Apparent Conflicts in the Classification
of Miasmatic Symptoms
All the articles we have carried over the last few months on Miasms
largely agree on the grouping of miasmatic symptom expression. While
some symptom expression in these miasmatic classifications tend
to overlap, there are symptoms that seem to belong to one miasm
in one article and another miasm from another's point of view.
Hahnemann on the other hand, clearly demarcated his groups. Conditions
that followed an infection of Gonorrhea or Syphilis were put into
those venereal miasmatic expressions, anything else was included
into Psora which he called the most destructive miasm. This Psoric
expression was subdivided into Latent Psora, Primary Psora and Secondary
Psora. In secondary Psora (fully developed Psora) he included a
vast number of diseases (all detailed in the CD as well as in the
Organon) many of which today, based on other derivations of miasmatic
concept (Part II and III) have been reclassified into Sycosis, Tubercular
or Syphilis.
Understanding this from another perspective, "secondary Psora"
is an unclear in the clinical entity, given the multifaceted, multimiasmatic
and complex disease conditions we are faced with. There are a percentage
of cases that are largely Psoric and remain that way without ever
developing underlying non-Psoric traits. But most people do not
fall into this category. They instead express complex diseases and
mixed miasms. Also, if Psora had a latent, primary and secondary
manifestation due to a history of suppression, most surely Sycosis
and Syphilis would also over the centuries develop latent, primary
and secondary manifestations. And why not?
It would be best not to get into academic arguments. Rather to
my mind, a conceptual derivation from Hahnemann's Chronic diseases
that would be most helpful with clinical management is the one that
understands Hering's Law of cure in tandem with Miasmatic expression.
Hering's Law of cure is a chronological, logical and natural process
of disease cure verified over and over again in nature as well as
in homeopathic management. Miasmatic progression of disease is opposite
in direction to this Law of Cure. Hence Miasmatic improvement has
to be parallel in direction to the Law of Cure. Both the ICR's Disease
Evolution and the Genetic/Embryological approach of Dr. Vijaykar
follow this logical line of thought.
The proof of the pudding is in eating it, and both have shown that
this concept works clinically, inspite of some differences in symptom
classification. This is because the basic concept of disease development
and its miasmatic expression are a linear process that can be perceived
by the alert and trained homeopath. Matching the remedy to this
perception is an art that one can gain with experience. Rules for
matching the remedy remain exactly the same as Hahnemann stated
- the predominant picture is matched with a similimum remedy that
also covers that miasmatic expression in its (miasmatic) proving
symptoms.
How do we know whether the remedy covers that miasmatic expression?
One way out is to use the rubrics in the repertory for Psora, Sycosis,
Syphilis. But these are extremely large rubrics and would really
get us nowhere with repertorization or even understanding the miasmatic
background of a remedy.
So we need to miasmatically analyze the provings in the Materia
Medica of that remedy to find out its miasmatic scope. This is an
avenue that needs to be explored in depth - the ICR have done so
in remedy groups.
Vijaykar has also pointed out a method of understanding the multi-miasmatic
expressions of polycrests (see Part III) and other well proved remedies.
Reproving remedies to record symptoms with a miasmatic concept of
disease evolution in mind is another possibility (as I mentioned
in Part II) of obtaining reliable information in this regard.
Or otherwise re-arranging well recorded proving material of every
prover where available right from Hahnemann's day, in terms of onset,
duration and progression of symptoms experienced during a proving
is another possibility of observing miasmatic progression of a remedy.
Mental Symptoms vs Physical Symptoms for Miasmatic Classification
On the whole, physical symptoms and pathological expression are
more reliable to decide on the predominant miasmatic expression
than mental symptoms. This is because pathology is fact, whereas
mental expression is open to the judgment of each individual homeopath,
his prejudice and his perception or the lack of it!
A discussion with a colleague on a public list revealed to me that
a rejection of moral absolutes by some, in todays relativism has
left us floundering on what constitutes moral and immoral behavior.
Hence acceptable or unacceptable behavior that arises out of the
depraved moral sense of the Syphilitic miasm, or the manipulative
tendencies of the Sycotic miasm, or the natural tendency to abide
by the moral code in the Psoric miasm, can have as wide a range
of interpretations as there are homeopaths!
