Just wanted to update a little on our day. It seems silly sometimes to just post and post about our lives, though I know some people are reading and do appreciate your prayers. Your notes and comments have been sweet too. :-)
I took Joshua to the renal ultrasound appt today a little after noon. We took our bag with a game (thanks Rebecca as we have had a lot of fun with this!), puzzle book and more. Joshua worked on lunch on the there. I learned a lesson that I'm sure will be repeated. We are carb counting now and administer his insulin (one of them) based on the number of carbs he has eaten. Since he slept in late and hadn't had a shot yet, I wanted to be sure he got one at lunch.
I made a lunch, counted the carbs and figured he could take the food with him. Well, about 5 min down the road, I realized he didn't have about half of his food. So we turned around and went back. I weighed the cost of being late (they wanted us there 15 min early) versus what not having the food would do to his body. I choose the food. He could not afford another low. As it turned out, our timing worked out just fine too.
The ultrasound was long. I asked the sonographer if she would be interpreting the results and she said no, it would be a radiologist (dr) who would then talk with our ped. I sat at the end of the bed while Joshua had the test done. Up until that point, I realized that I had felt light about this appt. I really viewed it as just something to cross off the list, not really searching for a problem if that makes sense.
Well, as we were sitting there, I saw her go back to an area that she had already studied and measured. It was then that I felt fear seep into my mind and heart. I knew that she was looking at something, though I didn't know what. I knew not to ask as they can't tell you anyway. My mind started racing with things that could be wrong. I know that there is a link between diabetes and kidney problems, but surely not so soon.
I thought about how people sometimes comment that I am "strong". I don't always feel so strong. I think handling trials has made me realize how very weak that I am. I probably thought I was strong before I had been tested. Now, I know better. I think that being strong is sometimes just doing what you have to do. You do what you have to do for your children. That is part of being a parent. You don't always have a choice. I also know that my strength comes from God. I can't imagine doing any of this without Him. He is faithful and always with us.
So, I began to pray in that little dark room. Praying for our brave little boy who has been through a lot in the last two weeks. Praying for health. Praying for his body to be fine.
When the testing ended, she had us wait as she wanted to check with the dr to make sure she had gotten all the pictures that were needed. Then she asked us to wait for the dr. to come talk with us. I began to feel nervous again - thinking that this must mean bad news.
The doctor came out to talk with us. She had been unable to reach our ped and didn't want us to have to wait to hear the news. (That was very considerate!) She told us that his kidneys look healthy and that they did find one thing that wasn't normal. The collection area of his left kidney is too large. They aren't sure why. It could be that this is normal for him or it could be a sign of an obstruction. I left thinking that this was the end of it.
When we got home, we got in a poke and then a snack. Then I headed up to take a nap. I got in a short one before the phone rang. It was our ped. She talked more about the results of the test. She doesn't want to let it go in case there is something wrong. She wants another test (CT) done to see if there is an obstruction in his kidney. This is unrelated to his sickness and his diabetes. This is just another something going on in his body.
She told me that she was trying to find out if insurance would cover the test before getting it scheduled. She wants it done tomorrow. I'm guessing we'll get a phone call in the morning to set it up.
I also got a call from the endo wanting to know how Joshua was doing. We were both very pleased with his numbers today. Most in the 100s and one in the 200s. No lows!!! Yippee!!! This new med seems to be doing a better job. She again said what a great job we are doing taking care of Joshua. She is confident that we could move to an insulin pump soon if Joshua would like that. We'll definitely consider this, but first I want to get rid of the sickness.
Christopher, Daniel and Joshua are all feeling better this evening. They all slept a good bit today and were able to eat supper. Roger just told me that he is feeling a little queasy. Praying that he doesn't get sick too!!! Praying that Eliana would be spared as well.
As always, thank you for praying. I'm off to sleep now.
Love
Leslie
Wow, Leslie! You guys have sure been hit hard in the last little bit! You are (all) always in my prayers. We've been out of town, but are back at this point. Please call if there is anything we can do!
ReplyDeleteLove,
Lea.
Strength: Knowing when to ask for help when you need it.
ReplyDeleteStrength: A Mother doing all she can for her child
Strength: Relying on God to hold you up when you are too weak.
Strength: Moving on, day after day, not knowing what the future holds
Strength: Walking through fear
Praying for you dear friend.
Leslie,
ReplyDeleteI'm catching up with your posts. Wow, your family has been through a lot. I hope that you can continue to find time during the day to post updates, we will read as often as you post.
We pray for your good health to continue to care for your children. Your strength is an inspiration. We praise God for wisdom in the doctors to see what was the diagnosis. Although we are far from you in miles, our hearts are close and we are prayerful for your family.
Thank you friends!
ReplyDeleteLea - good to hear from you. I hope you had a great vacation and hope to see you sometime soon (when we are all well).
Sheri - thank you friend! I think the same of you now too! (((Sheri)))
Thank you too anon friend. If you see this, I'd love to know who you are. :-)
Love you all,
Leslie