PeterKoziol
Arthritis and Multiple Sclerosis--The Cause May Be in the Blood
------------------------------------------------------------------------
Changes in the shape and function of common microorganisms may explain the
 origin of
certain autoimmune diseases. A live blood analysis provides the startling
 evidence--and
points the way towards successful treatment.

Many theories are put forward to account for the development of autoimmune
 diseases
such as rheumatoid arthritis and multiple sclerosis, both of which are marked
 by the body's
strange destruction of its own tissues, as if they were foreign, even
 dangerous, matter.

Physicians believe rheumatoid arthritis is caused by, variously, food
 allergies, nutritional
deficiencies, intestinal permeability, genetic susceptibility, or
 microorganisms. For
multiple sclerosis (MS), proposed causes range from food sensitivities, yeasts,
environmental toxins, and dental mercury amalgams to fatty acid deficiencies,
 stress, and
the herpes virus.

A new theory may dispel the cloud of uncertainty surrounding both diseases and
 the
baffling nature of the autoimmune response itself. This theory holds that the
 cause may be
fairly ordinary bacteria that have changed their body structure and activity
 and become
what microbiologists now call "stealth pathogens" or cell wall deficient
 organisms. These
pathogens can be seen through darkfield microscopy in living blood samples of
 patients
with
rheumatoid arthritis or MS.

However, according to Philip Hoekstra, Ph.D., director of Therma-Scan, Inc., a
blood-imaging and specialty diagnostic company in Huntington Woods, Michigan,
 you
can only begin to understand the clinical relevance of these pathogens if you
 study living
blood without any preconceived ideas.

"Most blood testing starts with too many preconceptions, but if you simply
 remove your
biases and allow the blood to show you what is going on, you can see a whole
 story. Every
cell has a story to tell. You can physically see these microorganisms. You may
 not be able
to identify exactly what they are, but you can tell fairly quickly whether
 these
microorganisms are at a problematic level and affecting the immune system."
 This in turn
sheds new
light on the process of autoimmune diseases, Dr. Hoekstra adds.

Understanding the Autoimmune Response
Dr. Hoekstra disagrees with the prevailing concept of an autoimmune disease;
 that is, for a
mysterious reason, the immune system starts attacking itself as if it were
 suddenly crazy. "I
do not believe that in the wisdom of the body the immune system goes 'nuts' and
 targets
the body's tissues for destruction. Rather, I see this as collateral, secondary
 damage while
the immune system is actually seeking out a specific, though somewhat hidden,
target."

To explain his new model of autoimmune activity which is based on extensive
 laboratory
observation, Dr. Hoekstra relies on a hunting metaphor. Hunters with torches
 move
through the woods in search of a raccoon. In pursuit of the elusive raccoon,
 the hunters
accidentally set fire to trees and the hunting dogs damage much of the
 undergrowth. In
fact, they nearly trash the entire woods, creating a tremendous amount of
 collateral
damage, says Dr.
Hoekstra.

"Let's see the dogs as immune system antibodies (out to digest foreign matter),
 the hunters
as white blood cells, the woods as the body, and the raccoon as a specific
 microorganism,"
he comments. "In pondering this analogy, it occurred to me that in an
 autoimmune disease,
the immune system is probably tracking down a specific, targeted microbial
 agent."

The quest to identify this elusive microbial agent in rheumatoid arthritis has
 occupied
rheumatologists for over one hundred years, but it has been a quest marked by
 numerous
false starts and dead ends, partly because it has been based on misleading
 animal studies,
says Dr. Hoekstra. But when you start looking with wide-open eyes at the living
 blood of
humans, as a researcher you are brought a lot closer to an accurate
 identification of that
microbial "raccoon."

