And just like that my 24 hours in New Orleans is complete.
If you want to get to the good stuff, here’s the link for my slides, data, and additional resources I provided after my presentation – http://snider.io/aade2015.
Unfortunately, I’m not sure if I can call my presentation a success. I thought I was invited to speak about Twitter data and show off some cool graphics to a crowd that understood the basic mechanics of Twitter, but was looking for more insight into what the diabetes community has done and continues to do on Twitter. I completely underestimated the amount of time I should have spent covering the basics.
“How many of you are actively on Twitter?” For some reason I didn’t interpret the lack of hands in the air as a sign that I needed to slow down and focus on the simple stuff first:
What is Twitter? How do you sign up for Twitter? What the heck is that “#” symbol? What is an impression? How do you use Twitter? Why should I use Twitter? How do you Tweet? How do I follow you? Who should I follow? Why does this thing need my phone number? Help?!
I’m presenting at the annual meeting for the American Association of Diabetes Educators (#AADE15) on Friday at 11 am. If you’re going to be in New Orleans, swing by Room R06-R09 and check out the awesome pictures I will use to distract the audience from seeing how nervous I will be.
I will share my entire slide deck for “The Social Network: Using Twitter to Understand Health Conversations and Visualize Data” along with relevant notes and data referenced Friday morning on Twitter and Facebook, and later here if you want to see what the fuss is about.
Part of my deliverables to the audience will include a #dsma how-to and a quick guide to common diabetes hashtags. My goal after my hour in the spotlight has concluded is to empower the educators in attendance to feel safe and confident in joining in the conversations that are taking place online. I don’t necessarily think that every medical professional needs to actively engage in tweetchats every week, although that would be cool; but I believe acknowledging, respecting, and following these conversations is a great way to better understand what people with diabetes think and feel.