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Creating Waves of Awareness

Introduction 2009:
This article was first published more than 15 years ago, yet it has not lost its significance. It does not condemn vaccination, but raises important issues and draws some valid conclusions.

ARTICLE:
Th. Quak. Translated by Hans Weitbrecht

Much has been, and still is, reported on complications following vaccinations. Among others, the literature describes the following (rare) Vaccination Induced Side Effects (VISE) of the MMR and polio vaccinations: Local erythemas (inflammation of the skin), Fever, Irritability, Tiredness, General rashes (acute urticaria), Conjunctivitis, Arthropathies (Arthritis like Symptoms), Peripheral tremor, Cough and/or coryza, Post-vaccine meningitis (aseptic meningitis), Guillain-Barre syndrome, Brachial neuritis (Pain of the nerves of the underarm), Anaphylactic shock (sudden collapse, live threatening), Multiple sclerosis, Chronic arthritis.

Most feared are lasting damages like the consequences of a post-vaccine meningitis and life threatening diseases like anaphylactic shock. The short lasting smaller side effects are usually interpreted as the normal reaction of the immune system to the attenuated disease (i.e. the vaccine) and therefore regarded as harmless. Since, according to available statistical data, the "side-effects" of the real diseases are much more frequent than those of the vaccination, the following conclusion is commonly drawn: vaccinations prevent more damage than they cause and are therefore of considerable benefit to society.

Side-effects of vaccinations

Legally, only symptoms, which appear within a certain well-defined time (normally a few days or weeks) after the vaccination, and thereby suggest a causal link to it, are considered to be side effects of the vaccination (VISE). Symptoms that develop slowly or only after considerable time are difficult to link to the vaccination because of the multitude of other environmental influences to which the patient is exposed in this period. Since data on these delayed effects are difficult or impossible to treat in a statistically meaningful way, these side-effects are not recognized as caused by the vaccination: up to the year 1991 "only" 1870 patients in Germany filed claims based on VISE under the BSeuchG [21] (German bill for the prevention of the spreading of infectious disease). According to Buchwald [31], until 1992, 3407 cases of VISE have been legally confirmed in Germany. This corresponds to a prevalence of 4.3 per 100,000 .. For the population of Germany this translates into about 170 confirmed VISE per year. The number of filed claims is of course much higher.

Gathering data on long-term VISE requires very expensive and labour intensive observations over long time periods. Those would only be useful, however, if comparable groups of vaccinated and unvaccinated subjects were available for long term study. Many ethical and forensic problems arise at this point. Furthermore, it is difficult to find a sufficient number of unvaccinated people. There are no long-term studies comparing vaccinated and unvaccinated groups.

An important factor in the assessment of how frequently VISE occur is that: how much attention is given to the observation of VISE and how frequently side-effects are brought in connection with vaccination in general. The editorial of the J. Med. Microbiol. [11] comments: "The rate of post-vicinal meningitis varies between studies and may be dependent on how hard the investigators try to uncover such cases." This comment was made with respect to a study on the MMR vaccination in the United Kingdom. In this study the authors show that the risk of aseptic meningitis is not, as previously thought, between 0.4 and 10 per million, but rather between 100 and 11000 per million vaccinated[16]. This is a shockingly high number of complications [32], since in this case everybody, without exception, comes into contact with the (attenuated) virus; not just a part of the population as with the naturally occurring disease.

Between the introduction of the MMR vaccination in the UK in 1988 with the so-called Urabe-Mumps-Strain (sold under the brand names Pluserix and Rimparix in Germany before they were removed from the market in 1992) until the realization of the high risk involved, several years elapsed until this strain was replaced by a different one (Jeryl Lynn) in 1992. It is generally assumed that this strain does not, or not as frequently, lead to aseptic meningitis, even though cases of meningitis have already been reported for this particular vaccine [26].

Vaccines

Surprisingly, there are different strains of the vaccines in use against the same disease.This is the result of different production methods. All vaccines in use today contain live, attenuated viruses (as do measles, polio, rubella, influenza, yellow-fever, chickenpox).

The "transmutation" (attenuation) of a virulent wild strain into a vaccine is today still an empirical process. The virus is subject to several passages in various cell cultures under non-optimal growth conditions. Through this process the virus changes some of its specific properties, yet it remains however a "live" virus. The mechanism involved in this attenuation is unknown. Following that, a few safety investigations are made and the reactivity and efficacy is tested on laboratory animals and volunteers.

This process basically has not changed since the early experiments with vaccines during Pasteur's time. Pasteur, for example, developed a rabies vaccine [52] by cultivating the virus in rabbits and "attenuating" it through variable length of exposures to air. It was this still incomplete method that made Pasteur famous and at the same time ill reputed since many people died from rabies caused by the vaccination itself [57].

