Treatment combo Sessions of Modern Medicine in Digital format

Treatment combo Sessions of Modern Medicine in Digital format - J

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) Jaundice
2) Jaundice Chronic Idiopathic
3) Jaw Diseases
4) Job Syndrome
5) Joint Diseases
6) Juvenile Spinal Muscular Atrophy

* Jaundice can occur in babies, children, and adults. Jaundice is not an illness in itself, but a medical condition in which too much bilirubin - a compound produced by the breakdown of hemoglobin from red blood cells - is circulating in the blood. The excess bilirubin causes the skin, eyes, and mucus membranes in the mouth to turn a yellowish color. Because bilirubin is processed by the liver, the symptoms of jaundice may indicate damage to the liver in adults. If the cause is not identified and treated, it can lead to liver failure. In newborn babies, though, jaundice is common because they have extra red blood cells that begin to break down soon after they are born and their liver is often slower to process bilirubin.

* Jaundice Chronic Idiopathic or Dubin-Johnson syndrome is a condition characterized by jaundice, which is a yellowing of the skin and whites of the eyes. In most affected people jaundice appears during adolescence or early adulthood, although a few individuals have been diagnosed soon after birth. Jaundice is typically the only symptom of Dubin-Johnson syndrome, but some people also experience weakness, mild upper abdominal pain, nausea, and/or vomiting.

* Job's syndrome, or hyperimmunoglobulin E recurrent infection syndrome, repeated staphylococcal infections of the skin due to impaired immune defenses.

* Juvenile spinal muscular atrophy is a rare neuromuscular disorder characterised by loss of motor neurons and progressive muscle wasting, often leading to early death. Spinal muscular atrophy manifests in various degrees of severity, which all have in common progressive muscle wasting and mobility impairment. Proximal muscles and lung muscles are affected first. Other body systems may be affected as well, particularly in early-onset forms of the disorder. SMA is the most common genetic cause of infant death. The juvenile form usually manifests after 12 months of age and describes people with SMA3 who are able to walk without support at some time, although many later lose this ability. Respiratory involvement is less noticeable than in SMA1 and SMA2, and life expectancy is normal or near normal. The symptoms vary greatly depending on the SMA type involved, the stage of the disease, and individual factors; they commonly include: Areflexia, particularly in extremities. Overall muscle weakness, poor muscle tone, limpness or a tendency to flop. Difficulty achieving developmental milestones, difficulty sitting/standing/walking. In small children: adopting of a frog-leg position when sitting (hips abducted and knees flexed). Loss of strength of the respiratory muscles: weak cough, weak cry (infants), accumulation of secretions in the lungs or throat, respiratory distress. Bell-shaped torso (caused by using only abdominal muscles for respiration) in weaker SMA types. Fasciculations (twitching) of the tongue. Difficulty sucking or swallowing, poor feeding.