Bacteria in an Altered State
Quite often, when he examines a slide of blood using darkfield microscopy, Dr.
 Hoekstra
can quickly surmise the patient's entire health history. If the platelets are
 "sticky," or clump
together, there is a high probability the person suffers from headaches.
 Similarly,
variations in shape among red blood cells tell him a great deal about a
 person's
biochemistry, their nutritional intake and nutrient levels. "We are committed
 to patient
education
here, so patients sit with me while I analyze their living blood sample,
 watching its shapes
and movements on the video monitor."
Patients new to the information-gathering potential of darkfield microscopy
 often liken the
technology's remarkable ability to reveal detailed health histories to a
 crystal ball, says Dr.
Hoekstra. "There is no psychic intuition here--it's all there in the blood for
 us both to see.
With our specially equipped microscopes, we can look for many things that are
 commonly
missed in routine blood studies. The goal is to get more than routine
information about a patient's condition so that it might be used in a holistic,
 preventive
way."

It doesn't take long--watching the blood for 20-40 minutes--to get to the heart
 of the
problem, says Dr. Hoekstra. "Then I can show the patient different features in
 the blood
that are probably linked to their health problem. You can see features of
 chronic viral
infections, such as herpes, cytomegalovirus, and Epstein-Barr, that cause shape
 changes in
the white blood cells called lymphocytes."

In the case of rheumatoid arthritis, Dr. Hoekstra has found that virtually all
 the patients he
has studied have had significant amounts of a bacteria called Propioni
 bacterium acnes.
"This is the genus and species of the organism we believe is responsible for
 propagating
and perpetuating this disease," says Dr. Hoekstra. "It is a very common
 bacteria in an
altered state of being--it's cell wall deficient."

The bacteria was first identified and described in 1981 by G.A. Denys at Wayne
 State
University in Detroit, Michigan. "This bacteria is passed transplacentally,
 from mother to
fetus, and this may be responsible for rheumatoid arthritis showing up in
 generations in a
single family," says Dr. Hoekstra.

Why this bacteria is prevalent in seemingly all cases of rheumatoid arthritis
 is not clear;
overuse of antibiotics may be a factor encouraging its growth. "The use of
 antibiotics is
one of the most potent ways of inducing cell wall deficiency; bacteria seem to
 do this as a
survival mechanism."

In other words, when a bacteria is transformed into a cell wall deficient form,
 it assumes
different characteristics from the whole or native type of microorganism it
 used to be, Dr.
Hoekstra explains. "The organism remains intact except it loses its cell wall
 and its
antigenic characteristics, enabling it to function as a cellular chameleon."
 When it loses its
antigenic signature, the bacteria is able to mask itself against destruction by
 the
immune system's antibodies which can no longer recognize it as an antigen
 (foreign
protein).

Dr. Hoekstra's mentor, Lida Holmes Mattman, Ph.D., also of Wayne State (now
 professor
emeritus of biology), confirmed the causal role of P. acnes in a laboratory
 experiment. Dr.
Mattman extracted the bacteria from the synovial fluid (which lubricates
 joints) of human
arthritis patients, and injected it into chicken embryos. The chicks then
 exhibited
symptoms of rheumatoid arthritis. When she treated the chicks with antibiotics
 known to
disable
P. acnes, the disease disappeared.

A different bacteria, operating on similar principles, seems to be the organic
 cause of
multiple sclerosis, says Dr. Hoekstra. It's tentative name--not yet widely
 accepted by other
microbiologists--is Borrelia mylophora, so named because its characteristics
 seem to
resemble those of Borrelia burgdorferi, the bacteria believed responsible for
 Lyme disease.

In multiple sclerosis, the myelin sheath covering nerves gets eaten away by the
 immune
system, explains Dr. Hoekstra. "That is exactly like the hunters' torches
 setting fire to the
forest. Most of the destruction of the myelin sheath takes place from actions
 of the white
blood cells and their antibodies. But their primary target is not the myelin
 sheath at all. It's
the Borrelia mylophora bacteria, running around in the nervous system. B.
mylophora has an extremely high affinity for the myelin sheath. It loves it."

Unfortunately, the myelin sheath sustains a lot of collateral damage as the
 immune cells
attempt to find and destroy the microbe, Dr. Hoekstra says.

As with rheumatoid arthritis, the work on identifying a possible microbial
 agent in
multiple sclerosis has been under way for many years, since 1913. One of the
 difficulties is
that the microbiologist must be very patient, able to culture a blood specimen
 and keep it
uncontaminated for as long as nine months before a positive bacterial
 identification can be
made, explains Dr. Hoekstra.

