children with ASD had atypical fear noted in service records compared to 6 % of children with ASD symptoms but no ASD diagnosis. Three articles met search criteria and addressed excess or absence of fear. All three of these articles were published in the United States between 1990 and 2011 and were two cross-sectional studies and one case–control study. In these studies, females with ASD had more specific phobias than males with ASD (Gadow and DeVincent, 2012; Matson and Love, 1990) and more unusual fears (Mayes et al., 2013). One study conducted by Matson and Love (1990) found more fear in typically developing female children compared to male children and no significant difference in fear between typically developing female children and female children with ASD. Given the sparse amount of research on this topic, further exploration is warranted to understand sex differences in fear among persons with ASD.
Safety Issues (Self-Injury/Elopement)
About 50 % of children with ASD engage in self-injurious behavior (Richards et al., 2012; Baghdadli et al., 2003; Duerden et al., 2012). Four studies met search criteria and three pertained to self-injurious behavior. All three of these studies were cross-sectional designs with two being conducted in Europe and one in the United States. No difference in self-injurious behavior was found between males and females with ASD (Richards et al., 2012; Baghdadli et al., 2003; Duerden et al., 2012).
Elopement, also known as wandering off, is a rising concern among parents of children with ASD. One online survey addressing elopement met our search criteria. This survey was conducted in the United States in 2013 and found that 49 % of parents reported that their child with an ASD wandered off at least once after the age of four years (Anderson et al., 2012). Results also found that sex did not influence the prevalence of elopement, although children with more intellectual impairment were more likely to elope (Anderson et al., 2012). Few conclusions can be drawn since there is little research on elopement and other safety issues in children with ASD and associated sex differences.
Psychiatric Domain
Anxiety/Mood Disorders
Symptoms of anxiety and mood disorders are more prevalent in children with ASD than in typically developing children (Worley and Matson, 2011; Nicholas et al., 2008). Among children who met a surveillance definition for an ASD, 55 % had abnormal mood or affect compared to 26 % of children with at least one symptom of an ASD but no ASD diagnosis (Schendel et al., 2009). The Special Needs Autism Project in the UK found 44 cases of emotional disorder per 100 children with ASD (Simonoff et al., 2008). Moreover, among eight-year-old children who met a surveillance definition for an ASD, 3 % had anxiety, 2 % had emotional disorder, 2 % had mood disorder, and less than 2 % had obsessive-compulsive disorder (OCD), depression, bipolar, or oppositional defiant disorder (Levy et al., 2010). Nine studies were found that met search criteria and addressed anxiety or mood disorders. These nine studies were published between 2005 and 2012 and included five cross-sectional studies and four case–control studies. Four of the studies were conducted in the United States and five were conducted in other countries.
The literature on sex differences in co-occurring anxiety or mood disorders and ASD is mixed and dependent on cognitive abilities. In some studies, females with high functioning autism were at greater risk for internalizing psychopathology than both male children with ASD and typically developing female children (Solomon et al., 2012; Mandy et al., 2012). These studies are supported by a Finnish report that found female children with ASD had lower scores on a test associated with major depressive disorder compared to male children with ASD (Mattila et al., 2010). Other studies found no sex differences in the of co-occurrence of anxiety or depression in children with ASD and varying cognitive abilities (Quek et al., 2012; Gadow et al., 2005; Park et al., 2012b; Simonoff et al., 2008; Mayes and Calhoun, 2011; Lai et al., 2011). In the general population, females have more panic attacks, generalized anxiety disorders and males have more social anxiety (American Psychiatric Association, 2013). Based on this review, the current literature is inconclusive on whether a sex difference in children with ASD and co-occurring anxiety or mood disorders exists, although a few studies suggest more anxiety and mood disorders in females than males with ASD.
Schizophrenia is a mental disorder that involves delusions, disorganized behavior, disorganized speech, hallucinations, and restrictions in the range and intensity of emotions (American Psychiatric Association, 2013). Schizophrenia typically presents between 18 and 30 years of age with earlier onset associated with male sex. Lifetime prevalence of schizophrenia is near 0.2 % (American Psychiatric Association, 2013) The prevalence of schizophrenia in eight-year olds with ASD is less than 1 % (Levy et al., 2010). Two articles met search criteria and addressed schizophrenia. These two articles were published in 2005 and 2010 and were both case–control studies. Review of the two studies found conflicting results on sex differences and the co-occurrence of ASD and schizophrenia or schizophrenia spectrum traits. A parental survey of 6 to 12 year olds with ASD found schizophrenia spectrum traits to be twice as prevalent in females compared to males (57 %: 28 %) independent of ID (Gadow and DeVincent, 2012). Conversely, in a group of 6 to 12 year olds with ASD and ID, schizophrenia was more common in males than females (Tsakanikos et al., 2011). Again, the literature is relatively sparse due to the late onset of schizophrenia and the rarity of co-occurring schizophrenia: future research is warranted.
Medical Domain
Birth defects/Chromosomal Disorders /Genetic Disorders
Population-based surveillance data from the 2008 ADDM report found that among children with ASD, less than 1 % had a co-occurrence of fragile X syndrome, Down syndrome, chromosomal disorders, or other genetic and congenital diagnoses (Levy et al., 2010). It is likely that these rates are under-reported because investigation of ASD co-occurring conditions was not the focus of the ADDM surveillance effort. However, a cohort study of children in Georgia found a similar prevalence of chromosomal disorders and Down syndrome in persons with ASD (Schendel et al., 2009).
There were four studies reviewed that met search criteria and addressed ASD sex differences in birth defects, chromosomal disorders, and genetic disorders: two systematic reviews, one case–control study, and one surveillance study. Co-occurring birth defects, such as impairments to the central nervous system, cardiovascular system, genitourinary system, or musculoskeletal system, appear more often in males than females with ASD. Among children with ASD, the male to female ratio was 9:1 if a child had a co-occurring birth defect and 3.6:1 if the child did not have a co-occurring birth defect (Schendel et al., 2009).
A review conducted by Reilly (2009) found that males with ASD have more co-occurring Down syndrome than females with ASD and the male to female ratio among children with both ASD and Down syndrome may be near the overall ASD prevalence ratio of 4:1. A review conducted by Wiznitzer (2004) found no difference between males and females with ASD and the co-occurrence of tuberous sclerosis. Clifford et al. (2007) found that about 70 % of males aged 5 to 80 with fragile X syndrome had co-occurring ASD while 23 % of females in the same age range with fragile X had co-occurring ASD. The difference in co-occurrence of ASD between males and females may suggest a greater association between the two conditions in males as compared to females.
It is important to note that birth defects, chromosomal disorders, and genetic disorders are rare and seldom studied. Therefore, the results on sex differences for co-occurring ASD and chromosomal and genetic conditions are inconclusive.
Head Size / Encephalopathy
Head size, specifically an enlarged head circumference or macrocephaly, has been associated with ASD (Wallace and Treffert, 2004). Three articles were reviewed that examined differences in head size between males and females with ASD. Studies include two case–control studies and one cross-sectional study. Two studies were conducted in the US and one study was conducted in Italy. A cross-sectional study by Fombonne et al. (1999) found no difference in head size between males and females aged 2 to 16 with ASD. Sacco et al. (2007) also found no difference in head size between males and females aged 3 to 16 with ASD. In contrast, Aylward et al. (2002) found larger head sizes in male adults and children compared to female adults and children with ASD, but the female sample size was low (n=9).
Abnormal Eating and Gastrointestinal Issues
In a population-based study conducted by Nicholas et al. (2008), about 54 % of children with ASD had an abnormality in eating, drinking, or sleeping, which is nearly 40 % higher than that of children with at least one symptom of ASD but no diagnosis (Nicholas et al., 2008). Some studies have shown an increase in certain gastrointestinal symptoms among persons with ASD, including constipation (Ibrahim et al., 2009) and diarrhea (Wang et al., 2006), while other studies found no significant increase in overall gastrointestinal symptoms or symptoms such as esophageal reflux, vomiting, and abdominal discomfort (Ibrahim et al., 2009; Wang et al., 2006; Valicenti-McDermott et al., 2007). However, little research on gastrointestinal issues has been conducted at a population level and no studies were found that compared males to females on gastrointestinal response. More research is needed to determine if there is an association between gastrointestinal symptoms and ASD and whether the association differs between the sexes.
Four studies were found that compared the sexes and addressed food selectivity. These four studies were conducted in the United States between 2006 and 2010 and included one case–control and three cross-sectional designs. In general, review of these studies found food selectivity and feeding issues to be more frequent in children with ASD than children without ASD (Valicenti-McDermott et al., 2007; Ibrahim et al., 2009), although limited research is available in this area. There was no difference between child sexes in over or under-eating in a study of children with high functioning autism (Worley and Matson, 2011) and no differences between the sexes in eating abnormalities in two studies conducted in children with ASD and varying cognitive abilities (Mayes and Calhoun, 2011; Horovitz et al., 2011). Based on this limited review, it appears unlikely that there is a difference in eating habits between males and females with ASD.
Seizures/ Epilepsy
Epilepsy and other seizure disorders co-occur in 5 % to 40 % of children with ASD and there is differential prevalence based on ID (Baird et al., 2008; Nicholas et al., 2008). This review found three articles that met search criteria and addressed seizures or epilepsy. These three articles were published between 2008 and 2013 and consist of a cohort study, one cross-sectional study, and one meta-analysis. Females with ASD were found to have more epilepsy than males with ASD; the male to female ratio drops to near 2:1 in children with ASD and co-occurring epilepsy, but this may be partly due to differential ID (Amiet et al., 2008; Bolton et al., 2011; Ben-Itzchak et al., 2013). There may be an increased likeliness in females with ASD to have co-occurring epilepsy or seizure disorder; however, the literature is sparse so a conclusion cannot be drawn. Further research is needed to enhance current knowledge of sex differences in children with ASD and epilepsy or seizure disorder.
Sleep Disturbances
In a systematic review of parental sleep surveys, sleep problems were present in 50 % to 80 % of children with ASD compared to 9 % to 50 % in matched typically developing children (Kotagal and Broomall, 2012). There were six articles reviewed that met search criteria and addressed sleep disturbances. These six articles were published between 2004 and 2012 and included two case–control studies, two cohort studies, and two cross-sectional studies. Four were conducted in the United States and three were conducted in other countries. Based on this review, some studies found no sex differences in sleep problems among persons with ASD (Liu et al., 2006; Wiggs and Stores, 2004; Mayes and Calhoun, 2011; Horovitz et al., 2011), one study found that female children with ASD have less sleep problems than male children with ASD (Sivertsen et al., 2012), and one study found female children with ASD have more sleep problems than male children with ASD (Hartley and Sikora, 2009). The minimal amount of research in this area leads to inconsistent results and prevents definitive conclusions on whether a sex difference exists in sleep disturbance.

