� #1
Old 07-01-2009, 10:27 AM
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Default Colloidal Silver Testimonials

I am providing a link to a website for my favorite colloidal silver product.
I have been tracking on this for quite a while and now they have some good testimonials available and you can read them here. It is demonstrating to be pretty effective for Morgellon's disease, really, the only thing effective that I have heard of.


If you have other colloidal silver testimonals please put them on this thread.

"Everything we hear is an opinion, not a fact. Everything we see is a perspective, not the truth." Marcus Aurelius
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� #2
Old 07-01-2009, 10:29 AM
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Default Multiple Sclerosis and Colloidal Silver

What follows is the story of Nancy Delise, who, over the years, has utilized retail colloidal silver , colloidal silver made with a basic generator, basic colloidal silver enhanced with H2O2
( orally ), and finally IV Silver ( Argentyn 23 by Natural-Immunogenics - Available only to MD's ).

Colloidal Silver: Oral Use

I drank 2 oz of Silver water twice a day - in the morning & at three PM. Day four I begin to drink 8 oz of Silver water two times per day. I seem to have more energy and the end of the day seems to come a little later. I do not drag as much to my car.

Day 12 The night paralyzation seems to be easing. I can get out of bed with more ease Day 14 thru Day 18 My fingers and toes are tingling more and more. My toes are aching. As the days go by my fingertips seem to be aching, also. Day 20 I seem to have surreal feelings in my fingers. It�s like a far away out of body feeling. They still ache.

Day 21, I am getting out of bed much easier and quicker. I climbed a ladder at work, and I am not nearly so tired when I leave work. I can actually walk to my car without holding on to the wall. I did some things on the floor at work, and was able to get up without too much trouble.

Week four, The bottom of my feet are tingling, and I could feel whiskers on Mike�s face (a surreal feeling). I could feel cool bathroom tile on bottom of my feet.

My legs ached all night. It was very painful, I wanted to scream out. My legs hurt a great deal. The next morning I was able to walk further than I had in years. Mike and I walked about four blocks that morning. I feel stronger and stronger every day.

Week five, More and more feeling in both fingers and toes every day. Less surreal and more natural. Both toes and finger get cold.

Week 10, Seem to have small changes every day. Again my toes ached for several days, then I had more feeling in my toes. It�s as though I have a non feeling pad at the bottom of my feet, but feeling all the way around. Like an animal�s paw with the padded bottom. It seems I hurt for a few days, then something feels better.

Week 12, I feel like a caterpillar in a cocoon. I wonder if they have pain during the metamorphosis. The bottom of my feet are no longer numb, the fingers on my right hand tingle only at the very tips. I don�t even think about lifting a heavy container with my right hand. For years, I wouldn�t dare lift, or I would drop whatever I was holding. I poured coffee from a pot without even thinking about it, until I noticed myself. Doing it. There is NO WAY I could be working the hours I have this Christmas, if not for the water. Last year, I had to wear my cooling vest all day every day, and when I went home I could barely walk to my car. Some days I literally dragged my right leg to get to my car. I had to hold on to the building to get around the corner and into my car. When I got home I actually crawled on my hands and knees to get up the steps. This year I never once had to wear my cooling vest. I walk normally to my car at the end of the day, and the steps are not too much of a problem. I still go up one leg only, but it is stronger. The fatigue is minimized, also. I�ve worked many more hours this year than last.

Week 14: I started making my own water about three weeks ago, and I�ve had to send samples to San Antonio for testing. It seems the probe they sent me was not working to full potential, and for about a week I was drinking water with very minimal amounts of silver. After the week I KNEW IT!!! I was regressing. Things were not working so well, again. I was regressing. Thankfully we figured out the problem and within a couple of days I was back on track. Thank God. This set back has convinced me even more. As if that were possible. I have my life back. I will never give up silver water. Week 20: Christmas Week. I had 16 people for dinner Christmas eve. I had 7 people for dinner Christmas day, I worked 11 hours the day after Christmas, and I had 14 people for dinner the next day. That is four days out of four I entertained at my house. I can�t remember when I did something like that. I still have night paralysis, but not nearly as bad as it used to be, and I have a lot of stiffness still when I sit a long time, but nothing near as bad as it used to be. My energy level is very high.

August 2002

My MS Update This is the second anniversary of my long, but wonderful journey with colloidal silver (CS). I am a 59-year-old female who had relapsing remitting MS for 31 years. About 1995 it changed to secondary progressive MS. Thus began my long road of decline. Everyday I got worse. When I discovered CS I could barely walk. I was beginning to use a cane. I could not even go up on the curb without aid. My prognosis was grim. I had some knowledge of the great properties of silver, so the idea of CS intrigued me. I researched CS. What did I have to loose?

I began drinking 16 oz per day. In about three weeks I began to notice a difference. You already have a log of my first year�s progress. I seemed to reach a plateau about this time. I did not improve, BUT I never got worse.

