What happened to theincrediblejy? They started with such high hopes and production values. If MMS was a miracle cure, surely they wouldn't have just stopped posting videos after 3 months and disappeared? Where are the videos of them being cured? Of course the scammers will have seen this too and we're bound to get some fake "i've been cured" videos, but if MMS was REALLY a miracle cure, which should have come 1st? The cured or the not cured? It's been 14 years.
After 14 years there is still not a single verified case of anyone being cured by mms of a serious illness like aids or herpes. MMS is a scam, google mmsdebunked for more info,
@mykitchen51 WHO PAY YOU JIM HUMBLE? I'm just a guy who got tired of reading about this scam. The fact of the matter is it doesn't matter who pays me or you, what matters is what evidence there is to support our claims. You could EASILY refute my claim if they weren't true, but you can't, so your only option is personal attacks and character assassination. It's not so easy for me to refute your claims even thought you have no evidence, but I don't think it matters, you can see for yourself.
@mmsfraud THE EVIDENCE IS MY FAMILY AND MYSELF. My granddaughter (3) had heart operation 3 times, she hurt a nerve that causes disease each year of her lungs, breathing with difficulty and the cure was with MMS. I am well on my prostate AND CHOLESTEROL by MMS. My wife 25 years suffering from allergies, fine. My wife's arthritis is well thanks to MMS and DMSO My son (38) with gastritis and colitis, cured with MMS To me that is MORE than 100,000 LABORATORY TESTS Tray MMS mmsfraud,
I don't know if you are still doing the protocol, but 10 drops of MMS is much too high for lyme disease. You should start with 1 drop, no more than 3 twice a day if tolerated. Please read before proceeding so as to not get extremely ill.
@halleyscomet take it from someone who has been fighting this horrible affliction in varying degree's of misery for over 10 years.... YOU ARE AN IDIOT you would have to be an even bigger idiot to think that with the explosion of the deer population over the past twenty years especially in certain parts of New England that you WOULDN'T be exposed to this disease I just wish I'd caught it sooner
@suechef99 I'm sorry my science based comment caused you to respond with such malice. My wife had Lyme disease many years ago. She was left with atypical arthritis as a result. She is not, however, trying to claim she has some kind of mysterious, scientifically undetectable "Chronic Lyme Disease." I would suggest you seek treatment from a competent doctor who will diagnose your actual medical condition instead of sweeping it under the rug with a vague, fictional diagnosis.
@halleyscomet ....terribly sorry H.C. I was giving you the benefit of the doubt when I suggested that your ignorant & unusually snotty dialogue had to be that of an insensitive "idiot" ... apologies ! now I have to admit that I am quite simply mystified. since you clearly believe in Lyme is it just the word "chronic" that you take exception to ? considering that your wife has been left w/a seemingly chronic & painful condition I wonder, has ignorance replaced the bliss in your home ?
@suechef99 "since you clearly believe in Lyme is it just the word "chronic" that you take exception to"
The arthritis is a consequence of the Lyme disease, but that does not mean she has a "Chronic Lyme" infection any more than someone with a chicken pox scar has "chronic chicken pox". The bacterium B. burgdorferi is no longer in her body. She doesn't have an active case of Lyme disease.
People left in an iron lung after a polio infection don't have "chronic" polio.
@suechef99 "Chronic Lyme disease" generally has two meanings.
1. Untreated infections of B. burgdorferi, a real medical problem.
2. People attributing a variety of problems, some psychosomatic, to an imaginary B. burgdorferi infection.
Unless you have an actual B. burgdorferi infection you don't have any form of Lyme disease. You may, like my wife, be suffering from the damage cause by a past infection. On the other hand, you may be misdiagnosing and thus mistreating another real problem.
you still CAN BUY MMS online.. there are some countries where FDA can not behave as they would want to... site is on purusonline . com and more detailed info about MMS itself i found on mmsdisinfectant . com. Many good videos there also. worth to check, if nothing else, i made myself a few years supply over at purusonline. =)
Hi everyone. I tried MMS to see if it would reduce the mucus in my lungs due to Cystic Fibrosis. I have been using it now for two months and Have seen no decline in mucus production yet. I will continue to use it and update on my condition if it improves or not. So far I'm thinking that this is a fraud but can't pass judgment until I have completed three months so that I can be completely sure of MMS and it's claims. I will Update on my health positive or negative.
