I have lived with this devastating and painfully horrendous virus for 47 years. After treatments with high strength CDS covering a period not exceeding 3 months overall, my genital herpes (HSV2) is completely cured.

It is now over 18 months since my treatment and not a sign of the HSV2 virus have I seen in that time. Previous attacks came every 2 months as regular as clockwork.

My story of how I succeeded with this cure was far too long for a testimonial, so in the interests of providing some really helpful feedback, and for those who would like to know the full story, it is 5 pages, I have presented a document which can be viewed at the following link.

A long story by “Ancient_Rider”.

For those of you who know nothing about MMS your starting point should be the book by Jim Humble titled “The Master Mineral Solution of the Third Millennium”. My document is based on the fact you already have a good grounding in MMS.

I contemplated considerably about making a long story of this, but given that many testimonials are rather short, one extra-long story should not hurt. I believe that some aspects of my story may just encourage someone, also in such a predicament, to have faith in the MMS (CDS). I wanted to show others that no matter how difficult their situation, or what turmoil herpes puts you through, this treatment works.

The Road to genital herpes.

I am now, in 2015, in my 70th year of age. At the ripe old age of 25, in 1969, a one night stand while I was backpacking through South America, saddled me with genital herpes. My first attack was devastatingly severe and painful, and being travelling and on the road at the time, made it more difficult. After that first fateful attack I never had another for 6 months, this time while I was on the road backpacking through Africa, but two months after that, when I returned to Australia the attacks started coming every two weeks.

At that time (1971) doctors in Australia knew nothing about it. After being fed every antibiotic in existence for several months on end, I was eventually sent to a specialist with gave me my life sentence news, and told me there is nothing more they can do for me. At 27 years of age I was totally devastated. This started a cycle of total depression from which I didn’t emerge for many years.

The Bad Effects of the virus.

Genital herpes can effect different people in different ways, for myself that was in the most triple severe category. There are those who probably think that this affliction is nothing more than a few inconvenient blisters. Well, unless you have been saddled with this debilitating problem you really have no idea. As for my attacks, they consisted of severe and agonising pain and swelling in the prostate, bladder and rectum, also affected was the skin with the nervous system surrounding the pubic region and thighs, becoming agonising to touch, and quite often attacking the sciatic nerve down the right leg, so one limped around for a week or more unable to walk properly.

The severe itching followed the initial pain 24 hours later, affecting an area about 150mm radius of the pubic region, an itch which is impossible to describe, and for which nothing provided relief. And last of all followed by the inevitable 10mm to 15mm circle of painful blisters, which usually appeared on either the penis, scrotum or in the pubic hairs. The blisters of course, if you did not take care of them, infection would follow, and the lymphatic system in the groin, would become swollen and painful. And all of this would be coupled with severe depression which triggered every time an attack came.

All in all a great package. At times, not many, three or four that I can remember, the attacks would lock themselves into the pain syndrome without ever leading to blisters or finality of an attack. The longest period I remember this happening was some 9 months in length and the pain never subsided until another major attack decided to eventuate and put things back to the normal horrid cycle.

In my first two years back home after travelling, herpes attacks came every 2 weeks, no doubt triggered by the severe depression/stress cycle this whole scenario had me locked into. A nightmare, ten days to get over one attack, four days of peace and the next would start. After that two year period I tried very hard to come to grips with my allotted course in life, and the attacks levelled out at every two months, as regular as clockwork, and for the next 29 years maintained that two month pace with the severity listed above never lessening over all that time.

My herpes caused cancer.

Then when I was 58, I was diagnosed with cancer of the rectum. Now as the rectum was one of the most severely affected areas with each attack, it was always my considered opinion that the cancer was caused by the herpes virus and blisters in the rectum that did not heal. Not too difficult to come to that conclusion given the severity of the herpes attacks on the rectum.

The inevitable and barbaric chemotherapy and radiation treatment, and I got through the cancer, and from that time, after cancer treatment, I went on to suppression treatment with aciclovir, three per day, to make sure the attacks did not come again. My thinking being, that if I could stop the attacks then the risks of cancer returning would be minimised.

Mind you at 58 that was the first time I ever heard of aciclovir. Given the fact that I was run a merry dance for five years when I was a young man by doctors, who of course told me it was incurable but always promised me hope, I never discussed herpes with any of them ever again until cancer diagnosis, when they told me that herpes can kill you when the immune system is killed off by chemotherapy. After that comment the decision to go on aciclovir at that stage was pretty easy.