Both P. acnes and B. mylophora are examples of stealth pathogens, of organisms
 with
deficient cell walls, capable of acting secretly in the body, creating disease,
 and hardly
leaving a trace.

Pushing Away Their Wheelchairs
Once you understand the nature of the organism causing an autoimmune disease,
 it's much
easier to develop an effective strategy against it, says Dr. Hoekstra. "We have
 a number of
multiple sclerosis patients who have pushed away their wheelchairs or thrown
 away their
canes and are walking now. And their vision has been restored," he adds.

Physicians use different strategies in dealing with the underlying bacteria.
 Dr. Hoekstra
cites the example of Phoebe, a 36-year-old woman with MS. After B. mylophora
 was
cultured from her blood, Phoebe's doctor prescribed a heavy dose (about 100 mg
 daily) of a
standard antibiotic called doxycycline. After four weeks, she was able to lift
 both hands in
the air, comb her hair without losing her balance, see clearly again without
 dizziness, and
move about without her cane; after six months (four of which involved
 continuous dosing),
Phoebe was free of all symptoms, says Dr. Hoekstra.he successful use of this
 antibiotic against B. mylophora was first verified by a physician
in South Dakota who reasoned that the symptoms of MS (which he had) were
 suggestively
similar to those of Lyme disease, which responds fairly well to doxycycline.
 After dosing
himself for three months with the antibiotic, he was symptom free.

However, the long-term use of antibiotics has many drawbacks, cautions Dr.
 Hoekstra. It
seriously damages the ecology of intestinal microflora and can lead to a
 condition of
microbial imbalance called dysbiosis. This in turn can be the foundation for
 numerous
diseases. As stated above, it can also facilitate the growth of more cell wall
 deficient
forms. To counteract this, Phoebe's doctor recommended a product called
 Probioplex,
made from
concentrated globulin whey protein.

"This is a source of passive immunity, like the concentrated antibodies in
 colostrum [breast
milk at childbirth]," Dr. Hoekstra explains. Phoebe used Probioplex as a
 gentle,
broad-spectrum, natural antibiotic (at a dosage of 1/2 teaspoon, four times
 daily) to
suppress the overgrowth of nonbeneficial bacteria, whose numbers may have
 increased
from the prolonged antibiotic intake.

Phoebe further supported her intestinal ecology by regularly taking supplements
 of
Lactobacillus acidophilus and L. bifidus (in refrigerated powder form). To
 offset the toxic
effects of the antibiotic on her liver and kidneys (which filter all the body's
 toxins), Phoebe
took high doses of vitamin C, typically 4.5 g daily in divided doses. She
 continued this
regimen for a month after the end of the antibiotics course, adds Dr. Hoekstra.

Often patients with MS have a problem with mercury amalgam fillings, says Dr.
 Hoekstra.
"Some MS patients seem to benefit greatly from having their mercury fillings
 removed."
Phoebe had her mercury amalgams replaced, a procedure that seemed to help her
considerably, he adds.

Halting Bacteria with Colloidal Silver
In the case of rheumatoid arthritis, a hallmark of conventional medical
 treatment is the use
of steroids, which can provide symptomatic relief, but no cure. The danger
 here, cautions
Dr. Hoekstra, is that such drugs "give a free and clear run to the bacteria
 involved
(Propioni bacterium acnes). If such a patient is ever to subdue this
 microorganism, they
must have a competent immune system, and to have this, they must be off the
 steroids."

Dr. Hoekstra notes that while it may seem daunting to an arthritis patient to
 surrender the
comfort of symptomatic relief from steroids, there are effective natural
 alternatives by
which inflammation can be diminished without suppressing the immune system. The
 herb
gentian violet, for example, is a nonspecific antimicrobial agent of benefit
 here. Other
helpful herbs include echinacea, goldenseal, and chaparral. A homeopathic
 preparation
called a
nosode can be cultured from the bacteria itself then reintroduced into the
 patient as a subtle
vaccine, says Dr. Hoekstra.

