Begun June 14, 2011
My mother is dying. It’s so bizarre. First everything is fine, then there is pain, then a fractured pelvis is diagnosed, and then dying – in the space of two weeks. Activity is frantic as caregivers are lined up, the house rearranged, and a story line develops that changes three or four times by the end of the day. Death moves quickly when one has decided to die.
Mom is heavily sedated right now – thank goodness. We called Hoffman Hospice yesterday since hospice nurses are always amazing, always available, and always knowledgeable. I knew deep inside that she wouldn’t make it, but mostly, Mom needed pain control and that’s one of many things hospice does well. Part of me thought, if the pain can be controlled…but the other part remembered… she’s not eating. She doesn’t want to eat. She doesn’t want to be alive.
Neither my mom nor my dad has ever wanted to live in an incapacitated manner. When mom was first home from the hospital, she realized she couldn’t move or walk without great difficulty and extreme pain, and she said she can’t live like that, she’s just a big lump, she doesn’t want to live like that. And I knew she meant it. Maybe if we could have gotten the pain controlled earlier…but thoughts like that are futile because it was what it was. A fractured pelvis can take up to a year to completely heal, and months until the severe pain goes away. Mom wouldn’t be able to do that. She always said it, and she meant it.
Mom actually asked me how long it would take to heal and I told her the bone can take a long time but the pain should be able to be controlled and might go on for a few months, but not as bad as now. She said, “Susan, I know I can trust you.” In retrospect, I realize she was deciding whether to live or die. She knew that asking Dad was impossible since he’s 93 and has loved her deeply for almost 70 years; she knew asking my sister was impossible since she is so emotionally invested that she’d just be encouraging. Not that I am not emotionally invested, but it’s different. I marvel at Mom’s clarity in this as she’d suffered from dementia for years and couldn’t remember one minute to the next. I’m glad I didn’t know the burden that was placed on me until afterwards. Burden is perhaps not a good choice of words, because Mom would never have intentionally burdened her children with anything. I’m glad I was truthful even though I made it a little rosier than it would have been in reality.
Yesterday and today, at least this morning, Mom kept telling my sister and me how much she loves us. Over and over again. She’d say, “I love you. I love you so much.” Every time someone visited, like Daniel, when he left she said “I love Daniel so much.” She was emphatic, making sure we really understood. She was saying her goodbyes and I knew it. She repeated to herself over and over, “It’s going to be all right, it’s going to be all right,” by which she meant it was ok to leave us, she was comfortable that Dad would be taken care of and we would be all right. She was convincing herself that she could safely leave us. This, too, I understood in retrospect.
This morning she described a beautiful green lawn she was seeing. She was looking for Grandma Betty, her mother. She was reaching out with her hands to things invisible to us.
My mother-in-law did that when she was dying, and a dear friend did that when he was dying. I read about it in a hospice booklet but now that I’ve seen dying people do it three times, I believe it. Dying people reach out to the unseen and recognize people who have passed before them. Reconnecting. Being helped over to the other side.
So my mom is dying. She’s on the hospital bed that was delivered today to her bedroom. She’s on oxygen, and when that was delivered this morning I said, “Oh, we’re not going to need that.” How fast things change. Within hours.
Mom’s been suffering from dementia and her personal hygiene hasn’t been good the last few years. Now she’s as clean as a baby. The “bath” nurse came. To move her to the hospital bed, hospice called the transportation team who knows how to do these things incredibly gently. Josh, the wonderful equipment guy, brought the bed and oxygen. Another nurse came and spent hours with us. And then the “bath” nurse came. Who would have known? She very gently bathed mom, washed her hair with real water and real shampoo, carefully put lotion on, and even filed her nails.
Tonight the “tuck in” nurse is coming to make sure everything is set for the night. Our night caregiver, Katie, will be here and we were all going to sleep at home in our beds. Now, that’s impossible. I will – I can hardly hold my head up now. But my sister is coming back – once it became clear what was happening, no way would she not sleep here.
While this was going on we were in a race to get our sister who lives in Alaska here in time. She had been planning to come on Saturday, but it all moved so fast and we realized she had to come – now. She got here by Wednesday afternoon; my husband raced to LAX to pick her up and get her here in time, and although Mom was not responsive when Janine arrived, I know she could hear and was aware that Janine was there. Janine had all day Thursday with her because Mom died on Friday June 17. (the link is to the obituary).
We have Sharon, someone dropped in our laps from heaven I think. She took care of a relative of my friend Pat in Utah and was highly recommended and she was available. How quickly we came to depend on someone who was a stranger just days ago. And Katie – she’s just 18 but she went from being someone new to a member of the family just like that.
Mom’s respirations are slow now. Partly from the morphine, but mostly because her body is shutting down. Looking at her, I just feel an overwhelming sense of relief and gratitude that the unbearable pain is gone. I’m fighting off the sense of loss that is trying to creep in. I don’t want to feel it or deal with it until I’ve done what needs to be done and can collapse.
To be continued…





































































































































































































































