TOPIC:

Hi@, back in 1997 I was diagnosed with a so-called autoimmune disease, “MS“. I learned pretty fast that people with “MS” are nothing else as cash cows owned by MS-ologists & Big Pharma and for that reason none of them is really interested in honest research to cure this disease. But back in 2008 quite amazing things happened. A game changer, called Prof. Zamboni (vascular specialist from Italy) and his CCSVI theory in MS came into the play and he met with some MS-activists on social network websites like facebook. Since that time things have changed dramatically. MS/CCSVI patients are getting more and more organiced every day and we are challenging the med. $Establishment$. We are taking influence on how studies get done. We are making politics and we are kicking asses as much as possible to save life.
To cut a long story short, since 2009 I’m diagnosed with CCSVI (vascular disease, obstruction of the veins which are draining the brain and the spinal cord => MS symptoms) as well and I’m trying everything to keep them open after I had my second angioplasty.
That’s why I became interested in MMS. Nobody knows for sure why people’s veins, who are suffering from CCSVI/MS are ‘collapsing’ again and again after they had a successful angioplasty. Is it an underlying infection with CPn or Lyme, which ends up in a chronic vasculitis with all the scare tissue or is it the surrounding biofilm of the bugs, which is interfering with proper blood flow?
I don’t know either but want find out! So I’ve started yesterday with the MMS-protocol 2000 and I got a proper Herxheimer reaction just after 5 hours and a dosage of 10drops.
Yes, I’ve learned my lesson pretty fast.
Best Arne (not a native English speaker)