2015 Millicent Holliday RN BEP Quintessential Health Care wwwquintessentialhealthnet 1 Goal To examine numerous topics pertaining to current pediatric health conditions with the intent of generating creative thought and conversation so that we the health practitioners can be more info ID: 930139
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Slide1
Unraveling the Complexity of Modern Pediatric Conditions2015
Millicent Holliday RN, BEPQuintessential Health Carewww.quintessentialhealth.net
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Slide2GoalTo examine numerous topics pertaining to current pediatric health conditions, with the intent of generating creative thought and conversation so that we (the health practitioners) can be more informed, thus allowing both parents and practitioners to assess and expand on the data presented. My goal with this presentation is to assist people to move away from fear-based medicine, and to provide starting points that allow for practical evaluation of benefit verses risk, as we navigate the health issue’s that impact our children in these days.
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Slide3Childhood Related Health issues that were not present, or were minimally present, 30 years ago…ADD/ADHDAllergiesAphasia (Language dysfunction)
Apraxia (Motor Speech disorder)AsthmaAtaxia (Involuntary muscle movement)Autism/Aspergers Behavioral DisordersDiabetes
Dyspraxia (Developmental co-ordination disorder)
3
Slide4Childhood Related Health issues that were not present, or were minimally present 20 to 30 years ago…EczemaGastro-Intestinal DisordersCandidiasis ColitisGERD’s
Leaky GutHypotonia (Poor Muscle Tone)Immune Dysfunction
IntussusceptionLearning DisordersMood DisordersMulluscum
Contagiosum
Nutritional Deficiencies
Gluten Sensitivities
Key Mineral Deficiencies
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Slide5Childhood Related Health issues that were not present, or were minimally present, 20 to 30 years ago…Nervous System DisordersBipolar DiseaseSeizures
Schizophrenia ObesityObsessive Compulsive DisordersPervasive Developmental DelaysTourette SyndromeSIDS
5
Slide6What is Happening to our Children?Why is there a global epidemic of increasing chronic disease and developmental disabilities?Why has the incidence of autism increased by more than 1700% since 1991?
Why is 1 child in 6 learning disabled?Why are 15 % of children now diagnosed with ADD/ADHD?
Ref. Andrew Moulden, B.A., M.A., M.D., Ph.D.
Slide7We have to Ask Why?Why did autism grow from a relatively rare incidence of 1 in every 10,000 births in the 1980s? 1 in 500 in the late 1990s.
1 in 250 in 2000. 1 in 150 in late 2000.“1 in 87 in 2014.” (cdc.gov)
David Kirby “Evidence of Harm”
Slide8Why?Why is 1 child in 9 asthmatic?Why is 1 child in 450 diabetic?
Why has the prevalence of eczema (Atopic Dermatitis) risen to impact 80% of children, with most children developing symptoms before 12 months of age?Why are infants and toddlers dying with “cause of death undetermined” on their death certificates?
Ref: Andrew
Moulden
, B.A., M.A., M.D., Ph.D.
Ref: March 8, 2004, Understanding Eczema, by Debra
Indorato
, RD, LDN., Vol. 16 No. 5 p. 35
Slide9Why?“Why did the CDC and the Food and Drug Administrations (FDA) allow mercury exposure from childhood vaccines to more than double between 1988 and 1992 without bothering to calculate cumulative totals and their potential risks?” “Why, for that matter, was there a corresponding spike in reported cases of autism spectrum disorders
(ASD)?
David Kirby
Slide10Statistics…About 1 percent of the world population has autism spectrum disorder. (CDC, 2014)Prevalence in the United States is estimated at 1 in 68 births. (CDC, 2014
)Five times more common in boys 1-42. Girls 1-189More than 3.5 million Americans live with an autism spectrum disorder. (Buescher et al., 2014)Autism is the fastest-growing developmental disability. (
CDC, 2008)Autism services cost U.S. citizens $236-262 billion annually. (Buescher
et al., 2014
)
1 in 6 Children have developmental disabilities/speech and language disabilities statistics taken between 2006 -2008
www.cdc.gov
http
://www.autism-society.org/what-is/facts-and-statistics/
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Slide11Finding the answers to all these questions can be like looking for a needle in a haystack.This age of information overload has successfully complicated the honest attempts of many people to find not only answers but solutions.
