Re: miasms - PSORA 2
Posted: Wed Jul 20, 2005 11:22 am
At 10:37 PM 7/18/2005, you wrote:
Chickenpox appears to be what Hahnemann called a half-acute miasma in
the Chronic Diseases sin that it is not self limiting in a short period
like the acute miasms as it may have prolonged sequels in the form of
shingles. Chickenpox, your example, is passed by droplets and contact with
skin lesions. That patient is most infective before the skin lesions
appear. In psora the vector of transmission is from host to host through a
primary skin infection. It is never passed by droplets and aspiration, etc.
This makes psora different from the childhood eruptive diseases like
measles, chickenpox, etc.
Hahnemann did not group together "everything" take causes skin
symptoms. For example, sycosis and syphilis have their characteristic skin
lessions such as condylomata accuminata (sycosis) and the chancre and
condylomata lata (syphilis). He also did not include acute miasms that have
skin eruptions. Where have to be a little more specific when making up our
revised lists of classifications. There is a different in the nature of
acute, half-acute and chronic miasms.
Hahnemann did, however, group together several chronic skin lesions. He
listed several vectors that transmit psora in the Chronic Diseases where he
gave examples like leprosy (Lepra and TB bacteria), erysipelas
(staphylococcus), pimples, boils (staphylococcus), herpes (herpes viruses),
tetter (tinea) and itch (mites). These are the transmission vectors by
which the disease is passed from by skin to skin or skin to infected
articles to skin. These are exclusively contact diseases that are not
passed by droplets like the childhood acute and half acute miasms like
measles and chickenpox. One must not mix the acute and half acute miasms
with the chronic miasms as their nature and transmission vectors are
different.
Yes, Hahnemann did list an number of vectors for psora but they all
share the same primary pathway of the disease, which is a cutaneous primary
eruption which acts as a medium for transmission from host to host by
contact not by droplets or aspiration. That is what makes the Psora
different than sycosis, syphilis, TB,. hepatitis or HIV/AIDS. Sycosis also
seems to involve more vector, for example gonococcus, HPV, clamdiya,
trictamonous, etc. It is very possible that some miasms include a group of
microorganism that share a similar band of susceptibility and pathway of
disease. There are some fungi that produce symptoms in the lungs that are
almost identical to TB. Miasms also tend to "piggyback" one upon the other
as seen in HIV/AIDS, etc.
So as you can see this areas is very interesting and needs to be
brought up to date. This is one reason why I keep my definition of miasms
in line with its original meaning as acute, half-acute and chronic
infectious diseases. When we de-link the miasms from infection and make
them the same as the primordial homeomeries we lose a very special aspect
of homeopathy, which is vitalist epidemiology. This study offers
preventative, abortive and curative remedies for active acute, half-acute
and chronic infections as well as the long term sequels and affects of
their suppression and maltreatment.
First of all, Hahnemann's original list of psora symptoms and its
secondary diseases in the Chronic Diseases in 1828 included some symptoms
of the pseudopsora-TB as well as sycosis. While constructing his first
group anamnesis he mixed up some of the symptoms miasms. In some cases he
may have been looking at mixed miasms without realizing it.
Hering stated that Hahnemann was separating the symptoms of psora and
pseudo psora and we know from Boenninghausen that he was working on new
list of symptoms for sycosis. Unfortunately, these symptoms lists have not
be recovered. What we see in the 1828 Chronic Disease needs to be corrected
and brought up to date. Hering, Boennighausen, J.H. Allen, Kent and others.
In the process the symptoms of psora and TB miasms have become more
clarified and the images of sycosis and syphilis expanded. Therefore,
anatural evolution of the pictures of the miasms have taken place although
a few new mistakes have been made along the way.
Now, returning to psora. Yes, there are four major vectors of psora
based on bacteria, fungi, viruses and mites. One might called these types
psora 1,..2.,, 3, and 4. And yes, this may be one of the reasons there are
so many antipsoric remedies! All these vectors share the fact that their
transmission is by host to host by skin contact or skin to infected
material to skin. They are not spread by droplets and contact like the
childhood eruptive infections like measles and others like smallpox, etc.,
which are all acute miasms. Chickenpox, however, has much longer sequels
than these acute miasms and may be a half-acute miasma that is a bridge
between the acute and chronic miasms. That you brought up this particular
example is rather astute. I have been contemplating its nature and
classification for some time.
Sincerely, David Little
---------------
"It is the life-force which cures diseases because a dead man needs no more
medicines."