PLEASE PLEASE PLEASE do internet research on using SEA SALT for curing Lyme. I had it for seven months before I was diagnosed, and doxycycline only made me sicker. I took a shot of about 1/2 teaspoon of RAW SEA SALT in a small amount of water, and in only hours I felt better than I had in months! I continued this maybe three times a day for several days and it ended my Lyme. I take this "shot" every now and then just to be sure it stays gone. IT WORKS. DO RESEARCH. TELL THE PEOPLE!!
Damn! You've got cognitive issues?! I could only hope to be as articulate as you in the film! I know, it's been edited together, but I'm still impressed. I identified with many of your conditions but don't think it's Lyme's. But there's an infection simmering away in my bod somewhere. If this MMS can give this lifelong chronic sufferer some relief, I'll be one happy(er) guy! Thanks for the blog!
Friend died, first they said she had Lupus, then Lymes, then doc said, "no, neither", so they treated her with CHEMO & pain killer drugs (script) once a month, (she couldn't walk or stand) It was breaking them. They don't test for parasites in this country, & she would often travel to tropical climates; I am sure she was misdiagnosed, but she was too "conditioned" to seek an alternative, I am sure it was parasites in her lymph which often mimic, Lymes, Lupus, or arthritis. Good Luck
Sorry about your friend, Houseitch, It's unbelievable the corruption and the incompetence out there in the medical industry. Lots of great professionals but also a lot of people who belong in jail for their malfeasance!
Exactly! Most people don't have a few extra million sitting in the bank for such a course of action. You can well bet though that if there was more money to be made by the FDA than the current drugs they market....someone would donate the cash for the "official" research. If you want something done sometimes you have to do it yourself! Cheers.
IF testing were done by the FDA I would pay thru taxes. Testing is done by the manufacturer. Truth is the FDA doesn't even oversee protocols, hence so many recalls once the truth becomes known.
Don't take drugs on the market less than 5 years. That's how long the recalls take. You don't want to be one of the unpaid guinea pigs who dies (or worse).
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.
I have been taking MMS for 3 days now. I have followed the recommended method. So far I haven't had so much of a sneeze. I watched all this guys videos. I can't see how MMS could possibly have made this guy so sick. If I went through all his videos, I could find at least 50 complaints. Complaints which I haven't seen anyone else make while researching MMS for months before I decided to purchase. I think this guy is taking some other medication at the same time, and not following MMS directions.
When I first started using the product, Superman tried to use more drops than he should have initially, as opposed to building up over time. Whatever you're using it for, may your process be fruitful and your healing complete....
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.
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.
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).
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.
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.
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.
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?
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.
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.
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.
Thank you so much for staring to share your experience! It is only through the network of lyme sufferers that we can get to the bottom of this terrible disease.
This has been flagged as spam show
Google " MMS on an empty stomach" to get MUCH information, and testimonies!
OK55OK55OK 3 weeks ago
What happened to theincrediblejy? They started with such high hopes and production values. If MMS was a miracle cure, surely they wouldn't have just stopped posting videos after 3 months and disappeared? Where are the videos of them being cured? Of course the scammers will have seen this too and we're bound to get some fake "i've been cured" videos, but if MMS was REALLY a miracle cure, which should have come 1st? The cured or the not cured? It's been 14 years.
mmsfraud 5 months ago
After 14 years there is still not a single verified case of anyone being cured by mms of a serious illness like aids or herpes. MMS is a scam, google mmsdebunked for more info,
mmsfraud 6 months ago
WHO PAY TO YOU F.D.A. OR BIG PHARMA?
