Remembering Lizzie

Facebook tells me that it’s Lizzie Hudson’s birthday. (Facebook uses a different name for her, but I’ll use this one to protect her family’s privacy.)

Facebook tells me that I should wish her a happy birthday. I dearly wish I could. I would like nothing better.

But Lizzie Hudson passed away three years ago at the age of 23, after losing her lifelong battle with Cystic Fibrosis.

Lizzie was one of my first patients, when I was a third year medical student, just starting out with my first rotation: Internal Medicine, which I eventually chose as my specialty. She started out as any other patient does. I woke her up, apologized for waking her up, and did my standard History and Physical initial patient interview. As a lifelong denizen of hospitals, she was quite used to this. She answered all questions cheerfully, honestly, and concisely.

And starting from there, she quickly became a favorite patient. She had this cheerful, unrelenting positivity that was just a delight. I would stick my head into her room whenever I was on her floor, sometimes only long enough to make faces at each other before I had to move on. When I had some down time, I spent it hanging out with her, wrapped in an isolation gown and nitrile gloves to protect my other patients from the resistant bacteria she was inevitably colonized with. We talked about hospital stuff. We talked about music and movies. We talked about her family and friends. We talked about religion, because she was a devout Christian and faith played a huge role in her life and she loved to hear about the role that my very different faith played in mine.

She was a delight. She was a pleasure. She got over her bout of pneumonia, and we sent her home.

Fast forward a year.

I’m a fourth year medical student, and I’m basically in hell. Winter is a sucky time for a surgery rotation, since you have to make sure that any unplowed snow doesn’t interfere with you getting to work on time. So I had slogged through about two and a half feet of snow at 3am, walking in a tire track in the middle of the road, which was REALLY bad karma, but the sidewalks were unpassable. I comforted myself with the fact that my black coat would stand out against the white snow, and I could always dive out of the way without getting hurt because of all of the snow on the ground. I was headed to work that early to pre-round: get a morning set of vitals and labs on everyone before the surgery team came in to round at 6am so we could be in the operating room by 7. It’s hard pre-rounding at 4am, because the nurses just don’t have the information yet. So it takes a LOT of time to pre-round, and you get in BIG trouble if you don’t have a piece of information when you’re asked for it.

So I’m panicking, running from patient to patient and computer to computer, trying desperately to get everything together in time. Then….DISASTER!

One of the computers I tried to use actually had a nurse’s work screen pulled up on it. I had clicked on a button before it even registered that it was not the usual interface. And then as the screen went blank, it registered on my sleep-deprived brain that the screen had been showing a medication reminder. And in that adrenaline rush where my mind called up every detail of that screen, I noticed the name of the patient: Lizzie Hudson.

No time, no time, no time! I tracked down her nurse, told her about my idiocy, was quickly forgiven and reassured, and I moved on to my next patient, jotting down Lizzie’s room number for future reference.

The end of the work day saw me exhausted but grinning like an idiot, leaning against Lizzie’s doorframe, my arms crossed. “Didn’t I send you home?” I asked. “Yeah,” she replied as if ashamed. “But I missed you, so I came back.”

We spent about an hour catching up, and many more hours over the course of the month just hanging out whenever I had some time. She was no longer technically “my” patient, but she was solidly my friend. Since we both had a messed-up sleep schedule (it’s hard to sleep in hospitals, either as a patient or as a larval doctor), we’d have wee-hours hangouts when I was doing an OB-GYN rotation that required me to stay overnight. I showed her how to break the hospital’s firewall (shhhhhh! Don’t tell!) and we traded favorite movies, TV shows, and even musicals. She kept on taking her oxygen mask off so we could talk more easily, and I’d keep a nervous eye on her monitor and tell her to put it back on whenever her oxygen saturation dropped below 90%. It never took very long at all.

Something I’ll always remember: One day, Lizzie’s nurse took me aside as I was coming out of Lizzie’s room. “I thought you should know,” she said. “A few weeks ago, Lizzie was talking about stopping treatment and going home. Giving up. She was depressed, and she had lost hope. But since you started coming by, I haven’t heard her talk like that again.” I just about started crying. The nurse hugged me. “I just thought that you should know,” she said.

I sometimes got in trouble with my team for spending time with Lizzie instead of sitting bored, waiting for them to give me something to do. I sometimes lost some sleep, making sure I stuck my head in to say hi before I went home for the day.

We had a lot of fun. We had a lot of laughs. We swapped embarrassing family nicknames. One day, she made me promise to come back to her room after work so I could hang out with her while her parents were around. The four of us had a grand time. It’s one of my favorite memories of medical school. Besides the general enjoying-of-each-other’s-company thing, I also learned more about what it’s like for a family with a member who has a chronic disease than I ever learned at any other time during my medical education. The Hudsons were such wonderful people! What a dear, loving family!

