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JDRF’s Mental Health and Diabetes Strategy – where we are now  May is Mental Health Awareness month, a national movement to raise awareness of the importance of mental health, and […]

Every two years, more than 160 children living with type 1 diabetes (T1D) gather in Washington, D.C., to meet face-to-face with some of the top decision-makers in the U.S. government. […]

Guest post from Devin Myers, RN Devin Myers is a health writer as well as a registered nurse. She has experience in various areas of nursing including critical care and hemodialysis. […]

Training the next generation of researchers and clinicians in type 1 diabetes (T1D) is a central goal of JDRF’s global research strategy. Support of these emerging leaders is essential to […]

Hi, I’m Joanna! Born and raised in Ottawa, I now call Toronto my home. I’m passionate about health and fitness, PR/communications, all things food, travel and family! When were you […]

I was living in Winnipeg; I’ve spent my whole life here. I was diagnosed at the age of 6, spring of 1974, it was the May long weekend. I was […]

National Volunteer Week takes place from April 24-30, 2022, as organizations across the country celebrate those who generously donate their time and talents to their community.   The National Volunteer Week […]

The type 1 diabetes (T1D) community has always embraced new technology – with insulin pumps, continuous glucose monitors (CGMs), flash glucose monitors (FGMs), and a variety of T1D-focused apps rapidly becoming essential tools for many people. It’s no surprise, then, that the T1D community has quickly adapted to accessing healthcare virtually.

Throughout my career as a Diabetes Nurse Educator I have been asked all kinds of questions from people living with type 1 diabetes and their families. I’ve taken this opportunity to answer the most common questions about type 1 diabetes management. Here are just a few of the ones I hear most frequently.

The first few months after Mirella Gallo’s 11-year-old daughter, Isabella, received a type 1 diabetes (T1D) diagnosis were very hard for her. “We were in shock and had no idea what it meant for her or our family”. With the support of Isabella’s nurses and doctors, the family learned how T1D would impact her day-to-day routine and her future. “We came to the realization that my daughter’s life would never be the same and that until a cure was found, she would be insulin dependent,” says Mirella.