Now that the year is almost half over, (NOT SURE HOW THAT EVEN HAPPENED!!) I figured I would update on how Abby Grace is doing in school and post a few pictures of some recent activities.
As far as comprehension, Abby Grace is really catching on with reading and writing. Things were hard at first, as she is left handed and seemed to be so backwards with everything. She was consistently reading and writing from right to left (she wrote her name ybba instead of abby). All of her letters were almost mirror image from what they should be. However, her teacher has been an amazing support and with lots of practice, all of those issues seem to be SO much better!!! She can read all of her sight words fairly quickly and can point them out in other books. I am so proud of her.
She is however, having a hard time with her energy and being excessively tired from the school day. We are working with her team of doctors and trying to figure out the best way to handle the situation and improve her energy levels. Poor baby girl, it just breaks my heart at how exhausted she truly is. When she comes home from school she eats a snack, and 3 out of 5 days will ALWAYS take a nap until almost dinner time. We eat dinner by 5:30 and she is in the bath after right that. 6:00-6:15 is bedtime and I will read to her for about 20-25 minutes. She is sound asleep by 6:45 every night, 7 at the absolute latest....and then I wake her up for school at 6:45am to get ready for the day. That is not enough time to spend with her every day! I think that has been the hardest part of this whole school thing. I miss her, and that's just all there is to it.
From a medical standpoint, she is so exhausted from all of the central apnea she continues to have. During the night she still stops breathing about 80-90 times. The doctors are not sure what is causing her central apnea and honestly there isn't anything they can really do to improve it, other than keep her on a strict schedule. Every time her brain doesn't send the signal to her body to breathe, she has an apnic spell and her body arouses itself as an effort to "rescue" itself. Mind you the spells are short in length, but when they happen so frequently, her body cannot get a restful sleep at night.
The original thought was that Abby's central apnea was a result of the damage from her Chiari, however now that we have 2 children (Abby and Owen) with unresolved central sleep apnea they are leaning towards some genetic issue that we have not been able to diagnose. So for now, we will just keep her on the schedule and try to keep her as rested as we can. Prayerfully, we will find a solution that doesn't require giving her a med, which I do not want to do.
I didn't mean to elaborate on that for so long, but that is our life for now so kudos to you if you are still reading!
Here are some pictures from fun stuff that has been happening at school!
Mrs Miller's Class
First Trip to the library. Abby Grace was SO excited!!


Pajama Day!!

Thanksgiving Feast

Seriously, how precious is that Pilgrim? Although she was less than thrilled with the style choices of the pilgrims!! HA!