Similarly, perceiving the mental symptoms as expressive of a particular
miasm at a point of time requires a little deeper and mature perception
of human nature and its foibles on the part of a homeopath, that
not everyone is capable of! Hardly reliable for miasmatic prescriptions,
unless solidly backed up by obvious physical pathology.
So I think it is best that homeopaths concentrate on recognizing
the predominant miasmatic expression through the pathology expressed
in the chief complaint of each patient first. This is the (only)
reliable clue to the predominant miasm, and hence the clue to the
correctly indicated, miasmatically similar remedy, that has this
pathology in its Materia Medica. Study of Part II of this article
series along with the other supporting Miasm articles will give
one an idea of the symptoms that indicate miasmatic expression.
The steps in the process of miasmatic management have already been
detailed above.
Other Theories around Hahnemann's Chronic Diseases
Many have interpreted The Chronic Diseases and tried to adapt it
to their methods of prescribing. One well known concept is to consider
every possible infective agent or miasma into a separate miasmatic
expression in itself. A colleague (Feras Hakkak) gave me some feedback
on his understanding of this concept, which I replied to from my
perspective. I have presented that discussion below and I welcome
feedback on how this idea could possibly work especially in terms
of long term (miasmatic) case management.
I have read other concepts from Ortega, Kanjilal, and others which
are close to the concepts I mentioned before. Variations include
whether the Tubercular miasm exists separately or not often it may
be understood as Psoric miasm compounded with Syphilitic expression.
But the fact that Tuberculosis is such a common chronic (incurable)
disease today that exists in every culture. Its inherited traits
are clearly discernible. It complicates many chronic diseases (most
commonly today - AIDS), with a very clear mental and physical group
of expressions, it stands on its own as a major miasmatic group.
Some others consider Cancer and Vaccinosis to be miasms. Both these
don't clearly hold their own for a couple of reasons (and there
could well be more):
1. What is the causative organism that could produce a Cancer type
expression?
My answer is that there aren't any. This is obvious because there
is no real expression of a cancer infection. But I'd be happy to
hear a convincing argument to support the idea of a "cancer
miasm" as Hahnemann intended miasms it to be.
Carcinosin has its own remedy picture. Every patient with clinical
Cancer does not have this pathological picture.
Many today though advocate using Carcinosin as a nosode for Cancer,
including Dr. AU Ramakrishnan. Whether this indicates that Cancer
should be a separate miasm will continue to be debated.
Cancer needs to be understood in light of the individual expression
in each case in terms of the diagnosis, pathology and prognosis.
These are analyzed as expressions of combined miasms or predominant
miasmatic expression: Psoro-Syphilitic, Syco-Syphilitic, Tubercular-Syphilitic,
etc.
Strangely, the complete repertory lists this rubric:
GENERALITIES; SYPHILIS; hereditary: carc.
2. What is the expression of the "miasm" Vaccinosis that
requires it to be a miasmatic group separate to Psora, Sycosis,
Tubercular or Syphilis and their various permutation and combinations?
Is the need to consider Vaccinosis as a separate miasm due to the
fact that it is caused by artificially modified miasma?
How does its expression differ from the basic miasmatic expression
of Sycosis? Questions again, that would help qualify if Vaccinosis
is a separate miasm or not.
Finally, I'd like to introduce a word about Rajan Sankaran's use
of the term "miasm" in his recent prescribing method and
search for the "vital" similimum. I would caution students
that his concepts though brilliant, do not directly co-incide with
Hahnemann's Theory of Miasms in terms of clinical analysis and management
of disease. series.
But he does borrow some conceptual ideas from Hahnemann which is
interesting and helpful in itself in the quest of determining that
"vital" similimum. The resemblance stops there! I will
present a perspective of his approach in a later issue of the Ezine.
As mentioned earlier, there is a concept of discovering more miasms
(that are clubbed into Psora) based on diseases caused by various
infecting miasmas that are known in Bacteriology. I spoke
with an Iranian colleague as I wanted to get a clearer idea of this
concept of Miasmatic management which the Iranian group of 'Hahnemannian'
homeopaths had, and seem to find helpful. I conclude this article
with an interesting discussion we had we had about this.
Feras: I think the story
begins with our observations regarding the acute epidemic diseases.
In such situations, although patients show various pictures, one
(or a few) genus epidemicus remedy will cure most of them. If this
is true, which seems to be, then we can conclude that a specific
type of microbe will cause a diseased state which can be cured with
one (or a few) remedy (remedies), but the manifestations in different
patients will be different due to their susceptibilities.
