Ok, so I used to get UTI’s a lot in my younger 20’s and 30’s – Then when I started taking better care of myself with raising kids, growing up, etc. they became less frequent. Until one time when I was 47, I got one so bad I had to be rushed to the ER – it came on so suddenly, very intense with a lot of blood in my urine, all within just a few hours. This was around the time I was going through a divorce, so I attribute it to the stress weakening my immune system and I was also taking too many anti-anxiety meds, etc. Right after I recovered from this UTI episode with their powerful antibiotics, I decided to make a change. Divorce final, moved into a new house, had a little money, so I quit my daytime job and began to research alterative medicine which I had always had an interest in, but never had the time really to explore. I began to use Oil of Oregano (OOO) regularly after discovering how well it treated things such as sore throats, etc. Since I started using OOO I never once had a recurrence of a UTI. Perhaps just that little ‘queer’ feeling in my bladder every now and again, and then I would up my dose of OOO and it would just go away. I am now 61, and was introduced to MMS two years ago. I rarely take it internally, in fact the smell repulses me, but I do believe in it. Mostly I use it in the bath, and for dental issues when they come up. Well, lately, there has been a lot of stress in my life, again, without going into detail, and last night, I went to bed feeling normal and awoke with a strong sense of a UTI coming on., I immediately went to my OOO, which I hadn’t really been taking regularly like I should, and took a several drop dose every hour for 3 hours with a full glass of water – but the UTI kept getting worse throughout the night. I decided to take some MMS. I started with a 4 drop dose, then 2 drops every hour for 4 hours after that. I finally was able to fall asleep, and when I awoke – the UTI was all but gone! I could tell by how intense the pain and the ‘urge to go’ was when it first began that this would be a doozy, but the MMS seems to have completely eradicated it from my system – in less than 12 hours. Now I suppose the OOO is also a contributing factor as well, but from my experience, this UTI was every bit as intense as the one that sent me to the ER years ago, and instead of that, I am sitting here, pain free and feeling quite well.

Nine months ago I got a respiratory illness after an international airline flight.  Since then, I have seen 3 doctors, one of them a specialist, had 5 courses of different anitbiotics, and a 6th course prescribed.  My blood work looked fine, with only minor increases in neutrophils, though PCR test showed mycoplasma pneumonia exposure.  Two weeks ago, when I began my experiment with MMS, I had brain fog, was too weak to do more than stand up for 10 minutes, and was essentially confined to bed or chair most of the time.  After 10 days of MMS at a maximum dosage of 25 drops per day(divided doses), and with antioxidants in between doses, I am once again on my feet, cooking and gardening. 

In addition to oral use,  I also made my own sinus irrigation solution of acidified MMS, d-Mannose, distilled water  and enough sodium bicarbonate to adjust the pH to 6.2.  When I used it the first time, my sinuses cleared immediately and the relief was near miraculous.   I note that a patent on a similar solution was granted and that the commercial product is called Snoot.  I also found several journal papers indicating an immune modulating effect for stabilized sodium chlorite.  In light of this evidence, how can FDA prosecute anyone for selling a useful and safe product?

I wish to mention that I had sinus surgery two years ago that did not help my recurrent infections.  My doctor did a CAT scan of sinuses and chest, so the diagnosis was confirmed.  The next course of action would have been an antibiotic a day…Something I did not want to take for sure.  Just think of the danger of c.dificile!  A relative died of that, and I am aware of the risks.

In these times of increasing numbers of antibiotic-resistant bacteria, cryptic organisms like mycoplasmas and clamydophila  pneumonia, MMS becomes a life saving tool, because there are few sucessful protocols available to mainstream physicians and patients thus suffer years of suffering and economic loss.  Surely, if one is entitled to life and liberty, that includes the pursuit of health.  FDA has a long record of advocating for commercial interests at the cost of  consumer health.  This needs to end. Let FDA turn its attention to dangerous drugs which kill hundreds of thousand yearly, and leave citizens alone to make their own health choices.

I’m a 25 year-old woman who is on the spectrum with many autoimmune symptoms, chelating to remove mercury using Andy Cutler’s protocol. That protocol helped reduce my symptoms immensely, but I felt I was at a plateau so I used MMS2 for about two weeks and it helped substantially in lowering the pressure and anxiety in my brain. I’m going to try MMS enemas very soon and will give updates.

