Lyme Disease Association of Australia

Lyme Disease Association of Australia The Lyme Disease Association of Australia is a small yet powerful registered charity and Australia’s peak patient body. This page is run by volunteers.

We are committed to achieving universal recognition and equitable treatment for Australian Lyme and associated disease patients. The LDAA is an association comprised of volunteers committed to making changes to how Lyme disease patients are treated – both medically and personally – to improve their health outcomes and to move the treatment of Lyme disease into the 21st century. HOUSE RULES:

The L

yme Disease Association of Australia (LDAA) reserves the right to delete, remove content and block users on our page if interactions are:

• Threatening, abusive, defamatory, obscene, indecent, malicious or disrespectful to patients, their families and or LDAA volunteers. Including comments that attack, condescend or are derogatory towards patients or volunteers and or their families.

• Unlawful, fraudulent, deceptive or misleading.

• Sends users to external websites that may include information that cannot be verified

• Offensive, derogatory or racist commentary including nudity

• Unauthorised commercial communications such as Spam

We DO welcome

• Personality - don’t be shy

• Passionate discussions and healthy debates

• Views and opinions if shared respectfully

• Issues that affect your community

We do NOT welcome

1 - Trolls: Bullying, personal attacks and nasty comments. Comments that are disrespectful to our community members or our volunteers WILL NOT be tolerated. Comments that are defamatory, condescending, derogatory or insulting will not be tolerated towards patients, their families or LDAA volunteers. Be respectful of other community member’s and volunteers feelings and opinions.

2 - Spam: Our page is not intended for the promotion of third-party companies. Do not post content that would constitute advertising, junk mail, spam, chain letters or any other form of unauthorised solicitation. If in doubt do not post on our page, simply send a private Facebook email to the editor.

3 - While we do our very best to moderate the community, the LDAA does not take responsibility for postings or discussions that have not been posted by our team. However, we do reserve the right to remove offensive or harmful posts and ban individuals from accessing the page.

4 - Finally, comments must comply with Facebook’s Statement of Rights and Responsibilities (SRR) and other policies. User content published on this page may be used by LDAA marketing materials and other social and/or digital platforms. A copy of the SRR can be found here - https://www.facebook.com/terms

If a comment on the LDAA page offends you - please report it to us via messaging the LDAA page and an admin will investigate your concerns. The LDAA social media volunteers have the right to remove anyone from this page with out notice if they breach any of the house rules. DISCLAIMER:

The above material, and all material offered in posts is for informational purposes only. The material (a) is not considered or should be used as a substitute for medical advice, diagnosis or treatment, nor (b) necessarily represents endorsement by or an official position of the LDAA or any other of its directors, officers, advisers or volunteers. Advice on testing, treating, or caring for an individual patient should be obtained through consultation with a physician who has examined that patient or is familiar with that patient's medical history. LDAA makes no warranty of any kind with respect to this website, including as to the accuracy, completeness, currency or reliability of the information contained herein, and all such warranties are expressly disclaimed. Thanks for your cooperation and taking the time to read this. We want this page to be a safe and educational place for all. Socials:
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2022 © Copyright LDAA Lyme Disease Association of Australia. All rights reserved.

Alpha gal (aka Mammalian Meat Allergy) - The tick may not be the whole story 🤔The explosion of cases raises many questio...
18/06/2026

Alpha gal (aka Mammalian Meat Allergy) - The tick may not be the whole story 🤔

The explosion of cases raises many questions that deserve careful scrutiny. For example:

❓Why have cases of alpha-gal syndrome risen so suddenly?

❓Why do some people test positive but have no symptoms?

❓Why do some people have very mild reactions while others’ reactions are severe, even life-threatening?

❓What role do mammalian-derived pharmaceuticals and medical interventions, gut permeability, microbiome composition, repeated tick bites, genetics, and environmental exposures play?

❓How often are symptoms complicated by histamine intolerance, mast cell disorders, irritable bowel syndrome, medication reactions, foodborne contaminants, mitochondrial and other metabolic disorders, and so on?

“Ironically, alpha-gal syndrome was not discovered because people reacted to steak.
It was discovered because cancer patients in the southeastern United States experienced severe reactions to cetuximab, a monoclonal antibody.”

