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ALS or Motor Neuron Disease 03 Nov 2019 23:46 #61621

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I have a friend, 53, recently diagnosed with MND.

I've seen lots of testimonials on Lyme disease which has many similar symptoms, but does anyone think it's worth a shot with the cd and dmso?

Feel like it's a race against time before it gets worse, her speech has already slowed right down. I've also told them to get a second opinion, ie that it's definitely not Lyme
Thanks

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ALS or Motor Neuron Disease 09 Nov 2019 01:19 #61635

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MND is a form of ALS. The attachments are way at the bottom of this post.

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ALS or Motor Neuron Disease 09 Nov 2019 11:06 #61636

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Can you explain what the pdfs are? Sorry, i'm new to the forum

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ALS or Motor Neuron Disease 09 Nov 2019 11:28 #61637

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PDF files are text documents that you can read. Most people use Adobe Reader to read them.

If you click on the two PDF files at the bottom of my post they should download and/or open in Adobe Reader if you have it installed.

acrobat.adobe.com/us/en/acrobat/pdf-reader.html

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ALS or Motor Neuron Disease 09 Nov 2019 11:37 #61638

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So, the first pdf shows some encouraging signs for use of chlorite, although i think it was used intravenously there, if i'm correct.
The second is a page from EU, approving the use of sodium chlorite against ALS, that is encouraging too
Thanks, i will show her and her partner.

I think the use of DMSO would help too, anyone?

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ALS or Motor Neuron Disease 22 Nov 2019 19:03 #61721

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EU, approving the use of sodium chlorite against ALS, that is encouraging too

Sorry but they quit. Apparently because of poor results in secondary trials. The drug "NP001" (sodium chlorite) was never approved. It had only a so called orphan status to allow for testing:

NP001 was an injected therapy that was being developed by Neuraltus to slow or stop the progression of ALS. There is currently no evidence of this investigative therapy still being considered a treatment candidate for ALS due to failed results from a Phase 2 trial.

This will not say MMS can't do anything for ALS patients.

There is a link between use of cholesterol lowering statin drugs and ALS. Low and wrong fat intake may also be involved. Simply because the nervous system depends on cholesterol to work properly. Our brains consist of 60% fat. Synapses are made of cholesterol, etc. we depend on healthy fats and cholesterol.

IF your friend would be on statins he may want to read the below article:
Statins and Amyotrophic Lateral Sclerosis
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ALS or Motor Neuron Disease 22 Nov 2019 19:45 #61722

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I think the use of DMSO would help too, anyone?


DMSO has strong regenerating properties. I would use it myself if I had ALS. Actually I use it for prevention already.

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ALS or Motor Neuron Disease 22 Nov 2019 23:37 #61724

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I have read that Stanley W. Jacob, MD, the 'father' of DMSO, ingested 30 ml (1 fl oz) (or it might have been 1 teaspoon) of DMSO daily. He died at age 91.
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ALS or Motor Neuron Disease 23 Nov 2019 08:39 #61729

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Believe it was 1 teaspoon daily for Stanley W. Jacob. But Jim Humble recommends 30ml for stroke and heart attack (emergency), in addition to MMS use.

From Jim's book - page 230:

"At the onset of a stroke, first off, mix 2 full tablespoons (30 ml) of DMSO diluted in 1/2 cup (4ounces/120 ml) of water. Drink it down immediately. This is the starting point of the Stroke Protocol."

This is to be repeated 3 more times in the course of the first hour.

Aimed at dissolving the clot causing the stroke while it's happening and start immediate regeneration of damaged brain tissue.
Should be a most effective first aid.

If there is any hope for reversing or stopping the progression of ALS it likely requires long term small dose treatment.
Any use of statins must be stopped. Dietary changes and use of nutriceuticals may be essential.
Most of the food consumed today, including official dietary recommendations, is there to make us sick. Big pharma is in bed with big food. This way MMS is doing nothing else than correcting some of the damage we do to ourselves.
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Last edit: by mart1n.
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