MIRACLE MINERAL
SUPPLEMENT
An Integrated MMS
Therapy
By Walter Last
Sodium chlorite is presently being
promoted as a miracle mineral supplement or MMS with superior antimicrobial
activity. You can appreciate its power from a statement by its discoverer, Jim
Humble, that all 75,000 individuals with malaria that have been treated were
cured within a day (1).This obviously is important not only for self-healing
but also for the drug industry and medicine which so far try to ignore or
suppress this development. However, there are also considerable problems
associated with using MMS. In the following I suggest to minimise these
problems by integrating MMS with other natural therapies rather than using it
as a stand-alone treatment for all conditions.
Conventional Use of Sodium Chlorite
In solution sodium chlorite (NaClO2)
is very alkaline and stable but when acidified it forms the gas chlorine
dioxide (ClO2) which smells the same as chlorine and probably is the strongest
all-round antimicrobial and parasite remedy. While it destroys all anaerobic
microbes and parasites, it does not damage the beneficial lactobacteria
of our intestinal flora. The only residue left in water, food, or in the body
after treatment with MMS is a tiny amount of table salt or sodium chloride (NaCl).
Acidified sodium chlorite is being
used in many countries, including
In 2003 the Australia New Zealand
Food Standards Code was changed to permit the use of sodium chlorite
acidified with citric acid or other food acids for antimicrobial surface
treatment of meat, poultry, fish, fruit and vegetables (3). The time between
mixing and application is less than 5 minutes, and chlorine dioxide levels do
not exceed 3 ppm. The safety assessment report
concluded that if properly used no residues would be detected in the raw foods
following treatment and prior to sale, and therefore there would be no
toxicological concerns.
In solid form sodium chlorite is
unstable and commonly mixed with about 20% sodium chloride. Commercially it is
produced and shipped in
Even in conventional medicine chlorine
dioxide has been shown to sterilise red blood cells for transfusion. It was
found that a solution of 2.8% sodium chlorite activated with 15% lactic acid at
a concentration of 1:100 killed all HIV in the red blood cells (4).
Furthermore, low concentrations of chlorine dioxide are also effective against
the influenza virus (4a).
Curiously, stabilized chlorite,
commonly called Stabilized Chlorine Dioxide or SCD, that does not generate
chlorine dioxide has been patented for intravenous use in the treatment of
autoimmune diseases, hepatitis and lymph cancers. It supposedly prevents or
reduces antigen activity and autoimmune responses (5).
A
weak solution of SCD is approved by the FDA and available in many countries as
mouthwash; it is also in some toothpastes. The idea is that colonies of
bacteria in the mouth produce acids that release chlorine dioxide locally to
kill these bacteria.
SCD
has a pH of about 7.5 to 8.5 and is in effect a weak solution of sodium
chlorite stabilized with sodium bicarbonate, and sometimes also with additional
hydrogen peroxide.
The
Wikipedia mentions for sodium chlorite
that a weak acid can be added to SCD to "activate" it and make
chlorine dioxide in-situ. SCD is used as a broad spectrum disinfectant and
anti-microbial, it is currently being used against bacterial and viral outbreaks
including MRSA,
Legionella, and Norovirus. Therefore, if MMS is not available a
suitable mouthwash may be used in about a 10 times larger volume or about 1 ml
of mouthwash for 2 drops of MMS.
MMS
Therapy
The discovery and initial developments
of MMS therapy were outlined by Jim Humble in a 2008 Nexus article (6). MMS is
activated to release chlorine dioxide by mixing with 5 drops of acid for every
1 drop of MMS. Originally lemon juice and vinegar were used which are now
commonly replaced by a 10% solution of citric acid. This is about 5 times more
acid and releases considerably more chlorine dioxide with a stronger
antimicrobial effect. After waiting for 3 minutes half to one glass of water or
juice is added and one may then drink it.
You may add herb tea or juice without
vitamin C, e.g. commercial apple or grape juice but not orange juice. The
initial strong and somewhat nauseating smell is now greatly reduced as the
chlorine dioxide remains dissolved in water rather than escaping into the air.
Do not take any antioxidant supplements close to MMS. If it is too acid for you
then partly neutralize the liquid with bicarbonate shortly before drinking.
Carefully add only small amounts of bicarbonate so that it still tastes
slightly acidic when ingesting.
Therapy can be approached in two ways.