Vaccine News – Adverse events following Haemophilus influenzae type b vaccines in the Vaccine Adverse Event Reporting System, 1990-2013

An interview with Robert Kennedy Jr. on vaccines
By Helen Branswell
In the early days of 2017, proponents of vaccination were deeply concerned. Donald Trump, who has long espoused a debunked link between vaccines and autism, was set to enter the White House. He met with environmental activist Robert Kennedy Jr., who has for years argued that vaccines can cause a range of developmental and other health conditions. Kennedy emerged to report he’d been asked to chair a commission into vaccine safety.
But seven months later, no such commission has been appointed and the crisis-mired White House has declined to say whether the plan has been shelved.
STAT contacted Kennedy to see where plans stood. He would only speak on condition that STAT publish the interview in a Q&A format. He argued that his assertions — which are disputed as a misreading of the scientific literature by many mainstream scientists — have been misquoted and misrepresented in the media.
Here is STAT’s conversation with Kennedy. It has been lightly edited, for length and readability.
The question I want to ask you relates to the vaccine safety commission that you had announced in January that you were going to head, after you met with then President-elect Trump. It’s been a number of months now, and there hasn’t been any further public announcement. And so we’ve been wondering: Where does this stand?
I’ve had no discussions specifically about the vaccine safety commission, probably since February. I’ve spoken to the White House about other issues of vaccine safety and had a number of follow-up meetings.

Study – The putative role of environmental aluminium in the development of chronic neuropathology in adults and children. How strong is the evidence and what could be the mechanisms involved?
The conceptualisation of autistic spectrum disorder and Alzheimer’s disease has undergone something of a paradigm shift in recent years and rather than being viewed as single illnesses with a unitary pathogenesis and pathophysiology they are increasingly considered to be heterogeneous syndromes with a complex multifactorial aetiopathogenesis, involving a highly complex and diverse combination of genetic, epigenetic and environmental factors. One such environmental factor implicated as a potential cause in both syndromes is aluminium, as an element or as part of a salt, received, for example, in oral form or as an adjuvant. Such administration has the potential to induce pathology via several routes such as provoking dysfunction and/or activation of glial cells which play an indispensable role in the regulation of central nervous system homeostasis and neurodevelopment. Other routes include the generation of oxidative stress, depletion of reduced glutathione, direct and indirect reductions in mitochondrial performance and integrity, and increasing the production of proinflammatory cytokines in both the brain and peripherally. The mechanisms whereby environmental aluminium could contribute to the development of the highly specific pattern of neuropathology seen in Alzheimer’s disease are described. Also detailed are several mechanisms whereby significant quantities of aluminium introduced via immunisation could produce chronic neuropathology in genetically susceptible children. Accordingly, it is recommended that the use of aluminium salts in immunisations should be discontinued and that adults should take steps to minimise their exposure to environmental aluminium.

Australia Bans Truth-Telling Mother From Country For Three Years…And It Backfired
The date was August 8th and the Vaxxed team had just wrapped up a two-week tour of Australia, where the communities of parents received their info with great interest. It was time for the team, consisting of a medical doctor, a scientist, a videographer, and a mother of a vaccine-injured son to pass through Australia’s Department of Immigration within the airport on the way to their flight to New Zealand. Three passed through unhassled, one didn’t. Vaxxed team member Polly Tommey describes what happened to her:
“I get taken to one side and that’s when two immigration police take me into a room and tell me that I’ve been detained and ask for my phone…and then they told me that I was in violation of my Visa and they took my phone and went right through everything in my phone. They typed in ‘Australia’ they went through every contact and every email that there had been with myself and the team. They took my phone away and photographed everything.”
In an instant Tommey was a persecuted individual who moments later would find out she was officially banned from Australia for three years. Next, it came time for airport security immigration officers to address one of the reasons Tommey was being harassed:
“Then they asked me about Vaxxed. Did I have a copy of it? Endless questions about Vaxxed being a very dangerous film with lies…I’m a mother recording stories from parents. And parents come to me to tell their stories. I didn’t seek them out, they come to me. And that is more of a threat than anything else?”
How did we get to the point where a mother can be banned from a western country for simply offering a voice to families?

The Wild Doc – What Officials Can Do To End Unnecessary Drug Overdoses/ Vaccine Awareness Month Brings New Confirmation That Vaccines Are Causing SIDS.

Relevant to the back-end profits (and back-end injuries) industry is generating from the autism epidemic. Abilify is in the class of second generation antipsychotics frequently pushed on individuals with autism by mainstream doctors as part of the $5 billion (and rising) “autism drug” market.

Dr.Russell Blaylock Exposes The Gardasil, HPV Vaccine Fraud
A shocking interview by Mike Adams (The health ranger) with Dr. Russell Blaylock who exposes to total criminal fraud of HPV vaccines and the vaccine industry.

Hear Why He Calls The HPV Vaccine a Crime Against Kids!
The HPV vaccine continues to be a hotly debated issue. Robert Scott Bell, popular radio host and homeopathic practitioner, discusses the theory behind the HPV vaccine and whether or not he thinks it’s safe.

The Health Ranger – Gardasil HPV Vaccine Hoax Exposed
This video exposes the truth about Gardasil and HPV vaccinations: They don’t work and may actually be dangerous to women. The FDA knew HPV did not cause cervical cancer in 2003.

