Drogen allgemein Anhang e
Vergleich: Siehe: Herstellen von Mittel
[Nils Metzger]
Seit einem Jahr liefen die Ermittlungen gegen das Netzwerk der mutmaßlichen Drogenschmuggler. Ausgangspunkt waren Pakete, die Ende 2022 am Flughafen Köln/Bonn inspiziert wurden. Versteckt in Bremszylindern fand man damals 59.000 Captagon-Tabletten, kurz darauf am Flughafen Leipzig 32 Kilogramm, versteckt in Duftkerzen.
Die Pakete hätten in die arabischen Golfstaaten, nach Saudi-Arabien und Bahrain gehen sollen. Nun stießen sie in einem angemieteten Garagenlager in Herzogenrath nahe Aachen auf ein Hauptlager mit mehreren Millionen Captagon-Pillen.
Das Amphetamin Captagon war vor Jahrzehnten vor allem im Sport-Doping
beliebt, es putscht auf und macht extrem abhängig. Doch seit einigen Jahren
erlebt es eine dramatische Renaissance in Folge des Syrien-Kriegs. Kämpfer
aller Seiten benutzen es, manche der Gräueltaten des Krieges werden auch auf
den Einfluss der Droge zurückgeführt. Auch bei an den Massakern in Israel
beteiligten Hamas-Kämpfern sollen Tabletten gefunden worden sein.
Hinter dieser Drogen-Welle stehe die syrische Regierung, betont der Islamwissenschaftler
Caspar Schliephack, der für die Konrad-Adenauer-Stiftung ein Papier zum
Captagon-Problem verfasst hat. Für Diktator Baschar al-Assad sei Captagon eine
"überlebenswichtige Einnahmequelle".
Das Assad-Regime baute die
Produktion von synthetischen Drogen massiv aus und erlangte so die Kontrolle
über ein Multi-Milliarden-Business.
Mittlerweile werden in Syrien synthetische Drogen wie Captagon im
industriellen Ausmaß produziert und professionell verschifft.
[Ratan Singh]
Abstract: A common hurdle in the
treatment of the mentally ill is the intolerable side effects of allopathic
psychiatric drugs (APD) because of their toxicity. Patients for this reason
take the APD irregularly or altogether stop them and drop out of treatment or
they try alternative therapists including homeopathic physicians. The homeopath
finds himself faced with two problems, that is, not just to alleviate the
symptoms of the original illness but also to alleviate the iatrogenic symptoms
caused by APD. In fact patients often come with the request to help them stop
the APD. Often the case is that patients have already struggled to stop the APD
but have had to return to APD intake because of drug withdrawal reactions. In
this article, a solution to this problem is proposed in the form of serial and
ultrahigh dilutions of APD. Such a dilution can be used without stopping the
APD or with slow tapering of the APD. Some evidence of beneficial effect of APD
dilution so familiar among homeopathic circles is cited as example of relief to
the patient who otherwise finds himself a prisoner of APD.
Keywords: Side effects, Toxicity, Serial Dilution,
Ultrahigh Dilution, Mental illness.
Mental health practitioners today face the problem of toxic side effects of
allopathic psychiatric drugs (APD). Many a patient suddenly drops out and stops
taking these drugs or uses them irregularly and searches for alternate
therapies. Orthomolecular psychiatrists, homeopathic physicians and clinical
psychologists often face this problem because often their patients are on
allopathic psychiatric drugs (APD) that hinder the effect of these alternate
therapies including the homeopathic medicines. Prousky has emphatically brought
to focus this predicament of alternate therapists. He says “…the orthomolecular approach will continue
to have limited efficacy in the treatment of schizophrenia because of the
brain-disabling and toxic effects that psychiatric medications possess”.
Allopathic drug companies attempt to address this problem of drug toxicity
by altering the molecular structure of the drug. But at the end of the day the
drug molecule is always heterotoxic. Therefore the patient’s immune system
mounts an attack on allopathic molecules. In any case the trials of APD is at
best for six months, but the patient is often advised to take these drugs for
her life and even during pregnancy and advanced age. Therefore the solution to
this quagmire has to lie outside the present day practice of allopathic
psychiatry.
