Skip to main content

All Done

We just got done talking to the doctors. Surgery is complete. Millie and Maggie responded perfectly to the procedure,no blips in heart rate or temperature. We're waiting for her to come out of anesthesia then we'll accompany her back to the hospital room. She may not remember much from today or even tomorrow the doctors were telling us, but I'll never forget her courage. Thank you to everyone for your prayers, support, and love.


  1. Fantastic! I hope recovery goes just as smoothly.

  2. This brought tears to my eyes. So happy!!! Praying recovery goes equally well. Give that wife of yours a big hug from me!

  3. Thanks for letting the world be a part of your journey! Amazing how quickly modern medicine changes. Miracles are all around us. Chidester Family, Friendswood, Texas

  4. Great! I have been worrying about them all morning!

  5. Oh yay! We are all so happy for you guys! The kids even remember to pray for the Killpacks every night! Sending love your way!!!

  6. Such great news! Been thinking about you all morning!!

  7. What wonderful news! We will continue to keep your family in our prayers.

  8. Oh I am so happy! I have been waiting to hear. We will continue to pray. Love you guys.

  9. Previous post- The Brown Family!

  10. Thanks for the updates! This one was wonderful!!! Been thinking about you today! So happy and grateful for Brave Millie and Strong Maggie!

    We love you guys!!

  11. Thanks for taking time to update us, Matt! We love your family so much and we are in awe of your courage! We are sending happy, healing, thoughts and prayers your way. I like what Michelle said, "Brave Millie and Strong Maggie!" Perfectly true. Go "20 and 37."

  12. We are so glad to hear the good news. We hope that recovery and post surgery care continue to go as smoothly. We pray for you every night!


Post a Comment

Popular posts from this blog

Building a Utah Valley Parade of Home

Our home is complete (mostly), and we are thrilled!  It makes my heart flutter every time we pull up. This home is the fulfillment of a dream, full of beauty and accommodation.  Davey zooms up and down the ramps with freedom.  We all have our "favorite parts" of the home, and I can't narrow mine down to one.

The Parade of Homes is happening now, and every day I get questions from friends, family and strangers asking about the parade process and where we purchased things.  I'll answer some of them on the blog.  Keep in mind, this is just our experience.  I'm sure it is different for everyone.

Why did we build a parade home?  ·Some of the subcontractors offered a discount price because their products or work would be featured.  It doesn’t necessarily mean it is cheaper to build a parade home, but it is possible to get more for your money.  For example, appliances.  We wouldn’t normally buy Bosch appliances, but with parade discounts the fancier appliances were the …

Cross-eyed Cuteness

Written by Matt.

We've had lots of appointments this week.

Thursday:  Millie and Maggie went to the Primary Children's in Riverton for an ultrasound on the kidneys and brain for Maggie.  Everything looked good. 
Friday:  Maggie's first follow up since her shunt surgery.  To us, she seems to be doing quite well except for her eyes crossing.  But as soon as the neurosurgeons saw Maggie, they said she needed to get an MRI.  He felt that it was urgent enough to do the scan that same day, but Millie was too sick to stay at the hospital and was lucky to drive home without crashing.  If you’ve never heard Millie crow up,  you’re missing out (it’s a mix between coughing and throwing up).  And we did an ultrasound on Davey's kidneys that day.  
Saturday:  The MRI.  Millie was still too sick to go to the hospital, so just Maggie and I went.  Maggie was charming as usual even on the required empty stomach and made instant friends with all the nurses and technicians.  I stayed wi…

Surgery and Nursery

Can't sleep.  Spina bifida does that sometimes!  On Tuesday Davey will have surgery at Shriners Hospital.  Some call the surgery a bilateral tibial rotational osteotomy.   I refer to it as fixing the feet forward.  Here's how he walks now.  See how he trips on his feet because they turn inward.  That's a result of being born with clubbed feet.  Hopefully in two months after his casts have been removed, his feet will face forward.   This is Davey's 8th surgery (I think).  It's difficult to know how he processes the thoughts of surgery.   He is most excited to have a slumber party with his dad at the hospital, and for his Papa from Texas to come and sword fight with him.  It's been a long time since Matt and I had one of our kiddos in an operating room...over a year.  I've appreciated the break and pray the doctors will have skill, wisdom, compassion and clarity as they care for my little boy.  
My heart is really heavy concerning Maggie.  Spina bifida does …