Live Lyme Awareness Events
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Experts say it’s time for the World Health Organization to classify wireless radiation as a “known human carcinogen,” after a review commissioned by the organization concluded there is “high certainty” evidence that cellphone radiation exposure causes two types of cancer in animals.
A systematic review commissioned by the World Health Organization (WHO) concluded there is “high certainty” evidence that cellphone radiation exposure causes two types of cancer in animals.
The WHO-backed review, published online April 25 in Environmental International, determined radiofrequency-electromagnetic fields (RF-EMF) emitted by cellphones and other wireless devices were linked to an increased risk of malignant gliomas in the brain and malignant schwannomas, or nerve tumors, in the heart in studies on animals. The review noted that both tumor types had previously been found in studies on humans.
The WHO’s review also concluded there is “moderate certainty” evidence that cellphone radiation exposure causes an increased risk of rare liver and adrenal gland tumors.
Ron Melnick, Ph.D, chair of the International Commission on the Biological Effects of Electromagnetic Fields (ICBE-EMF) and a former senior toxicologist in the National Toxicology Program (NTP), said in a statement:
“The evidence is now clear — cell phone radiation can cause cancer in animals in concordance with the tumor types identified in human studies of mobile phone users. As animal studies are essential for predicting cancer risk in humans, governments should develop science-based safety standards to protect human health.”
The WHO review prompted leading scientists with the ICBE-EMF on April 27 to call for “immediate policy action” to protect people from possible harm from wireless radiation exposure.
“Given this high level of certainty,” ICBE-EMF said in a press release, “government policymakers worldwide should immediately move to revise their RF radiation exposure limits to protect public health and the environment.”
ICBE-EMF is a “consortium of scientists, doctors and related professionals” who study RF-EMF and make recommendations for RF-EMF exposure guidelines “based on the best peer-reviewed scientific research publications.”
The group warned that delaying such revisions “could have serious consequences amid the global surge in the use of wireless communication devices.” (See link for article)
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**Comment**
The U.S. government has known for over 50 years that wireless radiation is linked to 23 chronic diseases, and the NIH redacted nearly 2,500 pages of records on wireless radiation studies after the Children’s Health Defense FOIA request.
They know.
Now we know keeping cell phones close to the body causes blood vessels to clump together (rouleaux formation), which causes slower blood flow which can lead to blockages in small blood vessels which can lead to stroke or heart problems. People with diabetes or COVID-related blood vessel damage might be at higher risk.
Up until now, rouleaux formation has been associated with infectious and inflammatory processes, connective tissue diseases, and some forms of cancer. It is quite common for Lyme/MSIDS patients to have this hypercoagulation requiring blood thinners at some point in their treatment.
Radiofrequency radiation exposure from cellphones, and likely other technologies utilizing wireless communication, can now be added to that list of things that can cause this abnormality of the blood.
For more:
**UPDATE**
The Florida House of Representatives last week passed the bill to ban and criminalize geoengineering and weather modification, Newsweek reported. The bill makes it a third-degree felony to release any chemical, substance or apparatus into Florida’s atmosphere to affect the weather or climate. It imposes a penalty of up to $100,000 for any person or corporation and up to $5,000 and five years in prison for an aircraft controller or pilot involved in such releases.

HHS Secretary Robert F. Kennedy Jr named the government agency responsible for covertly spraying US skies with chemtrails, during a recent appearance on Dr. Phil Primetime.
An audience member named Emily asked RFK about “the stratospheric aerosol injections that are continuously peppered on us every day. Bromium, aluminum, strontium, it’s sprayed in our skies all day long… I know you’ve talked to Dane Wigington about this. He seems to be one of the experts in the field. How do we stop it?”
Most politicians would’ve dodged the question or changed the subject. But not RFK Jr. — he met her gaze, stayed calm, and gave a straight answer.
“That is not happening in my agency,” Kennedy said. “We don’t do that.”
Then came the bombshell.
“It’s done – we think – by DARPA and a lot of it now is coming out of the jet fuel. Those materials are put in jet fuel. I’m going to do everything in my power to stop it.
“We’re bringing on somebody who’s gonna think only about that, find out who’s doing that and hold them accountable.” ~ Robert F. Kennedy
DARPA is the Pentagon’s secretive tech research arm, best known for developing experimental weapons and surveillance tools, including the mRNA technology behind the Covid jab.
(See link for article and numerous video clips)
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**Comment**
Please take the time to go to the top link for the various video excerpts. It’s all right there in purple crayon: our government is purposely spraying the sky with toxic chemicals.
In one video you will hear a pilot whistleblower explain how he believes a majority of the planes are remotely operated but that 80% or more of the pilots spraying are single. These “Indigo” pilots are chosen from the top ranks within the air force, navy, and coastguard.
