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Medical device for management of infectious diseases
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1
Medical device for management of infectious diseases
Hans W Giertz
Uppsa Research, Miklagard, SE-646 93 GNESTA, Sweden
Abstract. Here, infectious diseases (pathogens) are managed by electromagnetic energy
extinction using a medical device. This medical device is described; how to produce it, how to use it
and how to evaluate the clinical results. The air contains low frequency electromagnetic energy
created by the rotating earth. Pathogens absorb this energy by means of resonance. This supplies
pathogens with energy and it possibly supports internal biological processes. The absorbed energy
disturbs the immune system in the pathological area. Preventing pathogens from absorbing
electromagnetic energy restores the immune system and prolonged energy extinction destroys
pathogen processes leading to pathogen death. Energy extinction is achieved through
electromagnetic interference using a medical device containing an oscillator. The device is carried
by the patient during 2-3 weeks. The method is non invasive.
1. Introduction
The present paper describes how to
manufacture a medical device which extinct
electromagnetic energy in the air, thereby
preventing diseases (pathogens) from
absorbing electromagnetic energy.
Management of diseases is made by
prolonged (3 weeks) extinction of
electromagnetic energy. The paper describes
how to manufacture the device, how to use it
and how to evaluate the result. A theoretical
description is provided.
2. Manufacturing the medical device
2.1 Making the oscillator
1. Prepare an approximately 50 mm
long copper wire, diameter 0.5 mm.
Strip off insulation if necessary.
2. This copper wire shall be cut and
trimmed to one piece of conductor,
exactly 7.02 mm long, the trimmed
piece of wire is called the oscillator.
3. The oscillator is produced as follows:
4. One end of the wire is polished using
240 – 320 grit sandpaper. Make sure
that the polished end is perpendicular
to the wire.
5. The vernier caliper is adjusted to 7.2
mm. The wire is inserted into the
vernier caliper and cut to
approximately 7.2 mm.
2
6. The length is then measured using
the vernier caliper.
7. Excessive length is removed by
polishing the end (the cut end). The
wire is polished to the exact length
7.02 mm +/- 0.02 mm. Polish,
measure etc. Ensure that both ends
are polished. The final result, the
7.02 mm long copper conductor, is
the oscillator.
2.2 Making the enclosure
1. The enclosure is made using
Hammond Manufacturing 1551GBK
Plastic Enclosure, 50x35x20 mm
(2x1.4x0.8 IN); however, similar
enclosures can be used.
2. 4 holes, diameter 2 mm, are drilled in
the enclosure, 2 on each side. The
objective is to allow air and its
positive ions to enter the enclosure;
otherwise the oscillators will not
work.
3. Cut an approximately 0.2 mm thin
plastic sheet (e.g. PVC Report Cover
found in book stores) to the size
28x32 mm or to a size that fits your
enclosure. The fit shall not be tight,
allowing air to have access to both
sides.
2.3 Assembling the medical device
1. Glue the oscillator to the approximate
center of the plastic sheet. Make sure
to use little glue, the wire/oscillator
3
must not be covered with glue. Use
Loctite 406 or similar glue intended
for plastic.
2. Glue the plastic sheet (with oscillator)
to the two standoffs molded at the
bottom of the enclosure, ensuring
that the plastic sheet is spaced some
mm from the bottom. The objective is
to allow air to have access to both
sides.
3. Attach the lid using the two screws.
3. Using the medical device
1. The medical device is attached to the
patient during at least 2 weeks,
preferably 3 weeks. Preferably the
medical device is attached to the leg,
close to the knee, and switched
between each leg every second day.
Alternatively it can be carried in the
pocket, and switched between left
and right pocket every second day.
The medical device is positioned close
to the bed at night and elevated at
least 0.4 m from the floor (e.g.
positioned on a table). Do not sleep
close to the floor; energy extinction
does not work close to e.g. concrete
floor. Sleep preferably in a bed,
elevated at least 0.4 m above the
floor.
2. When not in use, the medical device
must be deactivated by wrapping it in
aluminum foil and preferably storing
it in a metal container/box.
4. Evaluating the result
1. Evaluation of clinical results is
performed using state-of-the-art
methods.
2. Complementary evaluation can be
performed as described in [2]
allowing continuous monitoring of
processes within pathogens during
treatment.
5. Short description
The rotating earth generates low frequency
electromagnetic energy having the periods
24/m·2n hours [2-4]. Pathogens absorb this
energy by means of resonance at, among
others, the period 24/5·216 hour (3.79 Hz) or
24/7·216 hour (5.31 Hz), depending on
pathogen type [5-8]. The medical device
destroys energy present in the air at these
two frequencies. This is achieved by the
oscillator [10, 11].