Slide12The overarching need today is for there to be a return to practicality relative to our children’s health issues.Parents need to have an in depth (or even cursory) understanding of how the immune system works so that they are more able to make informed decisions relative to their children's health.
There is the need for a deeper understanding of the miracle of the human body and its ability to counteract and expel even the most virulent pathogens.
Slide13Historical Vision…A major cause of the Roman Empire’s decline, after six centuries of world dominance was its replacement of stone aqueducts by lead pipes for the transport and supply of drinking water. Roman engineers, the best in the world, turned their fellow citizens into neurological cripples.
Harris L. Coulter, Ph.D.
Slide14History“Mad Hatter’s Disease”
Symptoms:Depression
Sluggishness
Acute anxiety
Irrational fears
Nervousness
Timidness
Blushing
Uncomfortable in social situations
Avoiding people
Easily upset
Trouble with movement and coordination
Agitation
Irritability & aggression
Slide15Acrodynia/Pink Disease-1930Acrodynia
, afflicted tens of thousands of children in the 1930s.
25% of
babies with pink disease died.
Resulted from exposure to inorganic mercury found in teething powder, calamine lotion and mercurochrome.
1
in 500 exposed children developed the disease.
Slide16Symptoms of Pink DiseaseLoss of joyfulness
Children stopped playing, laughing or smiling
Sad expression, melancholy even desperate
Aphasia (stopped talking)
Constant crying, cranky and moaning
Affectivity
modified
Lack of awareness of parents
No
response to kisses
Irritability
Hostility
Biting, hitting
Bizarre behavior
Alternating excitation and depression
Anger turned inwards, head banging etc.
Slide17Minamata Disease: 1950Named after
Minamata Bay in SW Japan. In the early 1950s, residents began noticing bizarre
behavior in cats. They convulsed and screeched in agony.
Then
people began to be affected, first noted in fishing communities located near factories that expelled waste, including mercury, into the sea.
Slide18Symptoms of Minamata DiseaseNumbness in arms, legs and mouth
Sensory disturbances Problems with hand-eye coordination and movement.
Generalized lack of coordination
Difficulty in walking
Fatigue
Tremor
Weakness
Seizures
Reduced or slurred speech
Diminished vision & hearing
Partial Paralysis
Jerking movement
Difficulty swallowing
Convulsions
Brain Damage
Death
Birth defects
Slide19The Iraqi Grain Incident-1971Persian Gulf in 1971 suffered a catastrophic drought which wiped out
their wheat production.Iraqi government imported 178,000 tons of drought resistant wheat seed from Mexico. The grain was treated with methylmercury (and in some cases
ethylmercury) as a fungicide, and dyed pink.
The grain arrived too late in
Iraq
to plant so villages ground it into flour to make bread.
Thousands of Iraqi consumed this bread, finding the pink color attractive and festive.
Slide20Iraqi Grain Incident SymptomsBurning and prickling skin
Fuzzy eyesightLoss of muscle coordination
Blindness
Hearing loss
Coma
Death
6000 people
hospitalized
450 deaths
Slide21Iraqi Grain Incident cont…Fetuses exposed possibly 10 times more sensitive to mercury
Symptoms of children exposed during pregnancy
Cerebral palsy
Mental retardation
Weakness
Seizures
Delayed development
Symptoms in older children
Seizures
Abnormal reflexes
Delayed development
Children
exposed to mercury in utero “appeared fairly normal at birth, with only slight abnormalities of reflexes and muscle tone, but later had seizures, long delays in learning to walk and talk, and severe
clumsiness”
Slide22Gulf War Syndrome 1990Many Gulf Was veterans suffered from bizarre symptoms on return to the U.S.A., like severe weight loss, GI inflammation, neurological damage, short-term memory loss, even tumors.
Mercury levels in there hair measured around 14 ppm (5ppm is considered mercury toxicity) Some veterans received as much as 800 micrograms of mercury in there military vaccinations.
IV chelation therapy has proved effective in resolving many of there symptoms
.
Slide23Mercury Safety LevelsMSDS (Material Safety Data Sheet) states that thimerosal is “Highly Toxic”, that there is a “Danger of cumulative effects. Avoid prolonged or repeated exposure.
The chemical, physical, and toxicological properties have not been thoroughly investigated.”
Slide24Dangerous DosagesEPA
cites safety limits for ethylmercury at 0.1 micrograms per kilogram per day.
