Elena~That link does not work. So if there is enough question &/or proof in lab work, and the allegations of those rendering patient decisions are corrupt with patents & conflict of interest, why aren't more news reporters, etc all bringing this to light?
Yes, I realize the big powers at work, but ALL in the back pocket of evil, when so many ailing? No group of powerful lawyers to slay the dragon?
I just don't get it. Isn't the CDC supposed to work for US?
And Elena, I see u & Dr MacD in the comments section of this April 2014 Medscape article (arguing quite well!):
"CDC/FDA Warning Against Unapproved Lyme Culture Test":
http://www.medscape.com/viewarticle/823840
I liked another comment given: "Don't forget, the CDC is a self-serving PRIVATE organization, much like the Red Cross; but unlike the Red Cross, suffering patients do not pay their salaries."
Here is a Nov 2014 Alzheimer's Weekly article,
"Lyme Disease & Dementia" with Lyme found in FL & GA:
http://www.alzheimersweekly.com/2014/05/lyme-disease-dementia.html
Post Edited (happyjo) : 7/22/2015 10:51:57 PM (GMT-6)