It's a virtual certainty that the "body temperature"
stuff that is discussed in the post linked-to, below,
is a determining factor in Immune 'System' function.
This is be-cause disease agents' 3-D molecular
energydynamics necessarily exhibit NL-P 'signatures'
that are unique functions of the disease agents' global-
ly-integrated wholeness - which is 'just' their 'TD E/I'.
Immune 'System' reactivity is, necessarily, 'driven' by
the the way that disease agents' NL-P 'signatures'
differ from the body's DNA-encoded NL-P 'sig-
The NL-P is =everywhere=.
That this is Necessarily so, opens a 'door' =wide=
to the advancement of Medicine.
In the not-too-distant future, =Star Trek= -like
disease 'scanners' will become commonplace.
What they will do will be to 'lock-onto' the
body's NL-P and scan for non-body-specific
NL-Ps, signalling each instance of the latter
I understand that this sounds like "too much",
but it's not - for reasons that were also dis-
cussed in the post linked-to below.
Each organism's interaction with WDB2T's
universal one-way-ness is unique, and how
to map this is also given in the post linked-to
Progress toward these scanning methodologies
will begin at the microscopic 'level', with tissue
samples, and, from there, this technology will
build-up to whole-organism 'levels', which is
doable because it's 'just' a problem in collective
signal analysis [and there are Scientists who've
already developed some Expertise with respect
to 'collective signal analysis' :-]
K. P. Collins
"k p Collins" <kpaulc@[----------]earthlink.net> wrote in message
news:GgtNb.8998$i4.8624 at newsread1.news.atl.earthlink.net...