Kati's bone in her jaw is exposed again. The surgeon at primary children's hospital wants to do surgery tomorrow. So, we are departing in the morning to take her up. The pain just hasn't let up. Thanks for your continued prayers.
- Glenn
Thursday, November 29, 2012
Saturday, October 6, 2012
Homeward Bound!
Leaving the hospital now. KT is not too swollen, just woozy from the drugs. We're going to bee-line it for home and get her comfortable in her own surroundings. The exposed bone was scraped, cultures taken, but the soft tissue was NOT closed over the exposed bone. It was left open to heal on its own so if there is any infection, it has a way out. Thanks for your prayers.
Friday, October 5, 2012
Surgery # 25
Katie's just now going into surgery. Late night! Looks like they will keep her overnight for observation. Cultures will reveal whether antibiotics are targeting all the right bugs.
Thursday, September 27, 2012
Next Friday Surgery
Since she has exposed bone at the back of her mouth, they will be able to do the surgery a week from tomorrow at Primary Children's under only local anesthetic, and since they’ll
be going through the mouth, it should heal very quickly. We’re encouraged by that. This
might be easier than we first thought – we’ll see. Katie asked a boy out for Sadie Hawkin’s
Dance on Oct 13th, and he just accepted, so she’s excited to get this
surgery over with and healed quickly enough to go. I hope it works that way! She is such a social butterfly! Thanks for the prayers and faith - it's doing the trick!
Wednesday, September 26, 2012
Osteonecrosis
After two weeks of increasing pain, we took Katie for another exam. Diagnosis: osteonecrosis in her facial bone. So we got word yesterday that Katie has to
go in for another surgery. The bone in
her face is dying, and has to be scraped again. Pam had to get her out of
school today to rush up to Primary Children’s Hospital so the surgeon can make
a plan for it. She, Katie, is
devastated. She’d been doing so well
since the surgery in June, and we’d hoped we were all done. So an extra prayer in her behalf would be
great.
Thursday, July 26, 2012
EFY

The reason keeping her PICC is so important is so they can do all the blood draws, CT/MRI contrasts, and IVs over the next year without having to poke her hundreds of times. She is what they call a "hard stick," in that her veins have rebelled over the years and do not like being stuck, so they recede deep into her and are so tiny anyway. Few technicians can get an IV started on her anymore.
She's happy, growing in strength, and looking forward to starting the tennis season on Monday. Thanks for your love and support!
Tuesday, July 10, 2012
Back to Cipro
We spent Sunday morning in the ER, where they did blood tests and a chest x-ray. Turns out KT's white blood cell count is quite low (1.4?), so they immediately took her off the cefapime and changed her back to Cipro. She was on that before. They also put her on 6 days of steroids. She says her throat still feels constricted, but she's doing okay and wants to keep doing the fun stuff, so we went to Space Center Houston yesterday and had a great time. We’ll follow-up with
infectious disease doctor in Provo next week when we get home from Texas.
Thanks for your prayers!
Sunday, July 8, 2012
Allergic Reaction?
In ER in Houston with KT. She's had some sort of allergic reaction to the iv antibiotic. She's coming around ok, but scared us for a minute there.
Friday, July 6, 2012
Thursday, June 14, 2012
Tailbone
P.S. We just found out a few minutes ago that Katie's TAILBONE is broken, and is so bad that she'll have to have it removed! Say what???? It's from an injury 10 years ago!
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