My mother may be dying. Five words that, when said to myself, feel like they don’t mean anything; at least not anything real.
My 94-year-old mother has been living here with us in Florida since last Thanksgiving. She had previously lived with my brother in Michigan for the past 14 years, minus the winter months with me, since my dad’s passing. But circumstances brought her to us for longer than the typical winter months, and now she is in her bedroom, in a hospital bed, and for all I know, she is dying.
Did I mention I work for hospice? I know about people dying. I’ve talked to them or their caregivers and I’ve offered words of reassurance. But what did I know? My dad was on hospice in the hospital where he died, but only for a few days, and it seems far removed from this. This is different.
Mom is now on our hospice. She has an angel of a nurse and a wonderful aide. She has all the accoutrements of a hospital room, but she’s home, with us. And instead of hearing the reassuring words I’d uttered to others, I have tunnel vision. I feel inept. Like I’m not doing enough, but I don’t know what enough is.
She surprises us. She’ll be totally wiped out and barely able to get up enough strength to use the bedside commode. She’ll be in bed all night and all day eating and drinking little to nothing. And then suddenly I’ll see her dressed, coming out of the bedroom smiling, saying, ‘Hi, Honey!’ She has raised 11 children, worked tirelessly in and outside the home, traveled near and far. She is part of that generation that feels she’s not supposed to stop.
I’ve been trying to keep my 10 siblings updated as much as possible. The challenge seems to be, though, that my dire narration is often followed by a ‘never mind’ report making me feel foolish, like I’m jumping the gun or something.
She says this is dumb. “This is so dumb.” “I just wanna feel better.” “If I’m gonna kick the bucket, I wish I’d just kick the bucket.” I have no response to that. Part of me wants her to join her beloved Charlie, whom she has had to live without for 14 years. Of course, the selfish part of me wants her to rally once again, to go to breakfast with us, to drive to the ocean and watch the surf. And it could happen.
Being on this side of hospice is eye-opening and humbling. I can do this part, caring for her, making her comfortable, accepting the thanks from my brothers and sisters for something I’d have fought them for. This part is easy.
I’m not sure about the next part. She’s the last of them. She deserves to go peacefully to her husband and loved ones gone before. My mind knows this absolutely. I want it for her, too.
But my heart…
I hope I’m as strong as I need to be.
One thought on “The other side of hospice”
Beautifully written Maureen. We all feel the same, but you are the one with her and seeing her. Have to say I’m a little jealous, but I am so glad she has you. I know you carry all the love and support from all of us and I’m grateful to the core for all you are doing for our dear mother. Remembering her smiling and singing with me at night brings me comfort. Just continue doing what you are doing and as one of the sibs, again I say thank you. Love ya!