Are Private Clinics "Cashing In" On False Lyme Diagnoses? (read caption)

I share my perspective on this topic as someone who got overseas testing for Lyme and has been to private Lyme clinics. Studies are underway to try and create a more accurate mainstream Lyme test, as the one used by the NHS and by hospitals in America only has a 50% accuracy rate.
The NHS doesn;t diagnose of treat chronic Lyme despite 700 peer-reviewed studies and articles showing that Lyme and co-infections can persist despite antibiotics. ILADS document showing references to over 700 articles: www.ilads.org/...
The NHS (and doctors in mainstream American Hospitals following outdated IDSA guidelines) as to deflect responsibility and save money by saying we all have ME/CFS as they do not want to be sued for not treating people.

[@user-jr4xp4cj1e]

Spot on. Very tragic.

[@jakemerchant-wq3tb]

you speak so well and articulately on all of this! could you maybe do some vlog-type videos on the channel?

[@Truerealism747]

I have heds cfs fybromyalgia yeaes decades grew up in farm i have autism adhd to lost my mum.ti severe ms heds my father had cfs niw ok 30 years later

[@ChronicAdvocate]

I'm so sorry that sounds horrible

[@Truerealism747]

@@ChronicAdvocate thankyou do you have pain daily