Treatment combo Sessions of Modern Medicine in Digital format

Treatment combo Sessions of Modern Medicine in Digital format - S

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) Salivary Gland Diseases
2) Salmonella Enteriditis Gut
3) Salmonella Infections
4) Salpingitis
5) Samter Syndrome
6) Sarcoidosis
7) Sarcoma Osteogenic
8) Scabies
9) Schistosomiasis
10) Schizencephaly
11) Sciatica
12) Scleritis
13) Scleroma Nasal
14) Sclerosis Hereditary Spinal
15) Sclerosis Systemic
16) Scoliosis
17) Scotoma
18) Scrub Typhus
19) Sepsis
20) Serotonin Syndrome
21) Sexual Disorders(General)
22) Sexual Male Erectile Dysfunction
23) Sezary Syndrome
24) Shock
25) Shock Septic
26) Short Bowel Syndrome
27) Shoulder Injuries
28) Sialidosis
29) Sicca Syndrome
30) Silicosis
31) Sinusitis
32) Skin And Connective Tissue Diseases
33) Skin Collagen Building
34) Skin Diseases
35) Skin Diseases-Bacterial
36) Skin Mole
37) Skin Ulcer
38) Skin-Infectious Diseases
39) Skin-Scar Tissue Healing
40) Smell Disorders
41) Spasm
42) Spastic Spinal Monoplegia
43) Spider Veins
44) Spina Bifida
45) Spina Bifida Occulta
46) Spinal Cord Diseases
47) Spinal Cord Inflammation
48) Spinal Muscular Atrophy
49) Spinal Stenosis
50) Spinocerebellar Ataxia Type-
51) Splenic Diseases
52) Splenic Rupture
53) Spondylitis Ankylosing
54) Spondylolisthesis
55) STD-Comprehensive
56) Stevens-Johnson Syndrome
57) Stiff Knees
58) Stiff Muscles
59) Stomatitis Aphtous
60) Strabismus
61) Strabismus Convergent
62) Strabismus Divergent
63) Stress
64) Stridor
65) Stroke
66) Stroke Follow Up
67) Strongyloidiasis
68) Subdural Hematoma
69) Sudden Hearing Loss
70) Suture Techniques
71) Sweat Gland Diseases
72) Swelling
73) Syndrome Disorders
74) Synovitis
75) Syphilis Congenital
76) Systemic Inflammatory Response Syndrome

* Salmonella Enteritidis (SE) is one of the most prevalent infectious bacteria and the leading cause of Salmonellosis in the world. Salmonella Enteriditis bacteria may be found in the intestinal tracts of livestock, poultry, dogs, cats and other warm-blooded animals. This strain is only one of about 2,000 kinds of Salmonella bacteria; it is often associated with poultry and shell eggs. Salmonella enteriditis bacteria causes food poisoning and gastroenteritis. Symptoms of Salmonella include fever, abdominal cramps, and diarrhea. Symptoms usually only last for a day or two, however, serious complications can result from salmonella.

* Salmonella infections are caused by Salmonella bacteria. Most people infected with Salmonella develop diarrhea, fever, vomiting, and abdominal cramps 12 to 72 hours after infection. In most cases, the illness lasts four to seven days, and most people recover without treatment. In some cases, the diarrhea may be so severe that the patient becomes dangerously dehydrated and must be hospitalized. Intravenous fluids may be used to treat dehydration. Medications may be used to provide symptomatic relief, such as fever reduction. In severe cases, the Salmonella infection may spread from the intestines to the blood stream, and then to other body sites; this is known as typhoid fever and is treated with antibiotics. The elderly, infants, and those with impaired immune systems are more likely to develop severe illness. Some people afflicted with salmonellosis later experience reactive arthritis, which can have long-lasting, disabling effects.

* Salpingitis is an infection and inflammation in the fallopian tubes. It is often used synonymously with pelvic inflammatory disease (PID), although PID lacks an accurate definition and can refer to several diseases of the female upper genital tract, such as endometritis, oophoritis, myometritis, parametritis and infection in the pelvic peritoneum. In contrast, salpingitis only refers to infection and inflammation in the fallopian tubes. The infection usually has its origin in the vagina, and ascends to the fallopian tube from there. Because the infection can spread via the lymph vessels, infection in one fallopian tube usually leads to infection of the other. The symptoms usually appear after a menstrual period. The most common are: Abnormal smell and colour of vaginal discharge. Pain during ovulation, Pain during sexual intercourse. Pain coming and going during periods. Abdominal pain. Lower back pain. Fever. Nausea. Vomiting. Bloating.

