question-circle Latest thoughts on Lyme and MMS1/MMS2/DMSO/CDS protocols ?

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22 Aug 2013 22:38 #35524 by MartyW
Many Thanks edga.

I did look into Rife machines a year or so ago, and after doing quite a bit of research, I finally realized I didn't have enough knowledge to make an educated purchase. But I'm still very interested in them and I'd love to know of one that I could trust and afford. They seemed to range in price all the way from less than $500 on the low end to many thousands on the high end. I was afraid of getting a cheapie that might not have the frequency generators working exactly right. I also saw that some machines had hand contacts only, while others had contacts for hands and feet, while others had uv connections for multiple accessories and those were sooooo expensive.

Could you possibly offer some specifics on the one that you purchased?

Many thanks again,
Marty

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25 Aug 2013 02:55 #35566 by Archer
I was watching a documentary online about Lyme Disease - it had nothing to do with MMS

BUT at the very end of the documentary the researcher finds that Lyme protects itself by creating a biofilm and then hiding inside of that protective film.

Which means antibiotics can't kill all the Lyme at the same time because some of them hide in their protective shields.

Now the interesting thing is if you look at water treatment systems that use the same chemicals used to make MMS one of the things they talk about is how good it is at breaking down biofilms.

I believe it is this ability of MMS to break down bio-films why MMS works in some situations where antibiotics fail.

This is also the reason I think it is very important to regularly clean out your sinuses with MMS / Salt Water - I believe harmful bacteria hide out in your sinuses.
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28 Nov 2013 20:33 - 28 Nov 2013 20:39 #37664 by Arrow
Marty, I was diagnosed with Lyme in October. I have not been using MMS due to my aversion to the smell and taste.

I started out with a dark field live blood analysis which showed lyme cysts. I treated with a colloidal silver called nutriasilver and also did LDM-100 to boost my immune system. Both of these I took 3 times a day. One hour before taking them I took the enzymes, but also added serrapeptase and nattokinase to work on the cyst. After 7 weeks of treatment I had another dark field microscopic analysis done and no cysts were found and candida was also greatly reduced. From 3 to 4 cysts per photo to none.

I still have to work on other parasites as it seems what I took didnt bother them much, nor did it really get to the bartonella and babesia. I also have used a rife machine daily. Im getting a better rife machine soon so that I can target in better on these other microbes better than the machinee that I have.

I will probably conitnue with the lyme protocol for several more months at least for there is no way to know if it is fully gone. I do feel quite bit better. You also have to do liver support and for some people kidney support and over all detox. My last blood work showed that I have a stressed out liver right now so Im working on that. Look into the Cowdern Protocol and nutramedix products.

I am finding more positive testimonials in the use of MMS for lyme, but no one is spelling out its effectiveness or not for the co-infections.

For cutting edge updates in Alternative Medicine visit www.HealthSalon.org
Last edit: 28 Nov 2013 20:39 by Arrow.

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23 Dec 2013 02:40 #38024 by FightInMe
I was tested through quest diagnostics a few weeks back for lime. They used the western blot test. As I have read it is difficult to diagnose so I will take it a step further and tomorrow be getting tested through IgeneX. They are a lyme specific lab that has been touted by many as the best in the US.

Im suspecting I may have lyme. I have been on MMS 2000 for almost 3 months. Doing baths, enemas daily. I also did a full round of humaworm with MMS.

I had a parrazapper machine that I unfortunately broke since I was advised to do a sea salt bath zap. The machine fell in the tub :( The GB4000 rife is in the 2,000 range, verrrry expensive. Any further information on how your wife did?

Arrow! I have read through your friends lyme protocol through Dr. West and have ordered the enzymes and will begin this protocol shortly.


Anyone have any experience with IgeneX lab and getting properly diagnosed? Or any further advice....


Scott

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23 Dec 2013 09:56 #38033 by masoomi
Hi
I also have lyme problem many years , i am using mms from 2007 , and now i am in parasite protocol for few months .

i have himalaya salt and Dr clark Zapper for 5 years . I have plan for collidal silver from Dr clark shop . I read all ur posted .

PLS put me in ur advise also .

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28 Dec 2013 02:12 #38115 by Parino
My nine year old son was diagnosed with Lyme and Hemslae Bartonella. We have purchased a GB4000. Can you give me the channels or frequencies your wife used and for how long? Thanks so much. Ann

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12 Jan 2014 10:30 #38611 by FightInMe
Edga-

Im hoping you can chime back in on your wifes experience with the gb4000 rife machine. I have seen it has been efective but have also seen the coil machine being effective.

Im sure many people would like to hear more information on your wifes success. Did she use mms as well, was she diagnosed with co-infections, how long did she use the rife gb 40000 for??

Arrow-

You seem to have a wealth of knowledge to share lets use this as a thread to keep updates on. Im using the marcozyme with MMS protocol that you have shared from Dr. West.

My Igenex results came back and Im waiting to get them interpreted by a professional. Doesnt look good though. My MD claimed its negative then had them faxed to me only to see positive on IGG and IGM western blot from genex standards but negative on both for CDC standards. I tested negative on Quests Diagnostics Western Blot one month ago.

I will update you guys next week on those results. In the meantime Im going on 3 1/2 months of protocol 2000 with baths (MMS2 or MMS1 w/ dmso) and enemas. Im at 10-12 drops per hour.
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12 Jan 2014 22:10 #38627 by FightInMe
PLEASE let me know the protocol your wife used Ed. I have read others having success with this rife machine.

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12 Jan 2014 23:27 #38630 by pam
Edga has not been on the forum since 9/2013 - my guess is that he's not going to get the requests for additional information.
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13 Jan 2014 00:05 #38631 by FightInMe
Pam- This was my original thought.

I did a reply to his original comment this second time hoping the would receive the request via email.

After years of health problems at a young age I have cornered my invisible opponent to lyme. I have to await a conformation through a professional but all signs are pointing so. :(

MMS will be a weapon against it for me, as I will not use antibiotics. The abx will just create more biofilm and cysts while mms will do just the opposite.

Pam- I have read a few testimonials on this site with the use of mms for lyme. Anything else you have heard through the years in regards to lyme and mms? or even rife for that matter?

thanks as always.

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