HPV Gardasil Vaccine Proves Lethal – 236 Girls have now Died
236 Girls have now died in America –
Irish Times 8.1.2012-Schoolgirl vaccine uptake of 82% beats target figures
236 girls have now died in America and the rest of the World, But the Irish Times keeps this quite, Irish Dr Kevin Kelleher, assistant national director of health protection at the HSE, welcomed the high uptake on Gardisil Vaccinations, he fails to give the facts also, says its excellent!
The 82 per cent uptake was “excellent” and was equal to or greater than those achieved in the first year of programmes in other countries such as the United Kingdom and Australia. He said the figures were great credit to the vaccination teams.

MMR gave our boy organ failure and then loss of legs #vaxxed #truth #science #Praybig

Why My Wife and I Decided Not To Vaccinate Our Daughter
Author: Jason Christoff
When my wife was pregnant we knew the vaccine issue was coming our way and we put it off as long as possible. As the day fast approached, I started to investigate and compile some information for my wife because she trusted that I would make sure she understood what the main issues were regarding vaccination. We had heard vaccinations were potentially dangerous but we didn’t know if that applied to all children or just some. We weren’t aware if vaccination was beneficial for some babies and maybe not for others. We were new to being parents and we didn’t want to make any mistakes. We certainly didn’t want our baby getting sick if we could do something about it proactively. We wanted our baby to have the most comfortable journey through life possible and if that meant giving our new born vaccines, so she could avoid disease now and in the future, then that’s what we were going to do. After researching for a couple of days, we were more than shocked at what we were uncovering.

Study – Neurological and autoimmune disorders after vaccination against pandemic influenza A (H1N1) with a monovalent adjuvanted vaccine: population based cohort study in Stockholm, Sweden.
Excess risks among vaccinated compared with unvaccinated people were of low magnitude for Bell’s palsy (hazard ratio 1.25, 95% confidence interval 1.06 to 1.48) and paraesthesia (1.11, 1.00 to 1.23) after adjustment for age, sex, socioeconomic status, and healthcare utilisation. Risks for Guillain-Barré syndrome, multiple sclerosis, type 1 diabetes, and rheumatoid arthritis remained unchanged. The risks of paraesthesia and inflammatory bowel disease among those vaccinated in the early phase (within 45 days from 1 October 2009) of the vaccination campaign were significantly increased; the risk being increased within the first six weeks after vaccination. Those vaccinated in the early phase were at a slightly reduced risk of death than those who were unvaccinated (0.94, 0.91 to 0.98), whereas those vaccinated in the late phase had an overall reduced mortality (0.68, 0.64 to 0.71). These associations could be real or explained, partly or entirely, by residual confounding.
Results for the safety of Pandemrix over 8-10 months of follow-up were reassuring -notably, no change in the risk for Guillain-Barré syndrome, multiple sclerosis, type 1 diabetes, or rheumatoid arthritis. Relative risks were significantly increased for Bell’s palsy, paraesthesia, and inflammatory bowel disease after vaccination, predominantly in the early phase of the vaccination campaign. Small numbers of children and adolescents with narcolepsy precluded any meaningful conclusions.

Injecting Aluminum Official Trailer
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In the early 90s, a mysterious muscular disease with symptoms that included severe muscle and joint pain began to surface among multiple patients in France. In 1993, a team of doctors in Paris discovered that these patients had developed a new disease called Macrophagic Myofascitis, or MMF, which occurs when the aluminum hydroxide adjuvant from a vaccine remains embedded in the muscle tissue and causes an immune reaction. Featuring interviews with patients, doctors, scientists, and influential politicians, Injecting Aluminum calls in to question the public health policies around aluminum in vaccines and examines aluminum’s devastating effects on the human body.

In vielen Ländern Europas dürfen Eltern schon jetzt nicht mehr frei entscheiden, ob, wann und wogegen ihre Kinder geimpft werden. Auch in Deutschland werden die Daumenschrauben angezogen, aktuell wird diskutiert, man solle Eltern, die ihre Kinder nicht impfen, das Kindergeld entziehen!
Da Impfungen schwere Nebenwirkungen haben können, darf kein Staat und keine Institution Eltern vorschreiben dürfen, welche Pharma-Produkte ihren Kindern einverleibt werden!
Um den drohenden Impf-Zwang zu verhindern, rufen wir zur Teilnahme auf und bitten um Unterstützung:
Demonstration am 16.9.2017 in Berlin

Vaccination must be voluntary!
In many countries of Europe, parents are no longer allowed to decide whether, when and what their children are vaccinated. In Germany, too, the squeeze are being drawn up, and it is currently being discussed that parents who do not vaccinate their children should withdraw child benefit.
Since vaccination can have serious side effects, no state and no institution must be allowed to require parents to have the pharmaceutical products incorporated into their children.
In order to prevent the threat of vaccination, we call to participate and ask for support:
Demonstration on 16.9.2017 in Berlin
For a free future of healthy people!

Movie Vaxxed gets up QUEENSLAND Health Minister’s nose
By Brent Melville
QUEENSLAND Health Minister Cameron Dick was either seriously misinformed, ignorant, or flat out lying when, in response to the touring movie Vaxxed: From Coverup to Catastrophe, he said “there is no shred of credible scientific evidence to support claims that vaccinations are dangerous” (Gold Coast Bulletin, 15/7/17).
The same with Victorian Health Minister Jill Hennessy who stated on Seven News in February last year: “There are no risks in vaccinating your children – the science is really clear”.
Dr Hooker, who joined the Vaxxed tour, says there are in fact more than 100 studies on PubMed on autism, neurological developmental disorders (NDDs) and vaccination. But here’s a few specific studies our blind, deaf and dumb health ministers and their advisers refuse to look at.
1. Neurological and autoimmune disorders after vaccination against pandemic influenza A (H1N1) with a monovalent adjuvanted vaccine: population based cohort study in Stockholm, Sweden. Conclusion in part: “… Relative risks were significantly increased for Bell’s palsy, paraesthesia, and inflammatory bowel disease after vaccination, predominantly in the early phase of the vaccination campaign…”.
2. Autoimmune disorders (AIDs) after immunisation with Influenza A/H1N1 vaccines with and without adjuvant: EudraVigilance data and literature review. From abstract: “Of the 50,221 adverse reactions received in EudraVigilance for A/H1N1 vaccines (adjuvanted: 46,173, non-adjuvanted: 4048), 314 were AID (adjuvanted: 276, non-adjuvanted: 38). GBS was the AID with the highest number of reports (125, adjuvanted: 109, non-adjuvanted: 16).
3. Serious adverse events rarely reported after trivalent inactivated influenza vaccine (TIV) in children 6-23 months of age. From results: “During 1991-2001, VAERS received 128,717 reports…A total of 14.2% of all reports described serious adverse events, which by regulatory definition include death, life-threatening illness, hospitalization or prolongation of hospitalization, or permanent disability.”
4. “Adverse events following Haemophilus influenzae type b vaccines in the Vaccine Adverse Event Reporting System, 1990-2013.” Study results found: “VAERS received 29,747 reports after Hib vaccines; 5179 (17%) were serious, including 896 reports of deaths. Median age was 6 months (range 0-1022 months). Sudden infant death syndrome was the stated cause of death in 384 (51%) of 749 death reports with autopsy/death certificate records. The most common non-death serious AE categories were neurologic (80; 37%), other noninfectious (46; 22%) (comprising mainly constitutional signs and symptoms); and gastrointestinal (39; 18%) conditions.”

Study: Vaccine Induced Inflammation Cause of Obesity Epidemic – Not Diet
Childhood obesity is now a reason why the state could take away children from their parents. The rationale is that if a child is obese, it is the parents’ fault, because they failed to feed them properly. It is assumed that all childhood obesity is a result of diet.
However, most of us have probably seen first-hand just how different children are when it comes to food and putting on weight. Some children can eat junk food most of the time and never add weight, while some children can eat a healthy, organic diet and still add pounds.
Dr. J. Bart Classen has published a study claiming that the evidence for the overwhelming problem of childhood obesity is not diet, but “vaccine induced inflammation.”

