We got to be in the chemo suite for the hour or so it takes to get Pentamadine. As you can see, Kayla was very into her movie while Miss Jenn tried to talk to her. And,. . . I really can't remember much more.
On March 20, 2012, we learned that our 4 year-old daughter, Kayla, has an optic glioma (tumor on the optic nerve) and would have to start chemotherapy immediately that would be weekly for 60 weeks. This is a record of our experiences during that time. . .
Tuesday, August 27, 2013
July 19th- Week 59
Even though chemo was done, Kayla still technically had 2 more weeks. For this visit, she also got pentamadine. We went in to the clinic the morning after we got back from Utah. Lily, Benson and Nathan all went to friends' houses. I can't remember a lot of specifics about this visit. . . I have been really slacking on keeping up. There must not have been anything too memorable happen. . . I think we met with Dr. Hansen. Kayla's counts were pretty low, but she still looked great. We had survived a trip to Utah and were heading out of town again the next week. Since she still has her port, we need to still be aware and call the clinic if she has any fevers.
We got to be in the chemo suite for the hour or so it takes to get Pentamadine. As you can see, Kayla was very into her movie while Miss Jenn tried to talk to her. And,. . . I really can't remember much more.
We got to be in the chemo suite for the hour or so it takes to get Pentamadine. As you can see, Kayla was very into her movie while Miss Jenn tried to talk to her. And,. . . I really can't remember much more.
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Hi Jayme, oh my goodness I am just getting time to catch up on blogs and sounds like you have lots of exciting news! Congrats to Kayla and to you guys on the next new baby! Wow, you're amazing.
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