I had the question below come up. Then my response is below. Anyone have any other ideas or experience?
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Good day, everyone,
I hope this e-mail finds you enjoying better health as a result of using MMS.
I am looking for info/experience on using MMS for Myasthenia Gravis.
Thank you in advance for your responses.
Wishing you all Greater Health.
Jaime
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Hi Jaime,
MG (Myasthenia Gravis) is supposed to be an autoimmune nueromuscular disease according to wikipedia. I cannot find anything mentioning this in Jim's writings. It is hard to find info on it, curezone has a forum on it
www.curezone.com/forums/f.asp?f=433 .
Based on what Jim says in his new book in all likelihood there are some pathogens involved in this disease, probably pathogens attacking the nerves. When that happens it looks like autoimmune and it affects the muscles. This is why Jim goes around claiming MMS can cure 97% of all diseases, it is because every time he tries it on something it works and the most likely explanation is that pathogens were involved. Even something like sciatica pain he says is pathogens operating on the nerves causing the pain. The MMS will cure it.
A person who has MG should use protocol 1000 unless it is life threatening. If so, then they should start on protocol 2000. Or if they try P1000 and do not get cured, then they should go to P2000. Also, DMSO is extremely good for the nerves, so it should be taken by mouth and possibly via the skin too. It could be mixed with some of the oral doses of MMS just prior to drinking also.
Have them try Protocol 1000 and take DMSO too if possible. Or they could just start off taking MMS2 and working up to 4-5 doses a day and see how that does.
Let me know how it goes, something here should work well.
Healing wishes,
Michael Harrah
