Treatment combo Sessions of Modern Medicine in Digital format - D
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Modern Medicine in Digital format

The most modern format of medicine of the Digital World

Treatment combo Sessions of Modern Medicine in Digital format - D

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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) Dandy-Walker Syndrome
2) De Lange Syndrome
3) Deglutition Disorders
4) Dementia Lewy Body
5) Dementias Transmissible
6) Dental Diseases
7) Dentigerous Cyst
8) Dermatitis
9) Dermatitis Exfoliative
10) Dermatitis Herpetiformis
11) Dermatofibroma
12) Dermatomycoses
13) Dermatomyositis
14) Dermoid Cyst
15) Desmoid
16) Diabetes Gestational
17) Diabetes Insipidus
18) Diabetes Mellitus Type-
19) Diabetes Mellitus Type-
20) Diabetic Ketoacidosis
21) Diabetic Neuralgia
22) Diabetic Retinopathy
23) Dientamoebiasis
24) Digestive System Diseases
25) Diphteria
26) Diplopia
27) Disseminated Intravascular Coagulation
28) Distichiasis
29) Diverticulitis
30) Down Syndrome-Symptoms Only
31) Duodenal Ulcer
32) Dupuytren Contracture
33) Dysentery
34) Dyslipidemias
35) Dyspareunia
36) Dyspepsia
37) Dysplasia Arteriohepatic
38) Dystrophia Brevicollis Congenita

* Dandy�Walker syndrome (DWS) is a rare group of congenital human brain malformations. There are three subtypes which affect multiple organs to varying degrees, but the fundamental abnormalities involve the cerebellum which controls muscle coordination. The adjacent fourth ventricle is often affected which can alter the flow of cerebrospinal fluid, increase intracranial pressure, and lead to multiple other brain function problems. The degree of disability varies but is typically lifelong. The key features of this syndrome are an enlargement of the fourth ventricle; complete absence of the cerebellar vermis, the posterior midline area of cerebellar cortex responsible for coordination of the axial musculature; and cyst formation near the internal base of the skull. An increase in the size of the fluid spaces surrounding the brain as well as an increase in pressure may also be present. The syndrome can appear dramatically or develop unnoticed. Symptoms, which often occur in early infancy, include slower motor development and progressive enlargement of the skull. In older children, symptoms of increased intracranial pressure such as irritability, vomiting, and convulsions and signs of cerebellar dysfunction such as unsteadiness and lack of muscle coordination or jerky movements of the eyes may occur. Other symptoms include increased head circumference, bulging at the back of the skull, problems with the nerves that control the eyes, face and neck, and abnormal breathing patterns. Dandy�Walker syndrome is frequently associated with disorders of other areas of the central nervous system including absence of the corpus callosum, the bundle of axons connecting the two cerebral hemispheres, and malformations of the heart, face, limbs, fingers and toes.

* Dementia with Lewy bodies (DLB) is a type of dementia that gradually worsens over time. Additional symptoms may include fluctuations in alertness, seeing things that other people do not, slowness of movement, trouble walking, and rigidity. Excessive movement during sleep and mood changes such as depression are also common. The cause is unknown. There is typically no family history among those affected. The underlying mechanism involves the buildup of Lewy bodies, clumps of alpha-synuclein protein in neurons. It is classified as a neurodegenerative disorder. DLB is the most common cause of dementia after Alzheimer's and vascular dementia. It typically begins after the age of 50. About 0.1% of those over 65 are affected. Males appear to be more commonly affected than females. In the late part of the disease people may depend entirely on others for their care. Life expectancy following diagnosis is approximately eight years. The presenting symptom of dementia with Lewy bodies is often cognitive dysfunction, though dementia eventually occurs in all individuals with DLB. In contrast to Alzheimer disease (AD), in which memory loss is the first symptom, those with DLB first experience impaired attention, executive function and visuospatial function, while memory is affected later. These impairments present as driving difficulty, such as becoming lost, misjudging distances, or as impaired job performance.

