DAVE'S JOURNEY

Diagnosed in Nov. 2006 with lymphoma, stem cell transplant 2007, continued treatment and then diagnosed in 2010 with AML (leukemia) as a result of prior treatments. This is his story.........



Tuesday, June 5, 2007

Right on Track

Things are progressing fast and today was a whirlwind of appointments. After having lab draw at 9:30, the next stop was to the clinic nurse for administration of 3 Neupogen (growth factor) injections. We then met with the nutritionist where we got an A+!!! Nothing like being graded on what I fix for Dave's dinner! I then went to a class on food preparation and safety while Dave went to the hotel for a break and to spend a little time with Ripley. He met up with me at 1:00 for a "Managing Care at Home" class, which was 2 hrs. of mind-boggling information. It's a good thing they gave handouts, or we would really be in rough shape! Then onto Dave's last appointment of the day, which was a pulmonary function test, he did well with that also. I did have a surprise waiting for Dave when he was through, as I managed to get him a free ticket to the Mariner's game tonight from the cancer center. Wow - was he ever happy about that! The SCCA occasionally gets free "suite" tickets so that immunosuppressed patients may attend a Mariner's game and not be in the huge crowd. Dave was able to go with a wonderful couple we met who are from Spokane. I elected to stay home with Ripley as he had been alone for most of the day. That's where Dave is right now and I know he is enjoying every minute of it. It's nice to have a little normalcy. Tomorrow is a HUGE DAY and a step in the right direction - they will start to harvest his stem cells. This procedure is called apheresis and takes approximately 3 hours. It may take several days of apheresis to collect enough stem cells (5 million) for the transplant. He will continue daily blood draws and growth factor shots during this phase.

1 comment:

  1. Dave & Jenn,
    The SCCA must be a remarkable
    medical facility.We have no doubt that you are getting the best possible care anywhere. It sounds like things are moving faster than we thought.That's wonderful.A Mariners game...huh. I bet that was a great break for you,and a well deserved
    one for you to Jenn.Good luck with the stem cell harvesting.You'll do great.
    Let us know what your address is unless you plan to find a different place.
    Jenn, thanks for putting together this blog.It makes
    it easy to keep up with Dave's.
    treatment and to stay in touch with you guys while your there.
    Love you guys Robin,Karen & Family

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