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Has anyone had good experiences with seeing a neurologist for ME? I have an appointment in a few months and am trying to be hopeful and also know what to ask.
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Myalgic Encephalomyelitis
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Thank you! I'll post an update after the appointment. My PCP referred me to a rheumatologist, but they declined to see me because my ANA and RF tests were negative š
I was diagnosed by a rheumatologist, but I'd be interested if they find anything to help! Good luck!
ā This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision
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One user shared their experience with a neurologist, saying, "My first neuro was amazing, super attentive, the last two were meh but still listened and were helpful." While this is not specific to ME, it shows that some people have had positive experiences with neurologists. It's important to be prepared with questions and information about your symptoms to make the most of your appointment.
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