TOPIC:

MMS and Wegener's granulomatosis (WG) 25 Sep 2011 09:06 #5687

Polak
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Hello! I received the following request.

"Suffering from Wegener's granulomatosis (WG) .Take 2 tablets daily medrol and medicines for blood pressure and kidneys. I applied monthly pulse therapy with methylprednisolone and endoksan to suppress immunity. Now my prescribed daily imuran and also suppress the immunity but I have not yet begun to take it. If MMS does not conflict with my treatment administered? Whether it can employ and which protocol?"

As far as I understood, the disease is an inflammation of blood vessels. This makes me think, is that MMS will help, or even cure this disease. But why the official medicine is trying to suppress the immune system, and how it will affect the intake of MMS, after he increases?
How things stand generally with the autoimmune diseases? Because MMS reinforced, and the official "medicine" is trying to suppress the immune system!

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Last edit: by Polak.

Re: MMS and Wegener's granulomatosis (WG) 26 Sep 2011 02:19 #5718

Michael Harrah
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Hi Polak,

If I had someone with that I would just recommend going very slow with protocol 1000. I don't think there is any way to predict what the effects will be between the disease, MMS and the medicines, except that we don't have reasons to think there will be a problem.

The example of MMS working for HIV people who are taking ARVs, and the fact that we don't have reports of drug interaction problems indicates to me this person's WG case will probably be similar. It seems there is not much to lose if they just go very slow and watch what happens.

Probably in one way or another there are pathogens involved with that illness or at least as part of that person's total burden on their system. In all likelihood MMS would help a great deal.

Just my opinion,

Michael

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Re: MMS and Wegener's granulomatosis (WG) 26 Sep 2011 04:46 #5723

Polak Topic Author Offline New Member Posts: 17 Thank you received: 5	Thanks Michael. I appreciate your help. I also thought to give these recommendations and will now do. If the person decides to cure with MMC and hold me informed, I'll write here.
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