* Samter's syndrome (or Samter's triad) is a condition that consists of the following three symptoms: asthma, nasal polyps (small growths), and a reaction against aspirin. Usually, the first symptom is rhinitis (nasal inflammation), with sneezing, a runny nose, congestion, and often a reduced sense of smell. This is usually followed by the development of asthma, and then the growth of polyps inside the nose. Polyps can cause sinusitis, post-nasal drip and obstruction of the airways. Finally, aspirin sensitivity develops. This can be quite serious, prompting asthma attacks and anaphylaxis (acute allergic reaction throughout the body), sometimes with hives and swelling of body-parts such as lips, tongue and neck. In some cases this swelling can be so severe that there is a risk of fatal suffocation. Patients often also react to other aspirin-type anti-inflammatory drugs, although acetaminophen or paracetamol is considered safe. The condition may be accompanied by an increase in certain white blood cells. Samter's syndrome may be acquired at any time of life, although it often affects people in their twenties and thirties.

* Sarcoidosis, abnormal collections of chronic inflammatory cells (granulomas) form as nodules in multiple organs.

* Sarcoma osteogenic (osteosarcoma) is a cancer that starts in the bone. It often starts in the ends of the bones where new bone tissue forms as a young person grows. Bones in the thigh, upper arm, and shin are the most common sites, but osteosarcoma can occur anywhere in the body. It usually develops during the period of rapid growth during adolescence, as a teenager matures into an adult. Osteosarcoma is the most common malignant bone tumor in youth. The average age at diagnosis is 15 years. Boys and girls have a similar incidence of this tumor until late adolescence, at which time boys are more commonly affected. The cause of osteosarcoma is unknown. Only rarely does osteosarcoma run in families. A defective tumor suppressor gene, allowing tumors to grow, has been linked to increased risk of this disease and is also associated with familial retinoblastoma, a childhood cancer of the eye. Children with familial retinoblastoma have a high risk for osteosarcoma in adolescence. Pain in the affected bone is the most common symptom. This pain may initially come and go and then gradually become more severe and constant. As the tumor grows, there may be visible swelling and limitation of motion. Tumors in the legs cause limping, while those in the arms cause pain on lifting. Swelling over the tumor may be warm and slightly reddened. Sometimes, the first sign may be a bone fracture. The tumor may cause weakness in the affected area of the bone. A fracture at the site of the tumor is called a �pathological fracture,� which occurs after what often seems like a routine movement.

* Scabies is a contagious skin infestation by the mite Sarcoptes scabiei. The most common symptoms are severe itchiness and a pimple-like rash. Occasionally tiny burrows may be seen in the skin. When first infected, usually two to six weeks are required before symptoms occur. If a person develops a second infection later in life, symptoms may begin within a day. These symptoms can be present across most of the body or just certain areas such as the wrists, between fingers, or along the waistline. The head may be affected, but this is typically only in young children. The itch is often worse at night. Scratching may cause skin breakdown and an additional bacterial infection of the skin. Crusted scabies is a more severe form of the disease. It typically only occurs in those with a poor immune system and people may have millions of mites, making them much more contagious. In these cases spread of infection may occur during brief contact or via contaminated objects.

* Schistosomiasis, also known as bilharzia or �snail fever�, is a parasitic disease carried by fresh water snails infected with one of the five varieties of the parasite Schistosoma. Found predominantly in tropical and sub-tropical climates, schistosomiasis infects 240 million people in as many as 78 countries, with a vast majority of the burden occuring in Africa. Schistosomiasis ranks second only to malaria as the most common parasitic disease. Schistosomiasis is transmitted by contact with contaminated fresh water (lakes and ponds, rivers, dams) inhabited by snails carrying the parasite. Swimming, bathing, fishing and even domestic chores such as laundry and herding livestock can put people at risk of contracting the disease. Larvae emerge from the snails and swim in the water until they come into contact with an individual and penetrate the skin. Symptoms of schistosomiasis are caused not by the worms themselves but by the body�s reaction to the eggs. Eggs shed by the adult worms that do not pass out of the body can become lodged in the intestine or bladder, causing inflammation or scarring. Children who are repeatedly infected can develop anemia, malnutrition, and learning difficulties. After years of infection, the parasite can also damage the liver, intestine, spleen, lungs, and bladder. Most people have no symptoms when they are first infected. However, within days after becoming infected, they may develop a rash or itchy skin. Within 1-2 months of infection, symptoms may develop including fever, chills, cough, and muscle aches. Without treatment, schistosomiasis can persist for years. Signs and symptoms of chronic schistosomiasis include: abdominal pain, enlarged liver, blood in the stool or blood in the urine, and problems passing urine. Chronic infection can also lead to increased risk of bladder cancer.

