Marsha I am always amazed with the self-righteousness of these so-called professionals. Just like our CS/Rife experience they repeatedly demand more proof. If you give them 100 examples/cures, they'll insist on 1000, being more comfortable with peer approval than anything new. Mainstream medicine practice proclaims through their professionalism, dedication and expertise in debunking anything other than the status quo. And these are the people who approve funding for research - now can you see how much money and time is literally wasted? Sad.
I can always pin down these people who say "there in no evidence" translation: we don't know anything about the subject so there is no evidence! I get thoroughly annoyed when as a lay person I have to do the the health professional's job and not even get payed for it while they sit around pretending to be experts. If I was Bill Gates I would sue them for negligence! The problem with any medicine is simply that you cannot depend on someone else. You have to do your own homework regardless of conventional or alternative approches to a given disease. The only thing going for conventional medicine is that it can deal with such things as broken bones and accidents admirably and here it can excel. However, when it comes to more complex issues it simply is no better, and frequently much less, than the less invasive alternate approaches. So conventional medicine has its place in straight forward situations, but in my opinion, its the biggest quackery this side of the moon. Where else can you sell a cure for any cost and not be held responsible for the results that may even cause further injury? If I buy something, should I not get something in return? Have we been had or what? Medicine from time eternal has been exploitive and those who don't, won't or can't get involved in their own sickness will always be at higher risk. Predictably, most of us have been conditioned to ignore massive side effects and even deaths form conventional medicine but not tolerate the slightest problem with alternative approaches! Just look at Don Tunney's work. All the butchered and poisoned patients who have come from the traditional efficacy and safety tested medicine. Many of these people have been given up to die but with AFFORDABLE Rife/Bare, Beck, Clark, CS, Oxygen/Ozone therpies and other modalities many still have extended their lives or even cured themselves. Just imagine if they had been treated prior to all the butchering and poisoning what the outcomes would have been. Double blind safety tests were never done for X-rays, ultrasounds etc. but that's OK since these have been peer approved - they must know something others don't right? Just look at chemo, mercury amalgams etc. The electromagnetic theory was well established in the 19th century so why are we so fixated with drugs in face of superior and generally safer electromedical options?? Marsha liked your reply - Pls feel free to forword this to the alt health group, JX and anywhere else. Just like crimials they won't respond when they are cought red handed. Chris Gupta At 07:12 PM 12/1/97 -0600, you wrote: >Dear Folks, I ust thought you might be interested in the goings on at >the alt health group, so here`s what I sent to the anti CS fellow: > Marsha Hallett <[email protected]> writes: >> >> > Oh, you blind people, and arrogant "doctors"! Don`t you see that I >> >would rather be blue for all eternity than suffer the miseries of >> that horrible disease called Lyme?? >> >Get down off your high horse, and, if you`re not willing to give CS >a >> >proper scientific trial, at least be quiet. MH >> >> You made the statement that "The modern electrocolloids, ... creates >> particles >> so fine that they don`t build up." I'm not sure that I understand >> why it is >> "arrogant" to ask for some proof of that statement. I can provide >> several >> dozen references ('cept I would have to type them in) that document >> the toxic >> effects of silver in various forms. All I'm asking is for you to >> provide >> evidence in the form of a "proper scientific trial", that the >> statements you >> make are anything other than advertisers' hype. >> >> Do you have some proof that CS cured your Lyme disease? How were you >> diagnosed? How was the existence of a "cure" determined? Since you >> say you >> are "generating" your own colloidal silver, how do you know that your >> CS >> generator worked and there was actually some silver in the distilled >> water? >> Since argyria can take up to two years to appear after the use of >> silver >> products, how do you know that you won't develop it in the future? >> >> I first became interested in "alternative medicine" when I >> coincidently >> encountered some absolutely preposterous statements about colloidal >> silver the >> same week that I met someone who was suffering negative consequences >> from using >> "electrocolloidal silver". I looked up the legitimate sounding >> "references" >> that were used to support the advertising hype and discovered that >> they were >> quite misrepresented. JX >> > > Dear JX, I am a grandma, and a now empty nested professional mother. >I`m no doctor, or scientist. I go by what I read, and if that is wrong, >and I suffer thereby, well, so be it. >I was sent the directions and info. on CS as the answer to a sincere >prayer for help. >It came, I tried it and my disease is totally gone. So, now I try to >help