Sarah was diagnosed with type 1 at the age of 7, 17 years ago, and also lives with multi drug-resistant epilepsy. She was diagnosed during a visit to the pediatrician.

After diagnosis, Sarah spent her summers at camp Nejeda, later becoming a counselor, which helped foster a good relationship with my diabetes as well as instill confidence. While in college, pursuing her BS in nursing, she began modeling and wanted her diabetes to be a focal point. This is when she started advocating more for type 1. Eventually, Sarah got to take part in amazing opportunities, such as opening the NASDAQ on World Diabetes Day as part of a Dexcom campaign.

Currently, Sarah is a nurse on a neuro/stroke step-down unit and loves the conversations that her diabetes tech starts.

This year, Sarah will be working towards becoming a certified diabetes care and education specialist.Sarah shares how it's essential for young people to see someone openly share the good, the bad, and the ugly of diabetes.

Sarah knows that she would be nowhere if not gifted her amazing family. Her parents came together with their strengths to keep little Sarah well. Sarah celebrates that she's able to wake up daily and do the things she does.

The Diabetes community means a great deal to Sarah. The comfort others have with reaching out and sharing with her is amazing. The DOC has been there for her through the ups, downs, and through grief.

During this recording, flowers are gifted to the Guarino family for their forever support during her diagnosis and continuing. Sarah's mother recently transitioned. She was and continues to be the answer to all of Sarah's "Whys."

Get to know Sara @runawaywithsara

On this episode, we get to smile with Arianna @ariannaiannaira

Arianna was diagnosed with T1D at age 11, more than 15 years ago. She also lives with PCOS. Ari is mother to the amazingly amazing Finn, who is two years old now.

During our conversation, Ari shares her gifts of life. This includes her sharing her new level of acceptance with newly diagnosed people by finding the diabetic online community. We also converse about grieving the life before, not only this diagnosis, but also of other obstacles we have endured.

Ari is a published research scientist in cancer research and a biologist with her BS from Lehigh University. She is also a creative who loves to sew and act. As she says, she is a Jack of All Trades, not a perfectionist. In school, she also minored in theatre and apparel design.

Recently, she enrolled in @Bluecirclehealth ,and this has helped her find the support team she needs.

My friend Arianna is someone we should all get to know.

Follow Ari on Instagram @ariannaiannaira⁠

On this episode we get to hear from Mary @t1dartistry

Mary is an ambassador for Eversense CGM and has been for 5 years! Mary was diagnosed with T1D at the age of 18, during her freshmen year of college.

On this episode Mary invites us into her world and her truths. This includes discussions regarding the birth of her son. Although, her the duration of her pregnancy was pretty smooth and she had the best glucose results, during the last few weeks things changed drastically.

Mary was given predisone at 37 weeks, which shot her blood sugar up! In turn, during her next stress test, she was told that her baby wasn't moving. Mary asked them to deliver her baby. She was denied, even though he weighed over 10lbs.

The next day, she went back and they delivered her baby, and his heart rate was only 25 bpm. He had meconium aspiration, which hardened his lungs and heart, and led to him not being able to breathe. Mary also had fibroids. She lost 2 liters of blood and ended up with Sheehan syndrome (when you lose your blood and pituitary strengths) and needed transfusions. Now, all of her hormones are injured forever because of that.

Throughout this conversation, Mary speaks to us! Everyone in the community needs to listen to the strength of this Queen!

On this episode, we head to the Midwest and visit Marcus in Cincinnati. Marcus was diagnosed with Type 1 Diabetes at the age of 15. This year marks Marcus' 25th year with Type 1 Diabetes (T1D).

His diagnosis was a true traumatic experience for a young, fit athlete, and for the first few days after diagnosis, he did fall into a state of slumber depression. This was until his dad tapped him on his shoulder and said, "Just listen."

25 years ago, Marcus' diagnosis was not what we see and know it to be today. He started with NPH and Regular insulin. There was no wiggle room back then. His parents were his greatest advocates during those early years.

He remembers making sure every time he went out of the house to go through his checklist of everything needed. Marcus owned his diabetes from day 1. A lot of this is because of his anger with this diagnosis.

25 years ago his mom was his CGM. She made sure that she understood what it looked like when his blood sugar would fluctuate.

Marcus and his wife were on the Netflix series "I Do," which aired in 2020, where he and his wife were given a second chance at their dream wedding.

Follow Marcus along his journey @marcouslacour

Step into the world of Jayla. Jayla is a 24-year-old Detroit native and recent graduate of Clark Atlanta University. With a career in radio and digital marketing, her aspiration is to become an influencer and advocate for individuals like her to thrive even with chronic illnesses such as Type 1 diabetes. Jayla was diagnosed with Type 1 Diabetes the summer before high school at the age of 14. With being diagnosed with Type 1 diabetes for 10 years, she’s navigated her health journey through community and advocacy throughout many of the rooms she’s stepped in. In the end she hopes to be able to teach others, reach out to others, and inspire others.

Jayla is the Miss Atlanta Clark University 2024-2025 and in May graduated Magna Cum Laude

Connect with Jayla on Instagram @indigoyah

In this episode, we journey to India to meet Khushi Ahuja, a global advocate for T1International. Diagnosed with type 1 diabetes at age 11, Khushi shares her personal story of navigating the challenges of her diagnosis, including an extended honeymoon period. She discusses the stigmas surrounding diabetes and the critical role community support has played in her journey. Khushi reveals how connecting with others who understand her struggles has been a lifeline, offering hope and empowerment. Her family has been instrumental in keeping her at her best, providing unwavering support. Join us as we explore the transformative power of community and the importance of mental health support in managing chronic conditions. #CommunitySupport #DiabetesAwareness #MentalHealthMatters

On this episode, we sit down with Sa'Ra, a passionate advocate and inspiring individual who has lived with Type 1 Diabetes since the age of five, 25 years ago. Sa'Ra's journey is deeply personal, as her mother's older sister, Joy, also had Type 1 Diabetes and passed away from complications at the young age of 43. Five years after her diagnosis, her baby sister (3 years younger) was diagnosed. Tune in for an empowering conversation that highlights the importance of support, love, and choosing joy in the face of adversity.

In 2019, Sa'Ra's advocacy continued when she spoke out publicly, which led to widespread media attention and connections to T1International. She was then invited to testify before the U.S. House Oversight and Reform Committee, where she passionately addressed the insulin pricing crisis.

Join us as we explore her journey of resilience, from childhood challenges to becoming a mother, and her unwavering commitment to advocacy.

Follow Sa'Ra via instagram @_SaRaJoycelyn @_SkipJoy

In this compelling episode of the Chronically Will podcast, we hear from Dee, a resilient Cuban-Jamaican born, Brooklyn-bred single mother, as she shares her journey of advocating for her daughter, Jayde Michele, who was diagnosed with type 1 diabetes at just two years old, only 6 years ago. Dee opens up about the challenges and triumphs of navigating the educational system, ensuring Jayde receives the support she needs to thrive. From managing blood sugar levels during school activities to fostering a community of understanding and support, Dee's story is a testament to the power of informed advocacy and unwavering love. Join us to explore how Dee's cultural roots and personal strength shape her approach to advocacy and learn how you can make a difference in your community.

Follow Jayde Michele's journey

Instagram @type1derfullyme