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Die Amyotrophe Lateralsklerose (oder Amyotrophische Lateralsklerose, Myatrophe Lateralsklerose, englisch auch Motor Neuron Disease; Lou-Gehrig-Syndrom, früher auch Charcot-Krankheit), kurz ALS, ist eine degenerative Krankheit des motorischen Nervensystems.
Die Ursache ist unbekannt.
Grundsätzlich gestaltet sich die Diagnosestellung schwierig, da u. a. kein spezifisches Kardinalsymptom die ALS beweist.
Amyotrophe Lateralsklerose – Wikipedia
As already mentioned, the EAP-salts seemingly also work in FA and in ALS.
Around 1975 many people from Europe and from the USA asked me if FA and ALS, as well as MS, would respond to the colamin phosphates (EAP-salts). At first I had the tendency to deny this, but many people having such a disease insisted on trying it. The results turned out to be positive on the whole, and sometimes even surprising. As a result, people suffering from these diseases are welcomed by us today. ALS is – according to our proper findings – apparently not an immuno*disease. There are, however, mixed forms with an MS – like manifestation observable. ALS was found to be frequent with those people exposed to aluminum contamination. This was first reported from the island of Guam. We have frequently found ALS in aluminum welders, in people eating frequently from aluminum foil especially when it had been heated or even burned on charcoal, in people living downwind from aluminum refineries, and in people who used underarm sprays based on aluminum hydroxide in a fluoride propellant for a long period of time.
Interessanterweise ist bekannt, dass Aluminium das Myelin in vielfacher Weise schädigen kann. Tierversuche haben gezeigt, dass Aluminium die Eigenschaften des Myelin verändern kann, seine Oxydationsrate beschleunigen und einen raschen Abbau im Ammonshorn und im Rückgrat verursachen kann.
Hier nach ALS zu suchen, ist nicht so einfach. ;-)