Routine childhood vaccinations among kindergartners in U.S. public and private schools were down the previous school year, according to the U.S. Centers for Disease Control and Prevention (CDC).
At the same time, the vaccine exemption rate increased from 3 percent to 3.3 percent for the 2023–24 year and increased broadly in 41 jurisdictions. In 14 jurisdictions, that figure jumped to 5 percent, it said.
Over the summer, a survey from Gallup found that “far fewer” people in the United States believe childhood vaccines are important. (See link for article)
Experts are onto them; however, and state the agency is using the report as “propaganda” to defend its vaccination program.
“The methods are shoddy, the data are untethered from reality and the conclusions are a preposterous fiction,” Toby Rogers, Ph.D., a fellow at the Brownstone Institute for Social and Economic Research, told The Defender. “This study is an advertisement on behalf of the pharmaceutical industry and it should be treated as such.”
Experts state the CDC relied on outdated disease and mortality statistics that led to “laughable” conclusions and ignored the real costs of adverse effects of vaccination.
Further, they reproduced the methodology from a 2014 paper Zhou and colleagues published in Pediatrics, estimating the health and economic benefits of vaccination for a single year, 2009.
“If there are two more conflicted journals to represent the benefits of the childhood vaccination program, you could not find them,” Mark Blaxill, co-author of “The Age of Autism: Mercury, Medicine, and a Man-Made Epidemic,” told The Defender.
Blaxill said:
“The profession of pediatrics is the delivery channel for the childhood immunization program, that’s why it exists. And the MMWR is put out by the CDC, which is recommending the program. So this is propaganda, and it is put out by those parties most interested in defending the outcome.” Source
Another perfect example of captured government agencies.
Kris Kristofferson’s shocking tale of Lyme-induced Alzheimer’s
By Dana Parish
Sept. 30, 2024
In 2016, I was floored by Rolling Stone’s cover story on Kris Kristofferson’s Lyme-induced Alzheimer’s.
Having almost died from heart failure after 12 “top” NYC doctors neglected to properly treat my own case of Lyme & Bartonella in 2014, I wanted every possible detail. I had a million questions.
I was introduced to Kris and his wife, Lisa, by a mutual friend, and honored that they trusted me to write an in-depth piece for my HuffPo column documenting his tumultuous health journey, from earliest symptoms of fibromyalgia and cardiac arrhythmias to severe memory loss, and astounding, significant recovery.
In light of the terrible news of his recent death, I couldn’t help but wonder if Lyme played a role, and felt compelled to shine light on this important story again. The media is largely ignoring it. Acknowledging the truth about chronic Lymeand the vastdriver of autoimmune, psychiatric and neurologic illness that it is, is touching the third rail.
I am also struck, again, by the uncanny overlap between chronic Lyme and LongCovid, from their dark politics and conflicts of interest, severe effects on the brain and body, to how they both can persist long after initial infection. It’s also notable that those with Lyme had worse COVIDoutcomes. There seems to be nothing a wily, misunderstood infection can’t do. Kris’s story is a perfect example.
I am forever grateful for the awareness he raised about Lyme and infection-mediated chronic illness. Sincere condolences to Lisa and the Kristofferson family.
Kris’s fierce, intuitive wife, Lisa, tells us how she shepherded him through a haze of missed opportunities and misdiagnoses and got him back.
When and how did Kris’s Lyme symptoms begin?
About 12 years ago he was diagnosed with fibromyalgia, which looking back, should have been the first indication that a test for Lyme was warranted. But we suspect he’s been infected with Lyme anywhere from fourteen to thirty years because he used to have these chronic muscle spasms, which is a common symptom.
We were in LA at the time, in Malibu, and I just don’t think doctors were looking for it or aware of it there then. But now we know it’s everywhere. There are signs on my local playground that say beware of ticks.
Can you describe his fibromyalgia?
He had massive, painful spasms all over his back and legs– it was so horrible- his nerve endings were causing golf ball-sized, painful contractions that we battled with acupuncture, heat and massage, then finally a spinal cortisone shot by a rheumatologist, and a low dose anti-depressant.
