MMS-Miracle Mineral Supplement Vs. Chronic Lyme Disease
theincrediblejy asked:
One man's documentation of his experience using MMS to treat Chronic Lyme Disease. …
Caroline
April 14th, 2009 at 2:59 am
Dutch
Official double blind tests done by the FDA cost tens of millions of dollars man, you wanna pay for it?
April 15th, 2009 at 10:43 am
Violet
Please submit MMS for double-blind trials.
Don’t use any other intervention while using MMS or you won’t know what is working from what isn’t.
Get trials authenticated.
Get the outcome published by a recognised authority.
April 15th, 2009 at 8:40 pm
Caroline
Your video is jumping around a lot! My Lyme rage is displeased! Ha. I am sorry you have been sick for so long.
April 19th, 2009 at 3:44 am
Sandra
Read material about how to use the MMS before using it. Sounds like (all your blogs)that you were using too high dose. You should start at 1 drop and ONLY increase the number of drops IF YOU DONT’ HAVE ANY BAD SYMPTOMS. For me, I am at day 5 and only doing 8 drops. I feel fantastic. Tons more energy, feel very well and sharp – the cold does not seem to bother me as much. Brief nausea, minor numbness, isolated precise head aches, which pass fast then feel great.Keep dose low & Work up gradiently.
April 20th, 2009 at 7:41 am
Annemarie
It’s not a treatment, it’s a cure.
April 20th, 2009 at 3:09 pm
Chris
hi my name is vero and i assume by the symptoms i have lyme disease could you please tell me how you combine the himalayan salt with vit.c do you dilute the salt in water and take strong doses of vit c? hope to receive a response soon thankyou.
April 20th, 2009 at 11:23 pm
Julie
Jeremy, I have two protocols for eliminating Lyme disease naturally, one with MMS, the other with Himalayan salt and vitamin C, usually takes a few weeks, but could take longer since you’ve had it so long. I’d be happy to share my experience with it. You can contact me via freshandalive dt com. This is not a sales pitch, no charge.
April 23rd, 2009 at 5:02 am
Tiffany
Wow that sounds exactly like my situation. No real pain but lots of nuero stuff. Do you have fatigue and/or lightheadedness?
I will look into the MMS.
April 25th, 2009 at 12:32 am
Janet
Do you keep a health journal? One that would have the products you’ve tried and the results, your symptoms, etc? (i just stumbled upon your vlog and i’m going to see how things go with this MMS therapy. Good luck from a fellow Lyme sufferer).
April 27th, 2009 at 2:18 pm
Michelle
This is so interesting. Thank you for making these videos! I am going to follow your journey. Good luck!
April 29th, 2009 at 9:28 am
Sherri
We are due any day ( officially last Thurs.).
How are you feeling?
April 30th, 2009 at 6:11 pm
Susanna
Hurbis, thanks (in advance) for the incredible meal that you keep promising me, and for caring enough to pretend that I didn’t drool in public. You are a true friend.
May 2nd, 2009 at 5:32 am
Daniel
Hey there, Mrs. Todd. First of all, I must apologize for the mini-fro/buzz I had going in the first video. I know how much unkempt cuts bug you professional coiffeuses. And secondly, thanks for the prayers and concern.
May 2nd, 2009 at 10:53 am
Violette
Sen711,
Thanks for commenting. And I would be very interested to hear about your experience and progress with MMS as well, so please keep me posted. If you don’t mind me asking, have you any coinfections that were confirmed positive as well?
May 4th, 2009 at 1:31 pm
Gerald
Thanks, Froto. Maybe the GOB or BG would be willing to keep me company if I’m a feeling a little too tired to get out of the house during this treatment.
May 7th, 2009 at 1:41 am
Chris
Mr. Quillo (and Henry),
Here’s to hoping this is the magic bullet that at least starts some forward progress. Thanks for the well wishes, and the compliment on the buzz cut.
May 9th, 2009 at 8:06 pm
Vichelle
I appreciate the prayers and support, bro. BTW, what day are you scheduled to become a father? I’m so out of the loop these days.
May 11th, 2009 at 10:56 pm
Tiffany
Muchos gracias, senor Harkins. This approach certainly beats the days of driving an hour each way to Dr. Baron’s and getting a lecture about not eating enough raw honey.
May 14th, 2009 at 5:40 pm
Sandy
Thanks, L-boogie. Maybe I’ll add a reenactment involving the plush spirochete as a visual aid.
May 17th, 2009 at 12:45 pm
Kevin
York…thank you for the education and thank you for endeavoring to help others.
May 20th, 2009 at 10:32 am
Bethany
Well spoken my friend! Thanks for being so open and honest about what you’re experiencing. Your perseverance is incredible! I’m praying that your body will respond to your treatment.
May 21st, 2009 at 6:29 am
Louanne
Hi, I am glad you are posting your experience. I started taking MMS for Lyme this May as well so it will be nice to keep up with your progress.
Take Care
May 21st, 2009 at 2:29 pm
Chase
I’m so glad that you’re sharing and documenting this treatment with everyone. You approach each treatment decision with thoughtfulness, insight, determination and logic, and that’s something that can only benefit other people.
May 21st, 2009 at 8:18 pm
Cam
Bravo my friend. I hope MMS is the magic elixir we’ve been waiting for you to discover.
Henry says, “Adaaabe deda. Coehdaa” Which translates to, “Hello. Nice hair.”
Your in our thoughts.
Cheers,
NQ
May 23rd, 2009 at 5:38 pm
Joanne
I’ll be staying tuned for updates & praying for your treatment.