A Generational Force In 1983 when Debbie Newman and her husband Dr. Stephen Newman first received then five year old daughter Emile’s type one diabetes (T1D) diagnosis, they were frightened but also familiar with the lifestyle. “T1D care has changed dramatically since I watched my father sterilize his glass syringes by boiling them in a […]
There is no harder working retiree in southeast Michigan than JDRF volunteer Marvin Daitch. Marvin was introduced to type 1 diabetes nearly 20 years ago, an event that would map a new course for his life, and even become a calling.
When Kevin Wehrenberg became concerned about the media’s portrayal of type 1 diabetes (T1D) during the nomination of Supreme Court Justice Sonia Sotomayor, he contacted the Los Angeles Chapter, wanting to discuss the issue. The chapter’s executive director was impressed and soon asked Kevin to join the local Board.
JDRF Children’s Congress, our flagship advocacy event, takes place in Washington, D.C., today through July 10. 161 of JDRF’s advocates, ages 4 to 17, will bring an important message for Congress to renew the Special Diabetes Program (SDP). This federal program, which currently provides $150 million per year for diabetes research, has made possible some […]
Final voting is open now through May 28, 2013, 12 PM EDT! Do you share our need for speed in type 1 diabetes (T1D) research progress? Then vote for one of the 10 finalists in the 2013 Our Everyday Heroes Race Car Design Contest, hosted by Ford Customer Service Division (FCSD). From now until May […]