According to the last video in the top link by Baxter Dmitry, a task force is being created to address chemtrails.
Go here for Geoengineering 101: History, Science and Global Operations Shaping Our Skies
In a startling joint investigation, Dr. Jane Ruby and Mike Adams have uncovered web-like formations, with interconnected fibrous networks, some with flagella-like appendages, translucent “diploid” structures with internal webbing resembling parasitic or fungal forms, and unidentified egg-like particles with complex, possibly reproductive features in Florida air samples —prompting concerns over their link to unexplained respiratory and immune disorders after unusual orange-yellow fogs descended over South Florida. The duo drew parallels to prior investigations, such as Dr. Jane Ruby’s work on vaccine contaminants and Adams’ research into graphene oxide in medical injections. Some structures bore eerie similarities to self-assembling nanoparticles observed in other studies. ~ Source
Now, after incubating chemtrail fallout for three weeks in warm saline solution, tiny organisms started swimming – self propelling, and moving independently across the petri dish. Source
Due to the recent Florida Senate Bill SB 56, which bans weather modification activities in Florida, the state just announced a Chemtrails hotline. Offenders will get a five-year prison term. The bill passed the full Senate and is now awaiting Governor Ron DeSantis’s signature.
If passed, the law will directly target controversial practices such as solar radiation management, cloud seeding, and other forms of geoengineering that are being deployed without public consent or oversight.
Examples of geoengineering:
Dennis Kucinich, a former U.S. Congressman, courageously introduced the Space Preservation Act (H.R. 2977) in 2001. His legislative proposal sought to prohibit the deployment of exotic weapons in space, including directed energy weapons, psychotronic devices, and, most controversially, “chemtrails.”
Geoengineering, chemtrails, or contrails are all the same thing: jets spraying substances, many of which are toxic, that linger for hours to days in the sky which alter the weather and affect the temperature on Earth under the banner of ‘climate change.’
But the nefarious experiment is also being used to relocate people from one area to another in something called the ‘weather wars.’ Whenever there’s a hurricane, uncharacteristic weather, or a firem the ‘climate’ alarmists begin to beat their drums on cue.
In a never-ending quest to destroy humanity, Bill Gates, who doesn’t vaccinate his own children but is hell-bent on vaccinating everyone else’s, also has a mission to ‘dim the sun,’ to supposedly counter the ‘climate emergency.’ Other schemes include stopping cows from farting and burping, limiting cars, and culling the ‘useless eaters.’ A few brave experts are telling the truth:
‘Climate change is a lie and a scam’ and green energy policies have made the climate worse – not to mention our health.
Think our government wouldn’t dare to do such dastardly things?
Read on:
May 1, 2025
By Project Lyme
For many people, May means warming temperatures and the anticipation of the coming summer (and a break from school). However, May also marks a significant time for those of us whose lives have been affected by Lyme disease and other tick-borne infections: Lyme Disease Awareness Month.
Lyme patients often face challenges in obtaining a proper diagnosis due to a lack of awareness, outdated viewpoints, and a lack of sensitive tests. Delays in diagnosis often lead to disseminated, difficult-to-treat, or chronic infection. Chronic or late-stage Lyme disease patients report delays of 6 months to 5 years or more, with some studies citing an average of 1 to 2 years. Factors include misdiagnosis (e.g., as fibromyalgia, chronic fatigue syndrome, or psychiatric conditions), nonspecific symptoms, and limitations in testing accuracy (e.g., false negatives in serologic tests). A 2018 survey by LymeDisease.org found that 60% of patients took over 2 years to receive a correct diagnosis.
Lyme Disease Awareness Month is a great opportunity for advocates, patients, and friends and family to raise awareness about how just one tick bite can change your life forever. Your advocacy can save a life or vastly improve a friend or loved one’s quality of life. Interested in getting involved? Take a look at our list of five easy ways to raise awareness for some ideas.
Out of the ashes of adversity, we rise not just for ourselves, but to guide others towards the light. Help us to educate others by connecting with us on social media (Instagram, Facebook, X, LinkedIn, and TikTok) and sharing posts. We will be publishing informative posts and videos throughout the month covering everything from what to do if you get a tick bite to best practices in tick-borne disease testing and treatment, as well as patient stories. Sharing posts with your network is a simple way to spread awareness that can have a big impact.
Do you have a medical care provider who is interested in learning more about Lyme disease and related infections? The 26th Annual ILADS Scientific Conference will be held October 9-12, 2025, in San Antonio, TX. Project Lyme is proud to support ILADS by providing grants to first-time attendees.
