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See all 29 customer reviews Mrs S J Brittain See all 29 customer reviews (newest first) on Amazon.co.uk It's easy to use. I have a cold so it's come at a good time I bought this and after a lot research, i realised that is not real vitamin C. So, i bought cherry vitamin C by Natures own. Am not happy reading this review I have had a lot of these and was giving them to a sick friend !!!!! Am not happy !!!! I have taken the capsules for some 14 days now (6 a day) because of cancer. Do not know the effect if any - by now, For those who have difficulty absorbing nutrients. Health & Personal Care > Diet & Nutrition > Vitamins, Minerals & Supplements > Vitamins > Vitamin C Amazon EU S.a.r.l. is certified organic according to EU Organic Food regulations by the control body LU-BIO-04I quit chelating around seven months ago to do liver and colon cleansing and just recently did my third annual hair test. When the results arrived, I was very upset to see my copper has gone back up.
It went from 560 to 170 to 280 (whereas the reference range is 11 – 30). First I’ll show you the results compared with my previous two hair tests and then show you all the questions I’ve wanted to answer. I’m documenting all this research because my memory is so impaired, it’s likely one of the things that caused me to drop the ball on lowering my copper! Why should I care about high copper? Is hair testing for copper a reliable indicator of body copper? According to Dr. Cutler, hair testing is “believed to accurately reflect body inventory” either when mineral transport is normal or deranged (when showing high/red). since all three of my hair tests have shown extreme high toxic levels of copper. What are the possible causes of high copper? Can my 23andme results tell me anything about my copper problem? and found out that of 8 SNP’s checked, I have 6 good and 2 not classified. This report cost five dollars and is really really interesting.
Here are a few tidbits from my report showing how awesome I will be once I detoxify my body: Wilson disease protein is associated with ATP7B gene [1] Wilson disease protein (WND), also known as ATP7B protein, is a copper-transporting P-type ATPase which is encoded by the ATP7B gene. ATP7B protein locates in trans-Golgi network of liver and brain, balances the copper level in the body by excrete excess copper into bile and plasma. Genetic disorder of ATP7B gene may cause Wilson’s disease, a disease in which copper accumulates in tissues leading to neurological or psychiatric issues and liver diseases. Wilson disease happens when accumulation of copper inside the liver causes mitochondrial damage and cell destruction and shows symptoms of hepatic disease. Then, the loss of excretion of copper in bile leads to an increasing concentration of copper level in urine and causes kidney problems. Therefore, symptoms of Wilson disease could be various including kidney disease and neurological disease.
[8] The major cause is the malfunction of ATP7B[8] by single base pair mutations, deletions, frame-shifts, splice errors in ATP7B gene. So, we can see in my case, 51% of the 35 ATP7B genes checked by this report have genetic variations – maybe I should consider copper chelation with pharmaceuticals… The GPHN gene provides instructions for making a protein called gephyrin, which has two major functions in the body: the protein aids in the formation (biosynthesis) of a molecule called molybdenum cofactor, and it also plays a role in communication between nerve cells (neurons). Gephyrin performs the final two steps in molybdenum cofactor biosynthesis. Molybdenum cofactor, which contains the element molybdenum, is essential to the function of several enzymes called sulfite oxidase, aldehyde oxidase, xanthine dehydrogenase, and mitochondrial amidoxime reducing component (mARC). These enzymes help break down (metabolize) different substances in the body, some of which are toxic if not metabolized.
Gephyrin also plays an important role in neurons. Communication between neurons depends on chemicals called neurotransmitters. To relay signals, a neuron releases neurotransmitters, which attach to receptor proteins on neighboring neurons. Gephyrin anchors certain receptor proteins to the correct location in neurons so that the receptors can receive the signals relayed by neurotransmitters. GPHN gene mutations cause a disorder called molybdenum cofactor deficiency. This disorder is characterized by seizures that begin early in life and brain dysfunction that worsens over time (encephalopathy); the condition is usually fatal by early childhood. At least two mutations in the GPHN gene have been found to cause a form of the disorder designated type C or complementation group C. This is the rarest form of the condition, affecting only a small number of individuals. The GPHN gene mutations involved in molybdenum cofactor deficiency likely reduce or eliminate the function of gephyrin. The known mutations impair gephyrin’s ability to perform one or both of the final two steps of molybdenum cofactor biosynthesis.
Without the cofactor, the metabolic enzymes that rely on it cannot function. The resulting loss of enzyme activity leads to buildup of certain chemicals, including sulfite, S-sulfocysteine, xanthine, and hypoxanthine, and low levels of another chemical called uric acid. (Testing for these chemicals can help in the diagnosis of this condition.) Sulfite, which is normally broken down by sulfite oxidase, is toxic, especially to the brain. Researchers suggest that damage caused by the abnormally high levels of sulfite (and possibly other chemicals) leads to encephalopathy, seizures, and the other features of molybdenum cofactor deficiency. How do people lower copper and treat copper toxicity? This is how I lowered copper the first time, in between my first and second hair tests: Some additional things I’m considering now include: Here are the copper chelators: Studies of excretion of Cu from sweat and urine and found that sweat is the most efficient way of eliminating Cu from the body – apparently 100x more Cu eliminated from sweat than from urine.
This would be very exciting for me if I were not exercise and heat intolerant! I’m not too interested in DPA and Trientine considering the side effects. Who wants to mess with new risky substances when minerals like zinc and molybdenum can do the job? What does Andy Cutler say about high copper? First, there are almost 3 pages about copper in Andy Cutler’s book titled Hair Test Interpretation: Finding Hidden Toxicities and I found it all very interesting and useful. after reading it, my conclusion is that I’m probably a typical case of someone with mercury toxicity, weak adrenals and weak liver all contributing to copper accumulation. Rereading HTI, I can see that I made a number of predictable mistakes: This is why you really want a coach to help you through chelation if you can afford it. A few excerpts and other comments made by Dr. Cutler: What can I learn on FDC about high copper? “I went to the Pfeiffer Treatment Center who specialize in copper problems last March.
Andy talks about them in his book. . . Here is what Pfieffer put me on to bring down copper: Why did my copper fall dramatically from test 1 to test 2? I believe it was due to: Why did my copper climb again? I foolishly stopped taking the high quantities of zinc and molybdenum before testing to make sure my copper was down all the way to healthy levels. I did this because Dr. Cutler talks about how fast copper drops and recommends hair testing once a year roughly. He might say somewhere to test more frequently with high copper but if so, I failed to pay attention. I assumed that my low copper diet would do the trick after seeing my good progress on the first test. You know what they say about assumptions. On the other hand… there is this guy Fernando who has been getting tested for three years and his copper and mercury levels have been going up steadily at the same time as he has been feeling better and better through nutritional balancing. He’s saying that the hair test copper going up shows that his detox is working.
My situation is probably a mixed one. How badly did I screw up? Badly enough that I wanted to cry and didn’t sleep the first night after receiving my results. I might have prolonged my suffering by close to a year. On the other hand, it’s very possible I would not have discovered liver and colon cleansing and maybe most importantly oxygen therapy. These are therapies that will help me have a more complete recovery and I’m certain will benefit my family in powerful ways as well. How about a little entertainment here too: There exists a high copper personality. Positive traits include a warm, caring, sensitive, emotional nature, often with artistic orientation and a child-like quality. Often high-copper people are young-looking. Many traditionally feminine traits are associated with copper such as softness, gentleness and intuitiveness. Do I really want to lose my personality? Imagine my wife’s surprise when I turn into an athlete and a jerk after my recovery!