About Ross –

I grew up in the 1960s and ’70s in a Southern California college town. The town had two proverbial “sides” that were marked less by class than by lifestyle. One side of town was populated by professors and students, most of whom were part of the counterculture, while professionals who commuted into Los Angeles for work lived on the other. I attended an “experimental” public grade school on the counterculture side of town in which teachers abandoned grades, tried all kinds of creative ways to engage kids in learning and often taught in a democratic way that favored individual strengths. Years later, I attended junior high on the “professional” side of town, which was as hierarchical as any other suburban public school and focused on things like teaching to the test, Scantron sheets and those dreaded blue-book essays. Success was, of course, measured by grades.

I excelled in my grade school because I exhibited everything my experimental school cherished: creativity, outside-the-box thinking and an eagerness to learn via new modes and methods. I couldn't read well, couldn’t spell worth a damn and I found math impossible, but, for the most part, I was a star student. I felt like I held life literally in my hands, and truly believed that I could master it. When I graduated to junior high, however, that feeling abruptly evaporated.

All the expectations at my junior high school played to my weaknesses. It was a humiliating time that was made all the more painful by being identified by school counselors as suffering from a severe learning disability. Deemed “defective” at learning at an age at which learning was the central societal expectation, I felt like a broken gadget on an assembly line of perfect models.

Shame set in, and I would lie in my bed at night feeling a terrified sense of helplessness.  I had once believed that I held the world in my hands, but I now felt that was wrong because I now knew that something was “wrong” with me.

Looking back at junior high and the ensuing years, I’m convinced that the label I was given was much more destructive to my psyche and ability to function than any supposed “disability.” I now have three books under my belt, have built two thriving companies with my own hands and have a Ph.D. behind my name, and I’m still not sure what that damning disability was, or if there really had been anything wrong with me at all. My guess is that I wasn’t any good at being “factory taught,” and that the problem was less about a “broken” brain, and more a matter of a poor fit. To put it in terms used by current mental-health activists, it wasn’t about what was “wrong” with me, but an issue of what “happened to me.” That lesson is a constant refrain in my professional life to this day.

I hold a master’s degree in social work from UCLA, and I’m trained as a psychotherapist. The Ph.D. in my title, however, is a stamp from my time at Brandeis University, where I was the first person to receive a joint doctorate in social-welfare policy and sociology. Truth be told, I went to Brandeis with the intention of a solo social-welfare degree, but quickly grew pretty bored with the policy stuff, and ended up hanging out in the sociology department most days. At that time, that marvelously storied department had a specialty in disability rights and in medicalization: the making of human behavior into medical problems.

It’s pretty typical to see the social sciences as a kind of continuum, with psychology, and its study of skull-bound traits, on one side, and sociology, and its interest in social states, on the other. Social psychology, the investigation into what happens when our psychological traits meet up with social states, sits at the middle of the continuum. I’m no pro, but I like social psychology a lot, and since adding it to my learning and interests, I tend to see the world from a trait/state-based lens.

When I try to help someone with their individual suffering, my mind often sees two things at the same time: their struggle with their own psychology, and what is happening around them in their life i.e., the strength of their connections, their sense of value in their community, the opportunities they have to give voice to their being on a daily basis—and the lack thereof. When I think about social experiences, my mind is attracted to how these experiences affect individuals, and so, here, too, I find myself focused on “problems of living.”  This is especially true when I think about oppressive elements in society, and my eyes orient to what it means for individuals to lack access to the deep connections their cultures can bring them, to their value as members of various communities and to their ability to freely say, “I AM.” I tend to think that oppression isn’t oppression unless it is felt, and I believe that it is felt when we are refused the social resources that are central to a meaningful individual experience. To put it another way, when oppression leaves its mark, that mark remains on both the psychological and spiritual life of an individual.

I know people are really worried about the way we silo areas of thought, and how we’ve done this with the social sciences. I, on the other hand, sort of like the divisions—they keep me limber and allow me to respect the sanctity of individual suffering over psychological habits, and they also keep me from becoming what’s called, “reductionistic” by reducing public problems into psychological issues. A person’s suffering is always “multidetermined,” which means that it’s not caused by one thing. But often one thing is hurting them more than other things, and letting my mind’s eye get a little narrow seems to help me direct my compassion, if that makes sense. While this way of “seeing” is not for everyone, and I certainly don’t believe that it’s the only or even the best approach, it’s definitely what guided me to write my first book, Parasuicidality and Paradox: Breaking Through the Medical Model, which focused on repeated suicidal gestures—behaviors typically viewed as intimate psychological events, that I posit are actuality the means individuals use to attain certain social/psychological needs that are otherwise inaccessible.

My interest in more state-based insights definitely drove me to create my company Ellenhorn, which works with individuals experiencing complex events of mind and mood—the sorts of things that psychiatry defines as “pathological”—in a way that views social state as equal to, if not more important than, psychological state when it comes to living an independent life. This company has gone national, with offices in Boston, New York and Los Angeles, and is the preeminent private program in the United States that serves people in their own homes. We work with the people other professionals might deem too “ill” to live in the community, and believe that a sense of purpose and belief in one’s own value as a community member are central to a person’s recovery. My focus on psychosocial states also inspired me to create “Shifting the Addiction Paradigm” conferences, an annual series that aims to change the current definition of addiction from something that is trait-based to something that is more state-based and connected to issues of attachment, social support and purpose. Another of my books, called How We Change (And Ten Reasons Why We Don’t), is a sort of anti-self-help book that explains how change is always related to the social and interpersonal states we are in. A focus on the middle ground between state and trait is also central to my current writing on the use of psychedelics for what others might consider psychiatric complaints and the role of this trend in the medicalization of human suffering. And it’s the reason a partnered and I created Cardea, a psychedelic-care program that blends trait/state thinking. Lastly, it’s the view I took when I wrote my most recent book, Purple Crayons: The Art of Drawing a Life, which represents my life-long interest in play and examines how acts of being original are the things that often bring us to a state I call “livingness.”    



Ross Ellenhorn, Ph.D.