This eight-month period he was in so much pain he could not work. Two years earlier he had spent six weeks in the woods in rural, remote Vermont making a film called Disappearances. He was on the forest floor for much of the shoot, being dragged in a makeshift sling and carried by his son in the film, because he had been “shot” in the leg.
So, after so many years, how did he finally get diagnosed with Lyme?
During the aftermath of that film, Kris was diagnosed with moderate to severe sleep apnea, warranting a bi-level CPAP machine, which he tried and refused to use. He had painful knees and annual knee shots, a pacemaker for arrhythmias–which we now know could be from Lyme–so much Advil for headaches that he got anemic.
After a year of iron supplements and seeing a hematologist, he just wasn’t healthy-looking so I took him to an integrative doctor, Mark Filidei, at Whitaker Wellness Institute. Upon examining Kris and watching the muscles in his forearms constantly twitching, he announced, “He’s got Lyme disease,” and ordered a blood test. The first test from LabCorp came back suspicious, the second test by IGeneX was positive. This was in February 2016.
Excellent that the doctor knew to go to a reliable lab for Lyme like IGeneX. I also like MDL Labs. Most physicians don’t know that the tests are only about 50% accurate at the major labs and that Lyme should be clinically diagnosed based on symptoms. What did you do when you found out his diagnosis of Lyme?
Well, we got the news when we were on tour in the UK and Ireland, so immediately upon landing in the US, I went to a local pharmacy and picked up Kris’s prescriptions for doxycycline and alinia. Soon after, we also started hyperbaric oxygen therapy (HBOT) and transcranial magnetic stimulation (TMS) of the frontal lobe.
At this point, did anyone refer you to a Lyme-Literate doctor?
Yes, luckily, Kris’s cardiologist did her residency in New Jersey so she understood the cardiac involvement in Lyme and said go to a Lyme specialist. We began working with Dr. Steve Harris in California, who added antibiotic intramuscular injections to Kris’s protocol and is continuing to treat Kris.
But before this, wasn’t Kris misdiagnosed with Alzheimer’s?
Yes, for the past three years, he was treated for Alzheimer’s by two different neurologists. He was on two drugs for it, Namenda and Exelon patches. But finally, a spinal tap and functional MRI ruled out Alzheimer’s, so he quit those meds and the antidepressant for fibromyalgia. They also tested him for Lyme disease in the spinal fluid and it was negative but the doctor explained to me that Lyme does not live in fluid, it lives in tissue. It bores into tissue so you would really have to do a biopsy of the brain to find it.
That’s what makes Lyme blood tests so unreliable. I always encourage people suffering with Lyme symptoms or an autoimmune illness that’s linked to Lyme like MS, RA, Alzheimer’s etc to seek a second opinion from a Lyme-Literate doctor.
Exactly. People need to know this! I can’t wrap my head around why this information is not more widespread! Since Kris was diagnosed, so many people–even close friends of ours–are coming out of the woodwork telling us their stories and they’re not being heard. This is why Kris and I are glad to come forward. If it helps anyone, then great.
Were you told Kris was going to die from Alzheimer’s?
Well, no, but eventually Alzheimer’s is fatal, as is life. What we were doing was keeping him on these medications that would keep him from declining further for long stretches of time and then he would get worse and then he would plateau again. We had a very fatalistic attitude than none of us were getting out of this alive.
Why did you start transcranial magnetic stimulation?
The TMS targets the frontal lobe of the brain that was abnormal on the MRI. His neurologist is such a proactive, positive person and when she said, “let’s do this,” I was so ready to agree.
Can you describe his memory symptoms?
He could always remember songs, music is deeply embedded in the brain. The first thing I noticed was that he lost his keen sense of smell. The next thing I noticed was his spatial awareness was off. Like, if he would come out of the men’s room in the airport, he would start looking around and having no idea where to go. I had to watch him constantly, it was very consistent with Alzheimer’s. And he would do these mini-mental status tests where they have you remember certain presidents and things like that, and he was consistently failing them.
Did Kris think he had Alzheimer’s?
Actually, he has been complaining about having memory loss to his doctors for about 12 years and my understanding of Alzheimer’s is that you’re not even aware you have memory loss. That was a big clue to me that maybe it was not really Alzheimer’s. He would say “my memory’s shot, my memory’s gone.”
