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TOPIC: Chronic Fatigue/ME/Fibromyalgia

Chronic Fatigue/ME/Fibromyalgia 24 Apr 2018 17:52 #58349

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I have had Chronic Epstein Barr Virus for 30+ years and have tried everything to get well. I discovered MMS online and thought I would give it a try. I am on the Protocol 1000 taking 1 drop 8 times a day and started the protocol about a week ago. I am confused about what/when I can eat. Does anything containing citric acid neutralize the MMS. Am I taking too much? My symptoms now are more exaggerated than before I started the protocol. Symptoms are brain fog, fatigue, nerve pain, mostly as the day progresses. I understand that the new protocol now uses HCL instead of citric acid to activate the MMS. Please help.
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Chronic Fatigue/ME/Fibromyalgia 24 Apr 2018 22:50 #58354

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Hi, vdol! Welcome to the forum. It sounds like you're doing the right thing. Understand that you're knocking off parasites and your systems have to remove the debris. As long as you're able to manage, keeep on , but if you find it's too much, cut the dose in half by sipping the 1 drop dose over 2 hours.
Sending you LOVE and HEALING as well!
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Chronic Fatigue/ME/Fibromyalgia 22 Feb 2019 13:46 #59824

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vdol52 wrote: I have had Chronic Epstein Barr Virus for 30+ years and have tried everything to get well. I discovered MMS online and thought I would give it a try. I am on the Protocol 1000 taking 1 drop 8 times a day and started the protocol about a week ago. I am confused about what/when I can eat. Does anything containing citric acid neutralize the MMS. Am I taking too much? My symptoms now are more exaggerated than before I started the protocol. Symptoms are brain fog, fatigue, nerve pain, mostly as the day progresses. I understand that the new protocol now uses HCL instead of citric acid to activate the MMS. Please help.


Dear vdol52, please let us know how you have found the MMS use and how it has affected your EBV
The mind is like a garden, if you do not cultivate it, you cannot harvest from it.

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