* Schizencephaly is a rare birth defect. It causes slits or clefts in the cerebral hemispheres of the brain. These clefts may appear on one or both sides of the brain. They may be filled with cerebrospinal fluid. The symptoms of schizencephaly can vary depending on whether it presents clefts on both sides of the brain, which are bilateral, or only one side, which are unilateral. Unilateral clefts almost always produce paralysis on one side of the body. Most people with unilateral clefts have normal to near normal intelligence. Bilateral clefts tend to cause more serious symptoms than unilateral clefts. They often cause developmental delays, including delays in learning speech and language skills. They can also cause problems with movement due to poor communication between brain and spinal cord. Other symptoms of schizencephaly can include: poor muscle tone, partial or complete paralysis, a smaller than normal head, accumulation of excess fluid in the brain, recurring seizures.

* Scleritis is a serious inflammatory disease that affects the white outer coating of the eye, known as the sclera. The disease is often contracted through association with other diseases of the body, such as granulomatosis with polyangiitis or rheumatoid arthritis. There are three types of scleritis: diffuse scleritis (the most common), nodular scleritis, and necrotizing scleritis (the most severe). Scleritis may be the first symptom of onset of connective tissue disease. Symptoms of scleritis include redness of the sclera and conjunctiva, sometimes changing to a purple hue, severe ocular pain, which may radiate to the temple or jaw. The pain is often described as deep or boring. Photophobia and tearing. Decrease in visual acuity, possibly leading to blindness.

* Scleroma nasal, chronic inflammation of tissues in the mucous membrane of the nose and upper respiratory tracts.

* Sclerosis hereditary spinal or Friedreich's ataxia is an autosomal recessive inherited disease that causes progressive damage to the nervous system. It manifests in initial symptoms of poor coordination such as gait disturbance; it can also lead to scoliosis, heart disease and diabetes, but does not affect cognitive function. The disease is progressive, and ultimately a wheelchair is required for mobility. Its incidence in the general population is roughly 1 in 50,000. The particular genetic mutation (expansion of an intronic GAA triplet repeat in the FXN gene) leads to reduced expression of the mitochondrial protein frataxin. Over time this deficiency causes the aforementioned damage, as well as frequent fatigue due to effects on cellular metabolism. The ataxia of Friedreich's ataxia results from the degeneration of nervous tissue in the spinal cord, in particular sensory neurons essential (through connections with the cerebellum) for directing muscle movement of the arms and legs. The spinal cord becomes thinner and nerve cells lose some of their myelin sheath (the insulating covering on some nerve cells that helps conduct nerve impulses).

* Scoliosis, causes a sideways curve of your backbone, or spine.

* Scotoma is an area of partial alteration in the field of vision consisting of a partially diminished or entirely degenerated visual acuity that is surrounded by a field of normal � or relatively well-preserved � vision. Every normal mammal eye has a scotoma in its field of vision, usually termed its blind spot. This is a location with no photoreceptor cells, where the retinal ganglion cell axons that compose the optic nerve exit the retina. This location is called the optic disc. There is no direct conscious awareness of visual scotomas. They are simply regions of reduced information within the visual field. Rather than recognizing an incomplete image, patients with scotomas report that things "disappear" on them. A scotoma can be a symptom of damage to any part of the visual system, such as retinal damage from exposure to high-powered lasers, macular degeneration and brain damage. Symptom-producing, or pathological, scotomata may be due to a wide range of disease processes, affecting any part of the visual system, including the retina (in particular its most sensitive portion, the macula) and the optic nerve. A pathological scotoma may involve any part of the visual field and may be of any shape or size. A scotoma may include and enlarge the normal blind spot. Even a small scotoma that happens to affect central or macular vision will produce a severe visual disability, whereas a large scotoma in the more peripheral part of a visual field may go unnoticed by the bearer because of the normal reduced optical resolution in the peripheral visual field.

