I’m Alive

Three weeks ago I woke up from open-heart surgery. The very first thing that I remember is the realization that I was alive.

I’ve had too little stamina to take on writing about this moment and the period afterward. Putting what I felt, and feel, into words has also escaped me. But I think I’m ready to give it a crack.

This last year has been a strange one. Coming to grips with my fragile heart and poor mortality prospects meant that I needed to get comfortable with the idea of dying. Not to expect it, but to reconcile with it. I think I’ve worked it out.

The morning of surgery, however, was a bit different. As most of the hair was being shaved from my body and various lines installed in my arms, I thought a lot about the trauma that was to come. I wasn’t worried about the aftermath. I wanted to really, really be prepared that I might not survive the surgery, and yet expect to make it out just fine.

That’s why, when consciousness returned, I was so pleasantly surprised to be alive! Despite everything done to my body, inside of me my spirit just soared. I thought, “I have another chance! ” My kids say the first words I said were not understandable…”wh..,” “w…,” “wh dd dy doo,” which they finally deciphered as “What did they do?” There were a lot of questions before the surgery. How much of my heart was viable? Are there any places on the left ventricle to run some new blood lines? How much of the heart is dead muscle, especially at the bottom tip–enough to warrant opening the heart and radically remodeling it? More blood lines and remodeling would be my best chance for surviving for a while with this heart, staving off a heart transplant for years.

“Everything. They did everything.”

For the first time in a year (I was diagnosed with Heart Failure on January 13, told I needed a heart transplant on January 14. Half of all heart failure patients die within one year of diagnosis.), I really had hope. I will never forget that moment, nor be more grateful for the gift of life.

My surgeons were ecstatic. It seems I may have a shot at more than just a couple years to heart transplant. One doctor even told me I could be running in 5 to 6 weeks! The lines running out of my body (neck, two tubes from chest, both arms, catheter, and tube down my throat) were insignificant compared to this new found hope. As each was drawn out of my body (okay, that was weird and yucky to feel something snake its way out of the inside and out through simple holes just below my ribcage…) I felt more free and complete.

I don’t remember much on the day of surgery. Whether I sat up or stood up…I don’t know. I do remember being asked if I could stand up and walk a bit shortly after the ventilator was removed. “Get up and walk?” I thought, “Damn straight! Get me outta here!” And walk I did as much, as often, and as long as I could for next 5 days.

On every walk I recall gripping the glass heart from the Whitty family. Nurses up and down the hallways would ask me what it was and I would explain. It never left my hand while I endured the various insults to my body. It was a connection to a spiritual community that really did give me strength and inspiration.

Twice I have stood at the sanctuary of St. Clare church receiving the sacrament of Healing. At first alone and just weeks before surgery with many hands upon my shoulders. Was my heart miraculously healed?

No.

But the dearest support of so many people, together with children, my Judy and my friends, people I don’t even know at Regence who read my blog and send their prayers and good wishes…all really and truly kept the miracle of being alive fresh in my newly remodeled heart.

Jan and Claire flew up from California to stay with me for 3 days. I had only just gotten out of the hospital. These two close and wonderful people loved me so much during those first few days that I will always be in their debt. We laughed (God that hurts) and talked and ate and shopped a bit. It is what healing looks like.

Judy, whose dad passed away just weeks before, encouraged and loved and fed and guided me through recovery. No longer able to do laundry or vacuum or much of anything, she picked up all the slack and still found the energy to laugh and to hug. Jenny and Pat hardly left my side. Even with the funeral of Nora, Pat’s mom, just a few days past, they plied me with dark jokes, videoed me walking the halls, Pat blogging entries for me to keep you all up to date, coming up wth important questions I wouldn’t have thought to ask doctors, reports from the outside world…each and every moment precious beyond words and energizing me to keep going.