So this forms the assumption that a specific microbe can cause diseases
which will be cured by one (or some) specific remedy despite the
fact that this microbe will cause different disease pictures in
different patients (due to different susceptibility factors).
So if our assumption (specific microbes causing specific diseases)
is correct, it will be sufficient to identify microbes, do epidemiological
studies, and find the symptoms that are caused by these microbes,
one by one.
Leela: I think Hahnemann differentiated clearly
between acute "maisma" and Chronic "miasma".
The difference between these two he explained by the inherent properties
of these miasma to affect the "constitution" (which is
his word in the CD). The acute miasma did not produce chronic "miasms",
though they could possibly modify their progress depending on whether
suppressive treatment was used.
Acute "miasmas" caused acute diseases, the expression
of which Hahnemann attributed to Psora (psoric miasm) mainly. He
also used the term half-acute miasma for Hydrophobia and Rabies
infection.
My observation is that the reason for the different totalities presenting
during epidemics is not only due to differing susceptibility but
also based on the individual response of the "constitution".
This in turn is dependent on whether there is a multimiasmatic background
in an individual rather than just Psora.
The chronic miasm is ultimately an expression
of a deranged vital force expressing a certain group of symptoms
based on the type of chronic miasma (broadly venereal or non venereal)
that it has been affected with. Then we have the contribution of
inherited traits of chronic miasms. This is furthur complicated
by artificial drug disease which causes modifications in disease
progression. So it would be the sum of all these expressions that
determine the predominant miasmatic expression, not simply the causative
miasma.
With this background, I find it a little
hard to understand how the assumption you mentioned above helps
clinically in miasmatic management.
Chronic disease expression (according to
Hahnemann) is different from acute disease expression. Acute disease
is an immediate reaction of the vital force to the acute miasma
resulting in resolution of the disease either by healing or death.
Immunologically, there is an ACUTE inflammatory response of neutrophils
and eosinophils. Chronic miasm, on the other hand expresses itself
after the chronic miasma has taken hold of the whole being of the
person, but there is can be no resolution because the vital force
has been deranged to an extent that does not allow spontaneous resolution.
The immunological response is a chronic inflammatory processes that
does not resolve adequately, like that of acute inflammation.
Feras:
The method used is: to exclude all the symptoms related to diet,
lifestyle, etc and among the remaining symptoms collect the active
ones and recognise the miasm (disease caused by a specific microbe)
which is dominant. The remedy will be known automatically. In fact
we have to see the miasm's picture in the patient (and we always
see a part of it not the whole picture), and the remedy for that
miasm will do the job. It’s like seeing a part of a friend’s
face and recognizing him! This is the core idea behind the miasmatic
approach of our Iranian friends.
If we adopt this view, then we will believe
that Hahnemann's Psora is a mixture of many miasms that has to be
separated. Then we will have one (or a few) remedy/ies for each
miasm, like what we have about Syphilis with Merc and about Sycosis
with Thuja.
Leela: Hahnemann has the similar instructions
for deciding on the miasmatic similimum which may be a specific
intercurrent remedy or else the chronic similimum.
I'm unclear how this means that these remedies represent various
"miasms" within psora. How does one decide on what constitues
the miasmatic expression is of a specific microbe/miasma in the
long term - is this based on bateriology? What would these miasms
be called? How is the patient's chronic symptom expression related
to a specific infecting miasma?
In present day investigations, one can do ELIZA tests to check
for the presence of specific antibodies in the blood which indicate
the history of specific infections. BUt would this be homeopathically
helpful? In homeopathy we're concerned with the symptomatic expression
of the individual at a point in time. Are you saying that one can
observe these symptoms as indicative of a history of causative microbe/miasma?
If I have understood this right, there would be a miasmatic expression
for Falciparum Malaria Miasma, Salmonella Miasma, Haemophillus Influenza
Miasma, Ascarides Lunbricoids Miasma, etc - whatever the pateint
remembers suffering from in his life. Following which, there would
be a specific remedy for each of these 'miasms' that have been clubbed
into psora?
What would be the expectation in terms of healing if this concept
(which sounds allopathic) is clinically useful? Are there clear
cases with results where this theory has worked to cure a microbe-specific
miasm in the longterm? How would this differ from what Hahnemann
termed "Isopathy" which he decided within his own lifetime
was not homeoapthically healing? I'll look forward to hearing more
about all this.
