This presentation deals with the prevention
and treatment of "blocked oxidation" which we consider
the prime cause of malignant, viral, bacterial, and allergic
diseases.
With our present knowledge it should
be possible to prevent and wipe out cancer and serious infectious
diseases.
We are in an era of destructive therapy,
powerful poisonous insecticides, fluoride poisoning and "embalmed
foods." This is an era of ignoring the principles of healthful
living and then attempting to cure everything by taking an array
of pills.
We believe that the so-called "accepted"
methods of treating cancer are no more successful today than
they were 40 years ago.
We are entering on an era of prevention
and simple effective treatment of malignant, viral, bacterial,
and allergic diseases.
Blocking of,(1)
or injury to the vital oxidation process (respiration) of the
living cells by oxygen deficiency or various toxic substances
we find to be the most important cause of malignant, viral, bacterial,
and allergic diseases. Effective prevention and treatment of
these diseases depends upon the restoration and maintenance of
the normal oxidation process. Knowing and eliminating the oxygen
deficiency and these toxic substances is of prime importance,
but once the blocking process or injury has become established
effective means must be taken to reverse the process and restore
normal oxidation. The condition will not return to normal simply
by elimination of the cause.
In malignant disease, (1,
2) when the oxidation process is blocked, energy is produced
by fermentation and viruses grow profusely in this condition.
For many years Dr. William F. Koch(1) and Otto Warburg (2, 3)
have claimed that blocking of, or impairment of oxidation in
the enzymes and cells allows fermentation of sugar and that fermentation
in these enzymes and cells is the PRIME CAUSE OF CANCER. Koch
(1) has also proved that blocked oxidation
in micro-organisms causes them to be pathogenic and parasitic,
and that when this condition is corrected these organisms become
non-pathogenic, non-parasitic, and non-virulent.
In so many of these conditions patients
have a low blood oxygen level as shown by blood oxygen studies.
Some are only 50% to 60% of normal as shown in this paper. As
part of this paper are the results of studies made in 1968 which
confirm studies by Dr. George Miley.(6)
Our clinical studies show that intravenous
Ultraviolet effectively increases the blood oxygen to normal
or near normal in most cases.
Increasing blood oxygen is important,
but when the oxidation process is blocked by certain amines it
takes a powerful oxidation catalyst to bring about normal oxidation
and eliminate the blocking substances. We now have an effective
oxidation catalyst which does this.(1)
In the treatment of these cases the following
are very important: 1. Intravenous Ultraviolet rapidly increases
the oxygen absorption of the patient bringing the blood oxygen
up to normal. The powerful oxidation catalyst stimulates the
use of this increased oxygen or the patient's oxygen at any level
to restore the normal oxidation process (cell respiration).
2. The diet of these patients is extremely
important, using foods grown with natural fertilizers and without
poisonous fertilizers and insecticides, and eating much of it
raw. Since so many of these patients are deficient in important
trace minerals such as magnesium and zinc it is important to
see that these patients are supplied with sufficient trace minerals
in chelated form so that they are readily absorbed.
3. Since much of the toxic substances
producing these diseases comes from the colon we use colonic
irrigations for thoroughly cleansing the colon of these substances.
Since the normal pH (of fresh stool) of the colon must be properly
maintained this is done with every means to promote the normal
physiology of the colon.
4. All factors for the most healthful
condition of each patient are carefully considered and treated.
Pasteur was the first to discover the
oxidation process or respiration in the cells and enzymes. Koch,(1) Warburg,(2) and
others have firmly established the fact that oxygen deficiency
and certain toxic substances block the oxidation process, and
that in this condition energy is then produced by fermentation
instead of oxidation. This is the pathological basis for malignant,
viral, bacterial, and allergic diseases.
The pathogenicity,(1)
virilance and paracitism of micro-organisms is due to the same
blocking of oxidation in these organisms. When normal oxidation
is established in these organisms they lose their pathogenicity,
virilance, and paracitism.
