Episodios

  • Episode 101: Angel's T1D Theme Music
    Dec 22 2025

    On this episode, we get to sit down with Angel @angelverses. Angel is a hip hop artist from Ohio who expresses and voices his emotions about living with diabetes through his music and skits. People may not relate to what he goes through with diabetes, but they will relate to the music and the messages.

    Angel was diagnosed with T1D almost 18 years ago at 14 years young. He is the youngest of 3. Angel was diagnosed while on vacation with his aunt. His Auntie noticed his changes.


    In this episode, we recognize and give flowers to Angel's family of love and support.

    Más Menos
    57 m
  • Episode 100: Screen It!
    Nov 8 2025

    On this episode we speak with Leah. Leah is a research assistant at Trialnet.org. but is also an MPH candidate in Epidemiology. Her drive comes from her family and friends. She's seen T1D up close and is passionate about early detection and making research feel human, accessible, and community powered. Her allyship speaks volumes!

    At Trialnet they test family members of people living with T1D for risks of being diagnosed. They start testing as young as the age of 2 for T1D autoantibodies, all the way up to the

    age of 40 if you have direct family members with T1D.


    Trial Net contributed greatly to the treatment of Teplizomab, Tzield® (teplizumab) which is s a CD3-directed monoclonal antibody approved for delaying the onset of stage 3 type 1 diabetes in adults and children aged 8 years and older who have Stage 2 type 1 diabetes. It works by attaching to proteins on immune cells, helping to protect the insulin-producing cells in the pancreas from being attacked. Tzield was approved in the US in November 2022 and is the first

    disease-modifying therapy for autoimmune type 1 diabetes.

    For more detailed information, you can refer to the official Tzield website or the FDA label


    During our conversation we speak about the misdiagnosis of adults with diabetes and the challenges in care because of the proper education and tools not being given to them. At Trial Net, instead of continuously monitoring a finger pricks, that we know the child hates, and parents hate as well, if you live with T1Dyou can just have this simple lab drawn to determine their future risks. It's a win-win for everyone! It's a simple blood withdrawal; it's not a lot. It's no more than a typical blood withdrawal from a lab. If they can get this done, you will have immediate direct knowledge of what to look for moving forward. Is my child going to have it or if

    they're not? Right.


    Visit Trialnet.org to get screened. It's 100% Free.

    Más Menos
    42 m
  • Episode 99: Marlaina's Reason Why
    Nov 5 2025

    On this episode we get to hear from Marlaina Goedel. 14 months ago, Marlaina was fully, functionally cured of living with Type 1 diabetes. The procedure was the first of it's kind in the world, performed by Dr. Pior Witkowski at UC Med. With this process they inserted donor islet cells into Marlaina's liver and used the new monoclonal antibody Tegoprubart as the main antirejection infusion.


    After 25 years of living with Type 1 and having dealt with too many hospitals stays to recall and far too many times having to be rescued by her loved ones, including her daughter she no longer lives with T1D.

    During this episode Marlaina shares answers to every question that you could think of answering. And as Marlaina mentioned, "We did it!" She took this step for us all, not because only her own experience with diabetes.


    Marlaina was a pure gem to record with and her story is story of hope for everyone. To-date there have been 12 people in the clinical trial after Marlaina's successful transplant. So far, everyone is on schedule to be insulin independent like Marlaina (6 in total during the second phase already are).


    You can follow Marlaina on Instagram @ilovemiley94

    Find her on Facebook at Marlaina Goedel


    Donate to support Marlaina continue this new life

    Más Menos
    1 h y 42 m
  • Episode 98: Serial Volunteer
    Oct 30 2025

    On this episode, we hear from Jisel. Jisel has been living with Type 1 Diabetes for 22 years, having been diagnosed near the end of her sophomore year of high school at 15 in 2003. Jisel is a wife, mom of two, and a self-proclaimed Serial Volunteer! Whether it's school events, work-related, or with her people, in the T1D community, you can find Jisel always lending a hand, foot, time, and dedication to the communities she serves.


    In this episode, Jisel shares everything else, plus diabetes, including how challenging it was for a 15-year-old young girl learning to advocate for herself as a newly diagnosed Type 1, and as an adult throughout her pregnancies.


    Jisel is not only someone you should get to know but she's someone that is making things happen in the diabetes space!


    Follow Jisel @jisel.p_andt1d

    Más Menos
    1 h y 42 m
  • Episode 97: Pt 2 - Now I'm Hot They All On Me
    Oct 1 2025

    In Pt 2, we dive more into Krislin's new life without T1D and CKD as of June 29, 2025.

    Diagnosed with Type 1 Diabetes at just 9 years old, ⁠Krislin⁠’s life was forever changed. By age 22, she faced diabetic retinopathy. At 26, Chronic Kidney Disease entered the picture. And yet, on the 20th anniversary of her diagnosis, something extraordinary happened. By age 29, ⁠Krislin⁠ was gifted the chance at a new life.


    Her story is one of resilience, heartbreak, and hope. So, grab your tissues and walk with Krislin. Love with Krislin. Live with Krislin. Cry with Krislin. Heal with Krislin.

