As of a 4 month post op update, she is doing great! And as you can see, healing quite nicely! We have also just dropped her PT down to every 3 weeks. She was measured today at PT, and her range of motion has gone from 10 to 30/40. Thats HUGE improvement!! Her PT guy does mostly cranial sacral massage/technique.
School ended, summer began with lots of rain… I mean, lots!! We have had some flooding in our area… our backyard is really big, so it was never got close to the house… and after this first flood in the pics below, the kids never played in it again… I was too worried about mosquitos.
We also started a garden, mostly seeds planted. It took awhile to get itself started due to all the rain, but has you can see… it is thriving now!! The kids are excited about all the veggies that are blooming.
In the CT pics above, the one is 2 days before surgery. Then the other two are her 3 month post op… its hard to see the change, and to the everyday person, your pretty much looking at hardware.
Kaylie wanted to send the doctors some cards, she is so thankful to both, but to Dr Rekate especially. After they received the CD, they reviewed it, along with the report that I emailed them a few days later. A Skype appointment was set, which was last week. It went VERY well. Everything looks great, and in place. She hasn't had but maybe a handful of headaches since the surgery. Which is Amazing!! She is happy, and herself. She is still in PT, and probably will continue that for awhile. She is still healing. On the CT there was a small pseudomeningocele formation. This is spinal fluid (kind of built up), he said over the spinal cord area of where her surgery was at, it just needs more time to heal. He is very pleased at her healing as well, and how her scar looks. And we will see him a year post op, unless something comes up!
We celebrated "great" CT results with Snow Cones! |
Cavity Free!!! |
We then headed to Dallas for a Rheumatology appointment. That appointment went great, the doctor we saw was great too, and they decided to test Kaylie for a few more things. Those results have come back normal, but the Rheum doctor told me to not always focus on the bloodwork, that things can come back normal… just not be showing up yet. But for now… things are good… so we are leaving it at that. We won't see her again, unless symptoms flare up more. One concern she had about Kaylie's EDS is her ankles, I guess they are "rolling" pretty bad… she suggested that Kaylie wear tennis shoes more often with special inserts to help strengthen and stabilize her ankles better.
Just the girls went down to Dallas. |
Waiting for the doctor... |
A couple weeks before the 4th of July, we got a new puppy!! Meet "Okie"! He is a chihuahua, you can't see his body below, but his body looks like a cow, spotted! His ears haven't come up yet, he still has a few more months for that to happen.
Coco, our other Chi, just loves him. They play all day, or at least until Okie zonks out!
Our 4th of July was very low key… we did the neighborhood thing, then went swimming, then saw a local fireworks show. It was nice, and relaxing.
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