I’m a senior network quality assurance engineer from Scandinavia. In February 2014 I desperately needed to find solutions for a series of symptoms. At the time I felt the life was running out of me despite dozens of alternative treatments for many years.

In my search I accidently stumbled over MMS. That probably saved my life. Today I have been on MMS since mid March 2014, thus in treatment with Protocol 1000 for 4 months. I’d like to express my gratitude for letting me learn about this divine treatment and to let you know what it did for me.

After a short time everything inside you feels natural, like something you have been waiting for for a long time. All human needs change. Sleep gets better. The need for eating and drinking changes to natural. You might even change personality. I did. I don’t know if it was for the better, but I certainly changed beliefs about many things.

The healing process is like a movie playing backwards, for good and bad. That means you will feel the pain and discomfort of diseases experienced earlier in life but fortunately it won’t last that long.

The process of taking MMS is, sad to say, dreadful when having a job and social life to attend to. I wish an easier but still as cheap method could be found. But I held my spirits up high when I by accident misinterpreted Clara’s Protocol (6×2) and took 6×6 (6 drops per hour in 6 hours). When taking that lot in the early stage it later turned out that this can be used as indication for what the solution can do for you.

In this case some very annoying conditions would disappear: pain in feet, neck, back and shoulders, the fog in my brain. And it did. While it did I was so relieved and so happy one might think I was on drugs. What a feeling. Though returning to normal after a couple of days, I had a taste for more after that experience as I knew everything was going to be better.

The easiest way to describe the healing powers of MMS is to show my own list of symptoms with comments.

Small Fiber Neuropathy – Unnatural pain in hands, arms, legs and feet. Trouble walking. Restless legs and feet make it almost impossible to fall asleep at times. Dozens of doctors were involved in the diagnosis. It turned out to be inflammation in the nerve fibers that transmit thermal information to the brain. It is connected to diabetes, which I didn’t have. Not cured but relieved to be endured. MMS was able to remove the pain and most of the restlessness in less than a month. Currently the condition is like when it started years ago with only disturbance in the feet.

Hypothyroidism – Low energy, bad digestion, ennui. Treated with T4 medicine which turned out to be insufficient but not recognized by endocrinologists. Only with T3 supplement the jar over my head went away, but life was still a struggle. Last check and bloodwork showed no change in readings. MMS cleans up a lot and life is easier already.

Paradentosis – Sore and bleeding gums. Loose teeth for years. Brushing, flossing, rinsing with chlorine, strong antibiotics, vitamins and minerals, even ultrasound treatments at dentist didn’t help. I would inevitably lose my teeth. Almost cured after less than a month without mouth rinses with MMS. The dentist had never seen anything like it.

Hypertension – No symptoms. Blood pressure is lowered around 15% which makes me believe that I can start removing some of the medicine.

Deafness in left ear – Due to inflammation of the eustachian tube connecting the inner ear with sinuses. Had it for years. Sometimes tinnitus with both high and low sounds. Cleared up the day after first dose of MMS.

Nasal congestion – In the left nostril only. Cleared up the day after first dose of MMS, though it returned occasionally during treatment.

Swollen eyelids after Graves Disease – Before hypothyroidism I had Graves Disease for a couple of years. The disease made my eyes almost pop out of the skull and left damage in the eye sockets. MMS removed the inflammation in about 5 weeks.

Strange pressure under left ribs – A disturbing condition examined earlier by my doctor without findings. No improvement the first month. The second month I coughed a lot and tightness in the diaphragm ceased. The third month it got worse with more diarrhea and coughing. By the fourth month it was better than ever.

Muscle and joint pain – Aching muscles and joints for years, probably related to hypothyroidism and calcium metabolism problems. Reduced about 80% in three months.

Confusion and lack of concentration – Episodes of mental numbness and difficulty concentrating on complex tasks. Disappeared in about two weeks.

