Swim With the Others

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This boy – y’all, he continues to amaze me. I guess I shouldn’t be surprised. Most kids are amazing. Most kids can remind us of things that we have forgotten as adults. Most kids can teach us things if we only stop to listen.

I know Hugh is not the only amazing kid out there. His sister is pretty amazing, too, with her unique fashion sense and sheer command of the world around her.

 

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I teach some pretty amazing kids. I know kids who are fighting battles of their own, some not as visible as Hugh’s, and I am always amazed at their strength, resilience, and joyfulness in spite of their circumstances. Kids are amazing in general, I think.

So I really should not be surprised when Hugh says things that make me pause and marvel at his attitude in life. But I still am.

Hugh is not the kind of kid who is competitive or naturally aggressive. He tried playing soccer one year and was much more interested in singing and dancing for the crowd than running after the ball. When we would tell him to try and go kick the ball with the others, he would look at us with a quizzical expression, as if that were the craziest thing he had ever heard. Why should he go get the ball when there were ten other kids chasing after it? He had much more fun lagging behind and waving to the crowd.

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Sports just aren’t his thing, so his dad and I were thrilled when he decided to join the swim team. And we were even more excited when we discovered he was a pretty good little swimmer, with his long legs and torso propelling him quickly through the water.

Swimming has been an excellent sport for him and he enjoys the camaraderie. I can’t say enough about his coaches, who have been so patient with him. It hasn’t been easy – we check his blood sugar regularly as he swims, wiping his wet and wrinkled fingers on a beach towel as he is dripping pool water on our heads. There have been times his blood sugar has spiked and we have had to leave early, other times I have sat nervously on the sidelines when his blood sugar is dropping low. His coaches understand there are days he feels great and days where he is sluggish and slow. They are encouraging and compassionate through it all, and it has truly been a great experience for Hugh.

So imagine what went through my head when I was helping Hugh get ready for swim practice a few days ago, and he tells me “You know, Mom, sometimes when I’m ahead of the others in the pool, I slow down a little bit to let them catch up. I want to swim with the others.”

Of course, the first thing out of my mouth was “Hugh! The whole point of swimming on a swim team is to be first! You can’t slow down! You have to go super fast and beat everyone else!”

He gave me that same quizzical look as he gave me when he played soccer. As if that made no sense to him at all. Why would he want to be out there way ahead of everyone else in the pool? Why wouldn’t he want to swim with all his friends?

It was only later that night that I began to think about what he had told me. Again, I really shouldn’t be surprised. That is my son – always wanting to be surrounded my people, having fun, enjoying life. He doesn’t understand the hurry of things. He doesn’t get that there are races in life and that people want to be first. He doesn’t buy into any of that.

And then I started thinking, you know, there are a lot of times I feel alone with this disease. I feel like none of my friends understand what it is like to have a child with diabetes. When I wake up in the middle of the night to check Hugh’s blood sugar and the fear grips my heart as I lean over the bed, watching to see if he is still breathing, the loneliness surrounds me. Not many people can sympathize with that type of fear. Diabetes can be a lonely and isolating thing. Sometimes it feels like I’m in a huge, dark pool and I am swimming alone.

But maybe, just maybe, I am not alone. If I look behind me there are others in the pool with me, and they have helped me time and time again. There are family members, too many to count, who live diabetes with us, day in and day out. There are friends, who will never understand, but who show up anyway and are not afraid to listen. There are other parents of children with diabetes, who lift us up and never let us lose hope. We are not alone.

Maybe I should take Hugh’s advice. Maybe life is not a race. Maybe I should slow down, let others catch up with me, and swim together.

 

 

 

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The Ungrateful Heart

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I always love this time of year. I cannot get enough of kids dressed as Pilgrims and Indians, sitting down at their little Thanksgiving Feast, bonnets made out of construction paper falling over the girls’ eyes, and Indian vests two-sizes too big on little boys. One of my favorite things to do with the little ones I teach is sit down and ask them what they are thankful for.

It’s not as easy as you think. Some of the kids have got it – “I’m thankful for my mommy and daddy and my home.” Perfect. This kid has been well trained.

Others need a little coaxing. “I’m thankful for my Nerf Gun”.

I smile and then gently say, “It’s ok to be thankful for our toys, but remember God has given us our family and food to eat and warm homes to live in. So tell me again, what are you thankful for?”

“My family and my home and my Nerf Gun.”

Close enough.

I love this process because the kids are so honest. At four years old, they don’t own much. But they know what they do have and that’s what their thankful for. It takes a little bit of training and maturity to realize what they are supposed to say – things like family, food, and health.

Most of the time I have that maturity. I am trained to say I’m thankful for God providing us with so much, for my kids, and my husband. But on my bad days, I’m like a four year old. I want to hold up all my possessions and show everyone what I have. On my really bad days I’m not grateful at all. And on my really, really bad days I want it to be you and not me who has to have a child with diabetes.

My ungrateful heart is something I am not proud of. I have thought that something must be wrong with me to be so callous and cold. I am slowly starting to realize, however, that gratefulness is not something we automatically show up with in life. We have to choose to be grateful. And that is hard to do on some days.

