Q. So you are saying the you personally have found that CDS is superior? Or works as well with no reactions?

A. Yes it is definitely proven to be superior to MMS in my own case. I’ve been taking MMS for over three years three times per day, every day in an effort to cope with a bone infection.

In my own trials, I’ve found CDS to be much more effective than the MMS in terms of keeping the effects of my infection in check. For example… When taking 15-18 drops, 3 x per day, I’d begin having pains again the mornings. However, when I take 5ml of CDS 3 x per day, I wake-up without any pain whatsoever. – Furthermore, I have had several instances where I did not take my CDS(while out on the road) and I remained pain free for most of the day. And so I’d say that the CDS has proven to be far more effective than the MMS in this particular case.

Q. Or works as well with no reactions?

A. When I began experimenting with CDS, I have taken as much as 15ml without any signs of nausea, diarrhea or malaise whatsoever. Whereas the MMS(on the other hand) has proven to run on a very sensitive line. For example… my maximum tolerance has always been roughly 21 drops. However, in the event that I would accidentally miss my juice/water to MMS ration, I would certainly throw it up.

Additionally, taking MMS can alter your ph. Specifically your urinary tract ph. Which may or may not be a problem for most people on the short term, but for those of us who need to take MMS on the long term, or are susceptible to certain types of stone(kidney) then this could be a bad thing. And so again, I’ve found that CDS does not affect ph as the MMS would.

PS. my wife recently got pretty sick with a cough which fell into her lungs. And so we decided to try a protocol 1000(slow sipping throughout the day) to see if it would help and she was able to tolerate 20 ml’s(or 60 drops of MMS) of CDS in a 1L solution without any nausea or effects. – And the the results were nothing short of astounding. Within 12 hours her cough had loosened-up and she was feeling much better. – This is far better than she’s been getting with antibiotic inhalers throughout her history with bronchial asthma and so I think CDS has proven itself there also.

So in short, I’d say, I’m a believer.

Hope this helps.

JohnB

Toothache resulting from a broken 4-face filling which fell out of my upper, left bicusped. In addition, two walls of the tooth broke and I can’t re-fill the tooth. Either pull it or get root canal and crown. Cannot afford that.

The first time my broken bicusped started to ache, I had a dentist xray it to locate problem. Found inflammation in root. Prescribed 10 day antibiotic dose, which killed my digestion. Two weeks after finishing that, the toothache returned. Now I resort to MMS because it was an infection. I didn’t drink MMS, I only applied it topically to the root of the tooth. I mixed up 10 drops of MMS with 10 drops of 10% citric acid, waited 10 minutes and added to one ounce of water. This was my topical mix. I put 2 drops of this on a bit of cotton, added 2 drops of pure liquid DMSO (for increased penetration) and placed the cotton between cheek and gum at the root of my broken tooth. I also put a bit of the cotton inside the hollow tooth, because I could. The pain disappeared for 2 weeks before returning. I reapplied the MMS/DMSO and the pain again disappeared for 2 weeks. I have repeated this for 6 months. Sometimes, if the pain doesn’t dissipate after one application, just do it again every 6-12 hours until the pain is gone. When I didn’t have any MMS, I substituted Molecula Silver and it worked as well; it is relatively expensive, but you don’t use much.

I lost my mother to cancer – didn’t know enough about MMS at the time to use it.

Am now trying to help my father overcome cancer of the esophagus. He was diagnosed 18 months ago; he is 82 and the docs were pretty grim faced about it all. But 18 months on here we are. I think the reason he is doing so well is because 2 years before he was diagnosed he was taking MMS off his own back, on the old regime of a 15 drop dose in the morning and one in the evening. I believe that has stood him in good stead. His tumour has not grown or spread since diagnosis. Doctors are a bit confused. BUT the tumour is still there and still dangerous. I have only recently got him back on to MMS – protocol 2000 without the MMS2 as he can’t swallow the capsules. Am persevering but it is hard sometimes and easy to give up when the MMS is making him feel bad. Sometimes the amount of things one could try with MMS is overwhelming too for the carer – should i do this or that etc. MMS1/MMS2/CDS/DMSO…swallowed, bathing, enemas etc. Great to have such choice but overwhelming sometimes too.

