For those who have a chronic illness like Type 1 diabetes, a natural disaster of this magnitude offers a whole new set of challenges like access to supplies, stress management and extra care precautions. 

We all want to help, but in the face of so much uncertainty right now we share with you some ways to support the Puerto Rican friends.

Aidbox is an email signature technology that leverages partnerships between businesses and nonprofits like Beyond Type 1, by creating a new ad space for businesses and a fundraising mechanism for nonprofits.

Coverage matters. Access matters. People matter. Graham-Cassidy endangers access to affordable healthcare for millions of Americans - especially the most vulnerable.

A new independent study reveals that not all BGMs on the market report clinically accurate blood glucose levels.

The word yoga means wholeness, completeness. Instead of seeing myself as incomplete, yoga has taught me that no matter what happens to my body, the one looking out through the eyes (the experiencer) can never be incomplete.

Running with diabetes hasn't always been pretty. It's been trial and error every single day. Within 10 days of my diagnosis, I had all the technology available to assist with diabetes management.

Who says camp is only for kids? Find out about “diabetes camp for adults” and why we know you will love the camp experience even more as a grown-up!

In the wake of Hurricane Irma, Beyond Type 1 has compiled resources for those in need + how to help if you're able!

Check to see if your infusion sets are affected by 9/11/17 recall!

A surreal SCUBA dive in the Philippines goes awry, landing a Type 1 diabetic in the hospital on a very remote island.

Twenty years after her diagnosis, Stephanie Kahn is readying to run a half marathon and a full marathon in the same year. While her training is readying her body, it's her mind she feels shifting as she finally comes to terms with talking openly about T1D.

Uruguay - On April 27, 2015, we received an uninvited guest who has now become a friend and lives with us at home.

There was no way our little girl would ever feel different or excluded because of a disease she did not choose.

Cole Eller was diagnosed with T1D when he was one. His mother spent four years waiting for the day he would ask why. Together they’re exploring the answer to that question by educating others.