You can say that again. It has been playing like the movie in my mind, with the cowardly lion staring at Dorothy in the Wizard of Oz.
I have had an eventful weekend amongst my heroes, my heart is heavy. My tongue is tied. I’ll try to share why. I saw so many. Perhaps I should call them butterflies. People bursting out of their cocoons. Families who had lost, people in the midst of their fight and those that had won. They all came out to stand up to cancer. They were smiling, they were positive, they believed and they made a difference. They hugged me and pulled at my heart. As I pulled on theirs. They reminded me of the battles I had lost, the ones that I am still fighting and the ones I had won. They said “Mo keep fighting the war”. Their eyes, tears and minds echo inside of me as I sit and write to you. They wanted our team to succeed. I am touched and humbled by my weekend experience.
I have stared into the eyes of my patients, wondering what it would be like to be in their shoes. I always say to them “I put myself in your shoes”. I’m really wondering now, would I trade places? Would anyone? Here they are faced with an illness that could end their life and they say, “I want to fight”. I see the cowardly lion trembling uncontrollably, yet displaying the power to stand up to the Wicked Witch.
I have used many analogies to help my patients see cancer as I do. A good friend of mine on Sunday reminded me and said “Mo you just know how to explain things to people- thanks for coming out”. I was looking at the golf course, the trees and the eager faces of people who took time out of their day to care. “I think I have an empty brain that facilitates things”, I said back. I use simple things to show a point. Thanks for making that point meaningful to me. I stood before you and you all had the courage to ask me questions. I hoped I showed you that no question is “silly” and every question is the researcher in you showing its innate curiosity.
What have they got that I ain’t got? It is a loud echo.
Courage Ride, Saturday, August 24, 2013, Kalona, Iowa.
For more photos from the Courage Ride, please visit the Sarcoma Iowa Facebook page.
The Steve Yates Melanoma Awareness Golf Tournament, Sunday, August 25, 2013, Waterloo, Iowa.
For more photos, visit our Melanoma Iowa Facebook page.
5 thoughts on “What have they got that I ain’t got?”
Dr. Mo — My wife, Jane, and I are good friends of XXXXXX. You know what a wonderful person she is, so I won’t offer any exultations, but recently, first on NPR and then PBS were segments of science programs exploring the potential of nanotechnology in delivering chemotherapy drugs directly to tumor cells. This, combined with genomic technology appears, from what was shared, to offer some real help in the not too distant future. As I recall, human clinical studies are anticipated to begin in a year or so. What does this offer XXXXXX so far as her sarcoma is concerned? I just have the feeling there will be some positive answers by the end of this decade. But, you’re the specialist. What do you think. Always hopeful, I remain, Jon B. Oakleaf, Moline, IL
As you are well aware I look forward to these blogs every Wednesday.. I think it takes great courage for you as a doctor to really write about how you feel as a doctor when looking at it that way..I know as a patient I feel a lot more connected with my situation..and with my doctor.. I know it’s been only since march since John and I have met you but I do appreciate how honest and real that you are with us.. Keep up the good work Mo and I have always believed god has a plan for all of us and yours is your calling.. Also you should write a book. I know I would buy it…
I will see you Friday..
Again I really thank you for your support and kind words. I stand as always with my patients in their fight.
I am sorry I had to miss this, but I’m so happy it was a success. You have the courage to go above and beyond when many others wouldn’t.
I think you challenge me to do what others may not, you are also pushing the limits of navigating treatment for people. I am happy to be that button you push.