I have since had an MRI and it showed that at this time Aug 2001, I no longer had MS. I have had no new lesions for well over a year. What I was working on at the time is to now repair the damage. Since the damage is to the myelin and not the central nervous system, I was quite confident I could improve.
1 year-6 months: Hydrogen Peroxide Added

I have researched adding hydrogen peroxide to the CS. One drop of H2O2 per 2 oz. of CS. I learned this would cause the tiny silver particles to break up into even more minute particles. After 15 minutes, the peroxide was evaporated out of the CS, so it is not harmful to the body, but the tinier particles of silver got into the blood stream quicker. All this time it was a slow process because by the time the silver got to the myelin where it was needed, it was so diluted, it couldn�t penetrate the lesions and kill the mycoplasma (MS virus). Within a week I began to feel old symptoms again. This is what I call a healing crisis: I would get symptoms of the MS as the virus was dying and the dying pathogen aggravated the nerves, so for 2-4 days I would feel like I was having varying degrees of exacerbation. After a short period, it would end and I was improved again.

If I had known about this earlier, I am convinced my recovery time would have increased a great deal.

1 year-9 months: I am sure there is a way to go even quicker��� I began to research IV drips. There are cases of HIV-AIDS infected patients going into complete remission after three infusions. I worked on this project for about six weeks. I finally found someone with a protocol of infusing CS intravenously. I also found a doctor willing to work with me and give this a try.

1 year-11 months: Colloidal Silver IV Administered

First IV: I had my first IV. By that evening I had my first healing crisis; my legs became extremely heavy (like they were 2 years ago). My fingers tips were still numb, but the numbness was extremely exaggerated. All was better at day four.

Second IV a week later: My legs are again aching a great deal, the numbness in my fingers is very intense. It almost feels like they are not attached to me. All better by day three.

Third, fourth, fifth IV: Each time I experienced a reverse of some symptoms I had either forgotten about over the last 40 years, or didn�t realize over the years were actually MS symptoms. I�ve practically no problems at all. I feel better then I have in 15 years. I will have no more IV�s, but I will NEVER stop drinking CS.

If I had known about the IV�s I probably would have had full recovery even sooner. I am quite sure the old lesions are going away. I am anxious for another MRI to prove this also.

TWO YEAR ANNIVERSARY: No more MS, no more symptoms. Most myelin repaired.

PS: My friend, also an MS patient is on the IV drip. She also no longer has MS (By her MRI), but she was sores than me, and not able to get out of her wheel chair. Since IV�s she has given up all her spasm medication and has begun to take STEPS ON HER OWN.

I would be happy to share what I've learned with anyone. Call me, Nancy Delise,Ph: ...... https://testimonials.silvermedicine.o...-argentyn.html

I called Nancy a couple of years ago and spoke with her husband. Nancy was killed in an Auto Accident but he stated that she was well for the last few years of her life due to the CS given by IV. He asked not to be called again and wished that the phone number was not all over the net.
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Old 07-08-2009, 12:39 PM
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Default Chalazion

I had a chalazion for 8 months that affected my vision because it pu pressure on the lens. A chalazion is an enlarged oil duct in the eyelid. It is usually back from the edge which distinguishes it from a stye. There is controversy about whether there is a microbe cause or not. Mine showed up just after getting out of the hopital for a blood clot in my leg. A few months after I contracted the chalazion my eye doctor detected a staph infection on the lid perimeter. We all know what a wonderful source the hospital is for staph. He wanted me to use antibiotics but I chose silver instead. He mentioned that there might be a connection between the staph and the chalazion. I tried lots of natural approaches to no avail. When I began flushing my eyes with silver (10ppm hydrosol) results soon appeared. I would fill an eye cup, hold it to the eye and blink for 15 seconds twice per day. It took maybe a month to totally eliminate it. I suppose it could have been coincidental. I sincerely doubt that. I have had considerable experience with silver and find it to have extrordinary antibiotic abilities.
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Old 07-15-2009, 04:25 PM
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Default NutraSilver for Morgellon's

Dear fellow Morgellons victims,

I'm writing on behalf of all the young people and the elderly with Morgellons who have been shunned, criticized, and outcasted by society thinking we suffers of this horrible disease are crazy. I personally knew absolutely nothing about this disease until I came home from school one day of September 2007 and noticed granule-like crystals on my hands. I also noticed clear fibers that appeared to be coming out of my hands as well. I went to the computer and typed in "black crystals on hands?" or something to that extent. I stumbled upon a few websites that had details of Morgellons symptoms and the blue, black, clear, and red fibers with granules coming out of hands, body, and or hair. I didn't automatically assume I have this disease after a couple months of thorough personal research I had whatever this bizarre disease was. Every single symptom I had matched everything I read. I had everything from the physical identification of Morgellons right down to all the mental and cognitive disorders of Morgellons; brain fog, I slept constantly, depression, insomnia at night (slept all through the days), lost a lot of weight, everything aliment you could imagine I had. But by far the worst symptoms was the anxiety that would come out of nowhere, it literally felt like I was even in my body at times.

