Clinic Day #14

September 24, 2009 I’ve yawned and rubbed my eyes through this entire day and just finished spray n’washing a mound of laundry, so I’m going to make this update brief and go to bed.

John took Tanner to Clinic today while I stayed home and tried to get done some of the things I keep not getting to recently. She just went in to have blood drawn for Counts and we were concerned she would have to get a blood transfusion if her Hemoglobin levels had dropped any more than the previous week. They had dropped some (down to 8 from 8.5). Somewhere around 13 is normal and below 8, they will consider transfusing, but the doctor thought that since Tanner wasn’t really experiencing many symptoms (i.e. her energy level is at it’s normal uncanny level) and she was not receiving any chemo this week, she did not need one. Again, we’ll watch her to see if anything changes, but they anticipate that level to be rising.

Her neutraphil level, which is the other level they watch carefully and is indicative of her infection fighting ability, was still great, although it had dropped 1500 points to 2000 from 3500 last week. Although the normal person would have between 5-10,000, 2000 is still excellent for a kid on chemo and they were pleased.

So, barring any unforeseen drops in levels, Tanner will begin the dreaded Delayed Intensification phase of treatment next Thursday by beginning steroids, receiving an IV dose of Vincristine and getting a lumbar puncture with Methotrexate. Nothing like starting with a bang.

Thursday is also the day of the Leukemia and Lymphoma Society’s Light the Night walk to raise money to find a cure for blood cancers. Team Tanner has raised $4,925 so far, just $75 short of our $5,000 goal. But, we don’t want to stop at our goal, we want Tanner’s team to be #1. (We were #2 at the point when they gave away the Taylor Swift tickets.) Sooooo, if you haven’t donated yet, but feel moved to do so, you have 6 more days to do it. Just go to and click on donate. Tanner is planning on holing a lemonade stand in the next week so she can donate to her team as well and… as long as her counts hold up and she holds up after a day of surgery and chemo… she will be allowed to walk with us and carry the white balloon!!! All of us who are walking will carry a red balloon in support of her. At first, she didn’t want to do this walk because she was embarrassed for people to know she has cancer, but now she is excited and hopes to be able to do it. She’s really started to accept that she has cancer and to believe that people still love and support her.

Brief post… I am just not capable apparently.

Good night,

2 thoughts on “Clinic Day #14

Leave a Reply

Your email address will not be published. Required fields are marked *