Jim Humbles recommendation is to start with a low dose and gradually increase
by 1 drop each day until a slight feeling of nausea develops and then cut down
by 2 drops. After several days you try increasing again, and so gradually work
your way up to 15 standard drops 1 to 3 times daily for about one week. But
many individuals do not get that far because they become sensitised, and nausea
starts already at low levels without sufficient antimicrobial effect.
Nausea can be reduced by taking the remedy
after a meal, but this also reduces the antimicrobial effect compared to taking
it on an empty stomach. It may be best to take MMS just before going to bed.
MMS works very fast, and people often become sleepy after taking a dose of MMS.
Also it is easier to cope with nausea if you can fall asleep.
An
alternative method with acute infections is to take a very high dose or even a
high double dose one hour apart and accept that you will feel nauseous and may
vomit for a day or longer. Nausea or vomiting usually starts 2 or more hours
after ingesting a very high dose, and by then the chlorine dioxide has already
been absorbed so that vomiting does not cause any loss in effectiveness. This
method has been used in the successful treatment of malaria, blood poisoning,
and other acute infections. It commonly clears the condition in one hit. For
details of oral MMS therapy see my Sodium Chlorite article (7) and also Jim Humble’s Standard MMS Protocol (8).
An
alternative method for intensifying the antimicrobial program or for overcoming
an infection is by taking 3 to 4 drops of acidified and diluted MMS every hour
and a half for several days. Temporarily reduce the dose if any nausea should
occur. You may do this by swallowing the MMS or with oral absorption or a
combination of both.
To quickly
stop nausea you may take 1000 mg or more of vitamin C, but this also stops the
antimicrobial activity. To avoid or minimize oxidative damage I recommend
taking MMS only in the morning and evening or only once a day and use a
combination of antioxidants, including vitamin C, at lunchtime or several hours
away from the MMS. To minimize unpleasant side effects try to alkalize the body
before going on a course of MMS.
The main
danger after a high dose of MMS is from low blood pressure and hypoglycemic shock due to fluid loss after vomiting and
diarrhoea. If this should happen take immediately a high dose of vitamin C to
stop the reaction, lie down, and drink lots of lightly salted and sweetened
water. A general recommendation for rehydrating after vomiting and diarrhoea is
a fluid made with 6 level teaspoons of sugar
and 1/2 level teaspoon of salt dissolved in 1 litre
of water, or alternatively use salted rice water. Also.
Individuals with G6PD deficiency, an enzyme deficiency with a tendency to
haemolytic anaemia, must avoid MMS and other oxidising substances.
If this MMS
program causes problems or is too difficult then you may try instead oral or
rectal absorption. If used for more than a few weeks, especially for cancer and
autoimmune diseases, then I recommend non-acidified MMS as explained below.
Other
Delivery Options
Because frequently nausea
causes individuals to stop using MMS before the infection or cancer is cleared,
different ways of using it have been explored. Most common among these is transdermal application. When bypassing the stomach nausea
is not normally a problem.
A given number of drops of
MMS are activated with 5 times more drops of acid, after 3 minutes DMSO is added
at the same rate as the acid. After another 3 minute wait the solution is
rubbed into the skin. A variation of this uses 10 drops of MMS and 1 tsp each
of acid and DMSO. This method has also been adopted for cancer treatment,
including by Jim Humble (9).
While this method does not
cause nausea, there is no real evidence that it works. There is even strong
theoretical evidence that it cannot work. DMSO can act as a mild oxidant, but generally, and especially in the
presence of stronger oxidants, it acts as an antioxidant. The main metabolite
when DMSO is oxidised is MSM, which may also be written as DMSO2. If you search
Google for DMSO +antioxidant you find expressions like: “DMSO-The King Antioxidant”
and “It turned out that DMSO was a powerful antioxidant…”
You just cannot combine the most powerful oxidant with a powerful antioxidant
and expect that they do not talk to each other.
However, I still regard it
as useful to apply activated MMS on the skin for topical treatment of local
infections and tumours. While MSM is less effective as a carrier than DMSO, it
does improve passage through the skin, and it is not an antioxidant, so it is
safe to use with MMS. But absorption will be slow, and therefore it is not
suitable for getting chlorine dioxide into the blood.
In contrast, absorption
through the mucous membranes will be fairly fast, and may give better results.
Possible absorption areas are the rectum, the vagina, and the mouth.
Rectal
absorption is similar
to using coffee enemas which is already firmly established in natural cancer
therapy. First you clean the lower bowel with an enema.
Then insert a small number of activated drops of MMS in a large glass of water.