———- Forwarded message ———-

From: German Ruiz

Date: January 23, 2012 23:21

Subject: MMS Testimony from Barcelona

To: desdeandreas@gmail.com

Hi Andreas, my name is Germain Ruiz and you’re writing a book of testimonies of people who have taken the MMS has healed. I think I might be a good testimony, but first I need some help, in mid-February I have an endoscopy and I probably will do a biopsy. In the process I have been living with the MMS and what I feel, I think there is every chance that that test out that I’m cured and then of course we’ll give you my testimony with the data you need, or video, such as you see it. But as I say, first I would like to tell me a bit to see what advice you can give me in my particular case and thus achieve the best result in the February test.

I’ve been taking the MMS four months following an ulcerated carcinoma of approximately 1 cm in the stomach that I was diagnosed this summer in late July, before you start taking MMS I had been doing 100% vegetarian diet was a mixture of macrobiotic Orthomolecular and some of Dr. Gerson. Supplementing the diet with various supplements and vitamins that I list below:

Milk Thistle 200mg tablets.

Graviola 500mg capsules.

Fermented Papaya 500mg capsules FPP.

Blazei capsules.

Vitamins “Source of life”.

When I learned that the MMS would not take vitamin C, nor will any good taking antioxidants at the same time, I just stuck with the vegetarian diet and stopped using supplements which I have listed above.

Currently only complement the MMS doing coffee enemas twice a week and continue my vegetarian diet.

Although MMS gradually has decreased the symptoms of suffering almost completely (stomach aches, backaches, stomach feeling empty all the time, cold sweats, etc.) which is wonderful, now I feel that the process stagnant and not just heal completely, I have a few sporadic small punctures in the stomach and chest. I’m doing 14 daily doses of MMS is the most that you recommend one of your videos will they be too many? I use acid is at 50%

I think many things, if you should pause for a while with the MMS and retake supplements, if I stop right now that all symptoms are gone almost completely and I just have to keep taking the MMS to the overall improvement, if I can take supplements while squaring MMS times such as those containing vitamin C and antioxidants that are interfering with the MMS, and so I guessing all the time.

Do I still not completely cured just because it is also an ulcer and acid in the MMS does not let it cure?

How do you see MMS enemas?

So finally I encouraged to write and see if you can help me with advice, and become a witness to your book, that would fill me with pride and make me very happy.

Thank you so much before hand any information or assistance. May God bless you,

Germain

Translated from Spanish:

Jim Humble,

Good morning sir, I am Estuardo Vargas and I live in Ecuador, they gave me two bottles, one of mms and another one of an activator that I tell you that has left me as new. I am 45 years old and it hurt everything now after 10 days of taking it.

My mother-in-law’s afflictions that she has diabetes and cancer to the uterus, believe me that she has lowered the swelling this with appetite to my wife no longer it hurts nothing and my 3 year old son no longer has allergies his invention is amazing.

It will be possible to show me the formula, I know where to buy the 100-pound sodium chlorite powder, the citric acid, the distilled water, the labels I have with their stamp and their photo, the bottles are made of dark plastic with a dropper.

The friends, the families of the kids that I support here, I have a rehab program for gang kids and giving them this product calms their anxiety and depression, it’s amazing how their invention works.
I have been doing social work for 17 years, it is a way of giving my good faith back to society, since I have been using drugs for 17 years and having left the gangs.

From Jim Humble’s MMS Newsletter:

You may recall that our Minister of Health in Mexico, Kerri Rivera, has been ministering to over 400 autistic children by working with their mothers using the Church’s cleansing water (MMS) and the Church’s Sacraments. Kerri has developed a number of her own improvements to the sacraments which have made them more effective, one of which is that:

Her mothers have been giving the drops for more than the 8 or 10 hours suggested in the sacraments. This seems to have an even better effect. You might be interested to know that Kerri is now working with more than 1000 mothers and all the children are getting good results. The treatment has been extended to ADD, ADHD, and Asperger’s Syndrome. The results throughout the world are fantastic. Kerri said that it would be alright to give you her email address so here it is: kerririvera@yahoo.com

…my grandfather is 59 with cancer. He was given less than 1 week to live. That was 3 months ago.

He was skin and bones, could barely talk, barely walk, barely eat (no solid foods), was in constant agonizing pain, and his kidneys were clogged with extremely high levels of creatinine (1000+). The normal creatinine level is 117. In 4 weeks (1 month) of using a Rife machine and MMS almost daily, his kidneys returned to normal. He gained weight, talks normal, walks steadily, even climbs stairs multiple times a day, eats like a horse (good healthy foods) and has only occasion pain which is relieved immediately using DMSO.

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