Four years ago, Ryan's life, and the life of our family ceased to exist as we then knew it. This time of year is a landmark for us, and it always causes me to reflect on just how far we've come.
.....
We were in St. George, UT, where Rick was running the St. George Marathon, and we were visiting friends and family. Ryan had just turned 6 years old the week before, and we were also celebrating his birthday with family while we were there. During the trip, I noticed that he was extra hungry that week--we would eat dinner, and 15 minutes later he would be asking for more food. I explained that away by all the activity, and the excitement of being on vacation. He was also really thirsty, but since we were in the hot desert, I figured it went with the territory. When he had to go the bathroom frequently, I associated that with all the water he was drinking.
When we got home though, those symptoms didn't subside. One particular day though, stands out so clearly. It was a Monday, and I had taken him with me to Joann Fabrics. We were there for a couple of hours, and during that time, he had to use the bathroom 7 times. Right then and there I knew something was not right, and I couldn't explain it away. That evening I called one of our best friends, who also happened to be Ryan's doctor. He made some room in his schedule the next day for us to come in, but during the course of our conversation, and the questions he asked, he told me he was almost positive what the diagnosis would be.
We showed up at the office, and after a blood glucose test, he informed me that Ryan was a Type 1 diabetic--that his pancreas has shut down and was no longer functioning, and that he would now be insulin dependent. I tried to be very strong, and not show my emotions--the ones that were quickly coming to the surface. I didn't want Ryan to see that I was scared for him, and that I already could see how his life was going to change.
I called Rick when we left the office, and of course, he was out-of-town on business. He immediately spoke to his boss, and got permission to come home. He left on a flight the next morning, and came home as quickly as he could. Meanwhile, the next day, Ryan and I went to the diabetes clinic. We met with an amazing nurse, who walked me through a very overwhelming scenario. I found myself thrust into a life of needles and medication, and faced with the daunting task of giving my 6 year old shots up to 6 times a day. I knew Ryan was so scared, and really had no concept of what was happening. I just wanted to hold him close, and let him know everything would be okay. I will never forget that first visit--the first time I had to give him a shot, right there with the nurse making sure I was doing it right, and with Ryan crying. I was crying too, even though I had promised myself I would try and stay strong. Even though I had had the nurse give me a shot first, to demonstrate how it might look and feel, he was shaking. Finally, we made it through, and we went on to meet with the dietitian. I received a quick tutorial on counting carbohydrates, and reviewed a sliding scale that would dictate how much insulin Ryan would need--both short-acting and long-acting. After 2 hours, we were on our own.
Wednesday, the day after our visit to the clinic, Ryan's blood sugar kept spiking. After numerous calls to the doctor, and injections of insulin, I couldn't get it to come down. Finally, I needed to take him to the ER. As I was backing out of the driveway, Rick started driving in. He was home, and I had never been so happy to see him. When we got to the hospital, they immediately went into action, and they were able to get him back down to where he should be. We were very lucky, and Ryan didn't end up having to stay in the hospital at all, and we were were able to take him home that night.
Gradually, our life adjusted to a "new normal". At home, we were quickly learning how many carbohydrates were int he foods we ate, and within a few weeks I could quote just about any food around! We discovered the best places to give an injection, and which angle hurt the least. In the beginning, every time Ryan took his blood sugar (a poke in the forearm or finger), he had to put a band-aid on it. Well, since we were doing this 6-8 times a day, you can imagine what his arms looked like! After hearing about that, one sweet family showed up at our door with a lifetime supply of band-aids, with all the fun characters all over them. It was gestures like this, by friends and family, that strengthened all of us, and kept us going through those first really tough weeks. Gradually we fell into a routine of shots, taking his blood sugar, and treating him for any highs or lows that occurred, and counting carbs. We dealt with birthday parties and play dates, all the while trying to maintain as normal of an existence as possible.
