Sunday, May 17, 2020

Happy Lungiversary to me!


It’s officially been 1 year since my successful double lung transplant! Happy lungiversary to me!!

The last few months have been emotionally intense. Obviously the whole world is in crisis right now, and everyone is struggling and suffering in various ways. I have the added bonus of being in a high risk category and getting to worry about yet another threat on the long list of things that could kill me. But in addition to that, I’ve spent a lot of time remembering what life was like last year during the months leading up to transplant. Thankfully my memories of what it was like to be slowly suffocating to death are faded, and most of that whole time period is a bit of a blur. But I do still remember that it was horrible to the point that I wished for death just so the suffering would end. During these last few months I kept thinking about where I was a year earlier, and being a little traumatized by the memories. It’s been worse during the last couple weeks, which is when I struggled the most and went into respiratory failure last year. Getting a taste of a slow and painful death takes more than a year to get over.

But on May 12th the memories were different. I remembered getting the news, and calling Katherine and my mom to tell them. I remembered waiting to be brought down to surgery, and then going down to pre-op. My memories of that day are also hazy, but at some point in the ICU afterwards I asked how long the surgery took, and wrote down all the times. 2:19 PM – into the OR. 4 PM – anesthesia. 6 PM – first cut. 12:17 AM – out of the OR. And 6:15 PM on May 13th, less than 24 hours after surgery – taken off the ventilator and extubated.

I didn’t have any sort of major celebration right after the transplant for multiple reasons. The immediate aftermath of a lung transplant is a crazy whirlwind of pulmonary rehab and testing and doctor’s appointments. It’s exhausting and stressful and painful, and putting together a party was not on my priority list. Due to heavy immunosuppression I also couldn’t be in crowded spaces, which makes it a little difficult to host anything. But most importantly, I was well aware that the first year after transplant is a critical and tenuous time, and I didn’t feel comfortable celebrating until I saw how things went.

As we got closer to the year mark with relatively smooth sailing, I started considering whether I should have a party on the actual lungiversary, or wait a month or 2 for my immunosuppression to be lowered so I could be around more people. Never did I imagine that all in-person gatherings would be cancelled anyway by a global pandemic! Initially I was too upset to plan any sort of celebration. Having life basically be cancelled and being cooped up in my apartment week after week with no end in sight didn’t exactly have me in a festive frame of mind. But as the date came closer, I started to wonder… Maybe we could do a drive-by celebration, as has become popular these days? Maybe a Zoom party? Maybe both?? So I flung it out to Facebook, and the enthusiastic response convinced me to go for it. And I’m so glad I did!! It was so wonderful to see everyone who turned out, both in-person (at a social distance of course!) and online. The car parade in particular was wonderful fun and really got me into a celebratory frame of mind! I got balloons and streamers, and printed posters for my balcony, and baked my specialty lung-shaped cookies for the occasion. Seeing everyone drive by cheering and honking, waving posters, streamers and balloons blowing in the wind, was absolutely amazing! And then I ended up on the news to boot! What an amazing way to celebrate the incredible gift of life!!

At the same time, I’m also keenly aware that while we’re celebrating, somewhere out there another family is mourning. Somewhere out there another family is coping with death instead of celebrating life, and remembering the tragic loss of their loved one. This is the duality of transplant: my life could only be saved if someone else died. I am so endlessly grateful to my donor and their family, and I will never forget their pain and loss. I will always wish there had been some other way.

One year. It’s amazing how much can change in just one year! I’m still recovering, and COVID-19 has thrown unexpected complications into that process. And of course life after lung transplant is never guaranteed, and I will always live with a certain amount of fear and caution and what-ifs hanging over my head. But, against all odds, somehow at 41 years old I’m still here, still laughing, loving, and celebrating. And hopefully I’ll have the opportunity to celebrate many more lungiversaries for many years to come!











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