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Major improvement of ulcerative colitis especially stopping of longterm bleeding, still none 12 months on despite only 6 weeks of use, also gradual lessening of diarrhea episodes to complete remission. I did use other methods subsequently to keep it in remission.
Also improvement of urine flow and gradual increase in wellbeing
Although I remain a big supporter/believer in MMS and what it can accomplish in the body,
I am going to go off it for a while (at least.) At only 6 drops once a day, it seems the MMS is
neutralizing blood sugar and blood pressure medication because both are going up.
I have been feeling more pain and other all-over crappy feelings, easily stressed out, with
palpetations at times.
My bp has been inching up steadily with no change in medicine. I have had my blood sugar medicine
changed because the one I was on was causing pitting edema. It seems that the new medicines have
had no effect since I was on the MMS at the time of changing.
Since I feel so bad, I am dropping the MMS and continuing with other good supplements.
Hopefully, this will help.
Just a “heads up” to those on medication.
A friend recently introduced me to their daughter (42yr old) who has suffered with COPD for years and recently had gotten terribly worse. Her mother asked me if I would call her daughter and offer help.
When I first called her she could barely hold a conversation and it was very hard to understand most of what she said.
She told me she had been unable to work for a month and was often unable to go from one room to the next without passing out, so little was her strength and breathing.
She had been told by her Dr. that the lower portion of her lungs was dead and the disease would only progress.
I sent her some MMS2 and she took 1 each hour for 3 doses. She quit because of a sever pain in her upper abdomin which began 45 minutes after the first dose. She continued anyway with 2 more doses before quiting.
The next day when I spoke to her she was 50% better. By the 2nd day she was breathing better and walking about.
Her doctor then took her off the high doses of Steroids she had been on and she is now, (5 days later) back to work and feeling better than she has in years!
When she attempted to tell her Dr. (she is part of a COPD study) what she had done to make the sudden change he only said “I don’t want to hear about that!”
What will he say when she continues to be well and the others in the study get worse?
Praise God for the MMS and thank you Jim for bringing this to our awareness!
Mark (Pennsylvania)
Here is my story, so far:
I have started with MMS1 in 04/2010 after I have learned about J.H. on the web. I have been a genital herpes sufferer since 1978. Long time. My outbreaks are not frequent, only 2-4 times a year. However, the number increases due to higher stress level, improper diet, lack of rest, ‘ bad marriage ‘ ( hmmm…), etc.
I have followed the MMS1 protocol by using the 1:5 ratio. I started low and increased it to 15 drops x 2/day. I had severe diarrea soon after starting but it faded away after few days. Intensive cleansing happened through my body but I followed the protocol. A week after I started the MMS1, I have experienced a severe outbreak, which was more painful and more spread. Previously, I only had outbreaks at the top my penis, but at this time it also appeared on the lower section, as well. I have continued with the MMS1 and the outbreak went away as normally it used to, after 2 weeks.
When I reached the 3×15 drops I could not take it very long. After few days, I stopped and went back to the maintenance level 6 drops x 1/day using the 1:5 ratio.
In August 2010, I had another outbreak, but I have not changed the daily portion taking. The outbreak was gone again after 2 weeks.
In September 2010, I have learned about the new ratio by using 1:1 mix with 50% citric acid solution (5 tablespoon citric acid + 5 tablespoon distilled water). This was a good news for me because I had difficulties taking the high dosage. I have also changed the water to carrots juice, which has no vitamin C and it makes it easier for me to drink the mix. Previously, I have only used filtered water and held my nose closed.
All, was good until October 2010 when I had another outbreak. I continued with the 8 x 3 x 3 per day protocol and I also applied the mix with DMSO gel to my penis directly to kill the virus there. The result was very severe pain and inflammation and it took me a week to get healed just from that irritated skin. The outbreak lasted for 10 days, at this time. I was very discouraged, at this time, and I went back to the maintenance level.
I started searching and reading again and I have learned about MMS2. I have immediately ordered two bottles and started again with the 8x3x3 per day MMS1 and 4×1 per day with MMS2. I had new hopes and I was hopeful that this combination will result something more positive.
Unfortunately, a week ago in December 2010, I got another outbreak and it is still with me. I have not stopped the MMS1 and MMS2, yet. But I am planning to finish MMS2 this weekend and go back to maintenance mode with MMS1. MMS2 is recommended only for 3 weeks, which will end this Sunday.