Ryan was also just a few weeks into kindergarten, and there was a lot to be done in order for him to go back to school. Teachers, staff, administration, and a para pro were all trained, a 504 plan created and implemented, and in general, things became more scheduled. Overnight I was on a first name basis with the principal, gym teacher, counselor, and secretary, and each of them played an integral part in the smooth transition that took place. His cute teacher wrote down in his special notebook every single thing he ate while at school, and I always smiled when I read "9 M&M's", or "55 goldfish". Other parents were so thoughtful and kind, and it showed in the type of snacks they brought to class. Room mothers brought sugar-free candy to parties, and all of this was done without putting Ryan in the spotlight or making him feel uncomfortable. I will always be so grateful to all the wonderful people that made a difficult situation much easier--they showed true compassion.
The real hero in this story? Ryan. We're talking about a child who was scared to get his hair cut--a child that would shake at the very mention of a shot during a well-child visit. His aversion to needles was deep, and when I first realized what this diagnosis meant for him, I was terrified. But he was incredibly blessed, and I believe a miracle occurred. After the first week, he was an old pro. He took everything in stride, never complained, and did everything that was asked of him. He learned how to take his own blood sugar that first year, and is now giving himself insulin with supervision. He learned addition and multiplication while calculating carbohydrates and insulin dosages, and learned how to read by looking at food labels. Less than a year later, he was able to go on an insulin pump, which has been fantastic. He is constantly an example to me, and I am so amazed by his strength and tenacity. Just yesterday I received a note from his teacher that complimented Ryan, and the way that he handled himself at school. He is such a wonderful boy, and I feel very lucky to be his mother.
Sure, the road hasn't always been smooth, and we have surely hit bumps along the way. But thanks to a very loving Father in Heaven, wonderful friends and family, kind teachers and parents, and each other, we are making it through, and we are each stronger for it.
14 comments:
what an amazing mom you are!! And a special boy Ryan is. I giggled at the lifetime supply of bandaids!
I remember when you had to take him to the ER and I can't believe it's been 4 years already.
And good thing he got over the bandaid thing, ey?
Wow, I can only imagine. Britney has had sugar in her urine a couple times and the doctors freak out and send me up to Primary children's for blood tests only to find her blood work is normal. So I have no idea and can't imagine if one time it turns out she isn't fine.
What an amazing story and even more amazing kid. Ryan is such a great boy and what an example and help he is and will be to so many others :)
Ok, I just cried through that entire post! It is always amazing to look back on experiences and to see the growth that has occured. He is such a wonderful boy. Thanks for sharing an inspiring story.
Wow, I remember when he was diagnosed. Cannot believe it has been 4 years. Our little neighbor who is in kindergarten is diabetic also and it amazes me to watch his strength and knowledge. Sometimes kids have to grow up too fast but they handle it so well. Ryan is a trooper and a sweetheart!!
What a hard thing to deal with. I cna feel your angst when you say "after 2 hours we were on our own". I've felt that way so many times...
What a road you have been down. Ryan is an amazing boy. You two make a great team!
Wow! What a story! I appreciate you sharing that. Ryan is a special boy who overcame something that really scared him and thats awesome!
Wow, what a journey. My brother also has Type 1 Diabetes, it's so much easier for kids nowadays than it was for him. You are a strong woman and I admire that you see the blessings in this.
I don't know why that struck me so much, but I am sitting her crying my eyes out. I think you are one of the best Mom's. I think that I would have gone insane with all the counting and food stuff. I am so impressed by you and Ryan. I love that Rick made it home just in time to leave. I love that Ryan is so strong and awesome. I also love those sweet people who do the little things like bringing band aides when you wonder how you can handle it all. Thanks for that inspiring story. It shows that there truly are angels among us. You are one of them:)
I think you are a hero too. I am not sure I could give one of my kids a shot. I have a hard enough time giving them medicine. I usually make Frank do it. Love you guys.
wow! what a tender post. it made me feel for you and for ryan. i'm glad he's doing so well!
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