And then Lizzie got better enough to go home, and she went home. And tracked me down on Facebook. And, like a good medical student/larval doctor, I made sure to consider the ethical implications before I accepted her “friend invite”. For about three seconds. I swear, three whole seconds! Aren’t you proud of me?

We stayed in sporadic contact as I worked my way through my last year of medical school, trying to get recommendations, interviews, a residency. She was in and out of the hospital, more and more often. It became clear that she needed a lung transplant, but that she couldn’t get one unless she increased her weight, which was next to impossible for her due to her condition. (Cystic Fibrosis is a nasty, unfair disease.)

And then we lost contact for a bit, because I was busy and she was dying.

I got a Facebook message from her one day, out of the blue, and I was excited because she had dropped out of my world for a while. And then my stomach twisted. Because the message was from Krissy, her mother. (Name changed to protect family’s privacy.) Lizzie had passed away, having never gotten strong enough for a lung transplant. Krissy invited me to her funeral. I don’t think she expected me to come, to be honest. But I did. As I filed in with her MASSIVE amounts of family and friends, Paul (her father, name changed of course) grabbed my hand. “Come talk to us after the service,” he said. I promised I would, and sat down to learn about the short life of my favorite patient. As expected, she was an unrelenting joy. I laughed with everyone else at the slideshow of her family pictures.

I learned that Lizzie had died drowning. The lung infections that had plagued her for her entire life had overcome everything her doctors could think of to try. Her respiratory status declined progressively, to the point where she could no longer breathe on her own.

Her last words pretty much define her as I remember her. Between gasps for air, right before she was intubated for the last time: “I can do this, Jesus. I can do this, but I’m going to need some help. Please, Jesus. I can do this.”

I still can’t understand why G-d saves the most devastating diseases for the best exemplars of humanity. I will never understand this. I’m not even going to try.

Her pastor told us not to mourn, because Lizzie was now walking with Jesus, who she had loved so dearly and had so dearly wanted to meet. And she was holding his hand with both of hers. And chattering his ever-loving ear off.

I am not a Christian. But this image of Lizzie is nevertheless the one I carry with me, and it gives me comfort. Because it reminds me of exactly who she was. And if there is any justice in this universe, it is a true image, because that would be what Lizzie would have wanted for herself.

I have never had the courage to remove Lizzie from my Facebook page. And as bittersweet as it is, I do like seeing her picture popping up on my news feed every once in a while, as Facebook obliviously advises me to say hello to her. I wish I could, Facebook. You have no idea how much I wish I could.

After the funeral, Krissy and Paul asked me if I had any idea how important I was to Lizzie during her last years. They thanked me for coming to the funeral, and thanked me for deciding to cross the line that separates “doctor” from “friend”. We’re still in (very) sporadic contact.

There is no way for me to know how important I was to her. But I can guess, extrapolating from how important she was…is…to me.

I miss you, Li-bi-by-bie. I’m so glad you were a part of my education, and a part of my life.

Happy birthday.

PS: I know it’s a delight to not have to worry about breathing anymore, but seriously, girl, stop and take a breath. If only to let poor Jesus get a word in edgewise.

Help me remember Lizzie today on her birthday by learning a bit about Cystic Fibrosis, and sending good vibes to the families it destroys. If the mood takes you, there’s even a place to support the search for a cure through the Cystic Fibrosis Foundation.

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Published in: on September 6, 2011 at 5:55 am  Comments (11)  

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11 CommentsLeave a comment

  1. This is beautiful. Thank you for sharing.

  2. Thank you.

    Elodea

  3. Except for the birthday discrepancy, Lizzie could have been my niece Leslie. Les passed away from CF 22 years ago…and yesterday. She taught me more about life and death and dignity than anyone else I’ve ever known. I’ve lost two nieces to that awful disease, and have two nephews battling it. Thank you for telling us about Lizzie.

  4. My friend’s toddler has CF. I considered sharing this post with her but if I’m sitting here crying what will it do to her? 😦

    • ❤ Cass ❤

      It's ok.

      RIP Lizzie. Breath easy.

  5. I didn’t want to post because I don’t have anything to say other than ‘I’m crying now,’ but it was a beautiful post so I wanted to say something and send good vibes someone’s way.

  6. Yeah, I’m crying now too. Thank you for sharing this story. I’m sorry for the loss of your friend. 😦

  7. What a great post. I’m a 3rd yr med student on an in-patient oncology service as part of my internal medicine rotation. I’ve started to experience the difficult situations of death and coping with these type of situations. So this post really hit close to home for me. Thank you for your post.

    • I’m glad you liked it, Mike!

      Best of luck with the whole being-a-larval-doctor thing, and hang in there! It’s hard…but I still think it’s worth it.

      Thanks for reading, and thanks for writing!

      Dr. G

  8. Thank you for this post. I appreciate it very much. Tears here.

  9. Beautiful. Kind of reminds me of a Grey’s episode, and I hope you won’t take offense to that. CF is less common in South Africa, although I had two CF kiddies onmy paeds rotation. Enjoyed discovering your blog.


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