Reclaiming Stolen Cellular Signatures
Autoimmune Disease: A Cellular Approach
Not all diseases designated as autoimmune are caused
by parasites. The immunesystem, upon occasion, does appear
to attack cells that belong to the body. We have observed this in
cases of alopecia, thyroiditis, and some skin disorders. There are
times when there may be a combination, and perhaps Crohn's is one
of them. The parasite remedies help but sometimes not completely.
The rest of the puzzle could be regarded as an autoimmune-like process.
Contrary to current theory, we feel that the autoimmune
process is not a situation where the immune system has mysteriously
turned against the body, so the designation of diseases that fall
into this category as "auto" immune is not quite precise.
Our observation has been that the process identified as autoimmune
occurs only when certain cells of the body have been divested of
Each person has a self-signature that is unique, different from anyone else, like a cellular fingerprint. Every cell
and every tissue holds a specific marker that signals that it belongs
to the body, and each individual's immune system is familiar with
the vibration of the self-marker of the organism it has been designed
to protect. The NK cells and cytotoxic T-cells are constantly waiting
in the wings, watching carefully, ready to zoom out and destroy
every cell and every protein structure that doesn't display the
self-identifying mark. No killer cell would even dream of touching
a cell that held the self-marker on it. The body's self-differentiating
marker is called the human leukocyte antigen, and it is generated
by a signalling system known as the Major Histocompatibility Complex,
If any cells belonging to the body are divested
of their self-marker, then the immune system will perceive them
as "non-self." In response, quite naturally the normal
protective defenses are roused. The brave defenders, the cytotoxic
T-cells and the Natural Killer cells are attacking what they always
attack---those foreign-looking cells that don't belong---and this
is their job. They aren't engaging in a strange or hostile autoimmune
response, they are just doing what they naturally do. What is abnormal
is that the self-marker, the human leukocyte antigen, has been stripped
away. Certain designated cells, once belonging to the body, have
now been revealed as non-self. They have become targets. An inflammation
process is invoked, engaging an immune response that is identical
to any other viral or bacterial infection, or any other invasion
by non-self organisms.
The next question to ask is this: why was the
human leukocyte antigen torn away, and why were these specific cells
targeted and put at risk? In the cases that we have observed, it
is a two-stage process.The Major Histocompatibility Complex, at
the first stage, seems to be partially compromised by a methylated
form of the amino acid histidine.
Evidently a metabolic error can occur that causes
histidine to become incorrectly attached to a methyl group, (CH3)
so it turns into methylated histidine. This attachment is initiated
by a heavy toxic exposure in combination with an emotional trauma.
The trauma may have a direct impact upon the biofield in an area
of the body that has become emotionally vulnerable, so the vibrational
connection to the body's biofield signature becomes a little tenuous.
This effect does not produce a noticeable change, so the susceptibility
of these cells can remain hidden for years.
A subsequent insult triggers the original cell damage to come to the surface. This is the second stage. At that point a symptom suddenly
occurs, apparently striking "out of the blue."
We have found that the triggering factor, in response
to a biochemical/emotional trauma, involves another process, this
time related to the amino acid valine. The second-stage event is
the introduction of a valine utilization disorder. The disruption
in the valine cascade appears when a metabolite of valine called
isobutyryl-CoA becomes deflected, and the pathway cannot proceed
to the next step, which should have been methylacrylyl-CoA.
Just as in the formation of methylhistidine, this
metabolic error is usually induced by a heavy exposure to acetone
or other solvents, agricultural spraying or related chemical exposures,
in combination with trauma. In some cases it can be precipitated
entirely by trauma. It seems probable that when the valine metabolite
isobutyryl-CoA cannot proceed, it would be likely to build up to
It is our belief that the presence of an excessive
accumulation of iosbutyryl-CoA literally tears off the human leukocyte
antigen from specific cells that have been previously damaged. Now
that they are exposed, they will come under immediate attack by
the immune system. This is not "auto" immune. The immune
system is protecting the body from what it perceives to be a foreign
When the fighters discover these exposed cells, they set up their usual defense posture. Matching memory cells are
stored in the spleen and in lymph nodes, and these have the potential
for duplicating millions more fighters, now programmed to attack
the unmarked cells. In this way the immune response has, in fact,
been recruited to attack the body's tissues, but only those that
have been divested of their natural protection.
To restore the self-markers to these vulnerable cells, methylhistidine needs to have its methyl group removed so that it
can become histidine again. Histidine needs to be "demethylated."
This can be done fairly easily by detoxifying the toxic substance
that initiated the change, and/or an emotional event or decision
that contributed to the change. However, that shift by itself would
not be enough to restore the self-marker. It simply would lay the
groundwork for another shift. The second shift comes about with
the resolution of the valine utilization disorder.