Hold for 10 to 20 minutes, expel, use again a cleaning enema, and then insert a
larger number of activated drops in a glass of water.
Try to hold for up to 30
minutes. You may be able to move around during this time but preferably just
sit or lie down. Protect the anus with some fat, cream, or Vaseline. You may
make the solution less acid by adding some bicarbonate as explained for oral
application.
Afterwards you may feel
weak for a while and have much bowel
activity for several hours, and possibly longer. With cancer and other chronic
conditions you may repeat this once a week with increasing numbers of drops.
This will be good with problems in this area, such as
rectal or prostate cancer, irritable bowel, and infections, cysts and cancers
of the female organs.
Vaginal
application is
suitable in case of vaginal thrush to kill the roots and spores of Candida that
will be embedded in the mucous membrane and may cause flare-ups. Start with 1
activated drop in a small glass of water and gradually increase on subsequent
occasions. If the acidity of the solution is a problem you may nearly
neutralise it with bicarbonate several minutes after adding the water. Also try
using the mouthwash solution.
Oral absorption is
my preferred method. I believe that just swishing acidified and diluted MMS in
the mouth may be the best general method to get it quickly into the blood, in
addition to clearing the head spaces. After using 6 activated drops this way
and keeping it in the mouth for about 20 minutes I now always have a pink
tongue on rising in the morning while before it used to be partly coated. A
fragile elderly woman who was afraid to swallow it just kept a few activated
drops in juice in the mouth for a few minutes and then spat it out. After doing
this twice she had much better mobility. This shows that the chlorine dioxide
went quickly into the circulation.
Keeping it in the mouth is not too unpleasant, and the taste buds soon
stop complaining. However, it is
advisable to nearly neutralise the solution with
bicarbonate to protect the teeth. This should not reduce the effectiveness very
much because the chlorine dioxide that produces the peak systemic effect will
have been released in the first 3 minutes. Furthermore after diluting it one
may still wait for several minutes for further saturation of the solution
before neutralising it.
To
1 part of MMS add 5 parts of 10% citric acid and after 3 minutes dilute with 30
ml or a big mouthful of water. Finally add up to 8 parts of a 10% sodium
bicarbonate solution to protect the teeth from acid attack. This gives a pH of
about 5 to 6, and one can keep it in the mouth for 5 to 20 minutes before
spitting it out. You make the 10% sodium bicarbonate solution by dissolving one
level spoonful of bicarb in 9 spoonfuls of water.
Instead of plain water you may also use herb tea or flavor with some fruit
juice, or sweeten with Xylitol or Stevia.
Mouthwash:
I also recommend that
you make yourself a mouthwash by diluting a teaspoon of MMS in 500 ml of water.
This is only slightly alkaline and tends to release small amounts of chlorine
dioxide in contact with acid-forming bacteria. It is also commercially promoted
as the most effective method of removing bad breath or halitosis. It does this
by oxidising smelly sulphur compounds in the mouth to non-odorous sulphates.
Swish a mouthful around for a short time, gargle, and spit it out. You may also
flavour the solution or make it weaker. Some people claim that regular use has
protected them from ‘catching’ infections.
Even more important is the observation
that the combination of occasional oral absorption of chlorine dioxide and
regular use of MMS mouthwash tends to eliminate pathogenic microbes and
inflammations in the mouth. Such microbes and inflammations, be they from root
canals, deep tooth pockets or gum inflammations and other periodontal
diseases, are strongly
implicated in the causation of
arteriosclerosis, heart attacks and other heart diseases as well as
rheumatoid arthritis, diabetes, prostate cancer and other cancers.
You may also combine the stronger
antimicrobial effect of oral absorption with the convenience of a mouthwash:
add a drop or two of lemon juice or citric acid to a teaspoonful of mouthwash
solution and immediately start swishing this in the mouth for a minute or two
before spitting it out. This has a relatively mild effect on the taste buds.
One teaspoonful of mouthwash contains about one drop of MMS.
Non-Acidified
MMS: Medical-type
patents describe the use of stabilised sodium chlorite in oral, topical and
intravenous applications for treating autoimmune diseases and chronic infections,
also hepatitis and lymphoma, and for neutralising the neuro-toxic
effects of acetaldehyde produced by Candida and other fungi. In these cases the
solution is not acidified! This is also suitable for kidney and bladder
infections.