Prevention of the devastating effects
of these diseases is one of the principle goals of this work
and study. Now that we know these causes of these diseases, it
is imperative that we put forth every effort to prevent them.
Treatment of all of these conditions
in the earliest possible stages is also our goal, when these
patients have not been subjected to destructive forces and treatments
which are so generally used in the treatment of these diseases.
TREATMENT OF BLOCKED OXIDATION CASE REPORTS
I. On January 17, 1969, Miss D.P.,
38 years old, white female, was admitted to Providence Hospital.
Past History: Eleven years ago a melanoma
was removed from the right upper arm. August 1968 subcutaneous
tumor mass appeared on the upper left chest just below the clavicle.
Excision and biopsy of this revealed malignant melanoma. Following
this she developed a tumor on the right chest at the same level,
tumor in the right axilla, abdomen began to become very large,
patient had marked difficulty in breathing, and constant cough.
There was gradual and painful swelling of the right thigh (all
at another medical center).
Present Illness: On entering the hospital
patient was in critical condition with marked difficulty in breathing,
constant cough, cyanosis, abdomen was very large and pendulous
containing a large amount of fluid in which there were large
tumor masses palpable throughout the abdomen, especially the
entire lower abdomen and lower right quadrant.
Extremities: The right thigh from the
knee to the hip was very swollen and painful, about twice normal
size.
Diagnosis: Generalized malignant melanoma.
Treatment: Patient was immediately given
ultraviolet blood irradiation (UBI) to overcome hypoxemia, the
oxidation catalyst (Koch Glyoxylide) intermuscularly, ultra mycro-wave
therapy throughout the body, diet consisting of raw vegetables
and fruits eliminating all meats and fluorides, colonic irrigations
to remove the toxic material from the colon, and large doses
of trace minerals especially magnesium and zinc with natural
vitamin C and natural vitamin E in addition to other natural
vitamin supplements. UBI treatments given on January 17, 20,
24, and once a week following this. Koch Glyoxylide given on
January 17, February 20, March 21, June 2, and July 17. Mycro-wave
given on January 17, 27, February 3, 6, 12, 19, 26, and once
a week following this.
Within three weeks the mass in the right
axilla had disappeared as well as the tumor of the right chest
wall, and the abdomen was becoming definitely smaller and the
tumor masses much smaller. At the end of six weeks of this treatment
patient had no difficulty in breathing, the right thigh was normal
size and no pain, the abdomen had returned to normal size with
no fluid, and the tumor masses were practically gone with only
very small evidence of tumor in the lower abdomen. Patient up
and about in a normal manner except for some weakness following
her long illness.
This patient will remain under treatment
in the hospital for another 2 or 3 weeks when she will be discharged
to go to her home in Utah with instructions to return in approximately
3 months for examination and further treatment for the prevention
of further development of malignant melonoma.
This type of case will need observation
over a period of several years to be sure as possible of success.
This case illustrates the very early
effective results of treatment of the whole program that we are
now using for the treatment of all malignancy. This treatment
is based upon the evidence (4) that cancer is due to hypoxemia
and blocking of oxidation with the development of fermentation
of sugars which causes the cancerous growth. It has been shown
that all cancers have one common factor, and that is, fermentation
of sugar in the enzymes and cells, replacing normal oxidation.
Reversal of this process back to normal oxidation is all important.
II. Mrs. A.F., age 64, white female,
entered hospital on April 21, 1953 with a rapidly developing
carcinoma of the left breast. A few years before this she had
had cancer of the right breast with a radical mastectomy followed
by x-ray therapy. On this occasion mastectomy with removal of
axillary lymph glands was performed, but not a radical mastectomy.
It was found that the cancer was penetrating the chest wall and
into the lung. Post-operative therapy consisted of x-ray therapy,
but principally the program of stimulating the oxygen content
and the use of minerals, particularly magnesium and zinc. At
first the UBI treatments were given at weekly intervals and after
three months they were given at monthly intervals and this continued
on for five years. She continued to take the zinc and magnesium
supplement and other general vitamin supplements.
