Using MMS1 and chemotherapy

Hello everyone, I’m new here. Me and my family are using MMS1 many years.
My mother (84) has got diagnosed adenocarcinoma G2 in the right lung two months ago. She’ll start chemo- and immune therapy next week. She’s taking MMS1 2 drops/dose as many times as she can endure every day, at least 5-6 times. Got prescribed folate acid prior to the therapy where it will also be used dexomethazone. 
I’d like to ask here how to combine MMS and chemotherapy, are there any rules about that? Does she need to stop it for a while?

I’d be very thankful for any experience, information or advice shared here. 

Hello,

Difficult position and difficult to answer.

Much work is to be done. I will just add my 2c as there are other helpful people here and they may answer your question better than I.

I personally have far more faith in Chlorine Dioxide than any therapy they offer. Having said that, unfortunately, the burden is on you. When you go to the hospital, they put it in and do all the work. For MMS/CDS, you have to do the work and you have to use the volume of Clo2 needed to do the job.

If she starts with what you mentioned, that is great and I would build on that quickly as much as possible. Switch to CDS if that helps her with the taste. More is more.

A lot is needed and some may interact with the chemo and be lost/used up on that but that would not stop me taking it. Having an acid at the same time if prescribed will also lessen the work that MMS can do for you, but that would not stop me taking it.

If you must use them, maybe separate a little. But don't lose time doing that.

If there were any negative effects or interactions, I personally would prioritize Clo2 over chemo or anything else.

I would just try to have as much as I could as often as I could and she will need that support from you it seems.

I watched a friend have extremely slow progress with chlorine dioxide due to them consuming far less than what was needed, they eventually stopped and then they submitted to the pressure to have immune therapy and suffered multiple complications straight away and ultimately died from them.

So I would say to keep going with MMS/CDS use as much as possible.


On a positive, it is really good she is trying it. I currently have family with cancer unwilling to even talk about Clo2.


Finally, it is not my place to say but I would say to keep away from chemo and other therapies if possible. But it is not always that simple.

I really do wish you all the best

-john

Byos wrote:

Hello everyone, I’m new here. Me and my family are using MMS1 many years.
My mother (84) has got diagnosed adenocarcinoma G2 in the right lung two months ago. She’ll start chemo- and immune therapy next week. She’s taking MMS1 2 drops/dose as many times as she can endure every day, at least 5-6 times. Got prescribed folate acid prior to the therapy where it will also be used dexomethazone. 
I’d like to ask here how to combine MMS and chemotherapy, are there any rules about that? Does she need to stop it for a while?

I’d be very thankful for any experience, information or advice shared here. 

Chemo has, at best, a 5% chance of recovery  from cancer. I would never use chemo for any disease. It kills everything - the good and some of the bad. 

For many years the sick-care cartel has offered (approved) three fixes for cancer: Cut, Burn and Poison. They know that CLO2 can cure cancer, but they won't use it. The reason is because once the public discovers that CLO2 cures almost all diseases, those MDs, also known as legally approved drug dealers, would go out of business. Big Pharma does not care about us, only in making $$$$. 

I can't tell you what to do, but you could do your own research into the many other ways to cure cancer. Try not to be a victim of the Sick-Care Industry. 

 

Thank you very much for the reply!