Treatment combo
Sessions of Modern Medicine in Digital format - I
The frequencies used in these sessions are based upon Rife
sets for resonant therapy devices masked in Algorithmic piano music.
More information regarding the items in the list is given below the list.
List of Treatment combo
Sessions of Modern Medicine in Digital format for problems/products available at
us for just Rs. 1,000/- for any 5 sessions from any one or multiple
Treatment combo Sessions for 30 doses per session (2 times a day for 15
days) in max 15 days.
1) Ichthyosis
2) Idiopathic Scrotal Calcinosis
3) IgA Nephropathy
4) Ileocolitis
5) Immunodeficiency Common-Variable
6) Immunodeficiency Severe-Combined
7) Immunologic Deficiency Syndromes
8) Impetigo
9) Incontinentia Pigmenti
10) Infectious Mononucleosis
11) Infertility
12) Inflammation
13) Inflammatory Bowel Diseases
14) Inflammatory Myopathy
15) Inflammatory Response
16) Influenza
17) Influenza Avian-HN
18) Insomnia
19) Insulinoma
20) Intermittent Claudication
21) Interstitial Cystitis
22) Intervertebral Disk Displacement
23) Intestinal Diseases
24) Intestinal Neuronal Dysplasia
25) Intestinal Obstruction
26) Intestinal Polyps
27) Intracraneal Aneurysm
28) Iritis
29) Iron-Deficiency Anemia
30) Irritable Bowel Syndrome
31) Ischemic Attack
32) Ischemic Heart Disease
33) Ivemark Syndrome
* Ichthyosis, dry, scaly skin.
* Idiopathic scrotal calcinosis, also known as idiopathic calcified nodules of
the scrotum is a cutaneous condition characterized by calcification of the skin
resulting from the deposition of calcium and phosphorus occurring on the
scrotum. However, the levels of calcium and phosphate in the blood are normal.
Idiopathic scrotal calcinosis typically affects young males, with an onset
between adolescence and early adulthood. The scrotal calcinosis appears, without
any symptoms, as yellowish nodules that range in size from 1 mm to several
centimeters.
* IgA nephropathy, kidney disorder caused by deposits of the protein
immunoglobulin A (IgA) inside the glomeruli (filters) within the kidney.
* Ileocolitis, also Crohn's disease is a disease that causes inflammation, or
swelling, and irritation of any part of the digestive tract—also called the
gastrointestinal (GI) tract. The part most commonly affected is the end part of
the small intestine, called the ileum. The GI tract is a series of hollow organs
joined in a long, twisting tube from the mouth to the anus. The movement of
muscles in the GI tract, along with the release of hormones and enzymes, allows
for the digestion of food. In Crohn's disease, inflammation extends deep into
the lining of the affected part of the GI tract. Swelling can cause pain and can
make the intestine—also called the bowel—empty frequently, resulting in
diarrhea. Chronic—or long-lasting—inflammation may produce scar tissue that
builds up inside the intestine to create a stricture. A stricture is a narrowed
passageway that can slow the movement of food through the intestine, causing
pain or cramps.
* Immunodeficiency common-variable, genetically determined primary immune defect
which affects B cells.
* Immunodeficiency severe-combined, affects B and T-cell mediated immunity
responses and often cytokine function.
* Immunologic deficiency syndromes, inadequacy of the immune mechanisms to
perform their function.
* Impetigo, also known as school sores, is a bacterial infection that involves
the superficial skin. The most common presentation is yellowish crust on the
face, arms, or legs. Less commonly there may be large blisters which affect the
groin or armpits. The lesions may be painful or itchy. Fever is uncommon. It is
typically due to either Staphylococcus aureus or Streptococcus pyogenes. Risk
factors include attending daycare, crowding, poor nutrition, diabetes, contact
sports, and breaks in the skin such as from mosquito bites, eczema, or scabies.