mykitchen51 5 months ago
@mykitchen51 WHO PAY YOU JIM HUMBLE? I'm just a guy who got tired of reading about this scam. The fact of the matter is it doesn't matter who pays me or you, what matters is what evidence there is to support our claims. You could EASILY refute my claim if they weren't true, but you can't, so your only option is personal attacks and character assassination. It's not so easy for me to refute your claims even thought you have no evidence, but I don't think it matters, you can see for yourself.
mmsfraud 5 months ago
mykitchen51 5 months ago
ANOTHER account created which has done NOTHING since being created but go on about how great MMS is, I smell a shill.
mmsfraud 5 months ago
@mmsfraud LOL! Talk about the pot calling the kettle black!
peri525 1 month ago
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@mmsfraud
the pharmaceutical industry does not test for the third world because it is NOT business for them.
This video IN YOUR PAGE was done by a professional who knows the pharmaceutical industry is losing money, with MMS.
YOU ARE ONLY interested in money, not health.
you are a scientist?
but very well paid by the pharmaceutical industry.
It's amazing that someone is sold for money to do evil.
mykitchen51 5 months ago
The best and first treatment for Lyme is colloidal silver enemas and salt douching.
loopba 8 months ago
This has been flagged as spam show
@loopba "The best and first treatment for Lyme is colloidal silver enemas and salt douching."
LOL! Good one. You forgot to add "yellow bile pills to balance your humors."
halleyscomet 7 months ago
ur hot. Except u really should shave ur mustache lol
renerdrat 9 months ago
I don't know if you are still doing the protocol, but 10 drops of MMS is much too high for lyme disease. You should start with 1 drop, no more than 3 twice a day if tolerated. Please read before proceeding so as to not get extremely ill.
medicinewomon 1 year ago
oww.too many iv things inserted in ya body...ummph..hehe
btw u hot..
aidifazhim 1 year ago
I don't know if you knew this or not but aspartame causes the same symptoms as Lyme disease.
Interesting.
Messianicvoice 1 year ago
"Chronic Lyme disease" is a psychological disorder, not a physical one. Any placebo will help if the patient believes it will.
halleyscomet 1 year ago
@halleyscomet How very scientific, thanks for the info Freud
MerkinMuffly 1 year ago
@halleyscomet take it from someone who has been fighting this horrible affliction in varying degree's of misery for over 10 years.... YOU ARE AN IDIOT you would have to be an even bigger idiot to think that with the explosion of the deer population over the past twenty years especially in certain parts of New England that you WOULDN'T be exposed to this disease I just wish I'd caught it sooner
suechef99 7 months ago in playlist Gesundheit
@suechef99 I'm sorry my science based comment caused you to respond with such malice. My wife had Lyme disease many years ago. She was left with atypical arthritis as a result. She is not, however, trying to claim she has some kind of mysterious, scientifically undetectable "Chronic Lyme Disease." I would suggest you seek treatment from a competent doctor who will diagnose your actual medical condition instead of sweeping it under the rug with a vague, fictional diagnosis.
halleyscomet 7 months ago
@halleyscomet ....terribly sorry H.C. I was giving you the benefit of the doubt when I suggested that your ignorant & unusually snotty dialogue had to be that of an insensitive "idiot" ... apologies ! now I have to admit that I am quite simply mystified. since you clearly believe in Lyme is it just the word "chronic" that you take exception to ? considering that your wife has been left w/a seemingly chronic & painful condition I wonder, has ignorance replaced the bliss in your home ?
suechef99 7 months ago
@suechef99 "since you clearly believe in Lyme is it just the word "chronic" that you take exception to"
The arthritis is a consequence of the Lyme disease, but that does not mean she has a "Chronic Lyme" infection any more than someone with a chicken pox scar has "chronic chicken pox". The bacterium B. burgdorferi is no longer in her body. She doesn't have an active case of Lyme disease.
