Hello. I am Calla Michalski, and I am a Type 1 Diabetic.
I have been suffering from this disease since I was just 10 years old.
I would like to express how difficult it is to live with Type 1 Diabetes. In no way can I say I have good control, but in order to gain better control of one’s sugar level, you must learn, and understand other people’s experiences. I try to avoid high and low blood sugars, but that is not always the case! I am just a typical diabetic, and I am just trying to make it through another normal day.
In 1998, I went to the doctor with my mom for my 5th grade check-up. Shortly after talking to him, the doctor told her that my blood sugar level was slightly elevated. He advised her to call my dad, get me to eat some sugar and then go to the emergency room. I remember stopping at a small little diner, eating the biggest piece of cheesecake in my life, and then going to the hospital. At that point, I was just happy to have my parents together, not arguing, and not going to school.
The doctors were frantically waiting for us to arrive. We casually walked in. I was put in the ER and remember hearing people next to me screaming after just getting into a car accident. The one of their friends didn’t make it. I wondered, why I am I here? What could be so wrong with me that I am in here next to all of this?
The doctors drew some blood. They ran a bunch of tests. They pricked my fingers a million and one times over. And gave me shots like it was going out of style. They asked a million questions:
- “Have you been drinking a lot?” — Now that you mention it, yes.
- “Have you been going to the bathroom a lot?” — I’ve been waking up 4-5 times per night, but didn’t think anything of it.
- “Have you started your menstrual cycles yet?” — My mom chimed in, “No doctor, she has not.”
Then, the doctor asked me if I knew what “diabetes” was? I remember responding, “I’ve heard of it, but I don’t know…” He started to explain to me and my parents that my blood sugar level was 630 mg/dL. I had no idea what that meant. I was then told I would have to take insulin shots multiple times per day and check my blood sugar before each meal for the rest of my life.
I was hospitalized for two weeks, and was given the training I would need for the rest of my life! The doctors would not discharge me until both my parents gave me a shot of insulin, and learned how to draw it up properly. My mom was hesitant. My dad is needle phobic. Since then, that has been the first, and only, shot either of them have given me! (This was the early days and insulin pumps were just starting to come out…. so there was no talk about it yet.)
In 2001, I began to participate in the JDRF Walk to Cure Diabetes, and created my own team called “Calla’s Crusaders.” Our goal is to raise money for funding the advancements in medical research for Type 1 (Juvenile) Diabetes and to hopefully, one day, find a cure! Click here if you’d like to learn more about my team or make a donation to JDRF to help improve the lives of those living with type 1 diabetes.
In 2006, I started on the OmniPod Insulin Pump. It was, and still currently is, the only insulin pump without any tubes or wires. The meter reads my blood sugar level and wirelessly communicates with the pump/pod attached to my body to give me the appropriate amount of insulin. I change the pump/pod every 3 days.
There is a small tube inside of the pump/pod that constantly gives me insulin. I bolus, or give myself a boost of insulin, each time before I eat in order to avoid a high blood sugar. If I don’t eat or snack regularly, I get low blood sugars. My insulin pump gives me freedom and I no longer need to take up to 6 shots per day! Click here to watch a video on how to change my OmniPod Insulin Pump.
In 2012, I started using the Dexcom Continuous Glucose Monitor (CGM). The receiver part looks like an old iPod turned sideways, but instead of playing music, it shows me a graph of where my blood sugars have been, where they are approximately at now, and in which direction they are headed.
I wear a small sensor and transmitter on a fatty tissue area of my body. The sensor is the sticky part that adheres to my body. The sensors get changed approximately every 7 days, even though I have worn it quite a bit longer. The transmitter is the grey part that sticks out and looks like a battery. The transmitter transmits my blood sugars wirelessly to the receiver.
The Dexcom has become quite the little lifesaver as it has woken me (and my husband) up numerous times throughout the night. It has helped me avoid many high and low blood sugars. It has also brought my hemoglobin a1C number down significantly. Click here to see how I change my Dexcom CGM sensor and transmitter.
My husband is a great big part of my life, and has helped me to gain better control of my diabetes. He wakes me up every morning to make sure I check my blood sugars, and is on top of my case when I eat things I shouldn’t be eating. In this blog, you may see me refer to him as my boyfriend or fiancé (as of 5/28/13), but that is simply because that particular post was before we were married (as of 8/8/14). They are all the same guy, I swear!
If you would like to participate in raising Diabetes awareness, or join in my efforts to support JDRF, please don’t hesitate to get in contact with me! I would also love to hear your stories in managing Type 1 Diabetes.