[Back in my surgery days, I had the experience of being the circulating nurse in a number of transplant cases in a large metropolitan Level 1 OR and was very uneasy with what I witnessed. My experiences are what made me take “organ donor” OFF of my driver’s license. Dr. Paul Byrne has finally connected all the dots for me. I refuse to willingly go to any hospital today. Sad to think doctors such as Dr. Byrne will soon all be but a memory. What a treasure he is.]
I found this stunning information on Dr William Makis’s substack here.
In the first 15 minutes, Dr. Byrne gives vital information if you want the real scoop about “brain death” and organ procurement.
0:30: “Brain death is a lie”.
3:00: How the term “brain death” was invented/coined at Harvard due to an illegal infant heart transplant.
4:30: “Brain death does not mean flat brain waves.”
5:00: Consciousness vs unconscious.
7:00: Transplant patients. Just because a person can’t tell you of pain, doesn’t mean they don’t feel pain. They give paralyzing agents, so the person can’t tell you of their pain.
8:00: Stating a patient has “brain death” is a way to get organs.
12:00: Organ transplants and procurement. You can not get a healthy organ from a cadaver, you can only get healthy organs only from living persons.
13:00: They want the organs from persons 16-30.
28:00: About clamping of the umbilical cord.
34:40: SIDS. There is a relationship with vaccines, a predisposition to apnea, and intercellular magnesium deficiency.
45:45: Check box medicine today with both doctors and nurses.
52:45: How to protect and preserve your life legally. Have in writing and notarize that you are refusing organ removal. Be careful of who you make your power of attorney. See Life Guardian Foundation.
1:01:40: The system of death in socialized medicine. How you answer their questions will determine if you get real treatment or palliative care.
One Of the First Special Care Units in the U.S.
Dr. Paul Byrne established one of the first special care units for at-risk infants at Cardinal Glennon Children’s Hospital in St. Louis in the mid-60s.
“Back then, there were no treatments for preemies and low-birthweight babies –the kinds of things we take for granted today,” he recalls. “I went to the administrator at Cardinal Glennon with the idea of creating a center where we could find ways to treat these babies. She said, ‘OK, let’s try it for a year.'”
After that first year, Dr. Byrne’s efforts had saved the lives of 30 babies. How? For starters, he partnered with engineers working nearby on the space program. They had developed a plastic cuff to fit around the fingers of astronauts, which could enable their blood pressure to be monitored during space missions. Together, they developed a spinoff that fit around the arm of a tiny baby: Before this invention, there was no way to monitor a baby’s blood pressure. (source)
Dr. Byrne and his team also pioneered new techniques for feeding these babies intravenously as well as specially-designed ventilators to augment their respiratory function. All were instrumental in helping such infants survive. Since preemies are so small, new, highly sensitive measurement protocols were also necessary to track their health.
“For instance, premature infants have very small total quantities of blood,” Dr. Byrne notes. “That required development of micro techniques to analyze blood. These micro-techniques that were developed for sick babies are now used for everyone. It was exciting for me to be able to participate in the development of what was then a brand-new field.” (source)
Many of this care is now commonplace in neonatal intensive care units.
“I retired a few years ago after practicing medicine for 55 years,” Dr. Byrne adds. “Yet, instead of a retirement party, I asked my family to have a ‘redirection party.’ My work has not stopped—in fact, I’m busier than ever! People have a way of finding out that I can help them in the cause for life and in their own difficult situations.”
Dr. Byrne loved to witness babies who had been deemed hopeless develop into healthy children and adults. The birth of Joseph in 1975—at a mere 24 weeks’ gestation— was one such miracle.
“He had a flat electroencephalogram or EEG—in other words, no brainwaves,” Dr. Byrne recalls.
The EEG is a common method of measuring brain activity at any age. The flat EEG of Joseph was interpreted as “consistent with cerebral death. Nonetheless, Joseph went on to be a straight-A student in school, build a brilliant career, and he’s now married and the father of three kids.”
“My medical philosophy is that the best doctors are the ones who work the hardest on the people who are the sickest,” he says. “What you try to accomplish for those sickest people first will ultimately have a beneficial impact on the rest of humanity.”
Organ Donor? Consider This Before You Sign!
During the early 1970s, Dr. Byrne witnessed the increased acceptance of brainwave cessation as a legally acceptable marker of death. Shortly after, heart transplants became available.
“The push to accept ‘brain death’ has a lot do with the push for viable organs for transplants and longer and longer wait times,” says Dr. Byrne. He noted that, following that first heart transplant, the medical community began lobbying elected officials for new laws that first codified “brain death” in the US.
This had practical reasons. Dr. Byrne points out that to transplant a heart or a liver, the donor’s heart, circulation and respiratory processes must be kept functioning for healthy vital organs to be removed. Organs from a cadaver are useless, he notes, because organs begin to decompose immediately after those functions cease.
“Now, when someone suffers a head injury or is deeply unconscious, there is a shift of emphasis from helping that patient recover to harvesting his or her organs for transplantation,” he says. The fact that viable organs are very valuable to the organ transplant industry can add a monetary incentive to the push to declare patients legally dead.
Forty-seven US states have passed the Uniform Anatomical Gift Act (UAGA) that presumes EVERYONE is an organ donor. This is in addition to those who have willingly registered as organ donors on their drivers’ licenses. This often creates a conflict, when the same individuals have also filed advance DNR (do not resuscitate) directives. In such situations, that previous DNR order will be overruled and the patient will be resuscitated in order for their vital organs to be usable for transplantation.
