Impfungen
http://www.narayana-verlag.de/homoeopathie/pdf/Impfungen-Sinn-oder-Unsinn-Torako-Yui.09179.pdf ?? 18.03.2013
"As well consult a butcher on the value of
vegetarianism as a doctor on the worth of vaccination."
Bernard Shaw
Anhang (Tinus Smits)
Anhang. 2 (Wolfgang Hannig)
Anhang. 3
Anhang 4 (Dr Patricia Le Roux)
Anhang C (Catherine O’Driscoll)
Dr Elizabeth Wright Hubbard: It took
considerable experience for me to be convinced that the chronic constitutional
remedy is the best prophylactic.
Kinderkrankheiten und Impfen:
Wird das Durchmachen einer für den Organismus notwendigen Kinderkrankheit durch eine konventionell Impfung behindert, so gibt es keine Möglichkeit, sich von dem zur Zeit aktiven Miasma zu befreien. In der Regel
kommt ein Schwellprozess in Gang, der nicht selten ins Chronische abdriftet. Außerdem ist immer wieder feststellbar, dass eine Impfung nicht vor der Krankheit schützt, sondern diese nach einer Infektion bestenfalls
gedämpft abläuft. Was aber im Allgemeinen unter „gedämpft“ verstanden wird, ist – mit der homöopathischen Brille betrachtet – sehr fragwürdig. Da ziehen sich Krankheiten recht häufig unterschwellig in die Länge, ein Ausschlag kommt nicht richtig heraus o. der Organismus des Kindes ist nicht imstande, ein vernünftiges Fieber hervorzubringen.
Der Organismus ist seiner Selbstregulationsfähigkeit weitgehend beraubt!
So können also auch Röteln geimpfte Frauen in der Schwangerschaft wieder Röteln bekommen. Im Gegenteil: Bei durchgemachten Röteln liegt die Möglichkeit der Zweiterkrankung bei 3% (Virologin Dorothy Hartmann),
bei Geimpften bei 80%!!!
Die Impfviren können das Immunsystem nicht in der Weise stärken, wie die natürlichen „Wildviren“. Das zeigt sich zum Beispiel auch daran, dass die Antikörperkonzentration nach Impfung geringen ist als die nach natürlichen Erkrankungen. So sind also auch Säuglinge geimpfter Mütter schlechter geschützt! Nicht zu vergessen sind auch die so genannten Impfversager, die gar keinen Schutz bieten.
Impfung ist – auch bei Kinderkrankheiten – nicht gleichbedeutend mit der durchgemachten Krankheit! Weder wird lebenslange Immunität erzielt, noch werden Reifeprozesse beobachtet! Es kann kein Miasma aufgearbeitet werden und die Möglichkeit zu erkranken, wird auch nicht beseitigt – das zeigen die Erkrankungen nach Impfungen.
Vermeulen: Mehr Impfschäden nach Impfungen im Herbst und Winter.
Männer 4x von Impfschäden häufiger betroffen
Effects of vaccination:
Apis: Sudden puffing up of whole body
Arn.: sooths effect of vaccination
Malan.: Dry rough skin remaining for years
after vaccination.
Sil.: Abscesses or convulsions (also Thuja).
Abscess in axilla, whole arm swollen, backache, nausea.
Mez.: Eczema and itching
Sars. Blood purifier after vaccination. Itching
eruptions on face and skin.
Ant-t.: When Thuja fails and Silica is not
indicated.
Sulph.: When Sulphur symptoms prevail.
Sep.: When Sepia symptoms prevail
Thuj.: aborts effect of vaccination
To prevent side effects Hyp./Led.
Impfung und Homöopathie Hätte Hahnemann geimpft? Dr. Johann Loibner
Repertorium:
Im aktuellen „Complete Repertory" sind allein unter den Hauptrubriken 28 Rubriken zu diesem Punkt aufgelistet.
Gemüt: Angst nach Impfung: thuj.
Kopf: Entzündetes Gehirn - Enzephalitis; durch unterdrückte Hautausschläge - Ekzem durch Impfung: bac.
Kopfschmerz durch Impfung: thuj.
Augen: Entzündet nach Impfung: thuj.
------------------------------------- Bindehautenzündung: thuj.
------------------------------------- Keratitis, Cornea: vac. vario.
Magen: Schmerz im Allgemein nach Impfung: Thuj.
Übelkeit nach Impfung: Sil.
Rektum: Durchfall nach Impfung: ant-t. apis, sil. thuj.
Stuhl: < nach Impfung: apisin. thuj.
Atmung: Asthmatisch nach Impfung: thuj.
------------------------------------------ Kind: thuj.
Husten: nach Impfung: thuj.
Glieder: Abmagerung obere Gliedmaßen nach Impfung: maland. thuj.
--------- Hautausschläge – Pusteln auf Unterschenkel nach Impfung: sulph.
--------------------------- wie Varizellen nach Impfung: syc-co.
--------------------------- Lähmung der Beine nach Impfung: thuj.
--------------------------- eiterende Fingernägel nach Impfung: Thuj.
--------------------------- Nägelgeschwür – Umlauf nach Impfung: Thuj.
--------------------------- geschwollen in Arme – Schultern nach Impfung: apis, thuj.
----------------------------------------------------- Oberarme nach Impfung: Sil. sulph. Thuj.
Schlaf: Ruhelos nach Impfung: thuj.
Schlaflos nach Impfung: mez. thuj.
Haut: Hautausschläge Allgemein nach Impfung: crot-h. maland. mez. sars. skook. sulph. vario.
------------------------------------- Ekzem nach Impfung: ammc. kali-m. maland. mez.
Allgemeines: Nach Impfung:
acon. ant-t. apis, ars. bac. bapt. bcg, bell. bufo, carc. crot-h. diph. echi.
graph. gun. hep. kali-chl. lac-v. lepro. Maland. med. merc. merc-cy. Mez. nat-bic. Nit-ac.
ped. phos. psor. Puls. rhus-t. sabin. sarr.
sars. sep. SIL. skook. Stram. SULPH. syc-co. THUJ. Tub. Vac. vario. Zinc.
--------------------------------
Diptherieinfektionen: diph. merc-cy.
-------------------------------- Gelbfieber: ars.
-------------------------------- Meningitisinfektionen: apis
-------------------------------- Pocken: maland. thuj.
-------------------------------- Typhus: bapt.
-------------------------------- prophylaktisch vor Impfung: sulph. thuj. vario.
-------------------------------- Spasmen nach Impfung: Sil. thuj.
POLIO-IMPFUNG. Beschwerden nach: bell. caust. gels. hyper. lath. merc. phos. phys. plb. rhus-t.
PUSTELN nach Impfung: crot-h. hep. psor. sil. sulph.
------------ am Bein: sil. sulph.
------------ juckend. Brennend: psor.
------------ Am Kopf: sulph.
RÖTELN-IMPFUNG. Beschwerden nach: acon. ant-t. apis. bell. gels. phyt. rhus-t. sulph.
RÖTUNG, Erysipelatös: apis.
RÜCKENSCHMERZ: SIL.
SCHLAFLOSIGKEIT: apis. CARC. mez. Thuj.
SPRACHVERLUST: carc. Thuj.
TETANUS-IMPFUNG, Beschwerden nach: all-c. arn. cic. HYPER. LED. mill. phys. plan. sil. tetox. Thuj.
-------------------------- bösartig: mill.
-------------------------- Nach Verletzungen: all-c. hyper. led. Plan.