* Scrub typhus, also known as bush typhus, is a disease caused by a bacteria called Orientia tsutsugamushi. Scrub typhus is spread to people through bites of infected chiggers (larval mites). The most common symptoms of scrub typhus include fever, headache, body aches, and sometimes rash. Most cases of scrub typhus occur in rural areas of Southeast Asia, Indonesia, China, Japan, India, and northern Australia. Anyone living in or traveling to areas where scrub typhus is found could get infected. Symptoms of scrub typhus usually begin within 10 days of being bitten. Signs and symptoms may include: Scrub typhus eschar. Fever and chills. Headache. Body aches and muscle pain. A dark, scab-like region at the site of the chigger bite (also known as eschar). Mental changes, ranging from confusion to coma. Enlarged lymph nodes. Rash. People with severe illness may develop organ failure and bleeding, which can be fatal if left untreated.

* Sepsis, blood poisoning, septicemia, is a systemic inflammatory response syndrome caused by an infection.

* Septic shock, a condition that results of severe infection and sepsis.

* Serotonin syndrome is a predictable consequence of excess serotonin on the CNS and/or peripheral nervous system. Hyperserotonemia may occur following therapeutic drug use, combination, overdose of particular drugs, or the recreational use of certain drugs. Excessive levels of serotonin produce a spectrum of specific symptoms including cognitive, autonomic, and somatic effects.

* Sexual disorders refers to problems that prevent from wanting or enjoying sexual activity.

* Sezary's syndrome is a rare special variant of cutaneous T cell lymphoma (CTCL) (mycosis fungoides) characterized by universal erythroderma, peripheral lymphadenopathy, and cellular infiltrates of atypical lymphocytes (Sezary cells) in the skin and in the blood. The disease may arise de novo or, less commonly, result from extension of a preexisting circumscribed CTCL. It usually occurs in patients older than 60 years and more commonly in males than in females. Patients appear sick, shivering, and scared and there is generalized scaling erythroderma with considerable thickening of the skin. Because of the bright red color, the syndrome has been called the "red man syndrome". There is diffuse hyperkeratosis of palms and soles, diffuse hair loss which can lead to baldness, and generalized lymphadenopathy. The disease usually shows cutaneous patches, plaques, tumors or generalized erythroderma (Mycosis fungoides). Pruritus is a common symptom. Extracutaneous manifestations are more frequent in the presence of locally advanced disease (cutaneous tumors). The presence of erythroderma with circulating malignant cells (Sezary's cells) in the peripheral blood (PB) and in the bone marrow is consistent with Sezary's syndrome, which is usually associated with lymphadenopathy.

* Shock, lack of adecuate blood flow to organs and tissues.

* Short-bowel syndrome is a disorder clinically defined by malabsorption, diarrhea, steatorrhea, fluid and electrolyte disturbances, and malnutrition. The final common etiologic factor in all causes of short-bowel syndrome is the functional or anatomic loss of extensive segments of small intestine so that absorptive capacity is severely compromised. Although resection of the colon alone typically does not result in short-bowel syndrome, the condition's presence can be a critical factor in the management of patients who lose significant amounts of small intestine. Massive small intestinal resection compromises digestive and absorptive processes. Adequate digestion and absorption cannot take place, and proper nutritional status cannot be maintained without supportive care. Today, the most common causes of short-bowel syndrome in adults include Crohn disease, radiation enteritis, mesenteric vascular accidents, trauma, and recurrent intestinal obstruction. In the pediatric population, necrotizing enterocolitis, intestinal atresias, and intestinal volvulus are the most common etiologic factors. Other conditions associated with short-bowel syndrome include congenital short small bowel, gastroschisis, and meconium peritonitis. Not all patients with loss of significant amounts of small intestine develop short-bowel syndrome. Important cofactors that help to determine whether the syndrome will develop or not include the premorbid length of small bowel, the segment of intestine that is lost, the age of the patient at the time of bowel loss, the remaining length of small bowel and colon, and the presence or absence of the ileocecal valve.

* Sialidosis is a rare lysosomal storage disease with two distinct clinical phenotypes. Type I sialadosis is the milder form with onset of gait abnormalities, progressive vision loss, bilateral macular cherry-red spots, and myoclonus in the second or third decade. Ataxia and seizures have also been reported in type I patients. Type II has an earlier onset with coarse facial features, dysostosis multiplex, short stature, developmental delay, mental retardation and hepatosplenomegaly. Type II patients may also present with a congenital-onset form associated with ascites and hydrops fetalis prenatally, an infantile-onset form with the absence of symptoms at birth or a juvenile form that has onset in late childhood and a relatively milder phenotype. Seizures, myoclonus and renal involvement have also been documented in type II cases. The frequency of diagnosed sialidosis in the general population is estimated at approximately one in four million live births.

