This past Sunday at church I noticed Faith singing along to the chorus with a little more gusto than she has in the past. She seemed a little more confident and really projected her voice once she caught on to the words that were being sung.
I must admit, listening to her sweet voice singing the words, "He is faithful, He is glorious, He is Jesus, all my hope is in Him. He is freedom, He is healing right now" was enough to cause tears to stream down my face. Later after thinking about it, I realized that part of her new-found confidence in singing probably has something to do with the integrative music sessions she has been doing with a music therapist.
Faith playing the xylophone
fun with shakers
Every couple of weeks, Jonnica comes into our home and spends about 30 minutes with Faith singing songs and playing instruments. I know how much Faith likes music so I was pretty sure she would enjoy doing this but an added bonus is that the music therapist also does worship at her church so she and Faith like the same kind of music! While Jonnica does fun songs with Faith like The Popcorn Song, Ravioli and The Shaker Song, they also sing songs like "This Little Light of Mine" and "He's Got the Whole World in His Hands."
The great part about this music therapy is that while it is super fun for Faith, it also helps her work on things like motor skills, cognition, communication, visual and auditory skills. Besides bringing instruments like shakers, bells and the xylophone for Faith to play, Jonnica also brings flashcards with letters, numbers, words and colors. One of Faith's favorite parts though is getting to play Jonnica's pretty red guitar.
working on more than just music
Of all the cool instruments, this is Faith's favorite!
We've only really begun the integrative music sessions this year but I am already noticing differences in Faith and how it is helping her. I'm just as excited as Faith is about this type of therapy and who knows maybe she'll be helping to lead worship one day at church!
Click on the video below to hear Faith and Jonnica's good-bye song.
Dear Cari, Faith is just the most beautiful little girl. I have never heard exactly what she has for a handicap is it spina bifida or CP or something else? It is only important to me when I tell others about youtwo it is good to have the facts straight. I can't wait to meet her sometime! Hugs, Betty
Music therapy looks like so much fun! I am in favor of any type of education or therapy that really engages kids, gets them excited, and enriches their lives!
Today marks Faith's 8th day of school and we are all adjusting to a new schedule. Faith has made huge strides this past summer in sleeping better and having more energy so we decided to have her go to school from 9:00 a.m. to 3:00 p.m. 5 days a week. This is a change as last year she did not go Tuesday and Thursday afternoons due to how tired and worn out she would get. Faith's first day of 4th grade School starts at 8:30 a.m. but we asked if it would be okay for us to get her there at 9:00 instead. This allows us to more time to get her first feeding into her before she even gets to school. Her aides noticed last year that when we brought her to school without any food in her tummy, she was pretty sluggish and tired upon arrival. Sometimes, after getting her to school she wouldn't start getting her feeding until after 9:00 a.m. which meant, that because she gets a feeding every 3 hours, her last feeding of the day didn't end until 10:00 p.m. Another advantage to
Last Wednesday I had my yearly doctor exam and when she said I should get my tetanus shot updated, I didn't think twice about it. The nurse said my arm would be sore for a couple of days, gave me a handout and stuck the needle in my arm. The next day my arm was sore and although I found it a little harder to pick up and carry Faith, I was glad the pain wasn't going to last long. Boy was I wrong! But not only was my arm sore, my whole body was. I felt achy and extremely tired. According to a medical site on the Internet, these were mild side effects of the Tetanus shot. If these were only mild side effects, I would really hate to have them at a moderate or severe level. On Friday, two days after getting the shot I felt so tired that I took a four hour nap after getting Faith off to school. Then on Saturday I took a three hour nap up until 7 o'clock but still felt tired and was able to go back to sleep around 10. On Sunday, finally the fatigue started wearing off and I didn
Today we said goodbye to our Special Tomato adaptive car seat. And special it was. It helped Faith stay safe and secure in our Hyundai driving her back and forth to therapy appointments, shopping excursions and many other activities. It also helped us through our time of not being able to afford an accessible van. Like all adaptive equipment , the special car seat was expensive and although it is the law that a child is secured in a car seat while traveling in a vehicle, neither health insurance nor Medicaid would pay for it. Thankfully, we were able to receive funds from the fundraiser, the Great American Bike Race ( GABR ) which helps families pay for services and equipment that insurance doesn't cover for kids with cerebral palsy and related disabilities. After doing research on the Internet and talking to Faith's physical and occupational therapists, we decided to go for the Special Tomato adaptive car seat. You would think something with that name would be r
Dear Cari,
ReplyDeleteFaith is just the most beautiful little girl. I have never heard exactly what she has for a handicap is it spina bifida or CP or something else? It is only important to me when I tell others about youtwo it is good to have the facts straight. I can't wait to meet her sometime!
Hugs,
Betty
Hi Betty, she was diagnosed with CP at 6 months of age. Blessings to you!
ReplyDeleteMusic therapy looks like so much fun! I am in favor of any type of education or therapy that really engages kids, gets them excited, and enriches their lives!
ReplyDelete