Life as a Leach

Abby's first day of kindergarten Favorite thing about school so far:  centers (especially the playhouse) Abby has the same wonderful teacher and assistant Caleb had in kindergarten, so we are thrilled as can be!  We also hit the jackpot with her one-on-one, who is the perfect fit for Abs.  We are so thankful for all they have already done to ensure that Abby has a safe and positive kindergarten experience! Caleb's first day of 4th grade Favorite thing about school so far:  math because we get to play games Caleb has two excellent teachers who are both very experienced in the subject areas they teach.  I know he will do well under their care.  He has made a few new friends and is enjoying being with one of his closest friends again this year.  He says the day flies by because they are working and having fun! The kids are riding the same bus that picks them up from our driveway and Caleb is taking really good care of his ...

While it was never our intention to bring Abby's wheelchair to school (except for field trips that required quite a bit of walking because she does get tired and winded), circumstances have caused her to have to be in it a lot more.  At this point, the pain from the kyphosis in her back is keeping her from walking much further than from the parking lot to the front door of a building.  This means that she is riding a lot more than usual. The wheelchair is at school, out of the way and available if she needs it.  The kindergarten classes are doing a lot of walking around the school this week learning their way around, so she will most likely be doing some riding. Since we have no idea what she'll be like after surgery, we've already planned for her needing to take her wheelchair to school.  Her bus is prepared to transport her, and school knows it's a definite possibility. For now, we are just thankful that she can walk when she needs to and that the wheelchair ...

Tomorrow will be the start of a new chapter in Abby's life.  I am absolutely thrilled with the teacher and one-on-one she will have.  It is the perfect situation and we are so thankful for these wonderful ladies! The magnitude of this milestone is not lost on me.  For a little girl who was never supposed to get out of the NICU, she is loving life and proving all of the doctors wrong. So if you see me crying tomorrow, know that they are tears of joy, thankfulness, and unbelief that we made it this far.

I realized I didn't post on here our updated surgery date.  If you don't follow me on Facebook, Abby's date was moved up to September 8th.  We were really happy about this because her kyphosis is getting worse and the concern for spinal cord injury is real. I'm so thankful that Abby gets to start school on time, even if it's just for a week.  She needs that little bit of normalcy and it's a "first" that should be celebrated! Speaking of normalcy, Matt and I talked the other night about our constant need to cram in as much normalcy as possible while we can.  Crafts, trips to the zoo, pool time...so much fun, so little time.  In my urgency to give them so much normalcy, I'm reluctant to just hang out and rest at home.  The rain today forced us to have a day at home.  After church, we got some things done around the house, the kids played Disney Infinity together, they went over to our neighbor's house for a little while, I made dinner, and we...

We met with Dr. Campbell and Dr. Cahill today.  Turns out, they've been talking about Abby a lot--just not filling us in!  So at least we know that the decision was thoughtfully made.  Dr. Cahill will do the surgery with Dr. Campbell assisting, since he is the one familiar with Abby's "interesting" anatomy. She has a complicated kyphosis and there's no perfect answer.  They will use a Shilla procedure, which is a new special cover that kind of expands itself as her spine grows.  This allows them to not have to fuse as much, therefore allowing for more spinal growth.  They will fuse T1-T6 (not in the c-spine as once thought).  Even with this procedure to limit the fusion, she'll be pretty little and the fuse could constrict lung development.  But the kyphosis already is anyway, so it's a toss-up. Not doing it would mean her kyphosis could sever her spinal cord, since it's progressed so rapidly.  That statement freaked me out a bit, so we are d...

We heard back from Dr. C that he wants to do a limited spinal fusion with instrumentation to correct Abby's cervical kyphosis caused by the last veptr surgery.  It was a 2-sentence email that left us with a million questions, so now we are going to CHOP on Friday (2 days from now) to have a sit-down and iron all of this out.  I think driving 8 hours in one day will be worth it if we get some real answers.  We emailed all our questions, but we are sure that those answers will bring about more questions...it's just easier to talk face to face and the nurse practitioner agreed. Abby is understandably sad and downhearted, but her cousins and I went to Five-Below while she was at PT.  They each picked out something to cheer her up, and it worked. :) We would appreciate your prayers for clarity and communication as we meet with the team on Friday!