What were the doctors saying?
Well, after I questioned it, one of the head injury specialists that we saw looked at me and said, with a sad look on his face, “You really don’t want this to be Alzheimer’s.” I said, “It’s not that I want it to be something else, it just does not feelright to me.” Also, Alzheimer’s patients often fight things and don’t want to do certain things and Kris has always been a very compliant patient. That was another clue to me. Subtle things.
Do you think he felt hopeless?
I don’t think he even knew to feel that way, he just kind of floated. He did a film with the director feeding him lines and a teleprompter, and he is such a soldier. He never gives up.
What has treatment been like?
We had tremendous improvement after the intramuscular injections of Invanz, the Doxy and Alinia, thirty days of hyperbaric oxygen and twenty days of TMS of the frontal lobe. How it all worked is impossible to say but I can tell you that twenty days into theTMS, his personality was back. Of course, we are not done but that’s where we are right now.
Did he have Herxheimer reactions?
Oh, God, yes. He had three episodes of the most severe herxing. I wish I had him under medical surveillance because it was so bad. The first time, he violently threw up all over the hotel bathroom- the shower curtain- and he was so confused, he kept asking, “What’s happening? Why is this happening to me?” He was so disoriented. I’m gonna cry thinking about it.
Then it calmed down til the next evening when he had another episode in the restaurant bathroom where he kept saying, “What’s wrong with me,” and the way he was saying it, it was like when a little kid is confused. He just didn’t know why. Then, his third episode gave him a tremendous amount of shaking and spasming in his body, and again, the next day, he was totally fine. It’s the craziest thing. And so scary, I almost called 911.
How is he feeling now?
He still has spatial awareness issues and short-term memory loss. He sometimes even forgets he has Lyme! He shook the hand of a lady the other day and she told him she had Lyme and he said, “Oh! Is it contagious?”
So, he really lives in the present and he feels good. We walked two miles yesterday. His physical health is incredibly good. All his symptoms of fibromyalgia, sleep apnea and twitching are now gone with the Lyme treatment. He has stayed off the two Alzheimer’s drugs and the antidepressant he was taking for the fibromyalgia. He is continuing to do treatment as needed. When I look back, his symptoms really should’ve caused his doctors to test him for Lyme and they missed it. Most doctors are just not looking for it.
It’s a balance trying to work with all these doctors and telling them that even if they don’t all agree, we have to keep Kris’s best interest and we have to acknowledge he is getting better with Lyme treatment. His internist does not trust the Lyme tests and doesn’t want him doing more antibiotics.
It’s alarming that so many doctors don’t seem to even want to understand the seriousness of this disease.
I know! You and Dr. Phillips did a great job of conveying that onyour Fox interviewlast week. Seeing that young girl on the special broke my heart. I don’t understand the stigma or lack of awareness. It’s like doctors don’t wanna touch it. I think what I am teaching doctors now is that there is no downside in testing for and treating for Lyme when you can’t find anything else that makes sense. Because not acknowledging Lyme can be so devastating.
I had one doctor say to me that unless you live in New Hampshire, you can’t have Lyme. I’m like, “Why won’t you acknowledge Lyme? What is it, a religion?”
With over five million Americans living with an Alzheimer’s diagnosis, I have to wonder how many actually have Lyme and not Alzheimer’s, and what it will take for doctors to look for Lyme before giving someone a sentence like that. Malpractice suits? Complaints to medical boards?
Sadly, the average doctor doesn’t even check or test for Lyme, it’s not the norm. But they should! And now, with treating it, Kris is doing so much better than he was three years ago. I couldn’t even get certain doctors to look at his blood test and agree it was positive. But once he got his clinical assessment from his Lyme doctor, they all seemed to finally agree. And then we got him off all the Alzheimer’s meds and it was like, “I’ll be damned!”
How was Kris able to function on the road before his Lyme diagnosis?
Right before he started treatment, he had two fainting episodes where we got really worried about him. We were in Ireland and he was walking through the hotel lobby doors and he fainted. I grabbed him and yelled for help. He was completely passed out. This happened two nights in a row at exactly the same time, after his shows, walking back into the hotel lobby.
