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My Battle With Schizophrenia: "Rats Were Eating My Brain"

Posted: 03/11/2013 3:52 pm

The UN General Assembly has just put out its 2013 report of the special rapporteur on torture and other cruel, inhuman, or degrading treatment or punishment. I was not surprised at the majority of the content (e.g., forced sterilization) but then I came to this on page 14: "absolute ban on restraints and seclusion."

What would they do with me now, were I re-hospitalized?

Over a period of six years (when I was in my early to mid-20s) whenever I was hospitalized for my schizophrenia, restraints and seclusion were used repeatedly, readily, and beyond necessity. Also, I was over-medicated, probably not for my own sake, but to make me a more manageable patient. I was lost in my psychotic world, to the point of bashing my head on the concrete walls on the psych ward. For this, I understand the use of restraints. However, they, along with seclusion, were over-used, to the point of being a punishment rather than for my safety.

By my 12th certification (forced hospitalization) for schizophrenia they would outfit a stretcher with restraints while I was still waiting in Emergency. As soon as I was admitted, they would call a Code White -- aggression -- and within seconds, it seemed, a group of four to five Security officers was there, holding me down as I flailed and kicked and screamed with rage as they restrained me. Wrists, ankles, chest; I couldn't even wipe my falling tears away.

I wept not only because of being tied up; I cried for the high doses of sedatives and anti-psychotics the nurses injected into me, for the strip-search, for the forced changing from street clothes into hospital pajamas in front of all those (mostly male) Security guards.

Then, the stretcher-bound, pajama-clad, medicated me was placed in solitary confinement.

This did not happen just once. Or twice. Try over dozens of incidents. Restraints would last hours, hours, hours; later, when untied, I would be locked in a seclusion cell for as long as a week at a time. Cell, not room: a thin mattress on a concrete "frame," silver toilet in the corner, camera, and a door with no knob on the inside reminds one of a jail cell.

They did all this because I was bashing my forehead bloody on the concrete walls. See, in my schizophrenia, I strongly believed that miniscule rats were eating my brain and, reminiscent of leeching, bleeding them out was most effective.

What else could they do?

Restraint and seclusion: banned?

What would they do with me now?

A short series of electroshock. They did try to get informed consent, but because I agreed to it on the basis of it electrocuting those brain-eating rats, they determined I was unable to make medical decisions for myself. So off to "treatment," their signature on the papers waiving my rights.

And then there are the forced injections. These terrified me, as I delusionally believed that they had more rats in them, enough to eat my entire brain. Nevertheless, amid my screaming cries, pleadings, and sheer panic, in went the needles. That absolute terror certainly falls within the guidelines that "fear and anxiety produced by indefinite detention, the infliction of forced medication or electroshock, the use of restraints and seclusion, and the segregation from family and community, etc., should be taken into account" (pg 16).

Much of what happened to me while held involuntarily could have been averted. For example, when well and on the "outside" I walk everywhere. Confined, I pace. This calms me, and lulls those rats to sleep, further decreasing my anxiety. The nurses, however, see it differently. They call it agitation, and agitation means you must take their PRN pills. Rat-filled pills.

So I decline; they insist.

But there are rats in them! I protest.

Erin, there are NO RATS in this medication. Now take it orally, or we will have to restrain you and inject.

No! No! No!

Look, see how agitated you are!

They win, with the help of security.

What trickle-down effects will banning such practices have? How enforced, and with what consequences? And how will they deal with acutely psychotic and delusional patients such as I have been?

What would they do with me now?

They are still allowed to declare me of "unsound mind" and a "danger to self," the exception to the ban. I will certainly admit that I was of unsound mind (rats?) and a danger to myself (bashing my head). They may detain me ("deprivation of liberty") but where does the line between sound and unsound fall?

What is abusive and what is humane? In the moment, I cannot tell; I am delusional. Somebody has to decide for me, and for many others, that forced treatment is more compassionate than neglect of persons with severe mental illness, neglect that leads many such people to live disconnected lives on the street or in jail.

