I’ve been staying in Searsport Maine for the past 2 weeks, closer to Louise than my home in Hyattsville Maryland. From here, the trip to see her at the hospital is just short of an hour (if you’re in a car I’m driving). An hour away from mom compares now to slivers of seconds over the thirteen-hour car ride north. My apologies for taking a bit of a French leave (http://en.wikipedia.org/wiki/French_leave) with regards to Louise’s updates. I will attempt to summarize Louise’s progress over the last few weeks without drawn out stories or details; the facts will be the vehicle and succinct the delivery.
Louise was in ICU (Intensive Care Unit) for a month after the accident. After the surgeries, the staff of the ICU continued to monitor her vitals for weeks until she was stable enough to move to a rehabilitation unit. On any given day, Louise’s temperature would spike, prompting another dose of Tylenol and plenty of inquiries: What was causing it? What did it mean? Did she have an infection? Was she going to be OK? Should we take her covers off? Should we put a fan on her? Every little bleep of the monitor was an alert that told us something was wrong. It told the nurses something different – to give her something to stop the beeping. And medication always stopped the beeping. Her heart beat out of rhythm on a couple of occasions (http://en.wikipedia.org/wiki/Atrial_fibrillation), which not only brought out the drugs, but the paddles as well. Thankfully they were not needed. If I had been there, perhaps I would have needed them. When her blood pressure fell, drugs fixed that too.
Louise had many tubes, needles and pegs going into and coming out of her body, providing a system of pathways for food, drugs and excretions. As a result of the shock to her body, there wasn’t as much stuff leaving as entering; and in her ICU bed, Louise lay swollen and puffy. To grasp her hand was like holding onto an over-inflated latex glove or the Stay Puft Marshmallow Man http://en.wikipedia.org/wiki/Stay_Puft_Marshmallow_Man.
Gradually Louise lost the fluids that gave her skin and flesh the appearance of a wrinkle-free newborn. Louise looked more like Louise. As she stabilized, her days in ICU became numbered. She would soon check into a new room where she would meet a new team of doctors, nurses and physical, occupational and speech therapists.
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When I arrived back at Eastern Maine Medical Center, I was blown away by Mom’s appearance; in her new bed, her blue eyes were there to greet me, her face no longer showing signs of recent trauma. I had received reports from Larry, Kim and Yvonne while away. I knew that the puffiness had given way to muscle and bone that had not resisted gravity in 5 weeks; Louise was now slightly underweight and losing muscle tone. There she was, though, moving her extremities, mumbling, sometimes saying words and slowly finding her way back to back to us.
This trip to see Mom was very different than the last. I now had the experience of time and expectation; the more time removed from the accident combined with reports of steady progress made the reunion less distressing. She looked great. I was happy. Her toes were talking, walking and tapping a mile a minute when I walked into the room. If she knew it was her son at the foot of her bed, then she must have been happy to see me. I talked to her and took in her new condition. I started to think about the next steps.
Louise has been, and is making progress. She’s been tracking people with her eyes, she’s responding to people speaking to her and she’s able to hold her head up while sitting. These are giant steps toward recovery. Every day there’s a new jumped hurdle. She’s been receiving therapy every day, multiple times a day from occupational, physical and speech therapists. She’s often tired but to see and hear her count to 5, then 10, and on to 14 does reflect continued development and progress; her every achievement feeds the hopes and wishes of her family and friends.
Some of you may be wondering how she can speak with a trach (http://en.wikipedia.org/wiki/Tracheal_tube#Tracheostomy_tube). She was fitted with a smaller device, which has a plug in it for preventing air from leaving or entering through her throat and allowing her to inhale and exhale through her mouth. This allows her to speak. And she has been speaking. When she’s alert, she can answer basic questions. She surprises us every day with new words and actions. She’s been saying the Hail Mary in French! And the jingle from Scooby Doo!
Louise started eating and drinking too - ice cream and applesauce from a spoon and water from a straw. Soon they will start giving her food more regularly.
They call today Mother’s Day. Louise and I are sitting next to each other looking out a large window into the sunny Bangor morning watching trees sway and clouds float by. I can’t imagine being anywhere else.