* Dentigerous cyst or follicular cyst is an odontogenic cyst - thought to be of developmental origin - associated with the crown of an unerupted (or partially erupted) tooth. The cyst cavity is lined by epithelial cells derived from the reduced enamel epithelium of the tooth forming organ. Regarding its pathogenesis, it has been suggested that the pressure exerted by an erupting tooth on the follicle may obstruct venous flow inducing accumulation of exudate between the reduced enamel epithelium and the tooth crown.

* Dermatitis exfoliative or erythroderma, an inflammatory skin disease with redness and scaling that affects nearly the entire cutaneous surface.

* Dermatitis herpetiformis leads to the development of itchy blisters and bumps on different parts of the body such as elbows, buttocks, kne es and back. It is an autoimmune disease. Medical research suggests that in Dermatitis Herpetiformis wheat intolerance is the main cause. This disease is caused when gluten in the intestinal tract sticks to some antibodies and starts spreading in the bloodstream. As the gluten rises to the skin surface, burning and itching symptoms arise. Eventually, papules emerge over the skin. The word ��Herpetiformis� commonly leads to the misconception that the Herpes Virus, which causes skin ailments, is the cause of this disease. But the use of the term is not because of Herpes involvement. It is a reference to the fact that the blisters appearing in this disease appears similar to those arising in skin conditions. In Dermatitis Herpetiformis Herpes Virus has no role to play. The disease is mainly caused by gluten sensitivity in the small bowel. It mainly develops in people who suffer from Celiac Disease, also known as Coeliac Disease. Celiac Disease is marked by the inability of the sufferer to endure gluten or wheat protein. In Dermatitis Herpetiformis Gluten Sensitivity is the main reason for the rise of all symptoms. The disease is mainly characterized by extreme itchiness. The development of rashes or blisters on the body is another prominent symptom of this condition. Dermatitis Herpetiformis gluten rashes are chronic which indicates that they remain on the skin surface for a long time. Usually, these rashes arise on different parts of the body and are of the same shape and size. Generally, the blisters are seen to appear together in a cluster. These are white or pink in appearance and the surrounding skin becomes red in color. Patients of this disorder also suffer from a burning sensation in the blisters that arise on their body. Scratching the papules can make them burst. In Dermatitis Herpetiformis weight loss may also happen in a few cases. However, the drop in body weight is not immediately apparent.

* Dermatofibroma, benign dermal nodules that represent a focal proliferation of fibroblasts; the overlying epidermis is slightly thickened.

* Dermatomyositis, muscle disease that involves inflammation and a skin rash.

* Dermoid cyst, overgrowth of normal, non-cancerous tissue in an abnormal location. Dermoids occur all over the body.

* Desmoid tumor is an abnormal growth that arises from connective tissue, which is the tissue that provides strength and flexibility to structures such as bones, ligaments, and muscles. Typically, a single tumor develops, although some people have multiple tumors. The tumors can occur anywhere in the body. Tumors that form in the abdominal wall are called abdominal desmoid tumors; those that arise from the tissue that connects the abdominal organs are called intra-abdominal desmoid tumors; and tumors found in other regions of the body are called extra-abdominal desmoid tumors. Extra-abdominal tumors occur most often in the shoulders, upper arms, and upper legs. Desmoid tumors are fibrous, much like scar tissue. They are generally not considered cancerous (malignant) because they do not spread to other parts of the body (metastasize); however, they can aggressively invade the surrounding tissue and can be very difficult to remove surgically. These tumors often recur, even after apparently complete removal. The most common symptom of desmoid tumors is pain. Other signs and symptoms, which are often caused by growth of the tumor into surrounding tissue, vary based on the size and location of the tumor. Intra-abdominal desmoid tumors can block the bowel, causing constipation. Extra-abdominal desmoid tumors can restrict the movement of affected joints and cause limping or difficulty moving the arms or legs.

