What you can pray for.

FEAR.

A lot of people are asking what they can do or how they can pray. Right now, fear is the main thing.

Kielah is a smart little girl. Way too smart for her own good. She asks questions even adults wouldn’t think to ask. She says things even adults wouldn’t think to say.

Some things I’ve been told/asked in the last four days:

·        I don’t want to be in a wheelchair.

·        Am I ever going to be able to go to daddy’s house?

·        Is it going to hurt?

·        Are they cutting my foot off? (Side note to say this question is because she knows the doctor has mentioned this before, and while it was mentioned Friday, it was in a “that’s an option but not recommended” type of way).

·        Am I going to get a shot?

·        Why can’t Bubba be in the surgery room with me?

·        Is it going to hurt?

·        What are they going to do?

·        Will I be able to snuggle with you before bed with my cast?

·        Will I be able to ride in a car?

·        Will I ever be able to go to gymnastics again?

·        Will I ever be able to go to school again?

·       Will I ever walk again?

We went to lunch after her appointment, and while me and her dad were sitting there, out of nowhere she said, “I’m really scared.”

This doesn’t mean she’s nonstop all day asking questions or voicing her fears. If she’s preoccupied, she’s fine.

If you know of any songs about fear (preferably that are new and catchy that she’ll like) please let me know! I want to make a playlist that I can play once we lay in bed to keep her mind from going there. 

*We have a GoFundMe account set up for the costs we will incur throughout this time. Kielah's Surgery

Surgery scheduled!

It’s been a while.

Hey guys, just an update after a long time without one! (Oops.)

We found out in February that Kielah would be having a SUPERhip surgery sometime soon, but her bone development wasn’t quite ready yet. It was determined by Dr. Herring (her surgeon) that it would be checked again in November.

Lately, Kielah has been having a lot of pain lately when she walks around for a little while. We determined this was because her prosthetic leg doesn’t fit correctly. We called last month to get an appointment to get it looked at, and, long story short, it was determined that we needed to have an appointment with her surgeon.

Fast forward to today…

Found out a couple of days ago that they were going to send us to get images done before we saw the surgeon. (Insert dramatic DUN DUN DUN here)

Kielah gets x-rays all the time. First one was when she was a few hours old. She’s a champ at them. However, x-rays mean he’s looking again to see if her bones are ready for surgery.

Once we got done with that, we went to see the surgeon.

Dr. Herring checked her how he usually does (range of motion, gets her to walk, basic stuff), and then says,

“Well the bone looks like our next step will be surgery.”

(According to the man who has made Kielah’s prosthetics since her first one, this is pretty much how I looked at her dad when he said it.)

I was nervous, but I’m still much more peaceful than before because I had prepared myself for an all-day surgery.

(Side note to say that I am forever grateful for Kielah’s dad. He’s really the best dad she could ever have, especially in this situation, and he’s really the best co-parent I could ask for in it.)

The surgery will essentially rebuild her femur head and hip socket. It’ll take 2.5 hours. We’ll be at Scottish Rite for two to three days, and after surgery she’ll be in a Spica cast for about six weeks and be in a wheelchair in this time. After the cast comes off, she’ll do physical therapy and have to relearn how to walk. Dr. Herring said she’ll be walking again by her birthday. (GOALS)

Specific prayers:

-       Peace for Kielah. She was in there when the surgeon was talking, and we would never hide it from her and blindside her on it. She’s understandably nervous.

-       That people don’t constantly bring up the surgery to or around her.

-       Finances for the trips necessary during this. Just through September 6^th, we will be staying in Dallas a total of five nights over at least two trips. That doesn’t include going back for checkups, cast removal, or physical therapy.

We are so thankful that y’all care about our baby girl so much.