Bad generic drugs.

I was on aciclovir, three per day for ten years with no attacks. Then I changed to a generic brand of aciclovir. After about a month on that brand the herpes virus found a way to start attacking again. I had it on good authority after that the generic brands are poor quality and not very good. They are usually made cheaply in Asian countries and should be avoided.

In short the generic did not work properly and allowed the virus to evaluate a way through the suppression. Even though I went back on to Zovirax (the original and the best), the attacks, although very minor, would come regularly. The new attacks were rather painful, could last for two weeks or sometimes only for twenty-four hours, but never created the itching or blisters of the original attacks, and eventually went away. Remember I was still on three per day Zovirax. These attacks mainly affected the bladder and the prostate.

The Road to MMS (CDS).

I first heard of MMS in 2007 but it was not until about 2013 that I started realizing that some people were having success with the eradication of genital herpes, as I was alerted by emails from Genesis2Church. I started following MMS much more closely at that point.

My wife on the other hand about this time was told to have root canal treatment for a tooth infection. As root canal is a fate worse than death and the only other option is to remove the tooth, she decided to try the MMS. After six weeks of that treatment the tooth problem was solved. She returned to the dentist who could no longer find a problem with the tooth. (She used the original MMS as detailed in Jim Humble’s book.)

So at last we had our own positive proof that MMS can solve major infection problems. But would it work on a virus, and one that was as dastardly and clever at hiding in the cells as was genital herpes, that was the big question?

My first treatment.

With my renewed minor virus attacks continuing, and the aciclovir not managing to prevent them, I decided it was time to do a course of MMS. Living in a remote country location and working outside and away from my house mostly every day, I was reluctant to get involved with the MMS mixing scenario. I also didn’t like the idea of getting any type of stomach problem while I needed my health to keep working, so I decided that CDS was my best option.

I purchased some concentrated CDS, 24000PPM from a Genesis2Church recommended source in Australia, and commenced to take the drops at a dosage rate of one drop CDS per one drop of the original MMS directions. At that point I stopped taking the aciclovir, totally removing any protection that they still provided. I quickly pushed up to 8 drops per hour and continued that dosage for ten hours per day for ten weeks.

The herpes virus reacted rather badly to the daily CDS giving me medium pain attacks occasionally, but never arriving at the itching or blisters. Most attacks lasted about 24 hours and they were gone. After the 10 weeks I stopped the CDS and waited to see what happened. After several weeks some minor attacks appeared once again to my disappointment. After a few of these I figured I need to do something else. I was not prepared to give up, I wanted this virus gone.

My second treatment.

About this time I was advised of an alternate method of taking the CDS. Approved or not I don’t know and I don’t really care, I was ready for something new. The instructions were to take the course with as many drops as you can stand over a two hour period instead of the ten hours like I did in the first ten week treatment.

The instructions were to take the drops every fifteen minutes for two hours. Two hours sounded good to me as I was always back in the house in later afternoons, so I made my two hours from 2:00pm to 4:00pm.

I quickly got my drops up to six per fifteen minute period but with the fifteen minute time frame could not get them higher. I did this for three full weeks. I did find the fifteen minute time interval somewhat difficult, you felt rather bloated with fluid and the taste of the drops started to become annoying. (Please note not as annoying as the original MMS.)

I did however find that the drops were more palatable if I took them in cold water from the fridge. You were always glad when 4:00pm arrived but it took a long time coming, but a nice cold beer about an hour and a half later washed the events from my mind.

On reflection after my first ten week CDS treatment I now believe the perceived attacks after that first course of CDS were simply harmonic reflections of the original herpes virus winding its way out of the energy spectrum.

Perhaps I did not need the second course, who knows, but as the virus is completely gone I’m not sorry I tackled that second course, better to be sure.

Alternate applications.

During the first ten week course I added two other methods to apply as much pressure as I could to the eradication of the virus.

First one was from information I received from Genesis2Church, and that was using a mixture of MMS and DMSO in water and rubbing that on the lower spine. I managed a few applications of that but in the end my skin reacted badly to that mixture breaking into severe itching so I abandoned that treatment after two separate attempts.

The second was from information I noted from the Genesis2Church Forums, and that was that some people were suggesting the hot and cold shower treatment on the lower spine shocked the virus out of its hiding place.

I used that hot and cold water treatment quite a few times. I have no idea of how much or how little these additional methods helped but any method had to be better than none in view of what I was trying to remove.