In the case of cowpox vaccination, which has been abandoned in our latitudes, the origin of the virus contained in the vaccine is not even known. The original vaccine from cowpox used to be transferred from child to child because there was no way of conserving it. Re-cultivation on cows was only successfully accomplished after several decades. In the meantime, attenuation of the vaccine had been achieved in thousands of human bodies -- a very dangerous process indeed, since not only the cowpox virus was transmitted but also all other infectious diseases of the person. "This vaccine is molecular-biologically significantly different from the chickenpox virus as well as the cowpox virus." [58]

Nowadays there are different vaccines,(depending the manufacturing processes), sold by various companies, all with differing properties. However, the molecular basis of the active principle is in most cases still unknown. The natural virus can not be distinguished by serological methods from the attenuated virus. The Urabe mumps virus and the Jeryl mumps virus are identical on that basis. Only through the modern technique of gene sequencing has it recently been possible to identify several differences. It is, however, still unknown why one strain is more reactive than the other. Also unknown is how these genetic differences come about during the process of attenuation. After all, the injection of a live, attenuated virus is a process involving many unknowns and non-predictables. Still this is taken as the as the lesser of two evils due to the alleged success fighting the so-called mass epidemics.

Reaction of the Immune System

It is important to realize that the reaction of the immune system to the injected vaccine is only known partially: "It has been observed frequently that antibody levels do not go hand in hand with immunity to the disease... The investigation of the second branch of immunity, the cell mitigated immune response, has been technically much more difficult and turned out to be very complex ... There exists now a large number of experimental data and insights into the different mechanisms of the cell mitigated immune response including their interactions among each other and with the humoral immune system. Despite that fact, we have only fragmentary knowledge about the concrete role of the cell mitigated immune response to an infection by isolated pathogens in the human body." [58, p270].

The following conclusions are of great importance:

1. The potentially disease-provoking properties of a vaccine are unknown (the structure of the genome is not known).

2. The reaction of the immune system to the injected vaccine is not known in any detail.

3. The interaction of the altered state of the immune system after the vaccination with other variables is unknown.

We don't know which long-term consequences may arise from this, because studies are mostly focused on short-term reactions to the vaccination. There are, however, indications of long-term side effects of the immunization.

Long-term Consequences

The occurrence of arthralgias ( muscular pain) has been documented since the first studies about the rubella vaccination [1-10]. Based on these studies the Institute of Medicine states: "The committee concludes that a causal connection exists between the RA 27/3 rubella vaccination strain and incidents of chronic arthritis in women." "Thompson et al. report: arthralgias in 1973 on 11 children with recurrent arthritis which lasted at least for 36 months after vaccination with HPV 77; other cases of potential arthritis have since then reported, some with the RA 27/3 strain." [12].

Arthralgias and arthritic affections occur frequently in connection with diseases for which auto-immune reactions 9 A situation where the immune system attacks healthy body cells) are responsible. Examples are Systemic Lupus Erythematodes (SLE), sclerodermia, Sharp-syndrome, polymyositis [23], or rheumatoid arthritis (Aids, Cancer). It would be advisable to study the connection between activation of the immune system and auto-immune diseases, since the number of diseases in this class is large and grows steadily with our increase in knowledge of their pathophysiology: Thyreoiditis Hashimoto. Primary myxedema. Pernicious anemia. Auto-immune atrophic gastritis. Morbus Addison. Premature menopause. Goodpasture syndrome. Myasthenia gravis. Sterility in men. Pemphigus vulgaris. Sympathic ophtalmias. Multiple sclerosis. Auto-immune hemolytic anemia. Primary biliary scirrhosis. Uclerative colitis. Sjogren syndrome, etc.

We know that immunizations can lead to deterioration in existing auto-immune diseases [23]. The symptoms that the body exhibits in these cases because of its specific predisposition, are an indication of a weakness in the regulatory system. They are usually overlooked in the "still" healthy person, yet probably present nonetheless (Coulter refers to these cases as "cracked eggs"). "It is generally advisable to abstain from active immunization with live vaccines in the cases of patients with auto-immune diseases or chronic inflammatory processes and vaccinate only in special circumstances and in the presence of strong indications." [23] Further:

"It is not aberrant to assume that immunizations, being a considerable interference with the regulation of the immunologic network, can influence the progression of vasculitic illnesses." 23]

Even direct side effects are known: "Ten of 1000,000 vaccinated Americans developed auto-immune post-vaccine encephalitis or peripheral neuritis (Guillain-Barre syndrome) one or two weeks after immunization with attenuated influenza (Flue-) vaccine." [64].

However, it has been difficult to prove that immunizations are actively involved in the emergence of auto-immune diseases, because these illnesses develop after a considerable latency period. Furthermore, studies, in particular if they are supposed to be predictive, have not been carried out so far.

Patho-Mechanism (Ways in which disease organizes itself)

It is high time to launch these important studies, since a patho-mechanism which might be involved in causing such auto-immune diseases has been known for a long time: the cross-reaction between foreign pathogens (or vaccines), and body chemistry and tissues, so-called molecular mimicri [59]. One can imagine such a relationship between body tissues and foreign matter on three planes:
[58]:

"1. Between two types of cells, tissues, or micro organisms (e.g., bacteria or viruses), if they use a similar or identical kind of molecule in their structure.

