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Laura Gillis

In May 1992, my life took a sudden and unexpected turn while I was working on a temporary office job assignment for a chemical manufacturing company in Westchester.

At age 37 I was physically fit and as healthy as anyone could wish to be. I was studying yoga and taking swimming classes at the Y. I could run a seven-minute mile.

By 1990 I was earning $17 per hour. The rent for my apartment was low. My time was free for pursuing extended bicycle trips that I planned, and as a temp I could take off whenever I wanted.

Soon after the assignment began at the chemical manufacturing company, I smelled chemicals. I sensed them passing through my cubicle. When I asked questions no one else smelled them, but I heard that many other workers had only lasted two weeks before leaving.

When 5pm came on my 11th day, I didn't believe I knew how to drive anymore; my hands were foreign to me. That evening my head hurt in a most indescribable way. I would just hold it and cry. My nose and throat were burning. My skin was flushed.

I called the office of the temp agency that night to say that I would not be returning to this assignment. Little did I know that my life as I knew it would never be the same.

Afterwards I was unable to tell anyone what I did or didn't do during the hours I was there because I couldn't remember. It took me years to recall that I was typing the names of the chemicals that I believed would appear on the product labels. I didn't think to walk out with a copy of what I was typing on that day.

Three months passed before I realized I wasn't moving. I was sleeping 15 hours a day; my waking life was a blur. My partner would often find me sitting staring into the horizon, not listening or finishing sentences. I had aches and pains running through my entire body. When I actually made it to the doctor's office, I'd often forget to even mention the symptoms which brought me there.

It was about time I pulled myself together, I thought, and then encouraged myself to start working again. Subsequently, I was fired from my next three assignments for making all kinds of errors. When my temporary work counselor was explaining why these assignments were ending abruptly I was in total disbelief. I had always prided myself on being fast, accurate and having the ability to walk into a new office.

However, all these taken-for-granted facts of life became part of my disability. They are elements of functioning that I can't control or rely on. I was once fast, now I am slow. I still dread being asked, "what's new?" or "where are you working now?" Admittedly, I am getting much better at turning this type of question around, so that I hardly ever answer.

My diagnosis was Toxic Ecephalopathy and a Reactive Depression, total disability. How strange it was to hear these words used when referencing me.

Not only was I injured, but I became further victimized and abused by a system that is like a massive machine, impossible to penetrate, that was destroying what life I had left. I have come to believe that anyone who files a Workers' Compensation claim is immediately placed under house arrest, guilty of malingering and trying to defraud the insurer. There may be the day that the private investigator comes calling at your door, searching for proof of your guilt. Your treating doctors are seen as your accomplices. All your rights are denied.

I began to question myself. Are you sure your injury is real? Was I really injured on the job? I would reread my doctors' reports and ask them if they were certain they were referring to me?

Eventually, near the end of eight years my second lawyer approached me with a deal and suggested, argued, then shouted that I accept a permanent partial disability at the rate of $170 per week. The deal was never going to get any better. I have to say that, for better or for worse, accepting this deal was the only way to get a piece of my life back, my sanity. It was the only way to end what virtually never ends - the Workers' Compensation Game. The financial cost to me was close to $12,000 in legal fees, so that I could receive $170 per week as compensation for being permanently and totally disabled.

Even after five Psychiatric Independent Medical Examinations, it was never recognized that I was in a stable, long term, same-sex-partnered relationship, which had now lasted 22 years. It wasn't noticed that the income that I lost after becoming injured impacted our lives, and that our equal contributory relationship suffered a major financial blow.

Women are real people. When a woman loses her income, her sustenance for life, it is a real experience. Women, whether single, married, gay/lesbian, with or without children contribute to the world. A woman's on-the-job, disabling injury has a real impact on her own life, the lives of those she shares hers with, and the society all of us live in. Its loss is really felt.