-------------------------- vorbeugend: ARN. HYPER. LED. phys. plan. tetox. Thuj.
TOLLWUT-IMPFUNG. Beschwerden
nach: agar. agav-a. anag. BELL.
calc. canth. cupr. cur. HYOS. iod. lach. laur. LYSS. scut. STRAM. verat
TUBERKULOSE beginnend: tub.
TUMORE: sil. thuj.
ÜBELKEIT: ip. SIL.
UMLAUF. Paronychie: sil. THUJ.
VORBEUGEND. prophylaktisch gegen erwartete Nebenwirkungen der Impfungen: arn. HYPER. LED. phys. plan. sil. sulph. tetox. thuj. vario
WACHSTUMSSTÖRUNGEN: BAR-C. CALC.
calc-f. CALC-P. CARC. ferr.
ferr-act. iod. irid-met. kreos. ph-ac. phos. sil
WINDPOCKEN, Infektion: acon. ANT-C. ant-t. ars. asaf. bell. canth. carb-v. caust. coff. con. cycl. hyos. ip. led. merc. nat-c. nat-m. PULS. RHUS-T. sep. sil. SULPH. thuj. vario
ZITTERN der Glieder nach der Zweitimpfung: thuj
Attenuierter Lebendimpfstoff
Lebendimpfstoffe enthalten abgeschwächte (attenuierte) Viren/Bakterien, die sich noch vermehren können und eine Immunantwort auslösen, in der Regel jedoch keine Erkrankung. Ein attenuierter Lebendimpfstoff
ist in der Regel deutlich wirksamer als ein Totimpfstoff.
In seltenen Fällen kann es nach der Anwendung eines solchen Impfstoffes bei der möglichen Vermehrung der Erreger zu einer Mutation in Richtung der nicht abgeschwächten Ausgangsform kommen, durch
die dann doch die Erkrankung eintreten kann. Beispiele hierfür sind die in Europa aufgegebene Polio-Schluckimpfung (hat sehr selten Impfpoliomyelitis ausgelöst), der MMR-Impfstoff/BCG/Gelbfieber.
Zur Typhus-Impfung stehen sowohl Lebend- als auch Totimpfstoffe zur Verfügung.
Lebendimpfstoffe werden unterschieden in:
1. kälte-adaptierte Stämme, die sich nur bei Temperaturen um 25 °C vermehren können, was die Viren auf die oberen Atemwege beschränkt, und
2. temperatur-sensitive Stämme, deren Replikation auf einen Temperaturbereich von 38 - 39°C beschränkt ist; es kommt auch hier nicht zum Befall der unteren Atemwege.
Totimpfstoff:
Totimpfstoffe enthalten inaktivierte o. abgetötete Viren o. Bakterien o. Teile von Viren/Bakterien/Giftstoffen. Diese können sich im Körper nicht mehr weitervermehren oder vergiften, wie es das Tetanospasmin
könnte, Aber sie lösen ebenfalls eine Abwehrreaktion (Immunreaktion) aus.
Beispiele sind die Toxoidimpfstoffe und Impfstoffe gegen Influenza/Cholera/Beulenpest = Haffkine/Hepatitis A./Masern/Mumps/Röteln/Typhus.
1. Toxoide: = entgiftete Toxine krankheitserregender Mikroorganismen. Diese Impfstoffe werden verwendet in denen Toxine die Krankheitssymptome verursachen, nicht die Erreger selbst (Tetanus/Diphtherie).
2. Inaktivierte Ganzpartikelimpfstoffe: Inaktivierung der Viren mittels einer Anwendung von Formaldehyd + beta-Propiolacton + Psoralen
3. Teilpartikelimpfstoffe: Zerstörung der Virusoberfläche mit Detergentien/starken organischen Lösungsmitteln
4. Untereinheitimpfstoffe o. Spaltvakzine: Oberfläche wird vollständig aufgelöst und spezifische Komponenten (Hämagglutinin- und Neuraminidase-Proteine) herausgereinigt. Eine andere Möglichkeit besteht darin,
die Untereinheiten rekombinant herzustellen. Untereinheitimpfstoffe sind wenig immunogen mit geringen Nebenwirkungen.
The live Mycobacterium tuberculosis vaccine
developed by Calmette and Guérin is not made of a contagious strain, but
contains a virulently modified strain called "BCG" used to elicit
immunogenicity to the vaccine.
Toxoid vaccines are made from inactivated toxic
compounds that cause illness rather than the micro-organism. Examples of
toxoid-based vaccines include tetanus and diphtheria. Toxoid vaccines are known
for their efficacy.
Not all toxoids are for micro-organisms; for
example, Crotalus atrox toxoid is used to vaccinate dogs against rattlesnake
bites.
Jedes 4e Jahr ist der Grippeimpfung nicht die reale Umständen angepasst.
Informationen: www.impfschäden.info.de
1. The problem of vaccinations and new vaccine
preparations:
We must try to understand why a child is
oversensitive and then expose the practical attitude to our everyday practice.
[Madeleine Bastide] Proposed suggestions, she
is professor in immunology University of Montpellier.
1st the
adverse effects obtained with certain vaccinations (Hepat B) are due to certain
relationships between viral antigens and self antigens.
2nd the
special method of preparing the vaccinating antigene (producer cells) may be
responsible for the wrong response of the body to the vaccination. Producer
cells are the basis for the fabrication of the
latest vaccinations. The Hep B
vaccination is cultivitated on cancerous, undifferential cells called producer
cells.
3rd the organism is not capable of analysing
the" strangeness" of those new vaccinations/so producing a self-immune
response.
Now back to the origins of the vaccinations and
Pasteur’s initial approach.
Sure Pasteur’s attitude to vaccination is now
been totally bypassed/swept away. Pasteur worked on a real identity: the
vaccine itself was the pathogenetic agent, and it was diluted or killed and
simply attenuated.
This is different in the new vaccinations. They
are genetically engineered/cultivated on producer cells/the pathogenic agent is
not found in these vaccination.
Pasteur’s principle of identity has been
abamdoned and so the immunity system has to adapt to a certain extent and
sometimes it responds in a perverse way. This explains the greater number of
accidents linked to
vaccination (connected with self-immune
diseases).
There is a real problem with the new
vaccinations.
The new vaccination against Hep A/Pert tends to
improve with each personal vaccination, but the immunity system can only try to
adapt as much as it can take and adverse effects may multiply.
Vaccination should only be done when there is a
complete agreement between the physician and the patient. This explains why the
character of legal obligation is not really acceptable from point of view of
the patients
freedom. We live in democracies/each family
should be able to evaluate the advantage/risk ratio, as in other pathologies,
decide on the vaccination or not.
Pert. has been implicated in the causation of
juvenile onset diabetes as the vaccine acts directly on the islets of
Langerhans/BCG is compulsary only in France (last country in Europe). It is an
interesting example because
the incidence of this pathology in France is
the same as in countries where the vaccination is not compulsary.
Vaccination program must be discussed with the parents/it
concerns their children and help them to take all aspects in consideration. A
vaccination program should be set up for their child as it is very important
for their
health, and each child is different and needs a
different approach.
To cure cases of oversensitive reaction to
vaccinations we can give antidotes to vaccination.
In a certain way we reverse what Pasteur would
have done 100 years ago on the perverse effects of the vaccination in order to
have an adequate response to vaccination.
We realise in pediatrics that most of our
patients with immunological disorders or allergic states, need antidotes to
their vaccinations to allow the action of the similimum.