* Sicca (Sjogren) syndrome is a long term autoimmune disease in which the moisture-producing glands of the body are affected.This results primarily in the development of a dry mouth and dry eyes. Other symptoms can include dry skin, a chronic cough, vaginal dryness, numbness in the arms and legs, feeling tired, muscle and joint pains, and thyroid problems. Those affected are at an increased risk (5%) of lymphoma. The hallmark symptom of SS is a generalized dryness, typically including xerostomia and keratoconjunctivitis sicca, part of what are known as sicca symptoms. Sicca syndrome also incorporates vaginal dryness and chronic bronchitis. SS may cause skin, nose, and vaginal dryness, and may affect other organs of the body, including the muscles (myositis), kidneys, blood vessels, lungs, liver, biliary system, pancreas, peripheral nervous system (distal axonal sensorimotor neuropathy or small fiber peripheral neuropathy) and brain. Some patients have gastric issues such as GERD, achlorhydria and/or gastroparesis, and chronic pain with accompanying fatigue and brain fog. The symptoms may develop insidiously, with the diagnosis often not considered for several years, because the complaints of sicca may be otherwise attributed to medications, a dry environment, aging, or may be regarded as not of severity warranting the level of investigation necessary to establish the presence of the specific underlying autoimmune disorder condition. SS is associated with a number of other medical conditions, many of which are autoimmune or rheumatic disorders, such as celiac disease, fibromyalgia, autoimmune thyroiditis, multiple sclerosis and spondyloarthropathy, and several malignancies, principally non-Hodgkin lymphoma.

* Skin mole, growths on the skin which happen when skin's pigment cells -melanocytes, grow in clusters.

* Small-cell carcinoma is a type of highly malignant cancer that most commonly arises within the lung, although it can occasionally arise in other body sites, such as the cervix, prostate, and gastrointestinal tract. Compared to non-small cell carcinoma, small cell carcinoma has a shorter doubling time, higher growth fraction, and earlier development of metastases. Small-cell carcinoma of the lung usually presents in the central airways and infiltrates the submucosa leading to narrowing of bronchial airways. Common symptoms include cough, dyspnea, weight loss, and debility. Over 70% of patients with small-cell carcinoma present with metastatic disease; common sites include liver, adrenals, bone, and brain. Small-cell carcinoma is an undifferentiated neoplasm composed of primitive-appearing cells. As the name implies, the cells in small-cell carcinomas are smaller than normal cells, and barely have room for any cytoplasm. Some researchers identify this as a failure in the mechanism that controls the size of the cells. Due to its high grade neuroendocrine nature, small-cell carcinomas can produce ectopic hormones, including adrenocorticotropic hormone (ACTH) and anti-diuretic hormone (ADH). Ectopic production of large amounts of ADH leads to syndrome of inappropriate antidiuretic hormone hypersecretion (SIADH). Lambert-Eaton myasthenic syndrome (LEMS) is a well-known paraneoplastic condition linked to small-cell carcinoma. When associated with the lung, it is sometimes called "oat cell carcinoma" due to the flat cell shape and scanty cytoplasm. Small-cell lung carcinoma can occur in combination with a wide variety of other histological variants of lung cancer, including extremely complex malignant tissue admixtures. When it is found with one or more differentiated forms of lung cancer, such as squamous cell carcinoma or adenocarcinoma, the malignant tumor is then diagnosed and classified as a combined small cell lung carcinoma (c-SCLC).

* Spastic spinal monoplegia is a syndrome associated with injury to the lateral half of the spinal cord. The condition is characterized by the following clinical features (which are found below the level of the lesion): contralateral hemisensory anesthesia to pain and temperature, ipsilateral loss of propioception, and ipsilateral motor paralysis. Tactile sensation is generally spared.

* Spider veins or telangiectasia.

