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Lyme Disease Symptoms Improved with MMS

Date Created: June 12, 2018
Author: Rob



Transcript:

Hi.

I am Rob. I’m from Grand Prairie. This is my wife Jennifer. She’s videotaping us.

Hi.

Hi.

I have something to say. Like I was supposed to say it for a few months.

I got diagnosed with Lyme disease. And I really do have Lyme disease because I got bit.

I went on a remote fishing trip. If anyone is from Alberta, it was Graham Lake, Vandersteen, Peerless Lake, Big Walleye, Seven Pounders. We caught them. We have proof.

But I got bit on my foot. And I was itching my foot with my other foot all weekend. I thought it was a mosquito bite.

I went in there with crocs with little holes on the top. So it was kind of stupid. But I wasn’t really concerned about ticks back then. But now I kind of know.

So when I got home, three days after I got home, I was deathly sick for 17 days. Stuck in bed. And I could hardly walk to the bathroom. Super dizzy. Tons of symptoms. Not really throwing up, just really nauseated.

I went to the doctor after about a week. It was really dangerous to drive. And it was just like crazy. The doctor diagnosed me with vertigo. Sent me home.

It just didn’t feel right. I’ve been big into sports and stuff, and I just knew that my body wasn’t right.

Anyway, long story short of that, I went to a naturopath. And they said, you could have Lyme disease, you know. Never thought of it.

17 days went by and I got better.

Basically, previously, a year before that, I was diagnosed with testicular cancer. That was another one to go through. I went through the chemo and all those treatments. So I wasn’t sure if I was run down from whatever and stuff.

So anyway, I got better. That was in August of 2017. And now it is June 12th, 2018.

And this February, my symptoms came back. I went to Mexico and got food poisoning. And I thought I had heat stroke or food poisoning and something else.

Anyway, after about a couple days of food poisoning, it just kicked into. I had really bad pains in my neck. And I was stuck in bed in Mexico for 11 days, scared to go to the country. And it was awful.

If I moved my head like three inches either way, I would want to throw up and it was nasty. So I got home and basically actually went home and went in an ambulance. The doctor diagnosed me with vertigo again.

So the doctors in Alberta don’t have a clue with what’s going on with Lyme. They’re starting to catch on a little bit. But I mean, I actually went to my doctor and brought him a list of 62 different symptoms I had. It was awful. I lost use of my elbows. I went blind in this eye for like seven minutes. I had cerebral palsy in this wrist, couldn’t use my wrist. Sometimes my body parts would fall asleep all the time. Joint pain, you name it, neck pain. It was awful.

Anyway, I have a friend that I was supposed to go see when I had cancer. And instead I chose to go take the chemo. But I went to Tijuana before and after my chemo just to try to get things helped with them. And I’ve seen phenomenal things down there.

So if you’re sick and considering things, Dr. Castillo, he does crazy stuff down there. There’s Dr. Cedeno I went to. I wish I would have did the chemo treatments with him. It’s called IPT, Insulin Potentiation Therapy. And it’s pretty phenomenal. And I wish I would have did it.

Because I’m really having serious issues with my feet now. It’s called peripheral neuropathy. And my feet burn and they’re numb and they hurt all the time.

So if you’re dealing with testicular cancer as well, make sure that you get those little frozen oven mitt things on your feet and your hands. For breast cancer, they put those on your feet and your hands so that the blood flow doesn’t go there, so you don’t have that side effect when you’re done. But I have it even with the chemo that I took. So I would suggest highly to ask about that if you’re doing chemo for anything.

But get back to the Lyme in February. This is about three months ago. It’s June. I got really sick and I counted, it was 34 days. So twice from the last time that I was basically bedridden. Couldn’t hardly sit up. I could eat laying down, drink laying down. And it was awful.

And I found out, and everybody has their secret formula that they’re trying to say, try this, try that. But I mean, this MMS stuff I’m talking about, the catch is you follow the money and the things. And everyone’s trying to push something on you. MMS costs about $20 for a year.

So if you can do the math, I know that there’s people watching this with Lyme disease. They went to the Mayo clinics. They went everywhere to try to get the solution.

I was three days taking MMS. Actually, they started me on something a little bit softer. It’s called chlorine dioxide, which is only five percent sodium chloride, if you know anything about MMS, but just Google it. Watch the YouTube videos. They’re true with Lyme disease. There’s not that many with Lyme disease. So that’s why I want to actually write this out.