It began to slowly but surely rule my life. I noticed the fibers everywhere in my home, friend�s homes, family member�s homes, these fibers were everywhere but I was one of the only that had symptoms to this extent. My friends and family had the fibers on there body and hair as well. My friends were the only ones who believed me about the fibers and knew I was sick. I tried to express to my mother and stepfather what was going on but surely my mother thought I was loosing my mind which I can completely understand because of how bizarre this disease sounds to the layman. Finally after convincing my mom I had this disease I stumbled upon a website called "NutraSilver". My mother personally thought I was crazy but my stepfather said "whether its in his head or not we can see if this helps"

So my stepdad bought a bottle of NutraSilver and it came with another for free. The first night I tried the NutraSilver I had to lie down in bed with my mother I trembled so bad. When I woke up the next morning I felt slightly better. I started to use the NutraSilver a couple times a day and just put some drops in my daily routine of drinking water. Everyday progressively got better, I started to forget completely about Morgellons and live my life. It ruled my life, I am an 18 year old male (at the time I was 17). I also stumbled across an amazing doctor and friend named Dr. Susan Kolb. I found her website when I was researching about Morgellons and even though I lived many states away and was very embarrassed I deciding to just call her and tell her what was going on. She talked to my parents, talked to my family and tried to express to them that this is a real disease. Still after all of that they still did not believe. She gave me great tips to get slowly but surely better as well. I slowly started being able to go to school more and focus more on my life. Everyday with NutraSilver and Dr. Kolb�s advice made everyday easier to get through. As last summer came along (2008), I was very confident I was Morgellons-free. I completely forgot about the disease and was able to live my life.

I moved into a new home, had a new life ahead of me and I felt like my life was finally back, unfortunately I ran out of NutraSilver around September of 2008 and was unable to purchase it again with the lack of my finances. I stopped using it all together. Around November or December my symptoms started coming back fully. I had brain fog again, depression, anxiety, fatigue; the fibers were coming out of my skin again. I was once again infected. They were around my new home and in my hair and body once again. I talked to Doctor Kolb at least once a month to keep her updated. With her help I personally discovered some things that helped in the mean time until I could get another credit card to purchase NutraSilver once more. My symptoms got so bad living at my new home I finally ended up moving back into my mother�s house where I first discovered I had Morgellons. I still felt horrible, I discovered something called Trilogy Cardio Essentials in my fridge that mom used to lower her blood pressure and things of that nature. It was recommended by someone who also used silver on a daily basis that ran a herbal store down the street from me. So I took a couple swigs every day unknowing the effect it would have on me. The next day I glanced at my hands after I was out of the shower. I noticed the fibers purging out like I had seen with NutraSilver; it was very scary.

I am still drinking it and it helps just as NutraSilver has. I have used many things to help with this horrific disease but I can honestly say NutraSilver, Dr. Bronners, and Trilogy Cardio Essentials has helped the most by far.
I�m sick of people ignoring this disease; even doctors are ignoring it. I know there are so many people that are struggling with this disease everyday, and I truly desire for them to live their life and again and take back what�s rightfully theirs.

My life is finally coming into view again, and I literally owe my life to a man named Russell at NutraSilver and a wonder Doctor by the name of Susan Kolb. I have never met a person so dedicated to seeing their patients or customers get better than Dr. Kolb
Without their help, guidance, and advice I'm not too sure how long I could have held out with all the depression and anxiety.
My final advice to any man, women or child with Morgellons is get NutraSilver, have a positive mind-set and lives your life again; I don�t want anyone to go through what I have been through with anxiety and depression.

Daniel W.

I will list my personal protocol for Morgellons;
Dr. Bronners Lemon Castile Soap ( you can use it for toothpaste, hair, body, lotion anything you can think of even laundry)
Acai berry
Borax laundry detergent.
Air Filter
Trilogy Cardio Essentials.
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� #5
Old 08-14-2009, 07:08 AM
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So, Danser, If one were to try Nutrasilver for a severe MRSA case what dosage would one do and for how long?
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Old 11-18-2009, 10:27 AM
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Check this out...

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� #7
Old 11-27-2009, 01:05 PM
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Robert is on a distinguished road

Hi, Colloidal Silver definitely helped me with anal fistula. Visit my site if you wish for more info.
oldtimedoctor dot com
Cheers, Robert
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� #8
Old 04-25-2010, 12:31 PM
Join Date: Apr 2010
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robinski21 is on a distinguished road

Colloidal silver is unbelievable. Helped me with more than one cold, I'll tell you that!
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