So far, we have found that isobutyryl-CoA can
proceed to methylacrylyl-CoA if it receives selenium and methionine.
Therefore when we offer these supplements to the body, presumably
the sequence can move forward. In that event, the human leukocyte
antigen either returns to the exposed cells, or what seems more
likely, the new cells that arise to replace the damaged ones will
all display self-protective markers, and are no longer at risk.
Emotional Factors in the Autoimmune-like Process
To summarize this: three things have
First you need to locate all the traumas that are
related, and release them through the meridians.
Then you need to demethylate the histidine.
And last, you need to suggest selenium and methionine
to coax the valine cascade to completion, thereby reducing the high
accumulation of isobutyryl-CoA. We had another client who indicated
that she required silica and methionine, so it appears that the
mineral requests may vary. The enzymes that bring about the shift
to methylacrylyl-CoA are evidently fairly complex.
We have traced what we perceive to be two major
possibilities, parasites and amino acid utilization disorders, that
can form the basis for what has been designated as the autoimmune
process. Significant emotional aspects need to be explored, in addressing
the etiology of these diverse difficulties. Unlike the issue of
parasites, which usually does not have an emotional basis, unresolved
traumas and out-dated beliefs and decisions can play a significant
role in creating the amino acid utilization disorders.
The methylation of the histidine, and the blocking
of isobutyryl-CoA happen in response to a combination of toxic exposures
and damaging emotional experiences. Personal issues need to be sleuthed
out, addressed, and processed on an individual basis. Out-dated
time-frames need to be brought up to date, so that the body's entire
bioenergy field can register the same age as the presenting age
of the client. Intrusions into the chakras by other people, as well
as invasions by spirit-beings, all need to be released. The reasons
for inviting or allowing such interference needs to be addressed,
and resolved. Then the biofield can claim its rightful cellular
clarity, and protect itself on its own terms, in harmony with the
We not only disagree that autoimmune-like illnesses are
a permanent affliction, fated to become progressively worse,
we also disagree with what seems like a flippant New Age psychological
theory that by "creating" this immune reaction, the client
is showing that she is "turning against herself " and
must therefore be manifesting deep hidden issues of self-hate. This
assumption is a set-up. It produces exactly what these people have
already decided she feels---self-doubt and self-blame.
Given that premise, the patient will probably
be referred to a therapist who feels that resolving self-hate is
a requirement for healing. In that case, the client is coached to
search endlessly for hidden reasons for her self-hate. Often very
understandable reasons for self-rejection do exist, and if so, it
would be useful to trace these things and process them. This might
change her physical symptoms, but not unless self-contempt
is really the cause. On the other hand, maybe she doesn't hate herself,
and is told that she is "in denial" because otherwise
why would she have an autoimmune disease? The New Age circular theory suggests
that if only she were just "ready" or "willing"
to face these issues, then she could get well, and her pain would
A promise has been held out, and it is a promise that can't
Implied here is that her illness is her fault. She could change the basis of her diagnosed autoimmune process if
only she would admit the "truth" and confess. Sometimes
it is ascribed to punishment for a past life crime that there is
no reference for validating, but because of this she deserves her
illness until she can become spiritually perfect and can "forgive."
This theory seems pretty far-fetched, for many people. If it's just a parasite, such a guilt-producing hassle is not even
remotely relevant. Not by any punishing karmic cosmic forces has
she come across a parasite! She is perfectly OK already. None of
it is her fault in this or any other lifetime! All she needs is
a parasite remedy.
For the conditions that allow the loss of MHC protection, the initiating situation of a toxic exposure might carry with it
an unresolved emotional situation as well. On the other hand, these
factors could have been experienced at quite different times, and
the problem might not surface until the second contributing source
had occurred. These would both have to be identified and resolved
so that the amino acid utilization disorders could find their way
back to the correct cascades. It would require detoxification as
well as some careful emotional meridian releases, and the updating
of old strategies and beliefs that are no longer useful.
Our experience suggests that the best way to approach it is to ask the body-consciousness to locate the age when the relevant
events happened, and resolve the fear, anger, or grief that conspired
to create the amino acid utilization disorder. Under skillful gentle
guidance, the client can allow the amino acid cascade unfold in its own way. She can resolve
her issues on her own terms, in her own time, with no guilt, and no promises intended.
We feel that it is essential to validate the client's
defense strategy as an appropriate solution for staying safe in
a threatening situation. At a time when she was helpless, she was
able to figure out how to protect herself, otherwise her emotional
survival would have been at risk. When out-dated helpless feelings
are recognized, reviewed, and processed with meridian releases,
the hidden emotional charge dissipates. Then the protective devices are
recognized as irrelevant, in current time. New awareness can bring
these once uncomfortable emotional events into the time-frame where
they can provide the tools for healthy forgiveness, and can kindle
the motivation for making healthy changes.