As you can see, I am not very successful. I have not lost my faith in MMS and I still think it can do the job. However, something must not work well for me. I live alone, so intensive sexual activity is not in the picture. I eat healthy as much as possible, although, I am a carnivore and I love meat. I try to compensate this with a huge bowl of salad everyday. I don’t drink, I don’t smoke, and I don’t have my stressing marriage anymore. So the picture is not that bad and I should have some success by now. My only sin is an Americano everything morning. Only one, no more.
So, any advice will be appreciated from you. Tell me where am I going wrong ?
I have not tried the MMS + DMSO topical solution and I would like to try it out. What I don’t know is: how many times a day can you do this ? what is the daily limit ? ( I have done the Stabilized Oxigen method from ‘ Never an outbreak again ‘ but it has irritated my lower spinal area very much. )
Do I still want to take MMS2 ? I hate it and it makes me feel terrible. Ever since I am doing the MMS1 + MMS2 I have dizziness. It is not serious but it bothers me.
I am still hopeful, even after 32 years, that a cure is possible. I don’t give up easily, but I need solid advice or source to go to the right direction.
Thanks.
{Subsequent post on 12/16/10}
Hmm. After reading this web site: http://www.bioredox.mysite.com/CLOXhtml/CLOXprot.htm
it seems that I have the answers to my non-success. My diet. I need to follow incorporate the information on this web site and try it again.
I will stay on maintenance dose for a while and when I have my next outbreak, I will try the topical DMSO method with MMS1.
MMS2 just makes me very uncomfortable. I’ll keep you informed.
{Subsequent post on 12/17/10}
…I was using MMS1 all the time. With or without outbreaks. Like I said. I stopped the 3x daily for a while and I was on 6 drops maintenance for about 2 weeks. After this, I started the 1×1 method and I did it until yesterday. I will be on maintenance for few days, to give rest to my body. I will resume MMS1 soon, but with the topical DMSO solution. I plan to go up to 15 drops x 1 at night with DMSO until I have another outbreak. Once that happens, I will increase the topical DMSO method to 3x per day and see what happens. If I can manage it, I will continue this for couple months. If, after that, another outbreak comes, I will incorporate MMS2.
Yes, I know it can be a whole year program, but I need to go easy. MMS2 really made me uncomfortable. I admit, I was very disappointed, when I had this outbreak last week. I have put so much effort into this MMS1 and MMS2 method. But it is possible that my diet prevents the effectiveness of the MMS.
I will regroup my diet and I will try to avoid food, which can reduce or eliminate the effectiveness of MMS. I think I can manage it , because I am planning to follow the 4 hours limit for the undesirable food items, before and after MMS.
{Subsequent post on 11/30/11}
I do use MMS1 when I have an OB and it goes away in 2-3 days. Before MMS, it took about 2-3 weeks. I use MMS1 topically on the sore for 3 minutes and I wash it off immediately. ( It will burn, if you leave it longer ).
My latest info is that the virus is not what you need to kill. It is the parasite, which carries it. The parasite lives within the cell and it is very difficult to kill. Once the parasite is eliminated, the virus will be easy to kill with MMS. To kill the parasite, you will need heavy doses for minimum 2-3 weeks. Before you can start the heavy doses, you need to bring your body up to a strong immune system level. Vitamins, probiotics, etc. The heavy MMS treatment will destroy good bacteria, as well. So, your body has to be strong to overcome this stage. Lot of rest, sleep, no stress, is also required. I have seen negative lab tests on a web page from a guy, who has this method. He helped others to eliminate the herpes and have negative lab tests.
The MMS people developed a new method to take the doses. It is based on generating the gas into chilled distilled/filtered water. In reality the gas kills the pathogens. With this method, the troubling acid taste can be eliminated and higher doses can be taken. The generated gas will be active for weeks in this water, as long you keep it in the fridge ( below 11 Celsius ). It is called now CDS. Google for MMS/CDS and you will find out more how to do this. There is also a YouTube video you can watch, how to generate the gas.
If you are still using the activated drops method, I don’t recommend to take more than 3 drops (MMS + citric acid each ) per hour. But you can go all day 8-12 hours, if you can handle it. It is important to do a treatment like this for at least 3 weeks, or more, when you have an OB…
MMS might not be the magic tool but it does do wonders to certain people. Only you can decide, if this is for you, or not. Search, research, and try. That is the only way to know, if it I can help you. I did and it did help me in different ways. If, some day, it will also eliminate the herpes in my body, I will be overwhelmed. If not, I will keep trying and do my best. Isn’t it life is about this ?
