Julie Mellae Exposes The Silent Lyme Pandemic

This is my story and that of others who dispute the claim that 'Lyme Disease does not exist in Australia'. Julie Mellae, Author

Julie Mellae - Ambassador, Lyme Disease Association of Australia

I am certain the swollen, pregnant paralysis tick embedded in the back of my neck was the near fatal blow. Unaware of what it was, I squeezed and pulled, delivering tick guts and toxins directly into my bloodstream, the mouthpieces still attached to my neck!

The consequences unfolded to become a book. I was spiralling into dementia, sick to the core of my soul, yet I realised there was much more to this hideousness than sick Lymies knew about. So, I took a journey into the unknown. The dark underbelly of the Lyme disease mafia corporations and minions.

(Source: Lyme Disease Association of Australia website )

Australia Urgently Needs A National Lyme Inquiry

According to the Australian Government, Lyme disease does not exist in this country and the penalty for doctors who correctly diagnose Lyme ‘disease’, is de-registration.

Could this have something to do with allegations from various sources that Lyme is directly related to historical CSIRO tick bioweapon research? Perhaps a national inquiry into Lyme ‘disease’ will be able to explore this and many other serious allegations being made by a sea of credible yet inaudible voices.

Julie Mellae: We Have Been Deliberately Hurt By Our Governments

Julie Mellae is an artist, Lyme survivor, author of Australian Lyme Crimes - A Global Disgrace, an Australian Ambassador for Lyme Disease Association Australia (LDAA) and working in collaboration with scientists in Western Australia.

Unable to access the medical care she needed, Julie became so ill from the debilitating effects of Lyme that she had to sell her home because she couldn’t meet her mortgage payments anymore.

7 years of suffering and 20 doctors later, the one doctor that correctly diagnosed Julie’s chronic Lyme condition, was unjustly and crudely deregistered. Despite her ongoing battle against relentless obstacles and close calls with death’s door, Julie managed to research, write and publish one of the most important books of our time.

Julie credits a naturopath for helping her stay alive and has grieved all the way through her horrific journey of discovery that we have been deliberately hurt by our governments.

---

Book Synopsis: Lyme Crimes - The Global Disgrace

Lyme disease was initially a mysterious rheumatoid type of disease discovered in 1976 in a cluster of children in Lyme, Connecticut, USA hence its name. Now known to be harmful to humans, this disease can be transmitted from human to human.

Estimated Lyme patients worldwide could be over one million; the numbers rising. The following story covers my personal battle with Lyme disease and the history of the collaboration of Australia, America and Russia in their modus operandi of biological warfare.

In this book, we look at Lyme disease's origins, the reasoning behind its denial and negligence by Australian doctors sworn to the Hippocratic Oath. We depict the actions and role of three main protagonists:

• Willy Burgdorfer Willy Burgdorfer, the borrelia namesake, discovered the causative spirochete of Lyme disease and also genetically modified ticks, force feeding them cocktails of viruses, bacteria, fungi etc, etc, etc.

• Dr Erich Traub, a Nazi scientist who was saved by the Americans, from a litany of war crime charges, due to his knowledge of viruses and diseases in Germany and Europe.

• The third protagonist, Dr Allen Steer, who named the condition, dodged the Draft and omitted vital evidence from his scientific papers to deny Lyme disease credibility.

We look at the action of governments and their various instrumentalities, which on the one hand seek to exploit sections of their own populations while at the same time resorting to manipulating decisions and laws for their own self -protection. It is the sickening story of lust for power, the fear of losing it, and the might agencies will bring to bear against the people who threaten these ambitions.

This is not hyperbole on the part of the author. At the time of writing this, we have all become aware that biological warfare is a fact that can no longer be hidden as it once was.

The highly mutating virus COVID 19 has practically brought the world to its knees, and we must assume it was 'released from the lab' in Wuhan, China. Dr Francis Boyle, an expert in bio-warfare, recently said: 'the Coronavirus that we are dealing with here is an offensive biological warfare weapon’.