Thank God it was there because it was caught on camera and the hotel was nice enough to give us the footage to show our neurologist. Since then, I’ve learned that that is failure of the autonomic nervous system, which Lyme attacks.
Did he have any neuropsychiatric symptoms? You mentioned depression earlier. Do you think this was related?
In 1988 he was first given a diagnosis of clinical depression and he went on an antidepressant for a while but it was also in a period of a life where things were difficult. As he worked through his issues, he went off of the antidepressant and then went back on a very low dose because of the fibromyalgia symptoms.
In terms of other psych symptoms, it was more that his confusion would trigger anxiety. He would ask, “where are we going, what are we doing?” That kind of repeated thing. And that still persists today to some degree. It seems like most of the damage is in his short-term memory and spacial awareness.
Did any of that get better?
Not so much his working, short-term memory yet, but his whole personality came back after three years. I could cry now thinking about it. We were driving back from his sixth HBOT treatment and he looks over at me and says, “Wow, I feel like I’m back.” And I looked right in his eyes and I said, “OH MY GOD, HE’S BACK! It was like, WHOA!”
When you say his personality is back, what was it like before his Lyme treatment?
I think describing it as flat is the best way to explain it. Because he is such a charismatic, funny, fun person and his intellect is so amazing. Over the course of treating him for Alzheimer’s, there was a slow slipping away.
Looking back over the years, how do you think none of Kris’s doctors caught this?
All these doctors were wonderful in treating him and caring, but nobody was finding the cause or connecting the dots. The neurologist suggested anti-seizure medications for passing out, the fibromyalgia doctor was giving him antidepressants for his body pain, his cardiologist gave him a pacemaker for his cardiac arrhythmias, his knees were sore, so he got annual shots from his orthopedist.
Nobody was connecting the dots at all.
It wasn’t until I took him to the integrative doctor, Dr. Filidei, that he looked at everything and said, “This looks like Lyme disease.” I’m just so grateful that he is so much better now. And I feel really lucky that our doctors are willing to work with our Lyme-literate doctor. I know that is not always the case.
I bet he saw the best doctors money could buy.
The most expensive doctors don’t necessarily buy you the best treatment, that’s one thing I’ve learned. It’s not like he’s immortal at eighty, but there’s not that big black void ahead of us anymore. He is so much better now than he was three years ago. We are back hitting the road again.
You must be so relieved, Lisa!
I am relieved! And now we’re at a point where we can acknowledge and look at each other’s deficits with humor. I am deaf in one ear and everybody is patient about that, and we laugh about it. It’s OK, everybody has a challenge.
We understand Kris’s deficits in spatial awareness and short-term memory loss and we laugh about it all the time. We laugh at him and with him and we make the best of it because Lyme is so tragic that if you don’t have something to counterbalance the sadness of that, it’ll take you down. The more we can get Kris to laugh, the healthier he is. Being on the road, the laughter, the music. It’s great medicine. And I understand that when you have Lyme disease, your quality of life will vary with each different person. You have to just do the best you can.
Also, I tell people to exercise because Lyme can only live in a low-oxygen environment. The more you get out and do some aerobic exercise to get oxygen flowing through your body― if you are able to do that― the better.
Do you have any Lyme symptoms?
Well, I don’t, but the doctor thinks I should be tested since it potentially can be sexually transmitted and he doesn’t want me to reinfect Kris as he’s getting better.
Are you happy with Kris’s care now?
Yes! The good news is that the doctors we have now support us going to a Lyme specialist and when they don’t know the answers to certain things, they tell me to ask him.
That’s really unusual and wonderful. Certainly, that was the opposite of my experience.
Yeah, what’s that about? Again, I just don’t get it. People are coming up to us all the time now with their Lyme stories and it’s just so tragic! Doctors are not looking for this and then people end up down the road so much sicker. It’s heartbreaking. I am fortunate my doctors are willing to admit when they are unsure about something and have Kris’s best interest at heart.
What’s life like now for Kris?
We’re on the road right now with Willie [Nelson] and the Haggard boys. Kris is doing what he loves, he’s eighty and he’s healthy – we just walked for four hours in the LA Zoo with our grandchildren.
