Motor neuron disease

Has anyone had experience with MMS and Motor Neurone disease? I have a friend with it and wonder if MMS could help her.
Thanks ,
Liliana

No knowledge of this in particular, but be assured that MMS helps EVERYONE!
Paul

Hi Liliana,

I have been corresponding with a 71 yr. old gentleman who has ALS (Lou Gehrig's disease) which is also called motor neuron disease. He is in a power chair by himself most of the day and cannot make it onto the toilet himself, so he cannot afford to get diarrhea or vomiting.

Therefore he has gone very slow in introducing three items in a protocol regimen we devised for his situation. He first started on pHenomenal water ( phenomenal-water.com/ ) and is taking one quart a day of the mixed water, which is about a half dose for his body weight. Then he added in a capful of DMSO taken orally with half glass of water morning and evening. Then he added in MMS2 capsules taken 3 times a day.

He introduced each item slowly over about a week's time. He has been on this regimen for a couple months and is noticing improvements, more strength and fewer prostate problems. Also, he went off the MMS2 for a week when one capsule broke open in his mouth and he was not close to water and so got a burned throat. In that week he noticed a regression, so he knows the MMS2 is helping.

He did not start with the MMS1 because of the difficulty in mixing the doses and thought the MMS2 capsules would be easier to start with. He has not encountered any nausea or diarrhea so there have been no accidents other than the burned throat from the MMS2 capsule that broke open.

If a person could take MMS1, I would highly recommend that but with ALS I would go very slow in introducing it and watch for gradual improvement. It seems there is a danger in ALS cases of giving them too much oxidation therapy. The dose needs to be just right it seems.

According to our research we also believe this condition is caused by viruses attacking the nerves and muscles. The best information out there seems to be that it is pathogen related, along with things like heavy metals.

This man had tried a great many natural therapies and expensive supplements before the MMS2, all of which did not help. So the improvement he is seeing is giving him some strong hope. There is a website ericiswinning.com where a long time ALS survivor says MMS works great. Here is another thread we have on ALS also genesis2forum.org/index.php?option=com_kunena&func=view&catid=7&id=2302&Itemid=66#2302 .

Michael

Michael,
Thank you so very much for your time annd knowledge in giving this information packed reply. It is very helpful and I appreciate it.
I am visiting my friend in a few weeks and I am hoping she will be open to looking at MMS, DMSO and Hemp oil. Luckily hemp oil will be available in her area and easy to acquire.
Blessings,
Mary