In Australia, we have seen the effects of Thalidomide, the British Nuclear testing in Maralinga and the ramifications and destructiveness it has wrought on families. We witnessed Australia's appalling response to HIV Aids in 1980.

Our government is guilty of many sins to humanity. And yet, the intransigence of political parties remains. Admit nothing. Do not own any responsibility. Dismiss, denigrate, destroy if necessary, those who challenge the status quo.

This is my story and that of others who dispute the claim that 'Lyme Disease does not exist in Australia'. Alongside the history of Lyme will be the history of the strategies used against those patients and researchers who are fighting to claw back the right to decent medical care. Indeed, that is not such a big ask. Then why is it?

Julie Mellae, Author, Australian Lyme Crimes - The Global Disgrace

---

Reviews

---

---

Onerous Truths Need To Be Told And Acknowledged

I discovered Julie Mellae in her February 2023 interview with cult survivor turned child protection advocate and founder of Truth Justice Freedom for Children, Gabbi Choong.

Julie’s revelations initially shocked me to my core, but lashings of onerous truths that need to be told and acknowledged, tend to have that effect. Thankfully, the shock eventually subsided and, as the saying goes: This, too, shall pass if you are willing to pass through it.

The following interview notes initially landed in a note-book I created in 2023 called Toward Absolute Truth and Justice. Fully loaded with widely unreported issues that should make most Australian politicians and media executives hang their heads in shame, I decided that Julie Mellae’s story, her book and efforts to raise public awareness about the hidden global Lyme pandemic, deserve, at the very least, to be told in a standalone article.

---

“It is beyond ridiculous that you’re getting bull’s eye type rashes in Australia and they’re ignoring it… I mean, that is medical abandonment. From a human rights perspective that is absolutely not acceptable.”

Dr Richard Horowitz, LDAA Patron
Eminent Lyme expert, Author and Consultant
to the Australian Department of Health

(Source: LDAA)

---

Lyme doesn’t exist in Australia. Even if you test positive.

• In the 1940s, the Australian CSIRO colluded with the Russian military at Sydney University on tick bioweapons. Australia was ahead of the game in this little-known Cold War race for bioweapons.

• There is no Medicare or Centrelink support available for Lyme sufferers. Australian doctors and nurses have not been trained in treating Lyme and the Government refuses to have a register because Lyme doesn’t exist in Australia. Even if you test positive.

• The estimated number of infected patients worldwide is over 5 million and growing. The number of infections in Australia is 550,000 plus.

  When Julie’s doctor tested her for Lyme, the results came back showing anomalies in her blood, but not Lyme. When she had her blood tested privately, Lyme was acknowledged.

• A scientist friend of Julie’s is asking why Australian labs don’t see what she is seeing in our blood - a rampant cesspit of disease and bacteria; and why Australian labs don’t write a note when the bloods have been tested that say, ‘she doesn’t have this but according to the lab report, she needs follow up.’

• Lyme is also an STD (sexually transmitted disease) which is partly why the number of babies being born with Lyme is increasing. Lyme allegedly crosses the placenta to the unborn child.

• Lyme can also be passed on without the tick. Borrelia bacteria has been found in tears, sweat, semen and vaginal fluids, proving it can be passed on easily from one person to another. Patented symptoms imply that this is not a natural phenomenon. Nature cannot be patented.

• COVID case numbers are far smaller than Lyme numbers and many people are reportedly recovering from COVID within 2 weeks. Corona is ‘kiddie stuff’ compared to Lyme, which is far more difficult to recover from.

• Independent scientists, medical specialists and researchers have noted that Lyme and COVID symptoms are remarkably similar.

• We are chronically ill to the point of death and nobody is believing us…because Lyme doesn’t exist in Australia. Our government is guilty of many sins against humanity. And yet, the intransigence of political parties remains. Admit nothing. Do not own any responsibility. Dismiss, denigrate, destroy, if necessary, those who challenge the status quo.