He doesn’t remember bypass surgery, and so many things, but recently, he did this big Q&A in front of 600 people and my daughter and I were scared to death about how it would go, but it turned out to be the best, funniest thing ever.
And that’s the deal now, Kris is totally present and sometimes we forget he’s battling anything. At times, he’ll still say, “where are we going, what are we doing,” but he really rolls with it now. That’s just how it is. He is right here, right now. We’re jamming with it. It’s such a weird, beautiful journey.
Dana Parish is a singer, songwriter, author, and a major advocate for Lyme disease patients. She co-authored the book Chronic with Dr. Steven Phillips. This interview and other writings are available on her Substack newsletter Third Opinion. Click here to subscribe.
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**Comment**
And that is a typical Lyme/MSIDS story – which can vary in little details but overall explains what a chronic/persistent case looks like.
Notice the vast improvement with treatment.
A patient would not have this improvement IF they weren’t infected.
Tick-Borne Diseases & Associated Illnesses: National Community Engagement Initiative
Tick-borne diseases are a serious public health problem. Join us at one of our engagement meetings to
Learn about relevant initiatives and developments
Hear updates from federal agencies
Provide input about patient concerns and priorities
Audience: The general public; patients, caregivers, family members, and advocates; clinicians and healthcare providers; researchers; funding organizations
Upcoming Meetings
Virtual Community Engagement Sessions
Three virtual sessions will cover the topics of mental health, diagnostics, and treatment. These topics chosen were by the public at the San Francisco meeting on June 11, 2024.
Meeting Goal: The purpose of this meeting is to engage the public—patients, caregivers, and healthcare providers, in particular—in an educational and informative session on the mental health and neurological effects of tick-borne diseases and associated illnesses and conditions (TBDAIC). Presentations by clinicians and researchers will provide insights into these complex and multi-faceted topics.
Meeting Objectives:
Validate the patient and caregiver experience.
Educate the audience about the nuanced mental health challenges of TBDAIC.
Describe potential neurological effects of certain TBDAIC.
Provide resources for patients and caregivers seeking help with the mental health effects of TBDAIC.
Furnish information to help healthcare providers recognize, treat, and proactively address the mental health effects of TBDAIC in their patients.
Meeting Agenda
Time
Agenda Item
1:00 pm – 1:15 pm
Introduction and Welcome Remarks
James Berger, MS, MT(ASCP), SBB Office of Infectious Disease and HIV/AIDS Policy (OIDP)
B. Kaye Hayes, MPA Office of Infectious Disease and HIV/AIDS Policy (OIDP)
ADM Rachel L. Levine, MD U.S. Department of Health and Human Services (HHS)
Clinician Perspectives
1:15 pm – 1:45 pm
Neuropsychiatric Aspects of Tick-borne Diseases and Associated Illnesses
Brian A. Fallon, MD, MPH Director, Center for Neuroinflammatory Disorders and Biobehavioral Medicine Director, Lyme and Tick-Borne Diseases Research Center at Columbia University
1:45 pm – 2:15 pm
Neurologic Lyme Disease in Children: Preview of an Ongoing Clinical Study
Lise E. Nigrovic, MD, MPH Senior Physician in Pediatrics, Boston Children’s Hospital Professor of Pediatrics, Harvard Medical School
2:15 pm – 2:45 pm
It’s Not Just About Avoiding Red Meat: Giving Voice to the Untold Implications of Alpha-gal Syndrome
Scott Commins, MD, PhD Medical Director, UNC Allergy & Immunology Clinic at Eastowne Professor of Medicine, Division of Rheumatology, Allergy, and Immunology, UNC School of Medicine
2:45 pm – 3:00 pm
BREAK
3:00 pm – 3:20 pm
A Clinician Toolkit: Improving Care for Patients with Prolonged Symptoms and Concerns about Lyme Disease
Grace E. Marx, MD Medical Epidemiologist, Centers for Disease Control and Prevention
Researcher Perspectives
3:20 pm – 3:50 pm
Brain Changes and Symptom Correlates in Lyme disease
Cherie Marvel, PhD Associate Professor of Neurology and Psychiatry, Johns Hopkins University School of Medicine
3:50 pm – 4:20 pm
Powassan Encephalitis: An Emerging Tick-Borne Disease of Human Health Concern
Saravanan Thangamani, PhD Professor of Microbiology and Immunology, Upstate Medical University, Syracuse, NY
4:20 pm – 4:30 pm
Concluding Remarks and Adjournment
James Berger, MS, MT(ASCP), SBB (OIDP) What did we hear today? What’s next: Upcoming sessions and Portland ME Public Meeting
I recommend reviewing that link above which includes a list of references that the CDC refuses to acknowledge along with the 363 references of chronic Lyme after antibiotic treatment:
And why would the CDC refuse to recognize/study chronic Lyme disease in great detail you might ask? Because a chronic relapsing seronegative disease does not fit the business model of vaccine development, patent royalties and pharmaceutical profits. (Follow the money) Chronic Lyme does not fit any vaccine model.
