August Was Moving Month

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It's been a while since I have put up a blog post. I also haven't been very active on Faith's Mom's Facebook page. That's because the month of August was dedicated to moving!  About 4 years ago, Faith and I moved from the apartment she grew up in, to a different one in northeast Bismarck. The primary reason for the move was to have underground parking so that getting her loaded into the van by myself during our cold, snowy winters would be less of a challenge. We also needed to find a place in which the elevator didn't break down on a regular basis!  One of our last sunsets at our old apartment  That place served us well, but the drive to her day program, which is located across the river in Mandan was time consuming, not to mention, expensive. I drove about 45 miles a day and used up a tank of gas a week!  Searching for a New Place  Before our lease ended, I began praying about finding somewhere else to live. A condo would have been nice, but surprisingly not a...
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The Rewards of Respite Care

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Faith and Kimberly at Kimberly's college graduation reception

Last night when I came home Faith was so excited to show me the Mr. Pumpkin Head she and Michelle had made. There it was on our bookshelf, right next to two Mr. Potato Heads. By the looks of it, Michelle and Faith had a blast. Once again, I found myself being very thankful for such wonderful respite care providers.

I think respite care providers are a must for anyone with special needs children. I have to admit, I felt a little guilty handing off my daughter to someone else while I went and did, well, nothing. But that was the point. When we found Michelle, we were at the top of our stress level. We both needed a break.

The difference between us and couples with non-special needs kids is they could just hire a babysitter or have friends and family look after their children. We on the other hand, need someone who has had special training to look after our special needs daughter.

Rob and I applied to have a certain number of hours a month that we would have respite care available to us. We did this through our disability case manager. When we first began, we had one respite care provider with just 20 hours a month. Now, we are up to two respite care providers for 45 hours a month. The increase in hours allows for Rob and I to spend more time together as a couple as well as have some precious alone time.

A couple of years ago after having just Michelle, we also found Kimberly, a college student majoring in early childhood development/special education. Since Kimberly knew she was going to be moving, she introduced us to Lindsey. I know of families who have a hard time finding the right respite care person for their child. Also, there is often a high turnover rate with respite care providers. These are other reasons I am so thankful. 

It seems as though the Lord has found us the perfect respite care providers who have come to love Faith just as she loves them. And what a huge blessing that is!

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August Was Moving Month

-
Image
It's been a while since I have put up a blog post. I also haven't been very active on Faith's Mom's Facebook page. That's because the month of August was dedicated to moving!  About 4 years ago, Faith and I moved from the apartment she grew up in, to a different one in northeast Bismarck. The primary reason for the move was to have underground parking so that getting her loaded into the van by myself during our cold, snowy winters would be less of a challenge. We also needed to find a place in which the elevator didn't break down on a regular basis!  One of our last sunsets at our old apartment  That place served us well, but the drive to her day program, which is located across the river in Mandan was time consuming, not to mention, expensive. I drove about 45 miles a day and used up a tank of gas a week!  Searching for a New Place  Before our lease ended, I began praying about finding somewhere else to live. A condo would have been nice, but surprisingly not a...
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My Tetanus Shot Ordeal: A Real Pain in the Arm

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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. My arm is still red and sore on day 2 after my tetanus shot. 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. ...
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Cari's Cardiology Update

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Normally, Faith is the one with all of the appointments but this week it has been my turn. On Monday I had my annual echocardiogram. On Tuesday I had my pacemaker device check and appointment with the cardiologist who comes to Bismarck from the Mayo Clinic in Rochester, MN.  The doctors who come are pediatric cardiologists who also specialize in adults with congenital heart defects (CHD). This saves anyone in the area who has a CHD from having to travel to Rochester each year. It is very convenient! (I do travel to Rochester to get my pacemaker changed, though!)  The Bible verse that has kept me going all these years! When I saw the doctor, we mainly discussed two things: my Fontan and my pacemaker. But first, a little background. I was born with double outlet right ventricle (DORV). Basically, this means both my aorta and pulmonary artery stem from my right ventricle. Because of this, my left ventricle does not really do anything, which is why this CHD is referred to as a sin...
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Faith's iPad

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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 gre...
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