Vaccines, not Diet, are Causing Epidemic of Obesity and Type 2 Diabetes According to New Paper from Classen Immunotherapies
MANCHESTER, Md., June 26, 2017 /PRNewswire/ — A newly published paper in June’s Journal of Endocrinology, Diabetes & Obesity, 5(3): 1107, by immunologist J. Bart Classen, MD of Classen Immunotherapies provides further proof of the dangers of vaccines. The paper reviews the growing evidence that many cases of obesity, type 2 diabetes and metabolic syndrome are inflammatory conditions and that vaccine induced inflammation is the cause of the epidemic of these diseases. Upon receiving a vaccine some individuals’ immune system becomes hyper active leading to autoimmune destruction of insulin secreting cells and the development of type 1 diabetes. Many other individuals produce increased cortisol and other immune suppressing molecules, to suppress the vaccine induced inflammation. This increased production leads to type 2 diabetes, obesity and metabolic syndrome. The new paper reviews evidence supporting vaccines, not diet, as a cause of the epidemics of obesity, type 2 diabetes and metabolic syndrome.

Study – Cause of the Obesity, Type 2 Diabetes and Metabolic Syndrome Epidemics, Vaccine Induced Immune Overload versus Nutrition Overload
There is an epidemic of obesity, type 2 diabetes, metabolic syndrome and associated conditions. Patients with these conditions often have markers of
increased inflammation. Many researchers have published that nutrition overload caused the epidemic of obesity and the associated inflammation which
leads to type 2 diabetes and metabolic syndrome. A contrasting view has provided extensive evidence that vaccine induced immune overload has caused an
epidemic of inflammation and this inflammation caused epidemics of obesity, type 2 diabetes and metabolic syndrome. The data reviewed in these manuscripts
provides proof that immune overload, not nutrition overload has been the major contributing factor for the epidemics and inflammation associated with the
epidemics. Several lines of evidence are reviewed including evidence that inflammation precedes obesity in many patients, the lack of inflammation in many
obese patients, an epidemic of inflammation in thin patients, and an epidemic of obesity in children under 6 months of age. The failure to control the obesity
epidemic is blamed on the focus on nutrition and ignoring the root cause, vaccine induced immune overload. Once a patient has developed metabolic syndrome
with type 2 diabetes providers are too frequently subjecting their patients to further immune overload by administering yearly influenza vaccines and many
other vaccines. This action makes metabolic syndrome more difficult to reverse. The plan to reduce obesity must be focused on preventing immune overload
and not blaming patients for their diet. The epidemic of obesity can be reversed through discontinuation of vaccine practices that result in immune overload.


Vaccine News – “It took me 7 years to teach him how to chew”

Big Pharma is the biggest, baddest, most dangerous drug dealer in the world.

Study – Clinical clues for autoimmunity and neuroinflammation in patients with autistic regression.
The charts of 206 children with ASD and 33 diagnosed with autistic regression variant were reviewed. The incidence of febrile illness in the 6 months prior to initial parental concern was significantly higher in the children with autistic regression compared with those with ASD (30% vs 0%; p<0.001). The overall prevalence of familial autoimmunity was also higher in children with autistic regression compared with those with ASD (33% vs 12%; p<0.001). Type 1 diabetes and autoimmune thyroiditis were both more common in families with children with autistic regression. Other non-immune risk factors did not differ between the two groups.
Our findings suggest that predisposition to autoimmunity, and immune/inflammatory activation, may be associated with autistic regression.

The Vaccine Science Contradiction
The modern human race has been thriving and evolving for at least the last 200,000 years according to Anthropologists. Vaccines have only been around for less than 200 years. So how did humans survive for the 199,800 years before that. The answer is that you are born with a fully functioning immune system, capable of self-immunization. Vaccines are not required for immunization. Your body does it automatically. Just like 10,000 generations of your ancestors who also survived without vaccines. If your immune system didn’t work automatically to keep you alive then you would have never been born.

The Amazing Dr. Franz from Orlando.
#gooddoctor #pediatrician #vaxxed #praybig

Episode 7 of The Truth About Vaccines is NOW PLAYING. Tonight’s episode is all about Vaccine alternatives and Freedom of Choice. Super important for you to see.

Aluminium Adjuvants Have Never Been Approved For Use In Vaccination
In a press release, describing Professor Exley’s latest paper, the founder of the Dwoskin Family Foundation, Mrs. Claire Dwoskin wrote:
“Research at Keele University led by Professor Christopher Exley aims to understand the toxicity of aluminum adjuvants in vaccinations and their latest findings are now published in Nature’s ‘Scientific Reports.
In a project funded by the Medical Research Council (MRC) and the Dwoskin Foundation the group at Keele investigated the relationship between the physicochemical properties of aluminum adjuvants and the immune response. Specifically, they show that the reaction of the aluminum adjuvant at the injection site will determine its subsequent fate and therefore its activity both at the injection site and away from the injection site.
One form of aluminum adjuvant which is most commonly used in vaccines is an aluminum hydroxyphosphate salt and is more toxic at the injection site than the second form of aluminum adjuvant, also commonly used in vaccines, aluminum oxyhydroxide salt. However, the latter is more easily loaded into immune reactive cells with the possibility to be transported throughout the body. It is suggested by the Keele research that this loading of aluminum into viable cells offers a mechanism whereby significant amounts of aluminum, a known neurotoxin, might be translocated throughout the body and even across the blood brain barrier and into the central nervous system.” [2, 3, 4]
Countless Childhood Vaccinations Contain Aluminum

Shingles Vaccine Zostavax Is Causing What It’s Designed To Prevent
April 19, 2017
By now I think most people have seen the commercials on television telling us that if we’ve ever had the chicken pox at any point in our lives, then the shingles virus is already inside of us. As it stands right now, there is a vaccine for shingles called Zostavax, but what we’re finding out now about this vaccine makes it seem like it might be pretty dangerous or at least cause some side effects that are actually the same as what we’d see from shingles. Ring of Fire’s Farron Cousins talks with Attorney Troy Bouk about the dangers associated with Zostavax

Dying 13 Year Old Diagnoses Her Own HPV Vaccine Injury that Stumped Doctors
April 20, 2017
Health Impact News Editor Comments
One of the true tragedies in modern medicine is the refusal to consider vaccine injuries when diagnosing or treating disease. The U.S. government acknowledges that people die and are injured by vaccines, as is evidenced from the Department of Justice’s quarterly reports on settlements in vaccine court:
However, medical students are given no training in recognizing or treating vaccine injuries, and no studies are ever conducted to find out why some children suffer from vaccines while others do not.
In this story out of the U.K., a 13 year old girl accomplishes something her doctors could not do, and that was diagnose her own life-threatening disease by researching all of the possibilities, without excluding vaccine injuries, something that apparently handicapped her doctors. She discovered that she suffered from an autoimmune disease after receiving the HPV vaccine.

Professor Hamamoto talks about the persecution he faces at UC Davis after speaking the truth to his students. #Vaxxed #DarrylHamamoto #SenatorPan #SB277 #OperationPaperClip
Camera, editing and sound by Joshua Coleman.

It took me 7 years to teach him how to chew
Nancy Kirkman’s son was severely injured by vaccines at 3 months of age. The family has been subjected to immense heartache and cruelty.
Interview recorded on February 2, 2017 in San Diego, California.