* Diabetes insipidus (DI) is a condition characterized by excessive thirst and excretion of large amounts of severely dilute urine, with reduction of fluid intake having no effect on the concentration of the urine. There are different types of DI, each with a different set of causes. The most common type in humans is the neurological form, called central DI (CDI), which involves a deficiency of arginine vasopressin (AVP), also known as antidiuretic hormone (ADH). The second common type of DI is nephrogenic diabetes insipidus (NDI), which is due to kidney or nephron dysfunction caused by an insensitivity of the kidneys or nephrons to ADH. DI can also be gestational, or caused by alcohol or some types of drug abuse. DI should not be confused with nocturia.

* Diabetes mellitus type 1 (also known as type 1 diabetes) is a form of diabetes mellitus in which not enough insulin is produced. The lack of insulin results in high blood sugar levels. The classical symptoms are frequent urination, increased thirst, increased hunger, and weight loss. Additional symptoms may include blurry vision, feeling tired, and poor healing. Symptoms typically develop over a short period of time. The classical symptoms of type 1 diabetes include: polyuria (excessive urination), polydipsia (increased thirst), dry mouth, polyphagia (increased hunger), fatigue, and weight loss. Many type 1 diabetics are diagnosed when they present with diabetic ketoacidosis. The signs and symptoms of diabetic ketoacidosis include dry skin, rapid deep breathing, drowsiness, abdominal pain, and vomiting.

* Diabetic ketoacidosis, occurs when the body cannot use sugar (glucose) as a fuel source because there is no insulin or not enough insulin. Fat is used for fuel instead. Byproducts of fat breakdown, called ketones, build up in the body.

* Diabetic neuropathies are nerve damaging disorders associated with diabetes mellitus. These conditions are thought to result from diabetic microvascular injury involving small blood vessels that supply nerves (vasa nervorum) in addition to macrovascular conditions that can culminate in diabetic neuropathy. Relatively common conditions which may be associated with diabetic neuropathy include third nerve palsy; mononeuropathy; mononeuropathy multiplex; diabetic amyotrophy; a painful polyneuropathy; autonomic neuropathy; and thoracoabdominal neuropathy. Diabetic neuropathy affects all peripheral nerves including pain fibers, motor neurons and the autonomic nervous system. It, therefore, can affect all organs and systems, as all are innervated.

* Diabetic retinopathy, common diabetic eye disease caused by changes in retinal blood vessels.

* Diaphragmatic hernia is a defect or hole in the diaphragm that allows the abdominal contents to move into the chest cavity. The following types of diaphragmatic hernia exist, Congenital diaphragmatic hernia, Morgagni's hernia, Bochdalek hernia, Hiatal hernia, Iatrogenic diaphragmatic hernia and, Traumatic diaphragmatic hernia. The diaphragm is the muscle between the chest and abdomen that helps with breathing. The opening allows part of the organs from the belly to move into the chest cavity near the lungs. A diaphragmatic hernia is a rare defect. It occurs while the baby is developing in the womb. Because the diaphragm is not fully developed, organs, such as the stomach, small intestine, spleen, part of the liver, and the kidney, may take up part of the chest cavity. CDH most often involves only one side of the diaphragm. It is more common on the left side. Often, the lung tissue and blood vessels in the area do not develop normally either. It is not clear if the diaphragmatic hernia causes the underdeveloped lung tissue and blood vessels, or the other way around. 40% of babies with this condition have other problems as well. Having a parent or sibling with the condition increases the risk. Severe breathing problems almost always develop shortly after the baby is born. This is due in part to poor movement of the diaphragm muscle and crowding of the lung tissue. Problems with breathing and oxygen levels are often due to underdeveloped lung tissue and blood vessels as well. Other symptoms include bluish colored skin due to lack of oxygen, rapid breathing (tachypnea), fast heart rate (tachycardia). Complications may include lung infections and other congenital problems.

