SYDNEY, AU / ACCESS Newswire / May 26, 2026 / Julie Mellae releases Australian Lyme Crimes The Global Disgrace exploring the corrupt history of Tick- Borne disease, also known as Lyme Disease, her advocacy and the psychological gaslighting and anguish of patients’ healthcare experiences.
Medically Abandoned Around The Globe. THE TICK PANDEMIC
Australian Lyme Crimes The Global Disgrace has announced the release of a new written work by author, researcher and advocate Julie Mellae, focusing on personal narrative accounts and the sinister history of Tick- Borne disease around the globe, officially at pandemic proportions and growing especially in the USA with the advent of tick boxes released onto farmland throughout the country.
The publication is framed around the facts of Military collusion, medical abandonment and explores how individuals reporting chronic symptoms associated with Tick- borne diseases describe challenges in receiving diagnosis and recognition.
The work includes a referenced statement attributed to international human rights barrister Geoffrey Robertson QC of London, who is quoted as saying:
“This story must be told.”
The book presents this perspective within a wider discussion of controversial interpretations of Lyme disease and related conditions across different countries.
Author Synopsis and Lived Experience Narrative
Julie Mellae is an Australian author, researcher, and Lyme disease advocate known for her work documenting patient experiences and examining the contested history and global discourse surrounding tick-borne illness, commonly referred to as Lyme disease.
Her publication, Australian Lyme Crimes: The Global Disgrace, presents a personal and investigative narrative that combines lived experience with broader commentary on healthcare system responses, diagnostic challenges, and the experiences of individuals reporting long-term, multi-system illness symptoms associated with tick exposure.
Alarmingly, Tick-borne disease and co-infections include Babesiosis, Bartonella, Erlichiosis, Rickettsia, Morgellons disease, Reactivated Epstein Barr Virus, Q Fever, Relapsing Fever, Mycoplasma (Patented), Brucella,parasite and skin lesions, Tularaemia, Rickettsia Helvetica and Anaplasmosis.
Science papers prove this is officially an STD transmitted by saliva, tears, semen, cervical fluid and breast milk, which can be passed on in utero to the developing baby.
Drawing on her own health journey and interactions within the Australian medical system, Mellae describes a prolonged experience of illness, misdiagnosis, and what she characterises as gaps in clinical recognition of complex tick-borne conditions. Her work situates these experiences within a wider international discussion on Lyme disease definitions, diagnostic criteria, and patient-reported outcomes.
The book also explores historical and scientific themes related to vector-borne disease research, referencing contested perspectives on the evolution of Lyme disease understanding and the development of medical frameworks across different countries. These elements are presented as part of the author’s broader investigative narrative.
A central focus of Mellae’s work is patient advocacy, particularly the experiences of individuals who report feeling medically unrecognised or dismissed when presenting chronic symptoms they associate with tick-borne infections. The publication highlights tensions between patient communities and institutional medical perspectives, as well as differing interpretations of testing protocols and disease classification.
Through this lens, Australian Lyme Crimes: The Global Disgrace positions itself as both a personal testimony and a commentary on the broader challenges of complex chronic illness recognition, healthcare responsiveness, and ongoing scientific discussion in the field of tick-borne disease research.
Bioweapons, Healthcare Systems and Patient Advocacy
A central theme of Australian Lyme Crimes The Global Disgrace is the lived experience of individuals who report being medically unrecognized or inadequately treated for persistent, often debilitating symptoms they associate with tick-borne infections. The publication frames these experiences not only as individual struggles, but as part of a wider, ongoing question about how healthcare systems respond when patient experience does not neatly align with established diagnostic categories. Why are doctors de-registered for treating Lyme disease? Why do so many patients feel their symptoms fall into gaps that official testing and protocols fail to capture?
Across these accounts runs a consistent tension between lived experience and institutional interpretation, between what patients feel in their bodies and what is formally recognised within medical frameworks. Why do different countries continue to present such contrasting positions on the existence and classification of Lyme disease?
These questions are not presented as isolated disputes, but as part of a broader global conversation in which science, clinical practice, and patient-reported outcomes do not always evolve in sync. The result, as reflected in the publication, is a landscape where uncertainty persists and where many individuals feel caught between competing narratives of illness and legitimacy.
The publication further reflects the author’s intention to document lived experiences and perspectives she states have been historically underrepresented in mainstream medical discourse. It weaves personal testimony with wider historical and investigative threads, including references to legacy biomedical research, international scientific developments, and evolving interpretations of vector-borne disease within global health discussions, offering a broader lens through which these patient experiences can be understood.
Public Discourse on Tick Borne Diseases
Tick- borne diseases, including those commonly referred to as Lyme disease, remain the subject of ongoing research and international discussion. Differences in diagnostic standards, surveillance data, and clinical recognition contribute to varying perspectives among healthcare professionals and patient advocacy groups. However, all agree we are very, very sick.
Publication Information and Availability
Australian Lyme Crimes The Global Disgrace is authored by Julie Mellae, who is identified as an Author and Global Lyme Disease Advocate. The book is available through the official website and associated media channels. Purchase information and additional content can be accessed at her website. Readers and media representatives can also reach Julie directly by email at jmellae@bigpond.com. Social media presence is maintained through Facebook.
About Australian Lyme Crimes The Global Disgrace
Australian Lyme Crimes The Global Disgrace is an independent publishing and advocacy initiative created by Julie Mellae. The platform shares written works and commentary focused on the corrupt military history, the Nazi scientists developing biologically altered ticks, personal health narratives, discussions surrounding the negligence of doctors refusing to treat or care for those acutely sick patients within healthcare systems, Globally
2026: Ticks continue to be laboratory manipulated to include bacterium, viruses, fungi and toxins and has now hit pandemic proportions which remains unannounced by mandating governments.
Contact Info:
Name: Julie Mellae
Email: Send Email
Organization: Australian Lyme Crimes
Website: www.australianlymecrimes.com/
SOURCE: Australian Lyme Crimes
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