Colloidal silver and the omega-3 group of essential fatty acids can also be
 used
successfully. Dr. Hoekstra cites the case of a 45-year-old carpenter with
 rheumatoid
arthritis. Over the course of four years, he progressively deteriorated to the
 point where he
could only price jobs, but was no longer able to do the manual work. He took
 colloidal
silver (an ultrafine liquid suspension of medicinal silver) for several months
 at the rate of 3
cc of
30 ppm colloidal silver per day for 60 days.

In addition, he took daily dosages of immune-enhancing herbs and vitamins.
 Specifically,
these were: esterified vitamin C (4 g), vitamin B complex, zinc (30 mg),
 vitamin E (400
IU), folic acid (1 mg), vitamin B12 (0.8 mg), fish oils (5 g), goldenseal (500
 mg),
echinacea (500 mg), and chaparral (500 mg). After this supplementation, he
 improved
spectacularly," says Dr. Hoekstra.

On the basis of the "disease stories" Dr. Hoekstra has read in the living blood
 of numerous
patients, he affirms a message of clinical hope. "We have made a serious crack
 in these
autoimmune diseases by showing that there is a cause involving microorganisms
 which
can be handled. People who have been dealing with what they've been told is a
 hopeless
medical situation should realize it is not at all hopeless."

--RICHARD LEVITON

An Introduction to Stealth Pathogens

While they differ in function, most of the body's estimated 100 trillion cells
 have many
similar features, including a defined cell membrane, or wall, separating the
 cell's inside
from the surrounding fluid outside the cell. The cell membrane is ultrathin
 (about
1/2,500,000 inch thick), composed of proteins and fats arrayed in a scaffolding
 of different
fibers, struts, and hollow rods. The purpose of the cell membrane is to
 regulate the passage
of materials into and out of the cell.

The term stealth pathogens refers to bacteria that have cell walls that are
 deficient in
shape, structure, rigidity, and/or layering. This feature enables such bacteria
 (CWD, or cell
wall deficient) to easily move DNA between cells and for groups of CWD bacteria
 to fuse
together and "facilitate genetic experiments," explains microbiologist Lida
 Holmes
Mattman, Ph.D., a leading authority in this field.

Such "genetic experiments" can include many of today's more baffling autoimmune
diseases such as MS and rheumatoid arthritis, along with other forms of
 arthritis,
septicemia, meningitis, urinary tract infections, heart valve infection, eye
 inflammations,
"and a host of other maladies," says Dr. Mattman. These organisms are
 "clandestine,
almost unrecognizable, and omnipresent," says Dr. Mattman. They are capable of
considerable shape-changing and
growth resulting in disease--hence the apt term, stealth pathogens.

In fact, the cell shapes produced by a diminished, discontinuous, or absent
 cell wall are
"almost endlessly variegated" and work their way into "all aspects of microbe
 participation
in life." They're known by various technical names, according to the degree to
 which
they've lost their cell wall: spheroplast, protoplast, L-phase, L-forms,
 transitionals, and
mycoplasma. According to some physicians, mycoplasma, which are unable to make
 any
cell
wall whatsoever and are highly divergent in type, may be involved in the
 initiation of
cancer.

SOURCE--Lida H. Mattman, Ph.D., Cell Wall Deficient Forms--Stealth Pathogens,
 2nd
Edition, CRC Press (1993), CRC Press, 2000 Corporate Blvd. N.W., Boca Raton, FL
33431.







<Picture: Disclaimer>Alternative Medicine Digest © 1996 by Future Medicine
Publishing




The above comments are my opinion. That and about $1.00 might get you a cup of
 coffee.
Sincerely,
Dennis
http://members.aol.com/midennis/index.htm



I really in light of the information that we have obtained in the last two
weeks, verifying the causality of these diseases to be microbial want to
encourage you to make some CS and try it--I sent you the body weight dosage
material.  What ppm did you get?  YOu can make this for pennies per gallon
once you are set up.  You will need alot of it and to buy it is costly I
understandd,  Some go on a maintenance .  I have upped my dose a wee bit
and did have a reaction to it and now have less pain.   I am just weak from
so long not able to use muscles without ripping the heck out of them so
slow to go.
Blesings,
Susan

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