If the bloquage state caused by vaccination on
a sensitive organism is not taken away by antidote, the result of a well
prescribed remedy will have no effect.
As a conclusion to these frequent problems, it
seems important to remember here that vaccinations initially have brought
progress and relief for severe diseases (small pocks!/Polio/Tetanus).
But vaccination can not solve all our health
problems/multiplying sophisticated vaccinations is leading to saturation of our
immunities.
It is also important to consider that
cancers/self immune diseases/AIDS are deeply linked to saturation of immunity.
Immunology as a speciality must be considered
the most holistically as possible. Its comprehension and function should lead
to a very different way of healing and open way to giving alternative medecines
their proper place
in this field.
2° Immunology and homeopathy:
We all know that the immune system has a
function of defense.
It is a system less systemisable as its
anatomical and functionnal process is present in the whole body
(thymus/marrow/ganglions).
This explains why several unconventional therapies,
far from a mechanical allopathic therapy, seem esp. well adapted to correcting
the impairments of the immunity system.
3 fundamental points that can help
us to understand this:
* The immunity system of mamals is totally
adapted to defending its own biological system/it is a hybrid system: ½
mechanical + ½ informational/it can produce double-faced molecules seving as
mediators between mechanics and information (cells that have a function of
representing the outside world to the body).
* The immunity system that works on the model
of the identy law (meaning pain curing pain) and that adapts to the defense
processes of the virus or the bacteria that is different from it, can then
develop wrong responses when vaccinations are made with cells identified as
agressor (virus/bacteria)
But if the law of similarity seeks to recognise
strangers, maybe the components of the vaccinations do not represent
sufficently the agressor . Therefore the immune system can reply in a perverse
way (self
immune
disease or allergy).
Vakzins
Attenuation (abgeschwächt) reduces the
virulence of a pathogen, while keeping it viable (or 'alive')
Ist counterpart is a vaccine produced by
'killing' the virus (= inactivated)
Examples of live vaccines include:
* viral: polio vaccine (Sabin vaccine),
Morb. Pert. rubella
vaccine/Varicellinum o. Varicell (= chicken pox vaccine)/yellow fever vaccine
* bacterial: BCG vaccine, typhoid vaccine
Viruses may be attenuated via passage of the
virus through a foreign host, such as: tissue culture/embryonated eggs/live
animals/the initial viral population is applied to the foreign host. In all
likelihood one of these will possess a mutation that enables it to infect the
new host. However this mutant will normally have a lower virulence in the
original host, as the rest of the genetic information for interacting with the
host hasn't changed, enabling it to infect them, but cause less damage, and so
it acts as a vaccine/in an attenuated vaccine live virus particles with very
low virulence are administered/they will reproduce, but very slowly/they do
reproduce and continue to present antigens beyond the initial vaccination, so
boosters are required less often. These vaccines are produced by growing the
virus in tissue cultures that will select for less virulent strains, or by
mutagenesis or targeted deletions in genes required for virulence. There is a
small? risk of reversion the virulence, this risk is smaller in vaccines with
deletions. Attenuated vaccines also cannot be used by immunocompromised (= mit
geschwächtem Immunsystem) individuals.
Advantages of attenuated vaccines: activates
all phases of the immune system (for instance IgA local antibodies are produced)/provides
more durable immunity; boosters are required less frequently/low cost/quick
immunity/easy to transport/administer
Disadvantages of attenuated Vaccines: Secondary
mutation can cause a reversion to virulence/can still cause disease, particularly
in immunocompromised patients (AIDS)/can be difficult to transport due to
requirement to maintain conditions (i.e. temperature) at which the virus can
"survive".
* Self-immunity can have a mechanic explanation
by the presence of true cross reactions against bacteria which, by provoking
antibodies responses would give way to self-immune disorders through antigenic
patterns.
In a different approach, to global awareness,
it can be a deeper disease in the organism, with a true loss of identity of the
patient, who’s immunity system in its function of protection of the living can
no longer differentiate, the self from the extraneous agressors.
The elimination process would therefore be this
error in identification on what an agressor can be.
We must try and go ahead in our thinking and
learning of homeopathy and realise how to feed the fire (sulfur fire of
course): this will then leed us to entire satisfaction.
Tinus Smits († 27-4-2010)
‡ Folgendes hat
anthroposofische Einschlüße ‡
Frei nach: Hans-Ulrich Albonico, M.D.
Swiss Campaign against Measles, Mumps and
Rubella Immunization
When the campaign was initiated in 1987, the
USA was cited as an example because 20 years of enforced vaccination in the
States had reduced the incidence of measles by 99%. Recent developments in the
USA give pause for thought, however.
Major measles epidemics have developed
repeatedly since 1982. Adolescents are increasingly affected, in spite of
vaccination, and so are infants, because mothers no longer confer adequate
immunity. Childhood diseases are more dangerous for both these age groups than
for other children. According to official statements, measles mortality has
increased by a factor of 10 in the USA. American experts refer to this as an
unexpected and partly inexplicable development. Warning voices are increasingly
heard among vaccination experts.
It may be said that the incidence in the U.S.
is still much lower than in the period preceding the mass immunization
campaign. One thing is abundantly clear there are compulsive elements to the
MMR immunization campaign that inevitably intervene profoundly in the sphere of
the individual. When obligatory immunization had enforced high levels of
compliance in many places, the unexpected epidemics necessitated rigorous
measures including quarantaine, exclusion from school, house-to-house
immunization. MMR re-immunization has already been made obligatory. Similar
reports are coming from other countries with high immunization rates.
Recent investigations in Switzerland and other
countries have also shown that in practice it is impossible to eradicate
measles, rubella and mumps. This deprives MMR vaccination strategies based on
mass immunization of young children of any kind of rational basis.
In Switzerland, measles, rubella and mumps
cannot be said to represent an emergency situation that would justify such
rigorous government intervention. Prevention of the serious complications of
these three childhood diseases relates to three entirely different spheres, and
a single combination vaccine cannot do justice to these.
The Medical Group for Differentiated MMR
Immunization and the Groupe Medical de Reflexion sur le Vaccin ROR are not
against immunization as such. They do, however, advocate a cautious approach,
taking account of the individual situation and of the specific problems of each
of the three childhood diseases, avoiding fundamental changes to their
epidemiology and respecting parents' freedom of decision.
The critical studies of the Swiss MMR
immunization campaign published in the two papers mentioned below result from
three years of fundamental research done by the Medical Group for
Differentiated MMR Immunization and the Groupe medical de Reflexion sur le
Vaccin ROR. Essentially they base on the following:
- Documents from the Swiss Federal Department
of Health (BAG) relating to the MMR campaign, especially information material
for the medical profession issued in 1987 and 1989.
- 30-page correspondence between the Group and
BAG.
- Detailed study of the specialist literature
on the subject.
- A. Tschumper and Th. Abelin's
study of the literature entitled Die Impfstrategien gegen Masem, Mumps und
Roetein (MMR-Impfung) im Lichte der epidemiologischen Literatur. Bern, December 1988.
- Correspondence and discussions with experts
in Switzerland, Germany, the USA - esp. the US Centers of Disease Control (CDC)
- on the subject of protective immunization, and Prof. Dr. D. Jachertz in Bern
(on matters of epidemiclogical concern).
- The professional experience of the c. 240
physicians in the two groups.
The Medical Group for Differentiated MMR
Immunization (est. in 1987) and the Groupe Medical de Reflexion sur Ie Vaccin
ROR (est. in 1988) include c. 240 Swiss medical practitioners whose aim is to
gain acceptance for a differentiated MMR immunization practice.
