Because of the public interest in this - which pushed the inquiry in the first place - the MJA has made the review freely available.
https://www.mja.com.au/journal/2016/205 ... -australia . Probably worth reading.
It is NOT just Australia refusing the results of the looney labs - these labs are unaccredited in the country in which they reside. See
http://www.nejm.org/doi/full/10.1056/NEJMra072023. Yes, chronic Lyme exists - but ALWAYS in patients who had acute Lyme disease first.
And really - one of the GPs in the earlier article said he had "130 patients" disabled by it. Duh. We have, what, a GP per 2,000 population? even assuming a GP/5000 and cutting it down to 100/Gp that makes, um, 500,000. (the paralysis tick is limited to the Eastern states but there's ticks most places. Even so, you could have this - or heck, call it 50,000) Now the US gets 300,000 a year of ALL lyme disease and only a very small fraction of those go on to chronic disease. Even those patients do not, according to the CDC, need intravenous or prolonged therapy. See
http://www.cdc.gov/lyme/treatment/ . So the Aust GPs demand to use a treatment that is not thought to be good practice by doctors expert in treating proven Lyme disease. And surely, with that number, you'd have to be seeing SOME people with acute disease, and no-one ever has. Apart from those who aquire it OS.
The "why does this work then" - um. Remember the various calls at times for publicly funded bizarre treatments? If you are told that this expensive and wonderful treatment will cure your (purely subjective) symptoms and you have to fight to get it, yes you might feel better for a while. Its called the placebo effect and keeps a lot of people very rich. Including, from time to time, those in mainstream medicine.
No-one is suggesting that the affected people don't have something wrong with them. Some of the media makes it sound like its up to the affected to prove they have this disease, but that's a bit unfair, its not just that "there's no proof" that its Lyme - there's been a lot of work done looking for Lyme - and it can't be found.
Me, I'm going with DEET!