TOPIC:

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

Polak
Topic Author
Offline
New Member
Posts: 17
Thank you received: 5

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!

Please Log in or Create an account to join the conversation.

Last edit: by Polak.

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

Michael Harrah
Offline
Platinum Member
Posts: 1209
Thank you received: 1554

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

Please Log in or Create an account to join the conversation.

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.
	Please Log in or Create an account to join the conversation.

Page:
1

Index

Questions on Usage, Discussion and Information

MMS, MMS1

MMS and Wegener's granulomatosis (WG)

Disclaimer: This forum provides general information and discussion about medicine, health and related subjects. The words and other content provided in this forum, and in any linked materials, are not intended and should not be construed as medical advice. If the reader or any other person has a medical concern, you should consult with an appropriate licensed Physician or other Health Care provider. Never disregard professional medical advice or delay in seeking it because of something you have read on this forum or any other linked materials. If you think you may have a medical emergency call your Doctor or 911 immediately.

The views expressed on this forum and website have no relations to any academic, hospital, practice or other institutions. This website is at times monitored. Anything the host finds offensive may be removed at his discretion. The host disclaims responsibility for anything posted by third-parties. Any statements on this forum/website related to Chlorine Dioxide, MMS or variations are not FDA approved to diagnose, cure, mitigate, treat, or prevent any disease.

MMS (Master Mineral Solution) is Sodium Chlorite 28% (22.4% Sodium Chlorite, 5.6% Inert Salts and the remainder water) plus an acidic activator (usually 50% Citric Acid or 4% Hydrochloric Acid) when combined produces Chlorine Dioxide.

License: Except where otherwise noted, content on this site is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.