Sugars in the School Yard

Graham Daugherty • March 19, 2020

This is part 3 of a 4-part blog series by Trystan H., a recipient of the Charlotte Tucker Scholarship.

A woman is laying on her stomach in a field of grass.

Managing type 1 diabetes is no easy task. Each day poses new challenges and tasks that must be met in order to stay healthy. Learning how to complete these tasks is difficult in any situation, and it is especially tough in school. Since I was diagnosed at eleven years old, I did not have to navigate preschool, kindergarten, or elementary school with the additional stress of diabetes. I was diagnosed in sixth grade, the beginning of my middle school years. Middle school is already a stressful time for young people (and their parents), but this diagnosis made middle school a lot more challenging for me than I thought it would be.

Making friends and fitting in was easy for some… not so easy for others. One of my first fears of going back to school after I was diagnosed was the fear of rejection. I was so terrified that everyone was going to think of me differently. I hated telling people that I had diabetes, and I avoided it at all costs for pretty much the rest of middle school. I began to become more open about it in high school, but back to middle school for now. Luckily, my best friend did not think of me any differently, and she went with me to the nurse’s office every day to prick my finger and take my insulin. The teachers believed that I should be able to go to the nurse by myself, so they instructed my friend not to go with me again, but that did not stop her. She would find a way to sneak down the hallway almost every day at lunch. I do not think my friend will ever know how impactful her daily support for me was. I truly believe that a silly story like this can show the power of friendship. I encourage you to surround yourself with people who will support you through any struggles that you have with diabetes. This friendship made all of my dreaded nurse’s visits much less painful and helped me get through the years when I wasn’t quite able to manage my diabetes on my own. I encourage you to reach out to others like my friend did to me. It could be life changing for someone.

Now let’s get to high school. At long last, no more daily visits to the nurse! It took me a while to be able to become truly independent with my diabetes. When I got to high school, I knew that it was well past the time for me to start doing things on my own, and let me tell you, the independence felt so good. I ate what I wanted to, which was not always a good thing, I avoided the nurse at all costs, and I let my diabetes influence me in minimal ways. At this point in my life, the independence was so nice, that my glucose levels started to go down the drain. I was focused on hanging out with my friends and, more specifically, my boyfriend, all of the time. Whatever they ate, I ate. I did not count my carbs as accurately as I should have, and I put my academic and social lives ahead while my health was on the back burner.

I look back and think of this stage as my rebellious stage in life since I was basically rebelling against my health. Another huge factor in my BG levels going downhill is a huge fear that I have: going low. I have always been terribly afraid of going low, especially while I sleep. In order to account for this, I would often make my blood sugars go high so I would not have to worry about a low. I do not recommend anybody do this. My A1C’s gradually rose until I realized what I was doing and how horrible it was for my body. Doctors could tell me over and over that I needed to take more insulin, but I did not listen until I understood for myself what I was doing. I choose to hear their advice, but not listen to it. Once it clicked in my brain how silly my little rebellion was, I felt foolish and unhappy with my choices. Since then, I have definitely become better about trusting my pump and allowing my levels to lower into normal amounts. High school opened up a lot of doors for me to gain independence and be responsible for my health, and, unfortunately, I abused my freedoms for a while. I am not proud of it, but it did happen and still does happen. I don’t ever have a perfect day where my blood sugars are 100% where I want them to be, but this is just a fact of living with diabetes, and it certainly does not stop me from trying to do my best.

At long last, I have arrived at college, woo hoo! I thought what I had in high school was independence! College has ten times more independence. There are fast food options within a five-minute walk in every direction around my dorm. I can eat anything and everything that I want. I can choose when to go out, when to go to class, when to relax, when to study, and on and on. Luckily, I have become wiser since high school, and I do not abuse my freedoms as much as I did a few years ago. College comes with a lot of opportunities to make bad choices, and not just for diabetics. You can choose to skip class and focus only on your social life and start failing. You can choose to throw away the hard work that you put in and party your life away. College also comes with many opportunities to make amazing, life-changing decisions. You can pass your classes and get a degree that will open up so many doors in the future. You can choose to go to the gym for free as a student any day of the week. You can be active in your social life and still thrive in academics. I am very thankful that I am focusing on eating better, studying hard, and trying to live a healthier lifestyle. I try not to abuse the freedoms that I have, but sometimes I still make mistakes. There is always room for improvement, and the farther along in my education that I go, the more I realize how important my choices are. I now use my independence to grow and tackle the challenges of diabetes every day.

