DMSO - The Real (MMS) Miracle Mineral Solution
DMSO - The Real (MMS) Miracle Mineral Solution
DMSO - The Real (MMS) Miracle Mineral Solution
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DMSO is the last part of the traditional MMS kit … it’s normally added at the end of making – however there is
much more to DMSO than meets the eye!
In 1866, Russian scientist Alexander Saytzeff isolated a most curious and peculiar chemical compound. It was
crystalline, odor-less, non-toxic and had a garlic-like taste when consumed.
At the time, Saytzeff had no way to predict that his discovery was going to prove highly controversial
throughout its entire medical history, that it was going to be tested in thousands of studies and provide
miraculous relief for numerous patients.
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I’m talking here about dimethyl sulfoxide (DMSO), an organic sulfur compound which was used only as an
industrial solvent, that is, until its medical properties were discovered in 1963 by a research team headed by
Stanley W. Jacob, MD.
DMSO – Click Here (https:// amzn.to/ 2NjHTEC) is a by-product of kraft pulping (the ‘sulfate process’) which
converts wood into wood pulp leaving almost pure cellulose fibers.
As industrial as it may sound, the process simply entails a treatment of wood chips with a mixture of sodium
hydroxide and sodium sulfide, known as white liquor, breaking the bonds which link lignin (from the Latin
word lignum, meaning wood) to the cellulose.
DMSO is useful as a pain reliever and also in burns, acne, arthritis, mental retardation, strokes, amyloidosis,
head injury, scleroderma, it soothes toothaches, eases headaches, hemorroids, muscle strains, it prevents
paralysis from spinal-chord injuries and softens scar tissues.
In fact, it is useful in well over 300 ailments and is safe to use. You might think that a compound that has so
many alleged uses and benefits should be automatically suspect, so let’s have a close look at its properties
and the data available and we’ll shed some light in this miraculous chemical.
DMSO is an intermediate product of the global Sulfur Cycle which distributes bioavailable sulfur for all
animal and plant life (Parcell, 2002).
Sulfur compounds are found in all body cells and are indispensable for life, they are needed for a number of
chemical reactions involved in the detoxification of drugs and other harmful toxins, and they have potential
clinical applications in the treatment of a number of conditions such as depression, fibromyalgia, arthritis,
interstitial cystitis, athletic injuries, congestive heart failure, diabetes, cancer, and AIDS (Parcell, 2002).
Among the sulfur compounds, DMSO is probably the one that has the widest range and greatest number of
therapeutic applications ever shown for any other single chemical. It has around 40 pharmacological
properties that may be beneficial in the prevention, relief or reversal of numerous diseases (Morton, 1993).
Someone complained to Dr. Jacob of a splitting headache and gave him permission to apply some
DMSO after hearing of its capabilities. The headache was gone in minutes, came back in four hours, and
left for good after DMSO was applied a second time. Used for one purpose, sometimes it did another;
put on a cold sore, within a few hours it cleared up a woman’s sinusitis. A woman who had had a stroke
found after DMSO was painted on her painful jaw that she could now write with her paralyzed hand and
could walk better. (Haley, 2000)
Therapeutic Properties
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DMSO – Click Here (https:// amzn.to/ 2NjHTEC) is an effective pain killer, blocking nerve conduction fibers
that produce pain. It reduces inflammation and swelling by reducing inflammatory chemicals. It improves
blood supply to an area of injury by dilating blood vessels and increasing delivery of oxygen and by
reducing blood platelet stickiness.
It stimulates healing, which is a key to its usefulness in any condition. It is among the most potent free radical
scavengers known to man, if not the most potent one. This is a crucial mechanism since some molecules in
our bodies produce an unequal number of electrons and the instability of the number causes them to
destroy other cells. DMSO hooks on to those molecules and they are then expelled from the body with the
DMSO.
DMSO also penetrates the skin and the blood-brain barrier with ease, penetrating tissues, and entering the
bloodstream.
Furthermore, DMSO protects the cells from mechanical damage and less of it is needed to achieve results
as time passes as oppossed to most pharmaceuticals where increasing doses are required. It has a calming
effect in the central nervous system and it reaches all areas of the body, when absorbed through the skin,
including the brain.
That is, DMSO applied to one area often leads to pain relief in some other location due to its systemic effect.
It acts as a carrier for other substances or drugs and it also potentiates their effect. In fact, certain drugs
dissolved in DMSO, such as corticoids, antibiotics and insulin, may be used in a lower dose than usual without
reducing their therapeutic efficacy and in addition, their undesirable side effects are greatly diminished. Also,
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drugs are able to pass through the blood-brain barrier which is usually impenetrable.