2. Between two antigen molecules if, on their surface, they have besides different also identical determinants.

3. Between two determinants, if they are sufficiently similar to react with the same antibody. In this case the group homologue to the antibody will react strongly while the differently configured determinate (F1 generation) will yield a weaker reaction."

All these possibilities apply to vaccines or their constituents. If one introduces antigenes into the body (e.g., through vaccination) which have similar structural groups as some body tissue, even if the similarity is only partial, the production of antibodies in the sense of an auto-immune reaction is possible. A well known medical example for this process is the cross reactivity between poly-saccharine of the cell membrane of beta-hemeolytic streptococci and the human cortical valve during rheumatic fever. In this case, damage to the valve can occur by means of antibody production.

One may remark that the natural infections can trigger autoimmune reactions, too. However, it needs to be pointed out that vaccination induced infection differs from the natural one in three ways, and therefore possesses a different antigen makeup from the latter:

1. The pathway of infection is different from the natural disease (i.e., direct confrontation with the antigenes by intramuscularly injection).

2. The time of infection is determined by the time of vaccination (e.g., all children in the third month), not by the susceptibility of the body or the "random" contact with the virus (readiness of the immune system).

3. The vaccine is an artificial product with additives modifying the action of the pathogen (modified antigen makeup).

For these reasons, vaccination and natural disease are difficult to compare with respect to their risk potential. Both harbour their own risks.

Another point should not be neglected: it is possible to develop tolerance to certain antigenes, the exact opposite of what has been described so far [27]. This principle is exploited by desensitising techniques used therapeutically against hay fever and allergic asthma: the patient is injected with small doses of the allergen (pollen, dust mites, etc.) in order to make them adept to it.

In a similar manner, the body may develop a tolerance for things that it would normally eliminate due to their harmful nature. Along these lines one could imagine a weakening of the immune response against certain pathogens, e.g., cancer cells:

"A derailment of the immune system may be responsible for the development of various tumours." [60] "Animal experiments have shown that the foetus, with its immature immune system, can develop a tolerance by exposing it to antigenes." [61] However, the exact time when the immune system has matured fully is unknown, and "other factors like age, genetic background, and nutritional status" [27] are also relevant to the induction of a tolerance.

Furthermore, the exact mechanisms leading to a antigen tolerance are still mostly in the dark. Therefore, according to current understanding, there exists a real possibility to develop a tolerance to surface antigenes of tumour cells induced by vaccines exhibiting a cross-reaction with tumour antigenes. As a consequence, tumour (cancer) cells would not be effectively recognized by the immune system and hence also not fully eliminated.

Especially when one thinks about the DTP immunization (Diphtheria, Tetanus, Whooping cough), which is given in the third month, such reactions seem possible. We don't yet fully understand the highly sensitive interplay between fight and tolerance in our immune system. What consequences our interference from outside bears is impossible to predict. Further study is badly needed in this area since we know of numerous other mechanisms involved in the development of autoimmune diseases (e.g., formation of immune complexes after infection following vaccination [64], etc.).

Purity of Vaccines

Another important issue is the purity of the vaccine. As already shown, several vaccines (MMR, polio) are produced by attenuation in living organisms or cell cultures (kidney cell cultures of monkeys). Despite the utmost cleanliness strived for, it is technologically impossible to exclude all possible risks of contamination entirely.

One such risk is, for example, the infestation of the sample by various viruses (slow virus, BSE, retro- viruses, onco-viruses, etc.) or mycoplasms (candida), all of which are difficult or impossible to detect because of their specific properties. "Virus contaminated cell cultures are a significant problem of the bio-industry." [28] In addition, the latency period of diseases caused by these contaminants is long enough. A causal connection is almost impossible to detect.
Live vaccines possess a higher risk of contamination with microorganisms than other vaccines. Oncogenetic (Cancer-causing) viruses are, for example, present in mammalian cell strains used in vaccine production. [64]

Live vaccines attenuated by conventional procedures are commonly carriers of unknown genetic modifications. Particularly when these modifications are only minor, like localized mutations, the danger of back mutation into a pathogenetic virus is possible. The difference, for example, between the Sabin strain and one of the virulent poliomyelitis strains is only the addition of one nucleotide. The mutation into neuro-virulent strains occurred with rabies vaccines and Sabin-polio strains (oral vaccination) of types 2 and 3 [64]. Another drawback of live vaccines lies in their possibility of complementation or recombination with closely related wild strains or vaccine strains. The likelihood and possible consequences of this are totally unknown.

Reference [64] poses important thoughts to the issue of vaccination risks.
Because vaccines are applied million-fold on entire populations, overlooked viral contaminations, back mutations, new mutations of the attenuated vaccine, or insufficient attenuation of the pathogene may have disastrous consequences for a large number of people. [30] Big immunization accidents happen not infrequently. Here are a few examples taken from the history of medicine: 102 people contracted encephalitis and 17 died 1944 in Brazzaville due to a yellow fever vaccination. A yellow fever vaccination contaminated with hepatitis virus was conducted in the US in 1942. The consequence was 28585 cases of hepatitis and 62 deaths. In 1955, the so-called Cutter incidence: 250 cases of polio and 10 deaths, due to active pathogenes in the vaccine. 1960 in Berlin, within four weeks there were 25 cases of paralytic poliomyelitis reported, after using an insufficiently attenuated vaccine. [56] Finally, 1988-92 the increase in encephalitis cases after MMR vaccination.

