Category: Toxicity

MMS used to treat malaria in African villages

Categories: , ,
November 27, 2011

I personally know a group of people who go to africa every year, freeing water from underground mines to make availble to african villages, and they also give mms to every person they meet who has malaria, they say most people get cured just like that.

I dont belive MMS is a miracle cure for everything. But it sure works for malaria. Maybe it works only as an anti-protozoan agent, maybe it only works against some germs. But it does work.

The End.


My experience with Miracle Mineral Solution MMS - Day 7

Michelle
November 23, 2011

Transcript:

Hi I’m Michelle and I have been taking the product MMS Miracle Mineral Solution and actually I think the name has changed to Master Mineral Solution.

For seven days I’ve been taking it. I’ve been taking three drops an hour and that’s the one-to-one ratio.

What else? Let’s see. I’ve had a little diarrhea, a little nausea, but mostly I haven’t had any issues.

I do feel like I have a little bit of energy compared to normal, but at the same time I, especially at night and in the morning, I feel sick, like kind of like a cold, respiratory type cold. I don’t know if that’s to do with the MMS, but I do feel a little more energy and I have noticed that my skin is clearer.

So that’s nice. I’ve actually been making a small solution and wiping it on my face, you know, a couple times a day and if my skin gets too dry then I’ll skip a day.

So as of now things have been going great.

I’m going, actually today I’m trying a new way. I’m going to do, raise the amount of drops every hour. So the first hour today I took three drops and I just took my second hour of drops and that’s four drops. So I’ll just increase it hourly for eight hours or ten hours, somewhere around there.

The only issue that I am having is the eating thing. You’re not supposed to eat with it. It’s supposed to be like an hour or two hour window when you’re eating and so it’s really hard when you’re on the protocol of taking it all day to be able to eat.

Because I think that some of the food kind of deactivates, or not necessarily deactivates, but the MMS attacks the food instead of the pathogens in your body.

So anyways, like I said, that’s about my only issue right now.

I will check back in with you as soon as I get a chance and I will keep you updated.

Thanks. Bye.


MMS use associated with reduced pain and redness in breast cancer survivor

November 14, 2011

I am a girl of 40 years, I was diagnosed with breast cancer 3 years ago, I have echo chemotherapy, 2 times, radiation therapy and also twice removed quirurgucamente me. three years after my oncologist told me that there was more to do, just give me chemo podtrian to stop the disease, I would stay for 4 to 5 years. you can imagine my state of mind, on the floor started looking for my mother that I could heal and found mms, I started using it recently as 12 days, the 4 day gave me a kind of redness in the area where assume that this, plus a rash something suspicious, I thought immediately that something was pasandon in my body, fill me with joy and hope again. gradually disappeared pain and inflammation, giving just a little rash and disappearing. I started taking 5 drops, vomiting alprincipio much thought I would die, but never worse than when I got the chemo, lower the dose to three drops every hour for 8 hours, now takes 6 drops MMS1, and three capsules MSS2, I hope to increase the dose of the capsules, but are still very heavy patra me. I know I am healing, I have no pain or swelling, the redness is disappearing, I just hope that every day is better and actually be able to live more years. have more news when it publishes, but since I already know I found the cure for the animal that had died and that eta ¡¡¡¡¡


Bladder infections resolved after switching to MMS treatment

November 8, 2011

08.11.11 – constant bladder infections

I had 13 months continuous bladder infections again and again bacteria still cause pain, it was terrible. Both of the family doctor as well as several varieties of urologists, I got the antibiotic, including a 6-week duration of therapy. In addition to various side effects I had little success when things “well” ran, I had 2 weeks of rest, then went the whole process starts over again. Even an inpatient hospital stay did (again, except much antibiotic) had not, after 2 weeks I have the same germs back to where I was treated. I was in despair ….