DMSO promotes the excretion of urine and functions as a muscle relaxant. It boosts the immune system,
increasing the production of white cells and macrophages that destroy foreign material and pathogens in
the body. It also has anti-bacterial, anti-viral and anti-fungal properties.
DMSO also increases the permeability of cell membranes, allowing a flushing of toxins from the cell.
DMSO has radioprotective properties against lethal and mutagenic effects of X-rays in cells, cellular
systems and whole animals. It also has cryoprotective properties, meaning that it is capable of protecting
against injury due to freezing.
DMSO has also been shown to have cholinesterase properties (Sams, 1967), in other words, it inhibits an
enzyme from breaking down acetylcholine, increasing both the level and duration of action of this important
neurotransmitter.
Acetylcholine is responsible for learning and memory and is also calming and relaxing. Acetylcholine is also
a major factor in regulating the immune system, acting as a major brake on inflammation in the body.
As a source of sulfur, DMSO aids in heavy metal detoxification. Sulfur binds with toxic heavy metals
(mercury, lead, aluminum, cadmium, arsenic, nickel) and eliminates them via urination, defecation and
sweating.
DMSO- Click Here (https:// amzn.to/ 2NjHTEC) is sold in health food stores, mail-order outlets, on the
Internet, and in most countries around the world.
It is used by millions for its health benefits yet in the U.S., DMSO has FDA approval only as a preservative of
stem cells, bone marrow cells, and organs for transplant, and for interstitial cystitis – a painful inflammatory
condition of the bladder which is very difficult to treat with other therapies.
That DMSO has not found favor as a remedy for other medical conditions is partly due to the inability to test
it in double-blind experiments.
Blind studies, as the name suggests, requires that a study be done without knowing which patient is taking
the placebo or the drug. In the case of the DMSO, a blind study is impossible since the peculiar garlic-like
taste and smell (no matter the route of application) gives it away and no satisfactory placebo could be
devised that would mimic this particular effect of DMSO (Steinberg, 1967).
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The FDA and ‘big pharma’ would prefer we remain dependent on their drugs,
If you search for DMSO on the U.S. National Library of Medicine (pubmed.gov), you’ll get almost 30,000
indexed results, making it one of the most studied compounds of our time.
Yet, we are led to believe that DMSO can’t pass the required regulations for its approval in other medical
conditions even though its effectiveness and low toxicity profile is unquestionable.
You see, DMSO is a common chemical that can be manufactured cheaply. No drug company can get an
exclusive patent since it is also a natural compound, therefore there is no significant financial return.
“ I don’t care if DMSO is the major drug of our century and we all know it is, it isn’t worth it to us” [CBS
TV show 60 minutes with Mike Wallace, The Riddle of DMSO].
If DMSO were to be approved by the FDA, it would be competitive and drug companies would be unable to
hold the patents. In the words of the director of the Bureau of Drugs of the FDA, J. Richard Crout, M.D., “DMSO
is a low toxicity and safe compound (…)
I think that it is a fact of life that drug companies are not going to invest in something unless they think there
is some financial return” [CBS TV show 60 minutes with Mike Wallace, The Riddle of DMSO].
Despite restrictions on the use of DMSO, thousands of Americans purchase it on the ‘black market’ each year,
its popularity due not to publicity, but rather ‘word of mouth’.
When you have something that relieves all kinds of ailments, including some life-threatening ones, people
naturally recommend it to friends and family!
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In Perspective
In the 1960s, research with DMSO – Click Here (https:// amzn.to/ 2NjHTEC) on humans was temporarily
halted after certain animals treated with DMSO were found to have changes in the eye lens.
Some of these changes resembled those seen in aging dogs (Gordon, 1967), but nevertheless, research was
gradually restarted after no evidence was found of eye changes in humans.
As Daniel Haley reports in his book Politics in Healing: “ Tests in rabbits, dogs, and pigs (but not humans) had
shown some problems.
When quantities of DMSO equal to about ten times the maximum human dose were given every day over a
period of six months, slight changes in the lenses of the animals’ eyes would result, enough to produce a slight
nearsightedness.
This is the typical rough edged way pharmaceutical-sponsored-studies work, in attempt to find a toxic or
adverse reaction at a certain concentrations to focus on.
They can then fabricate statistics and data that focus on mechanisms of action at toxic doses (much like the
recent 2020 HCQ scandal) and publicize the scary story to the media who then help the pharmaceutical
companies retain their profits and market dominance, it’s not cold conspiracy, it’s just business as usual.
