mms side-effect ？ help 。。。 The renal hamartoma

My mother and I both used MMS to treat hepatitis B, but something happened. My mother and I both had renal hamartoma after taking MMS. I found it about half a year later, and my mother was found about 2 years later. At first I thought my hamartoma might be caused by other things, but when my mother also had it, I thought it might be a side effect.

This makes me feel sad and scared, because MMS can inhibit hepatitis B virus, and my mother's liver cirrhosis is gone. But our antigen hasn't turned negative yet. If the hamartoma grows, it is also dangerous. Can someone answer that? thank you

 

How could CLO2 (MMS1) cause this? CLO2 is just an oxidizer. 

rarediseases.org/rare-diseases/pten-hamartoma-tumor-syndrome/

"The PTEN hamartoma tumor syndrome (PHTS) is a spectrum of disorders caused by mutations of the PTEN tumor suppressor gene in egg or sperm cells (germline)." 

"When the strictest diagnostic criteria are used, patients with a personal and family history of Cowden syndrome (CS) features have up to an 85% chance to have a PTEN mutation."

Sounds like this ailment is hereditary. 

I don't know, but it was found by B-ultrasound after using mms1，，I didn't find it in the previous physical examination。

If MMS1 caused problems like you describe, they would have surfaced years ago. That has not happened. A simple oxidizer can't have caused renal hamartoma. 

Because this is a benign tumor, do not do B ultrasound will not find。And after I found renal hamartoma, I continued to eat mms1 (CDS) for several years, and he became a few millimeters bigger

Ojrain, ClO2 is not too different from the oxidants generated by the immune system - oxidants known to devour cancer/tumors. I suggest you to do some research on the main cause of cancer, which is lack of oxygen (an oxidant).
Chances are your condition would have been worse without using mms "for years"..
I would suspect lifestyle, diet, vaccines and other "medication", and possible environmental causes. Not mms.

wrote:

rarediseases.org/rare-diseases/pten-hamartoma-tumor-syndrome/
[...]Sounds like this ailment is hereditary. 


 

Not saying it can't be hereditary, but have a look at the supporting organizations on the website you quoted from. Some of them are known to be part of the cancer industry. This industry tends to look for explanations for different diseases that can't be cured, only treated. "Unfortunately, it got to be your genes. If you have the money we can make you suffer some less".
If it were my renal hamartoma I would research in some other direction. That will increase chances for actually solving the problem IMHO.  

wrote:

Ojrain, ClO2 is not too different from the oxidants generated by the immune system - oxidants known to devour cancer/tumors. I suggest you to do some research on the main cause of cancer, which is lack of oxygen (an oxidant).
Chances are your condition would have been worse without using mms "for years"..
I would suspect lifestyle, diet, vaccines and other "medication", and possible environmental causes. Not mms.

thank you 。 I don't live with my mother ，And it was found after using MMS. There was a physical examination every year, but it was not found before