The Establishment Cover-up of Chronic Lyme Disease

 Commercial viability is driving the research agenda in too many cases. Not what’s medically necessary and what’s medically useful. 

Heather Callaghan
Activist Post

In 1980, the government started allowing patents on living organisms such as pathogens. Perfect timing for scientists to make a mad dash for parts of newly-discovered Lyme and keep the information locked away to protect future profits.

These so-called experts continue to research Lyme disease with federal funds, then start private firms and obtain patents. They write guidelines for insurance companies and HMOs so that the disease doesn’t exist (yet) or require coverage. Not only do Lyme victims spend hundreds of thousands for medical treatment, but they can’t be covered for Lyme! (more…)

The Lyme Disease Health Crisis Rages On

‘What have you heard about tickborne Lyme for the last 30 years? That it’s rare, scary, acute, treatable? The government warns about its spread and implores people to go to a doctor upon seeing the telltale bulls-eye rash.

So, what happens when they actually do?

Many have researched the controversial beginnings of Lyme disease, but this article focuses on what happens to victims when they contract it, and the ongoing cover-up in the mainstream medical community and the CDC itself. ‘