I have Type 2 Diabetes. Three months of treatment with MMS showed no improvement in my fasting blood sugar, which I checked every day.
I had hoped that MMS would cure my type2 diabetes when I started over 2 years ago, no luck. However what I did find was that it would dramatically reduce my blood sugar shortly after taking it. My neuropathy in my feet greatly improved, it’s not totally gone but it became a lot more bearable. Recently I developed deep cracks in my heels which I managed to heal in about a week by bathing them every night in a basin of warm water with 10 drops activated.
{Continued on a subsequent post…}
I noticed an improvement [of my neuropathy] within a few days of starting taking MMS. At that time I was on the old protocol(working up to the 15 drops level).
Dear all,
I am please to share this visual photo which is the best proof to see MMS is working in killing pathogens.
Frankly, this guy is getting a disease that I don’t even know what cause it. It simply happen overnight after a shock fever and cold. Once wake up in the morning, he found his body full of wet bubbles from one side of his face till his shoulder and chest. He even unable to move his hand cos it will be very painful.
When they ask him to show it, he show to me and all I do is ask him, do you want to try my way or you want to go to hospital. Then he decide to let me try cos it is free.
I begin with letting him taking MMS2 orally for 4 times, one cap every 2 hours on day one. The next day he told me his pain is gone, so I ask him to continue taking MMS2 at the same dosage. At the same time I bring the activated MMS1 10 drop spray to spray on his skin area.
On the third day I was amazed with the progress of the skin, so I decide to take a picture of it. I continue ask him to take MMS2 orally at the same dosage for another 3 days. On the 4th day I again spray his skin with activated MMS1 10 drop spray.
On the 7th day morning I see all his problems is dry up so I take another picture of it to prove that MMS is actually working, but we may not know it if our disease is inside our body. It work very fast indeed. No wonder Jim said even cancer or HIV can be cured.
I believed this picture is very important to show how MMS is working. A lot people who know him does not believe that this kind of disease can cured in just 6 days.
Anyone here may use the picture to share to anyone you wish so that many could have benefits from it. This person will be around me for long time, so he can be reach by letting me know. He is Myanmar origin.






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
MMS Tackles Hepatitis C and Wins 5th April 2010 by Arrow Durfee Posted in Disease, Revolutionary Therapies, Oxidative Therapies, MMS Information
This post comes from www.natmedtalk.com and is a great story of the use of mms for hep. c. If you ever had doubt about using mms for this disease this may lead you to rethink your position.
You can read the original post at the forum on this page.As stated by the poster known as Hobo:
As some of you might already know from my former post on here, I found out that I had Hep.C a year ago, when my stomach filled up with fluids, [ascites] and my belly button ruptured from the large amount of fluids, which I was taken to the hospital, where they drained 7.2 liters of fluid out of my stomach, and put me on diuretics.I had also become very weak and ended up in a wheel chair for some time.
After initial blood screening and CT scan, I was told that I had end-stage Hep.C and given 6 months or less to live. From that point I was referred to a Liver specialist who told me that I was too far in the 4th stage to be considered for the standard interferon treatments and the 6 months or less, was re-confirmed… that I should just go home to get my ducks in order. Nothing short of a liver-transplant would help.
Over the past year I’ve researched and have treated myself at home with herbs. to slow down the progression of the virus, and from a years worth of trial and error testing with herbal treatments, the most effective I’ve found to help control the virus is with a liver formula herbal blend called:Xiao Chai Hu San, which I made into the 00 sized capsules. This with other basic herbs like Milk Thistle etc. helped a lot, but though I’ve heard of those cases where Hep.C virus was healed with herbal methods, I’ve never been able to stop the virus with herbs, even with my best efforts to do so. This lead me to continue “Searching”…and lead me to run across the news about the MMS.
NOTE: I would also like to mentioned that after reading several of the post on here about MMS, I wanted to give the MMS a “True Testing” for myself, without any outside influences, so I stopped taking any herbs while taking the MMS, though I did continue taking supplements of Vitamin B-12,B-6 etc.but not within an hour of taking any MMS. My Goal was to let the MMS stand-alone upon it’s own Merit. I’m not one that buys into or puts a lot of faith in blown-up advertisements or claims by others. Is MMS for real? And if so, just how good is it? And how effective is it without any help from outside sources like herbs or etc. taken along with it? I don’t drink, and stick to a healthy diet. ~ So here’s my results of finding the answers to these questions.