The main beneficial effect with
autoimmune diseases may be due to an ability of sodium chlorite to control the pleomorphic microbes which are not only a root cause of
autoimmune diseases but also of cancer. Therefore after a short period of using
acidified MMS, autoimmune diseases as well as cancer may be treated
periodically with non-acidified MMS. This is much less damaging to antioxidants
in the body than prolonged use of acidified MMS, and the incidence of nausea
will be greatly reduced.
As an average dose try 5 to 10 drops
(or half a ml) of MMS once a day after the evening meal or at bedtime in a
drink. In this way you may use vitamin C and other antioxidants until
mid-afternoon without interfering with the action of MMS. However,
non-acidified sodium chlorite. just like acidified MMS, does react with and
reduce the glutathione in body cells. Therefore use it only for limited
periods, e.g. for one week every other week, and limit this program to 6 to 10
weeks (3 to 5 cycles) before a longer
break of one or more months. Alternatively use it 5 days a week for 3 to 5
weeks. During breaks use higher amounts of other antimicrobials instead, such
as Olive Leaf Extract or Lugol's solution.
Intravenous
MMS
Intravenously MMS commonly
has been used without acid activation. Jim Humble has had it many times, and
also used up to 2 times 30 acidified drops orally without getting a reaction.
But recently he had one
acidified drop intravenously and that caused a Herxheimer
reaction. He believes that acid activation increases chlorine dioxide release
by up to 300 times. Next day another drop did not cause a reaction but 2 drops
the following day reacted again. The same happened with further increased drops
(10).
The effectiveness of
antimicrobial therapy can often be judged by its ability to trigger a Herxheimer reaction. This is caused by the waste material
of a large number of microbes being killed suddenly. It consists of extreme
fatigue, chills, diarrhoea, muscle and joint pains, and other flu-like symptoms
for several hours or days. During a reaction you stop the antimicrobial therapy
and instead have a high intake of good quality water, juices and herb teas.
The question now is what
kind of microbes resisted an extremely high double dose of 30 oral drops but
then readily died from one acidified IV drop? The oral doses would have cleared
these microbes from the blood and lymph system, and probably from most tissue
and organs. I can think of only one explanation, that these were so-called nanobacteria. They attach to blood vessel walls and protect
themselves with a calcified shell, and in the process also calcify the tissue,
thereby causing arteriosclerosis and related symptoms (11). Even one drop of
acidified MMS would have caused a high peak concentration of chlorine dioxide
in the blood vessels, apparently enough to penetrate the calcified barrier of
some nanobacteria.
Few individuals in Western
countries will have the opportunity to use IV MMS therapy, and I also regard
this as a rather inefficient way of dealing with tissue calcification. There
are better ways, such as preventing the formation of nanobacteria
in the first place, and then dissolving existing calcifications with magnesium
chloride and lemon juice or cider vinegar. Deprived of their calcium protection
the immune system can then easily deal with the nanobacteria.
Integrating Therapies
Often individuals
find it difficult to continue with the MMS program because of frequent nausea.
This is especially a problem with advanced cancer and other long-term
conditions. Therefore I generally recommend a program of intestinal sanitation
and antimicrobial therapy with milder agents before starting MMS therapy. This
will remove most of the toxic load with less discomfort than by starting
immediately with MMS. As part of this preliminary program I recommend a period
of intestinal sanitation with garlic, psyllium, sodium bicarbonate and probiotics, followed by a 3-week course of Lugol’s iodine solution (12).
In the case of
cardiovascular diseases and arteriosclerosis it has been suggested that with MMS therapy
cholesterol deposits may be removed too fast and lead to a weakening of the
affected blood vessels. To avoid or minimize problems it has been recommended
to take high amounts of vitamin C, up to 10 g daily in divided doses, for
several weeks before starting MMS therapy. This is to strengthen the blood
vessels and make them more elastic. Some other nutrients to improve elasticity
are lemon juice, green juices, copper salicylate,
magnesium chloride, MSM, and N-Acetylglucosamine.
For cancer I believe that MMS
treatment as a primary therapy has shown good results only with lymph, blood
and skin cancers. It will be much more effective to integrate MMS therapy into
a holistic program as outlined in my article The Holistic Solution to Overcoming Cancer (13).
With colds chlorine dioxide kills the virus but does not stop the
beneficial mucus release. This can be stopped with the Sugar Cure: Keep a
teaspoon of fine sugar in the mouth until it is dissolved, then spit out and
take another teaspoonful. Continue with this for one or two hours and repeat on
subsequent days as required. The sugar draws mucus combined with lymph fluid
from the lymph glands and so gradually clears the headspaces, see Instant Cure of the Common
Cold.
