My Progress So Far

Just re-read the cancer protocol (2000) and JH says not to go over 12 drops of MMS1 per hour. Tomorrow I'm going to back off to the 12/hr and start upping my MMS2 dosages. I've been dinking along at 1-2 size 3 capsules a day. Maybe that's why my progress has not been as effective or rapid as I would like...

It is not sugested any more to use baking soda, as it has a counter effect, go with CDS instaed. Good luck!

Hi Peterjurt,

I'm not using baking soda at all in my MMS preparations -- right now I'm using distilled water and a splash of grape juice over the top to mask the taste (no vit c or ascorbic acid added). Thank you for the Good Luck wishes!

Blessings,
KJ

It's been a bit since I posted here so I thought I'd give an update. I had an MRI on Tuesday (what a freaky experience that is...) and am still waiting to hear back the results. My QT practitioner found a virus in my joints and when she cleared it, wow that made a difference in a big way! I'd say the swelling is down about 50%, but the pain is still there so there's still more going on. I'm doing the 12 drops per hour of MMS 10 hours a day, and also size 3 capsules of MMS2 4-5 time per day. Also the Borax (about 25 teaspoons a day for the systemic candida), and the Lugol's, 3 drops per day. I forget what else -- it seems that there are a million things to remember every day, every hour, every half hour what to take next. Overall I feel pretty good though. Still eating meat, which I never thought I would do or be able to tolerate as well as I have. I'm learning how to cook it by recording Ina Garten's cooking show. Love her! She's my new surrogate mom

Just working every day to stay focused on what needs to be done next...

Hi KJ, You've really made progress on your doses. Well done you, i know exactly what you mean about trying to remember it all, phone alarm forgotten to be set and it's all out of whack. I've had to chill out about it all really and not feel it's all gone wrong if I've missed a dose or so. From all the varying protocols or experiments on different doses times a day if I'm still getting it in me regularly that still doing something. I saw one study on people with cancer working on getting up to 15 drops 3 x a day and some of them still made progress.

I am amazed at how well you've got it all regimented down. I pickled myself one dose of MMS2 so ended up taken 2 x size 3 capsules within 10mins. I was fine. I have a chart i keep on the fridge or take with me so i know where I'm at with everything sort of. LOL

Living in between dosing is a little like those short tea breaks at work. LOL

I've been taking Kelp for supplementing iodine. Would kelp not give enough then? I've heard about iodine, medical that if it's injected directly into the tumour over a 3 week period the tumour will be gone. I haven't been able to find out the amount or anything and can't remember if that was once a week or daily.

The food thing is a biggy, sounds like your doing well. I was a meat eater but for a while now even before all this i've been really not wanting to eat meat. I kind of figured from looking into Brain Peskins the hidden story of cancer he's talking about getting essential fatty acids (EFA's) into the body. The Budwig protocol is doing that also as flaxseed is a parent EFA and more so then fish.
I'm getting that in my ever day and on top of the quark mix i sometimes ground up a tablespoon full of whole flaxseed and put it in a smoothie and it's actually really nice.

I remember reading that Jim had said to build up to the MMS2 for 12 hours bi-hourly which to me was 6 a day. My head does spin with all this information.

L&L

KJ and LL (Utopia)

Thank you for keeping us informed on how you are doing. I know what you mean about keeping an eye on the clock and get all the work
done in between. I also have a chart on the fridge to keep good track of things.

I posted my latest report on the Testimonials: Asthma thread.

I had to switch to CDS because the MMS1 and 2 were giving me horrendous nausea and diarrhea. I had no desire to do or eat anything anymore.

For 2 weeks or so I have been doing the CDS the "shot glass method", which is super easy to make. I am still doing very well, breathing has been
very good, I can walk fast uphill even, I can laugh and not cough anymore, lots of energy.

Even with all the wildfires in the state of Washington and Idaho causing so much smoke in the valley, I am still breathing ok. In the past I would have
to travel somewhere else because no steroids would mask the severe wheezing and suffocating feeling.

KJ I hope you get a good result from your MRI, and I am glad your QT practitioner cleared your virus.

I also eat meat but I used to be vegetarian, doing green smoothies and juicing etc. and getting worse and worse...

Best wishes to both of you! Evanir

Hi Utopia and Evanir!

Today is Saturday, and the Dr, who at first told me she would call me with the results, now says I have to (surprise) pay her for another office visit to get my results. I can only assume the news is bad given that she won't tell me over the phone. Infuriating. I don't need to be coddled, I just need the information. At this point I would be surprised if it wasn't cancer -- whatever it is has spread throughout my foot (toes, ankle joint), up to the knee, my left thumb is now involved, as is my jaw and my upper neck. I am coming to a real crossroads with the MMS protocol. It is helping me, I am certain of it -- but obviously it's not helping me enough. JH says not to go over the 12 drops per hour for the 2000 protocol, and I'm already doing that. Already doing the MMS2, the diet, the Borax, and the Iodine.

Not sure where to go from here. I feel good doing this protocol, but I need it to work faster than what's spreading in me...

Hi Evanir and KJ and all that has joined. OH MY KJ ...I'm so sorry. Please do not get discouraged. Maybe she found that it had cleared and wants to question you about it or something good.Never look at it as bad. JH has protocols for alot of stuff. You are doing what you can to work on this and are doing great. Please don't get discouraged. I found yesterday tha when I miss one day of my 2 a day doses of MMS2 I have issues breathing real bad. I missed the day before and wow I felt bad. I remembered I didnt do the MMS2 so I did yesterday and I could breath a little a little bit better for me I can tell the dif if its alot or a little. I had purchased some Colidal silver and some DMSO the other day and will be getting it next week. My son paid for this for me.Anyone who can guide me on how to take the DMSO and the colical silver please do give input. I would like to put it in my nebulizer if thats where I can use it at ??? YES ? can I USE my nebulizer that I use for me inahaltion stuff?

Hi Megg.

Because of your breathing problem, please be very careful taking anything new. If you do use dmso, I would advise going slow - maybe starting out with a very small amount - even just a drop to begin with, and then increasing very, very gradually. Also, I don't know if you can use it in your nebulizer.

All the best,

Scott

MOST DEFINATELY scott. I ALWAYS start out small as small as I can go and work up. This is how Pam has me going on everything so if you want to know whats hse is doing for me and hoe much I'm taking or whatever you can ask her. She is guiding me.I am sti;; reading up on DSMO. Haven't tried it yet. Pam isn''t too familiar with it so Iits up to me . I will talk to Michael and see what he says. Im sure just a little won't hurt lol . but yes I will be careful...thanks ...