I was diagnosed with Hep C genotype 1a back in 2005. Each doctor I went too just wanted to do some interferon treatment and if I didn’t take it they didn’t seem to want anything to do with me.

I finally found a doctor who would continue to monitor me all the while trying to get me to take the treatment. I told this doctor that a friend of mine had the same genotype and took the treatment 3 times and is no better off.

A friend told me about MMS around October 2008. God nudged me to listen to my friend and order the Miracle Mineral Solution. I did my first “cleanse” that November beginning with one drop twice a day and slowly building it up to 15 drops twice a day for a solid week!!! I went to the Doctor to get my blood tested after I completed the regiment. My viral load dropped from over 1 million to 750,000. I thought could it be? To double check I decided to do it again. I waited until the New Year, January 2009. I began again yet did not get tested for a new viral load. I did the treatment once again in March 2009. I went to get tested. As the Doctor was writing the orders for the blood work she said ” Are you ready to give up on this silly treatment yet?” I said, “No, not yet. If this doesn’t work I have other alternatives I’d like to try.” She said I was silly. Well people my viral load was 130,000!! I couldn’t believe it was soooo low. My Doctor immediately ordered an ultrasound!!! I refused because I had just had one in November. Next she had her asst. call me and let me know that the viral loads have a tendency to fluctuate. I told her that I doubted they fluctuate that much!! I took a break for awhile. I just started back up around the 15th May with 4-6 drops once or twice a day, depending on how I feel! I feel sooo much better.

Other uses: I found that if I burn myself I squirt the MMS full strength sans Citric Acid directly on the burn. I wait about 3 to 5 minutes and then wash it off. No sign of burn.

My kitten climbed into my fireplace when it was on. When the kitten got out her paws were coal red. I immediately doused the entire kitten, paws include with MMS. I waited a few minutes and washed her off. To be safe, since I was in panic mode, I did it again!!! I can tell you that her paws did not blister or peel. She is ok!!! Her singed whiskers are finally growing out!!! Thank God for MMS!!!

I use a solution of 15 drops of MMS 75 drops citric acid then I add water and put it in a 2-4oz bottle. WHen I break out I apply it to my face. It dries out the pimples. Don’t forget to wash it off. Sometimes I don’t wash it off and I use it for a week. My face will appear dry but before you know it that goes away and my skin looks flawless. My forehead has been broken out since I was in 7th grade. I am now 41 and this year my skin has been pretty flawless. I don’t know if it’s from the cleanse or from the application of the solution.

My daughter was on Accutane 2007-2008 to clear her acne. It worked, but eventually the acne returned although not nearly as bad. She now uses an MMS solution for her face. She is 15 and has a beautiful complexion now and if she has

I have also used it to stop cold sores as soon as I get one.

It is amazing what all this stuff is good for. I can only thank GOD for urging me to listen. I will be getting a new test soon. I’ll keep ya posted!!!!

If you’d like, you can let A know that there’s no need for anyone to “pass on the relevant information” to me because I can still see the thread. In any case, I do appreciate A’s concern but I can’t think of anything that anybody could say really at this point that would get me to stop taking it. I don’t want to go back to the way I felt before, even if the way I feel now is representative of a clinically unhealthier state – which I don’t see how it could be.

At this point I’ve been on the MMS 12 days and I just can’t think of anything I could see in writing that would rival what I am feeling. I am just feeling so much better in nearly every category; more than 50% improved in my more annoying categories – like my feet and my anxiety/paranoia, and I haven’t really run into any downswings in my “cycles” as I call them – the rollercoaster up and down that I was having before with my symptoms.

I definitely still have symptoms but they are all being lessened and except for one day when I didn’t really take care of myself and didn’t get much sleep I haven’t lost any significant ground since I’ve been on the MMS. And I still have a lot of ramping up to do to get to the 2 or 3 15 drop doses a day that are recommended all over the place.

Currently I’m still taking 12 drops once a day. I should probably be breaking those up into at least 2 doses, but it just tastes so gross that it takes a lot of convincing myself to take even just one dose…then afterwards I always think “oh that wasn’t so bad,” but the smell has become familiar and has started to make me queasy before I drink it. Interesting since I’ve still never felt nauseas or queasy after taking the dose.

