Treatment combo Sessions of Modern Medicine in Digital format

Treatment combo Sessions of Modern Medicine in Digital format - O

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) Ocular Motility Disorders
2) Ocular Retraction Syndrome
3) Oculoauriculovertebral Syndrome
4) Oculomotor Nerve Diseases
5) Oculomotor Paralysis
6) Odontogenic Tumors
7) Olfaction Disorders
8) Oliguria
9) Olivopontocerebellar Atrophies
10) Onchocerciasis
11) Ophthalmia
12) Optic Atrophies Hereditary
13) Optic Nerve Diseases
14) Optic Neuritis
15) Oral Health
16) Orthostatic Hypotension
17) Osteitis Deformans
18) Osteoarthritis
19) Osteochondritis
20) Osteogenesis Imperfecta
21) Osteomalacia
22) Osteomyelitis
23) Osteonecrosis
24) Osteopetrosis
25) Osteoporosis
26) Ostomy
27) Otitis
28) Otitis Interna
29) Otorhinolaryngologic Disease
30) Otosclerosis
31) Ovarian Cysts

* Ocular retraction syndrome or Duane syndrome s a congenital rare type of strabismus most commonly characterized by the inability of the eye to move outwards. Duane syndrome is most probably a miswiring of the eye muscles, causing some eye muscles to contract when they shouldn't and other eye muscles not to contract when they should. The characteristic features of the syndrome are, limitation of abduction (outward movement) of the affected eye, less marked limitation of adduction (inward movement) of the same eye, retraction of the eyeball into the socket on adduction, with associated narrowing of the palpebral fissure (eye closing), widening of the palpebral fissure on attempted abduction, poor convergence, and a head turn to the side of the affected eye to compensate for the movement limitations of the eye(s) and to maintain binocular vision.

* Oculoauriculovertebral Syndrome or Goldenhar syndrome is a craniofacial syndrome, which means that it causes certain abnormalities in the formation of the face and head. It is considered a rare disease and a congenital one, meaning it�s present at birth. Goldenhar is present in just 1 out of every 3,500 to 25,000 babies at birth. In people with Goldenhar syndrome, abnormalities appear mostly in the areas of the ears, eyes, and spine. This condition can also affect the structure of the face, and some internal organs. The severity of the abnormalities and symptoms varies by individual. The symptoms of Goldenhar and their severity are extremely variable from one individual to another. The most recognizable symptom is the presence of facial abnormalities, in particular hemifacial microsomia. These occur when the bones and muscles in the face are underdeveloped on just one side of the face. Those with Goldenhar may also have a cleft lip or cleft palate. Other characteristics of the syndrome include defects in the eyes, ears, and spine. This can mean growths on the eyes, small eyes, missing eyelids, small ears, missing ears, ear tags, or even hearing loss. In the spine, Goldenhar can cause incomplete development of vertebrae, or fused or missing vertebrae. Many people with the syndrome end up with scoliosis, or a curved spine, as a result. There are other less common, and less visible, symptoms as well. Between 5 and 15 percent of people with Goldenhar have some degree of intellectual disability. Some also have abnormalities in internal organs, which most commonly include congenital heart defects. Defects affecting the kidneys and limbs are rare.

* Oculomotor nerve palsy or third nerve palsy is an eye condition resulting from damage to the third cranial nerve or a branch thereof. As the name suggests, the oculomotor nerve supplies the majority of the muscles controlling eye movements. Thus, damage to this nerve will result in the affected individual being unable to move his or her eye normally. In addition, the nerve also supplies the upper eyelid muscle and the muscles responsible for pupil constriction. The limitations of eye movements resulting from the condition are generally so severe that the affected individual is unable to maintain normal alignment of their eyes when looking straight ahead, leading to strabismus and, as a consequence, double vision (diplopia).

* Odontogenic tumors are dental neoplasms of the cells or tissues that initiate odontogenic processes. Examples include Adenomatoid odontogenic tumor, Ameloblastoma, a type of odontogenic tumor involving ameloblasts, Calcifying epithelial odontogenic tumor, Keratocystic odontogenic tumor, Odontogenic myxoma, and Odontoma.

* Oliguria, low output of urine.