Good results, genital herpes cured.

I finished that second course many months ago and have not seen the slightest sign of the genital herpes virus since. At time of this writing November 2015 it has now been over eighteen months since I finished all treatments and not a sign of genital herpes attacks have I had in that time.

I do believe with absolute certainty, for the first time in 47 years I am now clear of the herpes virus.

Contact.

If anyone would like to ask a question you may send an email to:

ancient_rider@yahoo.com.au

This email box is not checked regularly but I will reply eventually.

End of Document.

Note: “Nová Regena” is a Czech publication (magazine/newsletter) that has featured content related to MMS (Miracle Mineral Solution/Supplement) and CDS (Chlorine Dioxide Solution).

Dear and beloved reader of Nova Regena,

I would like to share with you the story of my father and his fight with cancer. Therefore, I have decided, with his consent, to write everything what could help people suffering from this serious illness.

I am a 33-year-old mother of a 3-year-old little girl. I am also a wife and am perhaps living as every woman taking care of a small child and household. Obviously, I am also a classic prototype of the daughter loving her father completely blindly and for the whole life. He was whole my childhood and nearly all my memories are connected with my dad. As a completely little girl I called him ‘tatty’. It was always great fun with him, he always fulfilled everything he had promised, he always showed me the correct way, he had the patience of a saint with me and I am sure that he has brought me up well.

First of all, I would like to inform you of my dad’s health.

When he was 33 years old, he had a serious stroke after which the left half of his body became partially paralysed. I was born a couple of months afterwards. He was with me all the time and we also learnt to walk together. Approximately in six years he started working again. In xxxx he started getting the full disability pension and a year afterwards he had again a stroke, even if a weaker one, but it tormented him a little. However, he has been living with his partial paralysis since 1977 up to now.

For the last time (before I learnt that he suffers from cancer) I saw him in August 2010. He did not seem to me all right. When we were leaving him, I said to my husband that I did not like my father, that he seemed to me yellowish and swollen, that – in brief – he was at death’s door. I do not exaggerate, I really saw and felt it in this way.

On 3 November 2010 in the afternoon, my aunt – my father’s sister living with him in one house – called me and told me that he was in a very bad condition. She told me that he did not want to tell me anything in order not to worry me, but now he is already frightened. She told me that he suffered from the large intestine cancer, that it looked very bad. On the following day, I called immediately the Lužická hospital in Rumburk town in order to find out more. His attending doctor was Ms Dr. Kulhava. She told me everything she could. The most important information was that my dad’s large intestine was closing due to a tumour and there was a danger of his quick and painful dying due to vomiting his stool and subsequently also total poisoning. Then I called my dad immediately who was psychically down and out. He put a brave face on it and told me that he resigned himself to everything, but yet I know him and could tell that he was afraid like a little boy, that he did not want to die yet. I promised him to take care of him, that I would not leave him in it, that I would help him, that yet there was a chance of some treatment that can be effective.

On the following day, I arranged the hospitalization in the Central Military Hospital Stresovice, (Prague) for him. Hereby I would also like to thank very much to my sister-in-law, Michaela, who helped and advised me whom to contact. I would also like to thank very much to Colonel Prof. Dr. Miroslav Ryska, CSc. who found a very early date for my dad’s surgery that was finally performed excellently and my father recovered quickly after it.

When we took my dad home before his surgery, he was skinny, without life. I saw a broken man about whom I thought as a child that he is immortal, that he will be here for ever, that he has the biggest strength in the world. Yet I could have already known at my age that it is not true, so why I was so surprised? However, I had to be strong, strong for him, so that he could cope with everything better and get the support from me. Nobody knew that I had spent the whole nights crying and could not sleep. I feared so much for him!
At that time I still knew very little about MMS. I knew it nearly only from hearsay. Otherwise I was convincing my father to undergo chemotherapy, that I would arrange everything for him, that I would help him, that I would be with him all the time. However, the surgery has changed everything…….

