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Testimonials and Shared Experiences with MMS

A comprehensive listing of anecdotal reports of Wellness breakthroughs and results for use of MMS, MMS2, CDS, CDH etc, against different conditions.

For more MMS Testimonials: mmstestimonials.is

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Multiple Sclerosis (MS) and MMS 30 Oct 2019 08:40 #61605

Maria1 Offline New Member Posts: 1 Thank you received: 0	Thank you.. What is CDS? I have MS and im searching for cures
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Multiple Sclerosis (MS) and MMS 06 Feb 2020 22:40 #62372

Jenny_goodhealth Offline Junior Member Posts: 21 Thank you received: 3	Hi Melissa, How are you doing? Are you still taking MMS? Have you taken MMS2, any side effects? thx
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Multiple Sclerosis (MS) and MMS 07 Feb 2020 12:04 #62383

Jenny_goodhealth Offline Junior Member Posts: 21 Thank you received: 3	HAS ANYONE TAKEN MMS FOR LATE STAGE MS AND SUCCESSFUL REVERSED IT?
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Multiple Sclerosis (MS) and MMS 09 Feb 2020 08:27 #62395

Jenny_goodhealth Offline Junior Member Posts: 21 Thank you received: 3	HI MARIA, Our CDS product is a solution that contains the active chlorine dioxide molecule dissolved within a slightly saline base, with 2ml of CDS solution being equivalent to 1 drop of traditional MMS. (According to www.mms-supplement.com/buy-cds) duckduckgo.com/?q=cds+mms&t=h_&ia=web hope this helps.
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Multiple Sclerosis (MS) and MMS 23 Mar 2020 05:53 #63108

Buckhen
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New Member
Posts: 5
Thank you received: 1

Hi guys. I've just been researching mms properly for my personal use for this awful Covid 19 virus that's got us on lockdown. I'm a bit of a Q fan so came across the subject on Twitter then BOOOOOOM! WHAT A RESULT! Im seriously doubting that it can do what everybody swears it can?? On the other hand I'm furious we havent been told about mms before.

Anyways, My mother has MS she is 65. She was diagnosed 15y ago roughly. She is really, really struggling now and so is my father. . She is wheelchair bound and is beginning to loose short term memory and she can get a bit confused also? (Alzheimer's)??? I'm in the uk, and ust ordered some chlorine dioxide, www.ebay.co.uk/itm/264629879338
and some DMSO www.ebay.co.uk/itm/193211910657 just for me. There generic but 100% ok products. Then I found out about all the other diseases it can rid you off including MS. PEASE can anybody advise me what is best for my man? Is it too late for her? If not, what products are best and can we sort shipping?? Many thanks , Kevin.

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Multiple Sclerosis (MS) and MMS 23 Mar 2020 23:21 #63128

CLO2
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Administrator
Posts: 5555
Thank you received: 4390

Hi Kevin. What you really need at this point is Jim Humble's latest book and learn how to use MMS. If you have questions after reading the book, come back here and ask away!

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

The MMS and 4% HCL activator you purchased on eBay UK looks perfect! Wonder how long that seller will remain on eBay. Probably not long. Wonder if it will be delivered thru the postal service?

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Last edit: by CLO2.

Multiple Sclerosis (MS) and MMS 25 Mar 2020 08:29 #63188

Buckhen Offline New Member Posts: 5 Thank you received: 1	Thankyou so much. I've downloaded the book in pdf and just waiting for my products to be delivered. Theres a lot of people waking up to #mms. In fact theres a lot of people waking up to #q aswell. A lot of light in these dark days. Thanks again. I will post some updates if everything goes ok. The following user(s) said Thank You: CLO2
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Multiple Sclerosis (MS) and MMS 25 Mar 2020 08:47 #63189

CLO2 Offline Administrator Posts: 5555 Thank you received: 4390	And, post some updates if everything does not go okay! The following user(s) said Thank You: Buckhen
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Multiple Sclerosis (MS) and MMS 22 Jul 2020 00:48 #65283

su58643
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New Member
Posts: 1
Thank you received: 0

Hello Melissa!
That is great news! I have MS myself and just started the protocol yesterday. I took 1 drop per hour for 8 hours yesterday, 2 drops per hour for 8 hours today. And tomorrow i will be taking 3 drops per hour for 8 hours. And I have been adding 1 drop of DMSO per hour for eight hours as well. I don't think I,'m as advanced as you were, but my walking is rough and I'm often lethargic. And heat is like kryptonite to me. May I ask what your protocol was? This MS is destroying my life socially and financially. And if can share your diet I would greatly appreciate it. Thanks and again congratulations!

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Testimonials and Shared Experiences with MMS

Multiple Sclerosis (MS) and MMS

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MMS (Master Mineral Solution) is Sodium Chlorite 28% (22.4% Sodium Chlorite, 5.6% Inert Salts and the remainder water) plus an acidic activator (usually 50% Citric Acid or 4% Hydrochloric Acid) when combined produces Chlorine Dioxide.

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