I still lose a little more hair in the shower than usual, but the drain is not clogged after one shower anymore. Last night I did wake up sweating mildly a few times, and I’m not sure if that is a result of Babs or Bart or perhaps I was just too hot – I did remove my heavier down comforter at one point and woke up a few hours later to put it back on again because I was chilly.

My feet are still somewhat red/discolored (as they have been since mid-August), but I was getting like these ulcers on the bottom of my feet and the bottoms of my toes felt like the entire part that touched the ground was a giant blister for a few weeks previous to my starting the MMS.

The ulcers are completely gone, but there is still a mark from one, a sore that my doctor called a sign of endocarditis a few weeks ago – but that sore does not hurt anymore, and I had another one in my mouth on my gumline which is totally gone now. A few spots on my feet are still occasionally sensitive but it is no thing compared to what felt like total rope-burn over the entirety of the bottom of my foot before.

I must say also that I am still taking 200mg of Doxy twice a day and have been for about a month and a half and I have about a month left of that treatment. I’m also on Malarone, one 250/100 pill a day that I’ve been on for as long as I’ve been on the Doxy and I have never thought that it has ever done much but I will keep taking it since I spent 400 bucks on a two months supply.

I am also taking herbs, right now primarily Hawthorn, Spirulina and Chlorella, as well as occasional Cat’s Claw and the occasional whatever else. I’m becoming somewhat of an amateur herbalist, but what I mentioned by name are the only things I’m taking regularly.

Anyway, the Hawthorn could be at least partially responsible for the disappearance/ lessoning of my endocarditis symptoms, as it is supposed to be the best cardiac herb there is because it is (according to Stephen Buhner) the only herb or drug which slows the heart and makes the beats more powerful – in other words it makes the heart more efficient. All other cardiac herbs and drugs make the heart beat faster, more often; they’re stimulants and therefore can wear your heart out over time. Apparently Hawthorn makes your heart stronger and stronger for the longer you take it and so I wouldn’t be surprised if it is what’s getting rid of my endocarditis symptoms.

The Spirulina and Chlorella are basically for immune fortification and the binding of endotoxins, as well as for keeping my system cleared out – they’re great at taking out all the trash before anything can get clogged up – and even after stuff already has been clogged, like we saw with my lymph node problem about a week ago, which is now totally resolved as if it never happened.

Anyway, yes I am taking plenty of other stuff besides the MMS and I am trying to make sure that I eat right and get enough sleep. I’m a writer so I pretty much work from home on my computer and that’s a great plus for me because it means I don’t have to stress myself out over a 9-5 job; which would probably have killed me a long time ago…..

…..anyway, I just want to make sure everybody knows that it could be entirely a coincidence that all of this improvement has just happened to coincide with the last 12 days since taking the MMS since I am trying to do everything else right, and I am taking other things – but I would also point out that at this point it would be nearly impossible for anyone to convince me to stop taking the MMS for any reason. I plan to take it until I have been symptom free for two months, like many do with antibiotics. Then I’ll keep a bottle around just in case.

Sorry this has been so long, I didn’t realize I was going to be doing an update until I was halfway done haha. Oh well, I guess I get excited talking and thinking about my condition. Feel free to post any of this for those on LN if you’d like.

Take Care, Send all the LN’ers my best!

NatureLover

UPDATE FROM NATURELOVER 12/4/07

I am doing really well, actually! I stopped antibiotics almost 2 weeks ago and have just been doing MMS, acidophilus, hawthorn, spirulina and chlorella. I am doing really, really well.

I am really excited though, I am making a lot of progress, pretty rapidly. I did have a minor setback at first when I stopped the antibiotics but I was able to get that under control pretty quickly. My feet are in the best shape they’ve been in for a month or two!

I really have a lot of hope surrounding this MMS; it is the most effective thing I’ve taken. My endocarditis symptoms are still nonexistent. My feet are doing really well and I just feel better in general. I still do have symptoms but it seems like they are becoming more manageable and less incapacitating.

I am up to a 15-drop dose twice a day, which apparently most Lymies can’t handle. I find that I do get nausea when I take a 15-drop dose on an empty stomach.