With contact it can spread around or between people.Other factors can increase
the risk of contracting impetigo such as diabetes, dermatitis, immunodeficiency
disorders, and other irritable skin disorders. Impetigo occurs more frequently
among people who live in warm climates. Impetigo affected about 140 million
people (2% of the population) in 2010. Globally, impetigo affects more than 162
million children in low to middle income countries. The rates are highest in
countries with low available resources and is especially in the region of
Oceania. The tropical climate and high population in lower socioeconomic regions
contribute to these high rates. In children in the United Kingdom under the age
of 4 are 2.8% more likely to contract impetigo and rates decreases to 1.6% for
children up to 15-years-old. As age increases, the rates of impetigo declines
but all ages are still susceptible. Without treatment people typically get
better within three weeks. Complications may include cellulitis or
poststreptococcal glomerulonephritis. Impetigo is usually diagnosed based on its
appearance. It generally appears as honey-colored scabs formed from dried serum,
and is often found on the arms, legs, or face.
* Incontinentia pigmenti, rare genetic disorder that affects the skin, hair,
teeth, nails, and central nervous system.
* Infectious mononucleosis (IM), also known as mono, or glandular fever, is an
infection commonly caused by the Epstein–Barr virus (EBV). Most people are
infected by the virus as children, when the disease produces little or no
symptoms. In young adults, the disease often results in fever, sore throat,
enlarged lymph nodes in the neck, and feeling tired. Most people get better in
two to four weeks; however, feeling tired may last for months. The liver or
spleen may also become swollen. In less than one percent of cases splenic
rupture may occur. Infectious mononucleosis is usually caused by Epstein–Barr
virus (EBV), also known as human herpesvirus 4, which is a member of the herpes
virus family. A few other viruses may also cause the disease. It is primarily
spread through saliva but can rarely be spread through semen or blood. Spread
may occur by objects such as drinking glasses or toothbrushes. Those who are
infected can spread the disease weeks before symptoms develop.
* Infertility, sterility.
* Inflammatory bowel disease (IBD) is a group of inflammatory conditions of the
colon and small intestine. Crohn's disease and ulcerative colitis are the
principal types of inflammatory bowel disease. It is important to note that not
only does Crohn's disease affect the small intestine and large intestine, it can
also affect the mouth, esophagus, stomach and the anus whereas ulcerative
colitis primarily affects the colon and the rectum. Inflammatory bowel diseases
fall into the class of autoimmune diseases, in which the body's own immune
system attacks elements of the digestive system. Although the symptoms of
Crohn's disease and ulcerative colitis are similar, they are not identical.
Abdominal pain and diarrhea are common to both diseases as is loss of weight and
fever. Ulcerative colitis tends to be associated with more bleeding due to the
extensive erosion by inflammation of the blood vessels supplying the lining of
the colon. On the other hand, symptoms of obstruction of the bowel (pain, nausea
and vomiting, and abdominal distension) are more common in Crohn's disease
because the entire wall of the bowel is inflamed. The more extensive
inflammation causes more swelling than the superficial inflammation of
ulcerative colitis that can obstruct the flow of digesting food through the
bowel. Possible complications of IBD include: malnutrition with resulting weight
loss, colon cancer, fistulas (ulcers that go through the bowel wall, creating a
hole between different parts of the digestive tract), intestinal rupture (or
perforation), bowel obstruction. In rare cases, a severe bout of IBD can make
you go into shock. This can be life-threatening. Shock is usually caused by
blood loss during a long, sudden episode of bloody diarrhea.
* Inflammatory myopathy (inflammatory muscle disease or myositis) is disease
featuring weakness and inflammation of muscles and (in some types) muscle pain.
The cause of much inflammatory myopathy is unknown (idiopathic), and such cases
are classified according to their symptoms and signs and electromyography, MRI
and laboratory findings. It can also be associated with underlying cancer. The
main classes of idiopathic inflammatory myopathy are polymyositis (PM),
dermatomyositis (DM), and inclusion-body myositis (IBM).
* Inflammatory neuropathies like Guillain-Barré syndrome (GBS), chronic
inflammatory demyelinating polyradiculoneuropathy (CIDP), and related
neuropathies, are thought to be caused by direct autoimmune attack on peripheral
nerves. Features that suggest that a neuropathy is likely to be inflammatory
include loss of reflexes without muscle wasting, elevated cerebrospinal fluid
(CSF) protein, positive sensory symptoms such as pain or tingling, asymmetry,
and proximal weakness. Nerve conduction studies show features of demyelination,
especially motor nerve conduction block and temporal dispersion. Inflammatory
neuropathy has been arbitrarily classified according to the time from symptom
onset until maximal severity, where “acute” is less than four weeks and
“chronic” is more than eight weeks, with a rare intermediate “subacute” group.
