Jenna’s Lyme Video Blog
Video blog about chronic and/or neuro-Lyme
20 Responses to “MMS Vs. Lyme Blog- Day 15”
Leave a Reply
- Lyme Disease Resource
- Miracle Body
- New Reference Textbook on Chronic Lyme and Vector-borne Diseases
- Is the Western Blot Capable of More Accuracy?
- ITT/Cytokine Testing for Definitive Diagnosis of Active Lyme Infection
- Best Supplement for Chronic Lyme Disease
- Detox Those Nasty Neurotoxins
- Did You See Boston Chronicle’s Series on Chronic Lyme Disease?
- Is Lyme the Co-infection for Bartonella?
- Watch ILADS Conference live on Chronic Lyme disease
- Chronic Lyme Proven in Recent Medical Research
- Lyme Boost – Moose Dying In Maine from Ticks
April 19th, 2009 at 6:07 pm
Joanne
MMS does not kill off beneficial flora, the symptoms are from die off of the negative pathogens
April 22nd, 2009 at 1:24 pm
Franny
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
April 24th, 2009 at 6:34 pm
Julie
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!
April 26th, 2009 at 1:07 pm
Chris
Aloha!
Love your post! Thanks!
I can absolutely relate to your disorientation! and the weirdness in public. and all the moodiness and snappiness!!
liked your soap comment…ha- relate there too!
All those cognitive and neurological symptoms- ugh!! Man it’s tough stuff… so nice to be understood by others who are on this journey as well….
I am also doing MMS…been on it about a month now…I got up to 15 drops twice a day…and cut back to 12 twice a day now….
love and hugs~
Fawne
April 26th, 2009 at 8:04 pm
Daniel
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.
April 27th, 2009 at 9:38 pm
Annemarie
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
April 30th, 2009 at 1:17 pm
Janet
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
May 2nd, 2009 at 2:35 pm
Tiffany
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
May 4th, 2009 at 10:46 pm
Chase
My best wishes and success. I’m following you since day one as my girlfriend has Lyme too. Just one comment. Maybe all the reactions you are suffering will probably attenuate by helping your body detox. As I think most of those reactions are related to toxins been released (by the effect of MMS killing bacterias) in your body and flowing to your nerves & brain and so on..I suppose you are doing something about it otherwise I highly recommend you to pay attention to it. Good luck from Spain!!!
May 4th, 2009 at 11:04 pm
Marilynne
Wrote a comprehensive brochure with the help of 2 Lyme specialists. Great info. Will email to anyone.
Elaine in VA
May 5th, 2009 at 7:49 am
Louanne
Be careful dude, it sounds like you are taking so much that you have killed off your stomach flora. Make sure you eat yogurt, and do you need to take so much in one shot?
Good luck – the question is – is it working for you or not?
May 6th, 2009 at 7:26 am
Michelle
Hey JY … Thanks for another informational update. I look forward to your recovery. RH
May 7th, 2009 at 12:56 pm
Butch
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
May 10th, 2009 at 5:11 pm
Sherry
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.
May 12th, 2009 at 3:49 am
Julie
That’s a very interesting detail that I’ve read as well. I appreciate your input and advice, nate4kate, keep it coming.
May 12th, 2009 at 2:17 pm
Dutch
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.
May 12th, 2009 at 2:27 pm
Bethany
A true pioneer – thanks Jeremy
May 13th, 2009 at 4:52 pm
Tim
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!
May 14th, 2009 at 11:39 am
Annemarie
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!
May 15th, 2009 at 5:33 am
Annemarie
Not many people know that if you take MMS at a max dose for awhile it can clean the plaqe off the heart valves, and if you dont give it time to heal it can cause heart arteries to collapse this can be avoided by replaceing the Vit C in take in the middle time between MMS doses,
What do you use as a Activator? and what do you mix in?