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inclusion-body myositis 05 Jun 2012 23:47 #18318

  • mariannhvw
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Hello all,

I am trying to help a man who has become paralysed by this auto-immune disorder. We started of on protocol 1000, building up slowly to him managing 2 drops per hour , 8x daily. He didn't notice improvement so I considered adding MMS2 but before we even started this his nausea took over. We reduced the drops and had to keep on reducing. Now taking 1/2 drop doses, and sill poorly. We have started to add DMSO, too soon to say if that helps. I am also considering starting him with MMS1 baths but he only has access to a spapool. Has anyone got experience with that, how many drops for a big pool like that. I am also open to any other suggestions that may help him.
I am looking forward to receiving support from this super-forum

Peace Marianne

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Re: inclusion-body myositis 06 Jun 2012 01:49 #18323

  • pam
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He might be having a reaction to the citric acid. In which case, a move to CDS is in order. Also MMS2, going VERY SLOWLY - LOL, i've just finished working on Michael Harrah's site, and coordinating the Spanish and Greek input. He's got a very thorough MMS4 (from Jim Humble) link.

You could limit the MMS1 to baths and go to MMS2 for the oral.

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Re: inclusion-body myositis 06 Jun 2012 06:41 #18334

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Hi Pam, thank you. So if we go to the spa pool as a bath how many drops for that amount of water? Do you think we need to drain the water each time or can it be reused?
Thank you for your time.

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Re: inclusion-body myositis 06 Jun 2012 07:30 #18335

  • Michael Harrah
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Hi Marianne,

With someone who is paralyzed, the bath protocol and protocol 3000 are good ways to get the MMS in when oral doses become difficult.

It might be better to use MMS2 in the spa, then you would not have to drain each time. The MMS2 turns to hypochlorous acid which stays in the water unlike the chlorine dioxide which dissipates over time. I have used up to 2 tablespoons of mms2 in a bath full of water.

I don't know the volume of the typical spa versus the typical bath, but I would try 1 tbsp in a spa and go up from there. If he gets real itchy afterward, then it is too much mms2 and use less next time.

I think you can also mix the MMS1&2 in the spa. So when he is ready to get in, just put say, 1/2 tsp of activated MMS1 in addition to the MMS2 that is already in there. Then each time just put more MMS1 in because it will have dissipated out. Probably the dose of MMS1 could be increased quite a bit from there.

genesis2forum.org/index.php?option=com_kunena&func=view&catid=8&id=1951&Itemid=66#3368 mms baths testimonials
www.michaelharrah.us/Info-Sheets-Michael-Harrah/instructions-bath-protocol.html

Protocol 3000 would also be something to try since the pathogens seem to be in the muscles with that disease. If citric acid irritates his skin then use CDS or MMS1 with HCl for activation and go over the top with 70/30 DMSO.

For the oral doses of MMS1 you should try the MMS baking soda protocol if you have not tried that. Also the protocol 1000+ can make a big difference in getting rid of nausea. I had a terrible problem with nausea and when that protocol came out, it eliminated the nausea for me.

www.michaelharrah.us/Info-Sheets-Michael-Harrah/mms1-baking-soda-protocol-info-sheet.html Baking Soda Protocol info
www.michaelharrah.us/Info-Sheets-Michael-Harrah/instructions-protocol-1000.html Protocol 1000+ info

Michael
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Last edit: by Michael Harrah.

Re: inclusion-body myositis 11 Jun 2012 00:21 #18530

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Thank you bothe Pam andMichael.

We will keep working, using all the information provided and hopefully will be able to bring you good news one day soon.

marianne

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Re: inclusion-body myositis 29 Jun 2012 00:06 #19330

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Hello Michael,

The spa pool has a system that sends ozone through the water. This can not be switched off. Does that effect the MMS 2. My friend seems to think that he needs to keep adding the MMS2.

He can just magage to have a 1 drop per hour dose on protocol 1000. No progress yet, but he is a very determined man. So we can keep on trying new things. At least he is not deteriorating further at the moment so that can be seen as progress.

As he doesn't have a suitable bath for MMS1 use we will look at gassing or moving to CDS.

The only thing I am not sure about at the moment is that ozone so I hope you can answer that.

Thank you for your help.

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Re: inclusion-body myositis 30 Jun 2012 05:48 #19355

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Hi Marianne,

Sorry I would not have any idea if the ozone would react with the hypochlorous acid. I imagine is might or it might not. Maybe test the water with chlorine test strips and see if it goes down after putting in fresh MMS2.

Michael
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Re: inclusion-body myositis 30 Jun 2012 06:00 #19356

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Marian,

I think the concentrations of ozone would be very low..... unless he has a very high-end system... and you can literally smell strong ozone at the water level. I have and still use my 2 ozone machines here at home....(internally and externally)

I seriously doubt that the ozone would interfere with he MMS 2

Clint
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