The difference between GMT’s definition of what is occurring and the generally
accepted theory is that, according to Dr. Fernandez, it’s the molecules/ions in our blood
that become excited when irradiated. These molecules, in a hyper-excited state, travel
through the circulatory system and, upon collision with pathogens (viruses, bacteria,
etc.), are fragmented and destroyed. Dr. Fernandez describes these molecules as
“molecular missiles” that destroy pathogens upon collision. This theory was proven in a
Government-Approved Clinical Trial in HIV/AIDS, where Viral Loads demonstrated a
drastic change in viral load after a treatment, thereby proving that the excited irradiated
blood is the one that destroys pathogens.
The generally accepted theory is that irradiated blood, when returned to the circulatory
system, strengthens the immune system into a “superstate,” and it is this super immune
system that destroys pathogens. Dr. Fernández proved this theory, which had stood for
over 80 years, incorrect. What Dr. Fernandez proved was that our immune system
becomes more efficient at eliminating and clearing dead debris from the circulation, and
that in the case of viruses and bacteria, after 10 to 15 days, the patient will test positive
for Antibodies, thereby being “Naturally Vaccinated.”

The difference between GMT’s definition of what is occurring and the generally
accepted theory is that, according to Dr. Fernandez, it’s the molecules/ions in our blood
that become excited when irradiated. These molecules, in a hyper-excited state, travel
through the circulatory system and, upon collision with pathogens (viruses, bacteria,
etc.), are fragmented and destroyed. Dr. Fernandez describes these molecules as
“molecular missiles” that destroy pathogens upon collision. This theory was proven in a
Government-Approved Clinical Trial in HIV/AIDS, where Viral Loads demonstrated a
drastic change in viral load after a treatment, thereby proving that the excited irradiated
blood is the one that destroys pathogens.

The generally accepted theory is that irradiated blood, when returned to the circulatory
system, strengthens the immune system into a “superstate,” and it is this super immune
system that destroys pathogens. Dr. Fernández proved this theory, which had stood for
over 80 years, incorrect. What Dr. Fernandez proved was that our immune system
becomes more efficient at eliminating and clearing dead debris from the circulation, and
that in the case of viruses and bacteria, after 10 to 15 days, the patient will test positive
for Antibodies, thereby being “Naturally Vaccinated.”

Today, doctors are confronted with the reality of just how little they know about UV
Blood Irradiation and its therapeutic capabilities. It is only when speaking with
Radiologists, Nuclear Medicine specialists, Oncologists, or Hematologists that we
realize how common this subject is to them. Many physicians have asked themselves,
“Why is so little known about such an efficient therapeutic process as UV Blood
Irradiation?”

For GMT, it was the HIV Virus that first gained our attention; could Blood Irradiation be
effective against HIV/AIDS mutations that cause resistance to medications (retroviral
drugs)? Approximately 30% to 40% of the nearly 45 million people infected with HIV
are Intolerant to retroviral medications, and without treatment alternatives like PCI,
they have absolutely no hope at all.

After two decades, GMT has the privilege of being counted among the American,
Russian, German, and South American scientists who have been ardently working to
open the doors so that the medical community and the general population can better
understand and accept this process for curing diseases. Sometime in the near future,
the process of Irradiodynamics will be as standard as Pharmacodynamics is today.
The challenge is to get the academic field to take an interest in the use of this process
in real life, not just in the lab, where it has been for the last 50 years.

Since the COVID-19 virus spread across the globe like wildfire, devastating families,
communities, economies, and governments, we know that we will soon witness a new
era in medical modalities; an era where it will be possible to confront any potential
pandemic, such as the one that currently threatens humanity.
But COVID-19 is just one such outbreak; many other pathogens could threaten
humanity, such as the highly pathogenic Avian Influenza (HPAI) strains H5N1 and
H7N9. Without the PCI, pathogens such as the Avian Influenza strains are capable of
causing the devastating demise of millions of people in a matter of months, if not weeks.
With the urgency to find an alternative treatment for COVID-19, we may finally have the
scientists and doctors needed to conduct the necessary clinical trials so UVBI can be
accepted as a mainstream medical treatment.

Previously, UVBI has been delayed due to the following:

 Exorbitant treatment costs, such as with the antivirals used to treat HIV Aids
 Drug resistance
 Vaccine allergies
 Public uncertainty and refusal to take the vaccines and/or treatments

 The length of time and professional knowledge needed to conduct clinical trials
 The lengthy & expensive approval process required by universities and
government entities
 The resistance by many scientists who have found the process too arduous and
tedious.
 The existing resistance to competitive treatments, despite their issues, allows
other needed treatments to be studied

The good news is that the urgency of the pandemic removed many impediments and
cleared the way, dramatically shortening the time required and reducing some of the
resistance to conducting new clinical trials.  

The opportunity is here and now, allowing GMT’s PCI to gain acceptance from the
scientific, medical, and general communities.

In the future, we look forward to the honor and privilege of sharing our knowledge of UV
blood irradiation with doctors, medical students, nurses, physician assistants, and
others in the medical field worldwide.