The fundamental aspects are presented in
leaflets for parents published by the groups which are entitled "Masem-,
Mumps- und Roeteln- Impfung - Warum die Eitern mitentscheiden sollen" and
"Vaccination ROR - Parents vous etes con-ceme's" (MMR immunization -
why parents should have a part in the decision). They may be obtained from the
Secretariat, Postfach 3009 Bern, Switzerland.
Smallpox = Pocken
Tb. have been linked to the smallpox vaccine.
Iimportant in understanding the significance of
smallpox vaccination is that smallpox and other communicable diseases were
declining before vaccination programs were enforced. This may be attributed to the
sanitation reforms and nutritional teachings instituted around the mid-1800’s
as much as to the vaccination programs as these other communicable diseases,
for which there was no vaccination, were also declining at the same rate.
However the incidence of smallpox actually
increased once vaccination programs were instituted. In Jenner’s time, there
were only a few hundred cases of smallpox in UK. After more than 15 years of
mandatory vaccinations, in 1870/1871 alone more than 23.000 people died from
the disease. Later, in Japan, nearly 29.000 people died in 7 years under a
stringent compulsory (re)vaccination program.
This increase in smallpox deaths was associated
with a noticeable lack of protection - not the best combination of events. In
Germany over 124.000 people died of smallpox during the same epidemic. All had
been vaccinated. Additionally, (unaltered) hospital records consistently show
that about 90 % of all smallpox cases occurred after vaccination.
This lack of efficiency and increase in disease
incidence, while other communicable diseases were declining, led to the refusal
of smallpox vaccination by some countries. This resulted in a drop of the
incidence of the disease that is quite remarkable. In Australia, when 2
children died from their smallpox shots, the government terminated compulsory
vaccinations. As a result, smallpox virtually disappeared in that country (3
cases in 15 years). When UK began to reject vaccination, then the incidence of
smallpox deaths decreased accordingly.
Assumed is that vaccination has made a
difference in incidence. Facts: from 1923 to 1953, before the Salk killed-virus
vaccine was introduced, the polio death rate in U.S. and UK had already
declined on its own by 47% and 55% respectively. Statistics show a similar
decline in other European countries. When the vaccine became available, many
European countries questioned its effectiveness and refused to systematically
inoculate their citizens. Yet, polio epidemics also ended in these countries as
well.
Additionally, as with smallpox vaccine, the
number of reported cases of polio following mass inoculations with the
killed-virus vaccine was significantly greater than before mass inoculations.
Though these facts are readily available, the mass vaccination against polio
has continued with the result that most of the cases of this dread disease are
now attributed to the vaccine.
In 1976, Dr. Jonas Salk testified that the
live-virus vaccine, used almost exclusively in the US since the early 1960’s,
was “the principle if not the sole cause” of all reported polio cases in the US
since 1961.
The Federal Centers for Disease Control
recently (Feb. 1992) admitted that the livevirus vaccine has become the
dominant cause of polio in the US today. According to CDC figures, 87% of all
cases of polio between 1973 and 1983 were caused by the vaccine. More recently,
from 1980 through 1989, every case of polio in the U.S. was caused by the
vaccine. During this same time period, 3 of 5 people that caught polio during
foreign travel were previously vaccinated against the disease.
Begleitend zu Polioimpfung: Sagitario sagitifolia,
Is very similar to canine distemper. The
measles vaccine was introduced in 1963, yet in the U.S./U.K.from 1915 to 1958,
a greater than 95 % decline in the measles death rate had already occurred. In
addition, the death rate from measles in the mid-1970’s (which was several
years post-vaccine) remained exactly the same as in the early 1960’s (pre-vaccine),
e.g., .03 deaths per 100.000. Again, the
efficacy of vaccination in prevention of this disease has not been established.
According to a study conducted by the W.H.O., chances are 14x greater that
measles will be contracted by those vaccinated against the disease than those
who are left alone. According to Dr. Atkinson of the CDC, “measles transmission
has been clearly documented among vaccinated persons. In some large
outbreaks.... over 95% of cases have a history of vaccination...”
In addition, of all reported cases of measles
in the U.S. in 1984, more than 58 % of the school age children were
“adequately” vaccinated. In 1985, the federal government reported 1.984
non-preventable cases of measles. But 80% of these so-called “non-preventable”
cases occurred in people who had been properly vaccinated. More recent
outbreaks continue to occur throughout the country,
sometimes among 100% vaccinated populations. In
spite of the evidence for lack of efficacy of this vaccine it is still strongly
promoted. This continued use of a useless vaccine, is not without its price. It
has been determined that the measles vaccine may cause ataxia/learning
disability/retardation/aseptic meningitis/seizure disorders/paralysis/death. It
has also been investigated as a possible cause of or cofactor for MS/Reye’s
syndrome/Guillain-Barre syndrome/blood clotting disorders/juvenile-onset
diabetes.
Another additional harmful effect is that the
disease has changed form, and now affects primarily a different age group. The
peak incidence of measles no longer occurs in children, but in adolescents and
young adults. The risk of complications of pneumonia (3%) and liver abnormality
(20%) have increased as a result.
Before the vaccine was introduced, it was
extremely rare for an infant to contract measles. However by 1993 more than 25
% of all measles cases were occurring in babies under 1 year. Centre for
Disease Control anticipates a worsening of this situation and attributes it to
the growing number of mothers who were vaccinated during the last 30 years and
therefore have no natural immunity to pass on to their children.
Whooping Cough (Pertussis)
Pertussis vaccine been connected with juvenile
onset diabetes as the vaccine acts directly on the islets of Langerhans (= insulin-secreting parts of the pancreas).
1. hypoglycæmia, 2. diabetes. This emphasises
the link between candidiasis and diabetes + Cand assimilating/fermentating
sugar. Use of Foll. successfully in candidiasis underlines the connection with
female sex hormones.
Incidence and severity of whooping cough had
begun to decline long before the pertussis vaccine was introduced in the
1940’s. From 1900 to 1935, in US/UK, before the pertussis vaccine was introduced,
the death rate from pertussis had already declined by 79 % and 82 %,
respectively.
Some studies indicate that the effectiveness of
the pertussis vaccine may be as low as 40- 45 + evidence indicates that
immunity is not sustained. During an epidemic in 1978, of 85 fully vaccinated
children, 46 (= 54%) developed whooping cough.
During a 10 month period in 1984, the state of
Washington reported 162 cases in age 3 months to 6 years, 49% had been fully
vaccinated against the disease. In the same year, of the 560 cases reported to
CDC in the age bracket of 7 months to 6 years with known vaccination status, 46
% had received vaccine protection. In 1986, in Kansas, 1300 cases of pertussis
were reported. Of the patients whose
vaccination status was known, 90 % were
“adequately” vaccinated.
There are several known or suspected harmful
effects from this vaccine. Includeding SIDS (Sudden Infant Death Syndrome -
research shows that children die at a rate 8x greater than normal within 3 days
after getting a DPT shot), encephalitis (the pertussis vaccine is used in
animal experiments to help produce anaphylactic shock/to cause an acute auto
immune encephalomyelitis), retardation and
learning disorders/fever as high as 106 degrees
- with pain/swelling/diarrhea/projectile
vomiting/sleePY/high-pitched
screaming/inconsolable crying bouts/seizures/convulsions, collapse/shock.
