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Advice needed 31 Jul 2020 21:54 #65425

  • Georgie21
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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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Advice needed 01 Aug 2020 02:38 #65427

  • CLO2
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Advice needed 21 Feb 2021 20:07 #68020

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

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Advice needed 03 Jun 2021 22:47 #69271

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

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Advice needed 04 Jun 2021 03:19 #69276

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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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Advice needed 21 Nov 2021 13:17 #72653

  • Gandolfo
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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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