The UN is, at a certain level, one such somebody.

Interested in my experience with schizophrenia? My memoir, When Quietness Came: A Neuroscientist's Personal Journey With Schizophrenia, is available from Amazon.

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  • In any given year, one in five people in Canada has a mental health problem or illness.

  • Of the 6.7 million people who have a mental health problem, about one million are children and teenagers between nine and 19 years old.

  • Mental health problems cost at least $50 billion a year, or 2.8 per cent of gross domestic product, not including the costs to the criminal justice system or the child welfare system.

  • In 2011, about $42.3 billion was spent in Canada on treatment, care and support for people with mental health problems.

  • Mental health problems account for about 30 per cent of short- and long-term disability claims.

  • If just a small percentage of mental health problems in children could be prevented, the savings would be in the billions.

 
 
 
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03:00 PM on 03/12/2013
my mother had schizophrenia and so my childhood was dominated by this reality as father was not in our lives. she had two rounds of ect that i learned of only after her death which reportedly have 4 sessions each. who knows what possible effect that had on her long term? i never had a sense that she had any evaluation for long term effects. it is moving to me that this writer shares her experiences with the system. my mother could never talk about her experiences with me. i wish i could ensure schizophrenics could enjoy the dignity and respect they deserve.
09:52 AM on 03/12/2013
I was reminded of my four granddaughter who dislocated her first vertebrae and wasat risk of paraplegia or worse . Courageous surgeons dared to go in and pin and space her spine in order that she might have a normal life. The vest securing halo to chest they fitted was too big, thus had to be changed (prescribed by the head surgeon) . Explaining this to a wee smart girl.....impossible The operation had already rendered much pain and she was heavly doped. Grandparents (doc and nurse) went on an excruciating walk. We came back to haunting screams ( her parents were in the room ) ... team were still getting the new vest secured . Two mail nurses plus female one persisted. They emerged from the room sweating and stressed but they did it ! A healthy eight year old is now skating dancing etc. Thank heavens that they dared to restrain her! The future is now possible as it is for Erin who now has a life . Patricia Forsdyke.
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09:17 PM on 03/11/2013
its all so complicated. and horrendous. if you didnt have trauma going in you would have to coming out. lets hope decision makers like the UN actually improve something it all seems a bit of catch 22. i saw how they over-medicated my quiet granny...
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09:08 PM on 03/11/2013
Before I navigate over to Amazon, which one of you wrote the book?
11:47 AM on 03/12/2013
I am perplexed by your comment. The article was written by Erin Hawkes so why are you asking which one wrote the book? Is it because you still believe incorrectly that schizophrenia is a split personality?
06:39 PM on 03/11/2013
I don't have an insightful or experience based answer to give Erin. I just wanted to acknowledge that I'd read your article. heard what you had to say, and wanted to express some kind of sympathy and empathy for the unimaginable anguish that you've suffered, through your illness and at the hands of mental health practitioners. I weep for the pain that you have endured and I truly wish that we had more answers, better understanding, and much better treatment for all mental health illnesses. What I have seen of mental health care in Canada has shown me that there are a lot of well meaning individuals following the dictates of the wisdom of the day, working within the confines of government spending, and it is not nearly good enough.
10:24 AM on 03/12/2013
But, Erin has her life back thanks to forced treatment.And judging by her book she is functioning well and has a life. Not so has a young man reported in a national newspaper in the death column He did not survive the tortuous symptoms that were inflicted upon him by this cruel disease. Patricia Forsdyke.
04:34 PM on 03/12/2013
I don't believe you have the correct impression. She is explaining the abuse not justifying it. Forced treatment goes on and on, and has nothing to do with anyone's 'Life'.
07:31 PM on 03/12/2013
Trisham I think that I do understand the situation. There is always a fine line between abuse and action which will pemit life saving treatment. Sadly too many people are left to flounder in distructive delusions. see my earlier email . Patricia Forsdyke
01:08 PM on 03/12/2013
right on well spoken and i wish Erin my sympathy as well and hope we can become more aware of this condition.