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Patent US10105389B1 - Method & compositions for treating cancerous tumors - text
- Truthquester
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29 Sep 2019 15:35 #61437
by Truthquester
I'm Scott McRae, creator of "The Antidote" & CDH with CLO2's help (Charlotte Lackney)
- I did a CDH injection / Chlorine Dioxide (CLO2) injection / IV push of 10ml of dilute 50ppm CDH / CLO2 into my blood 3 times in 11 hours & did before & after blood tests that showed that it did NO HARM to my blood, liver or kidneys. This suggests the possibility that CDH / CLO2 is a potential LIFESAVING MRSA cure, VRE cure, CRE cure, AMR cure, Ebola cure, HIV cure, Cancer cure, etc., since it appears to be safe intravenously at 50ppm.
- Join our group on MiWi (was deleted off of Facebook): mewe.com/join/coronavirusebolasolutions
- Every ml of CDH contains 1 drop of MMS, so 1 drop of MMS = 1ml of CDH
- MMS is 7 to 10% activated in 30 seconds while CDH made with 4% HCl is about 50% activated in the bottle. This is why CDH is far less nauseating than MMS drops
Replied by Truthquester on topic Patent US10105389B1 - Method & compositions for treating cancerous tumors - text
Hi Lori.
First of all I'm not a doctor and so can only say what I would do and try to convey what I believe the patent is saying. As far as I can tell, the patent says what worked the best were multiple injections per visit directly into the tumor using what appears to be something similar to CDH at 200ppm. Sometimes it only took 1 visit and other times it took multiple visits. Keep in mind that in the patent they did this with mice, not humans, so the tumors were relatively small. I'm sure the larger the tumor, the more difficult it is going to be to get rid of it but the procedure should be the same in general.
Regarding CLO2's idea of applying 24,000 ppm CDS externally with DMSO - unless the tumor is on the skin surface (like skin cancer) or has erupted up to the skin, so that the skin is already broken, then I would not do this because if the skin is currently intact, with the tumor below somewhat, then the CDS at such a high strength is going to badly burn the skin if left on for very long at all - it will be like a bad chemical burn which will become very red and then probably peel and crack and become an open wound. The only way that I can see this not happening is if you just applied it and left it on for maybe 30 seconds and then quickly wiped it off. But if you did that, I can't see how it would do much good for a tumor which is somewhat lower than the surface of the skin - like a centimeter deep for example. But maybe CLO2 has had or heard of good success this way that I'm not aware of and so maybe it works. Hopefully he'll chime in if he thinks I'm incorrect about this.
Hope that helps,
Scott
First of all I'm not a doctor and so can only say what I would do and try to convey what I believe the patent is saying. As far as I can tell, the patent says what worked the best were multiple injections per visit directly into the tumor using what appears to be something similar to CDH at 200ppm. Sometimes it only took 1 visit and other times it took multiple visits. Keep in mind that in the patent they did this with mice, not humans, so the tumors were relatively small. I'm sure the larger the tumor, the more difficult it is going to be to get rid of it but the procedure should be the same in general.
Regarding CLO2's idea of applying 24,000 ppm CDS externally with DMSO - unless the tumor is on the skin surface (like skin cancer) or has erupted up to the skin, so that the skin is already broken, then I would not do this because if the skin is currently intact, with the tumor below somewhat, then the CDS at such a high strength is going to badly burn the skin if left on for very long at all - it will be like a bad chemical burn which will become very red and then probably peel and crack and become an open wound. The only way that I can see this not happening is if you just applied it and left it on for maybe 30 seconds and then quickly wiped it off. But if you did that, I can't see how it would do much good for a tumor which is somewhat lower than the surface of the skin - like a centimeter deep for example. But maybe CLO2 has had or heard of good success this way that I'm not aware of and so maybe it works. Hopefully he'll chime in if he thinks I'm incorrect about this.
