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MMS and Chronic Lymes 27 Dec 2011 18:24 #9612

  • Bobbie
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Hi All,

I've been diagnosed with chronic lymes. In Jim's directions he states over and over that only take as many drop of MMS so that you don't get sick, with nausea, pain, etc.

The lyme spirochete releases it's toxins into the body when it dies off, causing pain and nausea.

I recently was taking the protocol that required hourly doses of MMS for eight hours. I worked my way up to 10 drops every hour for eight hours, this was over the course of 2 weeks. During this period there was a lot of pain and nausea. I backed off when I realized the body needed a break and I wanted to feel good for Christmas.

Is it possible to cure this condition without experiening the affects of the die off?

My heart goes out to anyone that has this terrible disease.

God Bless All,
Bobbie
The following user(s) said Thank You: Michael Harrah

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Re: MMS and Chronic Lymes 27 Dec 2011 20:13 #9615

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Bobbie, I think it is possible, you just need to keep the dosing down to the level where you don't have a herx reaction. The die-off is going to occur, but the body can remove a certain level of toxins without throwing the system into a herx reaction. That's the level you want to be at. Once a certain amount of die off occurs, you may be able to ramp up further.

Do you have his newest book? He goes into lymes fairly thoroughly, I thought. He may even have the same data on his www.jimhumble.biz website.

Good luck!

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Re: MMS and Chronic Lymes 27 Dec 2011 20:39 #9618

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Thanks so much Pam. I do have his new book but he didn't address this particular subject pertaining to Lymes, at least not in the Lyme section.
Bobbie

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Re: MMS and Chronic Lymes 27 Dec 2011 21:42 #9619

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Maybe because the herxheimer reaction is so endemic to all the protocols?

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Re: MMS and Chronic Lymes 27 Dec 2011 23:06 #9621

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That's what I didn't know. Thanks for educating me.

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Re: MMS and Chronic Lymes 28 Dec 2011 00:29 #9624

  • Michael Harrah
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Hi Bobbie,

You can try different things to see if there is less herx. I had such bad nausea on MMS1 that I could not even take 1 drop an hour. But when I added the DMSO according to protocol 1000+ then it completely eliminated the nausea. Maybe adding DMSO will change things for you.

Also, now that I have CDS, it has eliminated the nausea/diarrhea problems I had with MMS1 & 2. Trying CDS could make a big difference for you. Or combining CDS with MMS1 and/or DMSO also. There are many things to try.

MMS2 may also be easier on you if you have not tried that.

Jim does say about Lyme that it takes a lot of MMS and persistence. This is the situation I am in also, and all these new approaches have been very helpful for me.

Michael

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Re: MMS and Chronic Lymes 28 Dec 2011 00:58 #9625

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Thank you Michael. I'm not familiar with the CDS. Is there a website where I can purchase it?

Also I've been a little hesitant about taking the DMSO internally, not knowing how much to take.

I appreciate your feedback!
Bobbie

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Re: MMS and Chronic Lymes 28 Dec 2011 20:38 #9648

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Hi Bobbie,

CDS is chlorine dioxide solution, the new type of MMS recommended by Jim in his recent newsletters and he has made a couple videos about it now. The latest one
.

You can buy it from Steve at keavyscorner.com/index.php?main_page=index&cPath=73 or you can email me (see my signature below) about it since I am providing it also. Steve is in Floriday and I am in Arizona, so whichever one of us is close to you will be able to get it to you the quickest. We're both making the same thing and it has to be shipped via UPS ground.

The DMSO is something to try, you only use as many drops of DMSO as you are using of MMS in your dose. So it is not very much but it can make a big difference like it did for me. It is called protocol 1000+ jimhumble.biz/index.php?option=com_content&view=article&id=49&Itemid=72.

Michael

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