And nothing, my friends, has changed.
But, I don’t mean to stop anyone from participating. Just know the score. Hey, let it rip and see what happens. We have absolutely nothing to lose. Also – it’s always helpful to know what the enemy is thinking.
Recently, scientists uncovered at least 55 undeclared chemical elements found in six brands of the COVID shots including toxic metals, radioactive elements and rare earth metals which are also called lanthanides which have unique electromagnetic properties that make up the cornerstone for the internet-of-things’ technologies including; smart phones, fiber optics, lasers, and electronic vehicles (EVs). They are also key components of quantum dots(See Microsoft patent for Cryptocurrency body activity data implants) and gene-editing nanoparticle technologies that are foundational elements of optogenetics.
Please watch this brief 3 minute video explaining COVID shot technology and how DNA is ‘highly programmable,’ as well as:
“In some embodiments, the small molecule is a toxin. In some embodiments, the toxin is from a chemical weapon, an agent of biowarfare, or a hazardous environmental agent. In some embodiments, the small molecule is conjugated to a polymer.” Source
Dr. Ana Mihalcea is examining the blood of COVID ‘vaccinated’ and unvaccinated people, alive and deceased. What she is finding explains how the mass experiment is going down.
“…Pfizer BioNTech COVID -19 injection when it was first put on a slide. And in the background you see all of this blinking lights and extreme activity. This is 100 times magnification. And here you see something has self-assembled that we call microchips, because we have done studies that these microchips are actually emitting what’s called a “MAC address phenomenon…” Source
Milhalcea has been observing this phenomena at room temperature over time. She finds the tiny nano/microrobots can move large conglomerates of materials. In other studies with Lantus Insulin she saw large hydrogel Islands, possibly contributing to the rubbery clot formation being found in the ‘vaccinated’ are being self assembled. At 4000x magnification she is finding blue fluorescent aggregates that have an orange rim. This is significant because COVID injected people and those exposed to shedding have fluorescent blue filaments come out of their skin and orange spots on their face. Source
According to Milhalcea, she is also findingundisclosed clot forming chemicals and nanotech in all the childhood ‘vaccines’ she has looked at, which makes her wonder if they just use the same ingredients but but slap a different label on the vials. She states the nanotech is at least 1000x smaller than human red blood cells. Source
Nanotech materials deployed against humanity isn’t new – enter Morgellons
Chemical Analysis Of Multiple Morgellon’s Fibers From 2007 By Dr. Hildegarde Staninger Sheds Light On Current Advanced Nanomaterials Deployed Against Humanity Via COVID19 Shots And Geoengineering
In 2007, Industrial Toxicologist Dr. Hildegarde Staninger, who is the Author of GLOBAL BRAIN CHIP AND MESOGENS Nano Machines for Ultimate Control of False Memories performed a detailed study of Morgellon’s filaments and chemtrail fall out. Morgellon’s is a propaganda name developed to discredit sufferers of militarized bio-synthetic geoengineering warfare – in medical circles it was called “delusional parasitosis”. Very few scientists in the world understood that it was far from that. Dr. Staninger was asked to analyze these filaments. The analysis was done by her and other laboratories including the Massachussetts Institute of Technology.
Project Contract Labs: AMDL, Inc., ACS, Inc., MIT, and Lambda Solutions, Inc.