others to get well again, too. If I get blue in six months, again, >so be it. At least I can now do things without pain, my mind is clear >again, and I`m not so damned depressed that I`m really considering >suicide. If I`m blue or grey, well, so what. Black folks put up with a >lovely shade of chocolate! Why not a nice slate-blue, instead of yucky >fish-belly white? : ) > Now, I`d be delighted if someone would do a proper double-blind >scientific study of CS. >Maybe then the truth, one way or the other, would come out. But I`ll >just bet it`ll never happen, because the money-grubbing pharmaceutical >companies can`t make any money off of it. By the way, I call doctors >arrogant, as they, by and large, will not treat people properly for >whatever disease. I`ve seen it in letter after letter in the Lyme NG, >and several others as well, including the Fibromyalgia group. (Now that >is the worst "diagnosing" of all, as FM ain`t a disease! Many of them >are misdiagnosed Lymies.) >Some docs seem to be too anxious to get the troublesome patient gone. >The thought of doing proper testing and diagnosis is beyond them. Others > >refuse to believe that Lyme can be in their state or locale, and some, >as in my own case, refused to believe that Lyme can recur after many >treatments of antibiotics. Gee, if antibiotics worked, there wouldn`t be > >all the lamentations on the Lyme NG about recurring disease after many >bouts >of IVs etc. > Ok, here is what happened to me: I was bitten on the lower leg by a >tiny tick in 1990. I was living in Arkansas, and we had deer running >across our wooded property all the time. >I got a bullseye rash, and upon seeing it, I knew what it was, as I had >just read an article on Lyme in a magazine. The rash is proof positive >of Lyme infection. The doctor agreed and gave me 10 days of 60 mg. >Doxycycline. >Naturally the disease came back. (This doc was the one who called my >dead gallbladder an ulcer, and who never bothered to xray my daughter`s >broken foot!) >The Lyme destroyed my gallbladder, which had to be removed in Jan. 1991. > >Over the next 5 years, I moved to 3 different states, due to the hubby`s >job. >I kept getting more ill as time went on. I had no idea that it was >third-stage disseminated Borreliosis. Finally, in Phoenix, AZ, I >realized that I kept getting the same symptoms, over and over, and >they were the same as the Lyme in Arkansas. I went to the library and >got 2 books about Lyme, which convinced me that the disease was never >cured to begin with. I had had 2 blood tests, both negative, and blood >tests for Lyme are notoriously inaccurate. The new LUAT, a urine test, >is much better, thank goodness. After 5 1/2 years, and 50 of the 60 >symptoms listed in the books, and severe depression, I prayed for help. >It came in the form of CS. >After 3 days of taking it, I noticed the joint pains were easing, and I >could close my jaw again. By one week, my mind was clear again. Now I >could think of something to say, and have it come out of my mouth >clearly. By a month, I felt better than I had in years. I could walk, do > >housework, and garden. The proof to me that the DD was gone was in July >of 1996, when I flew to California for a visit to my elderly parents. >Normally travel sets off a recurrence, as does stress of any kind. I got > >both of those on that trip. >No recurrance whatsoever, in spite of a stressful confrontation with my >deranged sister. > I had another similar trip in this past October, still no Lyme >symptoms. >I feel beyond doubt that my Lyme disease is cured. I also get no more >UTI`s which were frequent due to the gallbladder loss. A cold is gone in > >2-3 days. I cured an eye infection, and an ingrown toenail that had >infected with topical CS. I give CS to my old Pug dogs, and their bad >breath is gone, and they are peppier than they have been for years. >No placebo effect, that! (Neither is the curing of a uterine infection >in a mare I was told about recently.) > As to making CS, I use a generator that is made from 3 nine-volt >batteries, some alligator clips, distilled water, and 2 five-inch wires >of 14 gauge .999 fine silver. The silver does come off, as I can coat a >penny with it, making it look silver. This is the same method industry >uses to coat one metal with another, called plating. This just uses a >tiny charge. >If I shine a flashlight beam through my finished colloid, I can see a >cone effect. This is the silver ions reflecting the light. > As to silver being toxic, it is, when ombined with something else, such > >as in silver salts, or with a protein. I have no regard for Mild Silver >Protein at all. It is no electrocolloid. > As I mentioned, I am willing to be a test subject for Colloidal Silver. > >I had nothing left to lose, except my life, 18 months ago, and by then >losing it seemed pretty good. I was so miserable, and death wasn`t a bad > >idea! I`ll keep taking my CS, and if I do go gray, I`ll gladly let you, >and the world know. So far, so good, nailbeds and eyeballs still normal. > > The thing is, now I can sing, I can dance, I can garden and do >lapidary, and even sex is a good idea now. Lyme even takes that away. CS > >is worth it. >Thanks for responding, and I hope all this will be informative and >useful. >Sincerely, >Marsha > > >Anyway, CS believers, I have yet to hear back from this guy. Maybe I >hit a nerve, or something. >Input, anyone? >Marsha > > >
