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Reporting MS pain accurately
When a member of your medical team asks you to describe your level of pain on a scale from 1 to 10, what do you say?
I tend to downplay, if not flat-out forget, any pain that I experience chronically (on a daily basis), and I think most of us who have pain from multiple sclerosis do too.
Is it like I said above, we just don’t consider something we’re used to. Or is it a fear of not being believed because we’re not reacting to it the way a person experiencing it acutely would?
Do you tend to downplay chronic pain? What are your reasons?
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