Hence, this chemical analysis is the largest and most comprehensive chemical evaluation of these advanced nanotechnology fibers to date. Full chain of custody for legal purposes was documented. Please note that these results are of utmost importance for all of us working to find solutions for the self-assembly nanotechnology assault on humanity. In the filaments, no cells were found and these filaments were not consistent with any human tissue. Please note that all fibers contained high density polyethylene like the “Goldenhead” image above and had self assembly capacity. In phase 1 B a filament that came from the skin of an individual was chemically analyzed. It contained high density polyethylene with carbon silica in the square chips attached to the filaments ( note this is why Dr. Staninger had advised me against using Zeolite products) – as well as Aluminum, Copper, Sulfur, Calcium, Sodium, Carbon, Oxygen, Chloride and Phosphorus. The components are similar to those used in batteries! Note that gels (hydrogels) were excreted that did not melt over 600 degrees F! Also note that Dr. Staninger calls this an ARTIFICIAL LIFE FORM. (See link for article and pictures)
Telling excerpt:
Laboratory personnel would also compare the fibers with some other nanofibers reported to be carbon-silicon fibers with photoluminescent and other properties.
In short, the fibers had nothing ‘human’ about them. They were ALL of a manufactured nanotechnology to form a specific structure with an undetermined function.
A specimen had a high amount of sulfur with trace copper and contained sodium, aluminum, and chloride – all used as a battery or catalyst in creating a battery similar to the Edison Cell or Lead Cell.
Go here for more on Staninger’s chemical analysis that indicates organic polymer that MIT ‘could not identify.’
It’s important to mention here that Geo-engineering Watch Director Dane Wigington has been exposing the Federal Government’s Secret Weather Weapons System for decades and most recently with the man-made hurricanes Helene, Milton, and others in Acapulco, as well as the decimating fires in Hawaii which selectively burned some buildings and not others, and left trees standing.
The soft term for ‘climate change’ has become ‘climate instability’ to make it more palatable.
Weather’ and earthquakes can be targeted to specific areas as in war.
Go here to help fund the work of Milhalcea and scientist Clifford Carnicom who has cultured the polymers in a laboratory setting. (The National American Renaissance Movement is a 501(c) 3 Non Profit organizations and contributions are tax deductable).
This quote explains why this research is of vital importance:
It is a puzzle to put together that requires understanding of many different aspects of science, toxicology, nanotechnology, synthetic biology, polymer chemistry, microelectronics and medicine. This important research into the most clandestine military assault against humanitycannot (yet) be found in the peer reviewed literature. It is my desire that by making this important information available on my substack, other researchers will have a greater insight as to the mechanisms and components of what we are facing now. Many laboratories refuse to now do testing on COVID19 injections, rubbery clots or blood samples for fear of retaliation. This historic research done at reputable laboratories including at MIT gives us the possibility of drawing parallels to our current findings around the world considering this important background knowledge.
On a practical note for patients, Milhalcea states that since silica has been found to be an integral component of the Morgellons fibers, DO NOT use Zeolite products. Zeolite has silica which is a non ‘caking’ agent for mixing and on one of the COVID injection patents it states silica is a facilitator of nanotech assembly.
EDTA has been used for treatment of advanced nanomaterials for decades and has confirmed her own research findings.
Go here for excellent Morgellons resources including how to find a reputable doctor for it.
Go here or a free bookby Dr. Savely on Morgellons.
Perhaps now that people are increasingly becoming aware of government corruption and lies due to agency capture by Big Pharma, they will be more willing to believe there are untold numbers of people suffering with Morgellons that have been unbelievably gas-lit by doctors, friends, and family.
Stand for Health Freedom has created a Health Freedom Policy Blueprint which is ready to be delivered to statehouses across the country. This primer was developed in response to requests from current and future legislators and attorneys general. They wanted to know exactly what they can do to defend and expand health freedom.
The health freedom movement is not defined by party lines but instead by a shared, deep commitment to our five core values: informed consent, free speech, parental rights, religious freedom, and privacy. We support candidates who promise to promote and protect our freedom to determine how best to care for ourselves and our children.
Madison Area Lyme Support Group 