“Often I’ve worked with parents of students who go away to college, get into a car accident, and end up at the mercies of a medical system that wants their organs for a transplant patient,” Dr. Byrne said. Since few people have taken the time to study the issue, and since parents are often bewildered and grief-stricken at such times, it can become a complex battle to receive any form of life-extending care for such patients. (source)
“Not only do we have a culture of death in our society—it is a System of Death. If you end up unconscious and on a ventilator, the doctors at the hospital treating you will declare that your death is imminent, and by law, they have to notify the Organ Procurement Organization (OPO),” says Dr. Byrne. If you don’t want that to happen, Dr. Byrne strongly urges you to explicitly document your refusal in writing.
The Life Guardian Foundation website offers three key directives that can help you accomplish that objective: 1. a healthcare power of attorney directive, 2. a directive to protect and preserve life for a dependent minor or mentally incapacitated person, and 3. an organ donation opt-out form that can be carried in your wallet or purse.
“We have to work hard to protect life from its beginning until true death.”
What You Need To Know About Ghost Surgeries: Jack’s Story
“For the love of money is a root of all kinds of evil. Some people, eager for money, have wandered from the faith and pierced themselves with many griefs.” ~1 Timothy 6:10
***For the Full Spike Protein Protocol (including NAC) to protect from transmission from the “V” and to help those who took the “V”, go here.
Deep Roots At Home now has a PODCAST! We are covering everything from vaccines, parenting topics, alternative medicine. Head over today and like, share and download a few episodes! https://buff.ly/3KmTZZd
I am once again being shadow-banned over on FB. If you want to stay connected, here is one way…
Censorship is real. My Pinterest account was suspended, yet surprisingly, part of my main board is still available through this link, and it scrolls down a long way! Pinterest now sells space in boards for Temu ads so be careful! Temu’s In-App Web Browser Secretly Tracks Users.
You can also find me on Instagram, MeWe, and Telegram.
And please join me for my FREE newsletter. Click here.
©2024 Deep Roots at Home • All Rights Reserved
eugenia taylor
I volunteered to be a bone marrow donor in the late 1980s.I was told I would have to go into the blood bank once a month or two to donate packed cells. They had us on some machine that took the blood out, did something to remove what they wanted and returned the rest to us. I was told I might start feeling sick, and was to tell them because my calcium could get too low. Then they would give us some TUMS, those nasty chewable antacid tablets, which I cannot stand. So when I started feeling ill, I waited to tell them until I was really feeling sick. And then I refused the TUMS, so they had to stop returning the blood, which I was told would leave me too anemic to donate again for a couple of months.
A couple weeks later, I received a letter from the blood bank saying my blood had tested positive for Hep B, and that had been the second time they had gotten a positive result, and therefore under federal law, I was blackballed from ever donating blood OR ORGANS for the rest of my life. I was pretty POd as I felt that was not possible. I had been tested twice since then, once by a private doctor and once by the VA, and both of them had said my blood was negative for even exposure to Hep B. I called the blood bank and they had told me there were thousands of people in the area who had been falsely diagnosed with having had Hep B, but the way the laws are written, they are still blackballed.
After reading this article, I am actually glad that they cannot use my organs, now I need to figure out how to make sure they don’t yank them and do me in, before finding out they won’t be able to use them.
I have been aware for decades of the danger of being admitted to a hospital and them finding out I was a match for an organ recipient and them, then, rushing me out to gain access to my “parts.” And when you read now and then about people having organs harvested, and being brought out of comas by the pain of the surgery, you have to realize their brains were certainly not “dead.” This article is a confirmation of what I have strongly believed, based on just what I have observed or read about.
Both the VA and doctors seeing Medicare or Medicaid patients are required to ask those questions about end of life care. And I have even heard Dr Emanuel, one of the ethicists involved with Obamacare, come out and say, people who are no longer able to contribute (Financially) to society should not have limited resources wasted on them. He was the first I heard saying handicapped children who will never be “productive” members of society should also not waste resources keeping them alive, and even proposing “post-birth abortion,” the concept that parents of handicapped children should have the “right” to kill their children up to five years of age, if they feel they cannot adequately provide for them.
Jacqueline
Oh, Gena, I am not shocked by anything any longer. And you were just trying to ‘give back’. I wonder why they kept stating you were Hep B pos when 2 more credible practices refuted that.
That seems like discrimination or a way from keeping you from donating. Yes, we live in an upside down world..
Rham Emmanuel has stated some very evil things!
Sending love to you, friend!
Jacque
eugeniaT
That was not Rham Emmanuel, it was his brother, Dr Ezekiel Emmanuel, who Obama had made one of the ethicists with Obamacare, and who, obviously, does not believe human life is sacred.
What they told me about not being able to change the Hep B diagnosis was that the laws regarding that stated that if they got two positive tests, you were forever banned from donating organs or blood. She told me that if I were to donate blood or organs after that, they would be checked against the donor blacklist, and would be thrown out and not used. She said they could not do anything and it was a dilemma to the blood bank, because they had hundreds of willing blood donors just in our area, who were no longer able to donate, even through they could prove they had never had Hepatitis.
Jacqueline
Wow, that is crazy, Gena! And thanks for the clarification! So it was his brother!
Bless you, friend,
Jacque
Laurie A
I appreciate the time and effort you put into sharing information I would never hear elsewhere. Thanks for all you do.
Jacqueline
Aw, Laurie, thank you for your encouragement! Hugs, ~Jacque