As the calendar turned to September, I began to detect almost imperceptible signs that something was not quite right with Hannah. I can't even explain what I was seeing ... I really don't even know what it was specifically.  But I remember crying to Brad one night (actually several nights) that I felt like she was leaving us, bit by tiny bit. Then, as September neared its end, Hannah began to experience waves of nausea.  She had experienced queasiness and nausea on and off since prior to her diagnosis in February of that year, but this was different.  

We waited for a few days, thinking it would pass ... thinking it was due to the chemo drug she was taking five days out of every month (she was in the middle of those five days when it started). We also thought it could be a stomach virus, because there was a vicious one being passed around in our community at that time. But when it didn't pass, I called our oncology nurse at Arkansas Children's Hospital. She talked to our doctor, and they decided to move up her MRI appointment. Hannah had just had a clean MRI about seven weeks earlier, and she wasn't scheduled for another until September 29th, but five days before that, on September 24th, we found ourselves in the basement at ACH, getting ready for Hannah's turn in the tube. Today's episode describes that day.  

Thank you for joining me for another bonus episode of the While We're Waiting podcast in this year-long series in which I share our family’s experiences as our teenage daughter Hannah battled glioblastoma brain cancer from February 2008 through February 2009.  My desire is to process through the events of those twelve months with the perspective that 16 years has brought … and point listeners to hope in Jesus along the way.

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