* Olivopontocerebellar atrophy (OPCA) is the degeneration of neurons in specific areas of the brain � the cerebellum, pons, and inferior olives. OPCA is present in several neurodegenerative syndromes, including inherited and non-inherited forms of ataxia (such as the hereditary spinocerebellar ataxia known as Machado�Joseph disease) and multiple system atrophy (MSA), with which it is primarily associated. OPCA may also be found in the brains of individuals with prion disorders and inherited metabolic diseases. OPCA is characterized by progressive cerebellar ataxia, leading to clumsiness in body movements, veering from midline when walking, wide-based stance, and falls without signs of paralysis or weakness. Clinical presentation can vary greatly between patients, but mostly affects speech, balance and walking. Other possible neurological problems include spasmodic dysphonia, hypertonia, hyperreflexia, rigidity, dysarthria, dysphagia and neck dystonic posture.

* Onchocerciasis, also known as river blindness and Robles disease, is a disease caused by infection with the parasitic worm Onchocerca volvulus. Symptoms include severe itching, bumps under the skin, and blindness. It is the second most common cause of blindness due to infection, after trachoma.

* Ophthalmia is inflammation of the eye. It is a medical sign which may be indicative of various conditions, including sympathetic ophthalmia (inflammation of both eyes following trauma to one eye), gonococcal ophthalmia, trachoma or "Egyptian" ophthalmia, ophthalmia neonatorum (a conjunctivitis of the newborn due to either of the two previous pathogens), photophthalmia and actinic conjunctivitis (inflammation resulting from prolonged exposure to ultraviolet rays), and others.

* Optic hereditary atrophies are the end result of inherited optic neuropathies that damage nerve cells anywhere between the retinal ganglion cells and the lateral geniculate body (anterior visual system). The optic nerve contains axons of nerve cells that emerge from the retina, leave the eye at the optic disc, and go to the visual cortex where input from the eye is processed into vision. There are 1.2 million optic nerve fibers that derive from the retinal ganglion cells of the inner retina. The inherited optic neuropathies typically manifest as symmetric bilateral central visual loss. Optic nerve damage in most inherited optic neuropathies is permanent and progressive. Leber�s hereditary optic neuropathy (LHON) is the most frequently occurring mitochondrial disease, and this inherited form of acute or subacute vision loss predominantly affects young males. LHON usually presents with rapid vision loss in one eye followed by involvement of the second eye (usually within months). Visual acuity often remains stable and poor (around or below 20/200) with a residual central visual field defect. Patients with the 14484/ND6 mutation are most likely to have visual recovery. Dominant optic atrophy is an autosomal dominant disease caused by a defect in the nuclear gene OPA1. A slowly progressive optic neuropathy, dominant optic atrophy, usually presents in the first decade of life and is bilaterally symmetrical. Examination of these patients shows loss of visual acuity, temporal pallor of the optic discs, centrocecal scotomas with peripheral sparing, and subtle impairments in color vision. Behr�s syndrome is a rare autosomal recessive disorder characterized by early-onset optic atrophy, ataxia, and spasticity. Berk�Tabatznik syndrome is a condition that shows symptoms of short stature, congenital optic atrophy and brachytelephalangy. This condition is extremely rare.

* Optic Nerve Diseases, such as glaucoma.

* Optic neuritis, inflammation of the optic nerve that may cause a complete or partial loss of vision.

* Oral health, dental comprehensive, includes Periodontal disease.

* Orthostatic hypotension, also referred to as head rush or dizzy spell, is a temporary lowering of blood pressure, usually related to suddenly standing up.

