I was recently diagnosed with Chlamydia Pneumoniae (CpN). I've known for over a decade that I've had an autoimmune disorder but it's taken this long to finally get a diagnosis. It's now in it's chronic stage. I've done a TON of research on it and, what makes it sooooo problematic, is that it's covered in a biofilm and antibiotics simply can't penetrate the biofilm.
My Integrative Medicine Doctor recommends IV Ozone Therapy (ten sessions with a 10-Pass machine for a total about $6,000) but I simply can't afford it. I've been unable to work since 2012 and am on Disability.
Not sure what MMS protocol to use so starting small. But here's what happening: my symptoms get worse the more MMS I use. It's doesn't feel like a herx reaction: I'm not nauseous, no loose bowels, no headache, no fever, etc. I'm not experiencing any new symptoms; just an exacerbation of my current ones, which frightens me and makes me think that all the naysayers are right and I'm just poisoning myself with bleach.
I still believe in this stuff. I just need some reassurance.
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