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Hospice only gave us the information about how to administer the medication, not anything about who.
Every caregiver should have the ability to administer the medication, I think keeping a written record stops under or overdosing. The patient is being kept pain free and that is what should be the focus when deciding how and who should handle the meds.
Worried, I'll bet you have some insight on this issue?
If you have several family members involved in this family members care, than it's probably a good idea to keep a chart of when the morphine was given and how much. The most important thing is to keep them comfortable. Best wishes.
What I wish I knew then was to give my dad a few drops at a time instead of a dose -- wait four hours -- then another dose. When he was near to dying on his last day, the hospice nurse was there full-time, and she gave him a drop or two, then 15 minutes later another drop or two, and so on, which kept the level in his bloodstream consistent. He was never in any real pain anyway, but he was comfortable and that was so important to us.
Interestingly, I spent a night a short time later in a boat that had a solar pump which regularly pumped water out of the leaky bilge. It sounded exactly like the morphine driver, and gave me the horrors!