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My mom has had basal cell carcinoma twice once ten years ago and then ten years previous to that. They were removed with no issues she had no spread of cancer and didn’t need any other treatment than removing the growths. The other day she had a spasm in a back muscle and while I was putting an icy hot patch on there for her I noticed a little area that looked abnormal. So I grabbed the camera and took some macro shots. There was one main area and one tiny area that was almost unnoticeable and one mole that looked odd to me. When she looked at the photos she said they clearly are not currently basal cell carcinoma but may be a pre-growth.
She decided this would be a good watch item for the MMS treatment. She is currently working her drops up slowly and when she gets to full dose we will start putting MMS topically on these abnormal areas to see what happens.
She has been a nurse for over 50 years so you can be sure she is not risking her health in any way by waiting to see what happens with the MMS before seeing a dermatologist.
The biggest area it is close to the size of a dime.
It is hard to see that there are areas on the top of this mole that don’t look right. ![]()
I have been dealing with candida overgrowth for over 20 years now. For about the last 15 years I have had these extreme issues with my skin. At its worst I could lay in bed at night and just peel off skin left and right. The pieces would be about the size of half of a dime. Whether I did this or not my sheets would be filled with skin all the time and by the end of a day the inside of my clothes would be as well. It covers my entire torso and up the back of my neck, with a milder version on face arms and legs that is not really noticeable to anyone other than me.
I have used so many supplements over the years for the candida, but none did anything for the skin aspect of my symptoms and to be honest most just knocked back the candida far enough that I felt a little better (after the die off reaction). I have used garlic, pau d arco, caprylic acid, lactoferrin, massive quantities of probiotics, fungal defense, oregano oil, citronella oil, black walnut hull, colloidal silver, and several others that I am not recalling at the moment.
The most recent is Candex. The Candex is nice because there are no die off symptoms. When I take Candex (two at night, two in the morning) and stay on a very low carb diet (low enough to keep me in ketosis) The skin condition starts to clear up in 8-12 weeks. This is the only product, even in combination with diet that has accomplished this. However if I start to eat enough carbs to be out of ketosis, even if it isn’t a lot (like 50 grams) the skin stuff comes back in about 2 weeks. Candex alone without the diet restriction does nothing for the skin stuff.
When I heard about MMS I thought this is something worth trying, it is cheap too. The Candex costs about 60.00 a month and still requires me to be on such an extreme diet that I can’t maintain it for more than a few months at a time. My family started the MMS and we were working up in drops when my brother Randy hit the wall and got really sick. I hadn’t gone up in drops that day through a little serendipity. I thought if someone in the family was going to get sick it would be me. I know a thing or two about the herxheimer die off reaction, having been through it more times than I can count, in more than 20 years of attempting to wipe this stuff out. The whole family decided to back off and create a much slower MMS protocol for ourselves. Now I am on day 19 and am taking 6 drops. I’m about ready to go up to 7 drops but I am also on the verge of starting my period so I may stay at six for a couple more days as I often don’t feel well the day before and the first day of my period.
These photos are of my skin a couple of days ago. The light wasn’t wonderful but this is a little of what it looks like as it is dying out. I purposely have not been eating low carb to see what the MMS could do regardless of my diet. Considering the fact that I will not be at full dose of the MMS until I am taking 15 drops morning and evening this is quite impressive. This stage normally occurs around week 9 (63 days) of Candex and extreme diet restrictions. So at day 19 only (only 5 days of which I have been at the 6 drop level, which is considered just a maintenance level dose) my body is already this far along with no eating restrictions. Amazing! It has also cleared more in the last two days as well. Somewhere in my box of negatives I have some photos that were taken back in late 1999 or early 2000 that show it at it’s worst. When I can dig them out and get them scanned I will post them for comparison.
So at this point in time I would say the MMS is doing it’s thing quite well and I am looking forward to reporting more great results. I haven’t had any bad symptoms using the slow approach so things are looking good.
This one is from a year or so ago it wasn’t as bad as it gets but it shows better how it gets this patchy look. As it clears and the skin stops shedding so extremely it will have these large red welt like areas that will then start to clear one patch at a time leaving areas of clear skin until it is finally all gone.