* Influenza A virus subtype H5N1, also known as A(H5N1) or simply H5N1, is a
subtype of the influenza A virus which can cause illness in humans and many
other animal species. A bird-adapted strain of H5N1, called HPAI A(H5N1) for
highly pathogenic avian influenza virus of type A of subtype H5N1, is the highly
pathogenic causative agent of H5N1 flu, commonly known as avian influenza ("bird
flu"). In general, humans who catch a humanized influenza A virus (a human flu
virus of type A) usually have symptoms that include fever, cough, sore throat,
muscle aches, conjunctivitis, and, in severe cases, breathing problems and
pneumonia that may be fatal. The severity of the infection depends in large part
on the state of the infected persons' immune systems and whether they had been
exposed to the strain before (in which case they would be partially immune). No
one knows if these or other symptoms will be the symptoms of a humanized H5N1
flu. H5N1 is a subtype of the species Influenza A virus of the Influenzavirus A
genus of the Orthomyxoviridae family. Like all other influenza A subtypes, the
H5N1 subtype is a RNA virus.
* Insulinoma, tumor of the pancreas that is derived from beta cells and secretes
insulin. The secretion of insulin by insulinomas is not properly regulated by
glucose and the tumors will continue to secrete insulin causing glucose levels
to fall further than normal.
* Intermittent claudication, muscle pain (ache, cramp, numbness or sense of
fatigue), classically in the calf muscle, which occurs during exercise, such as
walking, and is relieved by a short period of rest.
* Interstitial cystitis, characterized by a feeling or need to urinate
immediately or frequently, often with pelvic pain. It is a chronic inflammatory
condition of the submucosal and muscular layers of the bladder.
* Intervertebral disk displacement, or spinal disk herniation.
* Intestinal neuronal dysplasia (or neuronal intestinal dysplasia or NID) is an
inherited disease of the intestine that affects one in 3000 children and adults.
The intestine uses peristalsis to push its contents toward the anus; IND
sufferers have a problem with the motor neurons that lead to the intestine,
inhibiting this process and thus preventing digestion. It can often be confused
for Hirschsprung's disease, as both have similar symptoms. It can be grouped
into NID A and NID B, with the "A" form affecting the sympathetic innervation,
and the "B" version affecting the parasympathetic innervation.
* Intestinal polyps, colorectal polyps occurring on the lining of the colon or
rectum.
* Iritis is the inflammation of the anterior chamber and iris. Iridocyclitis
presents the same symptoms as iritis, but also includes inflammation in the
ciliary body. Anterior uveitis includes both iridocyclitis and iritis. Anywhere
from two-thirds to 90% of uveitis cases are anterior in location. This condition
can occur as a single episode and subside with proper treatment or may take on a
recurrent or chronic nature. Common symptoms of Anterior uveitis: Burning of the
eye. Redness of the eye. Blurred vision. Photophobia or sensitivity to light.
Irregular pupil. Blacked out sclera. Floaters, which are dark spots that float
in the visual field. Headaches. Signs of anterior uveitis include dilated
ciliary vessels, presence of cells and flare in the anterior chamber, and
keratic precipitates ("KP") on the posterior surface of the cornea. In severe
inflammation there may be evidence of a hypopyon (inflammatory cells in the
anterior chamber of the eye). Old episodes of uveitis are identified by pigment
deposits on lens, KPs, and festooned pupil on dilation of pupil. Busacca
nodules, inflammatory nodules located on the surface of the iris in
granulomatous forms of anterior uveitis such as Fuchs heterochromic
iridocyclitis (FHI). Synechia (eye condition where the iris adheres to either
the cornea or lens).
