Fry Labs and the new protozoa

Hi, how many have used Fry Labs and are aware of their newly discovered protozoa? Anyone been tested/treated for it?

(Actually I think he discovered it years ago, and he's changed the designation a few times, but the latest, I think, is that it is a protozoa).

I'm curious b/c I tested for it 1 year ago but chose not to treat at the time b/c I'd not heard of anyone who'd gotten better from it (those that I'd communicated with were in the Interstitial Cystitis online community).

I'm working with a new dr. now and thinking about treating for it with Plaqunil.

Someone recently posted an interview with Dr. Fry about this. He says he can't get rid of it, but he can get it into remission. I believe he said an ultra--low fat diet is the way to starve it. Also magnesium is a big no-no as it literally helps strengthen the biofilm. Do a quick search for it--it's really, really interesting. I hope he gets the funds he needs to keep up his research. He's already mapped its DNA. If he can prove it is this Protozoa causing MS, Fibro and CFS, he'll win the Nibel Peace prize. God bless him and his work!

I did the whole panel through Fry Labs (all tests offered at the time, except Lyme) and it all came back negative. I was soooo disappointed.