Re: Advice on hospice social worker role Originally Posted by Spidey's mom
I mentioned that and she came back with "This is not acute care - this is hospice and it is different". And since she has more training than I do, I don't know what I'm talking about.
steph
Not been around this place (or anywhere in the social media for a while) but this caught my eye.
Anytime someone uses their experience as a cudgel it puts up warning flags for me. (I'm assuming the part about you don't know what you're talking about came from her). It also seems that being part of a team doesn't mean that you try and ride roughshod over someone trying to do their job, or that a SW, who should be good at interpersonal relations shouldn't be getting her feelings so hurt when you are talking about a exchange of perspectives among colleagues (and team mates).
One aspect that bothers me is that of role confusion for the patient -- it's hard enough for pts and families to know who is the best person to ask about "X" but when the professionals are making the lines even more blurry, it's worse. As others said, it sounds like a power trip to me, to at least some degree.
I don't think that "being a patient advocate" is solely the nurse's purview, but overall assessment and developing an appropriate approach to care IS.
Good luck with it all. Small communities/organizations can be particularly tricky to navigate -- you do need to depend across disciplines more, and it can become insular and claustrophobic. That said, using "hospice is different" as a trump card is B.S. Hospice is patient centered and family focused. You asking the patient for their OK was EXACTLY WHAT YOU SHOULD BE DOING -- you are giving the patient's needs and desires primacy.
You are still professionals with different scopes of practice, and different places where you are, and should be in control of the proceedings.
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