NatureLover

12/05/07

I have been unignorably ill since mid-August when I found myself in the Emergency Room with disseminated rashes all over my body; a few of them bullseyes – and a left foot that looked so crazy my PCP thought I had renal failure or diabetes, and she refused to treat me because she wanted my foot looked at in the ER.

I had been on antibiotics from mid-August until about 2 weeks ago. I do remember getting a rash before then and I was sick though I didn’t put the pieces together since before mid-August. I would say I was actually bitten anywhere from May to late July.

I did have a little set-back about a week after I stopped taking the antibiotics in which it looked like I was losing ground, but I didn’t lose ground to where I had been before I started taking the MMS, and I think that I was more frightened than anything else. I have been taking the MMS all the way through and I am continuing to improve.

It is slow but finally my range of symptoms has stopped expanding – whenever I thought I was improving with the antibiotics (except during the initial 3 weeks) it always seemed like my individual symptoms were getting milder but that there were getting to be more of them. Now it seems like the symptoms I do have are getting milder or slowly disappearing one by one and I have not noticed any new symptoms.

I do not think that my improvement is totally separated from the pharmaceuticals I took; I think just the opposite. For several months I would have been unable to cope with life in the absence of antibiotics, and I think the antibiotics I was on did significantly reduce the rate at which I was degenerating. I am not saying they didn’t help; they definitely did. I have no intention of saying that the MMS has done what it has done for me on its own. I can’t even definitively say it was the MMS, of course, but to me the coincidences just seem unignorable.

I won’t be writing anything in any peer-reviewed scientific journals (for among other reasons, I’m not a Dr. or a Scientist). The evidence I have that MMS has been beneficial to me is almost certainly not enough to convince anyone in the mainstream or any official sources; but the evidence is good enough for me, and good enough that I will tell people that MMS is PROBABLY beneficial for Lymies – at least in the short term.

I have seen somebody say “well, I would hate to see a post from you someday that said ‘mms gave me permanent brain damage,’ or ‘mms liquefied my internal organs’ or something like that. Well, I’d hate to see a post like that too. I don’t know much about Cl02, but I do know that it’s not natural and probably not the best thing to be consuming for long periods of time (or maybe at all).

But I would point out that 1) neither are antibiotics and 2) when I was making the decision to try this it was the LYME that was in the process of giving me permanent brain damage, and liquefying my internal organs. At least with MMS, if I see adverse effects I can stop taking it at any time and therefore stop it from doing more damage – with the Lyme I don’t have that option; as long as the Lyme lives it will increasingly do more damage.

If I knew that MMS DID give people permanent brain damage and that it DID liquefy people’s internal organs but that it would kill the Lyme for good – I would take it anyway until the Lyme was dead so that my real problem would be solved.

The problem with Lyme – as I see it – is not that the assaults my body endures on any given day are particularly devastating; my body has overcome some remarkable injuries that it has sustained from the Lyme. The problem for me is that the Lyme is alive and it keeps assaulting my body over and over again, and since that’s the case and I can’t seem to kill it with any of the conventional methods that I’ve tried, I have no problem trying something else that’s cheap (free actually for a sample bottle – a several month supply – if you go to the source Humble recommends in book 1) and reportedly effective.

When coincidentally or not I start healing like I haven’t healed since the first 3 weeks on antibiotics, I am excited to tell others who are still suffering about my experiences.

I will end this now but I am really excited, and hope everything is going really well for you!

NatureLover

UPDATE FROM NATURELOVER 1/26/08

I’m not doing that well at the moment actually. Not because of the MMS, but because I haven’t been very good about taking it for probably the past 2 or 3 weeks and I think the Lyme is reminding me now that it isn’t gone yet.

I know I was going to wait until I had been symptomless for 2 months before I stopped taking it but that didn’t happen as it just tastes so gross and I felt so good that I made the dumb mistake of pretending I never had Lyme; I stopped taking the MMS strictly and had a few nights of drinking and so forth to ring in the new year.

