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Hi David,
Edwin was actually speaking to Bruce in reference to Bruce's comment earlier. Because of the way the forum system works, sometimes it is easy to get confused about what/who someone is referring to. It is good you have not had any lung problems though.

Hi Edwin et al,

Yes, I'm finding that MMS2/Cal Hypo is an incredible tool for reducing lung congestion - possibly something that will have a profound impact on pneumonias, tuberculosis, etc.

Wouldnt it be best to start a new thread on MMS for Lungs, Congestion, etc. then keep adding to this Kidney Unrelated thread?

David, ultimately that's probably right, but on a forum, trying to keep everything "just so" is a labor of Sisyphus. We do the best we can, and if a new question is raised in a thread it makes sense to respond in place.

We'll get the congestion info over to the MMS2 department eventually...

BTW, I sent your posts on your Kidney Tumor process over to Jim Humble and Mark Grenon at Genesis II Church in the Dominican Republic, and I got this back from Jim:

Thanks, Bruce, very nice story.

With love,
Jim

I included your email address with the information in case they want to contact you.

Best, Bruce

Thank you Bruce. I hope my success story aids in any way possibe.

becareful about that.u can burn your lungsi did)

better to do a high colonic with activated mms,since it will be close to the kidneys.and iv activated mms,or a injection of activated mms(on you tube)

Hi David
Thank you for sharing your cancer story, it gives hope to everyone out there struggling with this disease and struggling also with medics who seemingly do not want to help/can't help/aren't interested in their patients at all in any meaningful way. And for you personally such wonderful news - cancer tumours shrinking-amazing, I am very pleased for you.

I lost my mother to cancer - didn't know enough about MMS at the time to use it.
Am now trying to help my father overcome cancer of the esophagus. He was diagnosed 18 months ago; he is 82 and the docs were pretty grim faced about it all. But 18 months on here we are. I think the reason he is doing so well is because 2 years before he was diagnosed he was taking MMS off his own back, on the old regime of a 15 drop dose in the morning and one in the evening. I believe that has stood him in good stead. His tumour has not grown or spread since diagnosis. Doctors are a bit confused. BUT the tumour is still there and still dangerous. I have only recently got him back on to MMS - protocol 2000 without the MMS2 as he can't swallow the capsules. Am persevering but it is hard sometimes and easy to give up when the MMS is making him feel bad. Sometimes the amount of things one could try with MMS is overwhelming too for the carer - should i do this or that etc. MMS1/MMS2/CDS/DMSO...swallowed, bathing, enemas etc. Great to have such choice but overwhelming sometimes too.

It takes real courage to share your story about cancer, to question the oncologists and to persevere with MMS in the face of all the naysayers.

So thank you for your feedback, it is very inspiring.
I will post feedback on our situation when we have news and thanks again.
Very best wishes.

yes it does help immensly in lung congestion.it saved me when i had the h1n1 swine flu.