* Dientamoebiasis is a medical condition caused by infection with Dientamoeba fragilis. Dientamoeba fragilis is a single celled parasite that infects the lower gastrointestinal tract of humans. As many individuals are asymptomatic carriers of D. fragilis, pathogenic and nonpathogenic variants are proposed to exist. It increases in conditions of crowding and poor sanitation. An Australian study identified a large number of patients, considered to have irritable bowel syndrome, who were actually infected with Dientamoeba fragilis. Although D. fragilis has been described as an infection "emerging from obscurity", it has become one of the most prevalent gastrointestinal infections in industrialized countries, especially among children and young adults. A Canadian study reported a prevalence of around 10% in boys and girls aged 11�15 years, a prevalence of 11.5% in individuals aged 16�20, and a lower incidence of 0.3�1.9% in individuals over age 20. The most commonly reported symptoms in conjunction with infection with D. fragilis include abdominal pain (69%) and diarrhea (61%). Diarrhea may be intermittent and may not be present in all cases. It is often chronic, lasting over two weeks. The degree of symptoms may vary from asymptomatic to severe, and can include weight loss, vomiting, fever, and involvement of other digestive organs.

* Diphtheria is an infection caused by the bacterium Corynebacterium diphtheriae. Signs and symptoms may vary from mild to severe. They usually start two to five days after exposure. Symptoms often come on fairly gradually beginning with a sore throat and fever. In severe cases a grey or white patch develops in the throat. This can block the airway and create a barking cough as in croup. The neck may swell in part due to large lymph nodes. A form of diphtheria that involves the skin, eyes, or genitals also exists. Complications may include myocarditis, inflammation of nerves, kidney problems, and bleeding problems due to low blood platelets. Myocarditis may result in an abnormal heart rate and inflammation of the nerves may result in paralysis. Diphtheria is usually spread between people by direct contact or through the air. It may also be spread by contaminated objects. Some people carry the bacteria without having symptoms, but can still spread the disease to others. The symptoms of diphtheria usually begin two to seven days after infection. Symptoms of diphtheria include fever of 38 �C (100.4 �F) or above, chills, fatigue, bluish skin coloration (cyanosis), sore throat, hoarseness, cough, headache, difficulty swallowing, painful swallowing, difficulty breathing, rapid breathing, foul-smelling bloodstained nasal discharge and lymphadenopathy. Symptoms can also include cardiac arrhythmias, myocarditis, and cranial and peripheral nerve palsies. Laryngeal diphtheria can lead to a characteristic swollen neck and throat, or "bull neck". The swollen throat is often accompanied by a serious respiratory condition, characterized by a brassy or "barking" cough, stridor, hoarseness, and difficulty breathing, and historically referred to variously as "diphtheritic croup", "true croup", or sometimes simply as "croup".

* Diplopia, commonly known as double vision, is the simultaneous perception of two images of a single object that may be displaced horizontally, vertically, diagonally (i.e., both vertically and horizontally), or rotationally in relation to each other. It is usually the result of impaired function of the extraocular muscles (EOMs), where both eyes are still functional but they cannot converge to target the desired object. Problems with EOMs may be due to mechanical problems, disorders of the neuromuscular junction, disorders of the cranial nerves (III, IV, and VI) that stimulate the muscles, and occasionally disorders involving the supranuclear oculomotor pathways or ingestion of toxins. Diplopia can be one of the first signs of a systemic disease, particularly to a muscular or neurological process, and it may disrupt a person�s balance, movement, and/or reading abilities.

* Disseminated intravascular coagulation is a pathological process characterized by the widespread activation of the clotting cascade that results in the formation of blood clots in the small blood vessels throughout the body. This leads to compromise of tissue blood flow and can ultimately lead to multiple organ damage. In addition, as the coagulation process consumes clotting factors and platelets, normal clotting is disrupted and severe bleeding can occur from various sites.

