#CWDTech 2013 Part One.

I’m a little late posting today… I stayed up late last night celebrating the Baltimore Ravens super bowl victory. Yay Ravens!

I didn’t get much sleep on Friday or Saturday either. The Great Spousal Unit and I were in Crystal City, Virginia (just across the river from Washington, D.C.) for the Children With Diabetes Focus on Technology conference. It was my first time at an event like this in at least a decade.

There is so much to talk about. I have to admit to suffering from a bit of information overload. Today, let me just talk about what I picked up from the sessions I attended. In part Two, I’ll try to cover interactions outside of the scheduled content.


So let’s start at the beginning. The opening keynote was a dynamic talk from Dr. Ken Moritsugu, a former Surgeon General and Deputy Surgeon General who is now serving Chairman of the Johnson and Johnson Diabetes Institute. Dr. Moritsugu explained in great detail the importance of being an informed health consumer. There’s a lot of misinformation out there, and we need to do our best to separate fact from fiction. According to Dr. Moritsugu, it’s important to “access, understand, and use health related information to make sound, thoughtful health decisions”. What does that mean? It helps to remember three things:

1. Consider the source – Are you reading something from the Centers for Disease Control or World Health Organization, or is it from the “latest dream cure” website that promises much and delivers nothing in the way of information?

2. Risk is relative – Sometimes, a headline can grab our attention. But there’s often more to a story than just the headline. So when you see something like “Scientists find a link between breastfeeding and Type 1 Diabetes”, do the research. Was the scientific study realistic? Was it done on a large, diverse sample size, or did the subjects of the story come from a smaller subset of data that really doesn’t apply in the real world? Sometimes, the answers will surprise you.

3. Don’t forget to communicate with healthcare professionals – This is great for me. Sometimes my endocrinologist has additional information on something I just read about quickly online. Sometimes, she can go back and check things out if I have a concern about something, and then we’ll discuss it either in an e-mail or at my next appointment. Hopefully, you can count on having a two-way conversation with your healthcare professionals to hash out the truth and deception in stories about diabetes.


Next we heard from Ed Damiano, PhD, who is Associate Professor of Biomedical Engineering at Boston University. He’s part of a large team working in Boston on bionic pancreas technology – known generally as the Artificial Pancreas. After visiting the University of Virginia’s Center for Diabetes Technology last year, I was interested in hearing the perspective of someone else working on the same technology. Let me tell you… it was no less fascinating. It was interesting to see the device they’re working with too. An iPhone (this is nothing new… UVA’s program uses an Android phone), with some cool characteristics. Among them are a bolus feature that doesn’t include a carbohydrate count. It simply asks you to say whether you’re eating a Typical Amount, Less Than a Typical Amount, or A Small Bite. The AP device does the rest. If something like this comes to market, carb counts could be a thing of the past. Is that crazy?

There’s more to this, of course. The team in Boston is still hoping for a better version of microdose glucagon to work in their dual-chamber device (which has already been approved for clinical testing). Tiny doses of insulin and glucagon are administered in the device to keep the patient in an appropriate range. Yes, there’s a lot more here that could probably take up an entire post, so I’m encouraging you to get more information on the work being done. When will something like this be available to all People With Diabetes? Right now, we’re looking at around 2017. And since that’s four years away, the timeline may still move a bit. But the progress so far is very encouraging.


Got a chance to sit in a great discussion with Kerri Sparling and Scott Johnson that delved into Diabetes Devices in the Real World. People talked about everything from social media to carrying cases for your diabetes supplies to how you carry and show (or don’t show) your diabetes devices in public. It was a lively talk involving a variety of PWDs and parents who had lots of questions, but also lots of super information to share. People were creating Twitter accounts on the spot and showing off their D-bags. I loved watching faces light up when they started to understand something that they didn’t quite understand before, or found sources of information that they weren’t aware of prior to this get-together.


Sunday morning’s closing keynote spoke volumes to myself and to Maureen. Sebastien Sasseville is the first Canadian with diabetes to summit Mount Everest. Not enough for you? Last year, he completed the self-supported Sahara Race in Africa, through the world’s largest non-polar desert, running 250km over seven days. He talked about both of these events and gave us some important insights. Most meaningful to me was when he talked about doing the Everest expedition. Over two months, their team had to start at base camp, then climb up to various camps before climbing back down again. They had to do this several times before making an attempt at the summit. The point was to acclimate the team to climbing at that altitude (can you really get acclimated to something like that?). The point is that while we have this constant “perfect diabetes management” goal in our minds, sometimes our path to that goal is filled with ups and downs that help us get used to what we need to make it all the way toward our ultimate goal. And what if we reach that goal: that perfect A1c, or perfect pregnancy with diabetes. What happens then? Sometimes, our goals change. Sometimes the bar gets moved. Both up and down. And that’s okay. And fear about the journey should not keep us from going after our goals.


It was an interesting 36 hours or so. Soaking up a lot of information and hearing from people living the lives that we’re all living. Sometimes inspiring, sometimes life-affirming, sometimes funny. I’m lucky this was close enough that I could attend.

In part Two, I’ll try to cover my experiences outside of the scheduled sessions.

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  • Mike Hoskins (@MHoskins2179)  On February 4, 2013 at 3:25 pm

    Sounds like a great time, Stephen. I’ve not had the pleasure of hearing Ed or Sebastien speak in person, but have talked to them and they’re good people. Of course, Kerri and Scott are golden peas, too. (wait, did I write that? WTF is a golden pea???) Anyhow, very much like what they all had to say at this event and everything they’re doing for our community. Thanks for sharing your thoughts on the CWD event!


  • Scott K. Johnson  On February 11, 2013 at 12:39 am

    Great summary, Stephen. Thank you. I’d also like to add that we very much appreciated your questions and comments during the session!


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