  Governments are hurting us. You can’t go on thinking that the party you vote for is going to do the right thing by you. Because they are not.

• 80% of Lyme patients suffer from Morgellons, which is also a patented bioweapon. An insect hormone is attached to the disease. We attract these insects to us but how they get into and out of the skin is something that Julie doesn’t quite understand yet.

• Up until 18 months ago, Morgellons were labelled as Delusional Parasitosis, even though you can feel things moving around in your body. It itches, stings and you can see flesh being eaten away.

• Julie had Morgellons coming out of her skin and asked her doctor what they were. Her doctor said she didn’t know and told her to ‘slap some sorbolene onto them’. When she had detox baths, bugs came out of her. She thought they were dropping from the ceiling but realised they were coming out of her. It was horrific.

• Julie found a patented cure that was not peer reviewed but included topical lactase. She is trying to develop a lactase solution to see if it slows down the Morgellons which are protected by a biofilm. Removing the biofilm disrupts their environment and makes it hostile.

• Julie felt herself going crazy but pulled herself together and started collecting specimens because she knew that one day, she would have to prove it to the world. A dismissive professor suggested she throw her specimens into the bin but she said no.

Interview Link: Gabbi Choong: Julie Mellae on Australian Lyme Crimes, a Global Disgrace

Lyme Crimes Book Link: Lyme Crimes - The Global Disgrace

---

2024 Update on Julie’s Health

Julie has advised that her lactase cure for Morgs (Morgellons) was terrific for some time but she stopped using it when she became too ‘clogged’ to keep it up. When she ceased using it, the Morgs began to ‘breed’ again.

“My body has been a breeding ground for mutant insects including ticks. Shocking to witness, the grief profound.”

The following images are what she discovered from her specimens.

---

---

Americans assumed Lyme was leaked from Milson Island, NSW

“Milson Island is Australia’s equivalent of the USA’s Plum Island. It started off as a military quarantine facility and merged into a MK-NAOMI bioweapons research facility. Lyme disease and Swine disease were being researched on Milson Island in 1961 to ’62.

When Lyme turned up in 1982, the Americans assumed there had been a leak on Milson Island.  Sydney University took over Lyme testing from 1988 to ‘94, tested 4,372 people and did not get one positive in that testing – because they used the ELISA test. Everyone tests negative to the ELISA test. It tests the immune system which is not stimulated by Lyme Disease. ELISA is the only test allowed under Medicare.”

Eyes Wide Open, Co-authored by Fiona Barnett

---

---

Silent Lyme Bioweapon Pandemic Inquiry - A Matter of Urgency

The Australian government is obligated to demonstrate a duty of care to the Australian people and cannot expect to keep getting away with it’s habitual masonic silence and ridiculously unrealistic view that challenging issues will simply go away.

Time to grow up and face the music.

Whilst on the topic of freemasons, I have also been advised that satanic ritual abuse (SRA) survivors have complained to police about Masonic rape abuse and finding military grade aerosol ‘bug bombs’ in houses and city high rise apartments. These canisters released nymph ticks, the likes of nothing previously seen in Australia.

---

---

Testimonies From Lyme Sufferers

(The following testimony excerpts have been sourced from the internet. No names are mentioned for privacy reasons. Nobody should be left to suffer in silence like this and resort to support groups for help because doctors and governments are failing them and their families.)

---

I was just recently diagnosed with chronic lymes disease, babesiosis, ehrlichia, and rickettsia. I am 23 years old and am in a wheelchair and have a feeding tube.

Side note: With this, I also have

- Gastroparesis (paralyzed stomach)

- Ehlers-Danlos Syndrome

- Tethered Cord Syndrome

- Chiari Malformation

- Cervical Instability

- Celiac Disease

- Connective Tissue Disease

- Mast Cell Activation Syndrome (MCAS)

- Median arcuate ligament syndrome (MALS)

- Postural Orthostatic Tachycardia (POTS)

- Dysatonomia

---

Does anyone in here feel like your just so unlucky…. To have so many different issues?