A 10
lb
or 5 Kg babies should not be exposed to more than 0.5 mcg a day.
In the late 1980’s, and all through the 90’s, at
two months many babies routinely receive
diphtheria-tetanus with 25 mcg
ethylmercury
Hib
shot with 25 mcg
ethylmercury
Hepatitis B with 12.5 mcg
ethylmercury
= 62.5 micrograms in a day.
By age 18 months many children have received a total of 237 micrograms of mercury, 175 micrograms received in the first 6 months when body weight is low and the immune and nervous systems not fully developed.
Slide25Foreign Foresight & Myopic VisionIn 1990 the World Health Organization began to investigate allergic reactions to
thimerosal.
In 1992 thimerosal
was removed from all childhood vaccines in Scandinavia.
In 1997 the European Union had begun looking into the preservative and it’s toxic effects.
June 29, 1999 in an address to high level American and European health officials, Jon Christian
Ryter
said “WHO was concerned that the accumulation effect of more than 200 mcg of mercury in a fetus or infant could cause moderate to severe brain damage that would result in a rise of learning impaired children”.
This alarmed FDA
officials,
who encouraged removal of mercury from
childhood
shots. But in order “not to jeopardize immunizations programs” it was considered advisable to eliminate it “on a gradual basis”.
David Kirby
Slide26What Caused the Dramatic Rise is Autism in the past30 years
In 1988 Hib vaccine was added to the childhood schedule, calling for four shots in the first year of life beginning at age two months. Some brands of
Hib vaccine contain 25 mcg of
ethylmercury
-each.
In 1991, hepatitis-B was added to the list, at that time all these vaccines contained 12.5 mcg of mercury. The schedule was 3 injections in the first year, beginning with a “birth dose”.
These vaccines added an additional 137.5 mcg of
ethylmercury
, during a
childs
first most vulnerable year.
In just three years, total potential exposure leapt from 100 micrograms to 237.5 micrograms.
David Kirby Evidence of Harm
Slide27Slide28Why the Hepatitis B Vaccine?In 1991 hepatitis-B was added to the childhood schedule. At that time all Hep-B shots contained 12.5 micrograms of mercury.
Three injections in the first year was initiated starting with a “birth dose”.
Slide29CDC’s Advisory Committee on Immunization Practices, June 2000The CDC’s Dr. Thomas
Verstraeten determined that the odds of there being a neurological outcome with each incremental increase in
thimerosal exposure is dramatic. (0, 12.5, 25, 37.5, 50, and 62.5 micrograms or more).
Verstraeten
stated “What these estimates suggest is that there seems to be an increasing trend, an increasing risk for any of these neurological developmental outcomes, with increasing
thimerosal
exposure among children who received the highest exposure, compared with children who received little or no mercury at all”
In Atlanta GA, July 2000 he also stated that children exposed to 62.5 micrograms were 35% more likely to have a neurological developmental disorder than children exposed to 12.5 micrograms.
Slide30Verstraeten’s Observations cont…
For ADD they found that a child that received 62.5 micrograms by six months of age was 30% more likely to develop ADD than a child who received 12.5 micrograms.Likewise children who received 62.5 micrograms of ethylmercury
by 3 months of age, compared with children who received 12.5 mcg’s, were 110% more likely to develop language disorders.
With autism the risk in the higher exposure group at 3 months were 69% more likely to develop autism than the baseline group.
Slide31BREAK…31
Slide32Neuro Toxicity & AdjuvantsHow Mercury Causes Brain Neuron Degeneration (University of Calgary)
Slide33Boyd Haley’s Research 2002He exposed mouse neuronal cells in a culture to
thimerosal (in the same 0.01 percent solution found in vaccines); aluminum and neomycin which is widely used in pediatrics and found in the MMR vaccine.
Haley measured the percentage of neurons that were still alive after 24 hours. There was also a control group of unexposed neurons (all survived after 24 hours).
In the aluminum exposed group nearly
90%
of the cells survived.
In the antibiotic group survival was
80%.
In the thimerosal group only
30%
survived after 24 hours.
When all three were mixed together the survival rate plummeted to less than 10% after 24 hours.
Slide34Boyd Haley’s Research cont.Body Haley’s team made another remarkable finding: In normal children elevated mercury levels in hair correspond to the number of dental amalgams in the mother. In contrast, autistic children have very low mercury levels in there hair even if the mother has a mouthful of fillings.
