The problem with type 1 diabetes organizations (this is a rant).

Disclaimer that I have to put, even though – duh: all thoughts and opinions are my own and not that of my employer’s. 

There is no space for competition or animosity among diabetes organizations if any of us are actually truly aligned to our purpose – wiping diabetes off the map.

I have been involved with both JDRF and ADA since my type 1 diabetes diagnosis in 1997. I have done advocacy, hill visits, fundraising events and volunteered with both. When Beyond Type 1 was founded more recently, I hopped on their amazing community app, have shared their resources, and attend their events too.

I have worked for JDRF for a little over 2 years and have as much respect for this organization, ADA, and Beyond Type 1 as I always have. I STILL use each organization’s resources and go to each organization’s events. I donate to and fundraise for each.

I’ve found that almost anyone I talk to who actually has T1D knows that not only CAN these organizations coexist, but they should. Continue reading “The problem with type 1 diabetes organizations (this is a rant).”

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19 years.

Lala Jackson T1DToday marks 19 years since my type 1 diabetes diagnosis. It’s meant a lot of needles. Guesswork when my life is on the line. Lost sleep. Insurance fights and ignorant doctors. Fear. An incredible weight that threatens to break me sometimes because this thing that so deeply affects my life and my well-being and my future is never going away.

But it’s also meant resilience. Empathy. Learning how to shine my light brighter for myself and others. Understanding the strength of my voice. Learning how to fight harder because, in so many cases, our lives depend on it. A deeper faith in myself and those who care for me. Having people in my life who seek to protect me in ways humans don’t typically have to do for one another.

But mostly, it’s meant learning that type 1 diabetes – that having a chronic illness – doesn’t define who I am. Continue reading “19 years.”