I have been using CLO2 in my eyes daily for 3 weeks, diluted. I had an infection in my eyes, throat and ears. MD gave me Z Pack which didn't work and then augmentin which didn't work. Gargled with H2O2 and baking soda which got Reid of the sore throat. H2O2 resolved the ear ache and chlorine dioxide resolved the eye infection.
I'm confused about the difference between CD and MMS. Can someone explain or direct me to an article that explains it so I can learn more? Maybe it's here in the article and I'm just missing it. TY.
Deni - Thanks for asking this. For some reason I cannot keep the differences between CD and MMS straight in my head. I've read so many articles, and yet . . . I'll check out CO's article and maybe it will stick this time?!
I will be ever a follower of these experts and support them with monetarily donations and/or passing their information forward. Along with me paying it forward what I have learned to others for free or asking them if they'd like to donate to the all the experts who made this happened. I am a new follower of Jesus Christ and following his ways, thanks to you all. Eternally grateful.
I have just started a cycle of cds 10ml/liter. I am toned by it and a disconcerting sense of oppression and fatigue disappeared in 3 days. It's amazing. I was already using dmso for the eyes. Now I will also use the cds spray since I have become familiar with the preparation. Maybe not together but alternating them. Thank you for what you are doing, I hope to be of help in the future, in the meantime I am making it roll
My son is fighting an incurable Pfizer "vaccine" injury which manifested in an (undiagnosed/misdiagnosed) case of Necrotizing Scleritis.
His opthalmologist saved his eye with high dose predisone but the disease shifted. ("Rheumatoid Arthritis' diagnosis.)
Another high dose "cancer" drug: Methotrexate. (Self injects into stomach...)
He's now on a 3rd drug, a 'biological".
Devastating. He is 28. Pfizered at 24.5 years old, finally correctly diagnosed on his 27th birthday.
I've looked at ALL the medical literature regarding Necrotizing Scleritis. It's horrific. Bleak.
I have MMS in stock. Zeolite. Organic Sulphur. 100% pure pharmaceutical grade DMSO. Colloidal silver. Castor oil. You name it, I have it.
I have NEVER read about anyone with my son's specific RA symptoms getting CURED, only constant repetitive blah blah blah (copy & paste or "Grok/AI") "drug treatments" which barely serve to keep these vicious inflammations at bay then BAM. Another "recurrence".
Have sent my son EVERYTHING I’ve ever discovered which might help him but after being told 'You're not a Specialist mum" he stopped replying.
My heart aches for my now "disabled" young son who has barely spoken to me in nearly a year. Sometimes
grief morphs into depression.
I know that I need to find a way to reach out to him one last time, with the suggestion of trying this MMS1/DMSO eye protocol.
I think he could possibly terminate the "RA" diagnosis/prognosis as well. (It's an autoimmune disease: INFLAMMATION. Caused by? No specialists can SAY!!! Only "prescribe" drugs for SYMPTOMS. what CAUSED the SYMPTOMS DOCTOR???
"Dunno."
No "cures" though, after decades of dis-ease. Only Big Time Rheumologists who dole out Big Harma Brand-Aids.
(But I beg to DIFFER with the "specialists", to my son's eternal chagrin, and always have disagreed. There ARE cures. Just not profitable cures for the "industry" and their professional medical drug dealers.)
Ok rant over.
I will find a way to save my son from a lifetime of pain and drugs and depression. He has already gained weight. He was nearly unrecognizable to me on his birthday.
Ultimate "Irony": He got jabbed so that he could be permitted to WORK OUT in his GYM "during Covid", after a full 17 months of being LOCKED OUT ffs!!
(Close the gyms but keep the WEED SHOPS and LIQUOR STORES OPEN Mr. 💩‐Eau???)
If there's a hell: perhaps he'll be reunited with his father there. 🤞
Oh, Canada!!! 😭
The pharmaceutical drug treatments
my boy is taking are causing severe bloating. Not so much weight gain as BLOATING.
And the "Rheumatoid Arthritis' that continually shifts to different joints, is
painful. (Luckily he hasn't lost his eyeball after 4 (or more?) bouts of NS. Up the dose. Here's a new drug as the old drug isn't working anymore... #Diabolical.)
So...