Then I found out about MMS, I have the book immediately MMS – worried the breakthrough, and read immediately thereafter started with MMS. It was mid-August 2011, I have taken since then NO more antibiotics, my urine test strips were okay and the pain continued to improve. I started with 3 X 1 drop per day, then increased to 1 drop every hour and then slowly increased to 3 drops every hour. I have kept 3 weeks and then reduced again slowly. Meanwhile, I am with 2 X 3 drops per day and this will take a maintenance dose to prevent continued. I can take a drop of good, except one had mild diarrhea, no side effects.

I can not tell you how glad I am to have come to MMS, for me it was the end of an ordeal.

Many thanks to Jim Humble, that he has passed on this knowledge.


HIV-positive individual uses MMS supplements alongside discontinued ARVs to

November 1, 2011

I am also in my 3rd week of doing both MMS 1 and MMS 2. In general I have been doing protocol 1000…but as of 4th week I very frequently take a 9th, and 10th dose of MMS1. I started MMS2 in the 4th week (4 times a day every 2 hours) there too I will occasionally take a 5th dose, just before bed. I am awaiting several lab results and should have lots of info to post on Nov 9th…which I will gladly share. (forgot to mention this is to treat HIV) i stopped all ARV’s on Sep 25, 2011. The same day I began MMS. Before starting MMS my VL was undetectable and my cd4 was 550… I got blood work done 10 days into MMS and also again 28 days on MMS…. i will have both results on Nov 9th…the day i see my doctor and admit that Ive stopped the ARV’s and trying an alternative thherapy…. I will keep you all posted. I am aware my results may be worse at first…i will stick with this for a while longer….in another month as I continue protocol 1000 along with MMS2 anf if my results do not show signigficant improvement I will decide to go back on ARV’s … My decision to stop ARV’s is because I fear the long term toxicity on liver and kidneys etc…. But if MMS doesnt improve my results then at least I was willing to try something unconventional, and will go back on meds hoping that I have not suddenly become resistant to them. i did not have any bad side effects in the 2 years on ARV’s …again my decision to try MMS is just to see if it really works and because of my concerns over long term use of ARV’s…only been on the meds 2 yrs….6 years HIV+

thanks!

{Later the same day…}

Im looking for the same or similar results without having to spend a lifetime of taking 3 different powerful medications every single day forever that are practically certain to eventually kill me through eventual liver or kidney disease.

Im also seeking truth, I have no difficulty beleiving that the 1800$ per month for my medications (that luckily government here pays for entirely) keeps making many companies richer and richer as the users health slowly but surely declines. I want to know if its true that possible cures and remedies are witheld from us so as to continue to accomodate pharmaceutical companies…when there are indeed much cheaper remedies.

I am willing to take the risk just to find out the truth.

{11/2/11}

I’ve lived in Toronto before moving to Calgary…but am from Montreal originally, spent my first 33 years there. I am staying the course but some days i have a hard time swallowing the mms…also tired of the taste…i wish there were pre-made 3 – drop gel caps or something… With all that i have read about mms and hiv in Jim’s words…i should be completely rid of it after 6 weeks of 8-10 hourly 3-drop doese plus 3 weeks of 4-5 Mms2 capsules taken 2 hours apart….the mms 2 is hard on empty stomach….can occasionally give a full body chill and burp up chlorine! Which is why it should work,… Will keep you posted, ill have a total of 3 results on Nov 9th…one pre- MMS and 2 on MMS at 10 days and 28 days….i think i will continue mms for 4 more weeks after nov 9th…if my results arent perfect after that, then Ive had enough…especially since it was originally stated that 3 weeks would be enough…and then combining mms2 is supposed to even bring back hiv negative results, which puzzles me because supposedly antibodies stay with you forever….there is some confusing info out there for sure…even statements directly posted by Jim leave me a little perplexed…. But i continue with my leap of faith hoping that this just might actually work…. Cheers!


Ulcer width reduced after 24 hours of MMS1 application

Categories: ,
October 25, 2011

…I’ve been spraying MMS1 on the [diabetic] ulcer now for about 24 hours and I am seeing miraculous results already. Where there was a gaping hole about 1 inch in diameter, I now have more of what I would describe as a slit, about half as wide. It was never painful because I had a stroke that has left almost no sensation in that foot – luckily. I’m going to try and document the healing as it happens with pictures, if I can get my phone camera to work. MMS is AMAZING!!!