The lens changes were not enough to cause dogs difficulty when running – they didn’t bump into things – and
in some cases, the changes disappeared after the massive DMSO doses were stopped. In no test at that time
or since has DMSO ever caused cataracts, either in animals or in humans” (Haley, 2000).
In fact, DMSO is effective for macular degeneration and retinal disease, both diseases of the eye.
This effectiveness was first discovered when patients with retinitis pigmentosa, a retinal disease, were taking
DMSO for certain musculoskeleteal disorders. They sensed that their vision had improved and some had
remarkable results (Morton, 1993).
As far as eyes are concerned, the evidence on DMSO is quite to the contrary. When several patients
treated with DMSO for muscular problems reported to Dr. Jacob that their vision had improved, he sent
them to Dr. Robert O. Hill, ophthalmologist at the University of Oregon Medical School.
Confirming the favorable changes, Dr. Hill began his own experiments with DMSO (after it was known
that the lens changes did not happen in humans). His research showed drops of 50% DMSO to be
effective in retinitis pigmentosa and macular degeneration, and presented a report on this at the New
York Academy of Sciences symposium in 1971. (Haley, 2000)
In contrast, the number of medication-related deaths in the U.S. is estimated at over 200,000 a year, making
medications the third or fourth leading cause of death (Pezzalla, 2005).
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I would however personally put them in first place along with the reality of the first publicised studies in
Iatrogencis, and not fabricated and hidden statistics of the more recent Iatrogenics studies.
Even common pain relievers called NSAIDs, examples of which include Advil, Motrin, Aleve and aspirin,
account for an estimated 7,600 deaths and 76,000 hospitalizations in the U.S. every year (Tamblyn et al,
1997).
Taking this into consideration, it is safe to declare that DMSO is among the safest substances in the
world today.
In fact, the classic test for toxicity -the LD-50 test – measures the lethal dose (LD) at which half of a group of
test animals is killed. The LD-50 tests for aspirin and DMSO show that aspirin is seven times more toxic than
DMSO (Haley, 2000).
DMSO is generally applied to the skin in a gel, cream, or liquid. It can be taken by mouth or as an intravenous
injection, in many cases along with other drugs.
Dosage
The usual oral dose of DMSO is one teaspoon per day of DMSO 70% (Morton, 1 993). But since it can trigger
detoxification reactions and DMSO’s total excretion from the body can take several days, it is best to do it
only once a week.
When you use liquid DMSO in the skin, let it dry for over 20 to 30 minutes before wiping the rest out. The skin
must be clean, dry, and unbroken for any topical use of DMSO.
The face and the neck are more sensitive to DMSO and no higher concentrations than 50% should be applied
there.
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Topical concentrations of DMSO should be kept below 70% in areas where there is a reduction of circulation.
When 60 to 90% DMSO is applied to the skin, warmth, redness, itching, and sometimes local hives may
occur.
This usually disappears within a couple of hours and using natural aloe vera, gel or cream, will help
counteract or prevent this effect. When 60 to 90% DMSO is applied to the palm on the hand, the skin may
wrinkle and stay that way for several days.
“My brother put some DMSO gel (70% dmso, 30% aloe vera) on his shoulders and lower part of neck
because he had muscle pain/soreness in that area, and it caused skin redness/irritation for a few hours,
although it did diminish the muscle soreness as well…
my grandma has rheumatoid arthritis that made her legs swell up and hurt continuously, and I had her
apply the same DMSO gel, and after about 2-3 days of applying it once a day, the swelling was 90%
gone, and I think within 4-5 days it was 100% gone, and she said the pain diminished as well.” – Michael
Shatskiy, Los Angeles, California, United States
Chronic pain patients often have to apply the substance for 6 weeks before a change occurs, but many
report relief to a degree that had not been able to obtain from any other source.
In general, the greater the chronicity of the disorder, the longer the treatment with DMSO must be employed
in order to achieve palliation (Steinberg , 1967).
Common health problems for which people will apply topical DMSO at home include acute musculoskeletal
injuries and inflammations.
The earlier DMSO is used, the more dramatic the result. A 70% concentration of DMSO mixed with water in
volumes ranging from 8 to 12 ml, applied on and around the injury in a wide area at least three times daily,
will have a healing affect in 4 out ot 5 people.
It provides rapid amelioriation of pain and increased mobility and reduction of inflammation when used
topically. You can see a positive response within 5 to 20 minutes and usually lasting for 4 to 6 hours.
(Steinberg, 1967).
