Hi! Last Tuesday my cat was feeling not so good and she was about 5 days like that, something with the stomach. I start putting 7 drops in a litre of water and my cat around the 6th day she was feeling better and the next day my cat was normal again. 

John

I’ve had chronic dandruff all my life. We are talking big snowflakes type of dandruff. If I didn’t wash my hair with a strong dandruff shampoo every other day, the dandruff would reappear a day later. The prescription shampoos didn’t do any good either. It got so bad that when scratching my scalp, I could actually get a millimetres worth of dandruff under my fingernails. If I rubbed my scalp and hair lightly, dry flakes would fall as if it was snowing.

I had tried all sorts of remedies specifically designed to treat this problem without any success. It is something I had learned to live with all these years. I’m 55 years old now and still had this problem until recently. Someone mentioned MMS on one of the forums online. With that I bought a copy of your book, read about MMS and actually bought a couple of bottles from your friend in Canada.

Since I didn’t have any particular health problems (or so I thought), I just took it for maintenance purposes. About 7-10 drops with half a tablespoon of vinegar in two ounces of water. I repeated this routine once or twice a week.
A few days ago after ingesting the MMS for about two months, I noticed that my dandruff was completely gone. I purposely skipped two days of shampooing and scratched my scalp just to test it, but I am happy to say “THE DANDRUFF WAS AND IS NOW COMPLETELY GONE !!!!”.

As a side note, I’ve also had better bowel movement since.

Thank you, this was a God send.
Bob NYC

(Note: I included this story to illustrate the point that most skin diseases, including melanoma, are or over come by taking MMS internally. Normally, one does not need to put the MMS on the outside. Please don’t use vinegar as the activator. Use instead, lime, lemon, or citric acid solution. See the FAQ’s on this site. Vinegar feeds Candida.)

I want to thank you from the bottom of my heart. It is almost two years ago since I got in touch with you and you decided to help me, although it was a risk you took. Thank you. At the beginning of the treatment, my son’s ATEC was 37. I was devastated, due to the fact that the family could very clearly see that something was very wrong and no doctor could. They told me to be happy and that not everything could always be 100% perfect. He was diagnosed with….nothing. It was very obvious that he was suffering, he cramped, had PANDAS and everything was going in the wrong direction. Many symptoms. Because of my gut feeling and you, the nightmare ended. In addition to this, your protocol also saved my life. I had rheumatoid arthritis and lyme disease and was in a much worse state than my son; I had already got many “treatments” including antibiotics, cortison and antidepressants. I had been in a heart clinic with almost heart failure. The result was that I had to go very very low and slow, to be able to treat myself and my son. My own experiences with hospitals, clinics and blind doctors helped him though. Without you, it would not have been possible, any of it. Today, after CD, enemas, BSO & co, and 2.000 photos of parasites from us both? He is starting grammar school this autumn, with red cheeks and a happy smile on his face and writing this, tears are running down my face. I cannot thank you enough, Kerri. Bless you for your Courage, for being you and never giving up. I myself quit my job, have now started two different healer educations and I am looking forward very much to starting to support people as well.

A big big hug, many mind-flowers sent to you and much love.

Dear friends,

I want to share another success story from the mother of my young friend Max.

Max is recovering from autism, with a peak ATEC of 126. He would actively avoid interacting with family members, was anxious and not potty trained.

Max has made remarkable progress in less than a year’s time on the protocol.

See the story in his mother’s own words.

Max is 12, he weighs 94 lbs. He’s been on the CD protocol since beginning of July 2019.

He’s always been up and down over the years, with his worst atec being 126.

– Constant meltdowns
– Living in a state of perpetual anxiety
– Soiling himself
– No attention span
– Zero social skills and zero desire to be social and interact with others. Actually putting his hand over his own mouth and running away into a corner to show you he doesn’t want to be spoken to and interacted with.
– Cold sweaty hands which would leave actual wet patches where he’d touched.
– Avoided eye contact: If you tried to look at him he’d move your face away so you’re not looking at him. Would try and escape out of a moving car if looked at..
– Poor sleep
– Violent, aggressive behaviour during the frequent meltdowns, pulling people’s hair out from the root and then feeling so upset with himself for behaving like that.
– Absconding: Trying to run into moving traffic to get away during meltdowns.
– Speech: Unable to speak in sentences of more than 3-4 words, usually to tell you what he wanted. Diagnosed as speech of 18-22 month old in May 2019.
– GI Problems: Countless food intolerances, vomit profusely if I tried to give him sulphuric foods. Chondroitin sulphate made him vomit horribly even just 1 drop.

ATEC and Treatment History:

Pre-Treatment: Summer 2018 was ATEC of 126 and he was back in nappies (diapers).

Pre-Treatment: April 2019 his ATEC was as low as 110.

Began Protocol:

May 2019: Started him on black seed oil May 2019 and saw symptoms start to improve immediately.

July 2019: By July his ATEC was 57 when started the CD protocol. [Wow! 50 Point ATEC drop in 2 months from black seed oil!]

February 2020: Now his ATEC is 27 and I believe continuing to go down as his speech is getting better.

If you saw him last April, you would not think this possible.

Major Gains and Improvements:

– Mood: He is now calm, very well behaved. There is no anxiety, no meltdowns.
– Speech: He can carry on a fairly good conversation going back and forth perhaps 5-6 interactions.
– Sleep: He sleeps perfectly.
– Social: His social skills are so much better, as is his desire to be social with us. He interacts, sits with us, laughs at jokes, asks to play, tells me he has friends.
– Aggression: No violence, no aggression.
– Self-Expression: Types every day in full sentences about his thoughts and feelings.
– Self-Care: Self help skills getting better and better.