A Long and Interesting Testimonial

October 16, 2011

I began protocol 1000 for HIV on Friday. This will be my third day. I have been following the protocol closely, although I may have eaten too soon before doing a dose at dinner time the first day. I am seeing in the FORUM that it is advisable to wait at least 30 minutes after a meal. Jim says to eat an apple though if nausea occurs.

I began with 1 drop the first 2 hours. Then went to 2 drops the next hour. By the 4th hour, I was up to 3 drops with no nausea. Haven’t had any effects at all yet, going into my third day. The doses turn yellow and have a strong chlorine odor, even after mixing with juice. I am mixing it with organic apple juice, no ascorbic acid added. The first 5 doses, I used a drink called NAKED, a green mix with spirullina and other greens. No ascorbic acid in that juice either, so I believe that I am following the protocol correctly. Perhaps the NAKED juice neutralized the mix? Clyde told me that he was using that brand of juice so I assumed it was alright.

I was just expecting some reaction but none so far. Keep in mind that I did complete a 5 day colon detox a week ago. I am taking my ARVS about an hour or more either before or after the doses. I will do a MMS bath this evening. Any comments or other suggestions?

I was planning on doing the protocol as Jim suggests. 3 weeks then maintenance dosing. You are saying here that it has taken ’40 odd days, 3-4 months for others.

I am not sure at this point just how long I should continue with the protocol as I am not ‘sick.’ Everyone says to do the protocol until you are well. That isn’t going to work for me as I really have no sick feelings from HIV. Just some stomach bloating and spleen swelling from the ARVs. I feel pretty good actually. Not at all like the people that you have been treating there with HIV who are most likely in pretty bad shape.

So, do you suggest that I do 3 weeks (including bath protocol when I can) and then maintenance doses every day (4-6 drops a day all at once, as Jim suggests in his book) and then wait several months to get lab work done and see how it goes? Keeping in mind that I am still taking the ARVs. Thanks.

{10/16/11}

…I just had lab work done (both CD4 and VL) last Friday. Began the protocol that afternoon. Will get lab work again sometime the end of January or beginning of February…doctor’s request. I am hoping that by then the protocol will have boosted my CD4 count. It’s around 400 right now. And perhaps, hopefully, the spike in VL from the MMS will have leveled off a bit so the test results don’t freak the doctor out too badly. HA!…

{10/23/11}

Just finished my 10th day. So far, I have had no adverse side effects to the protocol whatsoever. I am consuming the MMS1 drops with organic apple juice, as it has nothing added. The taste is like drinking apple cider from a glass that was washed and not rinsed out very well…kind of a ‘soapy’ tangy taste. Not bad at all.

I haven’t experienced fatigue but I am sleeping better…it’s a deeper and longer sleep period, which is good because I am usually awake after about 4 hours and then can’t go back to sleep. My Acupuncturist says that’s a liver issue. It’s getting better. Drinking water after every dose as well. Peeing a lot! Also taking extra vitamin C, my multivitamin and a couple of antioxidant supplements a couple of hours after my final dose.

It’s sometimes hard to get a dose in every 60 minutes, particularly at work. However, I am not concerned, Jim has said to back off and actually stop taking a dose if you have nausea, etc., so, I don’t think it will hurt if I miss a dose by an hour occasionally. I am trying very hard to stay with it on an hourly basis, however. I have also gone to as much as 10 doses in one day a couple of times and I am also taking a bath with MMS1 2-3 times a week.

My appetite has increased, although it wasn’t poor anyway.

The protocol is going well. I am still taking the ARVs. As I was not sick before, I’m not seeing any improvements other than those listed above. Having faith that MMS1 is destroying the HIV in my body.