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“Applying DMSO where it hurt to a six-year-old wasted from rheumatoid arthritis, in a half hour the child
could move her shoulder and turn her head for the first time in two years. Persuaded to try walking, she
managed a few steps and then burst into tears. “Why are you crying?” Dr Jacob asked her. “Because it
doesn’t hurt anymore”, she replied. (Haley, 2000)
“My brother has arthritis of the spine. He is in pain and bedridden more than half the time. When he is
treated with DMSO, he is able to lead a normal, active life… Just one application of this cheap, safe
DMSO changed my brother from a grimacing patient into an active, pain-free man in exactly 30
minutes!” (Haley, 2000)
June Jones, once quarterback and later coach of the Atlanta Falcons pro-football team, had a bursitis
calcification in his right shoulder. His career almost didn’t happen as he could hardly lift his arm, let
alone throw a football. But he was aware of DMSO and had used DMSO for sprains, like thousands of
others. He received a shot of DMSO in the shoulder and after using DMSO for 30 days straight, the
calcification disappeared. (Haley, 2000)
Stroke
Given soon after a stroke, DMSO can dissolve the clot that causes the stroke, restoring circulation and
avoiding paralysis.
Once DMSO gets into the body either daubed on the skin, given in I.V., or by mouth, it permeates the body
and crosses the brain barrier, so even taken orally it can improve circulation. Ideally it should be I.V.
Even though DMSO 40% causes a prolongation of bleeding time, it is still indicated for use in treating
embolic or hemorrhagic stroke.
DMSO is superior to any other treatment for wounds to the brain where a great deal of bleeding is present
(Morton, 1993).
One man who had a stroke at 7:30 AM refused to go to the hospital until after his wife had spoken with
Dr. Stanley Jacob, which didn’t happen until 6:30 PM. Starting at 7 PM the day of the stroke, she gave
him one ounce of 50% DMSO in a little orange juice every 15 minutes for two hours and then every half
hour for two hours.
The next day, her husband was better and soon returned to normal. A substance that can stop a stroke
as it’s happening is something many might want in their home medicine chest .(Haley, 2000)
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Angina, Heart Attacks, Injuries of the Brain and Spinal Chord
DMSO may help neutralize harmful effects on the heart and brain in medical disorders involving the head
and spinal chord injury, stroke, memory dysfunction, and ischemic heart disease (Jacob, de la Torre, 2009).
A 40% DMSO solution should be administered within four hours to be effective, within ninety minutes is best.
After I.V. administration of DMSO, there is an elevation in the amount of spinal cord blood flow to the
region of trauma. One of the first things that happens after spinal cord trauma is that a reduction of
oxygen and blood flow sets in, inasmuch as the blood vessels constrict or shut down…
Without some treatment, the tissue swells. Eventually, this leads to paralysis. In a cerebral stroke, the
animal will either become comatose or lethargic or die. With DMSO infusion immediately after injury (or
stroke) all this is prevented. – Dr. Jack de Ia Torre, professor of physiology and neurosurgery at the
University of New Mexico
Dr. Stanley Jacob has even given DMSO intravenously to people who were already paralyzed –
paraplegics – and some regained use of limbs. One man, quadraplegic, recovered enough to go
through college and then to work in a bank. (Haley, 2000)
Infections
When combined with antibiotics, DMSO will convert bacteria which are resistant to a given antibiotic to being
sensitive to that same antibiotic and probably a 80 to 90 per cent solution of DMSO will be required in order
to be clinically useful ( Pottz, Rampey, Benjamin,1967).
DMSO has been used to transport antibiotics to hard-to-reach areas of the body with excellent results, such
as the bone marrow and brain (Sanders, 1967).
DMSO can dissolve a virus protein coating, leaving the virus core unprotected with its nucleic acid exposed
to the immune system.
Applied topically, it alleviates the lesions that occur as a result of Herpes Zoster, shingles (Morton, 1993).
Placed into the nostrils or topically in the face, DMSO can open blocked sinuses within a few minutes and it
has been used with sucess in patients with polyps (Marvin, 1967).
DMSO can clear up gum disease and reduce tooth decay and their pain by painting it on the involved areas.
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“I have some pharmaceutical grade DMSO and I pour about two teaspoons in a glass in the evening, put
my 20 mg of doxycycline in it, add about 2 teaspoons of distilled water, and then swish it around in my
mouth for about 2 or 3 minutes and then swallow it.
