My Turn on the Table
I worked for a pain management doctor before I was told I couldn’t work anymore. We did procedures. Laid the patient face down on the table and poked and prodded, usually, along the spine. Often the needles were large. Over a half of a year, I saw people react very differently to these “procedures.” Some winced. Some screamed. Some cried. Some didn’t. I would be lying if I said the reaction of a patient didn’t lead me to some assumptions of their overall character.
This week I had my own “procedure,” a bone marrow biopsy and aspiration. The biopsy cuts away a piece of bone, the aspiration sucks up some of the liquid marrow. This is the second time in the past eight months I’ve undergone one of these. The first time was not even 24 hours after my initial emergency room visit. There wasn’t much time to really think about it. I remember it was painful but I couldn’t tell you about the pain. Nor could I recount specific emotions before, after or during. It has blurred into the pile of blurs that come along with any overwhelming experience.

This time I got to prepare for it. My disorder is no longer a surprise and neither are the tests needed. They gave me a packet weeks ago, telling me precisely what had to be done. Monday, March 1st, was to be a bone marrow biopsy and aspiration day. Monday came and I sat in the waiting area and waited for my name to be called out.
And it happened. “Sheehan,” a woman yelled.
She introduced herself and walked me back to the procedure room. There she instructed me how to lay for the procedure, then prepped me and told me we had to wait until her associate arrived.
My mind wandered back to my old job. Walking patients back, telling them what to expect while my mind ran through a checklist. The whole spiel was on autopilot. While prepping them, I never shook with nervous anticipation, but now lying here my leg wouldn’t stop. I was asking the nurse the same questions patients used to ask me. And there she was reassuring me with the same lines and the tone she will use to reassure everyone after me. With the first poke she steadied my leg with the same clinical touch she has and will use on all those before and after. I wonder what assumptions a shaky leg leads to.

It took maybe 15 minutes in all. They warned me of the sensation about to come, told me to breath at those more painful moments. Prattled off “just one more..” or “almost done..” And then they pulled out the one inch sample of bone. Something like a cork coming out of a wine bottle. The assistant steadied my leg and said “all done, you did well.”
That was my line too.
Those times I rolled my eyes and thought this patient is acting absurd are regrettable. Not because the patients weren’t absurd, many may have been the attention craving, drama queens assumed. The inclination to arrive at a conclusion regardless of the sample size is what’s really regrettable. If you think long enough there are a multitude of instance we do this everyday, at least I do. Too often I find myself failing to take into account that what’s routine and ordinary and run-of-the-mill for me, could be new or nerve racking or even terrifying for another person. But there are those infrequent times when the twists and turns of life presents an opportunity where you can, to paraphrase Atticus Finch,” climb in and crawl around in someone else’s skin.” Even if it’s just for a moment.
Mine was easy and obvious. Some of us are lucky. When those moments do happen, absorb them. You never know when it’s going to be your turn on the table.





March 6th, 2010 at 7:49 pm
Hi Matt,
My name is Denise and I am a book club buddy of your mom. A woman I greatly respect and admire and am so glad to know. As I read about your journey I have the utmost respect and admiration for you as well. The courage and positivity you express is a reflection of the strength of character you must possess. I will continue to log on and will be sending positive thoughts your way as you successfully go through each procedure.
many prayers and positive energy being sent to you and your family,
Denise
March 7th, 2010 at 4:22 am
I can only imagine what you had to go through. My son has had five bone marrow bio. Since he was diagnosed with aplastic anemia at the age of three. The first two he was lightly sedated. The last three he was completely sedated. I pray for you often. Hang in there, you are very brave. Cdchilds
March 7th, 2010 at 4:52 pm
Geez Matt, Brutal . “There is a lot of ugly things in the world son” Think that is Atticus??? Your thought of daily . Myself and family all have red and white Bravery bracelets on. Brave you are !
March 7th, 2010 at 11:39 pm
Ouch! oh, boy, that’s gonna leave a mark! And leave a mark it has, but not just of the physical, empirical, measurable type. It and all of its other antecedent experiences since your diagnosis have left indelible marks on your spirit…leading you to a more compassionate, deeply insightful and more thought-filled world/World view. I get a sense of the depth of these ‘marks’ when I speak with you and read your webpage. You have much courage. You are ever in my thoughts and prayers. X0 Aunt Michele
March 8th, 2010 at 4:11 pm
Hi-
I read your blog and wondered if you might help us spread the word about a series of blood drives being held by Remington College, the Sickle Cell Disease Association of America and America’s Blood Centers. The focus is on recruiting more minority blood donors.
Please help us get the word out if you can.
For more information, please see the release below or go to http://www.3lives.com/
Frank Wolff
Wellons Communications
407-339-0879 office
407-637-6000 cell
frank@wellonscommunications.com
March 10th, 2010 at 10:38 am
“I wonder what assumptions a shaky leg leads to.”
Yes.
“Too often I find myself failing to take into account that what’s routine and ordinary and run-of-the-mill for me, could be new or nerve racking or even terrifying for another person.
Important.
Thank you.
-cgw
March 14th, 2010 at 6:30 pm
Matt, it helps me to recognize my role more clearly in this world of nursing and my patients, when I see it through your perspective. Some times I get tired and less compassionate then I should be—I will try harder and better. jan