For those with a diagnosis of ME/CFS, what was your next steps with a neurologist?
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For those with a diagnosis of ME/CFS, what was your next steps with a neurologist? I had one that diagnosed me and requested some basic brain imaging that was fairly unremarkable, but then dropped my insurance. I'm about to engage with a new neurologist and wondered what I might suggest for continued discovery/treatment?
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R relay@relay.mycrowd.ca shared this topic
