Monday, June 11, 2012

About dang time




Freedom:  The condition of being free of restraints--- American Heritage Dictionary

            I know, a little behind with an update, but cut me a break—I have been enjoying watching round 6 in the rearview mirror.  So let’s play catch up, shall we?  Round 6 was Monday, May 21 and the following weekend—my usual let me visit the 10th floor weekend, was looming.   Oddly enough, the odds were stocked in my favor.  For the first time, Dr K was on call and I just KNEW I was not going to be able to take advantage.  Not to mention Billy was down and he said he would cross to the other side of the ER and take me if needed.  There was a part of me which really wanted to go because of those 2, but then again, the part of me which just totally HATES fluids was praying otherwise.  Starting Sunday afternoon, I became attached to my 3 thermometers ( yes 3—I lost 2, bought one , found one as soon as I opened the new one and 10 minutes later found the last one) but I made it through.  Monday dawned and I admit to taking my temp at least 20 times.   And yes, my temp did made it to the “I have to call” point (by .1), but since Billy was long gone and Mom would be the one driving, I took 2 Advil and went to bed.

      When I woke up on Tuesday, I was ready… I had made it through the tough days and Pedro was coming out—I was sick and tired of him.  Plus he hurt and I was afraid he was infected.  I called Susan and I was on my way.  I was so excited!  I get there and before I see Becca, they take my temp.  Dang thing was 99.2.  However, Becca orders a few things and all I hear is “after all of this, take the pic line out”, Yay!  Then Dr K walked by—I waved and smiled—he smiled, kept walking then did a double take and shook his head.   He turned around and I knew he was about to suck the joy out of me and I was not disappointed.  Becca finds me and the words “he doesn’t want the pic line out just yet” come from her. Ughhhhhhhhhhhhhhhhh….figures.  As I am trying to come with grips of the unexpected—something I have become familiar with the past few months--the two of them are poking their heads in the chemo waiting room.  Not my fault the “now what” came out – which of course made the others in the room laughed --they knew…it’s a cancer thing!  After Dr K questions me and yes,  I made sure to point out  this is normally  the day I am sent home from the 10th floor as my count is back up—something he is well aware of ….he says IF my white blood count is okay—then he will okay Pedro’s release but not before.  What could I do?  I tried to give a really sad look as I headed back to the blood draw room but didn’t work.  At least this time I got to wait near Susan—which worked out great as I knew the Yay the counts are good was meant for me! And we were on our way BACK to the chemo waiting room to GET PEDRO OUT!!!!!!!! 

            Let me tell you about the chemo room.  Obviously everyone is there for the same reason. Different cancers, so many different variations on the chemo, but there is a bond knowing we are all getting filled with the poison that will hopefully kill the cancer and prolong our lives.  The chemo nurses are amazing.  They are kind, caring and keep track of everyone which is not easy as there are so many chairs and usually all are filled.  They have a gift and it shows.   They become part of your life for as long as the chemo continues and from a patient’s point of view, it is so very important to have people who truly care and are gentle to boot.  I was hoping Brittany would be there, as she gave me my first chemo as well as 3 others.  But it was her day off and I got Crystal— my second choice.  She tells me what she will be doing and it will not hurt—but to remember I have to hold my breath and basically push just as she is taking out the last of Pedro.  Very strange… but it is to avoid an air bubble at the end—or so she says.  I still think she did it just to get me. Finally Pedro is out and in the trash.  Crystal looks at me, gives me a hug and says “bring on the radiation!” and shoves me out the door as we both started to tear up.

    I have enjoyed these past few weeks before starting on the radiation.  My arm is again my own, I am able to eat fresh, raw fruits and I just feel better.  Yes, I forgot last week was fatigue week as in my mind I was done with chemo, but I dealt with it.  I am looking forward to settling into my radiation routine and then my new normal—which does include my trusty day planner!

Jeremiah 29:11





           


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