Exhaustion – Only willpower allowed me to do daily activities. Energy returned partially after one month and continues improving.

Trouble falling asleep – Sleep sometimes took several hours to arrive. This is now much better.

Nightmares – Vivid dangerous dreams occurred twice a month. Experienced only once at the beginning of treatment.

No libido – The desire was gone. After about three months a small sign of recovery appeared.

Depressive state – Felt hollow, like a zombie living in a filthy and creepy world. After four months this feeling is almost gone.

Fungal attack – Frequent fungal attack on the left side of palate starting with sore scalp. Appeared only once during treatment and much milder.

Abscesses – Boils in different places. None experienced during treatment.

Bonking – Need for sugar after several hours without food, sometimes leading to near fainting. Has not happened for months even though my need for food has reduced.

EM

The following testimonial is excerpted from page 358 of Healing the Symptoms Known as Autism, 2nd Edition by Kerri Rivera, published in 2014.

The book outlines a protocol in which chlorine dioxide is a key component. More recent editions have since been released with updated information.

A link to the full book in PDF format is provided at the bottom of this page.

My son with autism is 31 years old. Although he is fully verbal, he had a lot of issues: SIB, aggression, he was not able to sleep.

We have been trying different kinds of protocols since he was 3 years old, unsuccessfully.

I heard about Kerri Rivera and the CD protocol last September. We started right away. We were continuously in touch with Kerri who kept giving us the faith, that even at that old age it is possible to heal and even recover.

In September, when we started CD he had an ATEC of 87, 4 months later we measured 63, and now, after 8 months, he has an ATEC of 28.

There are some SIB’s and aggression left, but it happens only rarely. If we could get rid of it, my son would be recovered.

He became an interested young man, his memory improved. He keeps giving proper answers to my questions, something he never did before.

I can see his real personality now: he became a nice, lovable, open-minded young man from a very sick raging, roaring, screaming, suffering boy.

There are no words to say thank you to Kerri to show us the end of the tunnel.

I think I’m on the best way to recover my 31-year-old son!

Mark, 31, Hungary

Summary:

Sue describes her daughter Natalie’s lifelong health struggles, including mitochondrial disease, repeated infections, hospitalizations, cognitive regression, autism diagnosis, aggressive behavior, immune problems, and seizures.

After years of medical treatments, DAN doctors, special diets, immune globulin therapy, and rotating medications, Sue says she discovered antiparasitic treatment and later the MMS protocol connected with Kerri Rivera. She reports rapid signs of calmness and awareness after the first very small dose, followed by gradual improvements, reduced medications, lower ATEC score, and longer seizure-free periods.

Transcript:

My name is Sue and my daughter has been very ill all her life, from birth actually.

She started, gosh, she started getting really ill at about two weeks of age. Pneumonia, different things happening to her, many hospitalizations, ear infections, many hospitalizations.

At any rate, we were told to get a muscle biopsy and we learned through that muscle biopsy that she has mitochondrial disease.

So we of course sought out the best doctors that we could seek at that time, that we could find at that time, excuse me. And we employed many, many different medical treatments on my daughter to try to help her feel better.

And part of those treatments were a lot of antibiotics, a lot of antibiotics over the years. And also the mitochondrial specialists at the time were telling us that you really should make sure that every single year you give that girl a flu vaccine and your entire family. Because, you know, she has mitochondrial disease and so she’s going to be more susceptible. She’s, you know, going to want to protect her.

So we did this. And every single flu vaccine that she was given, she ended up in the pediatrician’s office the day two later. And she somehow bounced back, you know, a little bit. But she was always weak, always fragile, always sick.

Ear tubes, always occupational therapy, speech therapy, you know, everything. She started to kind of get a little bit better with a lot of in-home nursing care and my quitting my job and a lot of care.

Somewhere around 2003, and we were getting more help for her. We were really excited. 2003, 2004, like, hey, she’s getting prepared to go into kindergarten, a special needs type of kindergarten, one for mildly cognitively impaired children, but nonetheless, a kindergarten in a general ed setting. And she was happy.