Undesirable reactions to vaccinations are often the consequence of toxic substances in the vaccine, "of contaminants which are not antigenes and have been introduced in the preparation of the vaccine (like, e.g., substances used in cell cultures on which the vaccine virus grows, or insufficiently purified bacteriological antigenes), or in-vivo replications of the viral or bacterial organisms. Hypersensitivity reactions may conceivably be due to additives to the vaccine, like, for example, neomycin in the MMR-vaccine or the mercury contained in Thimerosal, a preservative used in the DTP-vaccine." [25].

Development of Allergies

In today's paediatric practice(Children’s clinic) we try hard to delay a possible allergen contact of the baby in order to avoid hyper-allergic reactions later on (e.g. eczema, hay fever, allergic asthma, recently also hyper kinetic syndrome). A study of more than 2000 children showed that feeding them with cow milk during the first 9 months resulted in 7 times more frequent complaints of eczema afterwards [62]. Therefore, there are a large number of hypo allergic nutritional products on the market, used by many parents, even though the study could not confirm a connection between ingestion of milk protein and occurrence of eczema.

On the other hand, the children are already at a very early age aggressively exposed to foreign proteins (allergen’s) in the form of immunizations: BCG ( Tuberculosis) diphtheria, tetanus, pertussis, poliomyelitis, hemophilus influenzae, measles, mumps, rubella, meningitis and all the corresponding booster shots. Adding to this is the fact that the vaccines (with the exception of polio) come in direct contact with the blood circulation and hence are not subject to a antigen modification by, e.g., the gastro-intestinal tract.

Seeking to avoid contacts with allergenes on one hand, while massively promoting it on the other hand by means of vaccinations seems inconsistent. At least there ought to be studies aimed at investigating the connection between immunizations and subsequent atopias.

The Meaning of Childhood Diseases

What role the so-called childhood diseases play in the development of children has been subject of many discussions. Reports of developmental leaps are frequent, yet usually very subjective. There are, however, some observations that childhood diseases do not just harbour risks but can be quite useful.

In Annals of Tropical Paediatrics [53] the following case is reported: "1984 a 5 year old girl presented with a bad case of psoriasis( Form of Eczema). She showed large affected areas on her body and extremities, also involving to a significant degree her scalp. During the following year she was treated by Paediatricians and Dermatologists with coal tar preparations, local steroids, UV light, and dithranol wraps. Despite these therapies and two hospitalisations, the psoriasis was refractory and remained essentially unchanged until she came down with measles. As the measles rash began to spread over her skin, the psoriasis disappeared. Since then she has been free of psoriasis."

Another startling effect is described in Am. J. Med. Hyg.: "The prevalence of parasites and average density of malaria parasites is significantly lower in children who have had measles or influenza before the age of 9 than in the a symptomatic control group." [54]

An article taken from the Lancet, 1985, [55] may be of decisive importance: "Persons who have never had any visible indication of measles, i.e., never developed the skin rash of measles, suffer more frequently from non measles associated diseases." "The data show a highly significant correlation between lack of measles exanthema and auto-immune diseases, seborrhoeic (washing detergent related) skin diseases, degenerative diseases of the bones and certain tumours... We think that the rash is caused by a cell mitigated immune reaction, which destroys the cells infected with the measles virus. If this is correct, the missing exanthema may indicate that intracellular virus components have escaped neutralization during the acute infection. This may later lead to the aforementioned diseases... The presence of specific antibodies at the time of infection interferes with the normal immune response against the measles virus, in particular with the development of the specific cell mitigated immunity (and/or cyto-toxic reactions). The intracellular measles virus can then survive the acute infection and cause diseases manifesting in the adult age."
If the infection with measles happens at a time when there are already antibodies against the measles virus present, i.e., within the first few months after birth, or after administration of measles immune serum because of contact with measles, or after antibody production following vaccination, the immune system cannot react fully to the infection, leaving the virus the chance to become persistent.

If vaccinated children contract measles from the wild strain, the possibility exists that the infection will be overlooked in them, since they do not exhibit the typical signs of measles anymore. It is impossible to say how common these latent measles infections are; finding the connection between latent measles and a disease at adult age is impossible. If this suspicion proves to be true, the merit of the measles vaccination has to be re-evaluated entirely.

Level of Protection

A last word to the level of protection: parents who have their children immunized assume that they will not contract the diseases covered by the vaccine. Unfortunately this is not true to the degree that most parents assume.