“This clearly shows that autistic children do not handle mercury like normal children…, they do not excrete mercury very well.”
EPA states that mercury above 1 part per million (ppm) is a consideration for action.
A reading of 5 ppm means mercury poisoning.
International Journal of Toxicology
Slide35Boyd Haley’s Research cont…He found that
thimerosal broke down when exposed to light, releasing its ethylmercury
at a rapid rate. Thimerosal
without exposure to light caused
80%
loss of protein, but an even higher toxicity resulted in the
photolyzed
vaccine.
He also found that methylmercury was not as toxic to tubulin as the
ethylmercury
released from
thimerosal
after exposure to light.
He also found that the mercury laced shots were tenfold to a hundredfold more toxic than those without
thimerosal
. There was one outstanding exception the preservative-free MMR vaccine. It was as toxic as the
thimerosal
-containing vaccine. There was something in MMR that inhibited enzymes and brain proteins, as yet
undetermined.
Slide36The Perfect Storm Hypothesis
Chemical ToxinsFluoride +++Geopathic StressorsGMO’s
Glyphosatearticles.mercola.com/sites/articles/archive/2013/.../dr-huber-gmo-foods.aspxHeavy Metal Toxicity
Aluminium
Ethylmercury
www.youtube.com/watch?v=AB7Os0tos5k
Methylmercury
Mal-nourished
Mothers
Ultrasounds
Vaccines
http://articles.mercola.com/sites/articles/archive/2015/01/24/catastrophic-vaccine-reactions.aspx
36
Slide37Adjuvants…Aluminum is being implicated as interfering with a variety of cellular and metabolic processes in the nervous system and in other tissues.
Conclusion: Aluminum is eliminated from the body primarily through the kidneys. Infants kidney function (glomerular filtration rate) is low at birth and doesn’t reach full capacity until 1-2 years of age. Infants may not be able to effectively excrete aluminum, contributing to heavy metal toxicity.
Ref:
Zatta
PF,
Alfrey
AC (
Eds
). “Aluminum Toxicity in Infants Health and Disease” 1997 World Scientific Publishing
37
Slide38AdjuvantsDifferent vaccines contain a number of different ingredients that can be toxic for humans and cause serious health problems, such as:
Vaccination: The Neurological Poison So Common Your Doctor Probably Pushes It April 11, 2012 Dr. Mercola
38
Formaldehyde, a known cancer-causing agent
Phenol (carbolic acid)
Neomycin and streptomycin (antibiotics)
Resin and gelatin, known to cause allergic reactions
Polysorbate
80 (Tween80™), which can cause anaphylactic reactions, and may cause miscarriage and infertility (see the next section for details)
Triton X100 (detergent)
Slide39AdjuvantsAdjuvants can cause your immune system to overreact to the introduction of the organism you're being vaccinated against, leading to a break down in self-tolerance, i.e. your immune system attacks your own body as “other” Vaccine-induced immune challenges can lead to permanent alterations in brain and immune function, including serious, chronic inflammatory conditions Children are particularly vulnerable to toxic insults; a new report states that a “rigorous evaluation of the vaccine-related adverse health impacts in the pediatric population is urgently needed”
Vaccination: The Neurological Poison So Common Your Doctor Probably Pushes It April 11, 2012 Dr. Mercola
39
Slide40GMOs, Glyphosate & The Human MicroBiomeTwo studies published in the past six months reveal a disturbing finding: glyphosate-based herbicides such as Roundup® appear to suppress the growth of beneficial gut bacteria, leading to the overgrowth of extremely pathogenic bacteria.
GM agriculture may be contributing to the alarming increase, worldwide, in infectious diseases that are resistant to conventional antibiotics, such as Methicillin-resistant Staphylococcus aureus (MRSA) and Carbapenem-resistant
Enterobacteriaceae (CRE), which the CDC's director recently termed a 'nightmare bacteria.‘
Glyphosate
has been found to be toxic to human DNA at concentrations 450-fold lower than presently used in agricultural applications.
