Two-year $300 Million Special Diabetes Program Extended

In an overwhelming vote, the U.S. Senate approved a two-year extension of the Special Diabetes Program (SDP)—an initiative that accounts for roughly one-third of all federally-funded type 1 diabetes (T1D) research in the United States. “JDRF staff and our network of advocacy leaders and passionate volunteers all across the U.S. work tirelessly every day to […]

Meet Kimberly Roosevelt: JDRF 2015 Children’s Congress Chair

It is JDRF Advocacy’s great honor to announce that Kimberly C. Roosevelt, of Dallas, Texas, will serve as chair of JDRF 2015 Children’s Congress to be held in Washington, D.C., this July. Kim, a prominent JDRF Advocate and volunteer leader, and mother to 13-year-old Elizabeth who lives with type 1 diabetes (T1D), will welcome more […]

A song worth more than a listen

Korn releases exclusive download to benefit T1D research What can one voice raised against type 1 diabetes (T1D) do? If you’re Jonathan Davis, lead singer of acclaimed rock band Korn, one voice can reach millions to help people living with T1D. Jonathan’s young son, Zeppelin, was diagnosed with T1D just over a year ago, and […]

CGM-Medicare Bill Introduced in House

JDRF Commends U.S. Representatives Reed, DeGette and Whitfield for Introducing Continuous Glucose Monitor (CGM) Coverage Legislation JDRF commends U.S. Representatives Tom Reed (R-NY), Diana DeGette (D-CO) and Ed Whitfield (R-KY) for introducing legislation, H.R. 5644, the ‘Medicare CGM Access Act of 2014,’ calling for continuous glucose monitor (CGM) coverage by Medicare. This legislation (which now […]

You’re the make it happen type

Thank Congress for $150 million renewal of type 1 diabetes research funding JDRF is pleased to report that Congress has approved a one-year renewal of the Special Diabetes Program (SDP). SDP funding has helped realize some of the most groundbreaking advances in type 1 diabetes (T1D) research possible. JDRF advocates have played an integral role […]

Volunteer Spotlight: Kathy Stewart

A warm embrace Kathy Stewart doesn’t do anything half-heartedly. No Mentor Program? She’ll start one!  Need the Outreach Program to grow? She’ll do it! Or maybe you just need a compassionate ear after being newly diagnosed with T1D. She’ll give you her undivided attention. Ever since Kathy’s grandson Marston was diagnosed with T1D at just 14 […]

Volunteer Spotlight: Monica Oxenreiter

Check out this resume: Founder of Zip the Cure, JDRF Youth Ambassador, Walk to Cure Diabetes participant, Trial Net liaison, Promise to Remember Me Campaign advocate, JDRF Children’s Congress delegate, and regular public speaker on living with type 1 diabetes (T1D). It’s hard to believe that someone could offer so much before the age of […]

Volunteer spotlight: Michelle Crouse

Michelle Crouse, of the JDRF Alabama Chapter, has been a caring volunteer, a dedicated advocate, and, quite literally, the calm in a storm. Now her 13-year-old son Cameron, diagnosed with type 1 diabetes at age two, is taking up the family tradition with his own volunteer and advocacy work.

Advocates Testify at Senate Diabetes Hearing

Advocates Testify at Senate Diabetes Hearing

Senator Bill Nelson, of Florida, chair of the Senate Special Committee on Aging, and Senator Susan Collins, of Maine, ranking member of the committee, convened the eighth biennial Senate Diabetes Hearing on July 10. The culmination of Children’s Congress—JDRF’s flagship advocacy event—the hearing offers JDRF advocates young and old the opportunity to speak up on […]