Robert Malone unpacks these questions and more in his essay: https://open.substack.com/pub/rwmalonemd/p/alpha-gal-syndrome-beyond-the-tick

LDAA President Sharon Whiteman was recently interviewed on live TV!Sharon was invited to appear on live TV on The Countr...
17/06/2026

LDAA President Sharon Whiteman was recently interviewed on live TV!

Sharon was invited to appear on live TV on The Country Telegraph, a daily program dedicated to celebrating regional, rural and outback Australia while exploring the issues shaping our nation’s future.

During the interview with host Mike Ryan, Sharon discussed:

✔️ Lyme disease and other tick-borne diseases in Australia
✔️ The challenges faced by patients and families
✔️ The urgent need for better awareness, diagnosis and support
✔️ LDAA’s National Tick-Borne Disease Survey and how community participation is helping build the evidence needed to drive change

💥 Add your story to the survey here: https://lymedisease.org.au/national-tickborne-disease-survey/

We appreciate the opportunity to raise awareness of the growing impact of tick-borne diseases on Australians and the importance of collecting patient data to inform research, healthcare, and policy.

📺 Watch the interview recording here: https://www.thecountrytelegraph.tv

Thank you to Mike Ryan and The Country Telegraph team for helping bring attention to this important public health issue. 🙏

Thursday 18 June, 6.00am (AEST) 🎯Why Some Heal & Others Stay Stuck with Bill Rawls, MD Dr Rawls has spent more than two ...
17/06/2026

Thursday 18 June, 6.00am (AEST) 🎯
Why Some Heal & Others Stay Stuck with Bill Rawls, MD

Dr Rawls has spent more than two decades at the intersection of herbal therapy, cellular wellness, autophagy, and chronic Lyme recovery. This is his most comprehensive conversation yet on why herbs work — and why they work when other approaches fall short.

Register now 👇👇👇

Dr. Bill Rawls on why herbs, autophagy, and cellular health are the missing piece in chronic illness recovery. Free. June 17th, 4 PM ET.

Did your relationship survive Lyme? 🥺 🎯 🫂Chronic Lyme disease doesn’t just affect the person who is sick. It affects spo...
15/06/2026

Did your relationship survive Lyme? 🥺 🎯 🫂
Chronic Lyme disease doesn’t just affect the person who is sick. It affects spouses, children, friendships, careers, finances, and nearly every aspect of life.

In this podcast, Fred Diamond chats with fellow Lyme author Sarah Krivos, who now realises that while she was ill, she was pushing away the person who loved her most. She admits that she often lashed out at her husband, Dan. 😪

If you have loved ones who don't know how to help, seek out Fred Diamond's book “Love, Hope, Lyme: What Family Members, Partners, and Friends Who Love a Chronic Lyme Survivor Need to Know.” 🙌
Fred's book is available on Amazon and the e-version (pdf) is always free to Lyme survivors. PM Fred on Facebook or LinkedIn for your copy 🆓 🙏 💚

By Fred Diamond A Lyme advocate once shared with me that they estimated that 75% of committed relationships will terminate when chronic Lyme is involved.

In Australia, Alpha-gal syndrome is mostly referred to as Mammalian Meat Allergy. That nomenclature is seriously mislead...
11/06/2026

In Australia, Alpha-gal syndrome is mostly referred to as Mammalian Meat Allergy. That nomenclature is seriously misleading; it’s far more complex than a simple allergy to mammalian meat.

People living with this disease know that avoiding red meat is just the beginning as the data from tickbitedata’s survey clearly shows:

* 72.5% reported reactions to dairy
* 78.6% reported reactions to gelatin-containing foods
* 67.3% reported reactions to gelatin-containing medications
* 73.0% reported reactions from cross-contamination
* 87.9% reported reactions to small amounts of mammalian-derived ingredients

Reactions reported include gastrointestinal symptoms, cardiovascular concerns, skin manifestations, sleep disruption, anxiety, or significant impacts on daily functioning.

This disease can cause neurological symptoms such as brain fog, mental fatigue, headaches, dizziness, and tremors.

Tick Bite Data lays it all out here:
https://www.tickbitedata.com/post/alpha-gal-is-not-behaving-like-a-red-meat-allergy-in-our-data

The Educated Patient recently interviewed Dr. Charlotte Mao, infectious disease pediatrician and advisory board member a...
11/06/2026

The Educated Patient recently interviewed Dr. Charlotte Mao, infectious disease pediatrician and advisory board member at Bay Area Lyme.