Hope that helps,
Scott
I'm Scott McRae, creator of "The Antidote" & CDH with CLO2's help (Charlotte Lackney)
- I did a CDH injection / Chlorine Dioxide (CLO2) injection / IV push of 10ml of dilute 50ppm CDH / CLO2 into my blood 3 times in 11 hours & did before & after blood tests that showed that it did NO HARM to my blood, liver or kidneys. This suggests the possibility that CDH / CLO2 is a potential LIFESAVING MRSA cure, VRE cure, CRE cure, AMR cure, Ebola cure, HIV cure, Cancer cure, etc., since it appears to be safe intravenously at 50ppm.
- Join our group on MiWi (was deleted off of Facebook): mewe.com/join/coronavirusebolasolutions
- Every ml of CDH contains 1 drop of MMS, so 1 drop of MMS = 1ml of CDH
- MMS is 7 to 10% activated in 30 seconds while CDH made with 4% HCl is about 50% activated in the bottle. This is why CDH is far less nauseating than MMS drops
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- lori1
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29 Sep 2019 18:27 - 29 Sep 2019 18:33 #61438
by lori1
Replied by lori1 on topic Patent US10105389B1 - Method & compositions for treating cancerous tumors - text
Hi Scot,
The tumor is under the skin. when we touch it, we can feel it. Skin is not broken. So what you advice to cure it? injection, protocol 2000, surgery or what?
l really dont know what we have to do.?
The tumor is under the skin. when we touch it, we can feel it. Skin is not broken. So what you advice to cure it? injection, protocol 2000, surgery or what?
l really dont know what we have to do.?
Last edit: 29 Sep 2019 18:33 by lori1.
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29 Sep 2019 19:35 - 29 Sep 2019 19:41 #61439
by gabyher
I am really interested. Could you please give me an idea about the hardness of the tumor. As hard as an unpeeled banana or a peach or ...? Thanks
Hi Scott:
sorry to budge in,...could you please please please reply to my last post here:
mmsforum.io/goto/cdh-research/30833-cdh-intravenous-injection-of-dilute-cdh-to-cure-infections-of-the-blood-appears-to-be-safe-and-very-effective?start=36#61430
Thanks
Replied by gabyher on topic Patent US10105389B1 - Method & compositions for treating cancerous tumors - text
Hi Lorilori1 wrote: The tumor is under the skin. when we touch it, we can feel it. Skin is not broken?
I am really interested. Could you please give me an idea about the hardness of the tumor. As hard as an unpeeled banana or a peach or ...? Thanks
Hi Scott:
sorry to budge in,...could you please please please reply to my last post here:
mmsforum.io/goto/cdh-research/30833-cdh-intravenous-injection-of-dilute-cdh-to-cure-infections-of-the-blood-appears-to-be-safe-and-very-effective?start=36#61430
Thanks
Last edit: 29 Sep 2019 19:41 by gabyher.
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29 Sep 2019 21:01 #61440
by CLO2
Replied by CLO2 on topic Patent US10105389B1 - Method & compositions for treating cancerous tumors - text
Scott, I have used CDS as high as 10,000 ppm CLO2 concentration on skin with no problems at all. Recall that CDS is just CLO2 gas in water. There is no unreacted MMS or activator that MMS1 and CDH have.
Lori, if you try CDS, start with diluted CDS and if no problems, then reduce dilution until you are using undiluted CDS. This idea is the same that we always use when dosing MMS; start with low doses and work up.
We know that DMSO is an excellent carrier, so it will help carry CLO2 to the tumor. I had a diagnosed pre-cancer on my forehead a couple of years ago and I applied undiluted CDS with a Q-tip followed by DMSO on a Q-tip, a few times daily. In about 3 weeks time, the pre-cancer was gone and has not come back.
Lori, if you try CDS, start with diluted CDS and if no problems, then reduce dilution until you are using undiluted CDS. This idea is the same that we always use when dosing MMS; start with low doses and work up.
We know that DMSO is an excellent carrier, so it will help carry CLO2 to the tumor. I had a diagnosed pre-cancer on my forehead a couple of years ago and I applied undiluted CDS with a Q-tip followed by DMSO on a Q-tip, a few times daily. In about 3 weeks time, the pre-cancer was gone and has not come back.
