Tuberous Sclerosis
Tuberous sclerosis is a rare inherited disease which causes the growth of hamartomas on various organs of the body including kidney, heart, eyes, lungs and skin. This disease is caused by mutations to one of two genes which cause deficient hamartin and tuberin. Both of these proteins suppress tumors. In the past, there has not been an effective treatment for this disease. In our clinic this type of disease is treated with dual interferential treatments utilizing thermistor guidance. This treatment was invented, developed, and patented in this clinic. It is FDA approved for the treatment of chronic, intractable pain, increasing local blood circulation, prevention or retardation of disuse atrophy, and maintaining or increasing joint range of motion. This treatment is designed to create nerve chemicals which increase circulation, as well as, nerve chemicals which work throughout the patient to normalize the bodily functions. What sets our treatment apart from standard medical care is that this system is designed to work on the actual underlying problems of tuberous sclerosis rather than the symptoms of this disease
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