Thanks for this thread. I lost my dad to a rare cancer about ten years ago and there was no guidance when the dementia hit (it went to his brain) and even hospice was not helpful. Reading other people’s experiences I realize now that I’m not the only one in the world who went through similar. Hugs to you all. |
I’m replying to myself here. Now that I’m physically with my dad, I’m getting great information from his hospice nurse, who’s wonderful. But I still want my own detailed, warts-and-all, university-grad-appropriate, Pubmed-aware written guide, and I’m seeing other forum posts about the lack of such a guide. If anyone here is a hospice nurse or the like who would rather be a writer, there’s obviously a huge, unmet need for What Expect When You’re Getting to the End kinds of books. |
We also had a really good set of hospice nurses. They taught us practical things like how to do transfers from the bed to a wheelchair, wheelchair to car, bed to toilet chair etc. They also taught us how to change the sheets with the patient in the bed. And which sounds indicated pain versus disorientation.
I feel like there is a much for LPNs to run a sort of class for caregivers. A lot of these skills require physical demonstration. But there are so few people with the training available. I went to a baby care class when I was pregnant that was run by the hospital. It feels like there should be something like this available. |