Some examples:
A population in the Gaza strip, which was vaccinated to a density of 90%, suffered 2 outbreaks of poliomyelitis, 1974 and 1976. In these epidemics 34% and 50%, respectively, of all sick children had received 3-4 doses of the vaccine. The incidence of diseases was 18 per 100,000 [35].
Hungary had a vaccination program which reached a 93% vaccination density in the target population. A measles epidemic occurred in 1981. In contrast to earlier epidemics, the majority of the sick were vaccinated persons, i.e., about 60%.

During another epidemic between September 1988 and December 1989, there were 17938 cases of measles recorded (attack rate of 169 per 100,000), with the majority of cases reported in the vaccinated population (attack rates for the populations vaccinated in 1971 and 1972 were 1332 and 1632 per 100,000, respectively). The status of immunization was known of 12890 (76%) cases of measles. Of these, 8006 (62%) had been vaccinated. [29]

A measles epidemic broke out in an entirely vaccinated population of about 4200 students of three schools in the USA [38]. Further cases from the U.S. have been reported [46, 47, 48, 49, 50, 51]
Despite a vaccination density of 96%, Fife, Scotland, was afflicted by a measles epidemic in 1991/92. This was followed shortly thereafter by outbreaks of measles in other parts of the country, notwithstanding the high MMR vaccination density [45].

In Nashville, Tennessee (USA), occurred a large-scale mumps outbreak in the vaccinated population [43]. It has been shown that the immunization against mumps provides in many cases only a 75% protection [39, 40, 43]. Mumps is nowadays regarded to be a mild disease [41, 42].

In conclusion, we may say the following:

1. Vaccinations modulate the immune system. What exactly happens lies beyond the capabilities of today's scientific analysis.

2. In particular, long-term consequences of vaccinations are unknown because their existence is difficult to prove statistically

3. So-called minimal lesions [63] and their consequences are not included in statistical studies of vaccination-induced side effects.

4. Vaccinations do not give complete protection from the disease.

The decisive question one has to ask is whether the expected short-term benefit of vaccinations outweighs the potential long-term damage.

We all tend to concern ourselves only with the problems at hand. Illnesses and diseases, which threaten us, now are more important in our eyes than possible complaints in the future. The fear of post-measles encephalitis is bigger than the fear of the rheumatic pain of the 30 or 40-year-old adult. If, however, there is indeed a connection between vaccinations and autoimmune diseases or tumour growth, it is questionable whether the cost-benefit analysis of today is still applicable.

Considering that homeopathic treatment and prophylaxis can reduce the number of sequels in childhood diseases significantly, the practice of vaccination becomes even more doubtful.
Knowledge of the nature of chronic diseases as described by Hahnemann are prone to make the homeopathic physician very sceptical towards introducing pathogenes into the human body. (S. Hahnemann, Chronic Diseases, theoretical part)

Confirming Hahnemann's insights, the collective experiences of seasoned homeopathic physicians show that vaccinations pose an obstacle to cure, and that diseases frequently take their course after a vaccination. Furthermore, childhood diseases are usually managed easily, and unvaccinated children undergo a less complicated development as their vaccinated counterparts.