People left in an iron lung after a polio infection don't have "chronic" polio.
halleyscomet 7 months ago
@suechef99 "Chronic Lyme disease" generally has two meanings.
1. Untreated infections of B. burgdorferi, a real medical problem.
2. People attributing a variety of problems, some psychosomatic, to an imaginary B. burgdorferi infection.
Unless you have an actual B. burgdorferi infection you don't have any form of Lyme disease. You may, like my wife, be suffering from the damage cause by a past infection. On the other hand, you may be misdiagnosing and thus mistreating another real problem.
halleyscomet 7 months ago
@suechef99 Are you claiming to have an ongoing B. burgdorferi infection? What exactly do YOU mean by "Chronic Lyme Disease"?
halleyscomet 7 months ago
Your are absolutely adorable haha. Thanks for the the video trying to reasearch for my grandma who has cancer...Thanks!
kabakris 1 year ago
what is the new Protocol for MMS treatment? I bought some for my CFS and ADD so hopefully it helps out?
maikakai 1 year ago
How was the book cheese monkeys?
dartus2bits 1 year ago
you still CAN BUY MMS online.. there are some countries where FDA can not behave as they would want to... site is on purusonline . com and more detailed info about MMS itself i found on mmsdisinfectant . com. Many good videos there also. worth to check, if nothing else, i made myself a few years supply over at purusonline. =)
quepao76 1 year ago
This has been flagged as spam show
Hi everyone. I tried MMS to see if it would reduce the mucus in my lungs due to Cystic Fibrosis. I have been using it now for two months and Have seen no decline in mucus production yet. I will continue to use it and update on my condition if it improves or not. So far I'm thinking that this is a fraud but can't pass judgment until I have completed three months so that I can be completely sure of MMS and it's claims. I will Update on my health positive or negative.
weleplaya 1 year ago
This has been flagged as spam show
PLEASE PLEASE PLEASE do internet research on using SEA SALT for curing Lyme. I had it for seven months before I was diagnosed, and doxycycline only made me sicker. I took a shot of about 1/2 teaspoon of RAW SEA SALT in a small amount of water, and in only hours I felt better than I had in months! I continued this maybe three times a day for several days and it ended my Lyme. I take this "shot" every now and then just to be sure it stays gone. IT WORKS. DO RESEARCH. TELL THE PEOPLE!!
iLoveSydBarrett 1 year ago
What is the daily schedule with the meals(times b4 and after and frequency)?
I used it w/apple juice(no V C),it taste and felt different, too mild. I was taken it straight w/water b4 but it was a stomach cruncher.
BLEZZ68 1 year ago
im not to shuer what mms is,, But Can it travel into the brain ?
AlbertInSanAntonio 1 year ago
how do you feel now after using MMS?
rinaliebtdich 2 years ago
Damn! You've got cognitive issues?! I could only hope to be as articulate as you in the film! I know, it's been edited together, but I'm still impressed. I identified with many of your conditions but don't think it's Lyme's. But there's an infection simmering away in my bod somewhere. If this MMS can give this lifelong chronic sufferer some relief, I'll be one happy(er) guy! Thanks for the blog!
dethride 2 years ago
theincrediblejy HOW ARE YOU GETTING ON WITH MMS?
JUST HAVENT READ ANYTHING FROM YOU AND HOW UR GETTING ON
I HOPE U ARE O.K.
NO WORRIES.
christolz 2 years ago
Who edited this, someone with tourettes?
pocksuppet 2 years ago
Friend died, first they said she had Lupus, then Lymes, then doc said, "no, neither", so they treated her with CHEMO & pain killer drugs (script) once a month, (she couldn't walk or stand) It was breaking them. They don't test for parasites in this country, & she would often travel to tropical climates; I am sure she was misdiagnosed, but she was too "conditioned" to seek an alternative, I am sure it was parasites in her lymph which often mimic, Lymes, Lupus, or arthritis. Good Luck
Houseitch 2 years ago
Sorry about your friend, Houseitch, It's unbelievable the corruption and the incompetence out there in the medical industry. Lots of great professionals but also a lot of people who belong in jail for their malfeasance!
myspen 2 years ago
release this medicine and cure the world!
