TOPIC:

Hi everyone, I'm reaching out to this community because I need some advice and guidance. A close family member has been diagnosed with triple-negative breast cancer that has spread to her liver and bones. She’s currently undergoing chemotherapy and radiotherapy, but we’re exploring all possible avenues to support her treatment. Here’s a bit more about her situation:- Diagnosis: Triple-negative breast cancer with metastasis to the liver and bones.- Current Treatments: She’s about to start on chemo and radiotherapy, and taking medications for pain and other symptoms.- Symptoms:  She’s dealing with a lot of pain, fatigue, and has had a persistent fever for a while now. ​​We have some specific questions and would really appreciate your help:1. Effectiveness of MMS/CDS: Has anyone here used MMS or CDS for triple-negative breast cancer? What were your experiences and did it help?2. Dosage and Administration: We’ve read about different ways to take MMS/CDS, like oral doses and even intravenous use. What methods and dosages should we try?
​3. Injectable CDS: We’ve come across some info about using CDS injections. Has anyone tried this? Is it safe and effective?4. Combining with Conventional Treatments: Any tips on how to use MMS/CDS alongside chemotherapy and radiotherapy? Are there specific precautions we should take? We really want to do everything we can to help her in this fight and your experiences or advice would mean a lot to us. We know MMS is quite controversial, so we want to make sure we’re making an informed and safe decision. Thanks a lot for your help! Best,  Alex

Hi Alex. I treat my wife with a similar condition (breast cancer spread to the bones, liver is fine) since October 2023. She was 60 yo when started, now 61.
We first used oral MMS, for about a month. The usual protocols, first protocol 1000 (up to 3+3 drops every hour, 8 times a day), then 2000, and 3000 with DMSO. Clinical improvement was rapid, within 2-3 days had more strength, mental clarity and feeling better. Kept taking oral MMS in increasing doses, but after about a month there were stomach problems. No real vomit, but stomach pain and discomfort. Switched to CDS, 10ml/day at first, up to 20ml. Kept it for some days, but eventually stopped taking ClO2 about mid-November 2023 because of the stomach.
As long as she was taking it, she kept improving clinically. She also had issues from a huge uterine myoma (19cm, non cancerous) which was bleeding constantly for more than a year. For three weeks as she was taking MMS, it stopped bleeding at all. Ultrasound in November 2023 showed it had decreased in size to one third compared to July 2023. This was a major issue, because it was giving her anaemia, weakness and worsened the tumors condition. Slowly it started bleeding again as she stopped taking MMS/CDS.
Mid-December 2023 an iv port was installed at a central vein and since last Christmas she is taking CDS iv. Improvement is slow but ongoing after that. Uterus has stopped bleeding entirely for the last 2+ months. X-rays on March 2024 showed at least one bone lesion restored (healed) compared to November 2023. Bone spread (and accompanying pain) is not an issue any more, we don't even do regular scans to avoid the radiation. Breast tumor looks contained but still active. Antigen CA 15-3 was still positive at April 2024 but its value reduced, compared to November 2023. We are about to check again this month. She has some evening fever (morning temperature is normal). Recently we came in contact with a person with more experience in using MMS/CDS/CDI and realized that iv daily dosage was rather low. That's why improvement is slow and took so much time for the uterus to stop bleeding. For the last two weeks dose is increased to more that double and evening temperature has gone down 1-1,5 degrees Celsius towards normal.
Overall, better and faster results we had with oral MMS/CDS, as long as she was able to take it. In your situation, depending on her stomach condition, if you go slow and be cautious not to upset the stomach, you should have very good results, regardless of tumor location. In fact the liver should be the first to be positively affected as it has more blood flowing through it and is directly connected to the GI tract. If you do have a vein port installed (which you might have done already if you consider chemo), you can definitely use CDI safely and with good results. I can provide detailed info on that based on my wife's experience.
CHEMOTHERAPY AND RADIOTHERAPY WERE NOT EVEN CONSIDERED AS A POSSIBLE TREATMENT FOR US. NO TREATMENT THAT KILLS NORMAL HEALTHY LIVING CELLS WILL EVER BE CONSIDERED BY US. We didn't even use hormonal therapy, in which my wife's tumor found to be susceptible, because even this treatment has side-effects.
Hope to be helpful, have faith and don't fear. Fear is a bad advisor.

Pan

Glad to hear you are figuring out how to use it and getting good results, but MOST IMPORTANTLY not stopping and continuing as best and as much as you can.

Remember that "MMS" is MMS1 (CD) AND MMS2 (Calcium Hypochlorite).
(and some other things, like Bentonite Clay Protocol, etc.)

My brother and I did significantly better when we started using MMS2.

I have to do monthly or thereabouts Clay protocols to get rid of recurring mold & fungus issues, or it interferes with the MMS1 and makes it not work as well.

As usual, I suggest following the protocols in Jim Humble's "MMS Health Recovery Guidebook".
(IF you choose to go the MMS route)
And that would be for ALL Health Issues and Problems.
 

where's the best place to buy Calcium Hypochlorite or MMS2 drops? thanks

this is so amazing that you are using and seeing results with MMS/CDS. I absolutely hate big pharma who has zero intentions of making people better. Just dollars.

I would love to hear more about the person who has more experience with this stuff. Can you share that info?

Im completely rooting for you guys!!!!

mattcanride2 wrote:

where's the best place to buy Calcium Hypochlorite or MMS2 drops? thanks

There are many sources. I mention on my webpage, link below, where I get my products.
 

@ mattcanride2 , Nothing special, he just gave us the piece of information that Andreas Kalcker mentions about dosage of CDI to dogs, 5-10 ml per 50 kg dog. This helped me establish a dosage for my wife much bigger than what she was taking. She went to 14 ml CDS iv daily, and for the last few days she's at 20 ml daily, all diluted in 0.9% normal saline solution. He also pointed out to us sulforaphane through broccoli sprout juice, and my wife is started on this too.

Pan