* Spina bifida is a birth defect where there is incomplete closing of the backbone and membranes around the spinal cord. The most common location is the lower back, but in rare cases it may be the middle back or neck. Associated problems include poor ability to walk, problems with bladder or bowel control, hydrocephalus, a tethered spinal cord, and latex allergy. Learning problems are relatively uncommon. Most cases of spina bifida can be prevented if the mother gets enough folate before and during pregnancy. Adding folic acid to flour has been found to be effective for most women. Physical signs of spina bifida may include: Leg weakness and paralysis, orthopedic abnormalities (i.e., club foot, hip dislocation, scoliosis), bladder and bowel control problems, including incontinence, urinary tract infections, and poor kidney function, pressure sores and skin irritations, abnormal eye movement. 68% of children with spina bifida have an allergy to latex, ranging from mild to life-threatening.

* Spina bifida occulta is the mildest form of spina bifida. In occulta, the outer part of some of the vertebrae is not completely closed. The splits in the vertebrae are so small that the spinal cord does not protrude. The skin at the site of the lesion may be normal, or it may have some hair growing from it; there may be a dimple in the skin, or a birthmark. Unlike most other types of neural tube defects, spina bifida occulta is not associated with increased AFP, a common screening tool used to detect neural tube defects in utero. This is because, unlike most of the other neural tube defects, the dural lining is maintained. Many people with this type of spina bifida do not even know they have it, as the condition is asymptomatic in most cases. The incidence of spina bifida occulta is approximately 10-20% of the population, and most people are diagnosed incidentally from spinal X-rays.

* Spinal cord inflammation, different neurological conditions which results to individuals suffering from back pain. It may be caused by viral infection, bacteria or auto immune disease.

* Spinal muscular atrophy, group of inherited diseases that cause muscle damage and weakness, which get worse over time and eventually lead to death.

* Spinal stenosis, narrowing of the spinal canal that causes compression of the spinal nerve cord.

* Spinocerebellar ataxia type 3 (SCA3) also known as Machado�Joseph disease (MJD), is a rare autosomal dominantly inherited neurodegenerative disease that causes progressive cerebellar ataxia, which results in a lack of muscle control and coordination of the upper and lower extremities. Some symptoms, such as clumsiness and rigidity, make MJD commonly mistaken for drunkenness or Parkinson's disease. Machado�Joseph disease is a type of spinocerebellar ataxia and is the most common cause of autosomal-dominant ataxia. MJD causes ophthalmoplegia and mixed sensory and cerebellar ataxia. Symptoms of MJD are memory deficits, spasticity, difficulty with speech and swallowing, weakness in arms and legs, clumsiness, frequent urination and involuntary eye movements. Symptoms can begin in early adolescence and they get worse over time. Eventually, MJD leads to paralysis; however, intellectual functions usually remain the same. The pons (a structure located on the brain stem) is one of the areas affected by MJD. The striatum (a brain area connected to balance and movement) is also affected by this disease, which could explain both of the main motor problems cause by MJD: the tightening and twisting of the limb and the abrupt, irregular movements.

* Splenic rupture occurs when the spleen is placed under intense pressure/duress, strong enough to tear or separate the outer lining of the organ. A ruptured spleen accounts for 10% of all abdominal injuries. When a blunt abdominal trauma is present, the spleen is the most frequently and often the only injured organ. A splenic rupture typically results in severe pain and internal bleeding. However, some cases have exhibited only mild symptoms and symptoms may appear delayed as opposed to immediate presentation. The condition is usually caused by a sudden and direct blow to the abdomen, but spontaneous rupture is also possible if the spleen is enlarged or has been enlarged in the past, due to mononucleosis, infection, or chronic excessive consumption of alcohol. Some symptoms are: Right quadrant/left abdominal pain. Left shoulder pain. Severe or mild pain. Rebound tenderness. Muscle guarding. Nausea. Profuse sweating or hot and cold sensations. Abdominal distension or ecchymosis (bruising). Light headedness or syncope (fainting). Fatigue. Low blood pressure. Blurred vision.

* Spondylitis ankylosing, inflammatory disease that can cause some of the vertebrae in your spine to fuse together.

* Spondylolisthesis is is the forward displacement of a vertebral bone in relation to the natural curve of the spine, most commonly occurring after a fracture, and most often the fifth lumbar vertebra. Backward displacement is referred to as retrolisthesis. When occurring in conjunction with scoliosis, the shortened term "olisthesis," may sometimes be used instead. Symptoms of spondylolisthesis include: A general stiffening of the back and a tightening of the hamstrings, with a resulting change in both posture and gait. A leaning-forward or semi-kyphotic posture may be seen, due to compensatory changes. A "waddle" may be seen in more advanced causes, due to compensatory pelvic rotation due to decreased lumbar spine rotation. A result of the change in gait is often a noticeable atrophy in the gluteal muscles due to lack of use. Generalized lower-back pain may also be seen, with intermittent shooting pain from the buttocks to the posterior thigh, and/or lower leg via the sciatic nerve. Other symptoms may include tingling and numbness. Coughing and sneezing can intensify the pain. An individual may also note a "slipping sensation" when moving into an upright position. Sitting and trying to stand up may be painful and difficult.

