Meet the Colorado doctor helping Hispanic families with Type 1 diabetes

Graham Daugherty • July 25, 2016

By Joanne Davidso


First published by The Denver Post. See the original article by clicking here.


The roads that led Dr. Andrea Gerard-Gonzalez to the Barbara Davis Center for Diabetes on the Anschutz Medical Campus in Aurora weren’t all eight-lane expressways.

A few of them weren’t even covered in asphalt.


But each can be seen as a metaphor in the journey that brought her to Colorado, where she is making an important difference in the health of youngsters of Latin descent who are Type 1 diabetics.

As director of the Barbara Davis Center’s Hispanic/Latino Diabetes Care Team, Gerard-Gonzalez continues to develop and expand culturally appropriate ways to not only improve the delivery of diabetes care for the 800 youngsters with whom her team works, but to educate family members about the disease, eliminate stigmas and build a sense of community.

A woman in a floral shirt is taking a selfie in an office.

Ultimately, the 36-year-old endocrinologist hopes to see medical facilities in other cities adopt the model on which her program is based; she is also working to modify it for other ethnic cultures.


“In the United States, Hispanic children under-utilize diabetes care technology and have higher HbA1c levels than non-Hispanic white children,” explains Dr. Marian Rewers, the Barbara Davis Center’s executive director. “This is likely related to language barriers, cultural barriers and the limited availability of Spanish-speaking staff and resources.”nn(HbA1c, or glycated hemoglobin levels, are determined through a blood test that gives doctors an overall picture of a patient’s average blood-sugar levels over a period of weeks or months).


“It’s painful for me to see such a disparity in outcomes,” Gerard-Gonzalez says. “Just translating printed materials isn’t enough. You have to work with the people in ways in which they are comfortable.”


After graduating first in her class from the prestigious Universidad La Salle School of Medicine in her native Mexico City, Gerard-Gonzalez set out for Chiapas, one of Mexico’s southernmost states, to complete a two-year internship at a tiny clinic ill-equipped to meet anything other than the most basic medical needs.


It was located in what she says was an “incredibly beautiful area … out in the middle of nowhere.” The nearest hospital was two hours away, reached by negotiating a bumpy, dusty — or muddy — unpaved road where farm animals roamed freely.


Little did she know how well the geographic and cultural challenges she faced would prepare her for her current job.


“You arrive filled with joy and expectations about how you’re going to change things for the better, help nourish the society. But then you find that you don’t understand their language or culture — it was a mostly indigenous population and not everyone spoke Spanish — and that they don’t want you and don’t trust you.”

Three women and a boy are posing for a picture in a park.

Establishing trust and respect was difficult, she admits in an interview conducted during her lunch break in a conference room at the Barbara Davis Center.


She gained it after two touch-and-go medical emergencies — one in which she saved the life of both mother and baby during a complicated delivery, and the other involving a child who arrived at her clinic near death because of untreated diabetes. She was able to convince the child’s parents that he needed insulin to survive and that hospitals shouldn’t be seen as scary places.

A young girl with a tattoo on her arm is wearing a pink watch.

“One of the greatest things that I learned in Chiapas is that there are many right ways to do things, not just the one way you think is right. (That experience) taught me that we need to work with the culture of the communities we serve and make things appropriate for them.”


Which is exactly what she is doing at the Barbara Davis Center.

The “unique and innovative model” that she and her team developed includes family-style shared medical appointments, educational materials written in Spanish and activities that are culturally sensitive and appropriate. The goal is to reduce costs associated with treating high-risk patients and build a strong sense of community within Colorado Latino patients with Type 1 diabetes.


“We alternate one-on-one visits with 45-minute sessions where Spanish-speaking professionals talk about things like carb counting, healthy eating and the importance of exercise.”


At first, she said, “We thought 45 minutes would be too much time because Latin families — and we have patients not just from Mexico but from Puerto Rico, Cuba and Guatemala — tend to be very private about their personal stuff. They might not know what diabetes is, and so a parent can feel guilty because their child has it. Which is what we want to eliminate.”


To her surprise and delight, “The conversation never stopped, even when the 45 minutes were up. They’d leave the building, but we’d see them continuing to chat on the sidewalk and in the parking lot.”


When her internship in Chiapas ended, Gerard-Gonzalez and her husband, Alejandro Ayestarán, a civil engineer, made the difficult decision to leave Mexico and move to Miami, where she joined the pediatrics staff at Miami Children’s Hospital.