If I'm able to actually SEE him on
Mother's Day, am bringing my eye drops along. (Will test on myself all this week. Hopefully my own eyesight improves during this experiment.)
Wish I knew what that testimonial about the castor oil, in conjunction
with the CLO2, was about. (How to apply?)
Anyway: Thank you SO much for providing these wonderful
I saw on the chat that some people were talking about castor oil and eyes. I wanted to share some of my personal testimonies.
My testimony with putting ORGANIC castor oil in my eyes every night.
I suffered with very dry eye and had to use eye drops every 2 hours for many years. I heard Barbara O'Neil talk about Castor oil for dry eye. It does need to be organic.
I made sure my hands were very clean and put a drop on my pinky (smallest finger) and rubbed it together and then rubbed it on the inside of my eye ( eye balls) just before bed every night. I would also put just a small amount on my eyelids and underneath my eyes.
I would recommend you do a test patch first to see if you're allergic to it or if it makes your skin itchy.
It helps dry eye tremendously and sometimes I use it during the day off and on so that I don't have to use so much eye drops with chemicals in them.
I've been doing this for a couple of years now and have had good results. Every now and then I get a little bit of itchiness around my eyes and I stopped using it for a short while and then I can go back to it. If I wake up in the middle of the night and my eyes feel dry, then I just reapply.
Also because of the dry eye before I was using the castor oil, I had damage to my cornea which The Specialist told me was irreversible and caused some blurred vision because of the scratch on the cornea. With lots of prayers going up to Jesus for healing and using the organic castor oil in my eye (a very small drop in each eye) when I went back several months later for my checkup at the specialist they said there was no damage to the cornea and I gave the glory to God and to the natural products that He's given us to use. They had also told me that I had a small cataract in both of my eyes which was normal. But now they told me that both of them were gone.
Thank you so much for taking the time to read this and post more data re: Castor Oil. (I'd read about it somewhere but couldn't recall where or when, but will now email this comment to myself, copy & paste as well, plus take a screen shot so I don't lose it.)
Thank you ONCE AGAIN. 🙏❤️
Edit: If anyone ever wants to "save" a comment so that they can find it again, I recommend a screenshot (in case the article containing the comment goes "poof)', and #2:
Click on the 3 little dots of Author's Comment (top right) whereby you can "copy link".
IF you can,, suggest to your son to see an endocrinologist to get hormones checked. With the amount of steroids he's on and the weight gain/bloating, sounds like Cushings Syndrome, a side effect of the steroid use. Side effects from steroids is what led us to natural medicine 12 years ago when the topical steroids caused HPA Axis Suppression and heart murmur and growth delay and full body steroid induced eczema for my then 3yo son. He was only 3yo. Some people are more susceptible to steroid side effects.
Sorry it took me so long to respond. Myy son had a unique case where the topical steroids caused the issue and we were able to withdraw from those readily, though painfully. He was already through year of the withdrawal by the time I knew he had the HPA axis suppression, a different variation from Cushing. But I know of Cushing because of our experience.
Your son will need to see an endocrinologist to help him lower the steroids he is on. And then your son needs to find a functional MD who can help him treat all this stuff more naturally with diet. My friend in Albuquerque keeps his RA at bay with diet and low dose methotrexate (which your son could do with his RA doc if he wants to stay mainstream). I personally think my friend could stop the methotrexate (a low dose cancer drug - gross, I know, but better than steroids) , but neither he nor his wife have tried any of the MMS/CDS or anything else you have tried sharing with your son. If you could get him into see Dr. Kory, that would be amazing because he could be treating not only the inflammation but also the cause. RA can 100% be put in remission with diet and non addicting/non harmful supplements. I know lots of other people who have done that route.
Unfortunately, your son needs to be warned that the steroids are possibly causing Cushing Syndrome. And he needs to be warned that the side effects become worse with time as the body becomes more and more reliant on them and quits peoducing its own cortisol. sometime stopping the steroids can cause the skin to go crazy, which is how I know of Cushing. because we had people in our skin support group ending up there while withdrawing from their oral steroids. if the skin gets involved during withdrawal, it is going to be awful (see itsan.org - what my son went through).
your son is on quite a harrowing health journey. he is going to have to acknowledge there is a problem the doctors can't answer first. With him as resistant as you describe, I'd probably just send him a link to Cushing Syndrome and suggest he see an endocrinologist and let him come back to you after he has done that. Or not. Let him ask you what else he can do to treat the RA. Let him connect the dots that these drugs are a bandaid but worse because things are actually rotting and getting worse inside while you have it on. Sounds like you've tried and he's closed.