#VaxxedNation #VaxxedNationTour #RFKcommission #Truth #Science #Vaxxed #Tears #VaxxedTears

Baby’s Health Rapidly Declines After Receiving 13 Vaccines at One Time – Mom Accused of Abuse for Disagreeing with Doctors
April 20, 2017
Durenda and her son KJ on his 1st birthday, before he had 8 shots in one day.
by Health Impact News/ Staff
A young Georgia mother had no idea that a routine trip to the pediatrician’s office for her son’s 1 year check-up would change her son’s life forever, and leave her fighting the state for custody of her own son. When the nurse-practitioner told her that her son was a little behind on his shots and they would need to catch up, Durenda Whitehead didn’t question the need for the vaccines. She did, however, question the safety of giving 13 vaccines at once.
Durenda’s pediatrician assured her that it was fine:
I can give up to 20 at one time.
Durenda was unaware of a research study published in the summer 2016 edition of the Journal of American Physicians and Surgeons by Neil Z. Miller entitled, “Combining Childhood Vaccines at One Visit Is Not Safe.” In a press release, Miller wrote:
Our study showed that infants who receive several vaccines concurrently…are significantly more likely to be hospitalized or die when compared with infants who receive fewer vaccines simultaneously.
Baby’s Health Declines After 13 Vaccines in One Day
During his first year of life, little KJ had a few bouts with respiratory illness, but on January 16, 2017, he was healthy, happy, and active.

Study – Combining Childhood Vaccines at One Visit Is Not Safe
Neil Z. Miller

#VaXism NEWS
#Texas Well done Texans For Vaccine Choice!!
Thank you freedom Reps!
Zedler let TIP have it!!

Skip that Newborn Vitamin K Shot
How much synthetic vitamin K is in the shot? Shockingly, the national standard mandated by most states for US hospitals to administer is over 100 times the infant’s RDA of this nutrient. Since studies have linked large doses of vitamin K with childhood cancers and leukemia, this large dose of synthetic K administered within minutes of birth seems questionable at best.
The fact is that medical science still does not know that much about the metabolic fate of vitamin K. Little to no unmetabolized vitamin K shows up in urine or bile. This is disturbing given the fact that vitamin K is a fat soluble vitamin and therefore has the potential to accumulate in body tissues. More disturbing is that the liver of a newborn does not begin to function until 3 or 4 days after birth. As a result, this little being has very limited to no ability to detoxify the large dose of synthetic vitamin K and all other the dangerous ingredients in the injection cocktail including:

– Phenol (carbolic acid – a poisonous substance derived from coal tar)
– Benzyl alcohol (preservative)
– Propylene glycol (better known as “edible” antifreeze)
– Acetic acid (astringent, antimicrobial agent)
– Hydrochloric acid
– Lecithin
– Castor oil

The manufacturer’s insert included with the shot includes the following warning:
Severe reactions, including fatalities, have occurred during and immediately after intravenous injection of phytonadione [synthetic Vitamin K] even when precautions have been taken to dilute the vitamin and avoid rapid infusion ….
The manufacturer’s insert is no exaggeration of the risks. On October 17, 2013, a case of anaphylactic shock in a newborn from the synthetic vitamin K shot was reported making the possibility of death from this shot a a very real side effect
Anaphylactic shock due to vitamin K in a newborn and review of literature
Newborn infants are born with an immature innate immunity. They are less likely to develop anaphylaxis since their immune system is weaker than older infants and children. There are only a few reports of side effects after vitamin K injection in neonates although prophylaxis against hemorrhagic disease of the newborn with this drug has been in routine practice in all over the world for many years. We herein report a case of anaphylactic shock developing after the intramuscular administration of vitamin K1 in a newborn. To our knowledge, this patient is the first case of neonatal anaphylactic shock developing due to intramuscular administration of vitamin K1. We suggest the clinicians should be aware of this possibility of potentially fatal adverse effect occurring with intramuscular administration of vitamin K1.
Does this make any sense to you? It makes absolutely no sense to me. How could anyone say that this shot is safe and effective for newborns?

Is There Vaccine Cause-And-Correlation Regarding The Dramatic Rise In Children’s Chronic Diseases?
Posted on April 18, 2017
Since the introduction of CDC’s hyper-vaccine schedule, which saw children’s vaccines schedules increase from 10 to 69 vaccines after the 1986  National Childhood Vaccine Injury Act was passed into law, very young children are contracting chronic “old age type” diseases early in life—an anomaly heretofore not experienced demographically.
First off, obesity rates (2013-2014) for U.S. children between the ages of 6 and 11 years was 17.4% [1]  Three leading causes of death in children between 1 and 4 years of age were congenital malformations, deformations and chromosomal abnormalities. [1]   Mandatory pregnancy vaccines have impact upon growing fetuses.  For children 5 to 14 years of age, it’s cancer! [1]   However, according to Contemporary Pediatrics [2] 2014 published data, cancer was the second leading cause of death for children between 1 and 9 years of age (11.8% of deaths).  For infants, the third leading cause of death was sudden infant death syndrome (SIDS, 8.4%)—something that seemingly appeared in pediatric medicine context concomitantly with the increase in mandated vaccines, specifically with multi-valent vaccines, i.e., numerous vaccines given at one time.  However, the CDC’s information about SIDS claims vaccines do not cause SIDS.  Try telling that to many parents.
According to Focus for Health, 27% of U.S. children live with chronic diseases! [3]   That website asks the question, “Why are today’s children sicker than ever before?”  The answer: “While genes may play a role in obesity, asthma and ADHD, environmental and social changes are behind the surge, researchers said.”5 [Children Sicker Now Than in Past, Harvard Report Says] [4]   That Harvard Report found a fourfold increase in childhood obesity; twice the asthma rate since the 1980s; and regarding diabetes: White children’s rate was 26.1 per 100,000; black children, 25.4 per 100,000; American Indian youth, 25 per 100,000 including the highest rate of type-2 diabetes. [4] According to the CDC, one in six children in the USA has a developmental disability, which represents a 17% rise between 1997 and 2008. [7]
Furthermore, are you aware the cost of fully vaccinating a child has increased by 2,700% during the last decade?  Vaccines are extremely profitable for manufacturers, but very costly in terms of adverse health effects, medical bills for parents, and social issues (day care, school, jobs, welfare benefits, etc.) for infants, toddlers, teens and adults.

The Dangers Of Vaccines and Vaccination
Vaccines Are Unavoidably Unsafe
According to the US Food and Drug Administration, safety assessments for vaccines have not often included toxicity studies because vaccines have not been viewed as inherently toxic. Yet vaccines are legally defined as unavoidably unsafe.
It is not just childhood vaccines that come with substantial risk. Influenza vaccines, vaccines for sexually transmitted diseases, and others contain similar risks for adverse events. Also troubling is that vaccination is recommended now for pregnant women, even though vaccine package inserts clearly state they have not been tested on pregnant women, so the effects on the fetus can’t be known.
In the 1960s only a handful of childhood vaccines were given. The current CDC recommended vaccine schedule for children now has over 30 vaccines by the time a child turns 6 and an additional potential for up to 30 more by the time they reach 18. Could this increase be linked to our declining health? For example, currently:

    One in six children in the US has a learning disability
Over 50% suffer from some type of chronic illness.
Cancer is the leading cause of death in our children
Autism rates have soared from 1 in 10,000 in 1990 to 1 in 68 today

Since genetic mutations change slowly over generations, we must look to environmental causes for these changes. While other environmental toxins certainly are at play in these statistics, disregarding the potential role to the amounts of toxin injected into children through vaccines is not only bad public policy, it is bad science. By disregarding the role of vaccines in our statistics for infant mortality and chronic diseases, we could be doing more harm than good in mandating, or even advising, them.
Vaccine Adverse Effects: Known Risks
The list of adverse side effects for vaccines is long and troubling. A quick scan of the Vaccine Injury Table kept by the Health Resource Center for the U.S. Department of Health and Human Services reveals that compensation for injury is possible from a variety of the most common vaccines given to children.
Adverse events are the reason the Vaccine Injury Compensation Program has paid out over 3 billion dollars from 1988 – 2016 despite the fact that only 1 in 5 claims receives any compensation at all. Studies reveal that a small fraction of those injured by vaccines ever file any claim at all since most doctors reject the notion that a problem was caused by a vaccine despite the reality that such problems are listed on the manufacturers product insert. You can learn more by reading this fficial document: National Vaccine Injury Compensation Program.
Vaccines: Adverse Effects List
Various vaccines are linked to the following serious adverse reactions:

    Anaphylactic shock
Aseptic meningitis, meningitis
Bell’s palsy, facial palsy, isolated cranial nerve palsy
Blood disorders such as thrombocytopenic purpura (a disease that destroys platelets need for clotting)
Brachial neuritis
Cerebrovascular accident (stroke)
Chronic rheumatoid arthritis
Convulsions, seizures, febrile seizure
Encephalopathy and encephalitis (brain swelling)
Hearing loss
Guillain-Barré syndrome
Immune system disorders
Lymphatic system disorders
Multiple sclerosis
Nervous system disorders
Neurological syndromes including autism
Paralysis and myelitis including transverse myelitis
Peripheral neuropathy
Pneumonia and lower respiratory infections
Skin and tissue disorders including eczema
Sudden infant death syndrome (SIDS)
Tinnitus (ringing in the ears)
Vaccine-strain versions of chicken pox, measles, mumps, polio, influenza, meningitis, yellow fever, and pertussis
Vasculitis (inflammation of blood vessels)



Vaccine News – Scientists Prove Those Vaccinated for Shingles Can Infect Others with Chicken Pox

Vaccines and autism: a new scientific review
By Sharyl Attkisson CBS News April 1, 2011, 7:55 AM
For all those who’ve declared the autism-vaccine debate over – a new scientific review begs to differ. It considers a host of peer-reviewed, published theories that show possible connections between vaccines and autism.
The article in the Journal of Immunotoxicology is entitled “Theoretical aspects of autism: Causes–A review.” The author is Helen Ratajczak, surprisingly herself a former senior scientist at a pharmaceutical firm. Ratajczak did what nobody else apparently has bothered to do: she reviewed the body of published science since autism was first described in 1943. Not just one theory suggested by research such as the role of MMR shots, or the mercury preservative thimerosal; but all of them.
Ratajczak’s article states, in part, that “Documented causes of autism include genetic mutations and/or deletions, viral infections, and encephalitis [brain damage] following vaccination [emphasis added]. Therefore, autism is the result of genetic defects and/or inflammation of the brain.”
The article goes on to discuss many potential vaccine-related culprits, including the increasing number of vaccines given in a short period of time. “What I have published is highly concentrated on hypersensitivity, Ratajczak told us in an interview, “the body’s immune system being thrown out of balance.”
University of Pennsylvania’s Dr. Brian Strom, who has served on Institute of Medicine panels advising the government on vaccine safety says the prevailing medical opinion is that vaccines are scientifically linked to encephalopathy (brain damage), but not scientifically linked to autism. As for Ratajczak’s review, he told us he doesn’t find it remarkable. “This is a review of theories. Science is based on facts. To draw conclusions on effects of an exposure on people, you need data on people. The data on people do not support that there is a relationship. As such, any speculation about an explanation for a (non-existing) relationship is irrelevant.”
Ratajczak also looks at a factor that hasn’t been widely discussed: human DNA contained in vaccines. That’s right, human DNA. Ratajczak reports that about the same time vaccine makers took most thimerosal out of most vaccines (with the exception of flu shots which still widely contain thimerosal), they began making some vaccines using human tissue. Ratajczak says human tissue is currently used in 23 vaccines. She discusses the increase in autism incidences corresponding with the introduction of human DNA to MMR vaccine, and suggests the two could be linked. Ratajczak also says an additional increased spike in autism occurred in 1995 when chicken pox vaccine was grown in human fetal tissue.

Study – Theoretical aspects of autism: causes–a review.
Autism, a member of the pervasive developmental disorders (PDDs), has been increasing dramatically since its description by Leo Kanner in 1943. First estimated to occur in 4 to 5 per 10,000 children, the incidence of autism is now 1 per 110 in the United States, and 1 per 64 in the United Kingdom, with similar incidences throughout the world. Searching information from 1943 to the present in PubMed and Ovid Medline databases, this review summarizes results that correlate the timing of changes in incidence with environmental changes. Autism could result from more than one cause, with different manifestations in different individuals that share common symptoms. Documented causes of autism include genetic mutations and/or deletions, viral infections, and encephalitis following vaccination. Therefore, autism is the result of genetic defects and/or inflammation of the brain. The inflammation could be caused by a defective placenta, immature blood-brain barrier, the immune response of the mother to infection while pregnant, a premature birth, encephalitis in the child after birth, or a toxic environment.

Study – The history of vaccinations in the light of the autism epidemic
Autism has been characterized as a behavioral disorder since it was first described by Leo Kanner in 1943. The number of autistic children has increased over the last decade. The incidence of autism was 1 in 10000 before the 1970s and has steadily increased to 1 in 150 in 2008 with a male:female predominance of 4:1. The cause of this epidemic has remained unknown, but several hypotheses have been studied. Many of these suggest an environmental trigger, such as the ethyl mercury contained in the preservative thimerosal, which has been used in vaccines since 1931. Other possible triggers associated with vaccinations are chemical toxins and live viruses. James has published studies suggesting a genetic predisposition in the families of autistic children, exposing them to a deficiency in glutathione and an inability to detoxify heavy metals. Vargas has shown autism to encompass ongoing inflammation in the brains of autistic children. The Hannah Poling vaccine decision was a landmark case. Poling’s family was awarded funds for ongoing medical care of an autistic child who was found to have mitochondrial dysfunction exacerbated by vaccines that left her with autistic behavior and seizures. Several studies have emerged supporting the fact that a significant number of autistic children do have mitochondrial dysfunction. The impact that the Poling case will have on the ability of parents of autistic children to gain access to funds to enable them to properly care for their children remains to be seen.

Nurse Whistleblower Confirms NICU Pre-term Babies Being Injured by Vaccines
March 10, 2017
Another Nurse Whistleblower Confirms: Routine NICU Vaccine Injury Happening
by Jefferey Jaxen
Health Impact News
There is a quickening happening within the establishment medical community. An awakening that is challenging an unthinking, business as usual atmosphere.
Many within mainstream US medicine are arriving at the painful realization that their job is often to follow unethical orders and push the products of a monopolistic pharmaceutical industry.

If vaccines are safe, why has the US gov. paid out $3 BILLION to vaccine-injured families?
Sunday, March 01, 2015 by: L.J. Devon, Staff Writer
(NaturalNews) Vaccines are a very imperfect science, despite the good intentions of healthcare providers and parents seeking to protect their children from disease. Adverse, life-changing and deadly effects of vaccines are more common than ever. In fact, the US government has had to pay out over $3 billion to vaccine-injured families since 1986. Still think vaccines are safe?
The Vaccine Adverse Events Reporting System (VAERS) lists several negative outcomes of vaccines. Many of these side effects are worse than the diseases these vaccines are for! VAERS reports that the MMR (measles, mumps, rubella) vaccine is “linked to febrile seizures, which are a type of seizure that occurs in infants and young children in association with fever.” While these seizures hold no long-term consequences, they can be a frightening experience.
Worse yet, VAERS reports that a whole slew of vaccines, including MMR, varicella zoster, influenza, hepatitis B, meningococcal and tetanus “are linked to anaphylaxis.” Anaphylaxis shock can lead to sudden death. Many of these cases are under-reported, filed as SIDS, or sudden infant death syndrome.
Injection, regardless of vaccine type, is associated with loss of shoulder motion and fainting

Shingles Vaccine Side Effects
More Shingles Vaccine Side Effects
Here is a list of side effects the manufacturer claims:

allergic reactions, which may be serious and may include difficulty in breathing or swallowing
hives at the injection site
joint pain
muscle pain
rash at the injection site
swollen glands near the injection site (that may last a few days to a few weeks)

Before taking any vaccine, know and understand the potential for side effects. Read the labels and do the research. Treat vaccines the same as any medicine you might be prescribed.

