I’ve been badly poisoned by massive exposure to mercury and also to lead as a kid and even more later in industry. As I began taking out a lot of that mercury I also experienced very strong infection pains. That was a result of Herxheimer pains that occur whenever the body’s immune defense discovers a powerful infection. Part of my infection came from getting a ‘dirty’ blood transfusion.

After I had that operation I felt terrible and my heartbeat began skipping real bad. Then an electronic MSA test was performed which showed I’ve got Lyme Disease from my transfusion. After my healing progress stalled I began to take small doses of MMS and worked on up. I got as high as 12 drops of MMS twice each day in 60 drops of citric acid mixture. After about 2 months of doing that in approx.

late 2008 I quit using any MMS after my heart STOPPED skipping altogether. After 3 or 4 more months passed that heartbeat began skipping again, but not nearly as bad. Then I took the same 12 drop doses of MMS mixed with citric acid drops for the final 3 months of 2009 and that STOPPED my heart skipping once again. Now a massive amount of heavy metals have been removed so I started to take MMS some more now in July 2010.

The Herxheimer pains I’m now having after taking only 8 drops of MMS twice are now very STRONG indeed. The MMS is now getting to my infections and killing them which causes those pains. The mercury in me has been sequestering, or hiding, these infections so my immune could NOT have any affect and wasn’t able to cure them. That’s why mercury was being administered by doctors to patients in the 1800s who had syphilis – because mercury in the body will lock those infections within a matrix of mercury ions and that causes the infection symptoms to be milder.

Anyway, if somebody with Lyme Disease would like to get cured, give it a try!

First thing, I would recommend not to combine it with any antibiotic therapy. MMS is stronger than any other antibiotic.

Think it kills the spirochete form of Borrelia Burgdorferii very well and with enough patience also all the cyst forms, because they will convert into the active spirochete form and then will be killed too. You will recognize this very soon.

For myself MMS has helped a lot already after a course of 35 days. Before I started I have had tremendous pain in my joints, muscles and tendons and frequently horrible headaches and much more of this nasty Lyme symptoms, to much to describe them all here, but within a few days most of them all was gone. I was able to get rid of all painkillers.

I started with 3 x 2 drops a day and worked me up to 3 x 15 drops, by increasing every day one more drop, I have had really nasty diarrhea and stomach upset around 8 drops … so I reduced the dosage several times during the protocol to a bearable amount of drops and started after a few days to increase again until I reached this 3 x 15 drops for three days in a row only to keep, then my body told me to reduce again, so I went down with it to 3 x 14 a.s.o, each day 1 drop less per intake. When I reached the 3 x 5 drops, I reduced to 2 x 5 then to 1 x 5 and from there to 1 x 4 and finally to 1 x 3.

Now I am on 1 x 3 drops a day and I am fine . Will see when my body tells me to stop completely with the drops.

By the way I recommend to eat only vegetarian food whilest the therapy and allways 3 hours before the intake of the MMS, never use it on empty stomach! And you have to trink a lot of fresh water during the therapy!

Coffee and Vitamin C is forbidden.

Keep in mind the Sodium Chlorite is an oxidative stress for the body, so you have to take afterwards some good combinations of Vitamins and Minerals and of course some probiotic food too.

Good luck!

Juergen cool2

P.S.: Medicos tractat – Natura sanat!

I have chronic Neuro Borreliosis, in other words Lyme Disease in third stage.

The symptoms (some but not all) are severe headaches, especially in the back of the head. These headaches are caused by massive amounts of ammonia that is produced by the the Borrelia bacteria.

Furthermore pains in mussles, strong morning chills, low temp feavers, very!! foggy brain, paralizing feeling in palm of hands, changes in perception of length of extremities, stumbling walk, loss of congnitive function.

I am using MMS now for two months. The great thing about this product is that it kills the Borrelia quite fast and sufficient to have much less pain in the brain. I have been on painkillers for 18 months and had to stop, so fortunately MMS came allong.

At this moment I use 7 drops 5 to7 times a day, so that is quite a lot.

The last few days I started to note a difficult feeling in the liver, as if too much chlorine (or some chloor product) was accumulating in the liver.

That is why I have started to research what the long term negative effects might be of taking this amount of MMS.

7 times 7 drops is a little more that Mr. Humble suggests, for strong treatment protocol. So I’m taking this daily to have the pain reduced, it is one of the other at this moment.

