[Hi there! I’ve written a lot more about ICD and their policy decisions since this post. After they released their 2020 Internal Review, I did a three-part in-depth analysis, discovering plagiarism and a lot of lingering questions. Check out Part 1, Part 2, and Part 3. In the fall of 2021, I also published a look back at the review and how many of the promised changes they’d actually implemented. Spoiler alert: a lot of things are late or undone. You can read that here.]
Many of you, like me, have been following developments at the Institute for Composer Diversity this year. The organization, originally created (as I understand it) as an intentional programming resource for educators and directors alike, has grown beyond its initial constraints and begun positioning itself as a juggernaut of diversity in music, particularly in the wind band world. I’ve recommended ICD as a resource in the past—even put them on my master list of resources I co-sign—but, sadly, that endorsement has come to an end.
Here’s the thing: like most institutions, ICD has messed up in the past, often pretty publicly. That in itself isn’t the end of the world! But it has increasingly turned a blind eye to the concerns and critiques of marginalized composers ourselves—the very people they claim to represent. That continual unwillingness to listen, acknowledge issues, and work efficiently to correct them (or to correct them at all) has soured their name among many folks who carry with them more expertise through lived experience in diversity and inclusion than many on the ICD staff.
I’ve also grown increasingly frustrated at ICD’s continued positioning at Midwest and other high-profile conferences as an authority on intentional programming, when in reality they offer very little (if any!) information or best practices on establishing relationships with the composers referenced within their database. There’s no discussion of the fact that many of us make more on commissions than we’ll ever make in individual score sales, no talk about how many of us are self-published because publishing favors notoriety over financial success (and many of us can’t get a foot in the door with the big houses, anyway). There’s no discussion about trauma performativity or the conditions under which it might be appropriate and meaningful to ask a particular composer to write a piece that addresses a specific marginalization or violence. There’s not even any discussion of ownvoices and the importance of prioritizing diverse stories told by the populations they most directly impact. It’s just a database, accompanied by vague encouragement to make marginalized composers part of your ensemble’s stat sheet without any attention paid to how their work actually informs and influences your programming needs and wants.
The stats they suggest are pretty conservative, too. If you go to one of the live ICD presentations, you’ll hear someone (probably Rob Deemer, head honcho of the project) say these are suggested starting points, but if that important caveat is anywhere on their website, I have yet to stumble upon it. (The website does cite a “minimum” stat, but it’s very easy to skip over the importance of the word while trying to process the numbers that follow.)
Among my biggest personal struggles with ICD’s work, though, is that it essentially weaponizes its composers’ marginalizations and markets to band directors without providing any specifics about their work, artistic practices, areas of specialization (beyond instrumentation), or even specifics of identity that composers may wish to share, like pronouns and other information that may vary from the traditional expectations that come with certain genders. We are reduced down to data points on a sheet, names that are guaranteed to check an ensemble’s diversity box without paying too much attention to the specifics of our identities and how those important distinctions might inform our artistic work.
Over the past year, it’s become clear that in allowing non-composers and others to submit information on a composer’s behalf, the Institute has inadvertently outed many queer composers without their consent. This isn’t just careless administration; it’s doxxing. A failure to check in with composers and ensure they consent to specific information being featured on a very public, easily searchable website is a colossal breach of trust. How are we to assume an organization that outs us alongside our contact information actually values our work, when they can’t be bothered to even consider how the release of this information might affect our day-to-day safety?
I first heard rumors of an email that would be sent to featured composers to confirm their presence on the ICD databases several months ago. At the time, I figured I’d sit on my thoughts for a couple weeks, then, when the email arrived, decide how to best proceed. But, like I said, it was months, not weeks—a time span that included much of Pride month, when many of us in the queer community had to lock down our social media to protect from coordinated doxxing attempts. All the while, our information remained readily available on ICD’s website. By the time the email arrived (a little over a week ago), I had lost faith that the Institute cared enough about the composers on their lists to protect them proactively.
Below is a copy of the letter I sent to ICD in response to their request to confirm my information in their databases. I am posting it in full because I firmly believe that an organization whose main mission is publicly espousing a reductive flavor of intentional programming should be held publicly accountable. I’ll post some suggested best practices next week, but for now, here’s what I told them (please note my dig at website hits at the end was due largely to the emphasis on their own stats they place in their promotional material):
Continue reading “I’m Taking My Name Off the Institute for Composer Diversity”