References
1. HOWSON CP, Adverse effects of Pertussis and Rubella Vaccines. Washington, DC; National Academy Press 1991
2. BARNES EK, Joint Reactions in children vaccinated against Rubella. Sudy II: Comparison of three vaccines. Am J Epidemiol 19972;95; 59-66.
3. COOPER LZ, Transient Arthritis after Rubella Vaccination, Am J Dis Child, 1969,118; 218-25
4. HORSTMANN DM, Post-Partum Vaccination of Rubella-susceptible Women, Lancet 1970;2; 1003-6
5. LERMANN SJ, Immunologic response, virus excretion and joint reactions with rubella vaccine, Ann Intern Med 1971;74;67-73
6. SPRUANCE SL, Joint complications associated with derivates of HPV-77 rubella virus vaccine, Am J Dis Child 1971:122: 105-11
7. SWARTZ TA, Clinical manifestations, according to age, among females given HPV-77 duck rubella vaccine. Am J Epidemiol 1971; 94; 246-51
8. THOMPSON GR, Acute arthritis complicating rubella vaccination, Arthritis Rheum 1971;14;19-26
9. WALLACE RB, Joint symptoms following an area wide rubella immunization campaign: report of a survey. Am J Public Health 1972;62; 658-61
10. WEIBEL RE, Influence of age on clinical response to HPV 77 duck rubella vaccine. JAMA 1972,222; 805-7
11. FORSEY T, Mumps vaccines-current status, J Med Microbiol, 41,1994,1-2
12. STRATTON KR, Adverse events associated with chilhood vaccines other than pertussis and rubella, JAMA, May 25, 271, No20, 1602-1605
13. FORSEY T, Mumps vaccines and meningitis, Lancet, 340, oct 17, 1992, 980
14. GRAY JA, Mumps meningitis following measles, mumps and rubella immunisation, Lancet, July 8, 1989, 98
15. MORRIS K, Gauillain Barre Syndrom after measles, mumps and rubella vaccine, Lancet, 343, Jan 1.1994,60
16. MILLER E, Risk of aseptic meningitis after measles, mumps and rubella vaccine in UK children, Lancet 341, April 17,1993,979-994
17. BUSINCO L, Measles, mumps, rubella immunization in egg-allergic children, Annals of Allergy, 72, Jan, 1994, 1-3
18. HOWSON CP, Chronic Arthritis after rubella vaccination, Clin Inf Dis, 15, 1992, 307-12
19. WYATT HV, Vaccine associated poliomyelitis, Lancet, 343, March 5, 1994, 609-10
20. SUTTER RW, Adverse Reaction to tetanus toxoid, JAMA, 271, May 25, 1994, 1629
21.ZASTROW KD, Tetanus-Erkrankungen, Impfungen und Impfschäden in der Bundesrepublik Deutschland 1971 bis 1990, Dtsch med Wschr., 118, 1993, 1617-1620
22. PELTOLA H, Frequenzy of true adverse reactions to measles, mumps, rubella vaccine, Lancet, april 26, 1986, 939-942
23. KALDEN JR; GERTH HJ, Polymyalgia rheumatica und Grippe Impfung, DMW 1992, 117, 1259
24. FORSEY T, Mumps vaccines -current Status, J Med Microbiol, 41, 1994, 1-2
25. GILSDORF JR, Vaccines: Moving into the molecular era, J Pediatr, Sept. 1994, 125, 339-44
26. EHRENGUT W; Komplikationen "nach" Mumpsschutzimpfungen in der Bundesrepublik Deutschland, Monatsschr. Kinderheilk, 1989, 137, 398-402
27. FRIEDMANN A, Oral Tolerance: A biologically relevant pathway to generate peripheral tolerance against external and self antigens, Chem Immunol, 1994, 58, 259-290.
28. RIVERA E, A new method for rapidly removing contaminating micro-organism from porcine parvovirus or pseudorabies virus master-seed suspensions, Vaccine 1993, 11(3), 363-5
29. AGOCS MM, The 1988-1989 measles epidemic in Hungary: assessment of vaccine failure, Int J Epidemiol 1992 oct, 21 (5), 1007-13
30. BROWN F, Review of accidents caused by incomplete inactivation of viruses, Dev Biol Stand, 1993, 81 (1), 103-7
31. BUCHWALD G, Impfen- Das Geschäft mit der Angst, 1994, EMU-Verlag.
32. CLARE D, Families win support for vaccine compensation claim, BMJ, Vol. 309, 24. Sept. 1994, 759.
33. BERR C, Risk factors in mulitple sklerosis: A population based case-controll study in Hautes-Pyrenees, France. Acta Neurol Scand (Denmark), Jul 1989, 80 (1), 46-50.
34. WHITE PM, Prevalence of antibody to poliovirus in England and Wales, Br Med J, Nov 1 1986, 293 (6555), 1153-5
35. LASCH EE, Combined live inactivated poliovirus vaccine to control poliomyelitis in a developing country five years after, Dev Biol Stand, 1986, 65, 137-43.
36. SUTTER RW, Paralytic poliomyelitis in Oman: association between regi onal differences in atack rate and variations in antibody responses to oral poliovirus vaccine. Int J Epidemiol, oct 1993, 22(5), 936-44.
37. WYATT HV, Unnecessary injections and paralytic poliomyelitis in India, Trans R Soc Trop Med Hyg, Sept-oct 1992, 86(5), 546-9.
38. MATSON DO, Investigation of a measles outbreak in a fully vaccinated school population including serum studies before and after revaccination. Pediatr Infect Dis J, Apr 1993, 12(4), 292-9.
39. GUIMBAO BJ, Parotitis in postvaccination period, Med Clin, 1993 Apr 10, 100(14),559.
40. SUAREZ J, Prevalence of anti-mumps IgG antibodies in a pediatric population, Enferm Infecc Microbiol Clin, Mar 1992, 10(3), 130-4.
41. FALK WA, The epidemiology of mumps in southern Alberta 1980-82, Am J Epidemiol, oct 1989, 130(4), 736-49
42. ARDAY DR, Mumps in the US army 1980-86, Am J Public Health, apr 1989, 79(4), 471-4.
43. WHARTON M, A large outbreak of Mumps in the postvaccine era, J Infect Dis, dec 1988, 158(6), 1253-60.
44. AGOCS MM, The 1988-1989 measles epidemic in Hungary: assesment of vaccine failure, Int J Epidemiol 1992 oct, 21(5), 1007-13.
45. CARTER H, Maesles outbreak in Fife; which MMR Policy, Public Health, 1993 Jan, 107 (1), 25-30
46. MARKS JS, Measles vaccine efficacy in children previously vaccinated at 12 month of age. Pediatrics 1978, 62, 955-60.
47. MARKS JS, Measles outbreak in a vaccinated schoolpopulation. AJPH 1987, 4, 434-38.
48. HERSH BS, A maesles outbreak at a college with prematriculation immunization requirement. Am J Public Health 1991, 81, 360-64.
49. DAIVIS RM, A persistent outbreak of measels despite appropriate prevention an control measures. Am J Epidemiol 1987, 126, 438-49.
50. HUTCHINS SS, A school-based measles outbreak, Am J Epidemiol 1990, 132, 157-68.
51. GUSTAFSON TL, Measles outbreak in a fully immunised secondary-school population. New England Journal of Medicine 1987, 316(13), 771-774.
52. BENDINER E, From Rabies to AIDS: 100 Years at Pasteur, Hosp Pract, Nov 30, 1987, 119-142.
53. CHAKRAVARTI VS, LINGAM S; Measles induced remission of psoriasis, Annals of Tropical Paediatrics, 1986, 6, 293-294
54. ROOTH IB, Suppression of plasmodium falciparum infections during measles or influenza, Am J Trop Med Hyg, Nov 1992, 47(5), 675-81.
55. R(NNE T, Maesles virus infection without rash in childhood is related to desease in adult life. Lancet, Jan 1985, 1-5.
56. BEALE AJ, Hazards of vaccine production, FEMS microbiol let 1992, 100, 469-474.
57. CLARKE JH, Praktische Materia Medica, 1994, S.1455
58. BRANDIS H, Medizinische Mikrobiologie 1994, S.268.
59. BARNETT LA, Molecular mimicry: a mechanismn for autoimmune injury, FASEB J, Feb 1, 1992, 840-4
60. ROITT IM, Immunologie 1991, S234ff
61. CLAASEN, Innere Medizin 1994, S.464
62. KELLER/WISKOTT, Kinderheilkunde 1991, S.380
63. COULTER H., Dreifachimpfung, ein Schuß ins Dunkle (DPT—a shot into the dark)
64. KIMMAN TG, Risks connected with the use of conventional and genetically engineered vaccines, Veterinary Quarterly , Aug 1992, Vol 14(3), 110-118