This paper attempts to bring to light a solution to this urgent problem.
The proposed solution can be adopted with or without simultaneous use of APD
and with or without micronutrients and diet therapy or any other alternate
therapy. An advantage of this proposed solution is that, like all homeopathic
medicines, it is very cheap and easily affordable even by poor populations.
What I am proposing can be called Serial Dilution Protocol (SDP) and Ultra High
Dilution Protocol (UHDP) as used in homeopathy.
But unlike homeopathy, where the medicine is prescribed on the basis of
similarity of symptoms between the illness and the homeopathic drug, here I
propose the use of serial dilution, first used by Samuel Hahnemann for
medicinal purpose, of the very psychiatric drug that is causing the toxic side
effects. This I propose can be an additional therapy in the kit of a homeopath.
In fact such a procedure has been already used mainly by European homeopaths
under
the name Isotherapy. The late
homeopath Dr. Tinus Smits has used Isotherapy to successfully treat many
children suffering from autism spectrum disorder (ASD) Most of these children were normal at birth
but regressed after undergoing the allopathic vaccinations.
I have found the serial dilution protocol (SDP) effective even when used as
a standalone therapy in the case of cold turkey cessation of ongoing APD. I
will briefly describe both serial dilution protocol (SDP) and ultra high
dilution protocol (UHDP) and cite supporting research. Both these have been
found effective. So at present I do not prefer one over the other. My present
position is to start with SDP and let the clinical feedback be the guide for
the decision to later on use UHDP.
The SDP is as follows. A Starter or Mother Solution is prepared of the
offending substance that in our case is an allopathic psychiatric drug (APD).
The Starter is a saturated solution but liquid enough to be pulled up into an
injection syringe that has its needle removed. Just 1cc of the Starter is
pulled up in the syringe and poured into 4cc distilled water or any relevant
diluents such as 100 proof ethyl alcohol available with homeopathic suppliers.
This solution is labeled “1/5”. Again 1cc of 1/5 dilution is pulled up and
added to 4cc distilled water or alcohol and that is called 1/25 dilution. This
series of dilution by a factor of 5 can continue to whatever limit. The therapeutic
testing starts with about 3 or 4 drops of 1/5 dilution dribbled under the
patient’s tongue or anywhere in his mouth, preferably retained in his mouth for
about 3 minutes. Often children with psychiatric symptoms are not initially
cooperative. In such a case the drops can be dropped anywhere in his mouth or
applied on a soft part of his skin. Also it’s alright if the child swallows the
drops rather than retaining them in mouth for 3 minutes. The next weaker dose
of dilution is given after 10 minutes or 30 minute intervals. The drops of
serially weaker –in homeopathy called the higher potency–dilutions are poured
in his mouth at 10 to 30 minute intervals and signs of symptom improvement or
worsening noted. These intervals are changeable according to the situation such
that I have used 10-minute intervals, day-wise intervals (the dilution is given
two days in a week) or monthly intervals when for example hormone dilution is
used as therapy for premenstrual syndrome. The guiding principle is that what
gives exacerbation at lower dilution, e.g., 1/5, will give relief at a weaker
level of dilution e.g., 1/125. The goal is to find the exact dilution that
relieves or reduces the main symptom. Such a dilution of the offending drug is
called End Point Titration (EPT). I have
also used the dilution once a day for two days, for example Monday and
Thursday. Each week I would ask the patient how he felt during the week. If
there was relief then I might continue the EPT dilution as treatment and test
the other drug’s dilution starting with 1/5. It may be necessary to run two
drugs the same week but on different days. For example I am continuing the EPT
of APD Valium/Diazepam on Mondays and Thursdays; EPT of Imipramine
Hydrochloride on Tuesdays and Fridays. We don’t need to buy these allopathic
drugs. The patient already has them. Incidentally, for my ongoing patient I
have found the EPT of Valium at 1/125 but for Imipramine Hydrochloride I have
not yet found the EPT even at 1/10,000.
I am giving Valium 1/125 on Mondays and Thursdays with excellent
results. I give Imipramine 1/10,000 dilution on Tuesdays and Fridays but have
had no success yet. These data will be reported separately.