Samuel Hahnemann
Visit our website on Hahnemannian Homoeopathy and Cyberspace Homoeopathic
Academy at
http://www.simillimum.com
David Little © 2000
Chickenpox appears to be what Hahnemann called a half-acute miasma in
the Chronic Diseases sin that it is not self limiting in a short period
like the acute miasms as it may have prolonged sequels in the form of
shingles. Chickenpox, your example, is passed by droplets and contact with
skin lesions. That patient is most infective before the skin lesions
appear. In psora the vector of transmission is from host to host through a
primary skin infection. It is never passed by droplets and aspiration, etc.
This makes psora different from the childhood eruptive diseases like
measles, chickenpox, etc.
Hahnemann did not group together "everything" take causes skin
symptoms. For example, sycosis and syphilis have their characteristic skin
lessions such as condylomata accuminata (sycosis) and the chancre and
condylomata lata (syphilis). He also did not include acute miasms that have
skin eruptions. Where have to be a little more specific when making up our
revised lists of classifications. There is a different in the nature of
acute, half-acute and chronic miasms.
Hahnemann did, however, group together several chronic skin lesions. He
listed several vectors that transmit psora in the Chronic Diseases where he
gave examples like leprosy (Lepra and TB bacteria), erysipelas
(staphylococcus), pimples, boils (staphylococcus), herpes (herpes viruses),
tetter (tinea) and itch (mites). These are the transmission vectors by
which the disease is passed from by skin to skin or skin to infected
articles to skin. These are exclusively contact diseases that are not
passed by droplets like the childhood acute and half acute miasms like
measles and chickenpox. One must not mix the acute and half acute miasms
with the chronic miasms as their nature and transmission vectors are
different.
Yes, Hahnemann did list an number of vectors for psora but they all
share the same primary pathway of the disease, which is a cutaneous primary
eruption which acts as a medium for transmission from host to host by
contact not by droplets or aspiration. That is what makes the Psora
different than sycosis, syphilis, TB,. hepatitis or HIV/AIDS. Sycosis also
seems to involve more vector, for example gonococcus, HPV, clamdiya,
trictamonous, etc. It is very possible that some miasms include a group of
microorganism that share a similar band of susceptibility and pathway of
disease. There are some fungi that produce symptoms in the lungs that are
almost identical to TB. Miasms also tend to "piggyback" one upon the other
as seen in HIV/AIDS, etc.
So as you can see this areas is very interesting and needs to be
brought up to date. This is one reason why I keep my definition of miasms
in line with its original meaning as acute, half-acute and chronic
infectious diseases. When we de-link the miasms from infection and make
them the same as the primordial homeomeries we lose a very special aspect
of homeopathy, which is vitalist epidemiology. This study offers
preventative, abortive and curative remedies for active acute, half-acute
and chronic infections as well as the long term sequels and affects of
their suppression and maltreatment.
First of all, Hahnemann's original list of psora symptoms and its
secondary diseases in the Chronic Diseases in 1828 included some symptoms
of the pseudopsora-TB as well as sycosis. While constructing his first
group anamnesis he mixed up some of the symptoms miasms. In some cases he
may have been looking at mixed miasms without realizing it.
Hering stated that Hahnemann was separating the symptoms of psora and
pseudo psora and we know from Boenninghausen that he was working on new
list of symptoms for sycosis. Unfortunately, these symptoms lists have not
be recovered. What we see in the 1828 Chronic Disease needs to be corrected
and brought up to date. Hering, Boennighausen, J.H. Allen, Kent and others.
In the process the symptoms of psora and TB miasms have become more
clarified and the images of sycosis and syphilis expanded. Therefore,
anatural evolution of the pictures of the miasms have taken place although
a few new mistakes have been made along the way.
Now, returning to psora. Yes, there are four major vectors of psora
based on bacteria, fungi, viruses and mites. One might called these types
psora 1,..2.,, 3, and 4. And yes, this may be one of the reasons there are
so many antipsoric remedies! All these vectors share the fact that their
transmission is by host to host by skin contact or skin to infected
material to skin. They are not spread by droplets and contact like the
childhood eruptive infections like measles and others like smallpox, etc.,
which are all acute miasms. Chickenpox, however, has much longer sequels
than these acute miasms and may be a half-acute miasma that is a bridge
between the acute and chronic miasms. That you brought up this particular
example is rather astute. I have been contemplating its nature and
classification for some time.
Sincerely, David Little
---------------
"It is the life-force which cures diseases because a dead man needs no more
medicines."
Samuel Hahnemann
Visit our website on Hahnemannian Homoeopathy and Cyberspace Homoeopathic
Academy at
http://www.simillimum.com
David Little © 2000