Current normally propagates in a conductor
with almost the speed of the light. There are
two mechanisms involved in this process.
Electrons in a conductor drift with their drift
velocity, in copper the drift velocity is ≈ 1.5
mm/s. Injected electrons create a charge
gradient and coulomb forces, according to
[10]:
F = q1q2r/4 ε0r3
This creates a force gradient which acts on
nearby electrons and this creates a chain
reaction which propagates with almost the
same speed as the coulomb forces, i.e. the
current propagates with almost the speed of
the light. The current transport is always
conducted by electrons on the conductor
surface, called surface charge. When the
4
injected energy is extremely small, ≤ 1pA,
the gradient is also extremely small. The
surface charge attracts positive ions present
in the air [4] and the number of positive ions
is sufficient to neutralize the gradient of the
surface charge, i.e. the coulomb forces are
neutralized. Thus the current propagates with
the drift velocity of the electrons, i.e. ≈ 1.5
mm/s. The wave propagation in a conductor
at current ≤ 1 pA is described by the classical
wave propagation in one dimension [12].
One solution is a harmonic wave that satisfies
ξ = a·sin(ωt + δ), where a is the amplitude,
δ is the phase constant and ω is the angular
frequency. The phase speed is equal to the
velocity v of the current, i.e. the drift velocity
of the electrons ≈ 1.5 mm/s in copper.
Resonance and a standing wave inside the
conductor occurs when its length is equal to
one half wavelength (λ/2) or a multiple, i.e.
(λ/2)∙ 2q. A conductor with length L creates a
standing wave and resonance at [12]:
L = (λ/2)∙2 q= (T/2)∙2q∙v , q = 0, 1, 2, 3, 4….
T is the period. This constitutes a resonance
circuit or a forced damped oscillator having
the natural period T. The forced damped
oscillator has low impedance at its natural
period T and this destroys creation of
resonance and electromagnetic energy in the
air. Exact values and exact theory is not
disclosed because of IPR.
An oscillator with copper conductor length L
= 7.02 mm extinct electromagnetic energy in
the air with period 24/5·216 hour (3.79 Hz)
and 24/7·216 hour (5.31 Hz) within a radius of
5-10 m, depending on the precision wherein
the oscillator is produced.
Destroying electromagnetic energy in the air
prevents pathogens from absorbing energy
leading to management of the infectious
disease [1].
The medical device described here is
applicable on infectious diseases described in
[6] and in [8]. The medical device described
here cannot be used on cancer [7] and on
some diseases not covered by [6, 8]. Contact
the author in case of clinical tests on cancer
and on diseases not described in [6, 8].
The author recommends that medical
devices, manufactured to high standard and
covering a broader range of disease, are
acquired from the author. Such medical
devices are available for clinical tests.
6. Conflict of interest
The method and the medical device are
patent pending, refraining commercial use.
However, the medical device can be produced
and used for non commercial clinical tests.
References
1. Giertz HW. www.miklagaard.com Paper 8;
A method to destroy electromagnetic
processes in infectious diseases.
2. Giertz HW. Extremely low frequency
electromagnetic energy in the air. Journal
of Atmospheric and Solar-Terrestrial
Physics 2010; 72: 767-773. Paper 1.
3. Rycroft MJ, Israelsson S, Price C. The
global atmospheric electrical circuit, solar
activity and climate change. Journal of
Atmospheric and Solar-Terrestrial Physics
2000; 62: 1563-1576.
4. Israel H. Atmospheric Electricity.
Springfield: U.S. Department of
Commerce; 1973.
5. Giertz HW. www.miklagaard.com
Introduction.
6. Giertz HW. www.miklagaard.com Paper 4;
Electromagnetic resonance in bacteria.
7. Giertz HW. www.miklagaard.com Paper 5;
Electromagnetic resonance in cancer
tumours and metastases.
8. Giertz HW. www.miklagaard.com Paper 6;
Electromagnetic processes in virus and
autoimmune diseases.
9. Giertz HW. www.miklagaard.com Paper 9;
Etiology of autoimmune diseases, asthma
and Parkinson’s diseases.
10. Bleaney BL. Electricity and Magnetism.
London: Oxford University Press; 1965.
11. Melrose DB, McPhedran RC.
Electromagnetic processes in dispersive
media. Cambridge: Cambridge University
Press; 1991.
12. Jönsson G. Wave theory and optics. Lund:
Teach Support; 1999.
© Hans W Giertz 2011