What do you want from your caregiver(s) after being diagnosed?
November is National Family Caregivers Month. We thought it might a good idea to share here what you might want from your caregiver(s) so they know how to best support you through your breast cancer experience.
So, what are you looking for from your caregiver(s)? Information, emotional support, help with daily tasks, medical care, transportation, finances, planning, advocacy? What else? Share with us below!
Comments
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Hey All,
Bumping this. Would love to get the feedback!
Thank you!0 -
Food and transportation were helpful. Also since was not up doing housework doing those tasks as well was helpful.
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I would simply like to have more info on side effects. My trust in the medical community is already low and when I hear doctors minimize my concerns I can’t stand it. Yeah, you have an MD, but I know my body better. And I am the one who has to live with whatever happens to me.
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