Scientists Prove Those Vaccinated for Shingles Can Infect Others with Chicken Pox
Posted by Claire Dwoskin on Sep 17, 2015 3:30:00 PM
For many years, the US government and mainstream media have continued to blame the unvaccinated community for the spread of infectious disease. We are constantly being bombarded with statements like the one written by Philip Ross and published in the International Business Times, which stated:
“The American classroom has become a battleground for parents who are threatened by the growing number of children not vaccinated against measles, one of the most highly contagious viruses in the world. The ongoing measles outbreak in the U.S. that started at Disneyland and has spread to 14 states has raised concerns over the country’s rising anti-vaccination movement, including whether the decision to vaccinate against such a dangerous disease should be left to parents, and what constitutes responsible childrearing. Should a child whose parents chose not to vaccinate be allowed to share the same pencils and playground as children whose parents did?”
Although the International Business Times had attempted to present the public with a balanced review of the situation facing parents, it is questionable as to whether they presented any real evidence to support their claims and they left many readers with unanswered questions.
Shingles Vaccines Cause Chicken Pox in the Unvaccinated
In 2011, a team of scientists headed by Duane L. Pierson published the paper Varicella Zoster Virus DNA at Inoculation Sites and in Saliva After Zostavax Immunization.
Their paper discusses whether or not individuals vaccinated with the shingles vaccine can remain infectious with the chicken pox virus after they had been vaccinated. To investigate this concern in more detail, the team studied 36 individuals over the age of 60 who had recently been vaccinated with the shingles vaccine, Zostavax. The scientists discovered that although the vaccine was efficient in reducing the incidence of shingles in the elderly, many of the skin and saliva samples tested positive for the varicella zoster virus (VZV) DNA for up to 28 days after vaccination.
Note: Varicella zoster virus (VZV) is a neurotropic alphaherpesvirus. Primary infection usually causes varicella (chicken pox) in children.

Study – Varicella Zoster Virus DNA at Inoculation Sites and in Saliva After Zostavax Immunization
Inoculation site samples taken within 10 minutes after vaccination were positive for Zostavax VZV DNA in 18 (50%) of 36 subjects. The VZV DNA copy number per nanogram of total DNA ranged from 28 to 2.1 × 106 (Table 1), possibly reflecting the presence of infectious virus since no alcohol or other agent was used to wipe the skin after inoculation.
No saliva specimen collected immediately before immunization contained VZV DNA. During the first week after immunization, VZV DNA was detected in saliva of 21 (58%) of 36 subjects (13 men and 8 women). During the 28-day study period, VZV DNA was found in 11 (31%) of 36 subjects (5 men and 6 women) at day 14, in 10 (28%) of 36 subjects (6 men and 4 women) at day 21, and in 2 (6%) of 36 subjects (1 man and 1 woman) at day 28. Figure 1 shows the percent of immunized subjects who shed VZV DNA during the 28-day study period. VZV DNA copy numbers per nanogram of total DNA ranged from 20 to 248 (Table 1). Genotypic analysis of DNA from 9 random saliva samples revealed vaccine virus DNA in all instances (Table 1, bold); wild-type VZV DNA was not detected. In 15 (42%) of 36 vaccine recipients (6 men, 9 women), VZV DNA was not detected in saliva at any time during the 28-day study period.


Dr. Andrew Moulden: Every Vaccine Produces Harm
by John P. Thomas
Health Impact News
Canadian physician Dr. Andrew Moulden provided clear scientific evidence to prove that every dose of vaccine given to a child or an adult produces harm. The truth that he uncovered was rejected by the conventional medical system and the pharmaceutical industry. Nevertheless, his warning and his message to America remains as a solid legacy of the man who stood up against big pharma and their program to vaccinate every person on the Earth.
Dr Moulden died unexpectedly in November of 2013 at age 49.
Because of the strong opposition from big pharma concerning Dr. Moulden’s research, I became concerned that the name of this brilliant researcher and his life’s work had nearly been deleted from the internet. His reputation was being disparaged, and his message of warning and hope was being distorted and buried without a tombstone.
I prepared a series of articles as a tribute to a great physician and as a memorial to a courageous individual who was not afraid to speak the truth about medical corruption and a flawed healthcare system that does more to harm health than it does to cure disease.
This is the first in a series of four articles about Dr. Moulden — the man, the physician, and the powerful advocate for ending all vaccine use. In future articles, I will summarize his detailed scientific evidence, which shows how vaccine damage occurs. I will explain the common mechanisms behind vaccine damage and how vaccines harm the health of everyone who receives them regardless of whether or not they notice any adverse reactions at the time they take the shots.
Dr. Moulden stated:
What we have done to each other [with vaccines] has produced the most profound damage to humankind by humankind in the history of humanity. And the reason why we got here is partly because of:
Our arrogance in thinking that we know everything. In physiology and medicine we do not know everything!
[Our greed] to advance our own self-interest to make money, to sell products and to advance corporate alliances. Commercialization has overtaken the fundamental human value of “do unto others as you would have others do unto you.” When society turns toward this human value, then we would all be working together for the greater good of each other. [However, other values have become more important] I don’t care whose feet I step on or how I get there as long as my American dream is realized. I don’t care who has to pay for it on the way of getting there. [1]
Dr. Moulden’s Credibility
Was Dr. Moulden a crackpot as some sources claim, or was he a brilliant physician and researcher? This series of articles will set the record straight, and summarize the contribution that his work has made to medical knowledge.
When I evaluate the credibility of people who are unknown to me, I begin by seeking answers to a few basic questions. For example: Is this person offering opinion, or can he or she back up the claims with valid science? Does he have educational credentials? Are there other physicians and scientists who support his or her beliefs and recommendations? Is this person controlled by the pharmaceutical industry, allopathic medical associations, or the US FDA (US Food and Drug Administration)? And finally, what do Quackwatch and their friends have to say about the person?
Dr. Moulden had a PhD in Clinical Psychology and Neuropsychology. He had a master’s degree in child development, and was also a medical doctor. [2] His work was respected by other researchers who don’t march to the drumbeat of the pharmaceutical companies. Dr. Moulden was a threat to the pharmaceutical industry, and their Quackwatch family of 21 related websites treated him as an enemy. [3, 4]

Vaccine Contraindications: Six People Who Should Not Be Vaccinated
The debate surrounding vaccinations is a fierce one, and personally, I don’t like to argue about it. I’m happy to make the right choices for my family while you make the right ones for yours. (I personally have suffered adverse reactions to vaccinations.) It’s ok to have different opinions, really it is. But there are a lot of folks out there who think everyone should be vaccinated, period, and those who choose not to vaccinate should be penalized or worse.
Listen. I get that people are scared and there’s a lot of fear-mongering in the media. But let’s be realistic here: vaccinations are a medical procedure. There are risks. Vaccinations are not right for everyone. There are at least six types of people in particular who should avoid vaccinations, and below, I’ll spell it out.
Vaccine Contraindications
Just like a particular surgery or prescription medication won’t work well for everyone, vaccinations are not a good choice for everyone.
Some people, in particular, are much more likely to have adverse reactions to vaccinations, including:

– Those with an autoimmune disease
– Children born to a mother with an autoimmune disease
– Anyone who is sick
– Pregnant women
– Those who have previously had a reaction to a vaccination

One size does not fit all
Clearly, vaccinations are not the right choice for everyone, and each family should decide what is right for them and their children. When parents are aware of vaccine contraindications, they can make informed and safer choices for their children.
Please share this post so that other parents can learn about vaccine contraindications and decide if vaccination is right for their children.

USA: Highest Vaccination Rate in the World Has the Worst Health
That “worst health” label includes a ranking of 34th in the world with infant mortality. In other words, the USA has the 34th worst infant survival with its highest rate of vaccinations. Some are directly from multiple vaccinations administered.
But the USA leads the world in infant vaccinations, those administered during the first year after their births – 26 vaccinations during that time.
The only vaccination I recall receiving during early childhood, circa 1948, was the smallpox vaccine, the one that left a circle of shallow pockmarks on the upper arm, a non-ink tattoo that proved you had received that vaccine. Months later there was the booster shot which gave me a vacation of several days away from my first grade teacher while sitting out the chicken pox.
During Naval training the mass vaccination high pressure hand held gun that replaced syringes and needles was tried on us with the polio shot. I wound up with a vacation in the base infirmary with an extended period of the flu. Between those two, there may have been a tetanus shot or two.
From the Healthy Home Economist:

-In1950, there were 3 childhood vaccines typically given when a child entered school.
-In 1983, there were 10 recommended vaccines by the age of 6 years old (24 doses, 7 injections, 4 oral doses for polio).
-In 2010, the CDC vax schedule totaled 68 doses with more than half given by the time a child was only a year and a half old.
-In 2016, the schedule has increased to 74 doses by age 17 with 53 injections and 3 oral doses of rotavirus.

