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Blogs from JDRF and/or TypeOneNation
  • Advocacy Blog

    Thanks for Sticking with Us - Happy Volunteer Week

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  • Advocacy Blog

    Hello Instagram!

    • 0 Comments
    We have asked you to tweet us , follow us , pin us , and read with us ! Well I am excited to announce that we would love for you to ’gram us as well! JDRF Advocacy is excited to announce our newest social media neighborhood, Instagram ! The Instagram...
  • Advocacy Blog

    We Heart YOU!

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    Advocates, here we are, February 14, Valentine’s Day! Happy Valentine’s Day to you and to your #1! Here on the JDRF Grassroots team, we wanted to make sure you felt the love we exude for you today. We wanted to make sure you knew just how...
  • Advocacy Blog

    42 Reasons JDRF is Thankful for YOU

    • 1 Comments
    JDRF was founded 42 years ago, by parents of children with type 1 diabetes (T1D) in 1970. For the past 42 years, JDRF staff and volunteers have worked together to fund research aimed at finding a cure, better treating and preventing T1D. This year, the...
  • Advocacy Blog

    U.S. Congress Votes to Renew the Special Diabetes Program (SDP)!

    • 2 Comments
    Congrats again, JDRFers! As one of the final acts of the 112th Congress, the U.S. House of Representatives and U.S. Senate approved a broad bipartisan bill that included $150 million for the Special Diabetes Program (SDP), extending the program for an...
  • Advocacy Blog

    Special Diabetes Program (SDP) Funding Approved by U.S. Senate

    • 10 Comments
    Thanks to you and your advocacy efforts on behalf of JDRF! I am happy to report that early this morning (around 2:15 am to be more exact!), the U.S. Senate passed legislation which includes a one-year renewal of the Special Diabetes Program (SDP) at the...
  • Advocacy Blog

    Email Congress to Renew Critical T1D Funding

    • 66 Comments
    Help me tell Congress, “Renew the Special Diabetes Program (SDP)” by sending a quick email (…and thanks again to those of you that made calls earlier this month, use this email alert to follow up )! As you know, the SDP is a critical...
  • Advocacy Blog

    Giving Thanks - Family, Friends and the SDP

    • 1 Comments
    Good morning. As I have spent the last days preparing for the visit of my family for the Thanksgiving holiday, I have been thinking about what I am grateful for. As the National Chair of JDRF Advocacy and the parent of a daughter with type 1 diabetes...
  • Advocacy Blog

    Congratulations on the Final AP Guidance

    • 5 Comments
    After all of the work many of you put into making the artificial pancreas guidance from FDA a reality, I wanted to say thank you and congratulations! FDA released the final guidance and included nearly all of JDRF’s suggested changes – see...
  • Advocacy Blog

    World Diabetes Day Action - Call Congress

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    It’s a critical time for type 1 diabetes (T1D) research, and we need you to call your members of Congress today (or tomorrow, 11/15) and tell them “don’t stop now, renew the SDP!” The Special Diabetes Program (SDP) provides $150...
  • Advocacy Blog

    T1D and Veteran's Day

    • 4 Comments
    November is National Diabetes Month. We also celebrate Veterans’ Day and honor those who have served or are serving in the United States military. Captain Joseph Budzyn of Mokena, Illinois, an Eagle Scout and a 2008 graduate of the Air Force Academy...
  • Advocacy Blog

    The Time to Renew the SDP is NOW!