This in depth discussion highlights a review she co-authored examining the current evidence surrounding Lyme disease in pregnancy, as well as the important questions that remain unanswered.

As research continues to evolve, conversations like these help raise awareness, support informed decision-making, and identify gaps where further research is urgently needed.

Charlotte Mao, M.D., highlights significant unanswered questions about whether and how Lyme disease may be transmitted from mother to child during pregnancy and birth.

💥 Too many patients are told, “Your test is negative, so you don’t have Lyme.” 😣 This mindset is dangerous because it cr...
09/06/2026

💥 Too many patients are told, “Your test is negative, so you don’t have Lyme.”

😣 This mindset is dangerous because it creates diagnostic dead-ends. Patients who clearly fit the clinical picture are left without treatment, often bouncing from specialist to specialist.

😧 In the meantime, untreated Lyme can progress to affect multiple systems: joints, nerves, heart, gut, and even vision or hearing. By the time years have passed, recovery is often harder and slower.

🎯 Clinical diagnosis prevents these delays by empowering providers to treat based on the whole picture, not just lab paperwork.

👇 Get the full story

Negative Lyme test but still sick? Learn why Lyme is a clinical diagnosis and how symptoms, history, and testing limitations shape proper evaluation.

07/06/2026

🕷️ Regardless of the label, Australians are getting sick after tick bites, and our systems aren’t set up to properly detect or manage it.

🩺 Australians are left undiagnosed or unsupported, which means prolonged illness, financial strain, significant loss of quality of life and sometimes death.

✅ Australia urgently needs a coordinated national strategy for tick-borne diseases so patients can be diagnosed, treated, and counted.

🫵🏼 You can be part of the solution: learn how here: https://lymedisease.org.au/national-tickborne-disease-survey/

Dr Richard Horowitz offers his take on new Health and Human Services action in the US led by Secretary Kennedy 🎯 🤔 👀On w...
05/06/2026

Dr Richard Horowitz offers his take on new Health and Human Services action in the US led by Secretary Kennedy 🎯 🤔 👀

On why it's hard for chronic patients to get well, Horowitz writes:

"Treating the biofilm/persister forms of the bacteria was the key. The patients who are ill post dapsone combination therapy usually still need to address their mold, active Babesia, active Bartonella, microbiome imbalances with leaky gut and/or mast cell activation, sleep disorder, vitamin and mineral deficiencies, immune deficiency and/or autoimmune reactions, mitochondrial, hormonal, and liver dysfunction as well as the neurological and psychological dysfunction, autonomic system dysfunction with or without POTS, pain syndromes and deconditioning.

In other words, they still had inflammation coming from multiple MSIDS factors that still needed to be properly addressed for their health to improve. That is the rule, not the exception for those thousands of patients I have treated. So when researchers describe needing ‘pure Lyme disease cases’ for clinical trials, they are ignoring the reality of the situation".

There's a LOT in this article, and it's worth a look 👇👇👇

I am happy to see more attention is being given to Lyme disease by Secretary Kennedy.

📢 Have you been affected by Alpha-gal Syndrome (Mammalian Meat Allergy) or another tick-induced allergy?TiARA (Tick-indu...
05/06/2026

📢 Have you been affected by Alpha-gal Syndrome (Mammalian Meat Allergy) or another tick-induced allergy?

TiARA (Tick-induced Allergies Australia) is conducting an important national survey to better understand the impact of tick-induced allergies in Australia, including Alpha-gal Syndrome.

Your experience can help shape future research, improve healthcare awareness, and strengthen advocacy efforts for people living with these conditions.

✅ Takes just 8–12 minutes
✅ Completely anonymous
✅ Every response makes a difference

The information collected will help to:
• Improve awareness among healthcare professionals and the wider community
• Identify gaps in diagnosis, treatment, and support
• Support advocacy efforts and future research funding

Whether you have been directly affected, care for someone who has, or have relevant experience with tick-induced allergies, we encourage you to participate.

👉 Take the survey here: https://docs.google.com/forms/d/e/1FAIpQLScq6q2LjMhzqAmgN47xpkV2_3Ph02PQuVcg_YE4qpj-E-kn-w/viewform?usp=send_form

Please consider sharing this post to help us reach more Australians affected by tick-induced allergies.

Thank you for supporting this important work.

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Newcastle, NSW
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