My dad knows he's injured (has vaers report even) and I figured out recently he doesn't have "asthma" post v, but myocarditis, but he stopped the v conversation when I tried to tell him of my public speaking at a health district meeting Friday to get them removed. normally he'd be thrilled i was speaking at a public mtg and pleased I was carrying on his legacy. nope. not about this. so I didn't tell him about the ultrasound he should get to get a correct diagnosis yet. timing.
Praying for you and your son.
if you can figure out a way yo share phone numbers privately, im happy to chat by phone too. Sending you a hug. Gotta be hard to be closed out of your son's life like this.
Hi Heather, thanks so much for responding to my inquiry.
So sorry to hear about your dad and his current "mental block". I know you understand how difficult it is to get through brick walls.
We are in British Columbia Canada. He is firmly entrenched in the "Canadian Medical System". He works as a Care Aid to severely disabled humans... (Non verbal severely autistic, etc etc...)
My son has been self-injecting Methotrexate since his 2nd bout of Necrotizing Scleritis.(While he continudd with the prednisone that he'd been weaning off.)
In November of 2024, after his 2nd round of (posterior)
Necrotizing Scleritis: he was waiting for approval to be prescribed a monoclonal antibody by the name of
Amjevita.
Similar to "Humira". Taken via subcutaneous injection:
Anyway Heather, if you hit "subscribe" on my icon, I-ll usually receive a notification via email which will include your email addy.
I'll reply to that email and maybe we can chat via Whatsapp or whatever. (My cellphone provider charges an arm and a leg to call the States, or to receive calls from the USA.)
PS: Didn't see him on Mother's Day. No card but received a brief phone call.
He is feeling "ok". The biological which replaced prednisone is called Amgevita and seems to controlling his disease for now. (In tandem with the immunosuppressant Methotrexate.)
Thank you for all of your time and support. You are such an incredible soul ❤️🙏🏻 I am super grateful for your extra time you put in and every little detail, especially every instruction on how to or don't do, the exact measurements for each protocol you share. It definitely shows how passionate you are to help others help themselves/loved ones/friends/pets/children/ect...
I am so thankful for this article! I've been using MMS for a couple of years for various issues. I didn't know about the eye protocol. I will be starting this today for my astigmatism! (Been wearing glasses since grade school, now in my 50's.)
MMS isn't going to do anything for an astigmatism. An astigmatism has to do with eye shape and nothing else. Whatever shape your eyes are when you are born, that's what you have to work with. That's like saying "my fingers are too short so I'll use MMS to grow them longer". It doesn't work that way.
A lot of work went i to this article. And then you gave the recipes all the way down to making saline solution. I appreciate all you do. Thank you. ⚡️
A Godsend.
Agreed, Amen.
Thank you VERY MUCH!
I have been using CLO2 in my eyes daily for 3 weeks, diluted. I had an infection in my eyes, throat and ears. MD gave me Z Pack which didn't work and then augmentin which didn't work. Gargled with H2O2 and baking soda which got Reid of the sore throat. H2O2 resolved the ear ache and chlorine dioxide resolved the eye infection.
did you mix the H2O2 and baking soda together to make the gargle solution?
Yes, I use the same on my teeth. Alternatively you can gargle with diluted chlorine dioxide.
I'm confused about the difference between CD and MMS. Can someone explain or direct me to an article that explains it so I can learn more? Maybe it's here in the article and I'm just missing it. TY.
Lesson one of the free training course provides that information about the difference between CDS and MMS
Free Course 🧑🏼🎓➡️ http://bit.ly/UniversalAntidoteCourse 🧑🏼🎓
Bless you ~ I appreciate it ♥ Looks like a great course - I'm excited to learn whatever it offers (the problem is always retention)!
Deni - Thanks for asking this. For some reason I cannot keep the differences between CD and MMS straight in my head. I've read so many articles, and yet . . . I'll check out CO's article and maybe it will stick this time?!
