Fund A Cure with Paul and Alanna Nerland | Breakthrough T1D Minneapolis Gala 2024

About

In 2018, Alanna and I first crossed paths, and over time, I took it upon myself to educate Alanna about Type-1 diabetes, a condition with which Alanna was initially unfamiliar. Throughout our relationship, my parents had been exceptionally supportive, participating in charity walks and rides, with my mother continuing to advocate passionately for Breakthrough T1D. Their support was unwavering; they never intruded on my daily management of the condition, such as dosing or dietary habits. Alanna mirrored this support with similar dedication, packing snacks for low blood sugar episodes, preparing Gatorade for overnight needs, and even joining me and my dad on a JDRF bike ride in Saratoga Springs. I was the sole person in my immediate circle affected by T1D—until September 2020.

By then, Alanna and I had been living together for a while and in late September she wasn’t feeling well for about a week straight – lethargic, thirsty, getting up to use the bathroom multiple times in the middle of the night. She had tested positive for COVID and did not complain much about how she felt, so diabetes never even crossed my mind. However, when I checked her blood sugar one Sunday, the reading was 562. The revelation was overwhelming, as it seemed almost inconceivable that Alanna could also have Type-1 diabetes given the improbability. Coupled with the uncertainty surrounding COVID-19’s impact, there was hope it might be a temporary spike. Alanna was taken to the hospital by my sister and admitted. It absolutely crushed me that I was unable to be by her side due to COVID-19 restrictions. Reflecting on my own diagnosis fifteen years prior, which had been a traumatic experience even with family by my side, the situation was particularly agonizing.

Since her diagnosis, Alanna has exhibited remarkable grace. Like many, she faced the challenges of navigating the healthcare system and managing the high costs associated with insulin and supplies. Together, Alanna and I now manage our diabetes, supported by Breakthrough T1D, an organization devoted to Type-1 diabetes across the United States. Their shared aspiration is to find a cure and live free from the constant burden of diabetes. Both wear their diabetes, Alanna quite literally, with pride and are eager to educate others about the condition.

Breakthrough T1D has been an invaluable support system throughout the years, and its dedication to finding a cure is what fuels their commitment. The organization’s efforts in funding research provide hope for achieving their dream of living part of their lives without Type-1 diabetes. I have always enjoyed attending Breakthrough T1D events for the opportunity to connect with others who understand the lived experience of diabetes. Engaging in discussions about new technologies, different types of insulin, and sharing experiences with fellow T1Ds has been profoundly meaningful. Even simply witnessing other T1D’s wearing their CGMs or giving themselves injections provides an odd sense of connection. One thing I particularly appreciate about Breakthrough T1D is the work that my mother does with the advocacy group. I truly admire their steadfast commitment to ensuring that the Special Diabetes Fund continues to finance research and treatments. The Breakthrough T1D community, though small, is fiercely passionate and supportive, which is why Alanna and I remain devoted in our support of the organization.