Re: Sim.....II
Posted: Tue Feb 08, 2005 3:19 pm
Dear Andy,
First let me compliment once again on your ability to right long but matter
of fact replies. And I am fine here in UAE, thanx.
In fact there shouldn't have the need to say that much as my question is
entirely on the 'possible future application of Chappell's technology', and
your reply about that is sufficient for my purpose.
But I think I have one more point to discuss with you about what you said
below.......
((.........My sense is that tailor-making a remedy for an individual
characteristic
totality would be more difficult than doing it for the group totality of a
pandemic chronic disease. A group totality is a set of symptoms confirmable
with quite a bit of certainty from a large data set. An individual case may
hinge on a totality based on any number of symptom genres--some subtle, some
metaphorical. Making a remedy for an individual would, I think be much more
difficult than what Peter is already doing. Our traditional comparator
method of finding a match with what is in our materia medica catalogued from
the effects of potentized substances and forces/emanations on a population
of testers (in provings by dissimilarity or clinically by similarity) might
be easier........))
In my opinion the reverse of which is -or can also be- the truth. In
ascertaining the medicinal powers of substances when one proves them the so
called materia medica (MM) becomes more complete as the number and variety
of provers increase. Which brings out the fullest picture of the drug. At
the same time a more complete MM may become too general in editing (unless
we keep ALL THE SYMTOMS produced in proving and use them in comparing with
the sick) and at least in some cases that will hinder a perfect matching
when we try to find out the similimum in any case. This is besides the
handicap already provings (MM) have due to geographical/racial/..
constraint. Tailor making remedies will be a best solution to this.
Also tailor making an individual remedy will have only the exact amount of
difficulty as we face today in our accurate case taking. Because the
technology of converting it into algorithms and so on will be the same once
it is effectively pass the R&D stage. On the contrary if this particular
aspect cannot be mechanised (means peter or some like geniuses can do it in
their head only....) all this should be stopped soon. So in my opinion they
will be more effective and almost 100% sure to act.
Another thing is that even though Peter's AIDS is doing well due to its
peculiar evolutionary nature, cancer or MS will be more difficult to be
treated in the present peter style i.e. disease similimum due to the same
reasons stated above. That they have more complex nature across continents
(geographical/racial) due to different parameters included over thousands of
years' of evolution. (where as AIDS is a very young illness and it still
have more or less the same picture every where!). So creating disease
similimum for them requires more work as in your terms.
I will wait for your opinion.
I think within two days we will be discussing more as I have an outline of
something why Peter's method works and I will give that for your kind
consideration.
Regards,
Dr. Abdul Gafar.
--
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First let me compliment once again on your ability to right long but matter
of fact replies. And I am fine here in UAE, thanx.
In fact there shouldn't have the need to say that much as my question is
entirely on the 'possible future application of Chappell's technology', and
your reply about that is sufficient for my purpose.
But I think I have one more point to discuss with you about what you said
below.......
((.........My sense is that tailor-making a remedy for an individual
characteristic
totality would be more difficult than doing it for the group totality of a
pandemic chronic disease. A group totality is a set of symptoms confirmable
with quite a bit of certainty from a large data set. An individual case may
hinge on a totality based on any number of symptom genres--some subtle, some
metaphorical. Making a remedy for an individual would, I think be much more
difficult than what Peter is already doing. Our traditional comparator
method of finding a match with what is in our materia medica catalogued from
the effects of potentized substances and forces/emanations on a population
of testers (in provings by dissimilarity or clinically by similarity) might
be easier........))
In my opinion the reverse of which is -or can also be- the truth. In
ascertaining the medicinal powers of substances when one proves them the so
called materia medica (MM) becomes more complete as the number and variety
of provers increase. Which brings out the fullest picture of the drug. At
the same time a more complete MM may become too general in editing (unless
we keep ALL THE SYMTOMS produced in proving and use them in comparing with
the sick) and at least in some cases that will hinder a perfect matching
when we try to find out the similimum in any case. This is besides the
handicap already provings (MM) have due to geographical/racial/..
constraint. Tailor making remedies will be a best solution to this.
Also tailor making an individual remedy will have only the exact amount of
difficulty as we face today in our accurate case taking. Because the
technology of converting it into algorithms and so on will be the same once
it is effectively pass the R&D stage. On the contrary if this particular
aspect cannot be mechanised (means peter or some like geniuses can do it in
their head only....) all this should be stopped soon. So in my opinion they
will be more effective and almost 100% sure to act.
Another thing is that even though Peter's AIDS is doing well due to its
peculiar evolutionary nature, cancer or MS will be more difficult to be
treated in the present peter style i.e. disease similimum due to the same
reasons stated above. That they have more complex nature across continents
(geographical/racial) due to different parameters included over thousands of
years' of evolution. (where as AIDS is a very young illness and it still
have more or less the same picture every where!). So creating disease
similimum for them requires more work as in your terms.
I will wait for your opinion.
I think within two days we will be discussing more as I have an outline of
something why Peter's method works and I will give that for your kind
consideration.
Regards,
Dr. Abdul Gafar.
--
No virus found in this outgoing message.
Checked by AVG Anti-Virus.
Version: 7.0.296 / Virus Database: 265.8.5 - Release Date: 2/3/2005