So I guess it is about 50% solution. It’s really working on my mouth. That inflamed area of my jaw has
calmed down about 70% in just a couple of days. Or more, actually. I expect it to be completely soothed
by tomorrow after tonight’s dose of DMSO.” – L., Toulouse, France
A concentration of 50 to 80% put on two or three times a day will flatten a raised scar after several months. It
is of considerable value in superficial burns (Goldman, 1967) and when applied quickly to an injury, it can
eliminate any bruising.
“I have been applying it to my face for two weeks… I had a bout of acne in March, and this healed the
damage pretty well but what amazed me is that my hyperpigmentation (melasma) has also faded very
noticeably. In fact, it’s amazing!” – HG, United States
“I diluted a 50% solution and applied it topically to the inflamed lymph node. I applied it again this
evening. I am totally amazed! There is a noticeable decrease in the size of the node, in just two
applications! And it no longer feels matted. This node has been swollen for over 20 years!!! – Melissa
Medlock, Coldwater, Michigan, USA
Podiatry
DMSO can be effective in the treatment of painful corns, calluses, ingrown toenails, bunions, hammertoes,
heel spurs, and the inflammation of gouty big toes.
Topical DMSO can whiten telangiectasias, small dilated blood vessels near the surface of the skin. It can also
decrease the size of varicosities in the legs and the inflammation that goes with it, along with a relief of their
cramping discomfort (Marvin, 1967. Blumenthal, Fuchs, 1967).
Eye problems
One drop of a 25% DMSO solution (diluted in sterile physiologic or saline solution) once or twice per day is
useful for eye problems, including cataracts or glaucoma.
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“DMSO is amazing, I’ve also read various good results with using it in the eyes. Being the adventurous
type myself, today I diluted DMSO down to 30% and put 2 drops in one of my eyes that has been having
red spots around the iris.
The red spots diminished drastically. The only side effect was a slight burning sensation, similar to those
drops you get when one goes for a glaucoma test, without the side effect of dilated pupils.” – DZ, United
States
Headaches
DMSO – Click Here (https:// amzn.to/ 2NjHTEC) is highly effective in vascular headaches and in muscular
tension which so often goes with headaches. It may be used on hairy areas such as the scalp and it also may
be used near the eyes. A 90% solution is more effective (Ogden, 1967).
Mental Disorders
DMSO has been useful in the treatment of patients with the following diagnoses: (1) overexcited states (acute
schizophrenic reactions, manic phase of the manic-depressive psychoses, alcoholic psychoses,
symptomatic psychoses); (2) some symptoms of the chronic psychoses (autism, stereotypia, negativism,
abnormal behavior or delusional states) ; (3) severe neuroses (anxiety reactions, obsessives)( Ramírez, Luza,
1967).
McGrady called special attention to an extraordinary paper presented by Dr. Eduardo Ramirez and Dr.
Segisfredo Luza of the Ayetano Heredia University in Lima, Peru.
After extensive tests on animals and then on normal humans, Dr. Ramirez reported “injecting 50% or 80%
DMSO intramuscularly into patients with acute and chronic schizophrenia” and that “of the 14 acute
cases, every single one was discharged from the hospital within 45 days after the start of DMSO
treatment…
He said that 4 of the 11 chronic cases, one of whom has been ill for 14 years, were discharged
eventually, and the other 7 improved a great deal and were given occupational therapy… He observed
rapid decrease in agitation… recession of persecution feeling, a relatively sudden tendency to
communicate and to stay clean.., the wane of obsessions, return to alertness, and a calmness where
there had been restlessness and anxiety”. (Haley, 2000)
Genitourinary disorders
DMSO – Click Here (https:// amzn.to/ 2NjHTEC) has been used in the treatment of a number of patients with
various genitourinary disorders, including Peyronie’s disease, interstitial cystitis, acute epididymitis. Some
have obtained dramatic and gratifying relief of symptoms (Persky, Steeart, 1967).
Miscellaneous
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DMSO – Click Here (https:// amzn.to/ 2NjHTEC) in conjunction with other treatments has shown to regress
cancer in a very effective way (Ayre, 1967).
Intravenous administration of DMSO markedly reduces pathological intestinal permeability while preserving
the gut’s absorption capacities (Wang et al, 1996). Considering that gut permeability (‘leaky gut’) has a
fundamental role in chronic degenerative diseases, this is of great clinical importance.
DMSO also has excellent results in the skin of people afflicted with scleroderma, results which have never
been observed with any other method of therapy (Scherbel et al, 1967).
Mrs. Jean Puccio of Washington, DC testified at hearings of Senator Edward Kennedy’s sub-committee
on health in 1980 on her recovery from scleroderma.