And we gave her another flu shot in 2005.

[Crying]

She regressed so rapidly. She went from being, you know, mildly cognitively impaired, I’m sorry, to severely, multiply impaired classification in the school.

Sorry, I wasn’t prepared for this. Severely multiply impaired. She could no longer be in that mild kindergarten anymore. Mildly impaired kindergarten anymore. She could no longer be integrated with normal children. Not even the least bit.

She had to be moved to an autism classroom. And it was, you know, a classroom of five children and three adults. And she was the worst one in that group of five children. She could not function at all. Barely at all.

So everything fell apart. And this happened, it was September of 2005, she got that flu shot. And she was rapidly degressed. By October, November, December, she had fallen apart within a couple months.

And the school systems take a while to make the adjustments. But by that April of 06, they did make the adjustments to that very heavy, intense need for her supports. And in 06 of April, we got an autism diagnosis.

So we had the medical side and we had the school side of her deterioration.

So of course I sought out the DAN doctors and we went that route for years, very diligently for years. And actually I started the gluten-free diet in 05 because I was already sensing and researching, you know.

And so gluten-free, casein-free diet in late 05 and then 06 became all the DAN supplements folded in and all that, you know. And, you know, there was some improvement initially, but then it just seemed like over the years things weren’t improving. They were getting worse and worse and worse.

07, 08, more aggression, more irritability, not only towards the caregiver myself, attacking kids at school, attacking them, attacking para-educators. My little, at that time, probably roughly 45-pound little infant girl, excuse me, infant girl, was attacking like an animal and could barely stay in school.

We had to switch school systems to try to find even more support for her. So I was really frustrated.

Things degraded even more to the point where she needed immune globulin therapy every four weeks. She’d get an injection of immune globulin into her vein to try to give her some immune support to try to combat these illnesses that kept on reoccurring in her.

And then the DAN doctor at the time, very generous and kind man, he was trying so hard for her, he said, well, let’s try every three weeks now. That still didn’t do it.

So we made another change. We said goodbye to that doctor, thank you for all your efforts. We made another change to the local hospital because we felt that we needed the local hospital support in case things continue to get worse for her.

[Crying] Excuse me.

We got her with an immune specialist and he put her on weekly immune globulin, which is subcutaneous. It’s less invasive. You don’t have to find a vein. You just go under the skin. So then weekly therapies.

Still didn’t do it. She was still attacking. She was still uncomfortable, still not sleeping well. She was not having a quality of life at all that she deserved.

And I was on Facebook, not on Facebook, on email, a Yahoo group, a support group of moms that I try to research like all autism moms do. And this one gal was talking about the moon.

She seems like she’s lost it. I mean, I thought I had already lost it. And she’s talking about the moon. Okay, whatever. And I’d see her emails periodically.

And one time, there was this one evening that Natalie had such a bad evening of weird crying, weird crying in a way that we had never heard before. Almost like a possessed kind of cry before bed.

And I looked at her dad, my husband, I said, this is weird. Something’s weird. And that email I had just read, again, the earlier in the day, I ran down to my computer at that very moment. And I went to Farmer’s Almanac.

And it’s full moon. It’s full moon. And that’s that crazy, crazy laughter. And it’s full moon. I knew that that crazy lady, that crazy mom wasn’t so crazy.

So then I knew what I was dealing with, at least to some degree. And I contacted her doctor. And I was emphatic.

Her pediatrician, I said, we need to, we need to give her an antiparasitic. This is what I think is going on based on all the research I had done. Give her an antiparasitic medication.

Things started to improve. Reports home from school. Natalie did this or Natalie did that where she hadn’t been doing things before. She hadn’t had behavior of hitting or pulling someone’s hair or biting or pinching or kicking. Oh, I could name the behaviors.

