Tuesday, September 15, 2009

A little better every day


I can not believe how nice it is to be on this side of the transplant. Each day I am getting more strength and feeling better. (Remember the Beatle song on the Rubber Soul LP, "I have to admit, it's getting better, a little better every day .....). Well every day things are getting better!
Friday September 11, is my second birthday ; the day I got my new heart. Can not tell you much after they put me under the anesthetic. I remember someone said, "The heart will be here in 90 minutes." I remember nothing more that day.
Saturday September 12, I woke up in ICU. Still on all kinds of tubes for breathing and draining stuck in my body. I do not feel any pain from the large incision, which is weird. I can sleep again with out the use of a CPAP because the fluid behind my lungs is now gone (no more feeling like I am suffocating). I am starting to talk to family on the cell phone. I am interested in the score of the UW Huskie = U of Idaho Game.
Sunday, September 13 Tried to stand and felt like I was going to fall down. Legs are so weak it was a concern. Walked around 50 feet and was exhausted. Can not believe how weak I am. The Docs want me to eat more protein to build myself back up and help the healing process. This is still hard as I have nausea every day.
Thursday September 17. The Docs feel I could be ready to leave the hospital on Tuesday, which is 11 days after my transplant. My legs are still very weak but I am able to stand up now without help. I am down to 160 lbs. in weight. I hope this is the bottom. Eating more protein and exercise is what I need now.
The next few days Rosaline and I will get training on all of my medications and the issues with immunosuspression. After I am released from the hospital, we will be living in a small transplant housing apartment for at least a month near Seattle Pacific University. This allows us the frequent visits required to see the Doctors so they can monitor my new heart. It is a nice part of Seattle on the north base of Queen Ann Hill. Every day it is getting better.

5 comments:

  1. Rick
    You are THE MAN
    Take your time and get healthy
    Hope to see you soon

    Bob Fetterley

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  2. http://www.youtube.com/watch?v=RGpAFpW2THw

    SING ALONG EVERYONE! :P

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  3. Rick - Keely and Andrew Murdoch and I are enjoying some time together this weekend in Cashmere. I will be at the Wenatchee Salmon Festival this weekend. We are all elated with your progress. Keely & I look forward to you re-joining the committees! You know the fun never ends there! Of course a strong heart and immune system is a pre-requisite for the committee! Keep up the good work! :-)
    I spent lots of time today working to open a steelhead fishery around these parts... that should make some folks happy in the Valley!

    Thanks for the updates too!

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  4. Oh so good to be on this side of the transplant. I can't stop smiling when I think of the Tin Man of Wenatchee and his new heart. Heal away, Rick....Linda Bennion

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  5. This modern day miracle has me totally amazed!! Keep up the great progress Rick! We are all pulling for you!! Hope to see you soon!

    Cathi

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