Guest guest Posted March 8, 2011 Report Share Posted March 8, 2011 dear rachael, i have the fear that ccsvi is having the same impact as stem cells, ie false hope and i am not being negative i am staying with ldn for 12 months and by then the ccsvi proceedure will have developed fingers X for all those that try any proceedure where they think it will help their situation regards/peter/ms/primary progressive Hi are you talking about the CCSVI (Chronic CerebroSpinal Venous Insufficiency) procedure bing done around the world? It certainly is a HUGE deal to those of us who've fallen victim to 'MS'. :)I've had the procedure and am now again able to walk and ride my exercise bike - the procedure has varying results because it is different for each individual.It truly deserves the publicity when it has helped so many - getting the word out about it AND about LDN is how I spend most of my days in the effort to truly help others who have had the letters 'MS' written in their medical files. Good idea regarding sending through feedback or responses about LDN - it could work very well!Another idea would be to 'tweet' about it and get it out there in the same fashion as Charlie Sheen has been causing his 'tweets' about a lot of his weird oddities like Tigerblood etc to 'trend'.*shrugs*dunno - just an idea 'What we do in life, echoes through eternity.'MARCUS AURELIUS (121 - 180 A.D.) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 3, 2012 Report Share Posted February 3, 2012 Hi , hoping to be prescribed LDN in April. Hoping that my neurologist knows enough about it! As I am only on 2 drops of Lugol's 5 days a week I am taking a few Brazil nuts for the Selenium, 1g of vitaminC, a multi high in the B group vitamins and either 2 calcium-magnesium complex tablets or one Magnesium Forte. When I go up to three drops (originally planned to do this at the beginning of February) I will increase to 2g vitamin C. I do have supplements for Selenium (100mcg), B2 (100mg) and B3 (500mg) but try to get as much from whole foods as I can instead. I have found I am needing to increase my water consumption. I am using rainwater filtered through a Brita jug to remove the roof sediment. I am in Australia. Buying supplements from the US adds significantly to the cost. From earlier topics - are they Bromide boils or Halide boils? I was suffering from something similar which did not resolve until I started the Lugol's in water. I eat very little bread, and most of my furnishings are well aged. Even my loungeroom carpet is wool. I do not think my cleaning products contain Bromine. But our mains water is fluoridated as are most of the dental hygiene products. I note many medicines and anaesthetics contain fluorine. MS> > > Hi, could anyone confirm that iodine is important to take when> somebody has Multiple Sclerosis? I read that iodine is good for> mylein... I bought sea kelp tablets that contains iodine. I know i> could take drops, but im on hydrogen peroxide therapy and cant stand> one more thing to do drops..:-) Any experience shared would be> appreciated. Thanks x> > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2012 Report Share Posted February 4, 2012 http://www.fibromyalgiarecovery.com Gracia I did read Dr Brownstein's book. It seems that patients with MS or Fibromyalgia usually do have thyroid issues - so iodine and the companion nutrients may be helpful. I cannot afford to see many specialists (I have MS and am on a pension), and iodine supplementation is affordable. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2012 Report Share Posted February 4, 2012 Hi , Can i ask you how much do you mean under " multi high " in the B group vitamins? :-) And do you mean all kind of Vitamin B? Just wondering if im taking enough, and how much i should take as a maximum mg..? Im taking B12 and B-complex, not sure what dose is best though. Thanks in advance, all the best Orsi > > > > > > > > > I did read Dr Brownstein's book. It seems that patients with MS or > > Fibromyalgia usually do have thyroid issues - so iodine and the > > companion nutrients may be helpful. > > > > I cannot afford to see many specialists (I have MS and am on a > > pension), and iodine supplementation is affordable. > > > > > > > > MS > > > > > > Hi, could anyone confirm that iodine is important to take when > > somebody has Multiple Sclerosis? I read that iodine is good for > > mylein... I bought sea kelp tablets that contains iodine. I know i > > could take drops, but im on hydrogen peroxide therapy and cant stand > > one more thing to do drops..:-) Any experience shared would be > > appreciated. Thanks x > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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