It's 3:00 a.m. and a bright flashlight shines inside a cabin full of kids. "Who's going low???" a sleepy teenage counselor asks as he goes through the kids in the cabin, one by one, to locate the source of the alarm that sounded just seconds ago.
A year ago, when Shulamith's son Swen was diagnosed with Type 1 Diabetes, I immediately contacted my friend Teresa, whose son and daughter both have T1. Her son (the younger of the two) was diagnosed first, when he was only three, and her daughter when she was 14. Teresa was an immediate source of knowledge and support as Shulamith, Matt, and Swen began the diabetes journey that would last Swen's entire life. We will always be grateful to her, along with a college friend of Shulamith's with T1 and others within the diabetes community, who reached out in support of the Webster-Monsons as they learned to navigate this stupid disease.
When Teresa told her son, now grown with a wife and children of his own, about Swen's diagnosis, his response was, "He needs a pump and camp! That's what he needs."
Swen got a pump (no more shots!) six months after diagnosis, but all camps were canceled last summer due to COVID restrictions. This year, diabetes camps in Utah were back in session, and Shulamith was quick to register Swen. Swen was both nervous and excited. We were both nervous and excited for him. Before this past week, Swen had never been away from his parents overnight, other than to sleep at my house. But he braved right up and went to camp with high hopes and an awesome attitude.
It was a long four days for those of us left at home. We couldn't even monitor his glucose numbers because the goal of camp is to help diabetic kids become self reliant, teaching them to manage the disease on their own AND to give parents a much-needed break from all of it. Shulamith barely slept the three nights Swen was away. "What if he goes low at night and sleeps through his alarm? What if no one notices? What if he dies?" This is not typical of Shulamith, about whom I often comment that she's never had an anxious thought in her life. But with diabetes, the hard truth is all of those concerns are realistic. I worried more about Swen's emotional health. I figured a camp for diabetic kids that's been in existence for 60+ years probably has its shit together; they probably know how to take care of these kids. My anxiety was more along the lines of "What if he gets scared at night? Would he tell someone? What if he hates all the food there? What if he doesn't make friends and feels lonely? What if no one else understands his obsession with car washes?"
All our worries disappeared yesterday at 5:30 p.m., when Shulamith drove up to camp to pick him up. He was alive and well, and he LOVED camp!! He was so happy! They evidently structure these camps to give diabetic kids a fun-filled week to meet and make friends with other kids with T1. It's such a rare disease that kids can feel pretty isolated. No one else has to check glucose levels all day, every day or bolus insulin prior to eating almost anything. No one else has two pieces of apparatus attached to his or her body 24/7, a glucose monitor to track highs and lows and a pump to dispense insulin. Swen was the only T1 kid in his entire school last year; it's hard to always feel different.
At camp, T1 Diabetes is the norm. Everyone has it. Swen loved that they all checked their numbers together throughout the day and that other kids' alarms sounded periodically alerting them of highs and lows. That's possibly the part Swen hates most about diabetes; he gets super embarrassed when his alarm sounds right in the middle of school. But at camp, that happens to everyone! He made friends, got "crazy," went on hikes, watched movies, saw a snake (he was quick to tell me all about that), and enjoyed lots of unstructured time (his favorite!) The only part he wasn't fond of were the education classes, you know, where they teach kids how to manage diabetes. My guess is it felt too much like school.
I asked Swen what he liked best about camp. In addition to the things noted above, he mentioned staying up until 11:45 p.m every night, all the free stuff they gave him (note: no one loves to collect free crap as much as Swen), getting to buy stuff every day at the camp store, no siblings around, and not showering even ONCE the entire week.
So there you have it.
P.S. Swen loved diabetes camp so much that he's considering going again next week when the theme will be Pokemon. Jurassic Park was cool, but POKEMON!!