Sorry, it’s been too long since I’ve posted. Been consumed with pre-production and crowdfunding for The Green Bench. Here’s our video on why we care. Huge thanks to the family members willing to talk on camera as well as Sharon Dunas, former head of NAMI Westside and Dr. Stephen Marder, a psychiatrist who specializes in schizophrenia.
Please watch, share, donate. Thank you. All of us working on the film are passionate about reducing the stigma of mental illness.
A few years ago, The Green Bench was one of those rare writing events that arrived whole. Adapted into a short film, it’s a different story. The first draft I wrote was a literal adaptation – too one note, too depressing. The blessing and (if you’re not with the right people, the curse) of screenwriting is that it’s a collaborative process. Fortunately, I’m with the right people and they’ve been invaluable in shaping the film. If you’d told me even 6 months ago, I’d be writing, producing and acting in my own short film…well, beware of being coached by Craig Archibald. You may find yourself stretching into new territory.
For the short, I did more research and we had the great, good fortune to connect with Dr. Stephen Marder, an expert in schizophrenia (you’ll see him in our promo reel, coming soon). As a result, my language is changing. For example, like most of us, I don’t say “diabetics” or “arthritics” when referring to people with those diseases, so I’ve started paying attention to not using “schizophrenics” or ‘bipolars” etc. to categorize people either. Am taking far more notice in the script of the illness as it most often presents itself and not what we see on the streets – that’s a tiny percentage of the most severely ill. Despite what many movies and TV shows depict, visual hallucinations are rare. Most people with mental illness can function and many do very well. There are many high functioning CEOs, physicians, attorneys and so on with schizophrenia and other illnesses. But the stigma keeps the success stories in the shadows and this time around, I paid far more attention to the stigma and humanizing the person with the illness. Because it is an illness and should be regarded in the same way as diabetes, lupus, rheumatoid arthritis or other physical illnesses. Thanks to the collaborative process, the film version takes the audience along with the main character through the onset of her son’s symptoms.
Don’t get me wrong, I’m still proud of the flash fiction and it was loosely inspired by a real-life incident I’d heard of some years back, but for film, especially with its additional visual impact, I like the step back to the beginning, to the onset, to hope, to empathy.
We start crowdfunding soon on IndieGoGo for a shoot early next year, intending to go to the festival circuit. I want you to contribute to our budget (and you can be sure I will let you know our launch date!) We need to do everything we can to diminish the stigma and let families know that others share their journey.