Views: 996

Comment by Gina Tyler DHOM on December 12, 2009 at 1:52pm
Hans wrote:"Confirming Hahnemann's insights, the collective experiences of seasoned homeopathic physicians show that vaccinations pose an obstacle to cure, and that diseases frequently take their course after a vaccination. Furthermore, childhood diseases are usually managed easily, and unvaccinated children undergo a less complicated development as their vaccinated counterparts............................................."
My reply:
I fully agree! Good article,thanks for posting this.
more on this subject from the prespective of homeopathic practicioners see link
www.hpathy.com
searchbox; EZINE november 2008
entire issue on vaccine damage and how homeopathy deals with it. Many interviews-
Comment by Gina Tyler DHOM on December 12, 2009 at 1:55pm
the Amish children in the usa are not vaccinated-no symptoms of autism in these children.All other children vaccinated in the USA stats; one in every 67 kids have autism
Comment by Hans Weitbrecht on December 13, 2009 at 5:39am
Gina, thanks for the info on amish children. Dr. Guillermo, yes -- there is no scientiffic basis of vaccination.
Comment by Ranga Sai on January 12, 2010 at 10:47am
Nice one Hans.

Grateful to Hahnemann, atleast we are equipped with the means to annhilate the side effects.

:-)
Comment by Jennifer Hautman on January 29, 2010 at 4:43am
Viera Sheibner's work refers to the Amish children, amongst others...
http://www.youtube.com/watch?v=pyja3Dnv84Y&feature=player_embedded
Comment by Tanya Nolte on January 31, 2010 at 2:04am
The Australian Veterinary Association have referenced research papers, on their pages for their Policy on Vaccination of Dogs and Cats (http://ava.informz.net/ava/data/images/documents/ava-vaccination-po...), re adverse reactions from over-vaccinating animals and the length of duration of immunity as being longer than they had thought etc, so now don't insist on annual booster shots for dogs & cats but instead recommend only having to give boosters for core vaccines triennially or even less frequently. This is a grateful advance for animals in that a 13 yr old dog or cat will have had 4 booster shots rather than 12 during it's life so less of an onslaught on it's immune system! At least some recognition of the damage vaccines are causing is being demonstrated by this recent change of protocol.
Comment by Gina Tyler DHOM on January 31, 2010 at 9:26pm
Hi Tanya,Even one vaccine shot is TOO MANY. My pets NEVER get any vaccines.
Comment by Gina Tyler DHOM on January 31, 2010 at 9:31pm
Dr. Charles E Loops DVM - "The first thing that must change with routine vaccinations is the myth that vaccines are not harmful.
Veterinarians and animal guardians have to come to realise that they are not protecting animals from disease by annual vaccinations, but in fact, are destroying the health and immune systems of these same animals they love and care for Homeopathic veterinarians and other holistic practitioners have maintained for some time that vaccinations do more harm than they provide benefits.