In the 20 months prior to July 31, 1992 - 250
deaths and 7,200 adverse reactions linked to whooping cough vaccinations had
been reported to CDC. In addition, the US Public Health Service announced that
as of Nov. 16, 1992, some 3,200 pertussis vaccine claims against the US
government had been filed.
Vaccination question looked at from several
aspects. We have looked at the way in which I think that routine vaccinations
can result in the production of chronic disease in animals and I have made some
specific suggestions of the symptoms that result. Also, we have considered the
question of vaccine effectiveness with the surprising evidence that vaccines do
not actually protect populations from disease - though they do seem to modify
the pattern in which the acute disease manifests.
Lebendimpfstoffe enthalten abgeschwächte (attenuierte) Viren/Bakterien, die sich noch vermehren können und eine Immunantwort auslösen, in der Regel jedoch keine Erkrankung. Ein attenuierter Lebendimpfstoff ist in der Regel deutlich wirksamer als Totimpfstoff.
In seltenen Fällen kann es nach der Anwendung eines solchen Impfstoffes bei der möglichen Vermehrung der Erreger zu einer Mutation in Richtung der nicht abgeschwächten Ausgangsform kommen, durch die dann doch die Erkrankung eintreten kann. Beispiele hierfür sind die in Europa aufgegebene Polio-Schluckimpfung, welche sehr selten die Impfpoliomyelitis ausgelöst hat, der MMR-Impfstoff, der Bacillus Calmette-Guérin sowie Impfstoffe gegen Gelbfieber.
Totimpfstoffe enthalten inaktivierte o. abgetötete Viren o. Bakterien o. Bestandteile von Viren, Bakterien o. Giftstoffen. Diese können sich im Körper nicht mehr weitervermehren o. ihn vergiften, wie es das Tetanospasmin könnte, Aber sie lösen ebenfalls eine Abwehrreaktion (Immunreaktion) aus. Beispiele sind die Toxoidimpfstoffe und Impfstoffe gegen Influenza, Cholera, Beulenpest oder Hepatitis A.
Totimpfstoffe werden unterschieden in:
* Toxoide: sind entgiftete Toxine krankheitserregender Mikroorganismen. Diese Impfstoffe werden in Fällen verwendet, in denen nicht die Erreger selbst, sondern vor allem deren Toxine die Krankheitssymptome verursachen (Tetanus/Diph).
* Inaktivierte Ganzpartikelimpfstoffe: Inaktivierung der Viren mittels einer kombinierten Anwendung von Formaldehyd, beta-Propiolacton und Psoralen
* Teilpartikelimpfstoffe: Zerstörung der Virusoberfläche mit Detergentien o. starken organischen Lösungsmitteln
* Untereinheitimpfstoffe o. Spaltvakzine: die Oberfläche wird vollständig aufgelöst und spezifische Komponenten (Hämagglutinin- und Neuraminidase-Proteine) herausgereinigt. Eine andere Möglichkeit besteht darin, die Untereinheiten rekombinant herzustellen. Untereinheitimpfstoffe sind nur wenig immunogen, besitzen dafür aber geringe Nebenwirkungen.
Lebendimpfstoffe wirken effizienter als Totimpfstoffe, da sie neben humoraler Immunität (eine durch in den Körperflüssigkeiten zirkulierende Antikörper bewirkte Form der Immunität) auch bis zu lebenslang anhaltende zelluläre Immunantworten auslösen.
Allerdings sind sie etwas schlechter in der Verträglichkeit und bergen das (sehr geringe) Risiko einer Rückmutation in Krankheitserreger und damit der Auslösung einer (meist abgeschwächten) Form der Erkrankung, gegen die sie ursprünglich schützen sollten.
Ferner sind nach aktuellen Empfehlungen des in Deutschland dafür zuständigen Robert-Koch-Instituts Lebendimpfungen ab 3 Monaten vor einer und während der gesamten Schwangerschaft kontraindiziert. Dagegen können fällige Impfungen mit Totimpfstoffen den werdenden Müttern im 2en und 3en Drittel der Schwangerschaft bedenkenlos verabreicht werden; im 1en Drittel sollten zum Ausschluss jeglichen Risikos für das Kind dagegen nur diejenigen Totstoff-Impfungen vorgenommen werden, die individuell dringend indiziert sind. In der anschließenden Stillzeit sind Impfungen generell ohne Beschränkungen möglich.
Unterschiedliche Lebendimpfstoffe können ohne Weiteres simultan verabreicht werden. Bei nicht gleichzeitiger Impfung soll der Abstand zwischen zwei Lebendimpfungen allerdings mindestens vier Wochen betragen. Totimpfstoffe oder eine Kombination mit ihnen betrifft dies nicht.
Impfung mit Endotoxine: (= in der Apotheke frei erhältlich) Bestandteil der äußeren Zellmembran von gramnegativen Bakterien/Blaualgen. Im Gegensatz zu den Bakterien, aus denen sie stammen, sind Endotoxine sehr hitzestabil (Sterilisierung).
Endotoxine gehören zu den Pyrogenen, sie können bei Kontakt mit Schleimhäuten und bei Übertritt ins Blut bei Menschen und manchen Tierarten Fieber erzeugen/aktivieren eine Reihe von Signalwegen von immunkompetenten Zellen, die entweder zu einer Entzündung o. zu einem programmierten Zelltod (Apoptose) dieser Zellen führen können. Sie sind schon in niedrigsten Konzentrationen (unterer pg/mL-Bereich) biologisch wirksam.
http://www.remedia.at/homoeopathie/suche.html?q=&gruppe=21
Arzneien in Gruppe Impfstoff
6- facher Impfstoff
ACT-HIB-plus-DPT
BCG Vaccine
Beriglobin P*
Bovigrip.
Bovilis BVD-MD
Bovilis IBR Marker
Diph Pert Tet Vaccinum
Diph Tet Vaccine
Dipht Tet Pert Hib Vaccine
Dipht Tet Pert IPV HIB Vacc.
Dipht Tet Pert IPV Vacc.
Dipht Tet Pert Polio - Vaccine
Dipht Tet Polio Vaccine (Pert.: Effekten danach)
FSME Vacc.
Gelbfieber
Grippe 2010/2011 #1
Grippe 2010/2011 #2
Grippe 2010/2011 #3
Grippeimpfstoff 2001/2002
Grippeimpfstoff 2002/2003
Grippeimpfstoff 98/99
Haemophilus B - Hepatitis B Vacc.
Haemophylus influenzae B Vacc.
Hepatitis A + B Vaccine, Erwachsene
Hepatitis A + B Vaccine, Kinder
Hepatitis A Impfstoff für Kinder
Hepatitis-B Vaccine
Humaner Papillomavirus Impfstoff
Influenza Virus Vaccine
Meningokokkenimpfstoff
MMR Vacc.
MMR-Impfstoff
Pneumococcen Vaccine A
Polio Sabin
Polio Vaccine
Rota Corona Vacc.
Tetanus Vaccine
Typhus Impfstoff oral
Vaccininum
Varizellen Lebendimpfstoff
Liste von Impfstoffen und
enthaltene Zusatzstoffen:
Acel-Immune DTaP - Diphtheria-Tetanus-Pertussis Wyeth-Ayerst 800.934.5556
diphtheria and tetanus toxoids and acellular pertussis adsorbed, formaldehyde, aluminum hydroxide, aluminum phosphate, thimerosal, and polysorbate 80 (Tween-80) gelatin Act HIB
Haemophilus - Influenza B Connaught Laboratories 800.822.2463
Haemophilus influenza Type B, polyribosylribitol phosphate ammonium sulfate, formalin, and sucrose
Attenuvax - Measles Merck & Co., Inc. 800-672-6372
measles live virus neomycin sorbitol
hydrolized gelatin, chick embryo
Biavax - Rubella Merck & Co., Inc.