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30 Sep 2019 05:21 #61441
by lori1
Replied by lori1 on topic Patent US10105389B1 - Method & compositions for treating cancerous tumors - text
gabyher,it is a cartilage tumor. tumor is solid like a bone. it has also soft tissues like banana. it is on sternum area. My friend use protocol 3000 on the tumor now.
l think we have to try strong CDS. But l dont know how can l prepare it at home. ls there any link for 24000 ppm?
l think we have to try strong CDS. But l dont know how can l prepare it at home. ls there any link for 24000 ppm?
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30 Sep 2019 05:44 #61442
by CLO2
Replied by CLO2 on topic Patent US10105389B1 - Method & compositions for treating cancerous tumors - text
Lori, you can make CDS at home. But, you may want to buy a bottle to see if it is going to work for this tumor.
In which country do you reside? I can look for a seller of strong CDS for you.
In which country do you reside? I can look for a seller of strong CDS for you.
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30 Sep 2019 06:05 #61443
by lori1
Replied by lori1 on topic Patent US10105389B1 - Method & compositions for treating cancerous tumors - text
CLO2, We live in Turkey. There is no CDS here and it is impossible to buy on amazon. Because custom problems.
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30 Sep 2019 08:30 #61444
by CLO2
Replied by CLO2 on topic Patent US10105389B1 - Method & compositions for treating cancerous tumors - text
Okay. Then we need to help you make CDS at home! Since you have MMS and either 4% HCL or 50% citric acid, you can make CDS. It is late here, so I will continue this discussion tomorrow.
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30 Sep 2019 09:03 #61445
by lori1
Replied by lori1 on topic Patent US10105389B1 - Method & compositions for treating cancerous tumors - text
CLO2, thank you so much.l have MMS and 50% citric asit. l am waiting for your help. Good nights.
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30 Sep 2019 09:14 - 30 Sep 2019 09:17 #61446
by Truthquester
I'm Scott McRae, creator of "The Antidote" & CDH with CLO2's help (Charlotte Lackney)
- I did a CDH injection / Chlorine Dioxide (CLO2) injection / IV push of 10ml of dilute 50ppm CDH / CLO2 into my blood 3 times in 11 hours & did before & after blood tests that showed that it did NO HARM to my blood, liver or kidneys. This suggests the possibility that CDH / CLO2 is a potential LIFESAVING MRSA cure, VRE cure, CRE cure, AMR cure, Ebola cure, HIV cure, Cancer cure, etc., since it appears to be safe intravenously at 50ppm.
- Join our group on MiWi (was deleted off of Facebook): mewe.com/join/coronavirusebolasolutions
- Every ml of CDH contains 1 drop of MMS, so 1 drop of MMS = 1ml of CDH
- MMS is 7 to 10% activated in 30 seconds while CDH made with 4% HCl is about 50% activated in the bottle. This is why CDH is far less nauseating than MMS drops
Replied by Truthquester on topic Patent US10105389B1 - Method & compositions for treating cancerous tumors - text
Hi everyone on this thread/topic. I just got off a call with CLO2 where we talked about our differing thoughts and discovered why we are coming up with what appear to be different expectations of putting concentrated CLO2 on the skin.
CLO2 either sprays the skin with the CDS (CDS doesn't have any sodium chlorite in it like CDH does) or applies the CDS with a cotton bud followed by DMSO in another cotton bud. This approach doesn't trap the CLO2 at the site and allows it to evaporate or gas out into the air fairly quickly and doesn't cause any kind of a burn on the skin but he did say the DMSO can cause some irritation.
I use CLO2's approach (minus the DMSO) for general purpose skin sanitization, cuts, scrapes and wounds.