February the 9th, I was stuck in bed. That was my 34th day. And by February the 12th, I was back to work. Probably maybe not full time, but four or five hours a day. I have like three, four businesses and I’m a busy guy. And this stuff is miracle. It’s called mineral miracle supplement. And to me, it’s been a miracle.

So I’m not promoting it. I don’t get paid. I just feel like I want to tell you this because it’s phenomenal stuff.

I had to experiment with moving up and taking drops. You mix, they react together and you basically just mix it with your water. It tastes like bleach. They say it’s not bleach. So basically what it is, it’s chlorine dioxide. It’s an extra O2 molecule on the end of it. And it’ll burn your clothes. It’ll do everything that bleach will do. But they say it doesn’t hurt the gut bacteria in your gut. So it’s good. It’s good for everything. And it’s like a natural antibiotic.

I was kind of blessed that I didn’t actually take antibiotics at all with the Lyme disease yet. So maybe it’s working better for me. I’m not sure about everybody, because Lyme disease is nasty. And it’s something, you know, you don’t want to have.

But clearly, if you have it, this MMS stuff has saved me. I basically just exercised tonight and feel great. I still need naps. I still am tired. And, you know, I still have some symptoms, but I can live a normal life, mostly for the most part.

So anyway, I just wanted to kind of let you guys know that I’m up to about 15 to 20 drops a day. I’m lazy on it. Sometimes I take like eight drops in the morning and forget the next day. And then I can almost feel, I know I wanted to tell you about brain fog. And it’s not just brain fog. I can feel all the symptoms kind of rushing in through my neck into my brain.

I got to the point where I couldn’t perform a single task at work, couldn’t make a sandwich, couldn’t remember a meeting, couldn’t talk. My words were slurring. It was basically like I had a stroke.

But after day nine of being on this product, all those symptoms left my head. Just all of a sudden, it’s like it’s gone. And it’s been back a few times. But that’s because I haven’t been staying up with the stuff, because you start feeling good and then you just get lazy on your medicine.

So I look at MMS as medicine for me. It’s pretty much the only thing that’s helped me. I’ve tried a lot of stuff and I’m taking Lyme core and Lyme yeast and a few naturopath things too. I think that does maybe help me. Who knows what does.

But I know that it was about two weeks ago I went off of MMS because I read somewhere on YouTube that probably it’s not smart to stay on it the whole time for the rest of your life. But I know a guy that’s been on it seven years and he’s fine.

So I went off it just to see what would happen. And within two days it went back in my brain and I was already getting really sick and I was bedridden for about a day and a half. So then I upped that right away because I was getting sick. And it took me about two days, from Monday to Wednesday, to get better again.

So since then I’ve been just taking it religiously, 15 to 20 drops a day, trying to get it within every hour of the day as much as I can, as long as I can remember. And I’m feeling like 90 percent.

So I just want to let people know that if you have Lyme disease, if you have any kind of disease, a pathogen, bacteria, you can kill a cold, you can kill pretty much anything. Give it a shot. It’s like 30, 40, 50 bucks. I ordered some more online from the U.S. just now. I’m waiting for it because I’ve been on this for like three months. It’s been the best solution I’ve ever found.

So anyway, just want to let you guys know that it’s pretty important to me and I won’t go without it until, you know, hopefully I’ll get better. And I mean, the thing is, as they say, it probably won’t cure me. I’ve read in Jim Humble’s book and it’s saying that it’s not going to actually make it so that my Lyme disease goes away. But it just kind of keeps all the symptoms at bay and keeps you rolling.

So I don’t know really. I’m still considering trying antibiotics maybe after the summer. But I’m just kind of scared because antibiotics run you down. So right now, my immune system is pretty strong. I haven’t had a runny nose. I haven’t felt a cold come on since the very beginning of being on this. It also helps a lot of other things, too. So it cleans out your bacteria and your stuff.

So anyway, that’s my story. Check it out. There’s lots of web. The last website I just looked on was Jim Humble, J-I-M-H-U-M-B-L-E dot I-S. And then it showed me a place to order the stuff. And that’s where I ordered mine.

Okay. Thank you very much and have a great life.

Update (June 29, 2018):

Two weeks after this video, I felt 100% percent.

In the last week I haven’t needed or wanted a nap in over a week. Amazed at waking up without a pounding headache or no joint pain and feeling well-rested.

It’s a night and day difference.

Just a couple days ago i golfed eighteen holes, walked the course on foot, and then drove eight hours afterwards and didn’t get exhausted at all.

I hope this helps people overcome this infectious disease while letting them get back to their lives.

with love, Rob


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