Timothy McDonald, 27 years
type 1 · United States
Hey everyone! My name is Timothy McDonald. I'm 27 years old, and currently living in United States. I've been living with type 1 diabetes for 22 years.
Hello! Who are you? And tell us a little bit more about your diabetes.
I was diagnosed at 5 years old, so I had to grow up with it. My mom made sure to inform everyone she met about my condition (teachers, restaurant staff, cashiers, random people in public, etc.) However, I tried to be a bit more discreet with it. Growing up, I wasn’t allowed to bring my blood sugar kit, insulin, or even glucose tabs with me into the classroom. I had to run all the way across the school to the nurse if I ever ran into an issue with diabetes. Looking back, this probably wasn’t the safest thing.
For my parents, it was probably mostly emotionally hard. I don’t remember it too much, but I’m sure they were devastated. For me, it was just life. My personal biggest issue is financial. Even after 22 years, I do not have a pump or CGM, simply because I can’t afford them.
“My mom made sure to inform everyone she met about my condition.”
Timothy McDonald, United States
Your treatment
How do you treat your diabetes, did a lot change over the past years and are you able to manage it well?
Currently, I do things old school with multiple daily injections. I am using Humalog and Tresiba insulin. I have used quite a few, but it seems I have to take new insulins every time my insurance changes. The ones I remember include Regular, Lente, Ultralente, Humalog, Novolog, Lantus, and Tresiba.
Humalog and Lantus came out, which really helped with my control as a kid. Being on Regular and Ultralente at five years old was tough!
I don’t think I treat my diabetes badly at all, considering my relatively lax approach to treatment. In my teens, I got most of my support from my family or the internet. For some reason, my parents stopped taking me to the endocrinologist altogether from the ages of 14-18, so I had to fend for myself and get information wherever I could, especially if I disagreed with my parents about something diabetes related. Currently, I take care of it mostly by myself.
I have a doctor who fills prescriptions, but they don’t offer much detailed advice. I have my girlfriend, who may not know a lot about diabetes, but she’s great for emotional support.
Can you recognize the symptoms of a low/high blood sugar? Do you test often and can you tell a bit more about your experiences with low blood sugar?
Yes, I can recognize them. Lows come with various symptoms, including weakness, an adrenaline rush, shakiness, cold sweats, and splotchy vision. The weakness and adrenaline rush come with pretty much every low; the others are usually reserved for the 50s and below. High blood sugar gives me less pronounced symptoms that I’m less likely to notice. I only seem to get thirsty, blurred vision and headaches.
I test myself anywhere from 3 to 10 times a day. Some days are easy if I don’t take any risks, don’t exercise, and don’t eat any weird foods. Others have me on my toes all day, chasing highs and lows.
I eat a bunch of sugary food to treat a hypo, feel bad about myself 30 minutes later, notice my blood sugar is going higher than I’d like, and correct for the high.

Food and diet
How does your diabetes affect your eating and do you find being on a diet restrictive?
I work 2nd shift, so my eating schedule is pushed back. Breakfast is generally something small, like an English muffin, around 11 am. Lunch is around 5 pm and more varied, but I will admit that I eat more fast food than I probably should. I eat dinner around 1 am, which is often some kind of chicken dish. Occasionally, I’ll have something like a granola bar between lunch and dinner. I sometimes skip meals.
I vary my insulin dose for anything I eat because I base my dosages on the amount of carbs in the dish. High-fat/high-carb foods like pizza usually require a small shot before I eat and a larger dose after I finish. After 22 years, it’s not really a diet—it’s just what I eat.
I probably drink around 2 liters a day.
It’s frustrating with people not understanding. It makes me want to eat more of it just to spite them.
Do you believe that a plant based diet can improve diabetes? Did you ever experiment with this?
I’ve never tried it, so I wouldn’t know.
Do you have a hard time eating out in a restaurant? And what are you thoughts on making this easier?
The only types of restaurants I have issues with are Italian restaurants. It’s so easy to eat over 100 carbs from a single dish. I would prefer it if restaurants had accessible nutrition info.
“It’s frustrating with people not understanding. It makes me want to eat more of it just to spite them.”
Timothy McDonald, United States
Exercise and work
Does your diabetes restrict you from exercise or your daily job?
Currently, I mainly run and do body weight exercises a few times a week. In the past, I ran track, and at one point, I was a caving instructor.
I am a clean room technician for a precision optics manufacturer. Other than not being able to eat in the clean room, it doesn’t really affect my diabetes one way or the other.
Final
Do you have any positive or negative effects because of your diabetes?
Honestly, not really. I mainly just count my carbs, take my insulin accordingly, and exercise when possible.
The best part is that I can use the “my blood sugar is low” excuse to get out of anything. Who’s going to argue with that? The hardest part is my ever-changing insulin needs. It seems like any small change in my routine will cause me to have to change things around.
Nothing quite kills the mood, like your blood sugar dropping to 45.
I still live with my mom, so it is very difficult to try new diets to manage my diabetes better. If I buy something she doesn’t like, she’ll complain until I cave in and buy the same old stuff.
What is the best advice that you can give to non-diabetics, new diagnosed diabetics and diabetics?
For the most part I can do the same things you can, so don’t worry about me, I got this.
It gets boring. You may be scared and drowning in a tidal wave of information now, but you’ll eventually be able to do all of this without thinking.
Learn how to guesstimate carbs. Not everywhere has nutrition labels or a scale, so being able to eyeball things makes things a lot easier.
What would you ask the other diabetics?
What advancement in diabetes research are you most looking forward to?
Share your thoughts in the comments. I cannot wait to hear from you!
Ready to share your story with the world?
At Diabetic Me, we dive into the real-life of people living with diabetes, uncovering the challenges, triumphs, and everything in between.
If this story resonated with you, why not stay connected? Join our mailing list to discover more inspiring journeys.
Have a story of your own to share? We would love to hear it. Share your story.
4 comments
Moderated · newest conversations first
Share what worked for you. We remove individual medical advice, dosing instructions and anything selling a cure.
More stories
Matt Vande Vegte, 30 years
I am a certified personal trainer, nutritionist, author, and speaker. None of these things would have ever been possible without type 1 diabetes, which has allowed me to see the silver lining in some of life’s most difficult times and remain grateful.
Living with diabetes for 10 years
Natalia Skuza, 22 years
I was diagnosed just after my 21st birthday. I had been sick for years and doctors did not pick up on me having diabetes, until after my 21st I said; “enough is enough”. I went back for more checks, and I finally was diagnosed. It felt like a long time coming.
Living with diabetes for 1 year
Andrew Burgess, 29 years
I’ve faced a lot of hurdles throughout my life. The biggest thing is to stay less stressed, not care about anyone else’s drama, be yourself, be a diabetic, and you will live a great diabetic life. Don’t be in denial when you have time to overcome things.
Living with diabetes for 23 years
wow didn’t know that diabetes could be so tough, especially at school. why isnt there better support for this? seems like something should be done so kids dont have to stress about getting to their insulin.
hey Ely, reading your story really hit home for me. my daughter got diagnosed last year and it’s been a roller coaster for us both. can’t believe you had to go all the way across school for insulin, that must have been tough. we’ve had our own struggles especially with the cost of all the supplies. i really appreciate u sharing ur experience, makes me feel less alone in this. hope you find a way to afford the pump and cgm soon, sending u positive vibes!
Emily, your spirit is awesome! Ely’s story and yours reminds us we’re all in this together. Keep pushing, the community’s here for you.
has anyone found ways to make diabetes care more affordable? sharing tips could help a lot!