* Iron-deficiency anemia is anemia caused by a lack of iron. Anemia is defined
as a decrease in the number of red blood cells or the amount of hemoglobin in
the blood. When anemia comes on slowly, the symptoms are often vague and may
include feeling tired, weakness, shortness of breath or poor ability to
exercise. Anemia that comes on quickly often has greater symptoms which may
include: confusion, feeling like one is going to pass out, and increased thirst.
There needs to be significant anemia before a person becomes noticeably pale.
There may be additional symptoms depending on the underlying cause. It is caused
by insufficient dietary intake and absorption of iron, or iron loss from
bleeding. Bleeding can be from a range of sources such as the intestinal,
uterine or urinary tract. The most common cause of iron-deficiency anemia in
children in developing countries is parasitic worms. Worms cause intestinal
bleeding, which is not always noticeable in feces, and is especially damaging to
children. Malaria, hookworms and vitamin A deficiency contribute to anemia
during pregnancy in most underdeveloped countries. In women over 50 years old,
the most common cause of iron-deficiency anemia is chronic gastrointestinal
bleeding from nonparasitic causes, such as gastric ulcers, duodenal ulcers or
gastrointestinal cancer. Iron deficiency causes approximately half of all anemia
cases worldwide, and affects women more often than men. Iron-deficiency anemia
is characterized by the sign of pallor (reduced oxyhemoglobin in skin or mucous
membranes), and the symptoms of fatigue, lightheadedness, and weakness. None of
the symptoms are sensitive or specific. Because iron deficiency tends to develop
slowly, adaptation occurs and the disease often goes unrecognized for some time,
even years; patients often adapt to the systemic effects that anemia causes. In
severe cases, dyspnea (trouble breathing) can occur. Unusual obsessive food
cravings, known as pica, may develop. Pagophagia or pica for ice has been
suggested to be specific, but is actually neither a specific or sensitive
symptom, and is not helpful in diagnosis. When present, it may (or may not)
disappear with correction of iron-deficiency anemia.
* Irritable bowel syndrome, more common in middle age women, some symptoms are
abdominal, cramping, and changes in bowel movements.
* Ischemic Heart Disease, also known as Coronary Artery Disease, is a condition
that affects the supply of blood to the heart. The blood vessels are narrowed or
blocked due to the deposition of cholesterol on their walls. This reduces the
supply of oxygen and nutrients to the heart muscles, which is essential for
proper functioning of the heart. This may eventually result in a portion of the
heart being suddenly deprived of its blood supply leading to the death of that
area of heart tissue, resulting in a heart attack. As the heart is the pump that
supplies oxygenated blood to the various organs, any defect in the heart
immediately affects the supply of oxygen to the vital organs like the brain,
kidneys, liver, etc. This leads to the death of tissue within these organs and
their eventual failure. Ischemic Heart Disease is the most common cause of death
in many countries around the world. The major risk factors are smoking, diabetes
mellitus and cholesterol levels. Those with Hypercholesterolemia have a much
higher tendency to develop the disease. Hypertension is also a risk factor in
the development of Ischemic Heart Disease. Genetic and hereditary factors may
also be responsible for the disease. Stress is also thought to be a risk factor.
Some symptoms are: Angina pectoris, Acute chest pain: which can be associated
with acute coronary syndrome, unstable angina or myocardial infarction, Heart
failure -difficulty in breathing or swelling of the extremities due to weakness
of the heart muscle.
* Ivemark syndrome is a rare disorder that affects multiple organ systems of the
body. It is characterized by the absence (asplenia) or underdevelopment
(hypoplasia) of the spleen, malformations of the heart and the abnormal
arrangement of the internal organs of the chest and abdomen. The symptoms of
Ivemark syndrome can vary greatly depending upon the specific abnormalities
present. Many infants have symptoms associated with abnormalities affecting the
heart including bluish discoloration to the skin due to a lack of oxygen in the
blood (cyanosis), heart murmurs, and signs of congestive heart failure. Ivemark
syndrome often causes life-threatening complications during infancy. The exact
cause of Ivemark syndrome is not known. Ivemark syndrome is classified as a
heterotaxy disorder or a laterality disorder. These terms refer to the failure
of the internal organs of the chest and abdomen to be arranged in the proper
location within the body.