{10/26/11}

Finished my 13th day on p1000 today. Took 1200mg of vitamin C last night before bed, along with NAC, ALA and a multivitamin and extra magnesium and calcium. Woke up during the night with mild diarrhea. When I got up for work I had wicked diarrhea. Mostly water. Not sure if it was caused by the MMS or Vitamin C or a combination of both. At any rate, I got rid of some stuff.

Getting sleepy throughout the day. Taking MMS1 hourly at work and really do have a difficult time staying awake at times. It’s hard to get out of bed each morning. Feel like I could sleep in. Sometimes I have a mild fever off and on during the night (sweats), as well as some fast heart rate at times. Some minor lightheadedness at times. Things are moving right along. HA!

Have an appt. with my physician on 11/3. That will be the last day of my 3rd week on the protocol. Will see what my lab work is like that was done the morning of the day I began the protocol. Expecting VL to be undetectable and CD4 above 400 as it has been for months. Cheers!

{11/5/11}

I’m on the third day of my 4th week. Will finish the week and then go to maintenance doses daily. I am also taking Kalonji oil twice a day, as well as adding DMSO to my doses and taking MMS/DMSO baths. I must say that either the DMSO or the Kalonji Oil, or both, are really helping with some of the side effects of the ARVs, which I am still taking. My stomach has been severely bloated and hard forever it seems. Direct effect of the ARVs. The protocol that I am on is helping with that and I am not having diarrhea but 2-3 good healthy bowel movements daily. I find it difficult to pace the doses around eating, so I haven’t really worried about it too much. Staying away from Vitamin C as much as I can…and powerful antioxidants, until a couple of hours after my last daily dose. Also doing extra doses some days. Taking extra C and antioxidants along with vitamins as well after the last dose for the day. Have an acupuncture appt. on Monday. Will treat to move toxins out of the liver and spleen, etc. He is anxious to see how the protocol has affected me from his viewpoint.

Had my appt. with my ID specialist on Thursday. My lab work, which was taken hours before I started the p1000, was good. CD4 counts had gone down a bit…down to 276 from 320 or so. About 12%. Percentage is about the same as it has been and the doc was not very concerned. He knows that the CD4s can go up and down even hourly. He seems to swear by the VL test though.

My VL is tested with the latest PCR test, which can measure as low as 20 ppm. I believe that anything below 50 ppm is considered undetectable. My VL is 21 ppm. HA! So, is that 21 ppm of antibodies to HIV and other viruses? Doesn’t sound like my body is having to put up a fight against HIV does it? Keep in mind that these results were taken prior to MMS consumption. Makes me think that whoever interpreted the results just didn’t want me to be below the 20 ppm mark so listed it as 1 ppm over the minimum that the test can measure.

I also wonder if I had gone to get an Elisa and Western Blot test before starting the p1000, if I would have tested negative. You betcha!

So, if the protocol is killing all pathogens, then once the VL spikes and the blood is cleared of it all, I should really show up below that 20 ppm level. Makes me wonder though…if the PCR test is finding other things than just the illusive HIV, then I am obviously pretty clean of anything it seems. My liver and platelets are fine. Blood pressure a little high. 140 over 80. Not that out of range for me. The Kalonji oil might help with that.

My next lab work is scheduled for the middle of February. That will give me 3 months between the protocol and the lab work. I will continue to take Kalonji oil daily until I run out…about a month. Still on the ARVs and wondering if they are affecting the outcome of the protocol at all. Guess I will find out. If the MMS is actually neutralizing the ARVs, they shouldn’t be doing anything, right? Jim said that to stay on the ARVs, one needs to continue with the p1000 to neutralize them.

Will see how my next lab work goes. I didn’t tell the doctor what I am up to. Waiting until the next visit the end of February. Expecting my lab results to still be ‘off’ but hopefully not too bad. Keeping the faith.

{11/8/11}

Day 5 of my 4th week on protocol 1000. Although I don’t really find the taste that bad with apple juice, I am getting tired of it.

Had my acupuncture treatment yesterday. This form of Oriental Medicine puts special emphasis on the science and art of pulse diagnosis. Contemporary Pulse Diagnosis®, based on the work of John HF Shen, OMD and further developed by Leon Hammer, MD, provides the foundation for an in depth diagnosis and for preventative medicine.

