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This is why I don’t read my treatment plans in full anymore. The docs fill it out to sound worse than reality/focus on the bad stuff because the patient “looks more disabled” on paper for insurance to cover stuff/to get benefits/etc.
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"I don't know what I'm looking for."
"Why not?"
"Because...because...I think it might be because if I knew I wouldn't be able to look for them."
"What, are you crazy?"
"It's a possibility I haven't ruled out yet,"
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