A black and white photo of a person with an insulin pump on their stomach
By Dr. Holly O'Donnell April 3, 2026
Type 1 diabetes affects mental health in youth and families. Learn about risks like depression, anxiety, and distress, plus support options and when to seek help.
A young boy in a white sweater is standing next to a cabinet.
By R. Paul Wadwa, MD, Professor of Pediatrics at the BDC April 2, 2026
Type 1 diabetes is often misdiagnosed as flu, UTI, or viral illness. Learn key symptoms, DKA warning signs, and when to ask your doctor for testing to avoid delays.
Author and type 1  diabetic Madeline in a research lab
By Madeline VanOrman March 20, 2026
Follow one patient’s journey with type 1 diabetes from childhood diagnosis to college life, sharing challenges, independence, and finding support along the way.
Three young type 1 girls with CGMs on their arms.
By CDF Staff March 18, 2026
Donate your Colorado state tax refund to the Children’s Diabetes Foundation. Learn how to use form DR 0104CH to support T1D patients and families.
A group of people are posing for a picture in a living room.
By Stacy Robinson June 14, 2024
With Father’s Day just around the corner, I am thinking about my dad even more than I usually do. He was a special man who lived a remarkable, impactful life right up until the day he passed away at the age of 98, a little over a year and a half ago. He was a decorated World War II veteran, a bookie in Vegas during the Rat Pack era who married the love of his life between rounds of a prize fight, and who later went on to become a successful entrepreneur. Most importantly though, he was a devoted husband, father and grandfather.
A man and a woman are posing for a picture in a parking lot.
By Lindsay Klatt June 14, 2024
Author: Lindsay Klatt Being the dad of two daughters already has its highs and lows; having one of them (who admittedly was already a little feisty) diagnosed with type 1 diabetes makes him a saint. My wonderful dad navigated these challenges with such love and grace. As we approach Father’s Day and as I recently celebrated my 27th Diaversary, I reflect on the things he deserves to be thanked for. There are too many to count and no way to properly express gratitude for the additional struggles type 1 fathers face, but here’s a toast to a few of the things etched on my heart: Cheers to my dad who, when I was diagnosed, had the best balance of acknowledging the sadness of the event and being encouraging for the future. It made me feel seen to see him upset, and to see him determined. He has always maintained that balance I am so grateful for.
T1D patient Dylan Archer on race track.
By Dylan Archer March 8, 2024
Diagnosed with type 1 diabetes at age 8, Dylan refused to give up racing. Read his inspiring journey of resilience, technology, and championship success with T1D.
Two girl scouts are standing next to each other in a room filled with boxes.
By Graham Daugherty January 9, 2024
By: Sarah Hathaway On October 10th, 2022 I earned my Life rank in Scouts BSA and began focusing on what was once a faraway goal: Eagle Scout. I had some ideas for my project and I knew I wanted to do something that means a lot to me and benefits as many people as possible; this led me to think about the Children’s Diabetes Foundation. I am an advocate for the organization and I know CDF has made an impact on others just like me so I was hoping I could come up with a plan to help families affected by T1D. I reached out to the Community Engagement Manager, Sydney. I believe that she was really confused and might not have heard about Eagle Projects before so she asked all about what I was looking to do and we talked about different options for projects. I asked her about the newly diagnosed onset bags for people with T1D that I remembered receiving from CDF when I was diagnosed in 2021. This was last June and we were both volunteering at the T1D Strong soccer camp. As camp went on we talked a lot and I offered some more ideas and the plan started coming together. I started to talk to diabetes-related companies to get additional informational materials to put in the bags. I got in contact with Dino from Omnipod and he was very helpful. He sent me a lot of informational packets, games, and even fake Omnipods for new patients to try before spending a lot of money on new technology. Unfortunately, other companies and organizations were not as responsive but there was already a lot of helpful stuff from CDF to go into the bags. I also did a fundraiser before my Eagle Project workday. I set a goal to raise money to put a restaurant gift card in each new onset bag because I remember going to lunch together as a family when I was discharged from the hospital. I knew that families could use that gift card and not have to worry about where to go. As I was fundraising, I found out that the Scouts BSA district person that I was working with, Pat, was associated with KFC. Pat put me in contact with the Regional Manager of KFC and through this contact, KFC donated 100 gift cards for the bags. Finally, on November 11th, 2023, I was able to carry out my project. I had been planning this for months and I was both nervous and excited. Sydney was kind enough to be at the CDF office on a day that she does not normally work and was so supportive. We set up the office to pack the bags and then people started to show up to help. We were able to do the project and even though we were only going to make 100 bags, the group ended up filling about 150 bags in less than an hour! Sydney and I then did a community information talk to over 30 people about our experiences with T1D and answered a lot of questions. It was awesome to look out in the audience at my Scout friends, neighbors, teachers, and family.
Type 1 Diabetes teenager on soccer field
By Gracie Lambrecht January 9, 2024
Learn about a teenage T1D soccer player. Discover tips for managing blood sugar, using CGM and insulin pumps, and staying game-ready as an athlete with T1D.