A provocative open letter purportedly written by an anonymous Lyme disease “expert” has resurfaced, highlighting the ongoing struggle of millions of Americans suffering from Persistent/Chronic Lyme Disease (PLD/CLD) who face systemic barriers to proper diagnosis, treatment, and support. – – The letter was circulated within the Lyme community in May 2014 and posted on WhatisLyme.com. – – The Patient Centered Care Advocacy Group has republished this letter with permission from Lisa Hilton, fou…
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