Vaccinations represent a major assault on the body's immune system.... Vaccine induced chronic diseases range from life-threatening conditions such as auto-immune crises to conditions destroying the quality of life of an animal as in chronic skin allergies." more can be found at www.shirleys-wellness-cafe.com
searchbox; pets and vaccines lots of articles from holistic homeopathic vets
Comment by Gina Tyler DHOM on January 31, 2010 at 9:42pm
The Science of Vaccine Damage Pets that have been vaccinated and those that are NOT vaccinated-
A team at Purdue University School of Veterinary Medicine conducted several studies 1,2 to determine if vaccines can cause changes in the immune system of dogs that might lead to life-threatening immune-mediated diseases. They obviously conducted this research because concern already existed. It was sponsored by the Haywood Foundation which itself was looking for evidence that such changes in the human immune system might also be vaccine induced. It found the evidence.

The vaccinated, but not the non-vaccinated, dogs in the Purdue studies developed autoantibodies to many of their own biochemicals, including fibronectin, laminin, DNA, albumin, cytochrome C, cardiolipin and collagen.

This means that the vaccinated dogs —
but not the non-vaccinated dogs—were attacking their own fibronectin, which is involved in tissue repair, cell multiplication and growth, and differentiation between tissues and organs in a living organism.

The vaccinated Purdue dogs
also developed autoantibodies to laminin, which is involved in many cellular activities including the adhesion, spreading, differentiation, proliferation and movement of cells.
Vaccines thus appear to be capable of removing the natural intelligence of cells.

Autoantibodies to cardiolipin are frequently found in patients with the serious disease systemic lupus erythematosus and also in individuals with other autoimmune diseases.
The presence of elevated anti-cardiolipin antibodies is significantly associated with clots within the heart or blood vessels, in poor blood clotting, haemorrhage, bleeding into the skin, foetal loss and neurological conditions.

The Purdue studies also found that vaccinated dogs
were developing autoantibodies to their own collagen.
About one quarter of all the protein in the body is collagen. Collagen provides struc­ture to our bodies, protecting and supporting the softer tissues and connecting them with the skeleton. It is no wonder that Canine Health Concern's 1997 study of 4,000 dogs showed a high number of dogs developing mobility problems shortly after they were vaccinated
( book, What Vets Don't Tell You About Vaccines).

Perhaps most worryingly, the Purdue studies found that the vaccinated dogs
had developed autoantibodies to their own DNA.
Did the alarm bells sound? Did the scientific community call a halt to the vaccination program?

No. Instead, they stuck their fingers in the air, saying more research is needed to ascertain whether vaccines can cause genetic damage. Meanwhile, the study dogs were found good homes, but no long-term follow-up has been conducted.

At around the same time, the American Veterinary Medical Association (AVMA) Vaccine-Associated Feline Sarcoma Task Force initiated several studies to find out why 160,000 cats each year in the USA develop terminal cancer at their

vaccine injection sites.
3 The fact that cats can get vaccine-induced cancer has been acknowledged by veterinary bodies around the world, and even the British Government acknowledged it through its Working Group charged with the task of looking into canine and feline vaccines4 following pressure from Canine Health Concern.
What do you imagine was the advice of the AVMA Task Force, veterinary bodies and governments? "Carry on vacci­nating until we find out why vaccines are killing cats, and which cats are most likely to die."

In America, in an attempt to mitigate the problem, they're vac­cinating cats in the tail or leg so they can amputate when cancer appears.
Great advice if it's not your cat amongst the hundreds of thousands on the "oops" list.

But other species are okay—right? Wrong.
In August 2003, the Journal of Veterinary Medicine carried an Italian study which showed that dogs also develop vaccine-induced cancers at their injection sites.

5 We already know that vaccine-site cancer is a possible sequel to human vaccines, too, since the Salk polio vac­cine was said to carry a monkey retrovirus (from cultivating the vaccine on monkey organs) that produces inheritable cancer. The monkey retrovirus SV40 keeps turning up in human cancer sites.

It is also widely acknowledged that vaccines can cause a fast-acting, usually fatal, disease called autoimmune haemolytic anaemia (AIHA). Without treatment, and frequently with treat­ment, individuals can die in agony within a matter of days.

Merck, itself a multinational vaccine manufacturer, states in The Merck Manual of Diagnosis and Therapy that autoimmune haemolytic anaemia may be caused by modified live-virus vaccines, as do Tizard's Veterinary Immunology (4th edition) and the Journal of Veterinary Internal Medicine.6 The British Government's Working Group, despite being staffed by vaccine-industry consultants who say they are independent, also acknowledged this fact.

However, no one warns the pet owners before their animals are subjected to boosters, and very few owners are told why after their pets die of AIHA.
Comment by Tanya Nolte on February 1, 2010 at 3:33am
Hi Gina, oh I totally agree with you that even one shot is too many!!! My animals dont' get ANY shots or boosters either...period. I am simply happy that at least there will be less vaccines dolled out for pets in Australia while people are still learning about the alternatives they can take with the use of homoeopathy INSTEAD of vaccinating. I offer material such as you have posted here amongst others to my clients and recommend to NOT vaccinate but I can only guide and warn but not insist. Many folks are still quite resistant or too afraid to go the homoeopathic route yet so I am grateful for the new policy for much less frequent vaccines. I will be even happier for those who do choose to go NO Vaccinating!!! :)

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