800-672-6372
rubella live virus neomycin
sorbitol/hydrolized gelatin/human diploid cells from aborted fetal tissue
BioThrax - Anthrax Adsorbed BioPort Corporation
517.327.1500
nonencapsulated strain of Bacillus
anthracis aluminum hydroxide, benzethonium chloride, and formaldehyde
DPT - Diphtheria-Tetanus-Pertussis GlaxoSmithKline 800.366.8900 x5231
diphtheria and tetanus toxoids and acellular
pertussis adsorbed, formaldehyde, aluminum phosphate, ammonium sulfate, and
thimerosal, washed sheep RBCs
Dryvax - Smallpox (not licensed d/t expiration)
Wyeth-Ayerst 800.934.5556
live vaccinia virus, with "some
microbial contaminants," according to the Working Group on Civilian
Biodefense polymin B sulfate, streptomycin sulfate, chlortetracycline
hydrochloride, and neomycin sulfate glycerin, and phenol (obtained by
distillation of coal tar vesicle fluid from calf skins) Engerix-B
Recombinant Hepatitis B GlaxoSmithKline
800.366.8900 x5231
genetic sequence of the hepatitis B
virus that codes for the surface antigen (HbSAg), cloned into GMO yeast,
aluminum hydroxide, and thimerosal
Fluvirin Medeva Pharmaceuticals 888.MEDEVA
716.274.5300
influenza virus, neomycin,
polymyxin, beta-propiolactone, chick embryonic fluid
FluShield Wyeth-Ayerst 800.934.5556
trivalent influenza virus, types
A&B gentamicin sulphate formadehyde, thimerosal, and polysorbate 80
(Tween-80) chick embryonic fluid
Havrix - Hepatitis A GlaxoSmithKline
800.366.8900 x5231
hepatitis A virus, formalin,
aluminum hydroxide, 2-phenoxyethanol, and polysorbate 20 residual MRC5 proteins
- human diploid cells from aborted fetal tissue
HiB Titer - Haemophilus Influenza B
Wyeth-Ayerst 800.934.5556
haemophilus influenza B,
polyribosylribitol phosphate, yeast, ammonium sulfate, thimerosal, and
chemically defined yeast-based medium
Imovax Connaught Laboratories 800.822.2463
rabies virus adsorbed, neomycin
sulfate, phenol, red indicator human albumin, human diploid cells from aborted
fetal tissue
IPOL Connaught Laboratories 800.822.2463
3 types of polio viruses neomycin,
streptomycin, and polymyxin B formaldehyde, and 2-phenoxyethenol continuous
line of monkey kidney cells
JE-VAX - Japanese Ancephalitis Aventis Pasteur USA 800.VACCINE
Nakayama-NIH strain of Japanese
encephalitis virus, inactivated formaldehyde, polysorbate 80 (Tween-80), and
thimerosal mouse serum proteins, and gelatin
LYMErix - Lyme GlaxoSmithKline 888-825-5249
recombinant protein (OspA) from the
outer surface of the spirochete Borrelia burgdorferi kanamycin aluminum
hydroxide, 2-phenoxyethenol, phosphate buffered saline
MMR - Measles-Mumps-Rubella Merck & Co.,
Inc. 800.672.6372
measles, mumps, rubella live virus, neomycin
sorbitol, hydrolized gelatin, chick embryonic fluid, and human diploid cells
from aborted fetal tissue
M-R-Vax - Measles-Rubella Merck & Co., Inc.
800.672.6372
measles, rubella live virus neomycin
sorbitol hydrolized gelatin, chick embryonic fluid, and human diploid cells
from aborted fetal tissue
Menomune - Meningococcal Connaught Laboratories
800.822.2463
freeze-dried polysaccharide antigens
from Neisseria meningitidis bacteria, thimerosal, and lactose
Meruvax I - Mumps Merck & Co., Inc.
800.672.6372
mumps live virus neomycin sorbitol
hydrolized gelatin
NYVAC - (new smallpox batch, not licensed)
Aventis Pasteur USA 800.VACCINE
highly-attenuated vaccinia virus,
polymin B, sulfate, streptomycin sulfate, chlortetracycline hydrochloride, and
neomycin sulfate glycerin, and phenol -a compound obtained by distillation of
coal tar vesicle fluid from calf skins
Orimune - Oral Polio Wyeth-Ayerst 800.934.5556
3 types of polio viruses, attenuated neomycin,
streptomycin sorbitol monkey kidney cells and calf serum
Pneumovax - Streptococcus Pneumoniae Merck
& Co., Inc. 800.672.6372
capsular polysaccharides from
polyvalent (23 types), pneumococcal bacteria, phenol,
Prevnar Pneumococcal - 7-Valent Conjugate
Vaccine Wyeth Lederle 800.934.5556
saccharides from capsular
Streptococcus pneumoniae antigens (7 serotypes) individually conjugated to
diphtheria CRM 197 protein aluminum phosphate, ammonium sulfate, soy protein,
yeast
RabAvert - Rabies Chiron Behring GmbH &
Company 510.655.8729
fixed-virus strain, Flury LEP neomycin,
chlortetracycline, and amphotericin B, potassium glutamate, and sucrose human
albumin, bovine gelatin and serum "from source countries known to be free
of bovine spongioform encephalopathy," and chicken protein
Rabies Vaccine Adsorbed GlaxoSmithKline
800.366.8900 x5231
rabies virus adsorbed,
beta-propiolactone, aluminum phosphate, thimerosal (=
Natrium-2-(ethylmercurithio) benzoat = Zusatzstoff in Impfungen), and phenol,
red rhesus monkey fetal lung cells
Recombivax - Recombinant Hepatitis B Merck
& Co., Inc. 800.672.6372
genetic sequence of the hepatitis B
virus that codes for the surface antigen (HbSAg), cloned into GMO yeast,
aluminum hydroxide, and thimerosal (= Natrium-2-(ethylmercurithio) benzoat =
Zusatzstoff in Impfungen)
RotaShield - Oral Tetravalent Rotavirus
(recalled) Wyeth-Ayerst 800.934.5556
1 rhesus monkey rotavirus, 3
rhesus-human reassortant live viruses neomycin sulfate, amphotericin B
potassium monophosphate, potassium diphosphate, sucrose, and monosodium
glutamate (MSG) rhesus monkey fetal diploid cells, and bovine fetal serum
smallpox (not licensed due to expiration)
40-yr old stuff "found" in
Swiftwater, PA freezer Aventis Pasteur USA 800.VACCINE
live vaccinia virus, with "some
microbial contaminants," according to the Working Group on Civilian
Biodefense polymin B sulfate, streptomycin sulfate, chlortetracycline
hydrochloride, and neomycin sulfate glycerin, and phenol -a compound obtained
by distillation of coal tar vesicle fluid from calf skins
Smallpox (new, not licensed) Acambis, Inc.