Diagnosed in 1971, she was told that no medication would help, and that she would probably soon face
a wheelchair and early death. By the time she found Dr. Jacob (through word of mouth), she told the
Senators, “I was having difficulty breathing, walking, and eating”.
The disease “thickens the tissue and makes your skin so tight you cannot move. It was difficult for me to
drive, to turn the ignition in my car or turn my body”. Her dentist could not work on her for awhile
because she could not open her mouth. “Now I can open my mouth like anybody”, she said.
After her sensitized skin burned from topical application of DMSO, Dr. Jacob suggested taking it orally.
“Within six months”, she testified, “my condition reversed almost immediately. I can do anything
anybody else can do now” (Haley, 2000).
Hopefully, this brief overview of DMSO’s great capabilities has helped to illustrate how it is indeed, the cure of
our times. I’m convinced of its therapeutic power, both by my own experience and that one of scores of
people, not to mention the back-up of published scientific literature.
Its uses and applications make it a very handy compound to have on your medical shelf. In pure form, the life
of DMSO is indefinite, so it may be used for years.
Troubleshooting
The garlic-like body odor and taste in the mouth that some experience is attributable to a specific DMSO –
Click Here (https:// amzn.to/ 2NjHTEC) metabolite: dimethyl sulfide (DMS), a component of natural onion and
garlic flavors (McKim, Strub, 2008).
This can last for one or two days and in a small number of people, especially men, the odor can be very
pungent. Drinking enough water will help diffuse the smell. Other side effects – such as stomach upset,
headaches, dizziness, and sedation – are very likely related to detoxification reactions – Herxheimer
reactions – prompted by the DMSO.
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Only purified and properly diluted DMSO should be used. When you dilute a pure DMSO solution, always do
it in distilled water. When it is applied, the skin site as well as the applying hand should be thoroughly
cleaned before application.
This is of utmost importance as DMSO’s properties allow contaminants to be absorbed through the skin and
transported into the bloodstream.
DMSO is known to be one of the least toxic substances in biology (Parcell, 2002), so any serious side effects
should come from potential contaminants or the intake of concomintant drugs that DMSO will carry into the
body. Worth repeating again, DMSO and any substance dissolved in it, will penetrate the skin, the blood-
brain barrier, and other parts of the body very fast.
Remember also that DMSO – Click Here (https:// amzn.to/ 2NjHTEC) increases the effects of drugs like blood
thinners, steroids, heart medicines, sedatives, etc. In addition to that, acetone or acid contamination of DMSO
can lead to serious medical consequences.
Be aware of this problem when buying unreliable DMSO. A pure DMSO solution will turn solid (like ice) in the
refrigerator within 2 hours. If, when the frozen bottle is turned upside down, little rivulets of water flow through
the ice, you probably possess the veterinary grade DMSO. This is a 90% concentration. Ten percent is
distilled water (Morton, 1993).
Women are discouraged from using DMSO during pregnancy or breastfeeding, even though DMSO is used
to preserve frozen human embryos. DMSO can interfere with liver function tests and give a false reading.
That problem is easily solved by waiting a week after DMSO usage before taking the test.
Long-term use has been documented as safe. Eye damage, reported in laboratory animals, has not been
confirmed. Side effects such as skin rash and itching after topical application, breaking up of blood elements
after intravenous infusion, can be avoided in large part by employing more dilute solutions.
Despite these side effects, DMSO is used as a preservative for blood elements and stem cells (McKim, Strub,
2008).
When DMSO is diluted with water, heat is released. The bottle will be warm to the touch. This is a temporary,
harmless reaction.
Since DMSO causes dryness and scaling of the outer layer of the skin, skin diseases characterized by scaling
(psoriasis) could be aggravated by the use of DMSO.
But DMSO applied topically for only a few days has been useful in psoriasis. Prolonged use of DMSO for the
treatment of psoriasis is not advised however, as it can worsen the psoriatic condition (Engel, 1967), only
DMSO taken orally is suggested.
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“I’m happy to say that taking DMSO in conjunction with implementing the detoxification suggestions that
were given is starting to take care of many of my remaining psoriasis problems. A couple areas are still
being stubborn, but I’ve noticed a lot of general improvement.
Using DMSO topically also helped improve a patch of eczema that my wife has been bothered by for
quite a while.” – Peter Norquest, Tucson, Arizona, United States
DMSO2, a derivative of DMSO, is better tolerated and doesn’t have the odor and irritation side effects. Despite
this positive aspect, it hasn’t surpassed the effectiveness, fascination and popularity of DMSO.
It is also known as methylsufonlmethane or MSM, an entire topic for another article by itself!