With Influenza I recommend taking several high doses of MMS for only one
or two days and then taking instead high amounts of antioxidants and especially
sodium ascorbate, e.g. half a teaspoon in liquid
(e.g. fresh citrus juice) every 2 hours until recovered.
Some
individuals, especially with advanced degenerative diseases, may become very
weak on prolonged MMS therapy seemingly unrelated to die-back reactions. Also
the eyesight may rapidly deteriorate. I believe that this is mainly due to
antioxidant deficiency, and especially to lack of glutathione and superoxide dismutase.
This
again raises the question of the appropriate use of MMS therapy. In my article How to Overcome Autoimmune Diseases (14)
I show that most chronic degenerative diseases are associated with nanobacteria and pleomorphic
microbes that appear to arise from the inside, out of diseased body cells,
rather than from outside of the body. The main cause of this microbial uprising
is seen as the accumulation of toxic metabolic residues inside the cells,
especially affecting the energy-producing mitochondria.
Experience
shows that it is definitely beneficial to eliminate the higher bacterial and
fungal forms of this microbial overgrowth, and MMS is an effective part of an
integrated antimicrobial therapy. But it is generally not possible even with
MMS to eliminate the lower forms of nanobacteria and
endogenous viral particles. Even if one continues with a long-term MMS
maintenance therapy, these microbes will continue to rise up, and the
accumulating toxic residues will in time cause increasing health problems in
other ways. Therefore, the rational solution is to remove these toxic residues
by the time-honored method of raw-food cleansing combined with an effective antimicrobial therapy.
While some viral infections can be effectively treated with MMS, others
such as hepatitis C, Lyme disease and even HIV, while often showing
improvement, are overall much more resistant. On the other hand, there is good
evidence that high antioxidant therapy is very effective against viral
conditions. For instance there are countless publications in the literature of
Orthomolecular Medicine (http://www.orthomolecular.org) about the quick and
effective treatment of serious viral infections with very high amounts of
vitamin C. Also hepatitis C can be effectively treated with high amounts of
various antioxidants (15).
Therefore, I believe that it is much more effective to use both
treatments in an integrated way. With a serious or resistant viral disease I
would alternate a short high-dose MMS treatment with a longer period using high
amounts of a wide range of different antioxidants.
Oxidants versus Antioxidants
Besides
nausea also inflammations may arise as a side effect of MMS therapy. To
understand this effect we need to have a look at the function of inflammation
and the role of oxidants and antioxidants in this process. Inflammations
increase blood and nutrient supply to an area and are essential for the immune
system to work, and for healing of damaged organs and tissue to occur. If the
immune system is not strong enough to eliminate invading microbes and diseased
body cells, originally healing immune inflammations become destructive chronic
inflammations, and this is a symptom of our present epidemic of chronic
diseases.
Oxidants
support the immune system by killing microbes outright and by giving the immune
system more firepower. This results in increased inflammation and body acidity
when using strong oxidants such as chlorine dioxide. Therefore as during any
real health improvement various healing reactions, including temporary
inflammations, may develop during MMS treatment. This is beneficial for healing
in the long-term even if uncomfortable in the short-term. For a more detailed
explanation of this process called a healing crisis or healing reaction see www.health-science-spirit.com/healingcrisis.html.
Antioxidants
have the opposite role to oxidants. They protect our body cells and functions
from being oxidized. Oxidation needs to take place only in well established and
protected pathways to generate energy or to eliminate invaders and harmful
agents. If we step up the intake of oxidants, we also need to increase the
intake of antioxidants otherwise we may get unnecessary inflammations due to
irritation of tissues and other degenerative changes. An example of this is
deteriorating eyesight that may occur when using high doses of MMS for more
than a few days.
Jim
Humble’s position is that antioxidants are not
necessary with MMS therapy. He states: “You don’t have to protect the body from
the small quantities ClO2 generated by MMS. It simply does not oxidize any
beneficial bacteria or body cells. No side effects have been reported in
hundreds of thousands of clinical trials and tests (16).” I find this statement
surprising as even from a small number of users I received several
communications that I interpret as damage due to antioxidant deficiency.
Therefore I strongly disagree with the position of Jim Humble in regard to
antioxidants.