By the way what is your understanding about multi-miasmatic diseases?
Feras:
Mercurius is suitable to Syphilis miasm but it doesn’t mean
that it can’t be used for other issues. The same with Thuja.
I will ask my colleagues who practice with this style to present
their cured cases. This will show how it works.The problem is that
after Hahnemann nobody has done good research work to study miasms
epidemiologically, or I’m not aware of. It should be done
to support this style of practice. I leave this to my colleagues.
Maybe they have something to offer.
And about multi-miasmatic states. It is when
more than one miasms are active. Then you have two options. The
first one is to give a remedy that has affinity to both of those
miasms. The other one is to start with the more dominant one. But
I’m not sure about this and we’d better study it from
Hahnemann who has talked about this issue in Chronic Diseases, and
has given instructions as to which miasm should be tackled first,
etc.
Leela: Yes, Hahnemann had some specific instructions.
Part I of this series details that. But he may or may not have been
mistaken, in that there may not be any fixed rules about the sequence.
The general rule he put forth though, holds true always - treat
the predominant picture of symptoms and if one reaches a block,
treat the predominant miasmatic symptoms first.
Feras:
I don’t know how correct these ideas are, and I have not had
enough clinical experience to reject or accept them, but it is worth
investigating. Anyway, even if it is in line with truth, I think
it is a very tedious job to differentiate these so many miasms (microbes)
and make detailed lists of their symptoms.
Leela: I think I agree with you here. There seems
to be an awful lot of (investigative) work to prove that it could
be viable. It simplifies matters a whole lot if we put the (miasmatic)
symptom expressions into either one of the 3 (or 4) groups after
studying clearly what are the the expressions of each of these miasmatic
groups. Its a simpler procedure and one that every homeopath can
learn to do.
Feras:
It is really a "Western", "technology-based"
method and we could leave it to those who are interested. It is
obvious that there are some other methods that work well and do
not involve so much sophisticated expensive experimentations, and
I believe the more you keep things simple the better it will be.
So I think we’d better stick to simpler and more “Eastern”
methods like Sehgal, if we come to the conclusion that they work
satisfactorily.
Leela: Yes, I think if we focused on the properties
of miasma (microbes) as causative of miasm, we would not be doing
any justice to the art and science of homeopathy. We'd be looking
at homeopathy through the eyes of modern medicine! Its a paradigm
shift today to be actually looking at disease from the homeopathic
perspective instead, right at the outset!
If your Iranian colleagues have cases that have been followed up
for at least 5 years to show that this has resulted in miasmatic
improvement and what constitutes this improvement in the progress
of a case, we'd be interested in hearing more.
Its interesting that you mention Sehgal. I don't think he talked
very much about Miasms.
Feras:
In the method of the late Dr. M.L.Sehgal (Revolutionized Homeopathy)
there is no mention of miasms. His conception of disease is totally
different and his case-taking and case management are totally different,
accordingly. Here in Iran (and also in the world) seldom you can
find a “Sehgalian homeopath” but I believe his views
ARE worth studying deeply.
I will ask my friends to present their cases with the "Hahnemannian"
miasmatic approach (as understood by them). Would you do it too,
to in order that we see the differences and make comparisons.
Leela: Managing a case miasmatically as I understand
it (Part II and III), has very little to do with a specific microbe/miasma
causing the miasmatic state. The symptom expression at any point
of time is enough to plot exactly where on the miasmatic progression
towards health a person is. The similimum is always based on this
symptom picture (charateristic totality or miasmatic totality),
independant of the causative microbe or miasma.
But it is tempting to consider whether an isopathic nosode or a
microbe-specific remedy would be indicated at a point when a past
(acquired and suppressed) infection in the patients history rears
its head again as expected with Hering's Law of Cure. Still, whether
any of these would be indicated by the symptom picture at that point
is not clear. Whether it would help the case progress towards healing
is also something that needs to be clarified by repeated clinical
experience.
Thanks for your time Feras! Your input has been very enlightening
for me.
Dear readers, do write in if there are any clinically useful concepts
around the theory of miasms that you would like to share with us
or discuss. Thank you.
Dr. Leela D'Souza
http://www.homeopathy2health.com/
|