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Experiences with Care centers – Negative (for parents of kids with CF)
As much as we wish it were otherwise, we have poor experiences at some care centers. On the other hand, we have some fantastic experiences at some care centers. I don’t want this to be a spot to attack care centers, so please refrain from naming your center. But I want this to be a place to offer genuine critiques (again, please no naming specific centers) for how centers can be better.
- What are some negative experiences you’ve had regarding your children’s care centers? (This can be regarding normal visits, or it can be regarding hospitalizations. Anything negative, honestly.)
- How could this experience have been corrected or made better? Or even prevented?
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