Health:

– Heavy Metals: Had him tested January 2020 and the aluminium is pouring out of him in “breathtaking” amounts (doctors words).
– GI Issues: His digestion improving. He is now on 16 drops of chondroitin sulphate with no vomiting at all. He is very affectionate, gives me cuddles and says, “I love you Mummy,” typed, “I want to be with mummy forever.”

EVERYONE is noticing the complete turnaround in him – many people have seen him at his worst and cannot believe this is the same person. I have so many parents wanting to know what I’ve done so they can repeat the same for their autistic child.

I’ve been trying to heal him for 7 years since he was 5. Some things made him better for a while and then he’d crash back down, worse than ever leaving me in despair as to what can be done to help him.

This is the FIRST time not only is he getting better and better but he is maintaining it. He is progressing massively- it is a dream come true. ❤️❤️❤️

Just to clarify – his ATEC is now 27 as of February 2020.

It was 57 start of CD protocol in July 2019.

auIt was 110 in April 2019, with its lowest being 126 the year before. It has been 126 before as well, when he was 6/7 years old.

This email was received last year. This same lady, Marline, has reported being much more recovered since this report was sent as she has been on the MMS for over 6 months now. She told me that she considers herself well at this time. She writes the following:

“I have Multiple Sclerosis and believe the cause to be many pathogens. I have been lab tested and found to have Lyme’s, Chlamydia Pneumonia, Epstein Barr, Mycoplasms, Candida yeast, Blackberry mold plus many others.

I also have been chelated for heavy metals Mercury, lead, arsenic, cadmium and etc. I have responded to many treatments and have made progress to health. I have taken the MMS formula for over a month. I started out slowly because of the extent of my illness. I gradually increased my doses from 1 drop 1 times a day to now taking 5 drops 5 times a day.

I stayed at the lower doses for safety and to allow any plaques to dissipate and heal the tissues under the destroyed growth. I had a little nausea, passed foamy bowel waters (which I think was dead yeast). I am noticing many improvements including less edema in hands, feet, legs, arms, face, stomach and my lymph glands under arms are losing their swelling. My breathing is more productive. I am not having pains from being out of breath.

The age spots on the back of my hands are fading. My cuticles are losing the hardened ridge around the nails. My nails are losing the longitudinal and horizontal ridges and lumps. My skin and nails are glossy rather than dull.

I spoke to Jim and he recommended I could remain at current dose for two weeks then go on maintenance of 6 drops a day. I think I will try this but depending on continual recovery I may stay at the 5 drops X 5 times a day as long as I notice improvements. I believe MS to be a difficult disease and it may take longer to address with this treatment. Also I have lost 8 lbs and 6 inches from my waist and I am not dieting.

I am a monitor on the Good shape Histamine, LDN and alternative message board. This is an active and supportive message board. Many with MS but we address all immune disorders, Lupus, fibromyalgia, chronic fatigue, Parkinson’s, and ALS. I hope you will all visit us at. http://disc.server.com/Indices/148285.html#5271

Just an update on the MMS treatment of Poppi. The first two photos were 2 days after treatment started and the last two after 10 days of treatment … I can see a huge reduction in the tumour. This tumour grew to this size within 8 days of being removed from another mammary gland … it would have been massive by now … it has shrunk I would guess about 40% … I am continuing treatment of 8-10 doses a day at 2 drops of activated MMS. At night I am giving her slippery elm in food (at least 2 hours after the mms final dose for the day), as this helps settle her tummy after a tough day … hope this helps other people … will keep you informed … have a wonderful day.

MMS got rid of all my joint pains in approx 3 weeks and also my sun hives which would appear at the beginning of every summer. What is important to note about MMS is that the formula for it changed. When I first used it around 2010 it was two liquids mixed together, one of those liquids was 50% Citric Acid. This has now been replaced by 4% HCL – Hydrochloric Acid. The old formula with 50% Citric Acid caused a lot of stomach upset, whilst the new formula with 4% Hydrochloric Acid aids digestion.

Also the way people are told to take MMS has changed – instead of very high doses, people are now encouraged to have very low dosages – usually upto a maximum of 3 drops per hour for upto 8 hours a day.

A lot of the negative reviews of MMS were from the use of 50% Citric Acid – taking it with 4% HCL makes MMS much more gentle on the body. As others have said, when I first used MMS I noticed I was flushing out many strange things from my body in my stools. Some of which may have been parasites.

I also believe I flushed out mercury from my body from years of dentist fillings as a child. The smell I would get of my stools was exactly the same smell as being in the dentist chair having a new filling put in. I think accumulated mercury might have been the reason I had sun hives every summer and once flushed out the sun hives just went away and stayed away. Before MMS I had to be covered in head to toe with long sleeves or sun cream – now I can walk in the sun with shorts and a T-Shirt and no sun screen and I’m totally fine, I never burn now.

With regards to joint pains – my wrists used to click and my toes would click when walking, within 3 days of taking MMS the clicking stopped.

For those of you considering taking MMS use the version with 4% HCL in it not 50% Citric Acid and most of the negative things you read about MMS won’t apply.

Looks like we have helped save someone from having part of her guts cut out, she has/had Crohn’s and after 16 days on MMS is feeling better than she has for a very long time; early days still but looking good.