Skip to main content

Day One Post Surgery

Millie's doing so much better. They've taken her off the magnesium sulfate (the anti-contraction med) and now she'll take pills to prevent contractions. Her vision is no longer blurry and she can open her eyes. She's starting to move her legs on her own now and she's got more strength and stamina. She can start taking clear liquids and is enjoying her gourmet meal of apple juice, cranberry juice, chicken broth, and cherry jello. I'm excited to get the leftovers, YUM! Her surgeons keep coming in to check on her and are pleased with her progress. One of her IV lines was removed and she didn't even bat an eye (that may have been because she couldn't open them). She remains my hero. Hopefully she can have a restful night.

Comments

  1. I'm so glad to see that smile! Don't let Matt steal your jello.

    ReplyDelete
  2. Way to go Millie! So glad to hear things are headed in the right direction. We love you, and you will continue to be in our thoughts and prayers.

    ReplyDelete
  3. Millie is my hero as well. So happy to see that smile of hers! Yay for no more magnesium sulfate. Keep up the good work Millie so that we can see you soon!!! We miss you guys. Thanks for the awesome update. I'll be praying that the remainder of the updates be just as awesome!

    ReplyDelete
  4. It's great to see Millie smiling. Glad things are going so well.

    ReplyDelete
  5. I agree with everybody else! It is great to see your great smile! Love you!

    ReplyDelete
  6. Good to see that beautiful smile we all know and love:). Way to go, Millie!!!!

    ReplyDelete
  7. Thanks so much for the updates, Matt! I know its no surprise to you that she is a hero to so many of us! I'm so happy things are looking up and going so well! You guys are so prevail people and we are all behind you!

    ReplyDelete
  8. So glad that everything went well. What a blessing. Sure Matt..."apple juice"...

    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...