Bacterial infections and IPT
Like viral infections, bacterial infections have always been a
part of human life. Some kill us, while others take us out of action for a
while. Some annoy or irritate us, and others we never notice. Some
appear to go away after initial reactions, but can survive in a latent state, to
manifest again.
Our bodies and immune systems have complex interactions with
bacteria. Our health depends on a whole ecosystem of beneficial
bacteria. And other bacteria cause us problems. There is growing
evidence that many cases of cardiovascular disease, Alzheimer's disease, one form of
stomach cancer, and other chronic diseases may have a hidden bacterial infection
as underlying cause. That is why I am suggesting that a multi-pathogen
IPT (MP-IPT) protocol be considered as part of treatment for many chronic
diseases for which the causative infectious agent is not yet known.
IPT has been found, in over
130 doctor-years of experience, to
be extremely effective in treating a variety of bacterial diseases, as well as a
number of chronic diseases that could have bacterial origin. IPT
has been found to work well with a wide variety of antibiotics.
IPT-boosted antibiotics quickly and intensively kill bacteria, even in less
accessible tissues and compartments of the body. A quick and efficient
kill would give bacteria less chance of developing resistance to the antibiotics.
Not only does IPT kill bacteria, even in less accessible tissues, but it
apparently also rapidly reduces inflammation, stimulates the immune system,
stimulates the healing process, and helps the body detoxify or eliminate the
byproducts of bacterial death. Thus it is ideal for treating nasty, dirty wounds,
gangrene, frostbite, and other situations where there is stressed
and necrotic tissue.
Following are some of the known applications of IPT for treating bacterial
infections:
 | Drs. Perez Garcia 2 and 3 wrote in the 1992 patent about treating skin
wounds and burns with Madribon (Roche) and antibiotics combined in
IPT treatments.
|
| Here is a case of a streptococcus
pharyngeal (throat) infection successfully treated with IPT, in the 1992 patent.
|
| Here is a case of streptococcus
group A infection causing rheumatic fever in the 1992 patent. After 5
IPT treatments, all symptoms went away, a test for the bacteria was negative,
and there were no relapses.
|
| Here is a case of pneumococcal
pneumonia in the 1992 patent. The patient was well after three
treatments and seven days.
|
| Here is a case of osteomyelitis
(bone infection) in the 1992 patent. After 3 IPT treatments she
recovered.
|
| Here is a case of osteomyelitis (bone
infection) presented in Dr. Paquette's book.
|
| Here is a case of acute
gonorrhea salpingitis (pelvic inflammatory disease) in the 1992 patent.
After the first IPT treatment, pain was gone. And after the third
treatment, all symptoms
were gone.
|
| Dr. Perez Garcia 1 treated stomach and peptic
ulcers rapidly and successfully with IPT in the late 1940s,
and presented his results publicly in 1950. He was using antibiotics
to do this, long before the responsible bacterium was discovered in
1995.
|
| Dr. Perez Garcia 1 at the same time was treating appendicitis
using IPT alone, and with no surgery whatsoever. IPT was
successful in reducing pain and inflammation, eliminating the infection,
removing toxins, and assisting the tissues to heal.
|
| Dr. Perez Garcia 1 published a paper in 1945
about using IPT to treat infections by
typhus exanthematicus (typhus fever).
|
| Dr. Perez Garcia 2 had protocols in his 1975
practice for treating:
bladder/kidneys
infection, chronic
cervicitis/vaginitis, acute
bacterial/viral infections, |
| Based on Dr. Perez Garcia 1's experience with appendicitis and ulcers,
it appears that IPT would be ideal for treating such serious and difficult
infections as peritonitis (infection and inflammation of the membrane
lining the abdomen), septicemia (bacterial infection of the blood), gangrene,
frostbite, and deep traumatic wounds.
|
| IPT should be investigated as a possible better treatment for tuberculosis
and for Lyme disease.
|
| There is growing
evidence that much or most heart disease
and atherosclerosis is indeed caused in large part by infection with
the bacterium Chlamydia pneumoniae. If this is true, then
IPT could be an ideal way to treat and prevent heart disease by delivering
antibiotics more effectively into the walls and plaque deposits of the blood
vessels.
|
| IPT may be a more effective way to treat the deep abscesses,
inflammation, and bone and tooth loss which can comprise gum disease
(gingivitis).
There is growing evidence that bacteria from infected gums may migrate into
the bloodstream and cause cardiovascular disease, so this potential
application is not at all trivial.
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