What have you heard about tickborne Lyme for the last 30 years? People see a doctor upon finding the tell tale bulls eye rash, but then what happens?
Why do conventional doctors tell them it's in their head? Why won't they quickly test for it? Treat it? Acknowledge it? Why do medical boards shut down doctors who can treat and cure Lyme?
Click here for more information >>>Perfect timing for scientists to make a mad dash for parts of newly-discovered Lyme and keep the information locked to protect future profits.
The biggest blow in the Lyme cover up - the Infectious Diseases Society of America (IDSA). Doctors must follow their diagnosis and treatment guidelines or face punishment from state medical boards.
Click here for more information >>>The political-medical battle over Lyme (and Babesiosis) was left to the dogs from the beginning.
Many have struggled and found their own way, with alternative doctors and unconventional methods.
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Excellent article! Being a Lyme Sufferer, and an advocate promoter of "under our skin", a medical professional, and a person who had a "symptom list"/diagnoses list too long to mention (when it was truely "lyme"); My research had to error on the side of Mycoplasma. Lyme has been manipulated to the crystalline form (see Dr. L. Mattman), the mycoplasma is the carrier (look into the "mycoplasma" patent). And, as specified, this disease is easily and entirely "transmitable", through sexual contact; however, if you look at the history of Mycoplasma; it has been placed in mosquitoes for decades. Hence, if this mycoplasma carries the "lyme" crystaline form, how many are going to understand that a "simple" mosquito bite can potentially cause "lyme" down the road? Depending on "stressors" in a persons' life, the disease can take hold quickly, or 20-30 years down the road. And a person left to slowly waste away, both physically and mentally, for the years they have left. Speaking to one doc; they advised that "if they deviate from the outlined protocols", as specified in the "acceptable" journals, they will be called before their "respective boards". In order to "appear" they are charged a nominal fee (somewhere around $70,000.00), not including their legal fees in order to defend themselves. Unfortunately, "anyone" can "anonomously" report a doc (ie: pharma/insurance), without fear of reprisal. I think this may correlate with why doc's are so fearful of treating a patient with "lyme". This is definitely a "political" illness. It is designed to take our money, then our lives. It is very difficult to treat, and yes; everyone that even "thinks" they may have symptoms of "lyme" should hunt down "MMS". It is "lousy" stuff. It smells horrific. But it does work, if you follow the protocol (or take it slow). Jim Humble is avoiding coming back to the U.S. for obvious reasons! Please take advantage of his work and humanitarian efforts. Please do not rely on the FDA/CDC, or any other body to protect or improve your health! (as they get paid when the drug trust makes money, not when you are healthy!) PS: as a health profession; I have been "disciplined" more times then I can count; for "health teaching" patients about natural means of improving their health". When I queried "why" I was being disciplined; the response was "our facility doesn't make any money off patients when they are well!".
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