617.494.1339 in partnership with Baxter BioScience
highly-attenuated vaccinia virus,
polymin B sulfate, streptomycin sulfate, chlortetracycline hydrochloride, and
neomycin sulfate glycerin, and phenol -a compound obtained by distillation of coal
tar vesicle fluid from calf skins
TheraCys BCG (intravesicle -not licensed in US
for tuberculosis) Aventis Pasteur USA 800.VACCINE
live attenuated strain of
Mycobacterium bovis monosodium glutamate (MSG), and polysorbate 80 (Tween-80)
Tripedia - Diphtheria-Tetanus-Pertussis Aventis Pasteur USA 800.VACCINE
Corynebacterium diphtheriae and Clostridium tetani
toxoids and acellular Bordetella pertussis adsorbed aluminum potassium sulfate,
formaldehyde, thimerosal (= Natrium-2-(ethylmercurithio) benzoat = Zusatzstoff
in Impfungen), and polysorbate 80 (Tween-80) gelatin, bovine extract
US-sourced Typhim Vi - Typhoid Aventis Pasteur USA SA 800.VACCINE
cell surface Vi polysaccharide from Salmonella
typhi Typ2 strain, aspartame, phenol, and polydimethylsiloxane (silicone)
Varivax - Chickenpox Merck & Co., Inc.
800.672.6372
varicella live virus neomycin
phosphate, sucrose, and monosodium glutamate (MSG) processed gelatin, fetal
bovine serum, guinea pig embryo cells, albumin from human blood, and human
diploid cells from aborted fetal tissue
YF-VAX - Yellow Fever Aventis Pasteur USA
800.VACCINE
17D strain of yellow fever virus
sorbitol chick embryo, and gelatin
Adjuvantien für
Humanimpfstoffe
Bezeichnung/Handelsname Typ, Zusammensetzung/Aufbau Beschreibung, Verwendung
Aluminiumhydroxid Anorganische Verbindung, Gelstruktur. Aluminiumhydroxid bindet das Antigen durch Adsorption und setzt es langsam frei. Verwendung als Adsorptionsmittel in Tetanus-/Diphtherie-/Pertussis-/Hepatitis A-Impfstoff
MF59 Öl-in-Wasser-Emulsion. Squalen/Polysorbat 80/Sorbitantrioleat Nach Injektion geht MF59 schnell in das Lymphsystem über und beschleunigt die Aufnahme der Antigene in das Immunsystem. Verwendung als Wirkverstärker in Influenza-Impfstoffen
AS03 Öl-in-Wasser-Emulsion. Squalen/Polysorbat 80/DL-α-Tocopherol Verwendung als Wirkverstärker in Influenza-Impfstoffen wie z. B. Pandemischer Influenza-Impfstoff A/H1N1 (Pandemrix)
MPL Monophosphoryl-Lipid A (gereinigtes Derivat von Lipopolysacchariden aus Bakterienzellwänden von Salmonella minnesota). Bestandteil von kombinierten Adjuvantien (Adjuvant Systems, AS)
QS21 Oberflächenaktiver Stoff (Saponin) aus Rinde von Quill Verwendung als Matrix in den sogenannten ISCOMs (immunstimulating complexes) und in den kombinierten Adjuvantien
AS04 Kombiniertes Adjuvans.
Komplex aus MPL und Aluminiumhydroxid bzw. Aluminiumphosphat Aktivierung des Toll-like-Rezeptors TLR4. Bestandteil in Fendrix (Hepatitis B-Impfstoff), Cervarix (HPV-Impfstoff)
AS01 Kombiniertes Adjuvans.
Liposomen, MPL und QS21. Aktivierung von Toll-like-Rezeptoren, experimentelle Verwendung
AS02 Kombiniertes Adjuvans.
Öl-in-Wasser-Emulsion, MPL und QS21. Aktivierung von Toll-like-Rezeptoren, experimentelle Verwendung (Entwicklung Malaria-Impfstoff)
IC31 Kombination des Peptids KLK mit dem Oligodesoxynukleotid ODN1 Aktivierung des Toll-like-Rezeptors TLR9. Experimentelle Verwendung (Entwicklung von Impfstoffen gegen Malaria/Influenza/Tb)
CpG ODN Immunstimulierende DNA-Sequenzen (ISS) aus synthetisch hergestellten Oligonukleotiden mit CpG-Motiven experimentelle Verwendung in der Entwicklung von Hepatits B- und Influenza-Impfstoffen
ISCOMATRIX Hersteller: CSL Behring. Besteht aus dem gereinigtem Quillariasaponin QS21, Cholesterol und Phospholipiden der Zellmembran, welche unter geeigneten Bedingungen 40-50 nm große "Käfigstrukturen" ausbilden experimentelle Verwendung in Humanimpfstoffen (zugelassen in Impfstoffen gegen Pferdeinfluenza)
Virosomen Doppelmembran aus Phospholipiden (Liposomen), in die die die viralen Antigenstrukturen (z.B. Influenzavirus A-Hämagglutinin und Neuraminidase) eingebaut werden; rekonstituierte („künstliche“) Virushülle. Einsatz in Hepatitis A-Impfstoffen wie HAVpur und Epaxal
SALK-Vakzine (= Lebendvakzin des Polios/hergestellt mit Form).
Thimerosal (= Natrium-2-(ethylmercurithio) benzoat = Zusatzstoff in Impfungen)/Quelle: Remedia.at
Using Thimerosal as a remedy could be
considered allopathic thinking. It's treating the cause of the illness. In
homeopathy, sometimes "why" is not necessarily as important.
Classical homeopathy addresses the symptom picture and finds the one simillimum
to match. Unless you consider the thousands of children who have been vaccinated
with thimerosal containing vaccines and the resulting disorders the proving,
thimerosal would probably not be considered a simillimum.
Arguing that these children *are* the proving
of Thimerosal. And while it may or may not be their simillimum, is a false
picture of who they are. In other words, the thimerosal masks the true
constitution. Believing a person's constitution can change and never more so
than when an artificial substance has effected them. A person is completely
different drunk from being sober. The alcohol would cover up who the person
really is and what his real traits and characteristics are. Unless perpetually
drunk, the effects of the alcohol are temporary. This cannot be said for the
effects of Thimerosal (and other vaccines).
There are some homeopaths who have had
astounding success treating children (and adults) the very way described. Tinus
Smits has some truly impressive cure stories and his understanding of autism is
admirable (check out the new article on autism on his site, including a good grasp
of glutathione). And there are also homeopaths practicing what is considered
sequential homeopathy who address the vaccine insults. I cannot attest to their
successes as I have no experience of it although I have read reports of
improvements from other parents on various lists. But their approach is very
different than classical homeopathy.
Given my son recovered from an
"isopath" (the DPT remedy), I can only attest it worked for him.
However, it has been his "one" remedy for a little over 3 years. It
could be reasoned, the DPT remedy *is* his simillimum which some would argue is
the only way the isopath would bring true cure. As a side note, I find it
curious others refer to the DPT remedy as a nosode as it is not made from the
diseases themselves. It is made from one ingredient like other remedies. It is
made from the actual DPT shot with thimerosal. I know there are homeopaths who
feel this isn't good homeopathic practice and in their experience, people
treated with a nosode or anything other than a traditional constitutional
remedy may not experience the long lasting, permanent "cures" but a
temporary amelioration. Only time will tell if that is true for us.
In the mean time, it is my own personal opinion
that like anything else, with time, we learn to improve upon our knowledge. To
be rigid in treatment, may miss an opportunity for healing for many. Hahnemann
himself (the founder of homeopathy) revised his methods during his lifetime
leading to several editions of the Organon. (Note to newbies: the Organon is
the book written by Hahnemann outlining the principles of homeopathy and its
practice.) Water dosing was a "new" development from him which went
unnoticed for years and years. Now, many homeopaths will only dose in water
because it is seen as superior to dry dosing. This doesn't mean dry dosing
doesn't work. Of course it does. But what it means is that Hahnemann was
continuing to learn and improve upon his craft. I believe this type of learning
and growing should continue in homeopathy.
