this was in Time magazine - or at least in the online version
wasn't a bad piece, you could quibble over a few of the facts here and there - but the general thrust was in the right direction - it showcased the lives of people dealing with this illness for decades
the weird symptoms
the pain and suffering
the financial hardship
the social isolation
the doctors not believing patients
etc
it made the point that more recognition for chronic Lyme is coming now that there is an estimated 7% of the US population suffering with long COVID and there are big patient groups pushing for answers
long COVID is getting around $1bn thrown at it in terms of research funding in the USA alone
so it at least demonstrates that long lasting symptoms do occur with what are thought to be merely acute illnesses - and some of that research will spill over into benefit for Lyme patients
it also mentioned some of the recent developments in lyme research by people like Haystead and Lewis etc
( eg sounds like Lewis has set up a company to produce Hygromycin A)
link here
https://time.com/6974403/chronic-lyme-disease-research/