———- Forwarded message ———-

From: German Ruiz

Date: January 23, 2012 23:21

Subject: MMS Testimony from Barcelona

To: desdeandreas@gmail.com

Hi Andreas, my name is Germain Ruiz and you’re writing a book of testimonies of people who have taken the MMS has healed. I think I might be a good testimony, but first I need some help, in mid-February I have an endoscopy and I probably will do a biopsy. In the process I have been living with the MMS and what I feel, I think there is every chance that that test out that I’m cured and then of course we’ll give you my testimony with the data you need, or video, such as you see it. But as I say, first I would like to tell me a bit to see what advice you can give me in my particular case and thus achieve the best result in the February test.

I’ve been taking the MMS four months following an ulcerated carcinoma of approximately 1 cm in the stomach that I was diagnosed this summer in late July, before you start taking MMS I had been doing 100% vegetarian diet was a mixture of macrobiotic Orthomolecular and some of Dr. Gerson. Supplementing the diet with various supplements and vitamins that I list below:

Milk Thistle 200mg tablets.

Graviola 500mg capsules.

Fermented Papaya 500mg capsules FPP.

Blazei capsules.

Vitamins “Source of life”.

When I learned that the MMS would not take vitamin C, nor will any good taking antioxidants at the same time, I just stuck with the vegetarian diet and stopped using supplements which I have listed above.

Currently only complement the MMS doing coffee enemas twice a week and continue my vegetarian diet.

Although MMS gradually has decreased the symptoms of suffering almost completely (stomach aches, backaches, stomach feeling empty all the time, cold sweats, etc.) which is wonderful, now I feel that the process stagnant and not just heal completely, I have a few sporadic small punctures in the stomach and chest. I’m doing 14 daily doses of MMS is the most that you recommend one of your videos will they be too many? I use acid is at 50%

I think many things, if you should pause for a while with the MMS and retake supplements, if I stop right now that all symptoms are gone almost completely and I just have to keep taking the MMS to the overall improvement, if I can take supplements while squaring MMS times such as those containing vitamin C and antioxidants that are interfering with the MMS, and so I guessing all the time.

Do I still not completely cured just because it is also an ulcer and acid in the MMS does not let it cure?

How do you see MMS enemas?

So finally I encouraged to write and see if you can help me with advice, and become a witness to your book, that would fill me with pride and make me very happy.

Thank you so much before hand any information or assistance. May God bless you,

Germain

A glimmer of hope

Over the past six months I have been working with a group of terminally ill people. I was asked to provide some help when a drug, currently in Phase II clinical trials, provided not only a stop of the progression of this disease, but some people were actually regaining function that they had previously lost as a result of the disease.

The drug is NP001. It is made from a chemical that many may be familiar with, sodium chlorite.

The problem with a drug trial is that they exclude people from the trial. Efforts were made to broaden the acceptance criteria, some progress was made, but still many were left out of the trial. While the main reason was that they lived in an area that was outside the trial locations, another reason was the progression of the disease in their bodies.

NP001 is administered via IV injection. I explained that there is more than one way to get chlorite into the body and that while it is not as efficient as IV injection, drinking a solution of chlorite will result in some chlorite getting into the blood stream.

A group of these people suffering from this disease decided to run an experiment on themselves. Efforts have been made to get the medical community involved and these have not been totally successful, so far. They have provided support in the form of check ups and blood work designed to monitor for any adverse effects of participating in the experiment, but ethics and legal ramifications prevent them from getting too involved with this.

A research neurologist was kind enough to explain to me that anecdotal evidence over a period of days to weeks is usually thought of as being the result of the placebo effect. However, anecdotal evidence that continues to show positive results with the same people over a period of months to years is much harder to dismiss as placebo. Testing done that supports the positive effect also helps. I was also informed that when the results are spectacular the general bias is to question the original diagnosis.

This experiment is coming up on six months now. The positive benefits seem to be holding on, so I think there is now a glimmer of hope.

Keep in mind that the group involved in this experiment is small. There are about 35 people that are openly vocal about it, and about that number again that are quietly participating. Also, not everyone is showing improvement.

Not knowing a lot about this disease I asked the group this question.

Chlorite is a free radical oxidizer. It does nothing to rebuild the body. What are you going to do to rebuild your bodies after the progression of this disease is slowed down or stopped?

The answer I received was…………. Well, the question was not answered.

I asked again.

This time I was informed that nothing had ever been successful in stopping the progression of this disease, so this question had never come up.

During this holiday time it is very exciting to see this glimmer of hope permeate the group, and to see some of their focus change to how to rebuild the body.