Within a few months there was no evidence
of malignancy in the x-ray of the lung.
This patient is now living and well and
has had no evidence of recurrence of her malignancy.
III. Mrs. A.R., age 60, white female,
entered the hospital June 22, 1960 with a large tender mass in
the left abdomen which was thought to be a perinephritic abscess.
Upon operation it was found that patient had a large carcinoma
of the splenic flexure of the colon which had ruptured into the
abdominal cavity. There were melostatic nodules beyond the primary
growth. A Miculitz type operation was performed and in due time
closed.
Following surgery patient was placed
on an intensive program of ultraviolet blood irradiation, given
four in the first week and one each week thereafter for several
months. She was also given zinc and magnesium in adequate amounts
with other vitamin and supplements. Patient made a very excellent
recovery from the surgery and is living today. She kept up with
the blood irradiation treatment once a month for 5 years and
also the supplement therapy.
IV. Mrs. C.B., age 55, white female,
entered the hospital on January 4, 1954 with a nodular tumor
of the thyroid. At operation it was determined she had an adeno-carcinoma
and sub-total thyroidectomy was performed leaving very little
thyroid tissue. Following her surgery she was given UBI treatments,
four in the first week and one each week, following this together
with adequate magnesium and zinc therapy. This treatment was
continued once a month for 5 years. Patient is still living and
well and has had no recurrence of her carcinoma.
V. On April 30, 1969 Mrs. I.W., white
female, 50 years of age entered Providence Hospital for treatment
of a large tumor of the uterus considered to be carcinoma.
Past History: February 1968 patient found
to have cancer of the cervix and uterus and was given radium
and cobalt treatments for a month. In August 1968 she was examined
again and her doctor told her that she had a large cancer of
the cervix and uterus and that nothing could be done and told
her to "just go home and die." Following this she had
six months of laetril treatment. (All of this was at other treatment
centers–not here.)
On entering Providence Hospital, examination
revealed a large tumor of the uterus and pelvis, specifically
carcinoma. She was given ultraviolet blood irradiation on May
1, 2, 6, 14 and once a week following this. She was given Koch
Glyoxylide on May 1, 6, 26, June 6, 16, she was given mycro-wave
treatments on May 1, 6, 14, 19, 29, June 4, 9, and 30th. Along
with this she was given the diet of raw vegetables and fruits
together with adequate amount of zinc, magnesium, vitamin C,
vitamin E, vitamin B6. By June 24th examination revealed a marked
reduction in the size of the tumor with only slight discharge
from it and it was felt that it was possible to remove the tumor
surgically. Hysterectomy was performed on June 26, 1969 by Richard
C. Olney, M.D. and the entire uterus including the cervix removed
and the remaining right falopian tube. Pathological examination
of the specimen removed failed to reveal any viable cancer tissue
in the cervix or uterus. Patient has made an uneventful recovery
from surgery and is continuing on with a vigorous program of
treatment to assure as much as possible no recurrence of her
malignancy.
Blood Oxygen Saturation After Intravenous Ultraviolet
(Ultraviolet Blood Irradiation)
Hypoxemia is a common and serious
factor in so many diseases and surgical procedures. Correction
of this and bringing the oxygen saturation of these patients
to normal or near normal is vitally important in the treatment
of these diseases and the success of serious surgical procedures.
This report deals only with the blood
oxygen saturation changes following intravenous ultraviolet therapy
(UBI). (Ultraviolet Blood Irradiation is by use of the Knott
Hemo-Irradiator. A definite amount of patient's blood, 1 1/2
cc per pound of body weight is withdrawn from a vein, citrated
and returned immediately to patient after passing through the
Knott-Hemo Irradiator and thus exposed to a certain band of ultraviolet
light in an exact period of time, 10 cc in 20 seconds.)