Hey folks. I’m still early in my MMS journey but I thought I would share an experience that I had.
My sister Engtovo and I started out by taking one drop on day one and increasing the dose one drop a day. So on the 7th day I was at 7 drops. It was just an AM dose at this point. I had some, what I thought to be minor symptoms on the 4th, 5th and 6th days but wrote that off as no big deal. they consisted of very minor nausea for a few minutes, minor headaches, some “brain fog” etc. I figured that if the stuff was “really” working that I would experience some symptoms. After all, that is what happened with other things I have tried to use.
Well, on the 7th day my body decided that I wasn’t listening well enough and about 30 minutes after I took the dose the nausea set in. OK, I thought you have my attn. but that was just the beginning. shortly after the nausea set in I was kneeling in front of the porcelain. no more got done with that wonderful experience and I was sitting on the porcelain. This process continued for about 4 hours at 30 minute increments. nausea, followed by kneeling and sitting. Trying to say this without being too graphic. That pushed me pretty hard but the thing that affected me the most was that every time I was kneeling in front of the porcelain I would get these intense COLD chills. They would continue for the whole time I was “kneeling”. leaving me physically drained and then it was time for some sitting contemplation. At about the 4 hour mark I managed to get myself to the back porch where the sun was shining and I just laid there until I felt the urge to go back to the porcelain just to try and get myself warm again. It worked!
At about the 5 hour mark this stuff pretty much subsided but I was left physically drained and sore. It didn’t matter what position I tried, it was uncomfortable. It wasn’t until around 9 hours after my dose that I was able to keep any water down, and 11 hours or so after, that I was able to eat anything. It took about another 24 hours or so until I felt that I was past it all, and yet another 24 – 48 hours until I had my energy back fully.
Now some of you may be thinking that after reading this there is no way you would consider using this stuff. But that is exactly why I am choosing to share this with you all. I FULLY BELIEVE THAT I NEED THE MMS. My body’s response, even as intense as it was, told me I have some “bad guys” to get rid of. What I didn’t understand was that I needed to take it REALLY slow. Engtovo after seeing what I went through stepped back her dose and scoured the net looking for more info on MMS and any type of protocol for it’s use.
After hours of looking, she had gotten enough info to create the protocol listed here in these pages. It is a slow process where your listening to what your body is telling you. Any symptoms and you stay put at that level until you have a few days symptom free. Then you move forward. The original protocol works, and if you don’t mind feeling bad it is an effective way of clearing out the parasites etc. quickly. (the MMS was originally designed to deal with malaria. no taking it slow if you want the person to recover.) After my experience however, I am taking it slow. I figure it took several years to get to this point so I can give myself 3-5 months to get rid of it.
I have a theory that all the nasty parasites etc.. are what create our bodies to become acidic (body ph) rather than slightly alkaline which is what the body by it’s nature tries to maintain. that in turn creates the problems like Candida overgrowth, intestinal problems, vulnerability to cancerous growths, feel exhausted all the time, not to mention all the other “ailments” of our society. We are basically trying to live in a body that is hostile to live in. I won’t have a clear picture of all that until after the MMS process is complete and I’m doing the maintenance dose. I tested myself for body ph a few months ago and the number I had was 6.02 with 7.0 being neutral. So my body was acidic and I felt it. I’m thinking that after the MMS, my body will be slightly alkaline or close to neutral and that using a whole foods multi we found (see garden of life link) I can maintain a “healthy” body after that. I will be sharing my MMS experience here on the blog so people can have an idea how things are going. After the day 7 experience I went back to 1 drop and am now at day 19 of my total MMS experience and 5 drops. will most likely be starting 6 drops tomorrow.
Now I don’t know if my theory will hold true for everyone but sometimes the very simple things like that are the most true. If you think about it, if your feeding xx number of parasites throughout your body and they are taking away the nutrients you need to maintain your well being and their byproduct creates an acidic body where they thrive and you do not, then getting rid of them should allow the body to easily maintain optimum health, as that is it’s nature.
Until next time, Randy




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