[ii]
When combined with
adjuvants
and other so-called 'inactive' ingredients, the glyphosate-formulations are far more toxic than their component ingredients taken in isolation
March 28th 2013 at 5:00 am
Written By:
www.GreenMedInfo.com
Sayer
Ji
, Founder
40
Slide41GlyphosateResearch has demonstrated that pesticides and other agricultural chemicals are neurotoxic, capable of damaging your nervous system. According to the US Environmental Protection Agency (EPA), 60 percent of herbicides, 90 percent of fungicides, and 30 percent of insecticides are also carcinogenic.Most notably, as reported by Reuters,
the USDA does not test for one of the most pervasive and one of the most harmful agricultural chemicals of all, namely glyphosate:As has been the case with past analyses, the USDA said it did not test this past year for residues of glyphosate, the active ingredient in Roundup herbicide and the world's most widely used herbicide.USDA Claims Pesticide Residues in Food Is Safe—Here’s Why They’re
Wrong January 27, 2015 Dr. Mercola 1/27/15
41
Slide42GlyphosateThe researchers also note that previous studies show that glyphosate "disrupts the endocrine system and the balance of gut bacteria... damages DNA and is a driver of mutations that lead to cancer.“Ref: USDA Claims Pesticide Residues in Food Is Safe—Here’s Why They’re Wrong
January 27, 2015 Dr. Mercola 1/27/1542
Slide43Correlation between Glyphosate and Health Problems…The researchers searched US government databases for GE crop data, glyphosate application data, and disease epidemiological data, and analyses revealed "highly significant" correlations between glyphosate applications and the following health problems among the US population:
USDA Claims Pesticide Residues in Food Is Safe—Here’s Why They’re Wrong January 27, 2015 Dr. Mercola 1/27/15
Hypertension
Stroke
Diabetes
Obesity
Lipoprotein metabolism disorder
Alzheimer's disease
Senile dementia
Parkinson's disease
Multiple sclerosis
Autism
Inflammatory bowel disease
Intestinal infections
End stage renal disease
Acute kidney failure
Thyroid cancer
Liver cancer
Bladder cancer
Pancreatic cancer
Kidney cancer
Myeloid leukemia
MTHFR Mutations – Developmental delays, severe mental retardation, peri-natal death, psychiatric disturbancesMTRR/A66G – A marker for chromosome damage & developmental delays
MAO A / R297R Monitor clinical indication of abnormal serotonin and plasma tryptophan. Ref: 1999-2014 Doctor's Data, Inc.If Glyphosates potentially has the ability to impact your DNA, could it alter gene function as well?Could children with these genetic
predispositions be more prone to developing neurological deficits?
44
Slide45Genetic Polymorphism…Methylene-tetra-hydro-folate Reductase (MTHFR)The MTHFR gene provides instructions for making an enzyme called methylene-tetra-hydro-folate reductase
. This enzyme plays a role in processing amino acids, the building blocks of proteins. Methylenetetrahydrofolate reductase is important for a chemical reaction involving forms of the vitamin folate (also called vitamin B9). Specifically, this enzyme converts a molecule called 5,10-methylenetetrahydrofolate to a molecule called 5-methyltetrahydrofolate.
This reaction is required for the multistep process that converts the amino acid homocysteine to another amino acid, methionine. The
body uses methionine to make proteins and other important compounds
.
http://ghr.nlm.nih.gov/gene/MTHFR
45
Slide46MAYA Clinic & MTHFRPatients with severe MTHFR deficiency (enzymatic activity 0%-20% of normal) develop homocysteinuria, a severe disorder with a wide range of associated clinical manifestations, including developmental delay, mental retardation, and premature vascular disease. Seven unique
MTHFR mutations have been associated with homocysteinuria, all among patients who were either homozygous or compound heterozygotes for 1 or more of these mutations.www.mayomedicallaboratories.com
46
Slide4747Slide48Folate/B12In infants and children, folate deficiency can slow growth rate. Women with folate deficiency who become pregnant are more likely to give birth to low birth weight premature infants, and infants with
neural tube defects.The role of vitamin B12 and folate in depression is due to their role in transmethylation reactions, which are crucial for the formation of neurotransmitters
(e.g. serotonin, epinephrine, nicotinamides, purines, phospholipids).Low levels of folate or vitamin B
12
can disrupt
transmethylation
reaction, leading to an accumulation of
homocysteine
(
hyperhomocisteinemia
) and to impaired metabolism of neurotransmitters (especially the hydroxylation of
dopamine
and
serotonin
from
tyrosine
and
tryptophan),
phospholipids,
myelin,
and receptors.