On 18 November 2010, I arrived to the hospital in the late afternoon. My dad was in the high-dependency unit, he did not wake up from anaesthesia yet. I was looking at him, tears were trickling down my face, he looked like a baby. He was covered up to his neck, he looked so tiny on that bed… His mouth was opened, all these hoses of various sizes in him…… he was sleeping like an innocent baby. The world has turned round. I am already for him here, now I will take care, I say to myself… I stroked him and left to see his doctor. He did not know anything. He told me what a garden-gnome would also understand. So I left for home. At 6:00 p.m. my dad called me that he had woken up. I told him that I had seen him, that I had been there, that we had only missed each other. He was very glad that he had survived it and he thought perhaps that he had to call me and say it to me, that I did not perhaps call the whole day to the hospital, every ten minutes ?. When I came to visit him on the following day, he looked as if somebody had tortured him. He was in great pain, but unfortunately it could be expected after such a surgery. Fortunately, I caught the doctor assisting during his surgery (Dr. Pantoflicek), for which I was glad very much. However, what he told me was not optimistic at all. The tumour was too big, they removed as much as possible of it, one could make perhaps even a ball from that. He had multiple liver metastases. The reply to my question how long my dad would live was crushing – from 6 weeks to 2 months, with chemotherapy circa a half of year.

A half of year with chemotherapy? To suffer, vomit, not to live in any respect at least little worthwhile life and a half of year???? So this is not the correct way, that I understood immediately. However, I have never given up, and that characteristic I have inherited just from my father. So I told him in the hospital that I knew about a certain preparation that could be perhaps efficient also against his illness. Meantime, I had found out more information about MMS, and before my dad was discharged from the hospital I had MMS prepared at home.

On 28 November 2010, my father took MMS for the first time. He started with one drop every two hours. It lasted for the whole week. The following week he took one drop every hour. The following week he took by one drop more, then again by one drop more, until he reached the protocol 2000 (10 hours per day 3 drops of MMS1 and 4 times per day one capsule of MMS2). He stayed there for the whole week, however, it was not possible for a longer time. He had nausea, his whole body was burning, he stayed in bed and my aunt called me that it was perhaps his end. So I went there with my husband. My dad looked really terrible. He was still skinny, tired, dead beat. However, I noticed a certain change. He had a peachy complexion. Yes, exactly such. In this respect he looked ‘healthy’. I wanted to please him, so I said it to him. We discussed how to continue further. The way with MMS was not easy at all, my dad often hesitated. Preparing it every hour sometimes oppressed him psychically. Therefore, we started to prepare a daily dose in a bottle and divide it into ten portions. I also gave him good pineapple juice with which he diluted the solution, and it became easier immediately. It was very important that I suggested him the feeling that MMS is his ally, that they are fighting together against a big monster. And as my dad is a very upright man and is sometimes very outspoken, I knew that also in this case it would be necessary to choose really fitting shouts before taking MMS. I cannot perhaps specify it, it was really vulgar very much, but why, how it helped!!! Therefore, I would recommend to everybody strongly not to ‘caress’ cancer. Swear at it very rudely, if you can, it has an unbelievably beneficial effect on the mind!

The time passed and my dad found his way and dosing that suited him. For a long time he was taking one drop of MMS1 every hour, ten times per day, plus a quarter of capsule of MMS2 four times per day. He tried to eat as healthy as possible and reduced smoking as much as his habit allowed him.
At the end of March, we were both already curious whether MMS helped him and in what manner. Therefore, I agreed with his general practitioner, the doctor Dr. Lacinova to whom I also have to thank very much for her willingness and care of my dad, upon the blood tests with focus on the oncomarker level. I called her in order to find out the results on 1 April 2011 and nearly had haemorrhage ?

His liver was negative, oncomarkers proving the large intestine cancer were negative. The doctor was silent for a while, she did not perheps believe it herself. Then she repeated again and again that it looked good, very good, that it looked really perfect.

Then I made a lot of phone calls quickly, the first person who learnt it was just my friend who had introduced MMS to us and helped us so much. Thank you, Pavel, very much! Then I called my dad immediately and he was afraid as it was the All Fools’ Day. But yet it is no joking matter. My surprised aunt called me back if it was true, I assured her that yes, that they can celebrate. I wanted very much to shout it from the rooftops how powerful medicine exists here, what it can do. I called perhaps all people from my address book that my dad had overcome cancer without chemotherapy and any other available methods and medicines.

However, in a couple of days another apprehension appeared. What was actually my father’s blood count before? We found out that we maybe rejoiced prematurely, as the level of oncomarkers from which the large intestine cancer can be determined was within standards also before his surgery, even if higher than after MMS, but the difference was very small. I immersed myself in all various information on the Internet, I called to the hospitals where my dad was hospitalized to receive various information. We needed the test for another type of oncomarker that must be conducted together with the test for the large intestine. During the following week they conducted some sampling for my dad. And now we already know the result.
In order you can understand it better, here is a small explanation. I do not provide any units, they are not important in this respect. I am describing it as a layman so that every person could imagine it.

