She’s Hanging on Strong

Look at our girl 🥰

She’s doing very well this afternoon and sitting so tall.

Hehehe it was a little adventure trying to get her into her brace and in her chair all by myself, but I’m learning and thank goodness we both have alot of patience 😂 and humor.

😂🤣😂🤣😂 We are going to need alot of humor in the next few weeks. But we’ll be good.

We just finished Descendants 3 and she’s eating. Yep I got her to eat- taco in a bag never fails!

I’m pushing her to get those fluids down. We have to make sure her intake doesn’t get low. She’s still being treated for an active UTI, so fluids are important.

Wanted to give y’all an update on our girl.

Hope everyone’s having a wonderful afternoon.

Lots of love and hugs,

Alexis, Ceci and our family

~Spina Bifida Fighters and Survivor ~

Ceci’s medical needs wish list-

1st Night at Home

Good morning everyone 😊

I’m so happy to be writing this update to you, all from the comfort of our home.

The drive home was a little rough on Ceci but we made it safe abd sound.

She slept for 30 mins of the drive, so that helped. There’s a huge bump on I-74 heading home that I knew would be too much on her. We hit it and it woke her. But we were close to home so I was able to give her pain medication.

I stripped her bed and put clean blankets down and got get into her bed while I unpacked everything.

I had to have dad run out and grab a dry erase board for her room because they added 6 new medications to her already crazy medication schedule.

There’s so many things to keep track of right now. 2 sets of wound dressings for her back- one for the surgical incision that has to stay completely sealed that has to be changed every 2 days and the other for her skin tears that have to be cleaned and covered everyday.

I have to keep track of her urine output and track of fluid intake as well.

Lots of recording to do for the next few weeks but I’ll get it down 😊

I’ll continue to take unpaid leave from work until Ceci is able to do more for herself. Right now it’s all hands on deck and she need loads of help.

It’s very frustrating to Ceci because she can’t even adjust her body’s position in bed. Last night she had to wake me 5 or 6 times to reposition pillows and heat packs. I told her not to worry we’ll get through it but at one point she was crying because she was in pain and very frustrated.

I know it’s overwhelming for her. I can’t imagine being so restricted 😥

I just sent my babies off to school a bit ago. This is Aiden and Nicholas’s 2nd day back at school and I’m very grateful for my mom at this time.

Ceci can not be left home alone for any amount of time, so she’s coming in the mornings to take them to school and in the afternoons to pick them up and drop them off at home. Helps tremendously!

Me and ceci have been up since 6 after a long and not very restful night, so she’s ready to nap.

I’m going to fold some laundry and try to rest while she is.

I have many cheer mail calls to share later today so we’ll be back 😁

Please continue to keep this brave girl in your thoughts and prayers.

Lots of love and hugs,

Alexis, Cecilia Marie and our special family 💜

~Spina Bifida Fighters and Survivor ~

Amazon medical wish list for ceci’s needs-