I have hEDS, hashimotos, all the things that come with EDS like POTS, MCAS.

I have PSVT, SIBO, and Candida. As well as leaky gut, and I have Mold exposure as well.

I don’t even know where to begin as I have symptoms in every part of my body. They all come and go at random. Rarely do I get a day without at least 2-3 symptoms if not more.

I don’t know what was the chicken/egg in my health situation honestly. As I suspect I got Lyme from my mother…. I know that’s not a very popular thought. And not at all backed by science.

But I’m going to have my 4 kids tested for Lyme and if they are positive too I know I’ll have my answer - because realistically what are the odds we all have it? And my mother?

---

Went to the rheumatologist today. He told me that I have fibromyalgia. He also told me that there is no cure for fibromyalgia, and that I need to just “accept it”. He said that’s the first thing you need to do and then do yoga and see a therapist because fibromyalgia stems from past traumas.

Recommended giving me a trazodone prescription for sleep, but I declined, because I wanted to get a sleep study for sleep apnoea done before I shove another pill down my throat.

I didn’t mention the Lyme disease until he brought it up. He told me not to waste my money going to see a Lyme specialist. He said that years ago chronic fatigue, fibromyalgia, then it was Lyme disease, and now it’s long-term Covid as the latest trends…people just want to put something tangible to their “imaginary problems”.

Why is it that these doctors just want to blame something else and call it some sort of mystery diagnosis with no cure?

WTF did I listen to today? Was this really a doctors appointment?

…I wake up in pain and I go to bed in pain. There has to be some sort of relief in between. I am going crazy dealing with this every day.

---

I got Lyme disease five years ago. I treated with silver, monolaurin and enzymes and homeopathics. I was unable to walk due to neurological symptoms. 7 months of treatment=remission.

Last April it all came back. This time worse. I suddenly couldn’t walk and had to use a wheelchair, body pain, severe fatigue, brain fog. Started the same Lyme treatment as above but kept getting worse not better. I switched doctors who suspected mold. We had no visible mold but sure enough it was found in several hidden places.

We remediated.

And two months later I feel completely fine.

The mold awoke the llyne out of remission and it was blocking the Lyme treatment from working. Once that was gone my body was ready to detox it all.

Hope this helps and encourages someone.

(This new dr also did find pernicious anemia and treatment for that also helped. )

But mold was the ticket for me.

---

I’m 20 years old and I just found out I have Lyme after being mysteriously ill for 15 months! I’ve gotten blood work done 30 times in 2023, had 2 MRI’s, 2 echocardiograms, 2 heart ablations, 3 iron blood infusions, 2 in hospital procedures, and dropped out of college due to suddenly feeling sick / panicky.

I am on the autism spectrum and feel completely alone and don’t know what to do to get better. My body feels 80 years old and I feel like my immune system, heart, and brain are all betraying me!Like many others, I was misdiagnosed for over 17 yrs. In 2010, I was finally properly diagnosed with Lyme & several Co-infections.

For the next seven years, I found myself pretty much bedridden, experiencing every horrible symptom possible and fighting for my life. I was 32, a mother of five (who all also have Lyme) and couldn’t walk more than 5 feet without a walker, riddled in pain, having multiple seizures daily amongst many other unimaginable symptoms & loosing everything.

Doctors told me my brain would never function at higher than a 4th grade level ever again. The damage done to my brain from Lyme Disease was to great.

That WASN’T an option for me!

After a huge shift in my mind set and lifestyle, adding four years of IV meds and homeopathics, I kicked Lyme Disease’s ass & reached remission.

1 year ago, I graduated with my Bachelors degree with Honors. A year and a half before that, Obtained my AA with honors. Currently working a full time job, can keep my house clean, enjoy my children and their sports and have a new view at life through these eyes.

Remission IS possible! Keep fighting! Life IS worth it! YOU ARE worth it!

---

Additional Resources

---

Rumble Channel: Michael McDowall Ministries

---

Until next time.

(Image: Indigenous Civilizations)

---