My approach for skin cancer, moles, warts and other hard to remove stuff on the body's exterior has been to use full strength 3500ppm CDH (without DMSO) and trap the CLO2 at the site by saturating a small amount of tissue and then covering it and holding it in place using plastic packaging tape which doesn't allow the CLO2 gas to escape to the air. This method of mine does cause a chemical type of burn on the skin and is actually one of the goals of doing it this way. For example with a skin cancer and this method, the goal for me has been to use the CLO2 to penetrate and burn the cancer cells so that the cancer (or mole, or wart) is chemically burned and then it just falls off. So far it has always worked after 1 or sometimes multiple applications.
So we have been talking about 2 different ways of applying CLO2 to the skin and I think both have their purposes.
In the case of the 5 cm cancer tumor that Lori is talking about treating, which is below the skin, I personally think CLO2's approach might work but I wouldn't rely on it myself because 5 cm is a pretty big tumor and so I would want to hit it much harder and faster so as to not give it a chance to grow any larger. I would do that by injecting directly into the tumor as described in the patent, using approximately 200 ppm CDH.
In case you don't know how to make CDH Lori, here's a video that CLO2 made on how to make it:
And then you would also need to dilute it so here's a link to a real good dilution calculator (use the last one on the page):
www.endmemo.com/bio/dilution.php
Hope this helps. Let us know if you need any other assistance.
All the best,
Scott
CLO2 either sprays the skin with the CDS (CDS doesn't have any sodium chlorite in it like CDH does) or applies the CDS with a cotton bud followed by DMSO in another cotton bud. This approach doesn't trap the CLO2 at the site and allows it to evaporate or gas out into the air fairly quickly and doesn't cause any kind of a burn on the skin but he did say the DMSO can cause some irritation.
I use CLO2's approach (minus the DMSO) for general purpose skin sanitization, cuts, scrapes and wounds.
My approach for skin cancer, moles, warts and other hard to remove stuff on the body's exterior has been to use full strength 3500ppm CDH (without DMSO) and trap the CLO2 at the site by saturating a small amount of tissue and then covering it and holding it in place using plastic packaging tape which doesn't allow the CLO2 gas to escape to the air. This method of mine does cause a chemical type of burn on the skin and is actually one of the goals of doing it this way. For example with a skin cancer and this method, the goal for me has been to use the CLO2 to penetrate and burn the cancer cells so that the cancer (or mole, or wart) is chemically burned and then it just falls off. So far it has always worked after 1 or sometimes multiple applications.
So we have been talking about 2 different ways of applying CLO2 to the skin and I think both have their purposes.
In the case of the 5 cm cancer tumor that Lori is talking about treating, which is below the skin, I personally think CLO2's approach might work but I wouldn't rely on it myself because 5 cm is a pretty big tumor and so I would want to hit it much harder and faster so as to not give it a chance to grow any larger. I would do that by injecting directly into the tumor as described in the patent, using approximately 200 ppm CDH.
In case you don't know how to make CDH Lori, here's a video that CLO2 made on how to make it:
And then you would also need to dilute it so here's a link to a real good dilution calculator (use the last one on the page):
www.endmemo.com/bio/dilution.php
Hope this helps. Let us know if you need any other assistance.
All the best,
Scott
I'm Scott McRae, creator of "The Antidote" & CDH with CLO2's help (Charlotte Lackney)
- I did a CDH injection / Chlorine Dioxide (CLO2) injection / IV push of 10ml of dilute 50ppm CDH / CLO2 into my blood 3 times in 11 hours & did before & after blood tests that showed that it did NO HARM to my blood, liver or kidneys. This suggests the possibility that CDH / CLO2 is a potential LIFESAVING MRSA cure, VRE cure, CRE cure, AMR cure, Ebola cure, HIV cure, Cancer cure, etc., since it appears to be safe intravenously at 50ppm.
- Join our group on MiWi (was deleted off of Facebook): mewe.com/join/coronavirusebolasolutions
- Every ml of CDH contains 1 drop of MMS, so 1 drop of MMS = 1ml of CDH
- MMS is 7 to 10% activated in 30 seconds while CDH made with 4% HCl is about 50% activated in the bottle. This is why CDH is far less nauseating than MMS drops
Last edit: 30 Sep 2019 09:17 by Truthquester.
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