While currently developing a Cancer Patient Planner/Navigator packet, I thought I would reach out to all of you. What types of things would you have like to have been told, been given, not been given by your care team? Was there something you found particularly useful/ comforting, or an indiviudal who made a difference by something they did? I'm attempting to learn more to be the best caregiver/navigator I can, and any advice would be greatly appreciated.
Topic: General
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