Guest guest Posted February 7, 2007 Report Share Posted February 7, 2007 A backgrounder on the relationship between disease and wasting disorders puts things in perspective. Myopathies are part of a group of disorders that are marked by low mitochondrial ATP output; this causes cell senescence and cell wasting. What they call idiopathic (no cause) on the street is called toxin load in the textbook. A mitochondrial insufficiency is actually a systemic involvement that shows up in " weak areas " first for lack of a better term. It's the reason people often have more than one degenerative illness. Mitochondrial impairment, it is taught in med school, is promoted by toxins; this is why areas that are prone to irritation and toxin assault anyway are usually the first to go, and because the liver is the most able to recover it's the bowel, lung and kidney, the three organs most exposed to toxin load next to the liver, that are fairly common targets. The solution is to reduce toxin load and promote mitochondrial function; this involves in an approach that actively promotes restoration and metabolic increase. Symptoms of celiac may not be celiac. The same protein gluten occurs on the outside of candida albicans cells and causes the same symptoms; this is why the treatment for intestinal dysbiosis -- bad bowel bacteria and candida -- usually dramatically reduces the celiac issues. And part of the treatment is carb reduction anyway Duncan , " Raven " <NWRaven wrote: > > Prevalence Of Celiac Disease Increased in Cardiomyopathy > http://www.mercola.com/1999/archive/celiac_disease_and_cardiomyopathy. htm > Researchers in Rome, Italy, report that the prevalence of celiac disease is increased in patients with idiopathic dilated cardiomyopathy. Quote Link to comment Share on other sites More sharing options...
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