Below you’ll find a selection of media releases from the Lyme Disease Association of Australia. As always, should you have any questions or require assistance please contact us.
May 2020
- LDAA Ambassador – Andi Snelling (PDF, 272kb)
December 2019
- LDAA Ambassador – Tanya Dupagne (PDF, 314kb)
November 2019
- When Lyme gets too big, get help (PDF 365kb)
January 2019
- Australian patients in disbelief as government fails (PDF, 192kb)
June 2018
April 2018
- Social Media Explodes with Lyme Rashes (PDF, 224kb)
- Lyme-Ed – Patients provide training gap solution (PDF, 133kb)
- Scientific Advisory Committee Announced
March 2018
- Australian Research Pilot Funded (PDF, 295kb)
January 2018
- Dr Michelle Wills PhD evidence ignored by government (PDF, 410kb)
August 2017
- NHMRC Lyme-like research funding (PDF, 134kb)
May 2017
- Take a bite out of Lyme (PDF, 150kb)
March 2017
- Patients invest in research (PDF, 156kb)
January 2017
- Dr Richard Schloeffel OAM (PDF, 86kb)
November 2016
- Exposed – Evidence of an Australian Lyme Disease (PDF, 80kb)
October 2016
- If I die on your watch (PDF, 139kb)
September 2016
July 2016
- Lives lost to Lyme-like illness remembered on Red Shoe Day (PDF, 78kb)
- Murdoch University Pilot Study
May 2016
- New Ambassador announced at Federation Square (PDF, 81kb)
April 2016
February 2016
- Lyme Life Lost to Suicide (PDF, 137 kb)
- Medical Complaints Inquiry (PDF, 64 kb)
- The NHMRC Advisory Committee for Research into Debilitating Symptom Complexes Attributed to Ticks now has a webpage portal to follow the progress.
January 2016
- LDAA seeks action from Senate Inquiry (PDF, 133 kb)
- Lyme-like Illness patient media release (Docx, 103 kb)