One story in the book "Plan B" really impacted me because it was similar to our story. The difference was that this couple had already served on the mission field and had twins and their twins were born very ill. They survived but it was discovered after some months that they were both deaf. Their father was quoted as saying "This is not the way we thought parenting was going to look. This is not the way we thought ministry was going to look. This is not the way we thought life was going to work." I could relate to that. The author of the book follows that by saying:
"I think this is a difficult truth to grasp, but God loves you enough to strip you of anything that keeps you from him. And often these things that separate you are not bad in and of themselves. Often, in fact, they're good things-relationships, missions, jobs. But if for some reason they are keeping us from knowing God as we should, he may take them out of our lives." Then a few paragraphs later he says "Time and time again in your life you're going to feel as if God isn't showing up. You're going to feel as if God isn't healing, he isn't restoring, he isn't releasing his mighty power. These moments are crucial because God is trying to get you to the place where you can't handle things on your own, where you are willing to surrender your plans in order to receive his. He's trying to mature your faith."
I really think it was easy when I was in college, single, doing my own thing, traveling the world and the states serving in missions. I thought back then that my faith was growing. It was, and I will always be grateful for those days, for God's hand in places I lived, the opportunities I had, and the people he placed in my life in those days. I honestly feel though like he has grown my faith more in the past several years through marriage and through having kids, and having one with a disability to really grow my faith. He continues to do that.
Welcome to the blog of Wayne, Kelly, Micah and Gabriel Womack.
Tuesday, July 12, 2011
Thursday, July 07, 2011
Long but decent day at ACH
Some of you know that we had three appointments at Arkansas Children's yesterday for Micah. The first one was for Nephrology (kidney specialist) because he had an ultrasound about 6 weeks ago that revealed numerous tubers in one of his kidneys. We had been told when he was a baby that this would be a strong possibility as he got older. These growths (angiomyolipomas) usually occur in about 60 percent of kids with TS. They aren't problematic unless they grow or get to a point of hindering kidney function. So, what we were told yesterday is that though Micah has many of these tubers in his kidney, they are very small and are not threatening at all at this point. We will just have to monitor the situation and see the specialist again in a year.
The hardest parts of the day were Micah getting blood drawn (it took Wayne, myself and two other nurses restraining him and another to stick him with the needle). He just didn't know what was going on and the kid is so strong already at 6 years old! We had to hold him down for the ultrasound as well. After those appointments, he was fine.
We saw his neurologist in the afternoon and actually got in to see him a little early, which was a blessing! We really like Dr. Sharp and have seen him several times now. He explains things very well, he talks about options (medications) and asks what we want to do rather than saying "this is what we'll do". He is very good with Micah too and I think Micah is comfortable around him. He said in December it will be time to do a MRI of his brain to check on the tubers there and at that time a neuro-opthamologist will check for growths in his eyes and nerves around his eyes. We haven't done that since we lived in California.
All in all, it was a good day with a good report about the kidney. Also for all the waiting around and shuffling to different places, Micah did well. We had some sweet friends who kept Gabriel for the day and that was a HUGE help to not have to shuffle him around as well.
The hardest parts of the day were Micah getting blood drawn (it took Wayne, myself and two other nurses restraining him and another to stick him with the needle). He just didn't know what was going on and the kid is so strong already at 6 years old! We had to hold him down for the ultrasound as well. After those appointments, he was fine.
We saw his neurologist in the afternoon and actually got in to see him a little early, which was a blessing! We really like Dr. Sharp and have seen him several times now. He explains things very well, he talks about options (medications) and asks what we want to do rather than saying "this is what we'll do". He is very good with Micah too and I think Micah is comfortable around him. He said in December it will be time to do a MRI of his brain to check on the tubers there and at that time a neuro-opthamologist will check for growths in his eyes and nerves around his eyes. We haven't done that since we lived in California.
All in all, it was a good day with a good report about the kidney. Also for all the waiting around and shuffling to different places, Micah did well. We had some sweet friends who kept Gabriel for the day and that was a HUGE help to not have to shuffle him around as well.
Subscribe to:
Posts (Atom)