I have heard and experienced that Phenylbutyrate (Brands: Buphenyl and Ammonaps) is very good in reducing the ammonia ammount in the brain, it really helps. However Phenylbutyrate is expensive – you need 500 – 1000 mg a day – and can only be supplied through MDsubscription.

But MD’s are not knowledgable in this area and refuse to supply this to me. I live in Amsterdam, The Netherlands

So I’m looking for supplier or MD that is willing to sent it to me without subscription for a reasonable price.

Will continue use of MMS, I use ozone sauna for 2 hours a day to feel better when too much regular MMS is getting me ill.

My experience so far is that MMS does reduce very well the pain in the brain but has very little effect of killing the CWD forms as well as the cysts and spores forms that Borrelia uses to hide itself in the body. So it does kill the spyrocheet forms, but leaves the rest allone. This means that after about 3 hours you have to take it again to reduce the pains

…I am taking MMS but mixing it with DMSO to use in a trans-dermal preparation. DMSO is a great product in and of itself but it is also excellent as a carrier agent. It takes the MMS directly into the cells. When you use MMS in a trans-dermal preparation you can avoid the nausea and bad taste…you may get diarrhea but I never have. The set back is that it can burn the bejeesus out of your skin so you need to be careful.

I’m taking it for Lyme disease…so far MMS and DMSO has made me feel like a new person…physically and emotionally…

My husband has been [using] MMS for almost a year now. He had Lyme disease and Lyme rheumatoid arthritis in his hands. He has recovered 100% and is now building up his body with Magnesium oil spray…

I’ve had chronic problems since my early 20’s, Lyme most likely, with recent serious issues.

I have tried the MMS protocol using citric acid activator, DMSO and MSM water follow up. This is a transdermal procedure… absorbed through the skin. There was no nausea and only slight irritation, which the MSM water cleared.

Here’s a link where I got my usage info…

[link to www.new-cancer-treatments.org]

There are probably many sites with information on this, undoubtedly some are easier to read and follow, this is just the one I used for the “recipe”.

I can tell you that after 4 treatments only, there has been a remarkable improvement! For the first time in years, I can walk without pain. Other symptoms cleared or improved as well, but the joint / muscle pain is one that nothing had been able to improve.

I, for one, am convinced!

I’ve had slow, but steady improvement on salt & C which took me from mostly housebound, on a walking frame & dying, to traveling overseas last year & not well, but actually having a life.Throughout my 29 year Lyme battle I’ve had flickery vision with flashing lights and blind patches. Kind of like a permanent migraine. It has been torturous, very disabling & stopped me driving my car. I could not cope with glare or sudden changes in light & dark. I had to wear sunglasses a lot and also sleep with a small night light on. On waking, the flickering would be very bad and I presumed it was due to poor circulation. Eye docs and neurologists could not explain it, other than a rare form of permanent migraine or spasms in the tiny veins in the eyes. Magnesium did not help the spasms.

I have been on 5 drops of MMS morning & night for 7 months, stilltaking 2 doses salt & C during day.I have to tell you, the 29 year spasms are nearly gone!!!!!!!!! I have slept without a night light for 2 weeks with no problem!!!!!! I am driving again the last few months and finally without sunglasses!!!!!!!! I wake in the morning and can cope if a light is turned on suddenly!!!!!!!

Yahooooooo!!!!!!!!!!!!!!!!

I think the MMS is killing a virus or something that salt & C was not killing. I am also walking miles every day, my cheeks are pink and my circulation is so much better. People everywhere are noticing how much better I look. I am even feeling well enough to look for a part-time job soon.

Persevere. It is worth it.

Rosemary.

MMS is not toxic to healthy people. I another words, if you have no bacteria or viruses to kill, it simply does nothing, as it has no target.

The reaction to MMS is caused by the destruction of these pathogens. Once they are all or mostly gone, there is no reaction to it. I take 15 drops once a week, and I can’t tell any difference between taking it or not. But I have used it for several weeks in which I have taken care of most pathogens in my body. I do not have Lyme, but I do have Crohn’s disease. Most of my bad bacteria and parasites were in my intestinal tract.

My wife, on the other hand had a very pronounced reaction since she has Lyme disease. Her spine hurt terrible at first. When it got unbearable, she would stop taking it for a while. Now after much of it is cleared out, she really has very slight sensations if any at all. Her ankles are still sore at times, so she still has bacteria left, but it appears to be much reduced. I have been giving her 15 drops once a day.

D Bergy