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.

Comments

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

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

    ReplyDelete
  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

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

    ReplyDelete
  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!!!

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

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

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

    ReplyDelete
  9. Previous post- The Brown Family!

    ReplyDelete
  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!!

    ReplyDelete
  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."

    ReplyDelete
  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!

    ReplyDelete

Post a Comment

Popular posts from this blog

At The Moment

Josie was reluctant to go to school today.  Friday was her "worstest day ever" of kindergarten.  According to her account, nobody would play with her at recess.  "I would ask different girls but they said they wanted to play with somebody else."  Then on the bus ride home, a girl kept pulling her pigtails, sang a mean song making fun of her and yanked her backpack.  I asked Josie how she reacted.  Her response, "I just sat in the corner."   When Matt heard the story he said, "Nobody puts Josie in a corner."  Just like Patrick Swayze.  I think it's easier to say goodbye to a daughter being wheeled into an operating room than watch her venture into the great unknown of kindergarten. Speaking of surgery, we are still in limbo for Maggie's surgery... ETV-CVF .  We are scheduled for this Thursday, but I'll meet with the neurosurgeon on Wednesday and reevaluate whether or not we should proceed.  We don't know what to do...

Shunt Happens

On Thursday night, I couldn't get rid of a nagging concern.  Maggie's eyes were sunsetting.  This is where the  eyes turn downward with the white showing above.  It wasn't constant, and she wasn't showing the typical signs associated with brain swelling.  But the Spirit just kept working at me, and I decided to call the neurosurgeon at Primary Childrens.  He wasn't too concerned and told me to come on Friday for spina bifida clinic.  Once there, the doctor thought it was nothing because Maggie's fontanelle (soft spot) was still soft and of course Maggie wasn't sunsetting for him.  But I didn't want to go to Houston next week until I knew for sure she was okay.  So he ordered a head ultrasound.  Sure enough, the ultrasound showed significant swelling in the ventricles of  her brain.  A shunt is needed. Poor Maggie. I hate to see her go through another surgery.  When I'm at the docs office and get bad news,  I try to a...

Flippidy Floo Flah Folic

Last time I was at Shriners, one of the doctors asked if I had checked my folic acid levels after having Davey.  I responded that I'd never heard of anything like that and had not checked them.  The doctor then proceeded to say she had spoken with a geneticist about our family...two kids with spina bifida.  The geneticist said that I most likely don't metabolize folic acid properly, so that's why my last two children have spina bifida.  In summary, they thought that if I had checked my folic acid levels after Davey, I would have seen that something was wrong and could have prevented Maggie from having spina bifida.  As I listened to these burning words, I thought, "Do you know what you're saying?"  I turned away, bounced with Maggie, and wiped my tears. I'm often asked about folic acid.  It's an integral part of spina bifida prevention , and I should lecture about how everyone should take their folic pills.   But I'm not in t...