Guest guest Posted May 30, 2008 Report Share Posted May 30, 2008 I believe AI and this forum infers that you should consider additional supplements/treatments to kill the other pathogens that get released/activated or just become more noticeable with chelation Here are some things I believe have helped me in the last month Protocol One _Shoemaker -mold and other toxins treatment IN the last month, I have been following Shoemakers protocol at www.chronicneurotoxins.com. Shoemakers site lets you sign up take the VCS (Visual contrast sensitivity) test and receive his treatment which you can then give to a Dr to prescribe the cholestyramine/actos. IMO understanding the Cholestyramine binds these neurotoxins in our bile My eyes have been more sensitive while on his protocol and the first two days I had to stop as the head symptoms were too much (the Cholestyramine can make you constipated and when things back up its not good). However I am starting to feel better when I take the " C " (week 2) which tells me its working!!! IMO if we have mercury poisoning we in all liklihood have many other bugs/viruses.lymes/etc that it seems this protocol can help with Protocol 2- temperature Syndrome treatment for Thyroid see www.wtsmed.com; this is basically T3 supplementation for thyroid problems (low body temps). I know this has helped me, I do a daily bowel movement that is just toxic and very large every morning. My temps are now in the proper range of 98.60 and my understanding is that this temp range helps with all sorts of enzyme conversion etc in your gut(which is where 60-80% of our immune system is located)..ie must be helping with bowels as well However I do know that AI says to treat adrenals first and I have ben doing this for the past 8 months so I felt it reasonable to try the T3 treatment OTHER THINGS There are a few other things I am doing/planning to do that I will post later I am now at 25 mgs ALA every 3-4 hours and 20 mgs DMPS every 3-4 hours My ability to think clearly and handle more mental activities has improved significantly in the last two weeks I am still pretty fatigued but it feels like my brain is coming back I am 6 months post amalgam removal Keep the faith everyone, and thank you Andy, moderators and this group What a forum and protocol !!!! Quote Link to comment Share on other sites More sharing options...
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