A visit from Fr. Tom, a bouquet of yellow flowers from the St. Clare parish staff, Kelly’s dedication of one song to me that Sophe Lux performed, Jaye and Ashley and Caitlin singing in my room and bringing me Communion, Jim Whitty’s arm as he helped me back from Communion, and meals prepared and brought to our house by confirmation students and staff, organized by Anne Marie. Sr. Anna’s delight to find Judy at mass with me! My first long walk with Bob followed by lunch and listening to a talk by Joseph Grizzone, author of Joshua. Gifts and notes from Vernique and Phillipe and the Conti’s and so many friends. Janet’s calls. My dad’s daily calls. Cards overflowing our mantle…

Healing looks like that. Many hands. Many hearts. Many prayers.

Perhaps I wouldn’t have been able to accept this kind of healing at another time in my life. I’d like to think I could, but more likely I would be giving, not receiving. But today, 22 days since opening my eyes and finding myself alive, the thrill and promise of it hasn’t left me.

From the darkness of just a few years ago, when I was too hurt and anguished to hold onto life, to this moment filled with so much hope and affection and life…well, that my friends, that is a miracle. That is a miracle. I do believe.

Thank you. You have given me life and inspiration. Judy and I have hope.

I am alive!

Published in: on January 24, 2007 at 1:21 pm Comments (9)

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  1. Yaaaay to healing and your heart functioning better. Before you know it, you’ll be running- perhaps next year’s marathon with Gary and I? I love you – jenny penny

  2. Mike,
    Just wanted you to know
    I cary my elephant with me wherever I go.

  3. Mike

    What a wonderful blog this is. So glad you are moving on and maybe even run that next marathon. Yes, what you have been thru is a miracle and we are very thankful for it.
    Keep blogging away as you feel better. Make sure to give our love to Judy, Jenny and Pat.
    Love you all
    Veronique & Philippe

  4. By mushroom time, you will be ready for a walk in the woods. You can show me how to Bass fish!

  5. Mike – Speaking from the St. Raymond contingent, thank you for everything, especially the miracle of your life. Life is soooooooooooo good !!………
    When you are able, would you send me your snail mail address please..Much love to you and Judy, sues

  6. Mike,
    I am so glad to hear you are doing so well! I can really relate to a lot of what you have to say because of my own experiences with my stem cell transplant. Isn’t the power of prayer and the support of friends and family one of God’s greatest gifts? Keep getting better!

    Love,
    Judy

  7. Big daddy…what a year indeed. The fact that you made it through last year and your surgery in one piece is a testament to your spirit and will to live. So many others in your place would have opted to just throw up their hands in disbelief and defeat. Not you. You clinched up a couple of fists and prepared for the fight of your life (literally of course).

    Your post was eloquent, transparent, and emotional. Just as they have been throughout this experience. I celebrate that you are recovering. That you are on the other side so to speak. You will run. I know this because I know you. You will not let something even as major as open heart surgery or potential transplants deter you. You are an inspiring force to me as I am sure you are to many. I consider myself blessed to be witness to the amazing support you have received from those you mention and I am lucky to call myself part of Team Ashland.

    Get better, get well, and get running.

    pat

  8. Hello Mike–

    I ran into Pat and Jenny the other day by chance–they seem so happy together. They literally exude positive energy. You’re fortunate to have them, and they you (and I know you all know that). It has been heartwarming to watch “Team Ashland” (as Pat calls it) in action. Thanks for your generosity in sharing your journey with the rest of us. I already deeply appreciate every moment I’m alive, but your description of the moment you woke up from surgery helps me realize anew just how precious each day is! I’m so glad you’re still with us.

    From my heart to yours–I wish you the best possible strengthening/healing in coming weeks.

    Peace,

    Steve Eichenberger

  9. I had a heart transplant on 2/6/07 & am rejecting the heart. I have both cellular & vascular rejection. I am currently being treated by plasma -apheresis & gamma globulin therapy. I am insured by Medicare & they are refusing to pay for the treatments. They run $1,500 to $2,500 per series. has anyone had any experience with this problem in the USA>I had a heart transplant on 2/6/07 & am rejecting the heart. I have both cellular & vascular rejection. I am currently being treated by plasma -apheresis & gamma globulin therapy. I am insured by Medicare & they are refusing to pay for the treatments. They run $1,500 to $2,500 per series. has anyone had any experience with this problem in the USA>
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