His "Antineoplastons" Therapy Has Been Shown to Help Cure "Incurable" Terminal Cancer
July 22, 2011
Dr. Stanislaw Burzynski has cured hundreds of people of brain cancer over the past three decades from his Houston, TX clinic. The State of Texas tried and failed once and the Federal Government tried twice to convict him of any wrongdoing, with several of his grateful patients as witnesses testifying that the doctor cured them of cancers previously thought to be incurable.
Why has the government been trying to imprison a doctor who has cured hundreds of cancer patients, many of whom are still in remission 10 years after treatment?
The director of this film, Eric Merola suspects that it is because when his "Antineoplastons" therapies are approved for public use, it will allow a single scientist (Dr. Stanislaw Burzynski) to hold the exclusive license to manufacture and sell these medicines on the open market - before they become generic - leaving Big Pharma out of the game of profiting from the most effective, gene-targeted cancer treatment the world has ever seen.
Because Dr. Burzynski is now once again being sued by the State of Texas, the recently-released documentary about his work, his many triumphs both with cancer patients and with the State and Federal legal authorities - a film that is as infuriating as it is inspiring - has now free to the public. Please share this film with as many people as you can and carefully read the statement by the film's director, below.
Burzynski Movie Newsletter
July 21, 2001
A message from Eric Merola Director, 'Burzynski the Movie: Cancer Is Serious Business.'
The Texas Medical Board is trying once again to shut Burzynski's clinic down. In January 2012 they will take him to trial - again. We will be launching a new call-to-action to bombard Governor Rick Perry's office, with letters, emails, faxes, phone calls and DVDs to keep this trial from going forward. Please sit tight, we will have a fully targeted package to utilize to try to help fight this absurdity.
As a part of this call-to-action, we will also be asking people to bug all of our Congressman and Senators to open up a new hearing to force the FDA to allow the approval of Antineoplastons based on their completed Phase 2 FDA clinical trials. Almost all cancer drugs approved in the last decade were approved after only completing Phase 2 FDA trials, especially for brain cancer. To make matters worse, nearly all of these drugs were approved after completing Phase 2 without having saved a single life. Yet, Burzynski & Antineoplastons are credited with saving hundreds of lives in Phase 2 FDA clinical trials, including the lives of pediatric brain cancer patients - who have not only been alive for over 10 years - but are the first patients in the history of medicine to ever have been cured of their type of tumor.
There is no logical reason other than outright bureaucratic suppression to force Antineoplastons to enter Phase 3 trials without hitting the market first after completing Phase 2. Not to mention the $300 million dollar price tag that Phase 3 trials cost, which can be more easily paid for if the FDA would allow them on the market - allowing The Burzynski Research Institute, Inc. and other third-party distributors to profit from it, then turning that money into funding for Phase 3.
Allowing drugs to be FDA approved after completing only Phase 2 is not remotely unusual. What the FDA does is approve these drugs after Phase 2, then while they are on the market they simultaneously conduct Phase 3. But, not for Burzynski, Antineoplastons, or cancer patients that need this treatment now.
We will have a well-buttoned up fact sheet and form letters to write your local Congressmen and Senators to push this forward. The truth is on our side, and all we are asking is to make the FDA consider Antineoplastons no differently than they have considered any other drug on the market.
If we put the FDA on the stand today, we can not only expose this abuse of power - but participate in the first time in history the general public will be responsible for forcing a medicine into FDA-approval and into the public's hands. (That's almost as exciting as discovering a cure for cancer).
Please stay tuned and look out for our future email newsletter that will include this new call-to-action. We hope to have it up and out to you by late August. Encourage others to sign up so they too can take part in this historical event. To subscribe
to their newsletter, go here: www.burzynskimovie.com
ABOUT THE FILM
Burzynski, the Movie is the story of a medical doctor and Ph.D biochemist named Dr. Stanislaw Burzynski who won the largest, and possibly the most convoluted and intriguing legal battle against the Food and Drug Administration in American history.
In the 1970s, Dr. Burzynski made a remarkable discovery that threatened to change the face of cancer treatment forever. His non-toxic gene-targeted cancer medicine could have helped save millions of lives over the last two decades had his discovery not been criminally suppressed by the US government, as his therapy, called "antineoplastons," have been shown to effectively help cure some of the most "incurable" forms of terminal cancer.
This documentary takes you through the treacherous 14-year journey Dr. Burzynski and his patients have had to endure in order to finally obtain FDA-approved clinical trials of antineoplastons.
His story is yet another testament that fact can be far stranger than fiction, as the film exposes the powerful, unscrupulous forces that work to maintain the status quo of the medical- and pharmaceutical industry at any cost - including the lives of millions of people.
Dr. Burzynski resides and practices medicine in Houston, Texas. He was able to initially produce and administer his discovery without FDA-approval from 1977-1995 because the state of Texas at this time did not require that Texas physicians be required to adhere to Federal law in this situation. This law has since been changed.
As with anything that changes current-day paradigms, Burzynski's ability to successfully treat incurable cancer with such consistency has baffled the industry. However this fact has prompted numerous investigations by the Texas Medical Board, who relentlessly took Dr. Burzynski as high as the state supreme court in their failed attempt to halt his practices.
Likewise, the Food and Drug Administration engaged in four Federal Grand Juries spanning over a decade attempting to indict Dr. Burzynski, all of which ended in no finding of fault on his behalf. Finally, Dr. Burzynski was indicted in their 5th Grand Jury in 1995, resulting in two federal trials and two sets of jurors finding him not guilty of any wrongdoing. If convicted, Dr. Burzynski would have faced a maximum of 290 years in a federal prison and $18.5 million in fines.
However, what was revealed a few years after Dr. Burzynski won his freedom, helps to paint a more coherent picture regarding the true motivation of the United States government's relentless persecution of Stanislaw Burzynski, M.D., Ph.D.
Note: When Antineoplastons are approved for pubic use, it will allow a single scientist to hold an exclusive license to manufacture and sell these medicines on the open market - before they become generic - leaving PhRMA absent in profiting from the most effective gene-targeted cancer treatment the world has ever seen.