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MMS: sodium chlorite (NaClO2) 28%
MMS1 or Activated MMS: chlorine dioxide (ClO2)
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Re: Eosinophilic Fasciitis 13 Sep 2012 20:27 #23340

  • Macaddict08
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It's very simple... the clay has an incredible magnetic drawing power. While it may be drawing stuff 'up & put' of the area... more so, it is drawing nutrients and blood to the area afflicted, creating lots of circulation in that area... where as before, there wasn't much. Having the clay draw blood & lymph fluid, etc... to that area is very healing, and will break down scar tissue... which is one of the things that clay is known for, especially when it comes to varicose veins:

www.aboutclay.com/info/Uses/veins.htm

I think the combination of the clay and the MMS is a perfect match.

C
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Re: Eosinophilic Fasciitis 13 Sep 2012 20:42 #23342

  • KennethWalter
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Ok, thanks for clearing that up!

And thanks for the clay link, a former co-worker I know can use that for his legs!

I'll have to find his number.

kw
I recently came upon MMS and FGHP therapy at the same time. And NOW more recently, I stumbled into old therapies, like turpentine!
And I always support peoples right to choose whichever therapy they see fit to take!
augmentinforce.50webs.com/Turpentine%20Therapy.htm
youtube- daniels, why turpentine is good for your health most excellent info with instructions and warnings for proper preparation prior to using turp should you choose to do so.
diamond g in georgia was the best turp I found.
www.biologicaltherapeutics.com/documents/Scientists%20Trace.pdf
also check out the borax conspiracy about arthritis, worth your time to read.

;-)

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Re: Eosinophilic Fasciitis 14 Sep 2012 02:35 #23380

  • Evanir
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Herbal Power,

I also have an autoimmune condition that has some similarity to eosinophilic fascitis, mine is called hyper eosinophilic syndrome.

My Eosinophils got so high I almost died and was hospitalized several times in 2008. The doctors didn't find out what was causing
and just put me on steroids, but prednisone is destroying my health way too much.

I also had numbness in my hands and feet which is typical of high EOS. And I started having other problems like severe asthma.

The only thing I can say, is that the MMS1 and MMS2 and now CDS are the only things that have helped me a lot. I don't have any
numbness, the asthma is so much better and I have more energy. I also decreased the steroids considerably in just 6 weeks.

One thing I used to do before MMS was to take a lot of antioxidants hoping to get better, but they would actually make my condition
worse. I would feel more numbness, more wheezing etc.. I am sure you know that with MMS we shouldn't take them.

I think the diarrhea will get better if you use Calcium Bentonite Clay as Macaddict08 suggests here. Also Diatomaceous Earth. I use both.

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Re: Eosinophilic Fasciitis 14 Sep 2012 02:38 #23381

  • Evanir
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Herbal Power,

my last response to you I thought you were the one with the problem, now I see it is you wife.

My best wishes to her and do try the Calcium Bentonite Clay on an empty stomach.

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Re: Eosinophilic Fasciitis 14 Sep 2012 12:45 #23398

  • herbalpower
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Thank you all for your advise , we will try the clay to see if it helps

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