about the link
who we are
The Diabetes Link is the only national organization built exclusively for young adults living with all types of diabetes. This is a stage of life defined by transition: leaving home, starting school or a first job, and building independence. Managing diabetes through all of it looks nothing like managing it as a kid with parents nearby, or as an adult with a settled routine.
That in-between is where we live.
Through peer community, campus chapters, and resources built by and for young adults, we meet people where they are, at four-year universities, community colleges, trade schools, online, and in person.
Our community is built on real stories and real listening. Peers who've lived it lead our programs, shape our content, and set the tone for what support actually looks like at this age, because we know that the people who understand this stage best are the ones going through it.
our story
The Link was founded in 2009 by Christina Roth, who was diagnosed with type 1 diabetes at 14. As a student at the University of Massachusetts, she felt isolated. Her peers did not understand what it took to juggle classes, diabetes, extracurriculars, and a social life. She started the first chapter that year and quickly found other students like herself on her campus and across the country. As students founded chapters nationwide, the organization, then called College Diabetes Network, received its 501(c)(3) status in late 2010.
What began as a student group on a single campus revealed a much larger gap. Young adults making this major life transition had no dedicated support. Christina ran the organization after hours until 2012, when she left her job to lead it full-time. She stepped down as CEO in 2023. Board member Marie Schiller served as Interim CEO until Manuel (Manny) Hernández was named CEO in November 2024.
In 2022, the organization rebranded as The Diabetes Link to reflect a broader mission: serving all young adults with diabetes, regardless of educational context or type of diabetes.
Peer-centered.
Young adults are best supported by other young adults who have lived the transition.
Inclusive by design.
All types of diabetes. All communities. All life paths.
Evidence-informed.
Our programs and advocacy are grounded in research and the lived experience of young adults and their support networks.
where we are going
Establish national leadership as the authentic young adult voice.
Build the emotional trust and educational presence that make The Link the first place a young adult turns at diagnosis and beyond.
Expand to serve underinsured and underresourced young adults.
Reach beyond traditional campuses into community colleges, trade schools, and underserved communities.
Build operational agility and programmatic focus.
Partner strategically, prioritize what works, and respond quickly to a changing landscape.
Build a sustainable and diversified funding model.
Broaden the revenue base through individual gifts, grants, sponsorships, and earned income.
Become a best-in-class workplace.
Attract, retain, and develop top talent through competitive compensation, clear growth pathways, and a culture where every team member can thrive.