Pulse diagnosis is an exquisite and sophisticated means of understanding the whole person. The pulse reveals the patient’s constitution, previous illnesses, early insults to normal physiology, environmental stressors, trauma, lifestyle, emotions and behavior. Pulse diagnosis can also predict possible future pathologies with accuracy. This allows the practitioner to address the patient’s unique situation rather than a pattern, disease, or Causative Factor. This school is currently the only one in the United States teaching this sensitive and subtle skill. I am finding it very interesting.

The acupuncturist made the comment when doing my pulse that my liver and kidneys were not very happy. This was the first visit that I have had since on the MMS. He saw quite a few conditions/diagnosis that he had never seen in me before. He was concerned that the MMS might be rough on my liver/kidney and spleen. I thought that it might also be the DMSO. However, he is very excited that I am doing the protocol and has a few friends who are also HIV+ that he has told them about my journey. They are all interested in learning more and he wants to get a group together to discuss it. Great!

Two more days on p1000 and then I move to maintenance doses daily for a while. Will see how I am feeling. I only got about 4-5 hours of sleep the last two nights…computer virus that was a real problem. Had to finally get Microsoft technicians to spend about 7 hours on it. I am pretty burned out today. I am experiencing a slight headache. Could be from the acupuncture treatment as he really got my blood and energy moving in my liver/spleen/kidneys and stomach…helping to release some more of the toxins. Onward! Cheers!

{11/20/11}

Well friends, after doing 4 full weeks of protocol 1000 plus using DMSO at times, particularly in bath therapy, and beginning and continuing a maintenance protocol for going on 2 weeks, I have mustered the courage to stop taking my ARVs. Whew! I admit, it is a scary thing that I do! Almost as frightening as having to tell the doc!

I decided to write a lengthy letter to my doctor, disclosing my decision, (‘disclosing’ is a touchy issue with the HIV diagnosis, eh!?) rather than wait until my next appt. in late February. There are several reasons for doing it this way:

1. I am a coward. (I just didn’t think that I could deal with a face to face argument about it at this point but I am pretty certain that will come in February, if not before.)

2. I wanted to direct him to information on the Internet that he can study over the next couple of months, including the Reappraising AIDS channel on You Tube. I discovered it myself today and I think that he will find it very enlightening. All of the really juicy videos, including the latest documentary called “House of Numbers’ and extended interviews with the participants, is there. I also linked him to the Alberta Reappraising HIV web site, which has a ton of information, as well as a huge list of ‘re- appraisers’, many who are in the medical and scientific field.

3. After getting a response to questions about ARVs from Rev. Jordan on the Forum, and viewing some of the documentary videos on the internet, I realized that it was time to make a decision to go for the whole enchilada, so to speak, and stop poisoning myself, whatever the outcome. I can’t wait until February.

In my letter to my doctor, I stated that it is against everything that I know to be true to poison my body in an attempt to heal it. I told him that my decision is a final one and that if for no other reason, he should do his own research into the reappraisal theories to see what a scam the HIV industry has become. I told him that the medical establishment needs to realize that they have a lot of PR to do to save any credibility that they have as far as HIV=AIDS goes. More and more people are going to hear about the ‘other side’ of the HIV hypothesis and will see their theory for what it is…full of holes.

and so it goes. As of today, I am ARV free!! Cheers!

{1/21/12}

…I am doing really well…my stomach and spleen are healing slowly from being off of the ARVs. I haven’t spoken to my doctor but my case manager for AIDS has been very supportive of my decision.

I am still taking daily maintenance doses of MMS-6 drops activated twice a day. I am supposed to get lab work done the end of January in preparation for my doctor visit in late February. Haven’t had any done since doing the MMS.

