Category: Twitching Muscles

Vocal cord paralysis improved with MMS use; voice clarity and coughing redu

December 21, 2009

21:12:09 Ms. S. reported (vocal cord paralysis)

Hello,

I salute all who have the courage to test MMS.

A good friend referred me to the book “The glove’s breakthrough”. I was curious but skeptical. All the information I got from the internet and got a video of a dear friend gave.

I’m testing now seven days beginning with one drop of MMS increased to 6 drops per day, and I can tell in just a short time significant changes in myself. 1987 I was operated on the thyroid gland and vocal cord paralysis have worn it.

I could not cough up before I took MMS correctly and therefore had always occupied a raspy voice. The phone was a disaster, especially as a clerk.

After taking only 2 drops of MMS, the situation improved. After a week, I took only 1 x 6 drops daily, it is my only became aware that I have a clear distinct voice, and not even this morning must hold quählenden coughing. I feel really liberated.

Then say I washed my mouth every night at 5 or 10 drops and must be: I have no bleeding and no more tartar.

It’s unbelievable.

Now I am suffering even to the nervous legs cramp. I am now at 7 drops, I take two times a day. The cramps and twitching muscles have been weakened, especially at night and I sleep wonderfully Duch again.

I will continue in any case and I will tell you.

I am grateful to Jim Humble for his great discoveries.

Gabi, Blankenfelde TF


Lyme disease with neurological symptoms shows improved fasciculations and f

February 8, 2008

{Part of original post}

I am a seriously ill person who has been diagnosed with both ALS and Lyme Disease…

I thought I had better qualify my previous statement. I now realize it sounds like I have both diseases whereas it is actually more of an either/or situation:

I am not sure if I have ALS or Lyme disease. I was diagnosed with ALS by a neurologist last May but 2 months later, I took antibiotics for an unrelated ailment (swollen glands) and I had a “Herxheimer reaction” (which should not happen to an ALS patient). Since August, I have been also given a working diagnosis of Lyme by an infectious diseases doctor (it can sometimes imitate ALS) and have recently had a weak/borderline positive Lyme test result from IgeneX labs in CA. So, my feeling is that I do have Lyme (with severe neurological manifestation of symptoms) and not ALS, even though I have been diagnosed with both.

{2/8/08}

I have been taking MMS for 1 month now. Currently, I am at 10 drops twice a day. I have had to stop and re-start twice due to extreme “herx” reactions. My goal is to get up to 15 drops 2x a day WITHOUT nausea. I got up to 15 drops before and had a violent reaction (the usual- vomiting and diarrhea) BUT I felt great for several days after the reaction subsided. I DO feel like it is getting to something toxic in my system and killing it.

I am still weak, have trouble walking and my hands are crippled from nerve damage. I do notice that some of my other symptoms are better or gone.

Better: fasciculations (twitching muscles), fatigue

Gone: tingling, facial numbness, blurred vision


FYI: Old Protocols


In the early days of MMS, a common protocol involved taking a 15-drop dose 3 times a day.  This has long since been improved in various ways.  Some of the older testimonials will talk about these 15-drop doses. Overall today it is not suggested to take such large doses in one shot, but rather much lower doses and on an hourly basis—which provides a more gentle and steady approach. Full details on how to properly use the various protocols can be found in the MMS Health Recovery Guidebook.
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