TOPIC:

Hi,

My brother in law has Acute myeloid leukemia (AML) and for some reason, neither he or my sister (who he is married to) is interested in MMS.
He was just told that his remission is ended and he needs chemo and has a 30% chance of surviving with this treatment.

Their plan is to ask if they can instead wait a few days and contact a group in Chicago to work up a profile and possibly give him a bone marrow transplant. They are in Syracuse, NY.

I am sure this is extremely stressful for them and I have tried to give them MMS1 in the past and tried to give them information, but my sister is a LPN nurse and I really don't know what they are thinking, but when I asked her to try MMS1, she said she tried it for a couple of weeks, but it doesn't fit into her lifestyle.

I feel like I am not communicating effectively or at all on this subject.

Does anybody know how I could find out about the effectiveness of MMS1 or MMS2 or the cancer protocol specifically on Acute myeloid leukemia (AML)?

I know Jim writes in his book that MMS is effective on leukemia, but I thought that if I had more specific information to offer them, that they might finally give MMS a real try on him.

Thank you all,
Joe

Joe, unfortunately, MMS is still in the realm of fantasy land for most , especially medical professionals. They will not even give it a chance since if it was that good, Dr's would use it in hospitals. They still believe that Medicine is there to cure people and all the current protocols are scientific and cutting edge.

Let them go in their ignorance, you will only belittle yourself insisting some more.
This is my opinion based on real life experience. ;-(

Hi Joe,

GB is probably right.

The way to treat it would be the CDS. Did you see in Mark's video that he mentions a cure of leukemia in 1 week (www.facebook.com/photo.php?v=10150991514880160.).

The thing is the people have to have some belief in it or they won't even take the dose every hour. Sounds like they are not the least bit open to it.

Michael

Usually, what I find with people, is that when they say it "doesn't fit into their lifestyle" - you have to ask them to clarify what they're talking about. Is it the hourly dosing? Is it the herximer reaction? Is it that they're so tied into the medical model that they are afraid/unsure etc. to try something else? Is it the taste?

Unfortunately many people will only move to alternative treatments as the very LAST resort. As long as they can focus some hope into the medical model, they'll follow that fantasy, because it's been so well sold to them - and particularly someone like your sister, who has a career in the field.

I have a friend who has lupis, but she keeps her numbers down with massive amounts of vitamins - is she "cured"? No, neither of us think so. Her only concern is her badly damaged finger nails, which look so bad. but she's doing something else with DMSO for now. MMS 1000 is inconvenient - she has to do it every hour. It's not worth the effort - she can get to the gym and work out, she can go to dance classes, work in her garden, her numbers are in the single digits, yadda, yadda, yadda. Why should she take 3 weeks out of her life and do something 8 hours a day? Or, when you realize that she was around for the original protocol (ramp to 15 drops 3x a day), you can see why she would think it inconvenient <G>.

I know she has inflammation issues (you have to with Lupis, it's an autoimmune disorder) but as long as she's adapted to her current paradigm, she is not eager to make the move.

Here's hoping that when your brother-i-law and sister finally get to the point where they are willing to try, he can still be helped. And he may never be willing to try - all you can do is be an example, a shining light.

I told my sister aboud mms/cds and she is asking some questions.
If her husband wants to try the cds, what would be the protocol?

Off the Genesis II Church site at: genesis2church.is/mms-protocol-2000.html

Protocol 2000

PROTOCOL 2000 is for cancer and other life threatening diseases. It basically is taking as many drops of activated MMS each hour as a person can take without becoming any sicker, or feeling worse, or developing diarrhea. It must be done for 10 hours a day, for 3 weeks or until well. It is best to start off with only one drop an hour and quickly build up to as many drops as you can take.

You should be able to do the same with the cds. I would think that the difficulty would be getting it to them to try in the first place - unless you can make it for them and get it to them. If you need to ship it to them you might take a look at the "How to store cds" new topic that I recently started. There it shows a very good way to package it that should work very well for shipping. Pam has also mentioned there about a way to keep it cool during shipping too.

Another thought would be if they would be willing to see Mark's video - that might give them some encouragement to give it a try too.

Take care.

Here is the link to the storage container idea and shipping idea from Pam:
genesis2forum.org/index.php?option=com_kunena&func=view&catid=16&id=8997&Itemid=66

Ok, they are less than 1 hour drive from me, so I would drive and bring it to them if they let me.
Thank you. He's kind of in bad shape.
If they agree to try this, I'd really like to get word from Jim or someone from the DR on using CDS.
For the reason that he doesn't have much time left and I really need to know if this is how to use CDS.
I mean it looks to me like what you are saying is correct, but Jim would be the one who would know best.
Joe

Ok, So my brother in law asked me yesterday to bring him the MMS/CDS.
The doctor told him he has about two months to live without chemo and if he takes the chemo, he has about a 20% chance of surviving.
The doctor also is waiting for him to schedule chemo.
Last evening I brought over all my supplies for Protocol 2000, protocol 3000, bath protocol, bag protocol, which is listed on this page for leukemia:
www.genesis2church.is/mms/mms-protocol-list.html

I also gave them two 4 oz and one 2oz bottle of my CDS.

My CDS is probably a bit weaker than it could have been.
I made it the day before Jim's instructional video was released.

I did it according to Andreas Kalker. But after about 10 minutes, the reaction seemed to stop producing bubbles and I stopped and took it apart.
Then when I poured out the MMS, the fumes were very strong, so I kind of know that it could have been stronger.
It was still dark too.

Anyway, that is what I had and protocol 2000 says to increase the dose aggressively and that is what he has started to do.
The CDS I gave them is bright yellow and I do think that there is a good dose of CDS in each ml.

I have some tasks I need to do:

I need to obtain a 2oz baby bottle and I think it needs to be glass. I prefer glass, but I am in a hurry.
If plastic will do, maybe I can purchase locally. Otherwise I will order online, the glass.
Can someone give me any suggestions on a good choice for this? Or is the "Green Sprouts" bottle the one to get:
www.amazon.com/green-sprouts-Ounce-Preemie-Bottle/dp/B004K6LMQQ/ref=wl_it_dp_o_npd?ie=UTF8&coliid=I2UUKWDASKTZ52&colid=1KZLR6KXAXBDZ

Now, I have a more important choice to make.
The CDS is shown to have some advantages, but there is no protocol for CDS.
The leukemia protocol calls for MMS1.
My brother in law does not have time to make a mistake.
I know that Jim and Mark are reporting that there was a successful elimination of leukemia using CDS, but we need to know how to proceed.

My brother in law can judge how he feels and also will be getting a blood test in two days.
The abnormal young white blood cells are already increased in number and if they are higher, then he might start thinking of chemo.

We need to know how to judge if this is working.
Should he get better results right away, or should it be something else?

Joe