* Osteitis deformans or Paget's disease of bone is caused by the excessive breakdown and formation of bone, followed by disorganized bone remodeling. This causes affected bone to weaken, resulting in pain, misshapen bones, fractures and arthritis in the joints near the affected bones. Rarely, it can develop into a primary bone cancer known as Paget's sarcoma. Often Paget's disease is localized to only a few bones in the body. The pelvis, femur, and lower lumbar vertebrae are the most commonly affected bones. Paget's disease typically is localized, affecting just one or a few bones, as opposed to osteoporosis, for example, which usually affects all the bones in the body. A later phase of the disease is characterized by the replacement of normal bone marrow with highly vascular fibrous tissue. Paget's disease affects from 1.5 to 8.0 percent of the population, depending on age and country of residence. Paget's disease is rare in people less than 55 years of age. Men are more commonly affected than women. Many people with Paget's disease do not know they have the disease, because they have a mild case with no symptoms. In addition, when symptoms do occur, they may be confused with those of arthritis or other disorders. In other cases, the diagnosis is made only after complications have developed. About 35 percent of patients with Paget's have symptoms related to the disease when they are first diagnosed. The first manifestation of Paget's disease is usually an elevated alkaline phosphatase in the blood. Overall, the most common symptom is bone pain. Loss of hearing in one or both ears may occur when Paget's disease affects the skull and the bone that surrounds the inner ear. Treating the disease may slow or stop hearing loss. In rare cases, involvement of the skull may lead to compression of the nerves that supply the eye, leading to vision loss. Paget's may also cause gross deformities in the bones. Paget's disease is a frequent component of multisystem proteinopathy. Paget's disease may lead to other medical conditions, including: Arthritis, Cardiovascular disease, Kidney stones, Nervous system problems, Angioid streaks, and loose teeth. (See also below Paget Disease Of Bone).

* Osteoarthritis, or wear and tear arthritis is the most common type of arthritis.

* Osteochondritis, painful type of osteochondrosis where the cartilage or bone in a joint is inflamed.

* Osteogenesis imperfecta (OI), also known as brittle bone disease or Lobstein syndrome, is a congenital bone disorder characterized by brittle bones that are prone to fracture. OI may also present with shorter height, neurological features including communicating hydrocephalus, basilar invagination, and seizures, blue sclerae, hearing loss, or other complications. The fractures themselves can cause acute or chronic pain, reduced quality of life, and depression. .People with OI are born with defective connective tissue, or without the ability to make it.

* Osteomalacia, softening of the bones due to a lack of vitamin D or a problem with the body's ability to break down and use this vitamin.

* Osteomyelitis, bone infection caused by bacteria or other germs.

* Osteonecrosis, bone death caused by poor blood supply to the area.

* Osteopetrosis, literally "stone bone", also known as marble bone disease and Albers-Sch�nberg disease, is an extremely rare inherited disorder whereby the bones harden, becoming denser, in contrast to more prevalent conditions like osteoporosis, in which the bones become less dense and more brittle, or osteomalacia, in which the bones soften. Osteopetrosis can cause bones to dissolve and break. It can cause osteosclerosis. The cause of the disease is understood to be malfunctioning osteoclasts. Radiological findings will show a bone-in-bone appearance. Despite this excess bone formation, people with osteopetrosis tend to have bones that are more brittle than normal. Mild osteopetrosis may cause no symptoms, and present no problems. However, serious forms can result in stunted growth, deformity, and increased likelihood of fractures; also, patients suffer anemia, recurrent infections, and hepatosplenomegaly due to bone expansion leading to bone marrow narrowing and extramedullary hematopoiesis. It can also result in blindness, facial paralysis, and deafness, due to the increased pressure put on the nerves by the extra bone.

* Ostomy is a surgical procedure creating an opening in the body for the discharge of body wastes. Certain diseases of the bowel or urinary tract involve removing all or part of the intestine or bladder. This creates a need for an alternate way for feces or urine to leave the body. An opening is surgically created in the abdomen for body wastes to pass through. The surgical procedure is called an ostomy. The opening that is created at the end of the bowel or ureter is called a stoma, which is pulled through the abdominal wall.

* Otitis interna, an inflammation of the inner ear; can cause vertigo and vomiting.

* Otosclerosis is a condition in which there's abnormal bone growth inside the ear. It's a fairly common cause of hearing loss in young adults. There are three tiny bones deep inside the ear, which vibrate when sound waves enter. They transmit sound waves to the cochlea (inner ear), which converts them into signals that are sent to the brain. In otosclerosis, the stapes ("stirrup" bone) begins to fuse with the surrounding bone, eventually becoming fixed so it can't move. This means sound is no longer transmitted into the inner ear efficiently. Most people with otosclerosis notice hearing problems in their 20s or 30s. One or both ears can be affected. Symptoms of otosclerosis include: hearing loss that gets gradually worse over time, particular difficulty hearing low, deep sounds and whispers, speaking quietly because your voice sounds loud to you, finding it easier to hear when there's background noise (unlike many other types of hearing loss), tinnitus (hearing sounds such as buzzing or humming that come from inside your body), dizziness � though this is rare. The symptoms of otosclerosis can be hard to tell apart from other causes of hearing loss.