THANK YOU so much for all your hard work and generous heart!!! xoxo
You are welcome.
Your help, instructions and tenacity for humanity is God-sent!
Thanks for the wonderful work you put forth to help us all out here.
I will be ever a follower of these experts and support them with monetarily donations and/or passing their information forward. Along with me paying it forward what I have learned to others for free or asking them if they'd like to donate to the all the experts who made this happened. I am a new follower of Jesus Christ and following his ways, thanks to you all. Eternally grateful.
I have just started a cycle of cds 10ml/liter. I am toned by it and a disconcerting sense of oppression and fatigue disappeared in 3 days. It's amazing. I was already using dmso for the eyes. Now I will also use the cds spray since I have become familiar with the preparation. Maybe not together but alternating them. Thank you for what you are doing, I hope to be of help in the future, in the meantime I am making it roll
Brilliant DIY healing solutions...
My son is fighting an incurable Pfizer "vaccine" injury which manifested in an (undiagnosed/misdiagnosed) case of Necrotizing Scleritis.
His opthalmologist saved his eye with high dose predisone but the disease shifted. ("Rheumatoid Arthritis' diagnosis.)
Another high dose "cancer" drug: Methotrexate. (Self injects into stomach...)
He's now on a 3rd drug, a 'biological".
Devastating. He is 28. Pfizered at 24.5 years old, finally correctly diagnosed on his 27th birthday.
I've looked at ALL the medical literature regarding Necrotizing Scleritis. It's horrific. Bleak.
I have MMS in stock. Zeolite. Organic Sulphur. 100% pure pharmaceutical grade DMSO. Colloidal silver. Castor oil. You name it, I have it.
I have NEVER read about anyone with my son's specific RA symptoms getting CURED, only constant repetitive blah blah blah (copy & paste or "Grok/AI") "drug treatments" which barely serve to keep these vicious inflammations at bay then BAM. Another "recurrence".
Have sent my son EVERYTHING I’ve ever discovered which might help him but after being told 'You're not a Specialist mum" he stopped replying.
My heart aches for my now "disabled" young son who has barely spoken to me in nearly a year. Sometimes
grief morphs into depression.
I know that I need to find a way to reach out to him one last time, with the suggestion of trying this MMS1/DMSO eye protocol.
I think he could possibly terminate the "RA" diagnosis/prognosis as well. (It's an autoimmune disease: INFLAMMATION. Caused by? No specialists can SAY!!! Only "prescribe" drugs for SYMPTOMS. what CAUSED the SYMPTOMS DOCTOR???
"Dunno."
No "cures" though, after decades of dis-ease. Only Big Time Rheumologists who dole out Big Harma Brand-Aids.
(But I beg to DIFFER with the "specialists", to my son's eternal chagrin, and always have disagreed. There ARE cures. Just not profitable cures for the "industry" and their professional medical drug dealers.)
Ok rant over.
I will find a way to save my son from a lifetime of pain and drugs and depression. He has already gained weight. He was nearly unrecognizable to me on his birthday.
Ultimate "Irony": He got jabbed so that he could be permitted to WORK OUT in his GYM "during Covid", after a full 17 months of being LOCKED OUT ffs!!
(Close the gyms but keep the WEED SHOPS and LIQUOR STORES OPEN Mr. 💩‐Eau???)
If there's a hell: perhaps he'll be reunited with his father there. 🤞
Oh, Canada!!! 😭
The pharmaceutical drug treatments
my boy is taking are causing severe bloating. Not so much weight gain as BLOATING.
And the "Rheumatoid Arthritis' that continually shifts to different joints, is
painful. (Luckily he hasn't lost his eyeball after 4 (or more?) bouts of NS. Up the dose. Here's a new drug as the old drug isn't working anymore... #Diabolical.)
So...
If I'm able to actually SEE him on
Mother's Day, am bringing my eye drops along. (Will test on myself all this week. Hopefully my own eyesight improves during this experiment.)
Wish I knew what that testimonial about the castor oil, in conjunction
with the CLO2, was about. (How to apply?)
Anyway: Thank you SO much for providing these wonderful
testimonials of WORLDWIDE SUCCESS.
Hopeful. 🙏
Re: Castor oil
This was another testimonial about castor oil and it discussed how to use it in the eyes.