I’m still doing a thousand times better than I had been before taking the MMS, but I am a little down that some of my milder symptoms which had all virtually disappeared are coming back to me now. I have been getting back into the MMS recently and I hope to begin adhering strictly to two doses of MMS a day again starting tomorrow. I have also restarted doxycycline in the past few days and I think that is contributing to my overall sense of less well-being.

I’ve also heard that the full moon has an exacerbating effect on Lyme (I’m not sure if I believe that or not) and I have noticed the past few nights that the moon has been pretty close to full. Again, I’m not really sold on that being a factor but I thought I would mention it so others can make up their own minds.

I don’t know if the MMS actually kills the Lyme or just drives it into cyst form (probably a little of both I suspect, just like anything else, right?) But the one comforting thing is that as much as I have stopped and restarted the MMS, it has not lost its effectiveness; which is unlike any of the other medications I have used.

I’m so used to having to add things to the regimen when whatever I’m using begins losing its effectiveness. So far, nothing of the sort has happened with the MMS. It seems I follow patterns of wellness that match exactly (delayed one or two days) the patterns of how much MMS I have been taking, and it does seem that the MMS takes away symptoms faster than they return.

Hope you and everyone on Lymenet are healing well.

NatureLover

Just a quick update. I’ve been on MMS for about a month…still not past 13 drops once or twice a day. The large stubborn plantar wart between my toes is completely gone! My husband also realized that the small hard cyst he had on his hip has disappeared. Another friend has been on the MMS for only 8 days and she also had 5 warts near her ankle disappear.

Also, I was able to clear up a bladder infection using only the MMS. I can tell that I am having a large die-off of Candida…yet my craving for sweets is nearly gone. I feel quite sick if I eat sweets and I am very happy about that.

I just decided to try it. The dermatologist wants to cut the end of my nose off, anyway. What do I have to lose??? I followed everything Jim did.

I have to say that it did not burn, and thought that nothing was happening. After a few minutes I felt a slight discomfort, but it went away. The next day my nose was red, and then it formed a scab. The scab is still there six days later. I have just left it alone. I ran the skin cancer program on my rife machine, and got only minimal hits — fewer than normal. I’m still in the wait-and-see mode

I started out very slowly taking one drop of MMS and 5 drops of Lemon juice with some pure grape juice and purified water in the am starting last Friday. When I increased to 3 drops on Monday, I had a very itchy large red rash that looks like a burn, break out on my chest. (I have been putting some Lanacane on it, but it is still bothering me today.) I was also was taking the proboitic LB17 and wheatgrass but have stopped these. I have just stayed at 3 drops today, but I am wondering if I should stop if this isn’t going away. Has anybody else had a reaction like this?

(I forgot to mention I have had itching in my chest and jock itch for a long time. But I never had anything breakout on my chest before, so it would seem there is something in all this mixture I am taking that has upset my system. Any ideas would be appreciated!)

…I had red rash and itch on my thigh and abdominal area. A awhile back I had the same rash and itch on the same areas. I had skin candida (yeast) infection on those areas.

MMS brought the rash and itch back for a few days. I think what happened is this: I had candida at those areas but dormant. MMS killed candida and toxins released caused the itch and rash. It only lasted for about 3 days then it was totally gone…

2 years old, had a rash, mainly on her belly

I made a spray in a verstuivertje by three drops of MMS to make, with water added. I sprayde it every time I spared her, once or 5 per day. After a week it was red and I felt that it was less.

I took a daily ration for her, 1 drop per hour, so 8 drops for 8 hours, supplemented with apple juice. Every hour I gave her one eighth to drink, also I used the spray. After two weeks, the housing results disappeared.

Eva Hovers

My daughter Ronja, 2 years old had a rash, mainly on her stomach. She scratched it open and expanded. I think it’s a kind of mollusca were.

As stated previously before I used MMS for the first time I thought I was going to die. I was so sick I could barely work or think. IT is hard to describe but the first few weeks using mms (I increased 1 drop 2x a day — first week 2 drops 2x a day, 2nd week 3 drops 2x aday…etc) I saw IMMEDIATE improevement in my conditions. I had a warty mole on my leg that was oozing and I was going to go to the dermatologist to have it checked and it cleared up in a few weeks. {Dry Skin} {Dry eyes}