* Distichia is an eyelash that arises from an abnormal spot on the eyelid. This abnormality, attributed to a genetic mutation, is known to affect dogs and humans. Distichiae (the abnormal eyelash) usually exit from the duct of the meibomian gland at the eyelid margin. They are usually multiple and sometimes more than one arises from a duct. They can affect either the upper or lower eyelid and are usually bilateral. The lower eyelids of dogs usually have no eyelashes. Distichiae usually cause no symptoms because the lashes are soft, but they can irritate the eye and cause tearing, squinting, inflammation, and corneal ulcers and scarring.

* Diverticulitis, formation of pouches (diverticula) within the bowel wall.

* Dr. Hulda Clark Parasite General, Comprehensive.

* Dupuytren's contracture, abnormal thickening and tightening of the normally elastic tissue beneath the skin of the palm and fingers.

* Dysentery is a type of gastroenteritis that results in diarrhea with blood. Other symptoms may include fever, abdominal pain, and a feeling of incomplete defecation. It is caused by a number of types of infection such as bacteria, viruses, parasitic worms, or protozoa. The mechanism is an inflammatory disorder of the intestine, especially of the colon. The most common form of dysentery is bacillary dysentery which is typically a mild illness, causing symptoms normally consisting of mild stomach pains and frequent passage of stool or diarrhea. Symptoms normally present themselves after one to three days and are usually no longer present after a week. The frequency of urges to defecate, the large volume of liquid feces passed, and the presence of mucus, pus and blood depends on the pathogen that is causing the disease. Temporary lactose intolerance can occur. In some caustic occasions severe abdominal pain, fever, shock, and delirium can all be symptoms. In extreme cases, dysentery patients may pass over one litre of fluid per hour. More often, individuals will complain of nausea, abdominal pain, and frequent watery and usually foul-smelling diarrhea, accompanied by mucus and blood, rectal pain, and fever. Vomiting, rapid weight-loss, and generalized muscle aches sometimes also accompany dysentery. On rare occasions, the amoebic parasite will invade the body through the bloodstream and spread beyond the intestines. In such cases, it may more seriously infect other organs such as the brain, lungs, and the liver.

* Dyslipidemias, an abnormal amount of lipids (e.g. cholesterol and/or fat) in the blood.

* Dyspareunia, painful sexual intercourse, usually in women, due to medical or psychological causes.

* Dyspepsia, indigestion.

* Dysplasia Arteriohepatic or Alagille syndrome (ALGS) is a complex multisystem disorder involving primarily the liver, heart, eyes, face, and skeleton. The clinical features are highly variable, even within families. The major clinical manifestations of ALGS are cholestasis, characterized by bile duct paucity on liver biopsy; congenital cardiac defects, primarily involving the pulmonary arteries; posterior embryotoxon in the eye; typical facial features; and butterfly vertebrae. Renal and central nervous abnormalities also occur. Mortality is approximately 10%, with vascular accidents, cardiac disease, and liver disease accounting for most of the deaths.

* Dystrophia brevicollis congenita or Klippel-Feil syndrome, is a bone disorder characterized by the abnormal joining (fusion) of two or more spinal bones in the neck (cervical vertebrae). The vertebral fusion is present from birth. Three major features result from this vertebral fusion: a short neck, the resulting appearance of a low hairline at the back of the head, and a limited range of motion in the neck. Most affected people have one or two of these characteristic features. Less than half of all individuals with Klippel-Feil syndrome have all three classic features of this condition. In people with Klippel-Feil syndrome, the fused vertebrae can limit the range of movement of the neck and back as well as lead to chronic headaches and muscle pain in the neck and back that range in severity. People with Klippel-Feil syndrome may have a wide variety of other features in addition to their spine abnormalities. In some cases, Klippel-Feil syndrome occurs as a feature of another disorder or syndrome, such as Wildervanck syndrome or hemifacial microsomia. In these instances, affected individuals have the signs and symptoms of both Klippel-Feil syndrome and the additional disorder.


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