Whether it’s for Lyme Disease Awareness Month, in honor of your birthday, or another special event, if you have a Facebook profile, fundraising for a cause just takes a few simple steps. Click on the “Fundraisers” button located in the left-hand menu of your main Facebook page to get started. Then click the “select nonprofit” button and follow the prompts to create your fundraiser. And remember, when you raise money for Project Lyme, a 501(c)(3) nonprofit, you are making our mission to spread awareness, fund research, advocate, and support our community possible.
You can also support our important work by making a donation directly on our website.
A recently leaked FY2026 budget from the Office of Management and Budget (OMB) shows that the federal government may cut programs that help the United States prevent, detect, and respond to Lyme and tick-borne diseases. Although budget passbacks are a routine part of the Executive Branch’s annual budgeting process and usually remain confidential, these proposed cuts put millions of Americans at risk—including vulnerable children, families, seniors, and people with disabilities. Lyme and tick-borne diseases still lack reliable diagnostics, affordable therapies, and a cure. Now is the time to speak up.
Our advocacy partner, the Center for Lyme Action, has developed a quick, easy, customizable form to urge Congress to adopt their recommended funding levels for Lyme and tick-borne disease research in the FY2026 Labor, Health and Human Services, Education, and Related Agencies Appropriations bill. Share this campaign with your network to help maximize impact
Looking for a comfortable t-shirt, tank, hoodie, or a new coffee mug? Check out Project Lyme’s online shop and get your Lyme disease awareness gear today.
Opening up about your experiences not only raises awareness about Lyme and other tick-borne diseases; it also serves as critical testimony that Lyme can persist and cause devastating symptoms. Want your story featured across our social media? Reach out to us through our website today!
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For more:
https://danielcameronmd.com/bad-ugly-lyme-disease/
“I thought I was better… until I wasn’t.”
That’s what one of my patients told me after completing a standard course of antibiotics for Lyme disease. At first, she felt relief—less pain, more energy. But weeks later, the fatigue crept back in. Then the brain fog. Then the joint pain that kept her up at night. What began as a simple tick bite turned into a complex journey through symptoms, misdiagnoses, and delayed treatment.
When it comes to Lyme disease, patients deserve to know the whole story—not just the optimistic version. As a doctor who has treated Lyme disease for decades, I’ve come to describe it in three stages: the good, the bad, and the ugly.
Understanding these stages can change the course of your care—and your life.
Let’s start with the good news.
If Lyme disease is diagnosed early—usually within days to a few weeks of a tick bite—and treated appropriately with antibiotics, most patients recover fully. Many return to work, school, parenting, and sports without ever looking back. They remember the tick bite, the rash, or flu-like symptoms, but the story ends there. Life goes back to normal.
This is what we hope for every patient.
But unfortunately, not every Lyme disease story ends this way.
Now, let’s talk about the bad.
Some patients complete their antibiotics and still feel unwell. They may face months or even years of persistent symptoms:
• Fatigue that makes it hard to get through the day
• Brain fog that affects memory and focus
• Aching joints or nerve pain that comes and goes
This is often labeled Post-Treatment Lyme Disease Syndrome (PTLDS)—a term that can be both validating and limiting. Many patients feel dismissed when told there’s no further treatment option, only time and patience. Yet they’re still sick—and they want answers.
Sometimes, this “bad” outcome is not just the aftermath of Lyme—it’s a sign of a persistent infection, an undiagnosed co-infection like Babesia or Bartonella, or even a misdiagnosis.
And then there’s the ugly truth.
For some, Lyme disease doesn’t go away. It becomes chronic—a condition that disrupts every aspect of life. These patients often endure:
• Severe, unrelenting fatigue
• Chronic pain or neurological symptoms
• Anxiety, depression, and even cognitive decline
• Loss of income, relationships, and identity
They see specialist after specialist, undergo test after test, and are often told, “There’s nothing more we can do.” Some are misdiagnosed with fibromyalgia, chronic fatigue syndrome, or even psychological conditions.
This stage is often preventable, especially if we don’t delay treatment or dismiss symptoms when they don’t follow the textbook path.
Whether your Lyme disease experience falls into the good, the bad, or the ugly category, knowing the potential outcomes helps you make informed decisions.
Patients who understand:
• That Lyme disease can persist
• That co-infections exist
• That early treatment matters
• That healing may require time and patience
… are more likely to seek the right care, ask the right questions, and avoid falling through the cracks of the medical system.
If you’ve been diagnosed with Lyme disease—or suspect you have it—don’t settle for a one-size-fits-all answer. Listen to your body. Trust your instincts. And don’t be afraid to advocate for care that goes beyond the standard playbook.
Because Lyme disease isn’t just a rash and a few weeks of antibiotics. Sometimes, it’s a long road—and patients deserve guidance every step of the way.
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For more: