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Advice needed

Georgie21
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31 Jul 2020 21:54 #65425 by Georgie21

Advice needed was created by Georgie21

Hello all,
I hope someone may be able to help me in one way or another. I am here to try and find out more about mms and whether it could possible help out a family member who has been diagnosed with Parkinsons and Polycythemia Vera. I have come across Jim Humbles protocols but I am not sure which one would be best suited. Any help would be greatly appreciated.
Many thanks

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CLO2
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01 Aug 2020 02:38 #65427 by CLO2

Replied by CLO2 on topic Advice needed

MMS Health Recovery Guidebook

jimhumble.is/bookstore/mms-health-recovery-guidebook

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DonRaph
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21 Feb 2021 20:07 #68020 by DonRaph

Replied by DonRaph on topic Advice needed

Hi, my father also has Polycythemia Vera. Would you mind sharing the results of the treatment?

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KimAnnMc
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03 Jun 2021 22:47 #69271 by KimAnnMc

Replied by KimAnnMc on topic Advice needed

My husband is diagnosed with PV, as well. Just now becoming aware of MMS protocols...updates appreciated.

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CLO2
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04 Jun 2021 03:19 #69276 by CLO2

Replied by CLO2 on topic Advice needed

You could look into CDI (chlorine dioxide injection) protocol which is found in Andreas Kalcker's book, Forbidden Health, on pages 121, 166, 362, and on other pages. Use the search feature of your PDF file viewer to find all pages that mention CDI, which include testimonials.

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Gandolfo
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21 Nov 2021 13:17 #72653 by Gandolfo

Replied by Gandolfo on topic Advice needed

I have polycythemia Vera and am curious if any of you have had luck with mms. I’ve done the protocol 1000 and am now doing maintenance. My blood levels don’t seem affected much to my dismay. I do feel better on mms … more clear headed and more energy. Have you had success?

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