"Yes, I would dab it on the eyelash lines with a clean finger. Only at night, because it can make your vision a little blurry. Don’t double dip. 😊
If your eyes react OK with it, then you can add it as an eyedrop in your eye. This is a testimonial from a friend of mine."
Organic castor oil for eyes testimony.
"Dry eye relief, irreversible scratched cornea damage, cataracts.
I saw on the chat that some people were talking about castor oil and eyes. I wanted to share some of my personal testimonies.
My testimony with putting ORGANIC castor oil in my eyes every night.
I suffered with very dry eye and had to use eye drops every 2 hours for many years. I heard Barbara O'Neil talk about Castor oil for dry eye. It does need to be organic.
I made sure my hands were very clean and put a drop on my pinky (smallest finger) and rubbed it together and then rubbed it on the inside of my eye ( eye balls) just before bed every night. I would also put just a small amount on my eyelids and underneath my eyes.
I would recommend you do a test patch first to see if you're allergic to it or if it makes your skin itchy.
It helps dry eye tremendously and sometimes I use it during the day off and on so that I don't have to use so much eye drops with chemicals in them.
I've been doing this for a couple of years now and have had good results. Every now and then I get a little bit of itchiness around my eyes and I stopped using it for a short while and then I can go back to it. If I wake up in the middle of the night and my eyes feel dry, then I just reapply.
Also because of the dry eye before I was using the castor oil, I had damage to my cornea which The Specialist told me was irreversible and caused some blurred vision because of the scratch on the cornea. With lots of prayers going up to Jesus for healing and using the organic castor oil in my eye (a very small drop in each eye) when I went back several months later for my checkup at the specialist they said there was no damage to the cornea and I gave the glory to God and to the natural products that He's given us to use. They had also told me that I had a small cataract in both of my eyes which was normal. But now they told me that both of them were gone.
Praise Jesus!”
Oh my gosh, that's wonderful.
Thank you so much for taking the time to read this and post more data re: Castor Oil. (I'd read about it somewhere but couldn't recall where or when, but will now email this comment to myself, copy & paste as well, plus take a screen shot so I don't lose it.)
Thank you ONCE AGAIN. 🙏❤️
Edit: If anyone ever wants to "save" a comment so that they can find it again, I recommend a screenshot (in case the article containing the comment goes "poof)', and #2:
Click on the 3 little dots of Author's Comment (top right) whereby you can "copy link".
Like this one:
https://curioushumanproductions.substack.com/p/chlorine-dioxide-eye-protocol/comment/114589068
Cheers.
IF you can,, suggest to your son to see an endocrinologist to get hormones checked. With the amount of steroids he's on and the weight gain/bloating, sounds like Cushings Syndrome, a side effect of the steroid use. Side effects from steroids is what led us to natural medicine 12 years ago when the topical steroids caused HPA Axis Suppression and heart murmur and growth delay and full body steroid induced eczema for my then 3yo son. He was only 3yo. Some people are more susceptible to steroid side effects.
So sorry to hear that your toddler was affected!
Thank you very much Heather. I've never heard of that!
How was he then treated for Cushings Syndrome? (So glad I mentioned the rapid weight gain... my son looks like the photos I saw.)
Sorry it took me so long to respond. Myy son had a unique case where the topical steroids caused the issue and we were able to withdraw from those readily, though painfully. He was already through year of the withdrawal by the time I knew he had the HPA axis suppression, a different variation from Cushing. But I know of Cushing because of our experience.
Your son will need to see an endocrinologist to help him lower the steroids he is on. And then your son needs to find a functional MD who can help him treat all this stuff more naturally with diet. My friend in Albuquerque keeps his RA at bay with diet and low dose methotrexate (which your son could do with his RA doc if he wants to stay mainstream). I personally think my friend could stop the methotrexate (a low dose cancer drug - gross, I know, but better than steroids) , but neither he nor his wife have tried any of the MMS/CDS or anything else you have tried sharing with your son. If you could get him into see Dr. Kory, that would be amazing because he could be treating not only the inflammation but also the cause. RA can 100% be put in remission with diet and non addicting/non harmful supplements. I know lots of other people who have done that route.