So we were onto something. I was really pleased. And we kept on with these antiparasitic meds. We’d rotate very various ones.

I was lucky enough to have found a doctor who was willing to see my passion and trust me. And I told that doctor, I will bring her in for as much blood work as you want me to bring her in. You have to do this for me.

And so there was a relationship where he allowed me to rotate various antiparasitic and sure enough, she improved.

But there was still some strain there. And I couldn’t figure it out what it was. Why? Why it was still going on?

Well, of course, she was still on antifungals daily, antibiotics daily, antivirals daily, and now an antiparasitic daily, rotating whatnot. So she had very complicated medical life.

And I ran into a friend of mine at Costco, an acquaintance who also had a special needs child with autism. And we were just chit-chatting back and forth over the Costco shelves.

And I told her, I said, no, we’ve been doing some antiparasitic on Natalie and they seem like they’re helping. I said, but I was expressing to her, you know, that some kind of strain is still there. I can’t.

And this friend of mine explained, she said, you know, maybe they’re having a hard time coming out. I didn’t really know what that meant. Because I hadn’t had that much time to research coming out.

She goes, you know, coming out, coming out of, you know, in the poop.

So I said, well, she goes, you know, there’s this, this, this woman who I’ve connected with Sue on the computer and she’s from Mexico.

I’m like, I said, I think, I think I know who you’re talking about. I said that to my friend, because I had just again been on Google and I was looking for mineral water, because I felt like, well, maybe this missing piece is maybe Nellie’s not getting enough minerals supplementation.

You know, you’re on the gluten-free diet. You don’t know. You want to make sure that she’s safe.

And I had Google mineral water and up pop Andreas Kalcker video. And I watched these videos. One, this was, this would have been November of 2011.

And I watched these videos around Thanksgiving and I saw this Andreas Kalcker talking and talking. And everything he was saying was making sense to me somehow, even though I didn’t understand the science. It was making logical sense to me, but I didn’t know, can I put, employ that, that technique, that product on someone so sick as this little girl, so sick? I didn’t know.

And I had actually again Googled again on a different evening, sometime around November or early December timeframe of 2011. Mineral water, because I thought, I want to look into that a little bit And Kerri Rivera popped up.

And she was, she had a tropical background. It was a nice, she was pouring and mixing and showing, displaying how to mix this product that Andreas was talking about. I didn’t know that they knew each other necessarily at this point, because I was still learning.

But when my friend at Costco said to me, hey, I know this woman. I said, is she, she has this beautiful face and she’s smiling like this in her video. She goes, yeah.

I said, and she said, Kerri Rivera. I said, yes, that’s who I was talking to, or who I saw in the video.

Anyways, within a week, that friend at Costco got me connected with another friend who had some spare MMS. And I went over to her house and she showed me how to mix the first drops.

And it was July 9th of 2012. And I’ll never forget it, because I’m sorry.

One eighth of a drop. One eighth. She took that afternoon at my friend’s house and we came home.

And I was in the kitchen getting ready to prepare dinner. And Nellie was watching me. She was watching me. Sitting there calmly, calmly sitting and observing me.

And I had never, never witnessed that ever in my life from her. And I knew, I knew from that moment, that moment I saw her, I said this, there’s something to this.

And we found a way to help my daughter finally feel better. I knew.

Anyways, the shock of it all, but delight too at the same time. She went and I had her go jump on the neighbor’s trampoline like she always liked to do. And she jumped.

But it was different. I was watching her from the kitchen, you know, and make sure she was safe and netted trampoline, of course. She stopped jumping.

She was looking around and she looked in the neighbor’s house. She looked up at the birds. She looked down at the grass. And it was different. It was different. Ken, this is just one-eighth of a drop.

Normally, on the trampoline, she would just be constantly bouncing, constantly flapping, looking, you know, never ever ability to focus, not one iota. You know, she could never attend to occupational speech therapy very well, hardly at all, because of that too, you know, in her past.

