Sunday, October 12, 2008

Update from Kira's Mom

I’m so glad to be posting this update – and not just because it’s my first experience with blogging.

Kira has been home now for a week, and it is so wonderful for all of us that she is here. The hospital discharged her with several pieces of equipment as follows: Wheelchair, cane, walking leg brace, night boot, and bedside commode.

The wheelchair is being used regularly – not by Kira, but Ross enjoys playing video games from the chair and has also mastered several daring wheelchair tricks. It is very entertaining. We also have a scooter at the house that we’re test-driving for possible use by my mom one day, and we put on some amusing family parades from time to time.



Kira used her cane for the first 4-5 days she was home, but it became more of a nuisance than a help, so it has been cast aside.

The walking leg brace was custom made for her and it is hinged at the ankle. The purpose of this brace is to keep her foot and ankle positions stabilized while walking to reduce the risk of damaging her ankle and/or foot. Her foot muscles have a tendency to turn her foot inward and the brace corrects this. She wears the brace all day and it has helped her walking tremendously. The night boot is a soft blue stabilizer that she wears while sleeping.

The commode is being utilized as a shower chair and she is showering all by herself.

Kira has a number of prescriptions also. The least favorite is Heparin, which is a blood thinner that has to be injected into her abdomen every day for 2 weeks. Only a short way to go and she’ll be done with that.

Ross and Kira went on a little road trip yesterday. They drove up to Boomtown and had a great time. Here's Kira right before they left:



Thursday was Day 1 for outpatient physical, occupational, and speech therapy at Mercy here in Folsom. Several staff members remembered Kira from last year when she was caring for my mom and taking her to the same place for rehab from her stroke. She was pregnant at the time so they were excited to see Baby Ross when I picked her up. The occupational therapist asked that the baby attend her next session so she can get some pointers on caring for him until her right arm “wakes up” all the way. She will be attending therapy sessions twice a week.

Progress is being made all the way around. We’ve been doing a lot of massaging of Kira’s right arm and hand and she has very recently begun to move them a little bit voluntarily! Prayers and well-wishes are so very much appreciated and they are helping. It is so exciting to see the progress that she is making, and it is an honor to witness her strong will and her outlook on what she has been through. Being proud of her doesn’t even touch it. My daughter is my hero!

2 comments:

Our Family said...

So great to hear that you are making such wonderful progress, and that you have so many people that care about you. You are amazing!!!

Allison said...

Kira you are my hero too! You are amazing & you look great too!