MMS Experiment / Lyme Video Blog

Discussion in 'Lyme Disease Archives' started by Waynesrhythm, Jun 7, 2008.

  1. Waynesrhythm

    Waynesrhythm Member

    Hi All,

    I found these videos to be very helpful as I try to sort out which direction to go therapeutically. This man's extensive experience with so many things I've considered was insightful. And I've been experimenting with MMS just as he is (for about 6 weeks).

    These videos document a young man's experiment with MMS as he tries to address his Lyme. Of note was that he has tried almost everything to try to address his Lyme, including 3 years of antiobiotics. It's interesting to hear some of the symptoms he's dealing with, very many of which are similar to my own.

    Thought I'd post the 4 video blogs he has done so far in case anybody else might be interested. I found his story and experiences to be quite interesting.

    Regards, Wayne
    ...........................................................

    <a href="http://www.youtube.com/watch?v=7cOFJTzLnxk&NR=1/">Day 1 of MMS/Lyme Video Blog</a>.

    <a href="http://www.youtube.com/watch?v=cO4M3T1Dt84">Day 3 of MMS/Lyme Video Blog</a>.

    <a href="http://www.youtube.com/watch?v=YdHWkC-cSus&feature=related/">Day 9 of MMS/Lyme Video Blog</a>.

    <a href="http://www.youtube.com/watch?v=gfhNu3X7nSA">Day 15 of MMS/Lyme Video Blog</a>.

    <a href="http://www.youtube.com/watch?v=gNMTO0KCqH8">Day 22 of MMS/Lyme Video Blog</a>.
    [This Message was Edited on 06/13/2008]
  2. victoria

    victoria New Member

    weird that I saw your 'live' links yesterday, but today they're not...

    Anyway, here's also a site that offers a lot of references for MMS along with Dr. Hesselink's:

    http://www.mmssupersite.com/

  3. Waynesrhythm

    Waynesrhythm Member

    Hi Victoria,

    Thanks much for your MMS link. I'm going to check it out as soon as I finish this note.

    It is kind of weird about the links sometimes. Every time I create one, I check it out to see if it works. Often when I doesn't, all I have to do is click on the edit, and then re-post without making any edits.

    I just posted on my other MMS thread on the CFS/FM message board this morning on my latest developments. I'm feeling more and more optimistic about what MMS may be able to do for many of us.

    Regards, Wayne
    [This Message was Edited on 06/09/2008]
  4. wld285

    wld285 New Member


    Thanks so much for posting this. I have been reading alot lately about MMS.

    Linda
  5. Waynesrhythm

    Waynesrhythm Member

    Here's the latest installment of Jeremy's MMS/Lyme video blog.

    <a href="http://www.youtube.com/watch?v=gNMTO0KCqH8">Day 22 of MMS/Lyme Video Blog</a>.

    Wayne
  6. Waynesrhythm

    Waynesrhythm Member

    Here's the latest installment of Jeremy's MMS/Lyme video blog.

    <a href="http://www.youtube.com/watch?v=Utcb7cIEOCw">Day 40 of MMS/Lyme Video Blog</a>.

    Wayne
  7. victoria

    victoria New Member

    I'm going to get my son to watch these, lots of symptoms are similar to him... My son, my DH, my daughter and her BF are still doing the MMS too. Not much has changed good or bad, altho they're all working their way up on dosages... how are you doing?

    Victoria
  8. Waynesrhythm

    Waynesrhythm Member

    Hi Victoria,

    I'm continuing to back off on the MMS. I had gone from 12 drops/day down to six. And then have only been doing three for the past few days.

    Though I haven't experienced any kind of major detox, the MMS does seem to have sort of a low-level intensity to it. And when I back off, I'm able to relax a bit better.

    I still think this is a good thing I'm doing, but feel that going slowly will enable me to stick to it for the long term.

    Always good to hear from you.

    Best, Wayne
  9. buttercakes

    buttercakes New Member

    Thanks for posting the lynks, I have been looking into MMS, but have not heard any testimonies on it, it sounds pretty good. Good Luck, Sandie
  10. vcamlin

    vcamlin New Member

    Pardon my ignorance, but what is MMS?
  11. Waynesrhythm

    Waynesrhythm Member

    On Jeremy's new <a href="http://www.youtube.com/watch?v=AD1UfawPdes">Day 48 MMS/Lyme Video Blog</a>, he mentions how his hypercoaglation levels have improved since starting MMS. He had his levels lowered while doing HBOT, but then increased after stopping that therapy. His levels are now down to where they were while doing the HBOT. He seems to be continuing to enjoy improved circulation, which he credits to the lowered hypercoagulation.

    Hi Vcamlin - MMS is short for Miracle Mineral Supplement, which is a liquid of sodium nitrite. When mixed with citric acid, it becomes chlorine dioxide, a potent killer of many different types of pathogens, whether bacterial, viral, fungal, etc.

    It is fairly inexpensive and is being discussed on a number of blogs, with some remarkable testimonials on cure-zone. Things like hepatitis C, Lyme, cancer, parasites, difficult GI conditions like Chron's, ulcerative colitis, etc. have improved, often dramatically. I've been posting on my own experiment with MMS on the main CFS/FM Message board on a thread entitled <a href="http://www.immunesupport.com/chat/forums/message.cfm?id=1279713&B=FM">Jump Starting Mitochondria with MMS ? [DCA Notes]</a>.

    I started at 1/3 drop every other day back in April, and have recently been averaging about 6 drops/day. On Jeremy's MMS/Lyme video blog, he is currently doing 15 drops twice a day. Hope this little introduction to MMS helps.

    Buttercakes - Hi Sandie, thanks for your well wishes. I seem to be more optimistic as each day passes as I continue this experiment. Nothing else I've tried seems to have the potency that this seems to have. And the side effects have been minimal for me because of how slow I apprached this. No overwhelming detoxification to deal with.

    Regards, Wayne
  12. Waynesrhythm

    Waynesrhythm Member

    Hi All,

    Jeremy's latest installment:

    <a href="http://www.youtube.com/watch?v=NmRwh_vq4s0">Day 57 of MMS/Lyme Video Blog</a>

    Regards, Wayne
  13. Waynesrhythm

    Waynesrhythm Member

    Hi All,

    This is an interesting blog by Jeremy. He explains how he quit taking MMS for a few weeks but is still experiencing a worsening of symtoms that started when he started taking MMS.

    He lays out some theories on the above, plus talks about how something is improving with his immune system which is validated by some diagnostic tests he's doing.

    <a href="http://www.youtube.com/watch?v=j7nIRszc2Zg">September 4 MMS / Lyme Video Blog</a>

    Regards, Wayne
    [This Message was Edited on 09/06/2008]