But yeah, so she came in from the trampoline. I said, Natalie, what are you doing out there?

Because I did see her doing a little bit of what is referred to as tick spitting. She has a little, you know, so I did see that she would kind of spit towards the sunlight, but it wasn’t consuming her, which was amazing.

She came, I said, I said, what are you doing out there? She goes, it’s sensory. She said to me about the spitting. It’s sensory.

Sensory. So what this tells me is she, all those years, and I’m talking with occupational therapists or teachers and trying to explain to people that all that spitting thing is a sensory input thing. She needs that, you know, visual stimming and oral stimming. And it’s a sensory thing.

She’s, you know, she was hearing me all those years. And she told me, it’s sensory, mom. Never had she ever said before. Anyways, more confirmation.

So from there, the story continues, of course, that I employed the MMS protocol of Kerri Rivera’s. I took out all the antioxidants from the DAN protocol. It was basically you’re doing a 180 away from DAN to the Kerri protocol and took some time.

This takes time, especially with a fragile one, as fragile as my Natalie. And we started seeing more, more good reports coming from home.

It’s a little rocky because with someone so sick, you have to move very, very slowly up on the drops. I could only go up, you know, I couldn’t go up as fast as some children could go up.

But I was able to go up and, you know, pretty fast and correlate it with the parasitic protocol and adding those also in slowly.

She started July 9th was the first drop and her ATEC was a 79, I believe it was. And she’s still a work in progress. And it is currently, what is it, May 25th of 2013.

But she hasn’t had a full year because it was such a slow ramping up. She has not had that many parasite full protocol rounds yet. But she’s already at about a 40, I think the last measurement was a 46, I believe, ATEC, somewhere around there.

She is off of antifungal med. Again, she used to take it daily. She is off of antibiotics. Again, she used to take them daily and rotate them because they weren’t working.

She is off of antiviral. She is off of low-dose naltrexin, which is an immune modulator type technique …that is employed by the DAN [protocol]. She’s off of that.

She is… her seizures used to happen grand mal tonic-clonic, which is a very dangerous kind of seizure. They used to happen every two and a half to three weeks. Terribly dangerous.

She has had seizure-free days now. Her largest streak of seizure-free days was 105 days. Then she had a seizure, but we know what it was related to. It was related to a stop in an antiparasitic med that was too fast.

But now she is, again, ramping back up. She’s at seizure-free day 69 right now. And she’s going to continue to go. I feel pretty good about that.

We are lowering her seizure med. We have to go very slow. But the dream is that she will be off that seizure med next too. And then the dream after that is that someday maybe she will be off that immunoglobulin therapy, which would be awesome for her.

So she’s a very complicated case. And being 14 years old and highly compromised in many ways, highly infested. Well, whatever.

She takes a lot of time, but she’s getting there. And so we’re really excited and really hopeful now. We’ve never had this before in our life. Never thought we would ever see her feeling better and coming off of all these medications like this.

So that’s my story, and I’m sorry for crying so much.

The following testimonial is excerpted from page 401 of Healing the Symptoms Known as Autism, 2nd Edition by Kerri Rivera, published in 2014.

The book outlines a protocol in which chlorine dioxide is a key component. More recent editions have since been released with updated information.

A link to the full book in PDF format is provided at the bottom of this page.

Hi Kerri,

We’re now at 1/4th of a drop per oz and today my daughter for the first time EVER answered a “Where is…” question.

I was putting out the garbage and when I came back in I remembered I had forgotten to put away a black marker. When I found it was missing, I could only hope the property damage would not be too bad this time.

I checked the living room and the kitchen but could not find any traces. Meanwhile my daughter had taken the photo camera and was taking pictures of herself in the mirror. Amazingly she seemed to have a way better understanding of the thing.

I asked her twice where the black marker was, and after the second time she pointed towards the kitchen and said “There.”

SHE HAS NEVER DONE THIS BEFORE!