    Her mother always told her, “You have diabetes. Diabetes doesn’t have you.” And today, that truth has never been more real, because diabetes no longer has her.

    In 5th grade, Krislin’s diagnosis took a heavy toll on her young body. The innocent question, “Why me?” evolved into painful self-blame. “What did I do to deserve this? What did I do that was bad?” Even at 9, classmates asked cruel questions like, “When are you gonna die?”—questions that haunted her for years and silenced her voice about her condition.

    She carried guilt. She felt alone. Her childhood was marked by hospital stays and isolation. For years, she didn’t speak about her diabetes, not out of denial, but out of pain.

    But three months ago, Krislin woke up freer than she had ever felt. And today, her heart is with the community she leaves behind—the warriors who continue the fight against diabetes every single day.


    You’ll laugh. You’ll cry. I know I did. Because this isn’t just Krislin’s story. It's a love letter to every person living with diabetes. To every parent, every friend, every fighter. This is for you.


    Follow Krislin's Journey on Instagram ⁠@krislinwins⁠

    Más Menos
    1 h y 18 m
  • Episode 96: Pt 1 - Back Then They Didn't Want Me
    Oct 1 2025

    Diagnosed with Type 1 Diabetes at just 9 years old, Krislin’s life was forever changed. By age 22, she faced diabetic retinopathy. At 26, Chronic Kidney Disease entered the picture. And yet, on the 20th anniversary of her diagnosis, something extraordinary happened. By age 29, Krislin was gifted the chance at a new life.


    Her story is one of resilience, heartbreak, and hope. So, grab your tissues and walk with Krislin. Love with Krislin. Live with Krislin. Cry with Krislin. Heal with Krislin.

    Her mother always told her, “You have diabetes. Diabetes doesn’t have you.” And today, that truth has never been more real, because diabetes no longer has her.

    In 5th grade, Krislin’s diagnosis took a heavy toll on her young body. The innocent question, “Why me?” evolved into painful self-blame. “What did I do to deserve this? What did I do that was bad?” Even at 9, classmates asked cruel questions like, “When are you gonna die?”—questions that haunted her for years and silenced her voice about her condition.

    She carried guilt. She felt alone. Her childhood was marked by hospital stays and isolation. For years, she didn’t speak about her diabetes, not out of denial, but out of pain.

    But three months ago, Krislin woke up freer than she had ever felt. And today, her heart is with the community she leaves behind—the warriors who continue the fight against diabetes every single day.


    You’ll laugh. You’ll cry. I know I did. Because this isn’t just Krislin’s story. It’s a love letter to every person living with diabetes. To every parent, every friend, every fighter. This is for you.








    Más Menos
    58 m
  • Episode 95: Hope Is Home
    Sep 30 2025

    On this episode, we travel to Aruba to meet with Nurianne. Nurianne was diagnosed with T1D at 19. She is a graduate of the University of Aruba. Nuri worked as a full-time lecturer at the University of Aruba and was a researcher for the local Foundation of diabetes in Aruba concerning diabetes management on the island. Nurianne is passionate about helping others, as she started volunteering at the age of 12 and has been active in many social projects and programs since then. Nurianne has a special interest in children and their development.

    Since her diabetes diagnosis, she has dedicated herself to researching diabetes and health conditions. Nurianne aims at motivating and coaching people living with diabetes.


    In 2018 Nurianne participated as the representative of Aruba in the Miss World pageant and her advocacy focused on health for children and youngsters. In 2019 Nurianne joined the YLD program by the International Diabetes Federation to gain more knowledge in the field of diabetes so she can develop the appropriate skills to support others and do research.

    Nurianne has been a Ph.D. student in the field of Public Administration since September 2023. Her Ph.D. research is an extension of her passion for advocating for health and specifically invisible disabilities. Nurianne plans on conducting research on how communities of experience (support systems) can enhance health outcomes of people with hidden disabilities such as diabetes, ADHD, and endometriosis in Aruba.

    Más Menos
    1 h
  • Episode 94: On Bad Days We Smile
    Sep 25 2025

    On this episode we get to hear from Anchal . Anchal visits the Podcast from India. Anchal is 16 years young and was diagnosed with Type 1 Diabetes 7 years ago at the age of 9. Anchal, in most ways, is your typical teenager. She enjoys dancing, doing her makeup, and dressing up. These things are what bring her peace of mind when everything gets too much.

    Anchal aspires to be someone who can encourage and motivate more people like her. She wants to make life a little easier for them in any way possible. Anchal also hopes to become a clinical psychologist! She remembers how traumatic her diagnosis was and continues to be for her and her family, specifically her parents, who are also her superheroes, and how much therapy can help newly diagnosed families.


    During this conversation Anchal opens up about being a teen and how misinformed others are about her living with diabetes and how it does anger her at times.


    Anchal is someone we should all get to know because she will take on and over the world!!

    Más Menos
    53 m
adbl_web_global_use_to_activate_DT_webcro_1694_expandible_banner_T1