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August 30th, 2008
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eschipul

This year’s JDRF annual conference has asked those involved with JDRF to compose a “Commitment to a Cure” piece. They will be using these commitment items to display on the Commitment Wall in hopes of increasing interest, passion and the volume of responses at the conference. 

 

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Option #3

Tomorrow is the JDRF Promise Ball. I still haven’t figured out what I’m going to wear. Since it’s black tie, I wanted to wear one of the many evening gowns I have laying around (from prom and other balls). So last week, I tried on the main one I wanted, but I didn’t feel comfortable.

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Our team, Charlie's Angels, has been raising money for the Juvenile Diabetes Research Foundation since 2003 – the year Charlie was diagnosed.

 

For the first few years, we sent out our fundraising letter to friends, family and co-workers and did remarkably well. Last year, however, I started to feel uncomfortable asking the same people to give so generously yet again. I felt like they were investors in a cure that I was falsely promising. A cure that was "closer than ever" or "within reach" or "right around the corner." To be honest, I really don't know how close we are to a cure. But, what else can I do? I can't cure Charlie. I can only raise money and give it to the people who say they possibly can. I'll sell it like a snake oil salesman if I must.

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I have officially started my new job and I am excited about the potential that lies ahead. For a while now I have been chasing after the opportunity to work for this company and I'm at a point where I feel comfortable sharing more about it. While I am employed full time with my new job I will also continue to do some personal training and be a blogger for dlife. So anyway, enough of the dancing around,I am now a full-time employee of the Juvenile Diabetes Research Foundation (JDRF) and I am really happy about it.
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theo_pz

What an awesome, great, fabulous, wonderful time I had this weekend in St. Louis, MO. I attended a family retreat put on by the Juvenile Diabetes Research Foundation. The event offered people associated with our disease MANY opportunities. There were tons of kids, parents, and loads of helpful information. If you are someone who has diabetes or someone who has a relationship with a person with diabetes then I would highly recommend becoming a part of your local JDRF chapter if you have not already. There are literally hundreds of them around the globe and the nation and you will get everything you need from them.
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trehala

Many of you have read about my opportunity coming up to speak at a JDRF family retreat in St. Louis. I am stoked to be going and to be a part of the whole AMAZING experience. It's like the diabetic version of the prom for kids and adults. I'm getting really excited and I recently learned of some new information regarding the event. Not only will I be speaking to the parents of these children, in a breakout session for exercise and diabetes, but now I will also be speaking to a large group (approximately 100) of kids with diabetes ages 8-12!

Look out kiddos, here I COME!! (I'm thinking about having them do a short unexpected workout with me??)
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Kerri Morrone
Kerri Morrone, diagnosed with type 1 diabetes when she was six years old, doesn't let diabetes define her. It just helps explain some things.
Creator of the diabetes blog Six Until Me and an editor for dLife, Kerri is an awareness advocate and an active member of the diabetes community. She'd also like a kitten. (Read More)


Latest Posts: There Are No Rules! | Evidence | Pain Thresholds

Andy Bell
Andy Bell has lived with diabetes since the age of 14. He controls his type 1 diabetes by taking multiple daily injections. Andy is 27 years old now and despite his diabetes, still maintains a very active lifestyle. Andy works for the Juvenile Diabetes Research Foundation (JDRF) in the National Outreach Department.(Read More)

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