It might not work. These are some of the scariest words in the vocabulary of any creative and they are responsible for stifling the launch of countless projects that might have changed the world if they’d only gotten out of the front yard. As much as I’ve tried to turn my creative focus away from diabetes and towards the things that inspire, I feel like there is unfinished business. Inspiration means nothing without insulin when it’s literally keeping you alive. That’s why I’m using the platform and the talent that I have to try to make a ruckus about insulin access through a documentary project called Banting’s Ghost–that will amplify the humanity in this otherwise very data heavy issue.

Banting’s Ghost is the working title for this project and it will document the people who are struggling with access to insulin–not in a far off land but right here in the United States. I named this project for Frederick Banting, one of the lead researchers who discovered insulin in 1923 and promptly sold his share of the patent for $1. He was quoted as saying “Insulin does not belong to me–it belongs to the world”.

Our current situation has departed significantly from Banting’s altruistic vision. The system has run amok. The pharmaceutical industry has escalated prices that are untenable for insurers–who have responded by covering fewer and lesser quality options which is untenable for people living with diabetes who would like to survive. Community organizations cry, ‘research for a cure’ over the wailing of those people suffering because they can’t afford access to 20 year old drugs.

We are expected to believe that advancements will lead to access rather than the other way around.

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Who are these people suffering and struggling you might ask? Maybe you–like me and most of those who are vocal and have time and following to share our opinions online–are still able to bear the weight of the dysfunctional system and are struggling forward under the burden in hopes that the finish line is at hand. I’ve got news for you. It’s not. People who are struggling are not represented in diabetes advocacy–which is funded by the industry–directly and indirectly swaying those who might otherwise stand up and provide a check and balance.

I don’t have all the answers. I have the ability to tell stories. It’s a start. It’s a missing piece of the puzzle and I’d argue that it’s a really important one. I don’t think that homebrewing insulin is the answer or that the diabetes industry should be decimated. I think that productive conversations begin with some empathy–or at the very least the inability to ignore a public relations fecal hurricane of stories that amplify the value of people over the pursuit of the status quo. There are a lot of data, graphs and charts out there to show that this crisis is out of control. What’s missing is the living, breathing human element and that’s what I’d like to amplify through the Banting’s Ghost documentary project.

It might not work. How will it get funded?

True, it might not even get enough funding to leave the station, let alone gain the momentum it needs to create impact down the line. It’s a bigger task than I can execute on my own, I know that much. I’m asking that if you believe this project to be a worthy endeavor that you back it with a small financial contribution. That’s the only way it will fly. With a family to support and limited resources at hand–addressing a topic that is inherently unfriendly to the industry it’s not difficult to see that the “fly by the seat of my pants” approach won’t work this time around.

Still, I want to unfurl the Banting’s Ghost documentary project in stages, according to the financial support that is available as we progress rather than waiting until all the necessary funds are in place. The first stage is a photo documentary project (inspired by Humans of NY) which is the most time efficient manifestation. My goal is for that to lead into a series of mini documentaries in video format as well as podcast episodes.

It might not work. It’s something I’ve always wanted to try to contribute to the conversation in the diabetes community and the public and I am not afraid to fail–at least not so afraid that I won’t try. Will you help?

Stephen Richert is a photographer and filmmaker who happens to live with type 1 diabetes. You can see his professional portfolio here

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