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Old 06-30-2009, 07:42 AM
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Default Multiple Sclerosis Treatment

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: ...... http://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 07-07-2009, 11:27 AM
Mandrake Mandrake is offline
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Wow, I specifically came to this forum looking for information on Multiple Sclerosis (MS). Strange that yours was right on top of the catergory. How you doing by the way Arrowwind09?

The reason I am looking is because my sister in law has just been diagnosed with MS. This is some interesting information which I will definately consider in my research for information.

I have started a thread for MS sufferers to offer information about what has been successful in their management and treatment of multiple sclerosis, and to also form an informal support group.

You may visit the thread here http://www.natmedtalk.com/showthread.php?t=4207

I have also put a link to this thread in that post. Lets get the sharing of information on multiple sclerosis going .
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Old 08-08-2009, 11:43 AM
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MS and many autoimmune diseases may be helped with the following

1) Serious cut back on dairy protein and meat protein.
2) Eat CANNED salmon for your protein source (canned salmon is wild caught in alaska)
3) Take aloe vera
4) Tale ginger root, turmeric, fish oil.
5) If possible fast walk 5X a week for at least 40 minutes.

Give this 2 months to see results
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Old 09-22-2009, 07:22 PM
D Bergy D Bergy is offline
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I copied this post, with permission as it seemed one of the most important findings concerning MS that I have seen to date. I believe this may be the key to the whole MS question. It also explains the close relationship between Lyme Disease and MS, as Bartonella is a common Lyme Co-infection.


I just spoke at lenght with someone at Galaxy Diagnostics in NC. For those not in the know, A veterinarian, Dr. Ed Breitschwerdt has done some amazing work, identifying bartonella in animals with a new patented test. Dr. Breitschwerdt is also an adjunct Professor of Infectious Disease at Duke University Medical School.

The better news is that there have been some research trials that have yielded results beyond expectation in humans. Testing and then treatment has been done, specifically on individuals who have been dx'ed with MS.. Many tested have been found to have bartonella and have responded beyond expectations with treatment.

The testing is two tiered. First by PCR and then culture grown to overcome sample bias. Then it will be DNA sequenced. There are over 22 named species of Bartonellis and as many as 30 species, some yet unnamed.

Galaxy is now working on antibiotic resistance studies. Their problem is funding and Grants have been applied for both with the MS Society and NIH.

They are working very hard at the present time to get the test out commercially. They never expected the huge results that they have had in trials.

The worse case that they have seen was a woman who was infected with Bartonella Melonagris (sp). contracted from a sheep. Bartonella has even been found in dolphins!


This testing will be patient pay as the testing has not yet been FDA approved.

A very hopeful strand for all of us waiting for something definitive......

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