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Common Variable Immunodeficiency

Treatment No. : RD0153
Dosage & Instructions: 15 drops in 15 ml of plain water twice a day, mornings and evenings.
Composition:
Ferr lod D12+100C
Acid phos D12+100C
Sulphur lod D12+100C
Calc lod D12+100C
Acid nitric D12+100C
Treatment Type:
This remedy is a symptomatic treatment. A symptomatic treatment cannot eliminate the disease from its root but is able to considerably improve the patient's condition by easing his or her symptoms.
Contra-indications: None established
Special Instructions: Whereas this remedy can be safely used by teenagers, its use has not been evaluated in children under 12 years of age. Please do not administer to children under this age.
Storage: Store in a cool and dry place
Precautions: Keep away from the reach of children
Standard Packaging : 30 ml Drops

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One 30 ml bottle for $79.99
Two 30 ml bottles for $129.99

 

Condition Overview:

Common Variable Immunodeficiency (CVI) is a group of rare genetic (primary) immunodeficiency disorders in which abnormalities in immune cell development (maturation) result in a decreased ability to appropriately produce antibodies in response to invading microorganisms, toxins, or other foreign substances. The symptoms of CVI usually become apparent during the second to the fourth decade of life.

The term "Common Variable Immunodeficiency" is used to designate an immune defect in which there is a substantial reduction of the level of immunizing agents (immunoglobulins) in the fluid portion of the blood (serum). According to the medical literature, most individuals with CVI share common, distinctive symptoms and physical findings (phenotype) due to decreased levels of all major classes of immunoglobulins in blood serum (panhypogammaglobulinemia). Defective production of certain antibodies in response to invading microorganisms (antibody deficiency) and recurrent bacterial infections are also characteristic of CVI. Such infections often affect the upper and lower respiratory tracts and the gastrointestinal (digestive) system.

In some cases, individuals with Common Variable Immunodeficiency have an increased tendency to develop certain diseases characterized by abnormal tissue growths (neoplasms) that may be benign or malignant. In addition, some individuals with CVI may have an unusual susceptibility to certain autoimmune diseases. These disorders occur when the body's natural defenses against invading microorganisms mistakenly attack healthy tissue. The range and severity of symptoms and findings associated with CVI may vary from case to case.

It is thought that Common Variable Immunodeficiency may result from a combination of genetic defects or from different disease genes (heterogenous). In many cases, there is no clear pattern of inheritance. However, in successive generations of some affected families (kindreds), there is evidence that CVI may be inherited as an autosomal recessive genetic trait. In addition, a rare acquired form of the disorder has been described in the medical literature.

 

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