ASSHOLELA 2 years ago
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.
Darryld1 3 years ago
Official double blind tests done by the FDA cost tens of millions of dollars man, you wanna pay for it?
BarrybritpopfreekS 2 years ago
Exactly! Most people don't have a few extra million sitting in the bank for such a course of action. You can well bet though that if there was more money to be made by the FDA than the current drugs they market....someone would donate the cash for the "official" research. If you want something done sometimes you have to do it yourself! Cheers.
chshamus3xw 2 years ago
If they cannot patent MMS then they will NOT put any money into it.
Pharmaceuticals are there to make money.
warriorprince1010 2 years ago 2
IF testing were done by the FDA I would pay thru taxes. Testing is done by the manufacturer. Truth is the FDA doesn't even oversee protocols, hence so many recalls once the truth becomes known.
Don't take drugs on the market less than 5 years. That's how long the recalls take. You don't want to be one of the unpaid guinea pigs who dies (or worse).
flatherist 2 years ago
yes,lets let the "experts" authenticate it.we need their approval.
oh wait?
their system is the one we have now.
how many dead?
no,we dont need approval.
testamonials are enough.
johnnykatt2009 2 years ago
Your video is jumping around a lot! My Lyme rage is displeased! Ha. I am sorry you have been sick for so long.
barbyfirefly 3 years ago
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.
USABEAT 3 years ago
I have been taking MMS for 3 days now. I have followed the recommended method. So far I haven't had so much of a sneeze. I watched all this guys videos. I can't see how MMS could possibly have made this guy so sick. If I went through all his videos, I could find at least 50 complaints. Complaints which I haven't seen anyone else make while researching MMS for months before I decided to purchase. I think this guy is taking some other medication at the same time, and not following MMS directions.
Blegemoth 2 years ago
I use MMS, and I became nauseous only when I took too much at once. It balances out when the body adjusts to it...
timotds 2 years ago
Well, I am up to 5 days now. Tomorrow will be six. Still no reaction whatsoever.
Blegemoth 2 years ago
When I first started using the product, Superman tried to use more drops than he should have initially, as opposed to building up over time. Whatever you're using it for, may your process be fruitful and your healing complete....
timotds 2 years ago
It's not a treatment, it's a cure.
zigyzigy13 3 years ago 2
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.
FreshandAlive 3 years ago
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.
special1337 3 years ago
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.
LymeAwareness 3 years ago
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).
periwink 3 years ago
This is so interesting. Thank you for making these videos! I am going to follow your journey. Good luck!
curtsey 3 years ago
York...thank you for the education and thank you for endeavoring to help others.
krenton1 3 years ago
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.
theincrediblejy 3 years ago
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.
mrsjamietodd 3 years ago
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.
theincrediblejy 3 years ago
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
sen711 3 years ago
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?
theincrediblejy 3 years ago
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.
lillulabelle 3 years ago
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.
theincrediblejy 3 years ago
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
N8Quills 3 years ago
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.
theincrediblejy 3 years ago
I'll be staying tuned for updates & praying for your treatment.
wallacefilm 3 years ago
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.
theincrediblejy 3 years ago
We are due any day ( officially last Thurs.).
How are you feeling?
wallacefilm 3 years ago
Thanks for the post JY. I'm looking forward to hearing about your progress.
rharkins123 3 years ago
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.
theincrediblejy 3 years ago
Thank you so much for staring to share your experience! It is only through the network of lyme sufferers that we can get to the bottom of this terrible disease.
lschott12 3 years ago
Thanks, L-boogie. Maybe I'll add a reenactment involving the plush spirochete as a visual aid. :)
theincrediblejy 3 years ago