My daughter, Haylee Kate, was diagnosed with APML Leukemia, which is a rare form, on November 21, 2011 at 8 years old. I thought this would be a good way for me to get my thoughts and feelings out and to let others know about her ups and downs throughout her treatment.

March 14, 2012

3/14/12 - Local news interview

Haylee went down to clinic with Nonna today and went well.  According to Haylee, it's Child Life month at the hospital (and maybe everywhere?).  That explains the CNN interview.  My mom called me today because Lindsay said Beth Galvin from Fox 5 in Atlanta was at the hospital and may want to interview Haylee about the Child Life Specialists.  Turns out she DID interview her and she will be on the news sometime this week!  I'm supposed to get a phone call from Fox 5 letting me know when the story will air and as soon as I know, I'll post the information about it in case anyone wants to check it out.  I'm not sure if it will be online or not for those of you far away.  I'll look into it!  The CNN interview with Brittany is scheduled for next Wednesday during clinic.  I'll miss that interview, too but I've got to work when I can.  I'm thankful for my mom for giving me the opportunity to work a few days a week and for helping me out like she does and has been during our daily clinic appointments :)
I had the meeting with Haylee's school about the 504 plan.  Basically, it makes accomodations for her for test taking (like CRCTs) and for other reasons that may come up.  During CRCT week (if she's there) she will have the opportunity to be in a small group, have extended time to take the test, and frequent breaks if needed.  It was a good meeting but I wanted to be more prepared about knowing if she would be able to attend that week.  They are very supportive of Haylee and I couldn't ask for her to be in a better school than Auburn.  From the administrators to the front office staff to her teacher and former teachers....they are wonderful all around!!

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