The changes are not drastic, but incremental. No one has jumped out of a wheel chair and started running down the street. However, to someone who has lost function in their hands or arms or legs, suddenly having some function restored and seeing this restored function continue over time is remarkable.

On May 2 1939 Lou Gehrig benched himself after playing 2130 consecutive baseball games with the NY Yankees. His health had deteriorated to the point where he was no longer able to play well. Addressing the crowd before a July 4 1939 game, Lou Gehrig told people that he was the “Luckiest Man on the Face of the Earth.” Two years later on June 2 1941 Lou Gehrig died of amyotrophic lateral sclerosis.

ALS is the illness that the people involved with this experiment are suffering from.

This glimmer of hope started with the drug trial that lead to the oral experiment. The purpose of the experiment is to help people live long enough to be able to use the drug. There appears to be a willingness of the FDA to speed things along, but the process will most likely take a few years and people who are diagnosed with ALS have an average expected life span of three years. I don’t think the FDA can speed things along that fast.

In loose side to side comparisons it appears that the drug is far more effective. The oral solution helps and seems to be able to halt or radically slow down the progression of ALS, but the results from the drug trial seem to be better.

Six months is not a year, but it is more than a day or a week. Making assumptions on the outcome of a clinical trial in the middle of the trial is not the best thing to do. Extrapolating from the observations of a small group of people is also not the best thing to do. Still, I think there is a glimmer of hope.

Chlorite is not a cure for ALS, but it does seem to provide something that people suffering from ALS have in very limited supply – additional time.

If you know of someone that is has ALS, I invite you to cautiously share this glimmer of hope and have them watch the progress of the NP001 trial.

Tom

hello I’m here, I have almost a month and a half taking mms, and if it is working, incredibly in the sternum had a swelling the oncologist had told me was bone, and pear my surprise, one night I began to feel a few pecks at electric Within days after the formation deishicieron he had, incredible ¡¡¡¡,

know I have a long way to go, I would like to travel to India but economically I do not think I can afford it, I would like to know how much it cost and treatment best?

but I’m struggling with what I can, my mms droplets, and friends who give me lots of love and are so convinced as I am in my recovery.

I love life, love what I’m learning and I love every soul to me dadicado few minutes of your attention

07:12:11 – healing and strength of a woman 84 years after surgery on the heart

Because surgery and blood loss, she was very weak. She had been in the hospital of my daily 1 teaspoon powdered yarrow (St. Hildegard) to heal the wound, and one each 1x tgl astaxanthin capsules and Moringa. After initial difficulties, the wound healed inside and out well and the force was gradually turned back.

At first she could hardly get out of bed alone, let go a step on the stairs when she came into the rehab. After 3 weeks of rehab, she could walk 50 steps in a practice session and the Hb (hemoglobin) fell from 11 to 12 without any other iron supplements.

After another 3 weeks, she makes few that she has recently done three years ago or longer and is looking forward to it. When baking Christmas cookies she kneaded dough, for example, only one sitting down with about 2 kg and a mass of about 1 kg mass, although it has been years sensory disturbance in their hands and left a slight paralysis. The effort gave her pleasure and she had no pain the next day.

I’ve had some great results using the MMS1/DMSO on my hands. I play guitar, drums, and bass, which definitely adds up to a lot of tension and soreness in the hands and wrists, etc. When I drum, sometimes all it takes is playing one fast/challenging song to develop blisters. The friction between the sticks and your hands with acidic sweat between them is the perfect recipe for blistering. So yesterday I was practicing a song that requires very enduring 16th notes on Mr. Hi-Hat. ‘Everlong.’ Well that didn’t agree with my hands very well; got some unpleasant blisters during it.

So what I did was: I put a glass on its side, and activated 2 drops of MMS near the brim. Waited about 30 seconds, tilted it onto my hand, then rubbed them together. I don’t add water for this because I find that the ClO2 absorbs much faster into the skin without it. Besides, it’s a small application so I find it appropriate for that reason as well. The downside is that your hands will have an odor from this, but I just rinse them with water a few minutes after the last step. Then I uncap a bottle of DMSO, pour a small amount onto my hand and do the same thing. (4 or 5 drops worth.) After a few minutes of absorption, some areas might feel a bit sticky, so just rinse your hands thoroughly afterwards. I did this no more than 3 times since yesterday, and already the blisters are about 80% healed. Normally it takes days to make that much progress. I definitely plan on doing this more frequently for tension and soreness which it aids as well.

Happy MMS’ing!