I checked the kitchen and found the black marker next to the fruit. The pears, melon and mango all had black circles and stripes. I was a bit overwhelmed I should say.

Thank you, thank you, thank you for never having given up your search!

The following testimonial is excerpted from pages 428-429 of Healing the Symptoms Known as Autism, 2nd Edition by Kerri Rivera, published in 2014.

The book outlines a protocol in which chlorine dioxide is a key component. More recent editions have since been released with updated information.

A link to the full book in PDF format is provided at the bottom of this page.

Drum roll please…….my son is 17 years old. He’s been on mms for 5 months now, I’m so excited I don’t even know, could it be 6? I think we started late July.

He started with a 63…….he is now a 7. He went from 63 to 25 in just a few weeks, then a 13 a couple months later, now a 7. I feel like I’m cheating every time. I go back and look, argue with myself, nitpick….but whether he’s a 5, 7 or 9, it’s nothing short of a miracle because just one year ago, he was WAY over 100. The ATEC is not perfect, not even close. There are things that the ATEC does not show. All that is true, but this is incredible improvement that no doctor I know would have ever been able to accomplish. Been there, did that, spent the 425K+.

And no, it’s not just MMS, but that has been the main treatment and everything else we do supports MMS and general health because I believe that in the end, it’s a battle between your immune system…and all that’s attacking it. We are winning and I sure do wish they would STOP CALLING IT AUTISM. That alone hurts so many.

Here’s a little background on my son: Matthew was very high functioning from age 6-12. That was after diet since 3, floortime play therapy, some aba, AIT, IVIG, chelation for a year, OIG, years of infusions of glutathione, vitamin C, B-com, etc…immune stuff. Then he did very well GFCF ages 6-12, ran track (very well), 2nd degree black belt, boxing lessons, etc….Then puberty hit, and what I did not know about, Lyme and co-infections RAGED, and for around 3 years, I lost him cognitively, worse, worse, worse. At 15, he was like an advanced Alzheimer’s patient, ADVANCED, he had lost ALL short-term memory, it was horrible, he struggled to think and could not.

He became more and more violent; choking me, kicking me, did I say he was a blackbelt? Even though he lost everything cognitively, like the ability to answer a question, those karate skills popped back into his head and he nearly killed me…. really close a couple times.

That was a year ago when his ATEC was over 100. So, here’s what worked: 1. Low amylose diet helped with the constant urinating. (he acted like a diabetic and had 14 of 16 PANDAS symptoms so auto-immune) 2. Biofeedback helped calm him some. 3. Cholestyramine helped him psychologically – I could see him clear up mentally in minutes. (chemical/mold/dust sensitivities big time) By this time, his doc had him on Ketamine for pain. 4. PEMF (pulsed electromagnetic field device) stopped the pain in 6 weeks, got him off of Vicodin, which was not working anyway at double doses, and all the Ketamine. I hated drugging him. Got him off the psych drugs over 6 months time. Then he got a lot better but communication did not really come around until 5. MMS. BAM. Big improvements in communication and PERSONALITY. With MMS, even his laugh changed to a typical sounding teenager’s laugh, and for the first time in years, he can sit still and stop pacing, pacing pacing….the parasites were eating him alive….and now more recently, I know 6. Hydro-colonics is taking us to another level of clear communication. Now there’s lots of spontaneous language.

I write things on Facebook so that I can remember and maybe write a book one day. I don’t care how bad things get, believe me, your kids can get better and it’s amazing, they really do store up all this info that you didn’t think was there. It is there, and they will share it with you one day.

I hope one day Matthew can share his perspective with others. It’s just that it has taken a very long time for us to help him understand that the things he did back then were not in his control so I’m careful not to talk about it. For months he would out of the blue apologize and feel terrible, over and over. Then there’s memories of his dad losing it also….protecting me.