* STD Comprehensive, Herpes, Gonorrhea, Syphilis, Chlamydia, HPV, HIV Symptoms.

* Stevens-Johnson syndrome (SJS) is a form of toxic epidermal necrolysis which often begins with a fever and flu-like symptoms. Within a few days, the skin begins to blister and peel, forming very painful raw areas called erosions that resemble a severe hot-water burn. The skin erosions usually start on the face and chest before spreading to other parts of the body. In most affected individuals, the condition also damages the mucous membranes, including the lining of the mouth and the airways, which can cause trouble with swallowing and breathing. The painful blistering can also affect the urinary tract and genitals. SJS often affects the eyes as well, causing irritation and redness of the conjunctiva, which are the mucous membranes that protect the white part of the eye and line the eyelids, and damage to the clear front covering of the eye (the cornea). Severe damage to the skin and mucous membranes makes SJS a life-threatening disease. Because the skin normally acts as a protective barrier, extensive skin damage can lead to a dangerous loss of fluids and allow infections to develop. Serious complications can include pneumonia, overwhelming bacterial infections (sepsis), shock, multiple organ failure, and death. About 10 percent of people with Stevens-Johnson syndrome die from the disease, while the condition is fatal in up to 50 percent of those with toxic epidermal necrolysis. Among people who survive, long-term effects of SJS can include changes in skin coloring (pigmentation), dryness of the skin and mucous membranes (xerosis), excess sweating (hyperhidrosis), hair loss (alopecia), and abnormal growth or loss of the fingernails and toenails. Other long-term problems can include impaired taste, difficulty urinating, and genital abnormalities. A small percentage of affected individuals develop chronic dryness or inflammation of the eyes, which can lead to increased sensitivity to light (photophobia) and vision impairment.

* Stomatitis aphtous, mouth ulcers.

* Strabismus convergent or esotropia is a form of strabismus, or "squint," in which one or both eyes turns inward. The condition can be constantly present, or occur intermittently, and can give the affected individual a "cross-eyed" appearance. Esotropia is sometimes erroneously called �lazy eye,� which describes the condition of amblyopia�a reduction in vision of one or both eyes that is not the result of any pathology of the eye and cannot be resolved by the use of corrective lenses. Amblyopia can, however, arise as a result of esotropia occurring in childhood.

* Strabismus divergent, exotropia, divergent squint or wall eyes, is a form of strabismus where the eyes are deviated outward. It is the opposite of esotropia. People with exotropia often experience crossed diplopia. Intermittent exotropia is a fairly common condition. "Sensory exotropia" occurs in the presence of poor vision. Infantile exotropia (sometimes called "congenital exotropia") is seen during the first year of life, and is less common than "essential exotropia" which usually becomes apparent several years later. The brain's ability to see three-dimensional objects depends on proper alignment of the eyes. When both eyes are properly aligned and aimed at the same target, the visual portion of the brain fuses the forms into a single image. When one eye turns inward, outward, upward, or downward, two different pictures are sent to the brain. This causes loss of depth perception and binocular vision. There have also been some reports of people that can "control" their afflicted eye.

* Strabismus is a condition in which the eyes do not properly align with each other. This interferes with binocular vision because it prevents a person from directing both eyes simultaneously towards the same fixation point. It also typically affects depth perception. Strabismus typically involves a lack of coordination between the extraocular muscles. Strabismus is present in about 4% of children. Treatment should be started as early as possible to ensure the development of the best possible visual acuity and stereopsis.

* Stress is a feeling of strain and pressure. Stress can be external and related to the environment, but may also be created by internal perceptions. Humans experience stress, or perceive things as threatening, when they do not believe that their resources for coping with obstacles (stimuli, people, situations, etc.) are enough for what the circumstances demand. When we think the demands being placed on us exceed our ability to cope, we then perceive stress.

