Hope this finds you doing well and enjoying life. I would like to share my testimonial with you if that is OK!

A little background. I have COPD, chronic asthma, chronic bronchitis and emphysema in both lungs. I have been on oxygen for months and should have been on it much longer but doctors couldn’t seem to agree as to what was wrong. I was so weak before that to brush my teeth I needed to sit on a bar stool and lean onto the bathroom counter on my elbows because I didn’t have the strength to hold my body upright to simply brush my teeth.

I downloaded your books on 24/8(2007) and ordered the MMS the same day. I received the product on 28/8 and began taking it that day. That was on a Tuesday.

By Sunday 1st Sept I felt so good that I went shopping for several hours without an oxygen tank. By the following week I was totally off the oxygen, even at night and have been free of the oxygen tubes and tanks ever since.

The MMS has given me back my life. I can vacuum my floors, work in my yard and cook my meals, now. 🙂 and I can brush my teeth standing at the bathroom sink, like everyone else does. This is the best I’ve felt in years and I’m getting better everyday.

I wish to thank you for what you have done for me. I have sung your praises all across the Internet and also to friends and family. Lots of these people have ordered your books and purchased the product because they have seen the difference this has made in my life..

Again, thank you. Your product has literally saved my life.

I was a ’30 pack year’ smoker and managed to give up smoking using Allen Carrs book, it took several attempts but got there in the end.  I stopped when I was 40, I am now 48. For the first 5 years  it was respitory infection over and over, with lots of antibiotics. I was in a bad state of health in other areas as well, overweight etc. It was not until I was 45 that I noticed shortness of breath developing, and I was getting it while at rest. I started going to the gym but then found the harder I worked out the worse the illness became.

The doctors prescribed all the steroids drugs, Symbicort, Ventolin, Spiriva, the latter made my condition worse. I had a CT scan done and fibrosis was found, they didn’t know how progressive the disease was, needless to say, it was not looking good. The doctors declared there was not much more they could do.

I found The One minute Cure and Bill Munro treatment of inhalation of H2O2, The effect was immediate, I coughed up more rubbish that week than ever before, I continued with it for about 6 months. My condition was better but it was not a cure, I still felt tightness in my chest. I read a technical article on COPD and it said that the disease is a result of the body’s immune system attacking itself.

The damage is caused by the created superoxidents such as H2O2, which the body produces in the lungs, it reacts with catalyses in the tissues, killing any pathogens present but at the same time it removes elastine from the lungs making the tissues less flexible eventually causes them to collapse causing Emphysema. I found that after inhaling the H2O2 for some time that I had effectively used up the excess catalyses in the lungs. You know you have reached this point because you stop coughing up rubbish.

It was then a work colleague introduced me to Chlorine Dioxide, I started slowly but the reaction came on suddenly, I got the usual diarrhea and nausea, I stopped, I became very ill, I had uncovered a biofilm and developed a massive sinus infection and had general malaise for about a week, I eventually became good and then continued with Protocol 1000.

It had an amazing effect all over, it fixed my stomach complaints, fatty liver symptoms, reduced my blood pressure to normal levels and my cholesterol levels and Bgl’s have come back to normal.

I felt the best I had in years,I decided to stop the Chlorine Dioxide all together and see what would happen. During this time I went on to high dose Vitamin C with MSM. The MSM restored the elasticity to my lungs, they feel normal now, however after a month I started to get the congestion happening again in my lungs and a green sputum. I have since gone back on the Chlorine Dioxide and a maintenance dose on 3 drops morning and Night , this keeps the COPD in check.

I have a grin from ear to ear.

Go a good thing, Jim Humble!

Hi. My name is Victor Summers and I am suffering from HIV, Severe COPD, as the doc describes it, with emphysema and other stuff I will share as time goes by. Today I started with my first dose of the mms. I have read about half of the posts made and will finish them.

I wanted to use this thread as a way to keep record of my progress and let others use it as a testimonial.

