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PRESS RELEASE: LYME/CDC RALLY MAY 4th, 2018

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“To go against the dominant thinking of your friends, of most of the people you see every day, is perhaps the most difficult act of heroism you can have.”~~~Theodore White

Please SHARE with any and all of your local news media, social media, elected officials, family, and friends. Thank you and hope to see you May 4th!

FOR IMMEDIATE RELEASE Contact: Mirenda Campirano
Phone: 956-778-1130
Email: mirendajones@yahoo.com
 

Chronic Lyme Disease/ Tick Borne Disease CDC Rally

 

 Ground Zero in our fight to expose medical research fraud by CDC doctors regarding Lyme disease.

 Atlanta, Georgia, May 4th, 2018,

 

Hundreds of chronic Lyme patients from across the U.S and Canada along with family and friends will gather outside the Center for Disease Control (CDC) to demand justice, truth, and acknowledgment for those infected with “Chronic Lyme Disease.” In addition, a film crew will document the event. Chronic Lyme Disease is not recognized by the CDC or the mainstream medical community because most Lyme patients do not meet the current case definition despite clinical symptoms and serologic evidence. Lyme disease does not discriminate against sex, race, age, or occupation. This diversity of sufferers will be seen at the rally.

 

“Medical research fraud has led to the denial of this debilitating incurable disease we call “chronic neurological Lyme Disease,” thus patients are left with little to no access to health care, inaccurate tests, no valid treatments, no insurance coverage, no disability insurance, and little funding for proper research. We are passing this infectious disease to our children. I know, because I gave it to my son in utero, along with several tick-borne infections” (Mirenda Campirano RN, registered Nurse and Lyme Army organizer).

 

CDC defines Lyme disease as little more than arthritis, yet the science shows it is far worse. According to the science there are two outcomes of Lyme; arthritis and a neurological outcome that can lead to death and is similar to AIDS and cancer combined.  According to Kathleen Dickson, Former Pfizer Analytical Chemist & whistleblower for the failed LYMErix vaccine: “The case definition for Lyme disease was falsified in 1994; in the early Lyme vaccine trials the CDC discovered that the main ingredient in the vaccine – OspA caused Post sepsis disorder or the systemic disease we refer to as Chronic Neurological Lyme. The main ingredient of the vaccine – OspA or “outer surface protein A” is a fungal endotoxin and could never be a vaccine”.  The CDC officers at the time who held patents on the vaccine and test kits held a consensus conference in Dearborn Michigan where they changed the definition of Lyme Disease to the arthritic outcome only; by doing this, they made it look like their vaccine worked.  LYMErix was ultimately pulled off the market in 2002 after a class action lawsuit.  This falsified case definition and laboratory pathology used to validate the LYMErix vaccine became the basis of our federally approved guidelines for diagnosing Lyme Disease in the United States.

 

This fraud has led to the denial of millions of patients with the neurological Lyme outcome around the world. In countries like England where universal healthcare is provided by the government, former Parliamentary Under-Secretary of State at the Ministry of Defense Lord Astor is pointing the finger at the United States as the culprit in this egregious human rights violation.

“…what we do have is outdated National Health Service guidance, relying on guidelines written by the Infectious Diseases Society of America and supported by the CDC. According to the National Guideline Clearinghouse of America, the IDSA-CDC guidelines are not fit for purpose. They are outdated and do not take into account recent developments in the understanding of these complex infections” – John Jacob Astor VIII, 3rd Baron Astor of Hever.

 

The Lyme Army and Worldwide Lyme Awareness & Assistance groups are both grass roots activist groups made up of people fighting back against medical research fraud that prevents Lyme patients from getting the help they rightly deserve.  We are rallying at the CDC to demand a change in the case definition of Lyme Disease to include persistent chronic neurological outcomes.  The United Nations accepts that Chronic Lyme disease should have its own billable ICD Diagnosis code, and so should the United States NCHS (National Center for Health Statistics). Members of our advocacy group lobbied, unsuccessfully in our nation’s capital to have Oversight in Government send the 2-tier testing for Lyme Disease to the FDA for performance review.  The ELISA and the Western Blot do not meet FDA criteria for a valid test.  Why does the CDC perpetuate this fraud committed by past CDC directors?  The test for Lyme isn’t flawed – it’s fraud!

 

The world needs to know that the science provided to and approved by the FDA and CDC is based on provable research fraud, which must be investigated by the Department of Justice. Calling the Lyme disease debate a controversy diminishes the severe nature of this injustice. Lyme disease is a crime, and a human rights violation! This discrimination against patients afflicted with the neurological outcome a/k/a Chronic Lyme Disease has left the devastation of millions of lives in its wake. Learn the truth about the Lyme Crimes at www.overcominglymedisease.com or visit The Lyme Army Facebook page & the Worldwide Lyme Awareness & Assistance Facebook page for more information.

 

The Lyme Army & Worldwide Lyme Awareness & Assistance

 

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Jennifer

Jennifer is a true believer of Zig Ziglar’s quote, "You can have everything in life you want, if you will just help other people get what they want." Jennifer also has been on her health journey for the past 30+ years. She has been the patient of, and has worked with, some of the most top holistic doctors and healers of our time. After recently healing her body from the damage of Lyme disease, Jennifer has made it her passion to educate the public on Lyme and give them tools and resources so they too can get better. Jennifer is one of many caring administrators on the Facebook Group called, Lyme disease and Co-infections. Jennifer has been coaching and inspiring Lyme patients all over the world thru her blog and the Facebook group, to find caring doctors that will help them. Jennifer shares the knowledge she has gained thru her team of holistic doctors and from trial and error. She teaches daily and inexpensive techniques to detoxify and nourish the body from home, along with ways to limit our toxic exposure to things we eat and use daily. Because Lyme disease is like Cancer and Aids, and is not being recognized by the medical community, Jennifer has decided to share her story and the successful treatments she has used to restore her health and to stay well, in this toxic world. Check out her recently released book 'Overcoming Lyme DIsease' and the accompanying free workbook available on this site.

Jennifer HeathPRESS RELEASE: LYME/CDC RALLY MAY 4th, 2018

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