High homocysteine levels
in the blood can lead to vascular injuries by oxidative mechanisms which can contribute to cerebral dysfunction. All of these can lead to the development of various disorders, including
depression.
www.ask.com/health/vitamin-b12
48
Slide4949Slide50Cranial NervesThe cranial nerves are composed of twelve pairs of nerves that emanate from the nervous tissue of the brain. The motor components of the cranial nerves are derived from cells that are located in the brain.
The sensory components of cranial nerves originate from collections of cells that are located outside the brain. In summary, the motor components of cranial nerves transmit nerve impulses from the brain to target tissue outside of the brain. Sensory components transmit nerve impulses from sensory organs to the brain.
Slide51The Cranial NervesI
Olfactory
II Optic
III Oculomotor
IV Trochlear
V Trigeminal
VI
Abducens
VII Facial
VIII Vestibulocochlear
or
Auditory
IX Glossopharyngeal
X
Vagus
XI Accessory
XII
Hypoglassal
Neurotransmitters Make All the
Difference
Slide54MMR Vaccine
1955 Death rate in measles was less than 3 per 10 million that was 8 years before the measles vaccination
campaign
began in
1963
The vaccine court has ruled that the MMR can cause acute encephalopathy followed by permanent brain injury or death.
MINE (Measles-Induced
Neuroautistic
Encephalopathy) syndrome has a constellation of symptoms similar to autism.
Ref:
Dr
Sherri
Tenpenny
, “Saying NO to
Vacines
”, p 91
Slide55MINE & Subacute
Sclerosing Panencephalitis (SSPE)
SSPE is an extremely rare, serious complication of a measles infection. It is also listed as a possible adverse reaction to the MMR vaccine by manufacturer Merck & Co. (Feb. 2000).
Slide56SSPEThe virus can remain quiescent for years prior to erupting in the CNS as complications of SSPE.
Prior to 1963, when the measles vaccine was introduced, more than 500,000 cases of measles were reported each year. 60 Cases of SSPE occurred annually.By 1975, SSPE had dropped to 41 cases per year. Only 80 cases reported in the U.S. over the last 15 yearsHowever, since the late 1990s > 2,000 children have been diagnosed with MINE syndrome and many thousands more have been diagnosed with autism (1 in 166 children).
(2014 Autism 1 in 87)
Ref: J
Ped
Neurology. 2004: SSPE & MINE
Slide57MINEAll children diagnosed with MINE syndrome had the MMR between 12 and 21 months of age. There are no reported cases in unvaccinated children.
Prior to vaccination, none of the children showed any features of autism or any signs of enterocolitis. Vaccine-strain measles virus found in children’s blood and spinal fluid
Slow viruses: many autistic symptoms develop many months after the measles vaccine, an interval characteristic of diseases caused by “slow viruses” such as the measles virus.
Ref: Saying NO to Vaccines, Dr Sherri Tenpenny
Slide58Possible Adverse Reactions to MMR Issued by Merck & Co. (February 2000)Body as a Whole:
Panniculitis (inflammation of a layer of fatty connective tissue of the anterior wall of the abdomen)Fever Syncope
HeadacheDizziness
Malaise
Irritability
Cardiovascular System:
Vasculitis (inflammation of the blood or lymph vessels)
Digestive System:
Pancreatitis
Diarrhea
Vomiting
Parotitis
Nausea
Endocrine System:
Diabetes mellitus
Slide59Possible Adverse Reactions to MMR Issued in 2000 by Merck & Co…Ear:
Nerve deafnessOtitis media
Eye:RetinitisOptic neuritis
Papillitis
Retrobulbar
neuritis
Conjunctivitis
Slide60Possible Adverse Reactions to MMR Issued by Merck & Co…Haematic
and Lymphatic System:Thrombocytopenia (abnormal decrease in number of blood platelets)Purpura (hemorrhage into skin, mucous membranes, internal organs and other tissue)
Regional Lymphadenopathy (disease of lymph nodes)Leukocytosis (increase in number of leukocytes (WBC) in the blood, generally caused by the presence of infection)
Immune System:
Anaphylaxis
Anaphylactoid
reaction
Angioneurotic
edema (spasm or paralysis of blood vessels
Bronchial spasm (asthma)
Slide61Possible Adverse Reactions to MMR Issued by Merck & Co…Musculoskeletal System:Arthritis
Arthralgia (pain in joints)Myalgia (pain in muscles)
