I had on purple heels I could actually walk in, a glittery handbag large enough to actually hold the things I needed to bring with me, and a folded up piece of paper with the mini-speech I had written that morning. (I like to tell myself that I work best under pressure. Or panic. One of the two.)
|This is the "quick, take a picture of me before|
we forget" shot. Sassy!
I was asked a few months back if I would be willing to share my story as part of this chapter's "Fund A Cure" video for the 2012 Gala. A camera crew came to our house in February and we did things like play fetch with Billy (you'll notice that he suddenly has no interest in his favorite toy once cameras are rolling), go for a walk (of course it was super windy) and I spoke about my diagnosis, finding support online, and what parts of life with diabetes have been most difficult.
My previous impressions of Gala videos led me to be a little cautious - I wasn't interested in being portrayed in a feel-sorry-for-me, tear-jerker sort of way. I thought they did a nice job of sharing both my and another young woman's stories in a realistic but positive light. (And yes, you'll notice that I'm a huge JDRF supporter.) But, don't take my word for it - make some popcorn, grab a comfy chair and watch it for yourself.
I was also asked to say a few words (around 30 seconds to a minute) following the video's presentation. As Molly and I stood on stage, the video drew to a close and the emcee introduced us to the audience of over 400.
We received a standing ovation. I really, really didn't expect that - neither of us did. (And though I feel a little like it's boasting to even mention it, it's the first time in my life that I can recall it happening, so I kind of feel like it's okay just this once.)
I'm grateful for a lot of things from this experience: for the opportunity to bring an adult voice and story to the JDRF narrative; for the chance to work with such passionate people through the whole process; for the generous audience (they surpassed their fundraising goal for the night!) who contributed to the work of people much smarter than I.
Organizations like JDRF help to provide people like me with what I think is one of the most important things required to live well with type 1 diabetes (aside from insulin): hope. And on the days when I find some, I try to store it up like a squirrel would do with acorns for the winter. A bad day can hit at any time, and it helps me to turn it around when I have a stash of these reminders - of how far we've come, and how many people are out there working hard to end this disease.
What a great picture of you! It sounds like you had a great experience.ReplyDelete
Nice job, Kim.
beautiful video! i loved it!ReplyDelete
Great job! Great video!ReplyDelete
THIS MADE ME CRY. Damn you!ReplyDelete
This video was wonderful- definitely got teary. Bravo for making it so filled with hope and positivity.ReplyDelete
this was awesome Kim!!ReplyDelete
Wow. This video got to me. Seriously, I want to stand and give you an ovation. I've seen a lot of these JDRF videos through the years, and this has to be one of the very best - highlighting you and Molly and getting that Adult T1 perspective that's so often forgotten. Great job, Kim. Truly awesome, my friend. Thanks for being a part of this and sharing your story to make such a difference.ReplyDelete
Great job. I'm so glad to know you. Sad diabetes made your life and my life so tough, but... glad in a way because we get to meet the sweetest most awesome people because of it. Continue the work Kim. What you're doing matters. Hugs!ReplyDelete
Great video! Wow... you don't need much more validation than that to know you're making a difference. Congrats on what sounds like a super night! Bask in the light for a while... you've earned it.ReplyDelete
wow, that was such a lovely video of you and molly. i'm glad to hear you received such a warm response at the gala, it was well-deserved. you guys looked so cute on the night, thanks for the pics! :)ReplyDelete
First, nice dress (do you know how hard that was for me to admit?).ReplyDelete
Second, Aaron looks so proud of you in that picture.
Third, that is an awesome video and I love that your chapter included you to give a voice to the adults with diabetes and probably hope to the parents of the CWD that their child will be awesome when they get to our age. ;)
Wow, I love this! I've been a part of Team 1 (young people with T1D climbing Mountains over the world) since 2005, and we have participated in a few JDRF galas up in Canada. One year it was really frustrating because we came out to show that T1D's can achieve anything, and not 20 minutes later they had a video of a man saying that we need a cure because he wants to be able to dance with his daugher at her wedding (she was diagnosed as a toddler). It's nice to see something uplifting, showing that yes we need a cure, but people are thriving and living totally normal lives, even with diabetes. Awesome job!!ReplyDelete