TOPIC:

Hello folks,

I am a new member of this board, but not new to MMS. I have been using it for my Ulcerative colitis and my son's Autism for 2 months now. I am going slow and steady. Glad to say I see benefits.

2 days ago, my Dad got diagnosed with lung cancer and he is still undergoing tests to find the kind and severity of it. I am sure the medical doctors will send him through chemotherapy and stuff that will get him nowhere except a pretty difficult death. If he is to die, I want him to die peacefully and not in pain. His pain threshold is pretty low as it is. PET scan showed that he has lumps in right lung and a lymph node on right side of the neck.

I am looking at MMS as one of the options. I checked the website and there are few cancer protocols. I admit, I am so overwhelmed that I am unable to think straight and unable to absorb what I am reading, hence I am asking for help from those who have been through this. Please help me get up and running with this protocol for cancer. I did a quick search and I do notice that there is some pretty good threads there. I WILL read ALL of those threads, but I have to admit, at this moment, I am desperate to get him started and then tweak things as I come across.

I am using MMS1 (Sodium chlorite and HCl), Can he use the same thing or he needs to use something else (like MMS2). I am using Kerri Rivera's drop method and I am on 20 drops and DS is on 11 drops.
Do I need DMSO as well here?

Thanks a million for all help in advance.

(PS- If mods would like to move this topic to more appropriate section, please do so.)

Hey Lifesurfer,

Just read yr post and seeing you online makes me rush the article, I got from earlier posts, to you: www.cancertutor.com/dmso

You are exactly on the right track and you did all the work from MMS already, so ideal to help yr father!

Yes, to enter the cancerous lumps in his right lung, you will have to add a drop of DMSO ( a great carrier to make sure MMS can do its job where needed) to yr MMS protocol 1000. When you add the drop of DMSO it is called protocol 1000+.

Please inform your father not to take any chemo/death row....only 3% of success whereas MMS/DMSO will have a chance of 90%.

First read the above post and let me check for the exact protocol 1000+ if not already mentioned in the above post,

Regards, keep up with yr good job helping your father,

mmsinfo.org/protocols/protocol_1000+.pdf


Basically it is one drop of DMSO for each drop of MMS1

Hopefully start today and start slowly, like 3 drops activated per day, slowly moving to the 6 then 9 drops eventually 24 drops/day carefully listen to the reactions of the body...
If nausea: take less, but do not stop
Vomiting: reaction of the body that detox is going to fast (called herxheimer)

Do keep us informed,

Wish you strength and health

Thanks Simone.

I checked all of those protocols, but there is another protocol, 4000, that Jim Humble approved for cancer usage. So I was wondering, should I stick to 1000+ or consider 4000.

I have heard that people to 'drink' 1tsp of DMSO and I have no idea if thats a great idea (taking into account the stinging part).

Thanks again.

Hello lifesurfer,

Protocol 4000 is with MMS2 which is in capsule form. When we start with your father with protocol 1000+ (with DMSO) slowly we can see his reactions. If he can handle (that is to say no nausea, vomiting) once a week we can start giving him a MMS2 capsule.

Do start slowly, as a lot of cleansing is to be done. But if you stick to the protocol (preferably go along DMSO with the amount of drops per drop MMS) your father's lung cancer will be going better for sure. Is he willing to try?

Hi Simone,

I don't know if he is willing to try, but I am gathering all information. I am just waiting for his oncologist to tell him to use all very expensive, probably useless and very painful therapies. And that is the point I am going to make my hit. He is not an easy nut to crack. The other day, he left his Oncologist speechless with the questions firestorm.

If I have to convince him to use MMS, I should be well prepared with ALL evidence.

He is a pathologist himself, so you can imagine the brainwashing he has been through. If I prove it to him, he will accept it without a single question.

Hi LifeSurfer,

You mentioned that you have a child that you're using Kerri's protocols with so you know the importance of diet and doing colon cleanses too, etc.

Here is a video by a biochemist who has/had an autistic child. She talks about the amazing effects that diet alone had on her child and on herself. Maybe it will help in some way to convince your father that there are other alternatives.



My mom died of lung cancer awhile before I knew of MMS however she was such a believer of the "system" that I doubt if she would have tried anything "outside the box" anyway .

May your father be well,
Scott

Trust me Scott,

Nobody in my family is as 'diet freak' (as I am called in the family) as I am. Not only my son has Autism, but I have ulcerative colitis and I follow both of these much more religiously than anything else. I will get there too, but partial hammering doesn't work in my family. One HUGE hammer and get the job done.

I noticed 2 lung cancer testimonials on YouTube using MMS. I have emailed to the contacts suggested in those videos to check if I can talk to those folks myself to hash out few nitty gritty details. Lets see if I get an answer.

At this moment, my plan is to talk to either of those folks (if I am lucky enough) and collect as much information as I can. The make a detailed plan, collect supplies and get them on their feet.

You know Lifesurfer, what I did with my father (forestadium prostate cancer)?

First of all I gave him as a birthday present MMS. His answer was: I'd rather had a book....I did not react. I just sipped right in front of his face and then I said: now it's your turn...we'll do this together. Now the prostate cancer is gone. And he is a fan of MMS. Each week he takes his 6 drops. Also a really hard nut to crack. I love him though, that is the biggest reason he took the MMS. Love is the answer. And (only with family) a little push

Love always, Simone