Guest guest Posted December 8, 2008 Report Share Posted December 8, 2008 Hi , regarding the Colloidal Silver, notice the Mds always say (you look good, keep doing whatever you're doing). They never say (tell me exactly what you're doing so that I may tell others). But you can't blame them, they're overhead is very high. ...RP - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 9, 2008 Report Share Posted December 9, 2008 > when ever you read a statement about anything from The Food and Drug Administration, they condemn all natural treatment, they want to sell drugs. Colloidal Silver was the natural anti-biotic prescribed before any antibiotics were manufactured. Now that makes sense. I tell you, any time I hear something works I want to buy it right away. Then I read up on it and am not sure. My source for vitamins sells it. I'll ask the MS doctor next week. I'd be curious to know how much and how often do you all take it? I am also looking into DDAVP Nasal Spray (desmopressin). I am taking data on that (from the National MS Society web page) and also on LDN to ask him about next week. I wasn't all that thrilled at interferon but seem to have been having more trouble both walking and with bladder function in the past 6 months since my diagnosis with PPMS. I turned down the treatments offered (because, 1- interferon and 2- he said it isn't that helpful in PPMS). Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 10, 2008 Report Share Posted December 10, 2008 RP, I told my GP exactly what I was taking, he heard me loud and clear, it hurt his feelings when I told him it is the natural anti-biotic used up until 1943, did you know that? 15 years ago Doctor's and District Nurse's used to ask my advise on alternatives and vitamins for different MS problems. Seeing I was the healthiest MSer they had. Dr's used to learn about vitamins as well as drugs back then, but they wanted first hand info. They never say (tell me exactly what you're doing so that I may tell others). But you can't blame them, they're overhead is very high. ...RP Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 10, 2008 Report Share Posted December 10, 2008 , Here in UK the MS specialists either work or are sponsored by drug companies. That is all they will talk about. I always say would you ask a train driver to drive an airoplane. I take 20ml of CS morning and night, which is only a maintenance dosage. I should up it to three times whilst the flu bug is around. I'll ask the MS doctor next week. I'd be curious to know how much and how often do you all take it? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 10, 2008 Report Share Posted December 10, 2008 Hi , I'm not sure if you're aggreeing, or disaggreeing with what I said? ....RP Quote Link to comment Share on other sites More sharing options...
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