I have been on HIV meds for two years and my viral load is <50 (under 50) which is considered undetectable. My Tcell count is at 500 and something. I just happen to have noticed I have thrush today so instead of using the thrush meds I will look to see the progress I will make with mms. I will also be looking for my COPD to improve which is the biggest thing to me at this point because the HIV is under control but my COPD is really causing me lifestyle problems like being out of breath all the time, plus my chest is very tight to the point it hurts. I also have an enlarged prostate gland and I feel sharp pains coming from that area often (a few times a day.) So will also be looking for that to improve. I would like for this to be documented in the greatest way possible so I will cooperate with anyone in making that posible so we can have the proper documentation to prove the claims I believe I will be making :) I'm going to stay on my HIV meds for now just to see how this first step goes. I took 1 drop in citric acid with apple juice about three hours ago now and will determine tomorrow if I am going to increase it or not and will keep my progress posted here. There are other things wrong too and will mention them as I discover them improving (like my energy.) After reading so many of the posts already, I feel I know some of you and I am very impressed and am so very happy to make your aquaintance. {5/1/08} Day 2 of my MMS experience. Well, I woke up this morning feeling like crap. I could barely get out of bed. After taking my son to school I came home and slept till 2:45 pm. I havn't slept so soundly in a very long time. It reminded me of how I slept when I was a teenage boy. After being awake for a while I started feeling better and I also noticed my lungs seemed to be working better. I have not taken any of my albuteral today, which is highly unusual. I decided not to take my Spiriva and see what tomorrow is like. While writing just now I realized that the tightness in my chest is also much better. I also coughed up some nasty mucus today. My sinuses are dripping I think. There is a weird feeling in them anyway. My joints are hurting also. I had a white spot on my uvula which I noticed yesterday while checking to see if this weird looking bubble was still on my uvula, which it was, but the white spot is gone. The bubble (which looks like a blister) looks the same. It has been there for many years now. My doctors could not tell me what it is. They didn't have a clue. I had a brainstem stroke in 1999 so am anxious to see if my brain improves as a result of taking MMS. I have also been diagnosed with Peripheral Vascular Disease and my legs hurt most of the time and both of my feet have numbness in them. I will see if I experience any improvement in that area as well. I am sticking to one drop until I start feeling better. I'm still tired and feeling blah, like you do when detoxifying. The most important thing for me is getting relief from the COPD and emphysema. My lungs do feel better and I haven't ran out of breath today. And I walked up a hill at my son's baseball practice too. I wasn't even sure I was going to go because of how badly I felt this morning when I woke up, but by 5 pm I actually wanted to go with him. For any readers who may think it may be in my head, I don't care if it is so long as I get relief. I'm serious! LOL {5/4/08} Well, this is May 4th, and I am up to three drops and am feeling very well. Still sleeping like a log but my energy is back up. My COPD acted up yesterday and I had to use my albuteral, but today my lungs feel better again. I seem to be able to breath better -- like my lungs are bigger, if that makes any sense. Oh, well that may be because the tightness in my chest has subsided. Still coughing up green mucus, which started soon after I started using the mms. I feel my strength returning. Feeling more normal and more alive too. My brain fog, which I wasn't that aware of, is lifting and I am thinking better. Just now I noticed I am typing this note without any difficulty or hesitation on my brains part happening. I decided to stop taking my HIV meds. I hope that was a wise choice. But I can always resume them. I have stopped them before and restarted them. I have had chronic diahrea for several years so, for me, I will be seeing if in the long run that improves as well. I hope to see dead parasites soon :) I am also entering into this with a good mental state of mind so I have that on my side. I have a doctor's appointment coming up in a couple of weeks so it will be interesting to see what happens when they give me the "blow" test. Not sure what that is called, but it measures your lung capacity by blowing into this contraption. I failed it so badly the last time that I was diagnosed with SEVERE copd. You know. I am a happy fella and I don't like talking about myself so this is a labor of love, in a way, in hopes that it may help others if it helps me. I don't want people to look at me and think I am ill when my state of mind is so positive and, the truth is, I am not afraid of death. I do, however, want to see my little boy raised.

I began taking MMS approximately 2 months ago. I am 60 years old and have COPD (Chronic obstructive pulmonary disease) with chronic asthma, chronic bronchitis and emphysema. I was on oxygen 24/7.

I was not bed ridden, but life was a real struggle. To give an example of how weak I was; I had to sit on a stool and lean on my elbows to brush my teeth because I didn’t have the strength to stand or to hold my body upright while I brushed my teeth.

Each day when I opened my eyes in the mornings I dreaded making the effort to get out of bed. But in only one week after beginning the MMS drops I noticed that I didn’t need my oxygen all the time and that I had strength and could walk easily through my home without gasping for air. I was able to remove the stool and stand to brush my teeth. I opened my eyes each morning looking forward to the day. By the end of the second week I was completely off the oxygen.

I am a new person and getting better with each passing day. I do things now that I have not been able to do in a long time. I vacuum, do laundry and am also able to go shopping. I’m beginning to have a real life. MMS has proven to be a MIRACLE for me and has literally given me back my life. God bless and have a wonderful day.

I have been taking the MMS or Sodium Chlorite activated and diluted for 10 months. I started low and worked my way up. I experienced the usual bowel upset from the die off. I noticed improvements really quickly. Symptoms of MS spasms stopped in days. I noticed improved energy at 4 drops daily. I stopped having digestive problems. I had fewer attacks of REFLUX. Then my breathing improved and seemed to be easier and had less breathlessness. I stopped snoring at night. I slept better. I lost 12 lbs in the first couple of weeks. My edema cleared, Kidneys and bladder worked better, and I had a better flow. My balance became better. My stiffness went away. Several pre cancerous spots dried up and fell off. A long standing ear infection cleared. My sinus drained and I felt sinus was much clearer. It seemed that I was on the edge of being queezy or had Diarrhea every time I increased my drop amount. I took each strength for considerable time. Then I tried to move to next dose I always had to take an extra drop then drop back the next dose. Most of the time I was able to move to the next level in about three days of trying. I think I had such a slow climb because I have a heavy load of pathogens and one of them is Lyme BB. I think I have lowered the pathogen load with the use of MMS. I am thankful to have disposed of most of my symptoms of MS which were still bothering me. I still have some pains and neuropathy which are much improved since I have taken the MMS. I have used many other treatments over the years. Many of the treatments removed symptoms and then the symptoms returned but at a lower intensity. I was doing ozone and chelation which were very expensive but they helped. I feel the MMS has accopmplished a lot and if I need to I can continue to take it forever. If it just controls the symptoms I will be greatful. I plan to stay on maintainance forever 5 drops activated with 25 drops Citric Acid 10% and diluted in 4 oz of water.once a day. I have prevented the flu, periodontial disease, toothaches, much pain and all that I have related to you above. I found MMS very productive for the amount of effort and the Financial price is incrediblely small.