For this study twenty-three patients
were selected at random regardless of the diagnosis in which
there was clinical evidence of hypoxemia. Patients were selected
in which there was no known condition which would interfere with
or change the outcome of these studies. Before the first treatment
of intravenous ultraviolet 5 cc of venous blood was removed and
immediately taken to the American Optical Oximeter and the oxygen
saturation was determined prior to the treatment. In this way
the oxygen saturation was compared with the day previously, and
the previous determinations, for the changes which could take
place following the intravenous ultraviolet therapy.
Normal oxygen saturation on the American
Optical Oximeter is 100% for arterial and 72% for venous blood.
The following is a brief review of the
cases in this study:
| Mr. L.H. Middle-aged man with lymphatic leukemia. |
| Venous oxygen 48% |
|
24 hours after 1 UBI 65% |
| Mr. C.G. Metastatic carcinoma of the lung. |
| Venous oxygen 54% |
|
24 hours after 1 UBI 66.5% |
| Mrs. E.H. Hysterectomy for uterine fibroid. |
| Venous oxygen 54.7% |
|
24 hours after 1 UBI 75% |
| Miss D.W. Laboratory technician. Apparent good
health, but heavy smoker. |
| Venous oxygen 50% |
|
24 hours after 1 UBI 64% |
| |
|
24 hours after 2nd UBI 81% |
| Mr. V.B. Acute severe respiratory infection. |
| Venous oxygen 48% |
|
24 hours after 1 UBI 65% |
| |
|
24 hours after 2nd UBI 81% |
| Mr. C.T. Severe diabetic with cerebral vascular
accident. |
| Venous oxygen 48.8% |
|
24 hours after 1 UBI 84% |
| Mrs. B.S. Acute mastoiditis and upper respiratory
infection. |
| Venous oxygen 47% |
|
24 hours after 1 UBI 71% |
| Mrs. H.M. Acute congestive heart failure. |
| Venous oxygen 32% |
|
24 hours after 1 UBI 56% |
| |
|
24 hours after 2nd UBI 70% |
| Mr. E.D. Asthma with acute myocarditis. |
| Venous oxygen 48% |
|
24 hours after 1 UBI 58% |
| |
|
24 hours after 2nd UBI 68% |
| Mr. A.V. Extensive malignancy of the ear and
side of the head. |
| Venous oxygen 52% |
|
24 hours after 1 UBI 60% |
| |
|
24 hours after 2nd UBI 66% |
| Mr. P.Z. Severe Diverticulosis of the colon,
myocarditis and acute respiratory infection. |
| Venous oxygen 53% |
|
24 hours after 1 UBI 60% |
| |
|
24 hours after 2nd UBI 66% |
| Mr. C.C. Patient in critical condition with intestinal
obstruction. Acute respiratory infection. |
| Venous oxygen 50% |
|
24 hours after 1 UBI 63% |
| Mr. R.D. Complete acute occlusion of the femoral
artery at the femoral region with impending gangrene of the leg. |
| Venous oxygen 38% |
|
24 hours after 1 UBI 73% |
| Miss A.W. Operated on for cholecystectomy and
appendectomy. |
| Venous oxygen 42% |
|
24 hours after 1 UBI 84% |
| Miss N.S. Coronary insufficiency. Respiratory
infection. |
| Venous oxygen 53% |
|
24 hours after 1 UBI 60% |
| |
|
24 hours after 2nd UBI 68% |
| Mr. W.H. Acute cerebral vascular accident with
severe acute otitis media and mastoiditis. |
| Venous oxygen 40% |
|
24 hours after 1 UBI 56% |
| |
|
24 hours after 2nd UBI 66% |
| Mr. A.C. Myocarditis, Acute respiratory infection.