I feel good…

{1/25/12}

DV, welcome to the Forum. I was diagnosed poz in 2000. Was generally healthy until I stopped ARVs in 2007 for 18 months. Came down with what was diagnosed as Encephalitis caused by Toxoplasmosis and was treated with malarial drugs for 9 months and also put back on the ARVs. That was about 3 years ago. I discovered MMS last Fall and began the protocol 1000 in October. Did that for 5 weeks then moved to a rather heavy maintenance dose (6 drops twice a day), which I am still taking daily. I also did 3 separate Malarial protocols after I completed the p1000. My main concern, believe it or not, is the Toxo, not HIV. Toxoplasmosis almost killed me and I don’t want to go through those migraine headaches/nausea/loss of equilibrium ever again.

I have not had any blood work done since around September, prior to my taking MMS, but I discontinued taking all meds around Thanksgiving. Notified my doctor that I was not taking the drugs again. Haven’t heard from him but I am pretty certain that he is concerned.

Just wanted to say welcome. I have been posting my journey and progress on this forum thread all along, if you are interested in reading it.

How do I feel? Pretty good. The protocol was easy…no adverse effects throughout the entire 5 weeks. I did get diarrhea from doing the Malaria protocol (15 drops twice, an hour apart), and passed some parasites (Toxoplasmosis?). The maintenance dosage twice a day is for the Toxo, as parasites can be difficult to get rid of. Bishop Humble personally told me that I have done more than enough of the protocols and that the ‘bugs’ should be all gone by now. I hope so.

Keep in mind that the Viral Load tests are monitoring ‘antigens or antibodies’ that your body has created, not the HIV itself. So, you will probably always have antigens for a slew of pathogens in your bloodstream. According to the AIDS Rethinkers, the Viral Load tests are not specific for HIV but also detect many other proteins and antigens to many things, ie, flu, etc. So, one may not ever test “Negative’. It is interesting to me though that my VL tests have been ‘undetectable’ for almost 3 years. Still not quite sure how that works, unless the ARVs have been killing off all pathogens in my body. ?

So, best of luck, keep the faith and feel free to privately email me if you want. I will try to answer any questions that I can. David Kiango on the Forum has been a great help to me with advice and an awesome ‘cheering section!’

Terry

{2/2/12}

Just want to let you know that I am doing well. Still receiving acupuncture biweekly. The school has done an extensive diagnostic protocol for me so that they can administer the best treatment. Things should begin to be more beneficial now. Last Friday, when they did my pulsing to diagnose my current condition, they were freaking out because they said that the ARVS had been ‘taking over my immune system’ and now that I have not been taking them since mid November, my pulsing was finally showing a much different situation…they said that I am now ‘on my own.’ My immune system is kicking in without the help of the meds and they could really see a difference in my pulses. Of course, they are checking pulses of heart rate, but also CHI, organs, and other things. They were very excited to see the change and amazed that it was so pronounced.

I get my lab work done tomorrow, I guess. Will be the first lab work since I began my journey off the meds and using MMS. Time has gone by very quickly since I first made contact with you and started my healing process with MMS back around early October. Thanks again!

I will post my lab results, although I am not really that concerned about them…looking more at the CD4 count than a VL. My hope is that MMS will have cleared out all pathogens and sent them on their way to pathogen ‘heaven.’ I still have not spoken to my doctor but will see him the end of February.

Juicing organic fruits and veggies every day, as well as still taking a maintenance dose (6 drops of activated MMS) twice daily for now. Waiting to see what the cd4 count looks like and then perhaps drop down to once every day or two. I turned 60 my last birthday and with my weakened immune system from taking ARVs, it seemed like a good idea to take the twice daily dose for a while. I am also doing Reiki self treatments, which really helps me, spiritually, as well as physically and mentally.

By the way, Bishop Jim wrote a personal email to me, saying that I had done plenty of MMS protocols for the HIV and the Toxoplasmosis and should have cleared out all the bugs by now. Just stay on the maintenance dose to keep any bugs away.

Cheers, my friend. Terry

{2/8/12}

Well, today I got a call from my drs. office. I was told that they had received my lab work (done last Friday) and they were confused why they got it.

