Guest guest Posted January 28, 1999 Report Share Posted January 28, 1999 : Thank you for taking the time to check my sitatuation. You mentioned hepatitis of the liver. I have been tested and came up negatibe. However, my Alkaline Phosphatase which is an enzyme produced in the liver, bone, and placenta that is released into the blood during injury or during normal activities as bone growth or pregancy is always on the low side. Also, I have three medium to large hemangiomas on the liver as well. Once a person has s Disease, don't they have to detoxify in a very specific way? I wonder what is to be done about that as I would not want to have continuous copper build up. ------------------------------------------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 28, 1999 Report Share Posted January 28, 1999 Hello Everyone, Would this cause color changes in the eyes? I swear my eye color has " lightened " over the years.... and the whites are more grayish then white. My eyes are a light 'celery' green (dont ask me someone discribed them like that LOL). Or might this just all be in my head? -- Kathleen ------------------------------------------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 28, 1999 Report Share Posted January 28, 1999 Hi , I didn't mean to imply that you have 's disease. People without 's also get the K-F rings when they are not properly metabolizing copper (and probably more likely if they are also supplementing it). Since hyperT seems to involve copper deficiency or inability to metabolize the copper in the diet which then causes the deficiency, it would appear that you have an inability to metabolize copper. Whether this is from the genetic problem which causes 's, from deficiencies of other minerals necessary for proper copper metabolism (iron, sulfur, molybdenum, zinc, vitamins, etc.), or from a toxic metal such as aluminum is unknown at this point. I think that 's is the least likely of the three possibilities. Of the remaining two, I think you should definitely consider aluminum toxicity. I'm planning on a longer post about aluminum, but I've seen studies indicating that aluminum causes low phosphorus levels. Since calcium combines with phosphorus to make bones, the lack of sufficient phosphorus causes the calcium to be unused and excreted. This appears to be the mechanism by which aluminum causes calcium metabolism problems, bone loss, and teeth problems. So your low phosphorus in addition to low copper (because it's not getting utilized) combine to strongly suggest aluminum toxicity. In 's disease, penicillamine is used as a treatment. Penicillamine is as degradation product of penicillin and is a chelating agent which chelates certain heavy metals like copper. I don't think that you have 's or need chelation. You probably need to supplement the minerals that work with copper and to supplement with the minerals which antagonize aluminum (My best guess right now is that these are: boron, silicon, iron, and phosphorus, in addition to copper.) Of course you don't want to supplement copper until the cause of the copper accumulation is understood and corrected. Hopefully I'll have the aluminum information written up soon. This may help make the picture a little clearer. ------------------------------------------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2008 Report Share Posted August 4, 2008 Holy catfish, there's a whole web site for 's disease. Here's more Kayser-Fleischer rings (it was spelt wrong by the original poster). http://www.wilsonsdisease.org/content_sub.asp@SUB_ID=56 & CAT_ID=14.html Jenn Quote Link to comment Share on other sites More sharing options...
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