The number of vaccines included in the current childhood vaccine schedule has quadrupled over the past 60 years, with several demanding multiple injections and boosters. During this exponential rise of CDC “recommended” schedules, the health of American children has plummeted.
Autoimmune diseases, learning disabilities, food allergies, chronic ailments, and childhood obesity have all risen. The overall health of this nation ranks very low compared to all other industrialized nations, dead last in most areas.
Vaccine false dogma is so heavy hardly anyone with authority, even in mainstream media, makes the connection between poor health with high vaccination rates. Instead, more, three added for 2016, are getting enforced by mandate or coerced by pediatricians who have the right to refuse medical care on kids who aren’t vaccinated.
Destroying Health with Vaccines is Good Business

50 Studies the AAP Avoided to Mention
There is a robust, worldwide body of published science from highly esteemed scientists questioning the safety of many different aspects of vaccines-how come we never hear from them? The majority of the most compelling science has been published since 2010. Below find 50 such studies to consider, sorted chronologically, and note that these studies only represent a portion of the published work implicating vaccinations in a wide variety of negative health outcomes.
The American Academy of Pediatrics made representations to President Trump in a letter dated 2/7/2017 that are utterly indefensible and inaccurate, as any rational review of the studies below quickly demonstrates. For example, the AAP wrote:
“Claims that vaccines are unsafe when administered according to expert recommendations have been disproven by a robust body of medical literature…we write to express our unequivocal support for the safety of vaccines.”
We contend that the AAP’s statements to the President are baseless, reckless, and easily refuted. The AAP’s letter alone supports the President’s desire to field a Vaccine Safety Commission and do all we can to make vaccines as safe as possible. Please click here for a list of all 50 studies detailed below.

Temporal Association of Certain Neuropsychiatric Disorders Following Vaccination of Children and Adolescents A Pilot Case–Control Study
New Quality-Control Investigations on Vaccines Micro-and Nanocontamination
Behavioral abnormalities in female mice following administration of aluminum adjuvants and the human papillomavirus (HPV) vaccine Gardasil
Autoimmune/Inflammatory Syndrome Induced by Adjuvants and Sjogren’s Syndrome
Combining Childhood Vaccines at One Visit Is Not Safe
Aluminum in Childhood Vaccines Is Unsafe
Aluminium in brain tissue in familial Alzheimer’s disease
Evidence that Food Proteins in Vaccines Cause the Development of Food Allergies and Its Implications for Vaccine Policy
Transcriptomic Analyses of Neurotoxic Effects in Mouse Brain After Intermittent Neonatal Administration of Thimerosal
A Dose-Response Relationship between Organic Mercury Exposure from Thimerosal-Containing Vaccines and Neurodevelopmental Disorders
A comparison of temporal trends in United States autism prevalence to trends in suspected environmental factors
A Population-Based Cohort Study of Undervaccination in 8 Managed Care Organizations Across the United States
Autoimmune/inflammatory syndrome induced by adjuvants (ASIA) 2013: Unveiling the pathogenic, clinical and diagnostic aspects
Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity
Autoimmune/inflammatory syndrome induced by adjuvants (Shoenfeld’s syndrome): clinical and immunological spectrum
A two-phase study evaluating the relationship between Thimerosal-containing vaccine administration and the risk for an autism spectrum disorder diagnosis in the United States
Human exposure to aluminium
Human Papilloma Virus Vaccine and Primary Ovarian Failure: Another Facet of the Autoimmune/Inflammatory Syndrome Induced by Adjuvants
Risk of Febrile Seizures and Epilepsy After Vaccination With Diphtheria, Tetanus, Acellular Pertussis, Inactivated Poliovirus, and Haemophilus Influenzae Type b
Mechanisms of aluminum adjuvant toxicity and autoimmunity in pediatric populations
Neurologic adverse events following vaccination
The spectrum of ASIA: ‘Autoimmune (Auto-inflammatory) Syndrome induced by Adjuvants’
Relative trends in hospitalizations and mortality among infants by the number of vaccine doses and age, based on the Vaccine Adverse Event Reporting System (VAERS), 1990-2010
Do aluminum vaccine adjuvants contribute to the rising prevalence of autism?
Maternal Thimerosal Exposure Results in Aberrant Cerebellar Oxidative Stress, Thyroid Hormone Metabolism, and Motor Behavior in Rat Pups; Sex- and Strain-Dependent Effects
Interindividual variations in the efficacy and toxicity of vaccines
Sorting out the spinning of autism: heavy metals and the question of incidence
Influence of pediatric vaccines on amygdala growth and opioid ligand binding in rhesus macaque infants: A pilot study
The immunobiology of aluminium adjuvants: how do they really work?
Hepatitis B Vaccination of Male Neonates and Autism Diagnosis, NHIS 1997-2002
Allergic Disease and Atopic Sensitization in Children in Relation to Measles Vaccination and Measles Infection
Long-term persistence of vaccine-derived aluminum hydroxide is associated with chronic cognitive dysfunction
Delayed acquisition of neonatal reflexes in newborn primates receiving a thimerosal-containing Hepatitis B vaccine: Influence of gestational age and birth weight
Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration
Post-vaccination encephalomyelitis: Literature review and illustrative case
Thimerosal exposure in infants and neurodevelopmental disorders: An assessment of computerized medical records in the Vaccine Safety Datalink
Delay in diphtheria, pertussis, tetanus vaccination is associated with a reduced risk of childhood asthma?
Hepatitis B triple series vaccine and developmental disability in US children aged 1-9 years
Comparison of Blood and Brain Mercury Levels in Infant Monkeys Exposed to Methylmercury or Vaccines Containing Thimerosal
Thimerosal Neurotoxicity is Associated with Glutathione Depletion: Protection with Glutathione Precursors
Activation of methionine synthase by insulin-like growth factor-1 and dopamine: a target for neurodevelopmental toxins and thimerosal
Abnormal Measles-Mumps-Rubella Antibodies and CNS Autoimmunity in Children with Autism
Macrophagic myofasciitis lesions assess long-term persistence of vaccine derived aluminum hydroxide in muscle
Detection and Sequencing of Measles Virus from Peripheral Mononuclear Cells from Patients with Inflammatory Bowel Disease and Autism
Annual Summary of Vital Statistics: Trends in the Health of Americans During the 20th Century
Iatrogenic exposure to mercury after hepatitis B vaccination in preterm infants
Effects of Diphtheria-Tetanus-Pertussis or Tetanus Vaccination on Allergies and Allergy-Related Respiratory Symptoms Among Children and Adolescents in the United States
Increased risk of developmental neurologic impairment after high exposure to thimerosal-containing vaccine in first month of life
Trends in Infectious Disease Mortality in the United States During the 20th Century
Detection of Measles Virus RNA in Urine Specimens from Vaccine Recipients


Read Actual Decisions and Award Amounts That Our Clients Received

Below is a selection of recent decisions of the United States Court of Federal Claims awarding compensation to vaccine injured clients of Maglio Christopher & Toale, P.A. through the National Vaccine Injury Compensation Program. Click on the case number to view the official decision document from the United States Court of Federal Claims. The decisions usually includes a brief summary of the case and lists the dollar amount of awarded damages. The names of our clients have been redacted to protect their privacy.

Damages decision based on stipulation; influenza (“flu”) vaccine; Guillain-Barré syndrome (“GBS”); Chronic Inflammatory Demyelinating Polyradiculoneuropathy (“CIDP”)

Joint Stipulation on Damages; Influenza Vaccine; Neuritis; Myositis; Polyneuropathy.