Carcinoma of the prostate. |
| Venous oxygen 34% |
|
24 hours after 1 UBI 48% |
| |
|
24 hours after 2nd UBI 60% |
| Mr. R. Stricture of the lower esophagus with
almost complete closure of the esophagus and marked dilation. |
| Venous oxygen 32% |
|
24 hours after 1 UBI 42% |
| |
|
24 hours after 2nd UBI 57% |
| Mr. B.S. Pericarditis, Cholecystitis and Pyelonephritis. |
| Venous oxygen 47% |
|
24 hours after 1 UBI 71% |
| |
|
24 hours after 2nd UBI 86% |
| Mrs. F.B. Severe neurosis. |
| Venous oxygen 29% |
|
24 hours after 1 UBI 83% |
| |
|
24 hours after 2nd UBI 86% |
| Mrs. R.B. Thrombophlebitis and Cholecystitis. |
| Venous oxygen 18% |
|
24 hours after 1 UBI 62% |
| Mrs. P. General carcinomatosis of pelvis from
CA of uterus and heavy cobalt treatments. |
| Venous oxygen 43% |
|
24 hours after 1 UBI 65% |
| |
|
24 hours after 2nd UBI 80% |
It is important to emphasize that
in so many pathological conditions there is a very marked hypoxemia
and that this is a very important factor in the diseased condition.
Whether it is an etiological factor or a result is not important.
It is important, however, that the blood oxygen saturation is
returned to normal as rapidly as possible, in the treatment of
these patients or in the performing of extensive surgical procedures,
as a matter of giving these patients one of the most important
factors in their defense mechanism and resistance.
SUMMARY
Hypoxemia and blocked oxidation followed
by fermentation of sugar in the enzymes and cells we consider
to be the prime factor in malignant, viral, bacterial and allergic
diseases.
A program of prevention and treatment
of this condition is presented which has proved in the past,
and is proving at this time to be very effective, in correcting
the pathological physiology which has taken place and returning
normal oxidation to the enzymes and cells for the recovery of
these patients.
REFERENCES
| (1) |
|
Koch, William F., M.D.: The Survival in Neoplastic
and Viral Diseases. Vanderkloot Press, Detroit, Michigan, 1955-1958. |
| |
|
| (2) |
|
Warburg, Dr. Otto, Director Max Tlanck-Institute
for Cell Physiology, Berlin-Dahlem (Nobel Prize 1931); "On
the origin of cancer cells," Science Magazine, Feb. 24,
1956, Volume 123, #3191. |
| |
|
| |
|
| (3) |
|
Warburg, Dr. Otto: "Revised lecture at the
meeting of Nobel Laurets," June 30, 1966, Landau, Lake Constance,
Germany. |
| |
|
| (4) |
|
Burk, Dean, National Cancer Institute, Bethesda,
Maryland: "The Prime cause and prevention of Cancer,"
Konrad Trietsch, Wurzburg, Germany, 1967; English edition by
Dean Burk. |
| |
|
| |
|
| (5) |
|
Olney, Robert C., M.D. and contributors: "Treatment
of Viral Hepatitis with Ultraviolet Blood Irradiation,"
Am. J. of Surg., Sept. 1955. |
| |
|
| (6) |
|
Miley, George, M.D.: "The Ultraviolet Irradiation
of Auto-transfused Blood: Studies in Oxygen Absorption Valves,"
Am. J.M.SC. 197:873, 1939. |
| |
|
| (7) |
|
Olney, Robert C., M.D.: "Ultraviolet Blood
Irradiation in Biliary Disease." American Journal of Surgery,
August, 1946. |
| |
|
| (8) |
|
Olney, Robert C., M.D.: "Ultraviolet Blood
Irradiation Treatment of Pelvic Cellulitis." American Journal
of Surgery, Oct. 1947. |
| |
|
| (9) |
|
Olney, Robert C., M.D.: "Role of Ultraviolet
Blood Irradiation Therapy, Not Technic, in Surgery." International
College of Surgeons Journal, 1949. |
| |
|
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