GI Update-
We are still fighting with gtube, but it is doing much better than it was before Christmas. As long as we can keep Casey from laying on it, we are able to maintain it as is. Hopefully we will be able to make it work long enough for some better veins to open up so the PICC will be an option when we need it. Only time will tell.
Ortho Update-
We ordered a new wheelchair for Casey a LONG time ago. We expected it around Thanksgiving, but the company was bought out, then there we other issues, long story short we have it scheduled for delivery Monday- YAY!!!! They came out to do a final fitting/measurements a couple weeks ago. We are very hopeful that she will fit much better and be more comfortable. It is of course all Casey, pink and girly as it can be.
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Not Casey's foot, just a Google Image- 4th Metatarsal |
Our poor Nissan van was about ready to die so we got a new van. We decided to go ahead and get one that can be modified with a rear entry ramp. It makes life much easier loading and unloading Casey. We are still getting used to it. We drove Nissans for so long, switching to a Chrysler is a big change. Without the new wheel chair yet, we are still adjusting where everything fits in the back. The new chair will make a big difference.

Nursing Update-
We are not back to having all of our shifts covered just yet. We have found a new nurse that wants to pick up our open shifts, but has other patients right now that conflict with our schedule. It looks like in about 3 weeks she will be able to pick up a few more. Then we should have at least 4 if not all 5 of our day shifts covered again. Right now we only have 3 days and I am not getting much done during the week. The extra 1-2 shifts will make a huge difference. Who knows, maybe I will be able to find time to post updates here more often.


We have decided that school is not working out for Casey. She had moved from the classroom to home-bound this year. Even being at home though just is not working. We had to cancel all the time for appointments, seizures, gi issues, etc. We decided that rather than pushing her to do school when she is not up for it that we would just pull her out. Now on her good days we can try to go to the library for story time, or do things that she really enjoys. It will be when she is up for it instead of on a set schedule that may or may not coincide with her good days. She loves to do arts and crafts, read stories, etc. I think doing it this way is going to be a lot more enjoyable. Tim said we need to find a "My Kids a 1st Grade Drop-Out" bumper sticker. I am pretty sure they don't make those.
That's about it for now. Hopefully we will have picture of a new wheelchair to post next week. Until then, we hope everyone is doing well.