My
view is supported by Dr Thomas Lee Hesselink (17). In
an exhaustive literature search he shows that chlorine dioxide kills the
malaria parasite by oxidizing its vital antioxidants, including glutathione,
alpha lipoic acid, and coenzyme A. He writes:”… no
amount of intraplasmodial glutathione (GSH) could
ever resist exposure to a sufficient dose of chlorine dioxide (ClO2). Note that
each molecule of ClO2 can disable 5 molecules of glutathione.” If parasites are
being killed by disabling their glutathione and other essential antioxidants
then the glutathione and antioxidant systems in our body will be just as
vulnerable.
I
believe that all those who live on a conventional diet, or who have an
infection or a chronic disease or who smoke or with advancing age are highly
likely to be antioxidant deficient. Any of these conditions will be made worse
by having persistent exposure to oxidants, be it from chlorinated water,
polluted air, fried food, or from a strong oxidant such as chlorine dioxide.
The
problem is not in chlorine dioxide oxidizing beneficial bacteria or body cells
but rather that it reacts strongly with a wide variety of antioxidants, and so
makes an antioxidant-deficient body even more deficient. There is evidence that
antioxidant deficiency is a main cause of the accumulation of oxidized waste
products and protein debris inside cells that lead to chronic degenerative
diseases and the uprising of nanobacteria and pleomorphic microbes (14).
Therefore,
I regard long-term MMS therapy without antioxidant protection as contributing
to the development of chronic diseases. It is important to increase antioxidant
intake when using MMS. However, oxidants and antioxidants should be separated
during the day or they may neutralize each other. Jim Humble recommends a
3-hour period of separation, and I agree with that. For instance you may use
MMS before breakfast and at bedtime and antioxidants from mid-morning to
mid-afternoon. However, my preference for long-term antimicrobial therapy is
alternating MMS, mainly in non-acidified form, with other antimicrobials as
outlined in the Ultimate Cleanse.
This
does not only apply to antioxidants in supplement form, such as vitamin C and
E, B-complex, coenzyme Q10 or grapeseed extract, Beta
1,3D Glucan and immune stimulants, but
also to food high in antioxidants, such as purple berries and juices, fresh
fruit, polyunsaturated oils, turmeric, black or green tea, cocoa and others.
Because chlorine dioxide reacts especially well with vitamin C, it is advisable
to take 1 gram or more when on a high dose of MMS for more than a few days to
protect oxidation-sensitive structures, such as heart, brain and eyes.
Conclusion
The discovery of antibiotics was hailed
as the greatest advance in modern medical history. I believe the internal use
of MMS is even more important. But just as antibiotics have a darker side by
causing dysbiosis and Candidiasis if improperly used
without a fungicide, so MMS carries the danger of causing health deterioration
if used without antioxidant protection.
In a more enlightened future when the
medical system refocuses on healing rather than profit the treatment of serious
infections may just require one intravenous infusion of acidified MMS. Until
then we have a variety of other methods to choose from.
I believe the most effective approach
for a serious acute infection is a high dose of 15 drops or a high double dose
of 10 to 15 drops, and just accept that you will vomit for a day or two. If the
problem is less serious then a double dose of 6 drops
followed by another 6 drops an hour later has been shown to be very effective.
Even this may cause nausea and some vomiting. Alternatively you may experiment
with absorbing a high dose through the mucous membranes of the mouth or the
rectum, depending somewhat on where the infection is centred.
With a chronic degenerative disease I
would alternate short periods of high MMS intake with longer periods of high antioxidant
intake from foods and supplements. In addition I would use other therapies such
as cleansing to remove the basic cause of the disease.
I would also apply activated MMS to
infected areas close to the skin. When starting on a health program I would
first attempt intestinal sanitation and reduction of any microbial load with
milder agents, such as Lugol’s iodine solution before
starting with a gradually increasing dose of MMS as in the standard
program.
Presently MMS is still available over
the Internet. There are 2 types with slightly different composition. The
product used by Global Light (http://www.globallight.net) and its
distributors is made from technical-grade sodium chlorite flakes containing 20%
sodium chloride, while the MMS from Stride into Health (www.strideintohealth.com) is a pure
sodium chlorite solution as used in the food industry. Nominally MMS is a 28%
solution of the flakes but because of its high sodium chloride content the
effective concentration of sodium chlorite is 22.4% which is the same in both
products. Also check for new protocols at www.jimhumble.biz.
REFERENCES
Disclaimer: The aim of this web site is to provide information on using natural healing methods in the treatment of illness and health improvement. The author cannot accept any legal responsibility for any problem arising from experimenting with these methods. For any serious disease, or if you are unsure about a particular course of action, seek the help of a competent health professional.