I ordered a bottle of MMS and after receiving it, I started taking it Mar.8th, 2010. But to not get ahead of myself here, here is my blood test results BEFORE and AFTER starting on MMS.
The results of my Liver panel blood test dated: …….Feb.3rd, 2010.~ April 2nd,2010.
ALT~{ SGPT } *85 ~*25 Normal Range: < 0 – 48 >
AST~{ SGOT } *54 ~*21 …………< 0 – 37 >
Alkaline Phos. *168 ~ *153 ……….< 20 – 136 >
Glucose ……..*130 ~*107 …………..< 65 – 115 >
Anion Gap ……*9.0 ~*16.0 ……….< 10. – 20.>
_______________________________________________________
Note: I started the MMS [Mar.8th], with only 1 drop per day for the first few days, and then started to slowly ramp up to 10 drops once a day on Mar.17th. ~Then I started to take more doses per day on Mar.18th.
Mar.18th= 12; 8; and 10drop dose for a total of 3 doses that day.
Mar.19th= 10; 10; 8; 10 drop doses. [Got mild stomach upsets]
Mar.20th= 10; 10 drop doses. Figured out that I needed a different juice
Mar.21st= 7; 7; 7;drop doses Started taking it with 100%pure Prune Juice
Mar.22nd= 7;7;7;7;3;3;7 drops. Read that more doses works better.
Mar.23rd= 9;9;9;9;9;drops. Being aggressive with hammering the virus!
Mar.24th= 7;7;7;7;7,drops. The ole’ stomach upsets again..dropping back.
Mar.25th= 5;5;5;5;5;5;5;5;5;5,drops. Hammering every hr. all day long!!
Mar.26th=5;5;5;10;5;5;10;10;8,drops. Being aggressive again!
Mar.27th=5;5;7;7;7;10;5,drops Feeling my oats and getting outdoors more
Mar.28th=5;8;5;6;5;5;5;5,drops. Having mild “D” every morning but okay.
Mar.29th=5;5;5;6;5;6;5,drops. Losing energy, toxic build up..
Mar.30th=5;5;5;5;5;7;5;5;5, ~Ignoring side effects, Enough of this Virus!
Mar.31st=3;3;5;4;5;4;3;4.~Had 2 big “D” dumps this morning! feeling sick.
Apr.1st=5;3;4;3;3;4, Spacing does out every couple hrs. or so now..
Apr.2nd=5;3;4;4;3;3.Had BLOOD TEST 2 hrs.after 1st dose this morning.
Apr.3rd=3;3;3;3;3;3;5;5, Planning to continue with lower doses….
Apr.4th=3;3;3;3;4. Will continue taking moderate doses like this now for another few months, so as to pick up any hidden viruses in lymph nodes, tissue, or tooth fillings.
*sleeping much better than before, better appetite too. Now that my blood test is established…I’m going back on some herbs to help clear out the toxin and to stiffen up my immune system too. Will see how that goes with my next blood test in May.
The above Blood Test stands on it’s own merits and needs no further proof as far as I’m concerned, simply because I’ve “NEVER” seen such a Normal reading with any of my blood-test over the past year, as I have with the MMS. And in such a short period of time too.
—It’s the REAL DEAL VIRAL KILLER ~ No doubt about it—
Haha. The FDA are plain evil. I’m glad I ordered my first bottle of MMS a few weeks ago. My mum got a terrible viral flu (chikungunya). She couldn’t walk. Four hours later after taking hourly doses of MMS she was fine. Amazing stuff. My dad’s autoimmune disorder which was causing water filled blisters to appear all over his feet…. cured. Then there’s the “house help” who has diabetes. Started dosing her and it is now under control. Need to find more people to heal. Dengue fever is rampant where I am. Wish I had MMS when I fell ill twice. Anyway don’t listen to the FDA. Also funny how Project Greenlife’s recall notice is dated the same day as when Jim Humble’s seminar in the Dominican Republic (Aug 9 – 13) was ending. Now Jim’s websites are gone too. jimhumble.biz and jimhumble.com. But I recovered jimhumble.biz using Google’s cache. Haha. I’ll be getting more MMS that’s for sure. I’ll also be making my own eventually. It’ll be easy enough to get the Sodium Chlorite where I live. Then there is Jim’s MMS2 (calcium hypochlorite) which turns into hypochlorus acid when activated with water. Check it out. Jim says it’s as effective as MMS1. Use both together for serious illness. Ok take care all.