One man’s documentation of his experience taking MMS to treat Chronic Lyme Disease.
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MMS Vs. Lyme Blog- Day 1517 comments to MMS Vs. Lyme Blog- Day 15Leave a Reply |
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Copyright © 2012 Jenna's Video Lyme Blog - All Rights Reserved |
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You are doing this wrong. You are not doing it how Jim Humble explains. Massive doses twice a day is wrong. You are to spread small dosages out thru an 8 or 10 hr time span. You are not to take more drops a day than is recomended.
MMS does not kill off beneficial flora, the symptoms are from die off of the negative pathogens
Hi Jeremy, Are you doing this on your own or under a doctors supervision? I’ve been dealing with Lyme’s many years and am looking for an alternative to antibiotics. Are there any success stories out there? Your journey with the MMS sounds scary. Especially all the floaters in your eyes. That would absolutely freak me out. I look forward to your recovery. Lori
Question : Why do you have these “valuable” videos in the Comedy section? These are absolutely helpful to fellow lyme sufferers. I can completely relate to your neuro symptoms! Thank you for being so honest and forthcoming in your experiences. This was a great idea!
I have had Lyme disease for 14 years and was always taken off treatments of antibiotics just as soon as the improvements came only to be knocked back down from the relapses. After being done that way several times the bacteria got resistaint to the treatment and I was left with out a doctor or any options. I started MMS 2 weeks ago and it is working just as good as the 30 day IV treatment I got the first time, only this time I’m not at the mercy of a doctor taking it away to early.
Waiting for your next video Jeremy. I have seen the day 15 one and expecting another update soon! Hope you are going ok and you’re not dead!
Just a question! Is Lyme considered to be a much more chronic deepseated condition than Malaria? How come they could deal with Malaria bugs in just a day or two but you guys are needing weeks/months of MMS?
I’ve been advised by my doctor to embark on MMS treatment soon, so just trying to find out all I can before I start!
Megan
Hi again Jeremy,
In case you’re interested, I’m sharing my MMS experience over on ProHealth’s CFS/FM message board. The thread I started is entitled “Jump Starting Mitochondria with MMS ? [DCA Notes]” username Waynesrhythm.
My post over there is rather long, and includes some information on some of the other things I’m dong for my own ME/CFS.
Again, thanks for your videos. It’s nice to see a kindred spirit doing some similar things.
All the Best, Wayne
Hey Jeremy,
Great videos. Could so relate to your description of the neurological and cognitive difficulties.
I started my own MMS experiment about 6 weeks ago, but have been going much more slowly than you. I’m now up to 12 drops/day. In the beginning was doing 1/3 drop every other day.
I believe I likely have Lyme, but probably a number of other pathogens could be involved as well. I’ll look forward to hearing more about your ongoing MMS experiment.
Thanks much, Wayne
Wrote a comprehensive brochure with the help of 2 Lyme specialists. Great info. Will email to anyone.
Elaine in VA
Hey JY … Thanks for another informational update. I look forward to your recovery. RH
Hi incredible Jeremy
I think you are very brave man and I am just thankful to found your blog. I believe this stuff and I am sure it will help you. Sooner or later you will be healthy again 
I am really considering to use MMS as I have chronic chlamydia and cant get rid of the fatique. But first I will be here cheering you up and watching your experiences. God bless you
Hi tulkuone. I’m sorry to hear that you’re feeling worse. How long were you experiencing symptoms before you were diagnosed? Was there any particular event that triggered their onset?
Frustratingly, my symptoms keep me from being able to do much of anything, so I haven’t worked for some time. Hopefully MMS will provide the relief we’re both looking for. Thanks for stopping by and for the encouraging words.
That’s a very interesting detail that I’ve read as well. I appreciate your input and advice, nate4kate, keep it coming.
Have recently recieved MMS – not yet tried it. ABX since diganosed in Nov 06 but have felt steadily worse since. Tried herbs, all kinds of supplements, gulatathione, some of Cowden’s stuff – including laser detox, acupuncture. Now considering MMS.
Have you been able to work? Can’t imagine how. I commend you on your courage and willingness to share your experience. Thanks again.
A true pioneer - thanks Jeremy
It is so nice to know there are others out there like you going through this too. It is so great for me while I am taking the MMS to find support, good info and encouragement from people like you going through the same thing! Thank-you!! Keep it up, you are going to make it!
Hi, Jer. You’re a good man for sharing your journey with the Lyme and chronic illness community. You are a great inspiration to me and undoubtedly many others who find solace in your video blog. Keep it up, brother!