Reviews
Reviews
I am concerned about how I will cope at home.
Continue ongoing.
No negative feed back.
Nothing to improve as the care team have been fantastic.
There have been some years really that have had to be requested as tests results did not came back machine.
(I can see that they are typing. They are open with me.)
They are patient with me.
They explain what is going on PT is happy that he will not be discharged until somewhere suitable is find for liken go.
Patient is concerned re his bed.
There are no sides to his hospital bed which makes maneuvering difficult. He has mentioned this to his consultant but feels nothing has been done.
At the great patient was told her cancer was treatable and then suddenly she was under palliative care, which shew as upset by.
There was no after care there. In contrast the treatment in the health has been much better.
2 daughters: they have been very proactive.
"I can't think of any way to improve things- patient daughter: we haven't had to chase anything up.
We felt supported and not stressed by the experience.
The gap between symptoms of care mouth and being treated for it was too long which ment I was unable to eat for a long time, and still struggling with this.
Also it took a long time for the mouth wash to arrive once it had been prescribed.
I can't fault the palliative care service but were sometimes lt down by the system.
Haven't seen my members of the team yet, but there's a meeting tomorrow.
Daughter feel pt was referred to palliative care early enough. Was admitted before Christmas to UMW but not seen palliative care team until this admission.
There seems to be a lot of confusion regarding whether pt has had an infection or not and family are not happy with this.
Husband feels pt should have been discharged after Christmas.