Wednesday, February 9, 2011

Our New Normal . . . . .

What is normal? It is so many different things to different people. Have you ever been over to someone's house for dinner and they are eating something you've never even dreamed of purchasing at the store, much less cooking into a meal? Or maybe they made something you are familiar with, but when you cook it, you do it just slightly different. What is a normal way of cooking a specific dish or what is normal food to one person, may be completely abnormal to another.

My version of normal in my home is - send the kids to school, go to work, come home to be with the kiddos in the afternoon, work out a couple days a week, Lifegroup ever other week, an occassional sporting event, church every Sunday, dinner as a family every night . . . .

Well, my normal has been interrupted and now, in the midst of all that we are checking blood sugar levels, counting carbs, calculating insulin dosages, and switching out some of our "normal" foods with our "new normal" foods, and praying with all the belief we can muster that God is going to perform a miracle so we can go back to our "old normal."

I am a blessed woman. I have a husband who loves me and three beautiful children, who despite their incessant bickering, are really good kids. My oldest loves to read and play basketball. My youngest is a fireball who keeps us laughing and not taking life too seriously. And my son (who falls in the middle) loves God's creation and enjoys making his own creations, or as he calls them, "projects." I wonder when God created the world if He considered it a project? I guess we humans are a constant project being worked on, aren't we?!

Well, I think our "new normal" is a reflection of a project God is working on in the Norris household. I'm not sure exactly what the lesson of this project is, but I am hoping we all learn it, and learn it quickly. I don't want to have to round any more "tragedy" mountains in order to be able to say, "lesson learned!"

God, I'm trusting You to speak clearly to me. I'm working dilligently to be still and hear your voice. I know it's sad that I have to work on being still, but it's how you made me, so I'm learning that one constantly! My efforts to help Caleb are in vain if You aren't involved, leading the way. Let us all, especially Caleb, see Your mighty hand in all of this, knowing that "everything works together for good for those who love the Lord. "

Friday, February 4, 2011

To Lara, Love God . . . . .

God gave me this scripture during a week of fasting regarding my place in the Children's Ministry. I felt He was telling me to hold on - it was all going to be ok, and not to give up. Little did I know that less than a week later it would mean even so much more.

On Monday, January 31st, 2011, my dear son, Caleb was diagnosed with Type 1 Diabetes. On Thursday, February 3rd, God reminded me of what He had showed me just a week prior. This is His love note to me . . . .

"I remember it all -oh, how well I remember - the feeling of hitting the bottom. But there's one other thing I remember, and remembering, I keep a grip on hope;

God's loyal love couldn't have run out, His merciful love couldn't have dried up. They're created new every morning. How great Your faithfulness! I'm sticking with God (I say it over and over). He's all I've got left.

God proves to be good to the man who passionatley waits, to the woman who diligently seeks. It's a good thing to quietly hope, quietly hope for help from God. It's a good thing when you're young to stick it out through the hard times.

When life is heavy and hard to take, go off by yourself. Enter the silence. Bow in prayer. Don't ask questions: Wait for HOPE to appear!" Lamentations 3:20-30

Lord, I am waiting for hope and I won't question Your sovereignty. I am believing for a miraculous healing in Caleb. War has been waged on my family by the enemy, but we won't back down. We are on the offensive, with You leading the march. Our heads are held high with our hope safely in Your hands.

Tuesday, February 1, 2011

I take it back . . . .

I take it all back - my complaining of the 3 weeks in a row with sick kids. I take it ALL back. Our family was hit with a landmine yesterday-the diagnosis of Caleb with Type 1 Diabetes. He's 10. God, did you hear me? He's only 10-no kid should have to deal with this! I have all these emotions raging through me - fear, rage, worry - you name it, I'm feelin' it right now. Most of the words I want to say would be inappropriate, but I'm sure everyone has thought of a few choice words now and then. Surely I'm not alone!

So, let me backtrack. . . About 3 weeks ago when Caleb was sick, he had a virus. No flu; no strep; just a virus. He's been over it - no big deal. Well, the past 4 or 5 days Caleb has had excessive thirst. I didn't think a thing of it at first, but one night this past weekend I was reminded of a conversation about a toddler at the preschool I used to work for, who was diagnosed with Type 1 Diabetes. She was suddenly excessively thirsty. My heart sank. I told Dennis that night we needed to get Caleb seen by a doctor. I didn't realize I should have probably done it immediately, but God's grace was sufficient and yesterday at 2:00 we were seen by our family practitioner.

Caleb did a "pee in the cup" test - which by the way he thought was hilarious! He'd never peed in a cup before. The results showed up with a lot of sugar in his urine, so then they did the finger poke. The result was "HI" which according to the meter means over 600. A normal level for sugars is 90-150 . . . Caleb was off the chart. The doctor looked at me and said, "this is not good." I knew. I knew before I took him in. God knew - that's why He reminded me of that conversation about my friend's child.

Based on the conversations I've had with the doctors, Caleb should have been in the Emergency Room. His numbers were off the charts, but he was remarkably well for as bad a shape as he was in. But, instead of the ER, favor abounded and we immediately headed to an endocrynologist who worked us into their schedule. They were fabulous! Both the doctor and nurse were Type 1 and had learned to deal with this since the 80's. We were handed glucose meters, needles, 2 different types of insulin shots, brochures . . . my head was spinning, Caleb was crying. It was awful, but through the awfulness, God's grace abounds!

When people say your life can change in an instant - they are right. I knew this, but having experienced, gives me a whole new perspective on situations my friends have gone through. I walked around in circles this morning trying to figure out what to do with myself. I'd gotten almost no sleep. The girls needed to get ready for school. Was I going to work or staying home? What to wear? Is Caleb going to school or are we going to monitor him? A cold front coming through, does everyone have jackets? Dennis is needing to get the truck to work for deliveries. Did the kids get their vitamins? Is Caleb ok? What's his blood sugar? Can he eat this? ??????????????????????????????????????????????????????????????????

My stomach still turns when I look at Caleb and see hurt in his eyes. He does NOT want this. He's old enough to know how life was before, but not quite old enough to heave a big sigh and just move on. As his doctor says, "shots suck!" I feel the same way - this really sucks!

However, as bad as this sucks, I know it could be worse. I have a dear friend who lost her daughter to a virus that attacked her heart. I have another friend whose daughter had a brain tumor. She's survived, but she will never be the same as she was before. I am reminding myself to count my blessings, as they are many. My son is a blessing and I am grateful he is still here with us. We walk on a little bruised, but we are not defeated. We raise our eyes to the One who knows exactly how we feel and reach for His hand as we move forward.