Tuesday, January 20, 2015

Show Your Scars Tour

I spent less than 48 hours in Vegas.
I didn't have a sip of alcohol.
I didn't drop a penny in a slot
Sleep was scarce.
Food was not.

Maybe out of desperation, I made the last-minute decision to head to Las Vegas for the annual Show Your Scars Tour(a weekend long event bringing together transplant friends, caregivers, donors and supporters of organ transplant). I needed to feel "not alone." I scrambled, reached out for help, hijacked my cousin's car and house, and went for it. I was going to Vegas; I was ALL IN.

I arrived late and joined the rest of the "Transplant Team" in the afternoon. I had trouble finding the group and after a failed attempt at one location and frustrating lack of confirmed details, I scoped out the second possible location, anxiously crashing the party as the remaining few finished lunch. I didn't know what to expect, and kept reminding myself that I was a big girl and would enjoy the weekend no matter what.  My ill-timed arrival and I were welcomed with smiles immediately.

Around the table, Cassie, Phil, Shelley, Mike and Mimi chatted me up, warm and inviting. I felt at ease. We didn't discuss a lot of transplant details, just some minor stuff to identify each other. Then we met more scarred friends for outside fun on the biggest ferris wheel ever - I think each pod held up to 30 people.

We spent 30 minutes circling the blue Vegas sky, taking pictures, getting to know each other and sharing hugs. Instant bonding. A pod full of giggling girls and a couple of boys who laughed along with us. I think more group selfies were taken than skyline shots.

Dinner a couple of hours later...even more warm, open and gracious folks. We smiled and laughed. I listened to some transplant histories. I shared some of mine. No one, not even Shelley, whose graft has failed and she's back on the waiting list, told a sad story. Every person at our tables was present and happy to be.

Aimee got emotional giving a toast. Mike teased Jake about his never-ending Facebook posts. Janet hugged new arrivals with genuine warmth. Darlene shed happy tears. Cassie shook her head, remembering how far Phil had come. Late-comers got a "Norm-from-Cheers" greeting. Paul subtlety got in one-liners you'd miss if you weren't paying attention. Lisa rolled her eyes playfully when her fake Happy Birthday dessert arrived. Mimi couldn't keep her contagious smile in check. I showed off my Scars-Are-Sexy shoes. Everybody posted pics on Facebook.

The rest of the evening and the next morning...the same. Smiles, Laughter. Appreciation. Repeat.

Too quickly, it was time for good-bye. A looong good-bye, an emotional good-bye. We hovered in the Peppermill parking lot for over an hour. I was in tears, and I wasn't alone.

I spent the flight back split between trying to catch up on sleep and trying to figure out why the Show Your Scars Tour was so meaningful to me. I've never been surrounded by a group of people affected deeply by something so many take for granted and no one was sad or regretful or angry or bitter. No one felt cheated. We ate and we joked and we laughed and we ate some more.


Looking back at the pics from the weekend, I'm still smiling, admiring each of us in our green Show-Your-Scar t-shirts. I'm so grateful for this time, to sit among people I admire and who don't need me to lead and be a shining example for the chronically ill.  I'm proud to look reflectively and introspectively at their faces, knowing we share an unspoken appreciation that eludes so many. We are people familiar with loss and strength and understand the power of living in the moment. 

Thank you for this moment, new and forever friends!

3 comments:

  1. It is awesome to hear you had a good time with some great people! It is also good to hear you are up and about. Reading your January 2014 post and this one now, it seems you turned a major corner. Enjoy!

    - Corwin

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  2. Hey Corwin! Thank you ! Wishing you nothing but good health, happiness and good h&h's!

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  3. Hi Michelle! I wanted to say thank you for allowing me to follow your journey. I have been on the KP transplant wait list for 16 months and enjoyed reading the pros and cons of your experiences. As usual, I have all kinds of questions/concerns surrounding the transplant and what to expect before and after. Currently, I am riding along that emotional rollercoaster that everyone gets to enjoy with each time the phone rings, I gasp hoping it is the transplant office and wanting them to tell me I am the primary candidate for a potential transplant. It helps me to know there are other people out there that are going through similar situations as me. :) Thank you again for allowing me to read about your journey!

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