The oncomarker proving the large intestinge cancer has the name C 19-9. Before his surgery, my dad had the level of 22.6. A healthy person can have the level up to 37. After the surgery and taking MMS, the level decreased to 22.34. As you can conclude yourselves, nothing what would predicate of his recovery.
The other onkomarker that should be measured at the same time with C19-9 has the name CA125. My dad had an increased level of it, the value was 49.6. The normal values are up to 35. And today? My dad’s current value is 14!!!

In addition, bilirubin that had the value of 4444 and often predicates of a bad function of the liver, in my dad’s case of multiple liver metastases (as I wrote that he was yellow everywhere – an increased bilirubin causes yellow skin), now he has the level of 8.4. The normal values are up to 24.
The whole blood count is negative, my dad is only missing a little of potassium, nothing that could not be resolved with a glass of fruit juice every day. We have already bought a juicer ?.

I am happy that I have my dad back, that he feels good and that it is again fun with him. We call to each other every day, we both already know that we must not lose a single day when we can exchange a few words. I love you, ‘tatty’, and I am proud of you that you have beaten that monster. I already think again that you are the strongest man in the world!

Finally, we have prepared a short interview for you, it will perhaps help you in many decisions and believing in MMS. Not only me, Dominika Waloszkova, but also my brave dad, Oldrich Kaspar, wish you good luck and especially health.

Was it a difficult decision for you to take MMS?

It was not a difficult decision for me. Anyway, I would not undergo chemotherapy as due to chemotherapy all my friends are dead and buried.

How did you endure it at the beginning?

At the beginning I endured MMS well. However, as I started increasing my doses, it became worse. At the moment when I reached the protocol 2000 and stayed there for the whole week, I was really feeling bad. I decreased my doses so that they would suit me. I have got used to it over time.

How did your food look like?

I ate really modestly. Vegetable, fruit, yoghurts, cheese, breads and rolls. Nearly any meat. I tried to eat as healthily and possible. At the beginning I had the appetite, for example, for streaky bacon and sausages. Gradually I have broken away from this habit and today I do not even miss it.

Did you feel any physical change after a certain time of the MMS treatment?

For me, MMS is a really miracle, I am not afraid of calling it like this. Every day I go walking, which did not crossed my mind before. I feel very well. If the weather permits, I spend the whole day outside.

Is it demanding to keep discipline and take MMS every hour?

I would say not. But I have to admit that at a certain moment it started upsetting me little, but a person can really get used to everything. I said to myself all the time: ‘MMS is my friend and we together will destroy that monster – cancer’. At Christmas I also received from you, Dominica, a small angel that I have hung in the window and never taken it from there. I chatted with him several times per day.

How did you cope with nausea and did anything help you against it?

It was often very unpleasant, but I am sure that it cannot be compared with nausea and undesirable effects after chemotherapy. It encouraged me and knowing that I could bear nausea better. I have never left out any dose, I only perhaps decreased it. I had always black coffee prepared. A couple of sips were enough and nausea was over. It helped especially after the MMS2 tablets.

How do you feel now?

Today I feel as a healthy person. I do all works, I only avoid great stress. I view everything from a completely different perspective as before. I have a much greater regard for life. I have three grandchildren and it also makes me happy.

What did the information mean for you that your blood count is all right?

It was a shock for me. I learnt it on the All Fools’ Day, so I hesitated a little bit (laughing). Than I only thanked to God for beeing lucky to take MMS. Of course, I have to thank to Jim Humble very much, and also to my daughter and son-in-law. And to my sister who took care of me with love, my niece and also Mr Pavel who always met with my daughter willingly and advised and helped us with MMS.

Will you continue with taking MMS?

I will certainly continue with taking it! I am convinced very much that it is a great medicine. Recently many people have asked me what I was taking and many of them would also try it. Only doctors talk them out of doing that. But I say that everybody can dispose of his health as he wants. Therefore, I took advantage of this free choice and do not regret anything.

……..

End.
MMS is Miracle. Send this text for more, more peoples, please!

My name is Lucia Barfield. My sister’s husband was diagnosed with Colon Cancer last year, and thanks to God and MMS he is fine right now.

And he is so grateful that he wants to be part of this blessing and pass it to many more. How can they do it?

They are in Cali, Colombia, South America.

Thank you for your attention.

Dear Jim,

You remember the case of my dad, which I write to you a while ago.

