Bless This Mess

Julianna's room was an absolute mess this past Sunday.  As I was trying to help her clean up and make sense of things, I noticed something written on her little schedule whiteboard.  Also, when I asked her who was responsible for the mess, I got a very interesting answer.  I was very amused, and I thought it was really special...  But I couldn't show her that, and I had to be firm and managed to tell her in between chuckles that she had to clean up her room.  I am not sure who of you out there will not be amused by this...

Very messy bed

Closer look at her sign

Very messy dresser (no surprise there...)

Closer look at the guilty bear, Amelia 

This bear was renamed Amelia after Andy and Mary Beth's little princess.  Amelia left a very lasting impression on Julianna after she saw her at her birthday party.  

Jack-O-Lantern

Below are pictures of Julianna and Jeff making their first Jack-O-Lantern together.  They had so much fun!  We were even able to roast the pumpkin seeds.  They were yummy!

Hard at work

Julianna and Mr. Jack

Learning to Share

We were finally able to deliver Julianna's donations to the Vanderbilt Children's hospital early this week.  In exchange for her gifts, Julianna got a private tour of the Children's hospital.  She really enjoyed watching the patients hold a "Teddy Bear's Clinic" and the Koi pond in the garden.  It is kind of ironic that I work at Vanderbilt, but that I had never seen the Children's hospital the same way I saw it that day.  I really am glad that we decided to support her in wanting to donate her gifts to the Children's Hospital.  I could really see the efforts of the hospital to help the patients and their families have a comfortable stay during what are really the most trying of times for them.  

I always feel bad whenever I see or hear about a very young child diagnosed with a terminal illness.  I could never understand why they were never given the chance to enjoy life.  A lot of our patients usually are diagnosed shortly after they are born.  Most of them live for 2 years or more, but it is always a life filled with pain and suffering.  I always wondered why they were allowed to suffer like that.   During our tour, I promised Julianna that she could share her gifts with the sick children every year.  Maybe in our small way, we can help improve the quality of life for these brave little angels.  Julianna also told me, much to my husband's disappointment, that she wants to be a doctor someday...so she can help the sick children get better.  Jeff pretended to be proud of her, but I knew deep down, he wants her to be a computer whiz just like him...We may hope and aspire differently for her, but I know that we will be proud of her no matter what she wants to be someday.  

Preparing her gifts...

Julianna loved looking at the costumes from Swan Lake

She enjoyed this model of the Children's Hospital a lot

In front of the Koi pond

The Little Gym Update

Julianna has been taking classes at The Little Gym in Brentwood since August.  She has really enjoyed it and has learned a lot!  She is more confident with her routines for her gymnastics and is really loving tap dancing and ballet during her dance class on Mondays.  She is also having a lot of fun learning about different sports during her sports skills class on Tuesdays.

She used to be scared of the balance beam and needed a lot of help on the uneven bars.  She can now do her flips with very little help.  She has mastered doing her forward roll and is now working on her cartwheel.  I am amazed at how well she has done.  I love the Little Gym because the instructors are very patient, and they make it fun for the kids.  The environment is never competitive.  I do not aim for Julianna to be a professional gymnast someday, if she wants to, I will be with her 101% of the way...but if she doesn't want to, then I am glad that I was able to let her try it and that it has helped her gain confidence.  She is also slowly learning that if she practices hard enough, she can do anything.  She takes pride with what she can do now.  Most important of all, she is having fun.  

Mommy's little gymnast

With Miss Ashley on the balance beam

Practicing her jump

Learning to tap dance with Miss Brooke and Kelly

No Sleep at the Sleep study

Last April, Julianna started showing signs of sleep apnea.  Her pediatrician noted that she her adenoids and tonsils were a little bit enlarged.  We decided to have her undergo a sleep study to see if surgery will be necessary.

It was great that the study was done at a hotel room, it is less intimidating (and had a more "homey" feel) than a hospital room.  They also had an LCD TV to help distract the patient while they hook them up to the monitors.  A big plus was the use of a night vision camera, this enabled us to turn off the lights in the room while she slept.  

As you can see in the pictures below, there were tons of wires attached to her.  She hated the probes near her nose the most.  She also had sensors on her chest and feet.  It was actually amazing that she got any sleep.  These pictures are not very good quality because they were taken from my iPhone.  I love this phone but it unfortunately, it takes very bad pictures.  

We will know her results in 3 weeks, but for now...I am just glad that it is over.  I didn't get any sleep at all because the sleep technician came in every two hours to fix the probe on her nose.  Argh!  Needless to say, Julianna and I slept in until 1 pm the next day!  

Getting ready to change into pajamas

Ready for bed!  Poor baby had to sleep with all the wires!