So I’m going to start small. And I’m going to be honest. I know there will be days when my ungrateful heart wins and I get weepy and mad. This is a process, after all.

I will still speak the words, even if my heart is not feeling them. For I believe that just speaking the words give them power.

I will adjust my crooked bonnet made of construction paper, grit my teeth, and utter the words of thanks that are in my ungrateful heart. Because if I search hard enough, they are there.

Thank you God, for the noise of my children.

Thank you God, for the music playing, the dog barking, the drums banging.

Thank you God, for the dances in the living room with just the four of us.

Thank you God, for what diabetes has taught me.

Thank you God, that diabetes is not winning.

Thank you God, for forgiving my ungrateful heart time and time again.

Thank you God.

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I hope I’m not alone in my struggle for gratefulness. Please share with me what you are grateful for and how you practice gratefulness (no four year old perfect answers allowed!)

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Tips for Happy Hauntings on Halloween

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Halloween . . . the one night of the year where kids can be anyone they dream of, adults loosen the rules and have fun, candy is abundant, and it’s ok to try to scare the little ones with ghost stories and scary masks. Not to mention all of us Southern girls get to decorate with pumpkins and fall leaves, drink pumpkin spice lattes, and pull out our winter boots (even though it’s usually about 80 degrees on Halloween here in the South, we wear our boots anyway).

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What’s not to love about Halloween?

A lot, if your child has Type 1 Diabetes. The word Halloween strikes fear in my heart for completely different reasons. I’m scared of candy with no nutrition labels, parties with only pretzel sticks and M&Ms, and of course, the blood sugar highs and lows that come with a night of no routine.

Last year was the first Halloween Hugh experienced with Type 1. While I am by no means a veteran (I’m sure moms who have many more years under their belt can tell you much more), I did learn a few lessons that I would like to share. I hope this helps those of you who have children or grandchildren with Type 1, but also hope these tips apply to all parents who want their children to have a safe and happy Halloween.

Tip #1: Be Prepared

I can’t stress enough how important I feel it is to be prepared. Of course, we can’t be prepared for everything that might happen, but a little planning goes a long way. I try to print out or download candy nutritional facts to have on hand for Halloween night. JDRF has a helpful Halloween candy carb count list here.I also try to pack snacks that might be helpful if we experience some blood sugar swings. Cheese sticks and protein paks are great if Hugh’s blood sugar is high and he is craving something to eat. A 15 gram snack is helpful if Hugh is dropping low, but is not in the danger zone yet. Something with peanut butter or cheese is always a great snack. I also pack lots of water for the night. Running from house to house makes all the kids thirsty, but I draw the line at giving Hugh sugary drinks. I usually make him flavored water and every once in a while give him Coke Zero for a special treat (especially if all the other kids are drinking sodas and other fun drinks).
Planning the night’s events with your host is also very helpful. Calling a few days ahead of time to discuss what types of food will be served, what time the kids will trick or treat, etc. is not only helpful to you, but a thoughtful gesture toward your host. She/He might not have everything planned out, but at least they know you will be attending and you have thought about the night’s events. It does take a little bit of extra work to plan ahead and it can be stressful at times, but I always say it is worth it. Hugh doesn’t know the planning that takes place before an event, and he shouldn’t have to. It’s my job as his mom to take care of these things ahead of time so he can have a fun and carefree night!

Tip #2: Offer To Bring Food

There is no better way to ensure there will be something at a party that Hugh can eat than to offer to bring something myself. I usually offer to bring pizza, hot dogs, sandwiches, etc. That way, I know Hugh will be getting some type of substantial food that will keep him full and happy (and I also know the carb count). I ALWAYS bring enough for everyone, not just Hugh. I don’t want him to be singled out as eating something different and we love to share!

Tip #3: Don’t Make it Complicated for Others

Hugh’s Type 1 diabetes is my responsibility, not others. I don’t expect to go to a party and for the host to have everything Hugh needs. Whether it is a church function, private home party, or school activity, I provide what Hugh needs to eat and drink. Of course, many people are thoughtful and ask if there is anything they can provide for Hugh. But, I usually decline and let them know that Hugh can eat most anything the other kids can eat. If he needs anything extra, I bring it.

Tip #4: Trick-or-Treat First

Most kids are eager to start trick-or-treating and I’m ok with letting Hugh trick-or-treat first and eat supper second. The reason I do this is because after Hugh eats his meal, I let him pick two or three pieces of candy for dessert. That way, I can give Hugh the insulin to cover his food and his candy all in one shot.

Tip #5: Have Fun!

Ok, I know this is easy to say, but not always easy to do. But as you are planning for Halloween, try to keep in mind that one night is not going to ruin everything. Hugh might have high blood sugar when he goes to bed, but we correct it and move on. I want Hugh to be a kid and to enjoy this special night with his friends. If that means allowing him to eat a few more pieces of candy, so be it. Halloween only rolls around once a year and I am not going to make it into a night of rules and regulations. Here in the South (and especially in Louisiana), we can turn anything into a party. Just bring together good friends, good food, and a few ghost stories – preferably told in a Cajun accent – and the good times start rolling. Diabetes or not.

Happy Haunting, Ya’ll!

 

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