March 23, 2012

Fork in the Road


Today was the end of the first leg of my journey towards transplant, and we can see the upcoming fork in the road.  Monday, we head back to MD Anderson for a bone marrow biopsy and meeting with Dr. O’Brien and the CLL team.  Wednesday, we’ll get the results of the biopsy and meet with Dr. Shah and the transplant team.  At that point, the decision will be made whether to continue on the Campath road for another round or to take the path directly to transplant.  It all depends on the level of disease left in my marrow.  Having been near 80% diseased marrow, Paul’s bet is on another round of Campath.  I’m ready to move on.  But this part is not our decision.

The past week or so could be classified as “side effect of the day.”  Some days I would have a rash.  Others I would have some light nausea.  Many brought increased fatigue, intestinal distress, or a return of the headaches.  Some weren’t bad at all.  And none have been as bad as the first week!  So for that I am immensely thankful.

I have taken time to read.  (I’m on my third book in four weeks.)  I have talked and Skyped with my kids and grandkids.  I have spent quiet times with my sweetheart.  I had a wonderful visit from a dear friend.  (Love you, Cheryl!)  I have enjoyed several mornings with my cousins, Al & Bonnie, who live around the corner from where I get my shots.  And I even felt well enough last night for my mom and Maxine, her neighbor and buddy, to come over for dinner and a game of cards.  I was pretty pooped out by the end of the evening, but it was a nice tired.

I have come to care deeply for the team at the good doctor’s office.  They are not only efficient but also very compassionate and caring.  It was a little sad leaving today not knowing if I’d be back anytime soon.  I’m sure that the same level of connection will happen with my transplant team on MD Anderson’s 11th floor.  Prayerfully, a year from now, these will be memories of a time when….  Memories that I will never forget.  Memories that will mold my future.


2 comments:

  1. Tamara,

    I am sorry I have to use "comment" to contact you, I couldn't find an email address. (but then again, I'm getting tired!)

    I am a cancer survivor, diagnosed in April 2008 with non-hodgkin lymphoma. In February 2009 I was declared cancer free and remain so to this day.

    I noticed you linked my blog on your side bar. Thank you very much!

    I am collecting Christian cancer blogs to have my readers link to. I would like your permission to link your blog, I do not have one for CLL and your blog is personal and you are in the midst of your journey.

    The purpose for The Voice is to offer an informative blog of articles and resource links from the Christian community.

    I had an auto stem cell transplant, so I know what you are going through in your mental preparation phase. I haven't read yet whether you are having an allo or auto. I have a great link on my side bar of a video for both, I wish a video to watch when I went in for mine! You can ask me questions if you'd like,too.

    God bless and now I'll start to read archived articles of yours!

    Cyndi Heath
    Lakeside, MT

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    Replies
    1. Cyndi,

      Thank you! I would be honored for you to link my blog. Paul Pavao directed me to yours. I am preparing for an allogenic SCT. I have a perfect 14 of 14 Male/47 match from Europe. PTL! We have studied extensively but I will definitely watch the video. I'm not sure anything can totally prepare us for what is to come. Everyone seems to have their own very unique journey. Blessings to you on the success of your transplant and being cancer free! I am looking forward to the day that I can say the same. Until then, we hang on to each other and to our Lord.

      Thanks again!

      Tamara

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