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    For the past few months, we’ve been stressing the importance of the Special Diabetes Program (SDP) , which has in one way or another changed the lives of every person living with diabetes today. Since Congress and the Administration created the...
  • Advocacy Blog

    WSJ Op-Ed by Woody Johnson Discusses Importance of Diabetes Research

    • 1 Comments
    In today's Wall Street Journal, you'll find an Op-Ed entitled "The Folly of Defunding Diabetes Research," authored by JDRF International Chairman and owner of the NFL's New York Jets, Robert Wood "Woody" Johnson, IV. If...
  • Advocacy Blog

    Tips to Children's Congress

    • 1 Comments
    We’re less than 2 weeks out from the last day to apply to the JDRF Children's Congress 2013 - Thursday, November 1 or T1D Day! If you know someone age 4 to 17 with T1D (type 1 diabetes) and has never been a CC Delegate, I hope you’ll encourage...
  • Advocacy Blog

    Role Models in Diabetes

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    The Children’s Congress 2013 (CC13) applications are due on November 1, 2012, the event will be held in Washington, D.C. from July 8-10, 2013 so don't miss your chance to participate! I also wanted to share another quick note from Angie Platt...
  • Advocacy Blog

    Apply to be a Children’s Congress Delegate Today! HERE'S WHY...

    • 2 Comments
    Every other year, JDRF brings children aged 4 to 17 years from all across the country to Washington, D.C. In face-to-face meetings with their lawmakers, Children’s Congress delegates help them understand the challenges of living with type 1 and...
  • Advocacy Blog

    Thanks to Type 1 Diabetes and JDRF

    • 10 Comments
    Yesterday, Angie Platt, Children’s Congress 2013 Chair, sent me the following so I could share her experience at the 2011 event with you, so be sure to apply by November 1 if you’re between the ages 4-17 . Hope you enjoy and be sure to leave...
  • Advocacy Blog

    James B on the SDP- From the NIHB Conference

    • 0 Comments
    Earlier this week I had the opportunity to connect with James Buckles, the Executive Director of the JDRF Rocky Mountain Chapter, who recently paneled a session for the National Indian Health Board (NIHB) Conference in Denver. James filled me in on his...
  • Advocacy Blog

    A Party to Beat All Parties

    • 5 Comments
    When my daughter was diagnosed with T1D, our family got a lot bigger; we became part of the JDRF family. What gives me great hope for a better life and eventually, a cure for my daughter, is that so many people share this hope for their loved ones, too...
  • Advocacy Blog

    Meet Jonathan, Children’s Congress 2013 Chair-Kid!

    • 7 Comments
    Meet Jonathan, Children’s Congress 2013 (CC13) Chair-Kid! Jonathan’s not only the Chair-Kid for CC13 but he’s also been keeping busy advocating for type 1 diabetes in all sorts of ways. With the support of his mom, Angie, the Chair of...
  • Advocacy Blog

    Help Us Tell the Story of Children’s Congress

    • 2 Comments
    Before you know it, the deadline to apply to Children’s Congress 2013 will be here! If you or someone you know is between the ages of 4 and 17 and are passionate about finding a cure for type 1 diabetes, then we want to hear your story. If chosen...
  • Advocacy Blog

    Meet the Newbie: Amanda McKinney

    • 3 Comments
    Join me in welcoming Amanda, the newest member to join JDRF Advocacy and our blog! Amanda started with the JDRF Capitol Chapter a year ago, a few months after she graduated college. Amanda is a born and raised Washingtonian. Over the past year, she has...
  • Advocacy Blog

    Who Motivates You?

    • 161 Comments
    My name is Camille Nash and I am the National Volunteer Chair for JDRF Advocacy. I’m also the parent of a daughter with type 1. As we start off the new fiscal year at JDRF this month, I want to welcome those of you that are new to our advocacy efforts...
  • Advocacy Blog

    NEW VIDEO: Why We Became T1D Advocates

    • 10 Comments
    During my three and a half years working on the JDRF Advocacy team I've been asked over and over again "Why should I become a JDRF Advocate?" To me it always seemed fairly simple--your Congressperson needs to hear from you about the T1D...
  • Advocacy Blog

    #JDRFac2012: Cure T1D!

    • 1 Comments
    #JDRFac2012 is a blog series to prepare JDRF’s ‘All for 1’ Annual Conference attendees for their time on Capitol Hill, and to educate you as readers on why JDRFers will be on the Hill on your behalf and how you can help . We’re...
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