Never before in our time, have our children
been subjected to such an assault to their vital force. The majority have been
injected with unclean antigens and adjuvants in the form of vaccine at birth!
Most major hospitals in the US made it policy to inject Hep B (which did
contain thimerosal) into babies within 24 hours of birth. Additionally, almost
all babies in the states are injected with Vitamin K which contains its own
adjuvants. Their immune systems are not only fully undeveloped, but they are
not even as yet fully incarnated. Add to that the routine use of ultrasound,
pitocin, brethine, and all the other drugs and interventions given to women
during pregnancy these days and it is no wonder we are facing a nation of ill
children. Couple that with air pollution, fish pollution, and the unhealthy
state of many diets, it is almost inevitable.
Moreover, as each generation evolves, I think
we are seeing children who are "more" of everything - more sensitive,
more intelligent, and more susceptible. We need to evolve with these changes
and how we address them.
This does not mean I think every parent should
run out and give their child Thimerosal remedy. It is so important to work with
a qualified homeopath who has the training and experience to know what to do.
We are only at the tip of the iceberg when it comes to treating spectrum
disorders. But I do think keeping an open mind is critical for success.
Zu den ältesten immunologischen Emulsionsadjuvantien zählen das inkomplette Freund-Adjuvans (IFA), eine mit einem Emulgator stabilisierte experimentell verwendete Wasser-in-Öl-Emulsion auf Mineralölbasis und das Adjuvans 65, eine Wasser-in-Öl-Emulsion mit Erdnussöl. Beide führen wegen ihrer ausgeprägt öligen Eigenschaften zu einer starken Gewebereizung.
Mit Gentechnik hergestellt sind Vaccin Hepatitis B und Vaccin Pertussinum
Impfungsnosoden:
DiTePo (Diphterie, Tetanus, Polio)
DiTePoPe (Diphterie, Tetanus, Polio, Pertussin)
MMR (Mumps. Masern, Röteln)
DiTe (Diphterie, Tetanus)
(alle Schmidt-Nagel)
Diph-pert-t.= Impfung DPT
Diph-t-tpt = Impfung DTTP
Impffolgen vorbeugen: Mit 1er Impfung warten bis Kind mündlich angeben kann, dass es Kopfschmerz hat. (ist meist 1er Beschwerde bei Impfschade).
Impffolgen Akut: Acon: FieBER, trockne Haut/DURST/Unruhe
Ant-t: Impfung während Atemwegebeschwerden wenn Thuj. versagt und Sil. nicht angezeigt ist.
Apis: Impfstelle HEIß/geschwollen/Ausschlag (Erypsel/schmerzlose Durchfall)/frösTELT + < warmes Zimmer/durstlos
Ars: SCHWACH/Atemnot/langsames FieBER/ängstlicher Ausdruck/unruhig
Crot-h: Haut entzündet/dunklen Bläschen/brennen
Echi: Impfung aus Tierserum/Blutvergiftung
Gun: Allgemein Empfinden SCHLECHT, Abszessen rezidivierend, Blutvergiftung
Hep: Abszess/Eiterung
Kali-m: AppeTIT + Essen = unverträglich/schläfrig nach essen, schwach + reizbar
Malan: Pustulösen Ausschlag/Kopfschmerz/Rückengradschmerz
Mez: Juckender Ausschlag = < Wärme/Waschen, Krusten + Eiter
Perla = Zuchtperle
Rhus-t: Ausschlag (Bläschen mit rotem Hof), BrenNEN + jucKEN
Sars: Hautausschlag trocken o. ätzEND, < waschen/nass-kaltes Wetter/Periode Kratzen lässt Juckreiz Ort wechseln, Abmagerung
Sil: Fieber, Hirn-/Ohrenentzündung, geimpftes Körperteil = geschwollen/Impfstelle entzündet, Abszess/Geschwür an Lymphknotem, Bläschen
Ohren/Gesicht/Beinen. Krampf
Thuj: durchfall
Vacc: Chronische Depression/Psychose/lauNISCH, weinerlich/vergesslich,
KopfSCHMERZ, schwach, Appetitverlust + Nahrungsmittelunverträglichkeit
Vario: Herpes + SCHMERZ, Muskeln tun weh/Fieber
Impffolgen chronisch: Bufo. Cars.
Syph. Stram. Tub.
After vaccination:
Mind: anxiety: thuj.
Head: Inflamed brain from suppressed eruption
(eczema) from vaccination: bac.
headache in general from vaccination: thuj.
Eyes: Inflammation (in conjunctivae): thuj. Of
cornea, keratitis: vac. vario.
Stomach: Pain in general: Thuj.
Nausea: Sil.
Rectum: Diarrhea: ant-t. apis, sil, thuj.
Stool: apisin. thuj.
Respiration: asthmatic: thuj. (children)
Cough: thuj.
Extremities: Emaciation of upper limbs: maland. thuj.
Eruptions: Pustules on Leg: sulph./like
varicella: syc-co.
Paralysis of lower limbs: thuj.
Suppuration of finger nails: Thuj.
Felon/onchyia/paronhia run-around: Thuj.
Swelling of shoulder: apis, thuj./of upper arm:
sil. sulph. thuj.
Sleep: Restless: thuj.
Sleepless: mez. thuj.
Skin: Eruptions in general: crot-h. maland. mez.
sars. skook. sulph. vario.
Eczema: ammc. kali-m. maland. mez.
Generalities: acon. ant-t. apis, ars. bac. bapt. bcg, bell.
bufo, carc. crot-h. diph. echi. graph. gun. hep. kali-chl. lac-v. lepro.
Maland. med. merc. merc-cy. Mez. nat-bic. ped. phos. psor. rhus-t. sabin. sarr.
sars. sep. SIL. skook. SULPH. syc-co. THUJ. Tub. Vac. vario.
after diphtheria injections: diph. merc-cy.
After Yellow fever vaccination: ars.
after Meningitis injections: apis
Begleitend zu Polioimpfung: Sagitario
sagitifolia,
After Smallpox vaccination: maland. thuj.
after Typhus: bapt.
Prophylactic: sulph. thuj. vario.
Convulsions: Sil. thuj.
Vaccinations: Use the Isode of the vaccination
given.
Wirkung: sycotisch
Allerlei:
Perla Künstliche Entstehung: Herstellung von Zuchtperlen geschieht durch Implantierung eines mit Epithelzellen einer anderen Perlmuschel beschichteten Zuchtkerns ins Muschelinnere („Wie Impfung“)
Sechsfachimpfstoff (= Hexavalente Impfstoff): Polio (Kinderlähmung)/Diphtherie/Tetanus/Pertus (Keuchhusten)/Haemophilus influenzae Typ B/Hepatitis B.
Durch Lebendimpfstoff kann bei der möglichen Vermehrung der Erreger zu einer Mutation in Richtung der nicht abgeschwächten Ausgangsform kommen, durch die dann die Erkrankung eintreten kann. Z.b. Polio-Schluckimpfung/MMR-Impfstoff/Bacillus Calmette-Guérin/Impfstoffe gegen Gelbfieber/Schweinegrippe.
Vorwort/Suchen Zeichen/Abkürzungen Impressum