Mandell and Scanlon cite successful treatment of alcoholism with -0.1cc
wine diluted in 1000cc of water. Mandell and Scanlon also cite cancer cases of
the late Dr. Lee who successfully treated cancerous tumours. Dr. Lee is quoted
to prepare serial dilutions from surgical specimen of the patient’s own tumour
of late stage inoperable cancer and successfully eradicate cancer using the end
point titration dose also called the neutralizing dose of the dilution.
The UHDP followers, almost all of whom are homeopaths, use dilutions much beyond
the Avogadro’s number. It is in their work that I came across an article that
is directly relevant to the problem
of toxic side effects of psychiatric drugs, although the said article was
on mice and the disease and medicine was not psychiatric. The researchers introduced trypanosome cruzi
(T. Cruzi) in mice. The mice were then divided into two experimental and two
control groups. Dependent measures were lab parasitological parameters and
clinical parameters such as weight gain etc. One experimental group received
the standard allopathic drug ponderal benznidazole (PB). The second
experimental group received PB and ultrahigh dilution of PB (PB + UPB). The
results were significantly in favour of PB + UPB than the PB alone or the
control groups. It was a well designed research. Also the side effects were
less in the PB + UPB group compared to PB group. Body temperature was raised in
PB + UPB group indicating activation of the immune system.
The SDP users are a small group and nearly all are allopaths. By contrast, almost all UHDP users are
homeopaths. The difference between SDP and UHDP is that by definition UHDP is
ultrahigh dilution, far beyond the Avogadro’s molecular number that is 10 to
the power 23. At that an ultra-high dilution allopaths believe that all traces
of the drug or substance in the solvent is lost. The main criticism against SDP
and UHDP advanced by mainstream allopathic medicine is that when there is no
trace of drug left in the solvent, how can that solution be of any medicinal value?
But some advanced research refutes this criticism. It has been discovered that
the memory of the solute stays in the solvent, for example water, as quantum energy
vibration. Be as it may, the ultraviolet (UV) spectrum of the solute has been
detected in the ultra-high diluted solution.
Discussion
The idea here is that the treating homeopath let the psychiatric drug
continue at its prescribed dose preferably under psychiatric supervision but
himself also gives an UHD of the same drug in parallel. The critics say that at
the UHD level, there is nothing of the original substance left that would exert
any effect. It’s beyond the scope of this paper to go into the intricacies of
the counter to this criticism but briefly I should mention two important
researches. In one research Benveniste the scientist, famed for his discovery
of the platelet formation factor, published an article revealing that he could
dissolve an antigen in water way beyond
Avogadro’s number, extract the specific electromagnetic signature of the
antigen and digitize it and send it as a file attachment with an e-mail from
France to a laboratory in Chicago where the signal was passed in water to make
new UHD. This new UHD was tested in the laboratory in Chicago on isolated heart
muscle of pig. The muscle gave the expected reaction to this reconstituted
solution in the Chicago laboratory. There was a flood of reactions to this
claim. The Nature editor himself went to Benveniste’s laboratory with his team
to first hand observe the process. There were claims and counter claims.
Results of several replications were mutually contradictory.
But another group of scientists, not involved in the Benveniste experiment
and not using e-mail transmission,
published another research in which the researchers showed that histamine does
exert its expected effect on basophiles even in histamine’s highly diluted
form. In conclusion the UHD research involving mice infected with Trypanosoma
cruzi mentioned above gives us hope that we can turn around the current
scenario in psychiatry for the benefit of our patients suffering from the
allopathic psychiatric drug side effects.
A legitimate pharmaco-kinetic position can be held that statistically there
is very little chance that a molecule of a medicine will get in contact with a
target organ in the body, but there is very high probability that the medicine
in the form of electro-magnetic vibrations or quantum resonance such as
obtained in ultrahigh dilutions always used by homeopaths can affect any organ
without causing toxic side effects. It is hoped that good sense will prevail in
allopathy and its drug companies such that all the allopathic medicines will be
made like the homeopathic medicines for the benefit of patients.