Sulfur is an element of the earth and it is essential to life, it as among the most prevalent elemenents in the
human body.
Allergic reactions to sulfur are not possible because sulfur has no protein component. When people are
‘allergic to sulfur’, what they really mean is that they are allergic or sensitive mainly to certain sulfur-
containing drugs or proteins, most notably sulfa antibiotics (sulfonamides) or to sulfites (preservatives used in
wines and some foods), or to foods with a high sulfur content (broccoli, cauliflower, garlic, onions, etc).
Many individuals with allergies to sulfa drugs, sulfites, or high sulfur containing foods (like the author) do not
experience problems taking DMSO, because apart from sulfur, DMSO bears no relation to these substances.
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Volume 243, Biological Actions of Dimethyl Sulfoxide pages 485–490, January 1975
Robert V. Hill
Department of Surgery
University of Oregon Medical School
Portland, Oregon 97201
This is a second report on preliminary work with dimethyl sulfoxide (DMSO) in the
treatment of certain ocular diseases. The first report was made in February,
1973, at the Science Writers Seminar in Ophthalmology, in Los Angeles.(1) The
retinal diseases reported on there were diabetic retinopathy, macular
degeneration, and retinitis pigmentosa. At that time, DMSO did not appear to be
very beneficial in diabetic retinopathy and macular degeneration, but did appear
to have some beneficial effects in retinitis pigmentosa.
Since that report was presented, further preliminary findings have given cause
for more optimism about the possible beneficial effects of DMSO in macular
degeneration, as well as in retinitis pigmentosa. Because of this evidence, the
author is of the opinion that more extensive, in-depth studies should be done on
these two retinal deterioration gr0ups.(2) Although the possible effectiveness of
DMSO on both of these groups deserves further study, the author has found it
possible to undertake an extensive, in-depth study on only one group at this time,
the retinitis pigmentosa group
PRELIMINARY INVESTIGATIONS
The first clue to the possible efficacy of DMSO in retinal diseases was discovered
inadvertently. Some retinitis pigmentosa patients under DMSO treatment for
certain musculoskeletal disorders felt that their vision had improved while they
were taking the drug. Because of their experience, it was suggested that the
author do a preliminary investigation on the effectiveness of DMSO in the
treatment of retinal diseases.(4)
Such an investigation was begun in 1972, after one patient who was suffering
from retinitis pigmentosa had a rather spectacular recovery of vision after
treatment with DMSO. This treatment consisted of topical application of 50%
DMSO in aqueous solution to the cornea by eyecup immersion, for 30 sec,
twice daily. When his DMSO treatment was started (February 10, 1972), this
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patient could see hand motion only with his right eye, and had a visual acuity of
20/200 (Snellen) in his left eye. Five days later (February 15, 1972), his vision was
measured as 20/70 + 1 in the left eye, and he could count fingers at 5 ft with
his right eye. Three months later, hisvisual acuity was 20/50 in the left eye.
This patient has continued his treatments daily, except for a 1-week trial interval
without DMSO. He noted that his vision began to get worse during this interval, and
when he restarted treatment, his vision returned to the level he had just before
dis- continuance. His most recent visual acuity measurement (January 2, 1974) is
still 20/50 in the left eye, and he is able to count fingers at 6 ft with his right eye.
The evidence of low toxicity gathered in the preliminary investigation was both
subjective and objective. The objective evidence of low toxicity was obtained by
serial fundus photography and by slitlamp photomicrography. No adverse tissue
reactions were noted. Subjective reports by patients on toxic side effects
included reports of temporary stinging (usually 20 to 30 sec) and occasional
burning and dryness of the skin of the lid.
Some patients also reported what might be called a glare effect. It was accom-
panied by increased sensitivity to light, or photophobia, in some, and was
reported as simply a blur by others. This phenomenon occurred within the first
month of the initial DMSO treatment, after some early improvement had been
noted by these patients. The glare or blur lasted for a few days or a few weeks,
and after its disappearance, the subjects again experienced subjective
improvement of vision. This improvement was expressed as improved ability to
get around at night, and improved visual acuity experienced as better perception
of contrast.
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SUMMARY
ACKNOWLEDGMENT
Inspiration and assistance in this study was provided by Dr. Stanley Jacob, of the
University of Oregon Medical School, Portland, Oregon.
For more information, please check this article at the Annals of the New York
Academy of Sciences (http://onlinelibrary.wiley.com/doi/10.1111/j.1749-
6632.1975.tb25391.x/abstract).
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Get a small glass bottle with a glass dropper. Make sure you clean it thoroughly
and/or boil it for a few minutes.