In his surgery for colon obstruction, the doctors found massive tumor grown through surrounding organs. They removed it but most his liver badly damaged.

The surgeon not give him a good prognosis. He said if my dad took chemotherapy, he might live 6 months and with no chemotherapy, just six, eight weeks.

In December 2010, my dad decided to taking MMS and no chemotherapy.

He started Protocol 2000. One drop of MMS1 every hour 10 hours a day and MMS2 capsule 4 times a day. The capsules just two thirds full. If he felt nauseous after third capsule, he didn’t take number four.

Now he is still with us two months later and managing very well. Full of energy, planning his life, going for walks nearly most days.

Today my daughter phoned me crying, she is so happy. She took my dad for tests when she found doctor to order them. My dad’s doctors refused to treat him when he refused chemotherapy.

Tumor markers – zero
Liver – completely clean, without any damage

He does not have cancer any more!

I cried on the phone with my daughter and now I’m sending you a really, really big thank you! You saved her granddaddy and my dad!

We have all documentation and have it translated in English and send it.

Jim, thank you!

John W, Czech Republic

I had discovered CD when arguing with someone on Twitter about the use of HCQ curing COVID. Someone posted the Quantum Leap video below my argument. I watched it and ordered it right away.

My husband and I took it for a month to prove its safeness as my sister’s father-in-law was just diagnosed with cancer and I wanted to help. Sadly, he decided not to take the CD.

Then my mother started feeling ill. Because she knew it was safe and felt comfortable, she started taking it right away. Then a week later she saw her doctor and they found a mass 7 cm large in her rectum and the doctors told her she would need a colostomy bag.

After about 3 months of MMS1 & MMS2 her mass shrunk to be superficial. They were able to remove it and could never find the cancer cells. Though it was in the muscle so the doctors kept saying it had to be cancerous.

I know God led me to this. Thank you, thank you for fighting for truth.

I want to testify to the fact that I treated my mum who had colon cancer stage 3 with mms and she’s now totally free of it in just 3 months. Also, my son has been suffering from asthma since when he was about 3 months old and now after doing the nebuliser therapy, he’s free from it. For about 2 years now, he has not had any attack

My son introduced a friend (55 y.o.) to MMS. He has an hereditary cancerous bowel condition requiring 6-monthly colonoscopies and diathermy of cancerous polyps (up to 40 each time).

After 3 weeks of MMS (as per protocol) his doctor has declared him to have a “clean bowel” and doesn’t need to see him for at least 2 years.

The same man also had a PSA reading which had increased sharply over the past 12 months, up to the point of recently being scheduled in for surgery for prostate cancer, something he did NOT want to do.

After 10 days of MMS, his reading came down into the normal range and so amazed his doctor that the doctor demanded to see all the literature he had on MMS. The patient, of course, is very happy that he didn’t need the operation after the MMS.

My son (35 y.o.) has suffered with debilitating prostatitis for 15 years. He took the MMS drops as per the protocol and after 10 days he has declared himself 100% cured.

His daughter (3 y.o.) went to a child’s party and caught a very bad throat infection. He and his wife thought long and hard about giving her MMS, as he said “It’s one thing to take it yourself, but another to give it to a child.”

After careful consideration they started with 1 drop, then 2 drops, then 3 drops, and after the 4 drop dose two days later she was up and running around. Normally a similar infection would have required heavy doses of antibiotics and a spell of 7 days or longer in bed. They weighed her and followed the protocol.

My partner has metastatic melanoma Stage IV with secondaries in lungs, liver, bones, chest wall and groin lymph nodes and began on MMS about 4 weeks ago. So far no discernible improvement, but we are hopeful and I will report his results as time goes on.

We understand there is no simple test to undertake to determine if the MMS is actually working on him or not, but he says, “where there’s life there’s hope.”

My father was diagnosed with the following mentioned above 10 weeks ago. He was not having any bowel movements, he did not have any appetite and he lost 43 pounds in 3 weeks.

When he walked from the bed to the kitchen and back he was extremely exhausted and all limbs were week.

I ordered the MMS for him and begun Clara’s 6 by 6 and increased it by one drop every day after one week.

After 3 weeks he was back outside working with the workmen helping to build our health detox spa.

He continues to use it as much as 5 times a week and he is very well indeed, thanks to MMS….

May the Rest of Your Life, be the Best of Your Life,

Richard Homer
(Bio-Feedback Consultant, 3D D-Tox Practitioner / Health Coach, Trinidad & Tobago)