Skip to main content

Faith's iPAD

There's a blog I read called Caleigh's Corner about a little girl with CP. Her symptoms are similar to Faith's except that Caleigh is nonverbal. One of the posts discussed Caleigh having her own iPAD along with a special language app to enable her to "talk." I saw the photos of Caleigh with her iPAD and thought how awesome that would be for Faith to have her own.

Then, a couple of months ago, during a visit with friends, Faith discovered the Apple iPAD for herself. I saw her with an app called Pocket Pond and how she could press the screen to make a splashing noise and the water ripple. She loved it! She also checked out a piano app where there are the actual keys of the piano. After she was done looking at it, she looked at me and said in the sweetest voice, "mommy can we please take that little screen home with us?"

I discussed the prospect of Faith having her own iPAD with her speech and physical therapists and they both agreed it would a great tool for Faith, educationally and therapeutically. They both encouraged me to apply for Great American Bike Race (GABR) funds to get Faith her own iPAD.

The funds went through and we excitedly made the purchase for Faith. Before giving it to her, we wanted to find as many useful free apps as possible and also download some of her Sesame Street videos. Finally, the day came for us to give it to her. She was soooo excited! She laughed and screamed, "I have my very own little screen!"

Faith playing Pocket Pond on her iPAD with it sitting on her lap
Over the weekend we've been trying to help her maneuver around on the iPAD. She's great about pushing the bigger icons but it's going to take some practice for her to touch some of the smaller ones. I really believe she'll get it though and it's going to be great for her fine motor skills. She needs to have an open hand to operate the touch screen and also be able to put her pointer finger in the right position. I've seen her do that several times this weekend and I'm so excited!

There are tons of apps out there - and I can't wait to be able to purchase some of them. Right now we have some learning apps that help her with letters, sounds, numbers and sight words. Another app called Dragon Dictation allows her to speak into a microphone and it puts the words on the screen - perfect for our little storyteller!

Faith playing with her iPAD while laying on the floor
She's just like her mom and dad and loves the computer and I really believe having her iPAD will help motivate her with learning and with attaining new skills. An added bonus is that it is so light and ultra portable so we can take all of her apps with us wherever we go!

Faith sitting at the table, playing the piano on her iPAD
We are so thankful to GABR for making this a reality for our daughter. There are many parents of children with special needs in other states who do not have funds available to make such a purchase. We can't wait for Faith to bring it to therapy to show everyone!

Having fun with the alphabet on her iPAD

Comments

  1. Invest in Ripple on eToro the World's Leading Social Trading Network!

    Join 1,000,000's who have already discovered smarter strategies for investing in Ripple...

    Learn from experienced eToro traders or copy their positions automatically.

    ReplyDelete

Post a Comment

Popular posts from this blog

Getting Used to Our New School Schedule

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

A Real Pain in the Arm

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

Goodbye to Our Special Tomato

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