Get some saline solution from the pharmacy (physiologic solution or sterile saline
solution).
Get a 10cc syringe from the pharmacy so you can measure the exact quantities.
With the syringe, put 30cc of saline solution into your small bottle. Then put 9 cc of
your pure 99.9% DMSO solution in the small bottle. Beware that you’ll have to
extract and pour the DMSO liquid with the syringe quickly and as you pour the
DMSO solution, you’ll feel a resistance in the syringe, so you’ll have to apply more
pressure. It might be easier to do it in two steps: first pour 5 cc of DMSO and then
pour 4 cc of DMSO.
Make sure your bottle is appropriately sealed and that nothing else enters the
solution.
As always, proceed with caution, do your homework, and consult a health care provider in case of doubts.
References:
Ayre JE, LeGuerrier J. Some (regressive) effects of DMSO dexamethasone upon cervical cells in cervical dysplasia and carcinoma in situ. Ann N Y Acad Sci. 1967 Mar 15;141(1):414-22.
Blumenthal LS, Fuchs M. The clinical use of dimethyl sulfoxide on various headaches, musculoskeletal, and other general medical disorders. Ann N Y Acad Sci. 1967 Mar 15;141(1):572-85.
Engel MF. Indications and contraindications for the use of DMSO in clinical dermatology. Ann N Y Acad Sci. 1967 Mar 15;141(1):638-45.
Goldman J. A brief resume of clinical observations in the treatment of superficial burns, trigeminal neuralgia, acute bursitis, and acute musculo-skeletal trauma with dimethyl sulfoxide. Ann N
Gordon DM. Dimethyl sulfoxide in ophthalmology, with especial reference to possible toxic effects. Ann N Y Acad Sci. 1967 Mar 15;141(1):392-401.
Jacob SW, de la Torre JC. Pharmacology of dimethyl sulfoxide in cardiac and CNS damage. Pharmacol Rep. 2009 Mar-Apr;61(2):225-35.
Marvin P. Interval therapy with Dimethyl Sulfoxide. Annals of the New York Academy of Sciences. Volume 141, Biological Actions of Dimethyl Sulfoxide pages 551 – 554.
McKim A.S., Strub Robert. Dimethyl Sulfoxide USP, PhEur in Approved Pharmaceutical Products and Medical Devices. Pharmaceutical Technology, May 2008.
Ogden HD. Experiences with DMSO in treatment of headache. Ann N Y Acad Sci. 1967 Mar 15;141(1):646-8.
Parcell S. Sulfur in human nutrition and applications in medicine. Altern Med Rev. 2002 Feb;7(1):22-44.
Persky L, Steeart BH. The use of dimethyl sulfoxide in the treatment of genitourinary disorders. Ann N Y Acad Sci. 1967 Mar 15;141(1):551-4.
Pezalla E. Preventing adverse drug reactions in the general population. Manag Care Interface. 2005 Oct;18(10):49-52.
Pottz GE, Rampey JH, Benjamin F.Ann- The effect of dimethyl sulfoxide (DMSO) on antibiotic sensitivity of a group of medically important microorganisms: preliminary report. Ann N Y Acad Sci.
Ramírez E, Luza S. Dimethyl sulfoxide in the treatment of mental patients. Ann N Y Acad Sci. 1967 Mar 15;141(1):655-67.
Sams WM Jr. The effects of dimethyl sulfoxide on nerve conduction. Ann N Y Acad Sci. 1967 Mar 15;141(1):242-7.
Sanders M. Discussion. Annals of the New York Academy of Sciences. Volume 141, Biological Actions of Dimethyl Sulfoxide pages 649 – 652, March 1967.
Scherbel AL, McCormack LJ, Layle JK. Further observations on the effect of dimethyl sulfoxide in patients with generalized scleroderma. (Progressive systemic sclerosis). Ann N Y Acad Sci.
https://www.cre8-health.com/dmso-the-real-mms-miracle-mineral-solution/ 19/29
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Steinberg A. The employment of dimethyl sulfoxide as an antiinflammatory agent and steroid-transporter in diversified clinical diseases. Ann N Y Acad Sci. 1967 Mar 15;141(1):532-50.
Tamblyn R, Berkson L, Dauphinee WD, Gayton D, Grad R, Huang A, Isaac L, McLeod P, Snell L. Unnecessary prescribing of NSAIDs and the management of NSAID-related gastropathy in
Wang XD, Wang Q, Andersson R, Ihse I. Alterations in intestinal function in acute pancreatitis in an experimental model. Br J Surg. 1996 Nov;83(11):1537-43.
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