Apparently, the dr. decided to drop me as his patient back in December when he got my lengthy letter telling him that I had gone off the ARVs. Apparently, his assistant was supposed to tell me this back then but never got in touch. She said today that she thought I knew about it already. Thus the confusion over why they got lab work.

So, all I know is what she told me. Apparently, he feels that there isn’t any sense in remaining my physician if I am not going to follow his advice and take the ARVs. Guess I was hoping that he would be compassionate enough to want to continue to monitor my health on my terms. NOT.

And I like the guy. Oh well. His choice. I still have my primary care physician to fall back on if I need medical care so I am not concerned. Just sort of wondering if I would be denied serious medical care if I refused to take the meds.

Feeling good. Still seeing the Oriental Medicine MD every two weeks or so.

So, I gave up the meds and now I am giving up the man who prescribed them to me every month for the last 2 years. HA! Kind of funny actually. Another part of the healing process.

I will report my lab results when I get them. Mainly interested in the CD4 count. The doctor’s asst. is mailing them to me. At any rate, I am feeling much better off of those toxic killers.

Cheers!

{2/10/12}

Ok, so I got my lab results back from the doc yesterday.

These dang things are almost impossible to understand but if I am reading it correctly (the doctor actually wrote some figures from the last result to show the difference,) my CD4 count is only 79, gone down from 231 the last time (which was before I started the MMS.

A question: If the ARVs were keeping whatever the VL tests were finding down to an undetectable level and then, once stopping the ARVs, that level goes back up, what is the VL test finding/monitoring? My viral load was undetectable before, like 21. Now it is over 400,000. I’m confused.

The thing is, Jim and David have both said that the VL will shoot up after the protocol and that a person needs to wait at least 3 months before getting any blood work or they would be disappointed. I didn’t really have that choice if I was going to ‘follow the doctor’s orders’ as he wanted me to get them done before seeing me the end of February. It was about 2 1/2 months and I am still on a maintenance dose of MMS.

Turns out that life took a turn, as noted in my earlier post. Not sure if or when I will be getting lab work again as he will no longer be my physician. Anyway, just told everyone here that I would post the results when I got them, so here they are.

Truth be told, I am feeling fine and I did so for over a year the last time I stopped taking the ARVs. Of course, that time I didn’t have MMS to support me or remove the virus…and for whatever reason, the Toxoplasmosis almost killed me.

I’m a little concerned (not much, mind you) that the CD4 count went down so low. I thought that it should be going up with the MMS protocol and the healthy diet, juicing, black seed oil, etc. Any comments?


Erysipelas improved after using MMS alongside standard treatment

October 4, 2011

04:10:11 – open legs and erysipelas

About 1 1/2 years my suffering began, legs open.

Through my GP I got the best dressings, ointments and Disinfektionsmittel to clean the wounds. To drain the legs H2O pills. However, it was getting worse and it caught fire, too. In pain I came to the hospital, where I got professional help and the wounds are closed, the inflammation decreased by ingestion of antibiotics by drip. After my discharge from the hospital had to be connected to another and the legs are compressed. To evil, I got another erysipelas which extended from the left toe to thigh. Now I should be hospitalized in order to once again re-treated with antibiotics. Now I decided since I had already made ​​good experiences with MMS in small things, this is also taken daily at a dose of 15 drops 3 times. After only two days back, the inflammation began to walk.

After 10 days, you had already holds off, I was able to reduce the dose to 5 drops, and my wounds have disappeared almost completely.

In my Umferld I’ve talked about MMS and could also help some people who even then ordered the MMS.

For example, bladder infections, surgical wounds, infections and much more.

I am glad to have such an effective way and thank Jim for Huble devoted work.

With warm regards, WS


FYI: Old Protocols


In the early days of MMS, a common protocol involved taking a 15-drop dose 3 times a day.  This has long since been improved in various ways.  Some of the older testimonials will talk about these 15-drop doses. Overall today it is not suggested to take such large doses in one shot, but rather much lower doses and on an hourly basis—which provides a more gentle and steady approach. Full details on how to properly use the various protocols can be found in the MMS Health Recovery Guidebook.
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