* Strongyloidiasis is an intestinal infection caused by 2 species of the parasitic nematode Strongyloides. The most common and clinically important pathogenic species in humans is S stercoralis. S fuelleborni is found sporadically in Africa and Papua New Guinea. Distinctive characteristics of this parasite are its ability to persist and replicate within a host for decades while producing minimal or no symptoms (individuals with an intact immune system) and its potential to cause life-threatening infection (hyperinfection syndrome, disseminated strongyloidiasis) in an immunocompromised host (60-85% mortality rate). The symptoms related to strongyloidiasis may reflect the nematode's systemic passage, its local cutaneous involvement, or both. During chronic uncomplicated infections, the larvae may migrate to the skin, where they can cause cutaneous strongyloidiasis, known as larva currens because of the quick migratory rate of the larva. Infection is clinically characterized by watery diarrhea, abdominal cramping, and urticarial rash. In malnourished children, strongyloidiasis remains an important cause of chronic diarrhea, cachexia, and failure to thrive.

* Subdural hematoma also known as a subdural haemorrhage (SDH), is a type of hematoma, usually associated with traumatic brain injury. Blood gathers between the inner layer of the dura mater and the arachnoid mater. Usually resulting from tears in bridging veins which cross the subdural space, subdural hemorrhages may cause an increase in intracranial pressure (ICP), which can cause compression of and damage to delicate brain tissue. Subdural hematomas are often life-threatening when acute. Chronic subdural hematomas, however, have a better prognosis if properly managed. In contrast, epidural hematomas are usually caused by tears in arteries, resulting in a build-up of blood between the dura mater and skull. Symptoms of subdural hemorrhage have a slower onset than those of epidural hemorrhages because the lower pressure veins bleed more slowly than arteries. Therefore, signs and symptoms may show up in minutes, if not immediately but can be delayed as much as 2 weeks. If the bleeds are large enough to put pressure on the brain, signs of increased ICP (intracranial pressure) or damage to part of the brain will be present. Other signs and symptoms of subdural hematoma can include any combination of the following: A history of recent head injury. Loss of consciousness or fluctuating levels of consciousness. Irritability. Seizures. Pain. Numbness. Headache (either constant or fluctuating). Dizziness. Disorientation. Amnesia. Weakness or lethargy. Nausea or vomiting. Loss of appetite. Personality changes. Inability to speak or slurred speech. Ataxia, or difficulty walking. Loss of muscle control. Altered breathing patterns. Hearing loss or hearing ringing (tinnitus). Blurred Vision. Deviated gaze, or abnormal movement of the eyes. Subdural hematomas are most often caused by head injury, when rapidly changing velocities within the skull may stretch and tear small bridging veins. Subdural hematomas due to head injury are described as traumatic. Much more common than epidural hemorrhages, subdural hemorrhages generally result from shearing injuries due to various rotational or linear forces. Subdural hemorrhage is a classic finding in shaken baby syndrome, in which similar shearing forces classically cause intra- and pre-retinal hemorrhages. Subdural hematoma is also commonly seen in the elderly and in alcoholics, who have evidence of cerebral atrophy. Cerebral atrophy increases the length the bridging veins have to traverse between the two meningeal layers, hence increasing the likelihood of shearing forces causing a tear. It is also more common in patients on anticoagulants, especially aspirin and warfarin. Patients on these medications can have a subdural hematoma with a minor injury. A further cause can be a reduction in cerebral spinal fluid pressure which can create a low pressure in the subarachnoid space, pulling the arachnoid away from the dura mater and leading to a rupture of the blood vessels.

* Sudden sensorineural hearing loss (SSHL), commonly known as sudden deafness, occurs as an unexplained, rapid loss of hearing�usually in one ear�either at once or over several days.

* Sweat gland diseases, abnormal function of the sweat glands.

* Swelling / edema, see which suits you better.

* Systemic inflammatory response syndrome (SIRS), a severe systemic response to a condition that provokes an acute inflammatory reaction indicated by the presence of some symptoms such as abnormal body temperature, and fast heart and breath rate.

* Systemic sclerosis, is an autoimmune disease of the connective tissue. It is characterized by thickening of the skin caused by accumulation of collagen, and by injuries to small arteries.There are two forms of scleroderma: localized and systemic. The localized (limited) form affects the skin of only the face, hands, and feet. The systemic (diffuse) form involves those and, in addition, may progress to visceral organs, including the kidneys, heart, lungs, and gastrointestinal tract. Signs and symptoms associated with limited scleroderma include calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, and telangiectasia.