Unfortunately, your son needs to be warned that the steroids are possibly causing Cushing Syndrome. And he needs to be warned that the side effects become worse with time as the body becomes more and more reliant on them and quits peoducing its own cortisol. sometime stopping the steroids can cause the skin to go crazy, which is how I know of Cushing. because we had people in our skin support group ending up there while withdrawing from their oral steroids. if the skin gets involved during withdrawal, it is going to be awful (see itsan.org - what my son went through).
your son is on quite a harrowing health journey. he is going to have to acknowledge there is a problem the doctors can't answer first. With him as resistant as you describe, I'd probably just send him a link to Cushing Syndrome and suggest he see an endocrinologist and let him come back to you after he has done that. Or not. Let him ask you what else he can do to treat the RA. Let him connect the dots that these drugs are a bandaid but worse because things are actually rotting and getting worse inside while you have it on. Sounds like you've tried and he's closed.
My dad knows he's injured (has vaers report even) and I figured out recently he doesn't have "asthma" post v, but myocarditis, but he stopped the v conversation when I tried to tell him of my public speaking at a health district meeting Friday to get them removed. normally he'd be thrilled i was speaking at a public mtg and pleased I was carrying on his legacy. nope. not about this. so I didn't tell him about the ultrasound he should get to get a correct diagnosis yet. timing.
Praying for you and your son.
if you can figure out a way yo share phone numbers privately, im happy to chat by phone too. Sending you a hug. Gotta be hard to be closed out of your son's life like this.
Hi Heather, thanks so much for responding to my inquiry.
So sorry to hear about your dad and his current "mental block". I know you understand how difficult it is to get through brick walls.
We are in British Columbia Canada. He is firmly entrenched in the "Canadian Medical System". He works as a Care Aid to severely disabled humans... (Non verbal severely autistic, etc etc...)
My son has been self-injecting Methotrexate since his 2nd bout of Necrotizing Scleritis.(While he continudd with the prednisone that he'd been weaning off.)
In November of 2024, after his 2nd round of (posterior)
Necrotizing Scleritis: he was waiting for approval to be prescribed a monoclonal antibody by the name of
Amjevita.
Similar to "Humira". Taken via subcutaneous injection:
https://www.drugs.com/uk/amgevita.html
Anyway Heather, if you hit "subscribe" on my icon, I-ll usually receive a notification via email which will include your email addy.
I'll reply to that email and maybe we can chat via Whatsapp or whatever. (My cellphone provider charges an arm and a leg to call the States, or to receive calls from the USA.)
Thanks again for replying. ❤️
I have 2 family members with RA. Can you point me in the direction of treatment using diet and supplements?
PS: Didn't see him on Mother's Day. No card but received a brief phone call.
He is feeling "ok". The biological which replaced prednisone is called Amgevita and seems to controlling his disease for now. (In tandem with the immunosuppressant Methotrexate.)
Thank you for all of your time and support. You are such an incredible soul ❤️🙏🏻 I am super grateful for your extra time you put in and every little detail, especially every instruction on how to or don't do, the exact measurements for each protocol you share. It definitely shows how passionate you are to help others help themselves/loved ones/friends/pets/children/ect...
Sending you so many blessings, love & light💛
Thanks so much for your encouraging words. God bless you.🙏🏻
Thanks so much for your prompt reply.
45 Comments, but only two are showing. Hmmm...
I am so thankful for this article! I've been using MMS for a couple of years for various issues. I didn't know about the eye protocol. I will be starting this today for my astigmatism! (Been wearing glasses since grade school, now in my 50's.)
MMS isn't going to do anything for an astigmatism. An astigmatism has to do with eye shape and nothing else. Whatever shape your eyes are when you are born, that's what you have to work with. That's like saying "my fingers are too short so I'll use MMS to grow them longer". It doesn't work that way.
I say it's worth a try. It couldn't hurt to try.
C
You are a blessing to us all..thank you
Thank you <3
Thanks CO as usual, a fount of CD knowledge!
3 questions on the eye topic:
1. The mix for the spray using CDS 3000ppm would be to add 2ml yes the equivalent you said to equal one activated drop of MMS1?
2. Do you recommend adding DMSO to the drops or the spray from the beginning or trying just the CDS first and then trying them both?
3. Those “SinuCleanse” packets I note contain sodium bicarbonate as well as salt, but that is ok for eyes?
Thanks for help.