Slide62Possible Adverse Reactions to MMR Issued by Merck & Co…Nervous System:
Encephalitis (inflammation of the brain…may be a specific disease entity caused by an arthropod-borne virus, or it may occur as a result of influenza, measles, German measles, chickenpox, herpes virus, infection, smallpox vaccinia or other diseases)Encephalopathy (any dysfunction of the brain)Measles inclusion body encephalitis (MIBE)
Subacute sclerosing
panencephalitis
Slide63Possible Adverse Reactions to MMR Issued by Merck & Co…Nervous System (cont’d)Guillain-Barre Syndrome (polyneuritis with progressive muscle weakness of extremities that may lead to paralysis; usually occurs after recovery from an infectious disease; has also occurred as a rare complication of immunization with influenza vaccine)
Ref:Taber’s Medical DictionaryFebrile convulsions
Afebrile convulsions or seizures
Ataxia
Polyneuritis (inflammation of multiple nerves)
Polyneuropathy (disease of multiple nerves)
Ocular palsies
Paresthesia (tickling, prickling or burning of skin)
Slide64Possible Adverse Reactions to MMR Issued by Merck & Co…Respiratory System:Pneumonitis
Sore throatCoughRhinitisSkin:
Steven-Johnson syndrome (see erythema multiforme
below)
Erythema
multiforme
(a form of macula showing diffused redness over the skin caused by capillary congestion usually due to dilatation of the superficial capillaries as a result of some nervous mechanism within the body, inflammation or some external influence)
Taber’s Medical Dictionary
Urogenital System:
Orchitis
Other:
Death from various and, in some cases, unknown causes has been reported rarely following vaccination with MMR; however, a causal relationship has not been established.
Slide65Pertussis Vaccination and Asthma: Is there a Link?Why is 1 child in 9 asthmatic?In a study of 450 children, 11% who had received the pertussis vaccination suffered from asthma as compared with only 2% of the children who had not been vaccinated.
Ref; JAMA. Aug 24-31 272 (8): 592-3 1994
Slide66Why are Childhood Allergies so Prevalent?The following vaccines and vaccine additives have been associated with an increase of serum IgE
, the antibody present in most persons with allergies:Aluminum; DT vaccine; Aluminum is eliminated from the body primarily through the kidneys. Infants kidney function (glomerular filtration rate) is low at birth and doesn’t reach full capacity until 1-2 years of age. Infants may not be able to effectively excrete aluminum, contributing to heavy metal toxicity.
Gelatin; Influenza;
Pertussis
& MMR vaccines; mercury (
thimerosal
)
Mercury
depletes glutathione, polarizing the TH2 dominance. Can induce a strong increase of
IgE
.
Ref
:
Zatta
PF,
Alfrey
AC (
Eds
). “Aluminum Toxicity in Infants Health and Disease” 1997 World Scientific Publishing
Why are vaccine manufacturers and those who administer them protected from liability by the government when their products cause injury?Why do so few parents know that they can report adverse reactions to the Vaccine Adverse Event Reporting System (VAERS)?
Slide68Between mid-1999 and January 4, 2004, a total of 128,035 adverse reactions were reported to VAERS (Vaccine Adverse Event Reporting System).Because it is estimated that only 1% of all adverse reactions are voluntarily reported, this figure may actually represent 1.28 million adverse reactions.During this same period, 2,093 deaths that occurred soon after vaccinations, were reported to VAERS
.
Ref: JAMA 269 and “Saying NO to Vaccines” 29
Slide69What can be done?Wait 2 years Draw blood titers No antibiotics or steroid x 4 weeks before a vaccineGive only one vaccine at a timeNever vaccinate a sick
childReport ALL “Adverse Events” to VAERSVaccine Exemptions:PhilosophicalReligious
Medical
Slide70Suggested reading…Evidence of Harm, by David KirbyA shot in the Dark, Harris L. Coulter & Barbara Loe Fisher
Multiple books written by Neil Z. MillerSaying No to Vaccines by Dr. Sherri TenpennyCallous Disregard by Dr. Wakefield Websites
www.mercula.comwww.nvic.org
www.greeninfo.com
www.iaomt.com
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