Being diagnosed with a chronic illness, specifically Type 1 Diabetes, is one of the most life-altering moments an individual could ever experience. It’s being told that you now will have to manage a disease that will require you to take insulin injections, finger pokes, and constant symptom monitoring for the rest of your life. Furthermore, if you should choose not to adhere to this, your risk of cardiovascular disease, nerve damage, kidney damage, eye damage, limb damage, hearing impairment, Alzheimer’s disease, and depression increase exponentially as compared to the rest of the population. Imagine being told all those things when you’re only a child.
That moment happened to me before I could even talk, I was nine months old when I was diagnosed with Juvenile Diabetes. My entire childhood consisted of hearing the risks regarding being one of the unfortunate children whose pancreas stopped working. Those risks aside, my childhood was different than the majority of my peers. I spent several hours per week in the nurse’s office, because I wasn’t permitted to treat my blood sugars in class. I would sit out from activities because my blood sugar was going low. This alone reinforced the idea that I was different from my friends.
All this being said, diabetes could have very easily become a prominent part of my identity-and for many diabetics, it is. Camp Hot Shots has been an imperative reason, however, as to why I can live my life to the fullest without letting my disease be an all-consuming factor.
In 1996, when I was diagnosed, Chris and Cory Harter decided to take on a momentous project- creating a full-blown children’s day camp for children with Type 1 Diabetes. The focus of this camp, called Camp Hot Shots, was twofold: 1) To educate youth to reduce the risk of diabetes complications and 2) To produce an environment that allows these children to have a normal summer camp experience.
I spent years attending this camp and loving every minute of it. It allowed me to develop independence and confidence in managing my disease. Then, when I graduated from being a camper, I was given the opportunity to become a counselor. Now, I have the privilege of volunteering for camp on the board of directors. Up until that point in time, I was ignorantly unaware of what it took to run this camp.
Camp Hot Shots takes place every June. Though it’s only three days long, it takes a small village to get it up and running. Chris and Cory Harter are the spearhead of this massive undertaking, every year without fail. To give you a glimpse of what this looks like, imagine the following: Needing a full team of medical professionals to volunteer their time, screening through dozens of counselor applications to find individuals who will prove to be good role models for campers, fundraising, networking with community partners, contacting medical supply companies for the equipment the children will need at camp, reassuring dozens of parents that their newly diagnosed child will be safe at camp…the list goes on and on. The Harters do it with smiles on their faces, because they know that the impact of all of these tasks is for a greater purpose.
Because of Camp Hot Shots, literally hundreds if not thousands of diabetic children in the Midwest have been impacted. I’ve seen the results of Camp firsthand in my own life and the lives of the friends I made at camp when I was a child and counselor. Diabetes is not an easy disease to live with, but it’s manageable with the right tools and education. The campers that have attended Camp have gone on to be lawyers, doctors, teachers, social workers, therapists, and more. Camp Hot Shots has enabled them and given them the confidence to do whatever they set their mind to, despite all odds. I am so incredibly blessed to have attended and volunteered at Camp Hot Shots and I am thankful for the irreplaceable gifts it has given me.
— Sarah Longhini, Counselor and Former Camper