“It was very hard to leave our loved ones behind,” she admits, “but my husband wanted to get an MBA and I had this great opportunity to get further training at one of the top children’s hospitals in the U.S.”


From Miami, the couple moved with their dog, Emma, to California, where she completed a fellowship in endocrinology at the University of California San Francisco. Three years ago, she gave birth to twins Sofia and Alex.


At the conclusion of her fellowship she was recruited by the Barbara Davis Center and the family moved to Colorado.


It’s a move she does not regret.


“I would have been a good doctor in Mexico but I might not have been able to make the impact I wanted to have. The Latin people are proud people and they don’t want to be judged, so we have to make them feel strong, to better understand diabetes and eliminate any guilt they may feel because their child has diabetes. We are able to do that here at the Barbara Davis Center.”


Joanne Davidson was The Denver Post’s society editor for 29 years before retiring in July, 2015. She quickly discovered she wasn’t ready for the rocking chair, so she dusted off her evening gowns and returned to the paper as a freelance reporter, writing feature stories and covering charitable fundraising events in the metro area. When she’s not attending a gala, you can find her out walking her dogs or sampling the food in one of Denver’s great restaurants.

A woman is doing a split with the words if i can just inspire one person
By Sasha Amiscaray April 15, 2026
TL;DR After 15 years of living with type 1 diabetes, Sasha shares her journey from diagnosis and denial to acceptance, advocacy, and a career in healthcare. Through challenges like fear of injections, managing diabetes as an athlete, and navigating school and college, she discovered strength, community, and purpose. Her story shows that while diabetes is difficult, it can also shape identity, open doors, and lead to meaningful connections and opportunities.
A black and white photo of a person with an insulin pump on their stomach
By Dr. Holly O'Donnell April 3, 2026
Type 1 diabetes affects mental health in youth and families. Learn about risks like depression, anxiety, and distress, plus support options and when to seek help.
A young boy in a white sweater is standing next to a cabinet.
By R. Paul Wadwa, MD, Professor of Pediatrics at the BDC April 2, 2026
Type 1 diabetes is often misdiagnosed as flu, UTI, or viral illness. Learn key symptoms, DKA warning signs, and when to ask your doctor for testing to avoid delays.
Author and type 1  diabetic Madeline in a research lab
By Madeline VanOrman March 20, 2026
Follow one patient’s journey with type 1 diabetes from childhood diagnosis to college life, sharing challenges, independence, and finding support along the way.
A cartoon illustration of a white monster with horns waving.
By Cheryl Lebsock March 18, 2026
A parent shares how naming type 1 diabetes “Frank” and reframing it helped protect their child’s identity, improve mental health, and strengthen family support.
Three young type 1 girls with CGMs on their arms.
By CDF Staff March 18, 2026
Donate your Colorado state tax refund to the Children’s Diabetes Foundation. Learn how to use form DR 0104CH to support T1D patients and families.
Young girl with her blood glucose monitor and insulin pump
By Hali Broncucia, Research Scientist at the Barbara Davis Center for Diabetes March 16, 2026
Learn the three stages of type 1 diabetes and why early screening matters, including how detection can reduce DKA risk and delay onset with new therapies.
A group of people are posing for a picture in a living room.
By Stacy Robinson June 14, 2024
With Father’s Day just around the corner, I am thinking about my dad even more than I usually do. He was a special man who lived a remarkable, impactful life right up until the day he passed away at the age of 98, a little over a year and a half ago. He was a decorated World War II veteran, a bookie in Vegas during the Rat Pack era who married the love of his life between rounds of a prize fight, and who later went on to become a successful entrepreneur. Most importantly though, he was a devoted husband, father and grandfather.
A man and a woman are posing for a picture in a parking lot.
By Lindsay Klatt June 14, 2024
Author: Lindsay Klatt Being the dad of two daughters already has its highs and lows; having one of them (who admittedly was already a little feisty) diagnosed with type 1 diabetes makes him a saint. My wonderful dad navigated these challenges with such love and grace. As we approach Father’s Day and as I recently celebrated my 27th Diaversary, I reflect on the things he deserves to be thanked for. There are too many to count and no way to properly express gratitude for the additional struggles type 1 fathers face, but here’s a toast to a few of the things etched on my heart: Cheers to my dad who, when I was diagnosed, had the best balance of acknowledging the sadness of the event and being encouraging for the future. It made me feel seen to see him upset, and to see him determined. He has always maintained that balance I am so grateful for.