Thankfully, Matthew has blacked out or forgotten a lot of it. He did say he remembers being locked in his room. We had to turn the lock around and sometimes lock him in there. Bad memories. We were all traumatized. But not anymore. He is a different person today but he’s always been the sweetest boy I know. I knew that, even back then. One day, he’ll probably talk more about it.

Translated Transcript from Spanish:

Hello. Today we are speaking with Dr. Icce Hernández Galán, a licensed homeopath with 22 years of experience in private practice using homeopathic metals, Bach flower therapy, emotional and mental therapy, and homeopathy for physical illnesses.

Today she brings a testimony about her own mother.

My name is Icce Hernández and I am speaking from León, Guanajuato, Mexico.

A few weeks ago my mother experienced an ischemic event, a cerebral infarction (stroke). She is 79 years old and had no illnesses and was not taking any medications.

On Thursday, August 13, she suddenly developed symptoms of a stroke. She lost her speech and had difficulty performing normal functions such as eating, writing, walking, and reading. She also had confusion and did not know what date it was.

She had difficulty coordinating movements and experienced memory loss, which made it difficult for her to take the CDS that we began trying to give her on Friday, August 14.

On Saturday, August 15, I attempted an enema with 10 milliliters of CDS but she could not tolerate it.

On Sunday, August 16, I asked my mother to try writing. The results showed she could barely write. She could not write her name or correctly trace numbers. I gave her exercises like those given to small children in kindergarten.

On Monday, August 17, laboratory tests were done including blood tests, urine analysis, and an electrocardiogram because I suspected cholesterol or triglycerides might have caused a blockage. However, all the tests were normal and the electrocardiogram was perfect.

On Tuesday, August 18, I decided to administer CDS intravenously. I prepared 400 milliliters of saline solution with 48 milliliters of CDS at 3000 ppm and administered it slowly.

Within about thirty minutes my mother began speaking again. She even began telling me about a movie she had found and was watching.

After that infusion I gave her another saline solution to hydrate her and allowed her to rest.

On Wednesday, August 19, we had our first appointment with the neurologist. The diagnosis was a cerebral ischemic event, but the neurologist did not find neurological damage.

After the first treatment my mother’s writing improved significantly. Her letters became clearer and more recognizable.

On Thursday, August 20, I administered a second intravenous infusion using 500 milliliters of saline with 60 milliliters of CDS.

Her speech improved further and we continued working on memory exercises.

After that I began giving it orally. I placed 15 milliliters of CDS into one liter of water. She drinks this mixture slowly every five to ten minutes during the morning and again in the afternoon.

Since that time my mother has improved every day. Her cognitive abilities have increased. She now speaks fluently, goes up and down stairs, and performs activities around the house that she had not done before. She no longer uses a cane.

Fifteen days after the event she was able to read and write normally again.

Here is her writing today. It says:

“Good morning. My name is María del Refugio Galán Gómez. I was cured with chlorine dioxide. Thanks to my daughter.”

This is what happened with my mother. It is emotional for me to share this because I was very worried about her.

In my practice as a homeopath I treat patients based on their symptoms rather than simply treating diseases. I applied this same philosophy in deciding how to use CDS with my mother.

I have also used similar treatments with patients who had COVID and low oxygen levels. They recovered quickly when taking it orally.

One of the principles of homeopathy is that the first duty is to preserve the life of the patient. We can use whatever therapeutic methods are necessary to save the patient’s life.

Thanks to this treatment my mother is now alive, coherent, mobile, and able to climb stairs in our four-story home.

Health Issues Mentioned:

Primary testimonial:

• Stroke / cerebral infarction (ischemic stroke)
• Loss of speech (aphasia)
• Memory loss
• Loss of coordination
• Cognitive impairment
• Difficulty walking
• Difficulty writing and reading

Associated symptoms:

• Confusion about time/date
• Reduced motor coordination
• Need for a cane

Other conditions referenced in discussion:

• COVID with low oxygen saturation
• Dementia prevention (mentioned)
• General neurological impairment after stroke