The reality of mental illness is much more than stigma.
It was a simple enough exercise. Take about 90 seconds and say how mental
illness affected you or your family. Do
it in groups of six and when I say time is up - move on to the next
person. The exercise was suggested by a
conference speaker who said a similar disclosure during an interview had given
him cause for concern about stigma. The setting was a
psychiatry meeting focused on stigma and we had all spent the morning listening
to presentations on the topic.
I really don’t like any professional meeting that resembles
an encounter group and think it should be actively discouraged. I think most people are like me – they go to
professional meetings to hear experts and passively absorb information. Further - I had just commented on the
psychodynamics of shame a few weeks ago in the seminar that I coteach and defined
the emotion has origins in disclosing information that could be embarrassing or
that others would potentially criticize you for. Of the 5 other people at my table – I knew
one professionally and had just met two.
I was the oldest person (by 30 years) and the only man. When they asked for a volunteer to start – I
volunteered. I did not think there could
be a more severe story, was thoroughly habituated to telling it over the past
50 years, and knew that 90 seconds was not nearly enough time to describe how
bad it really was. I was right on all
three counts.
“When I was 15 – I went downstairs and found my father
dead. Sometime after that my mother
began to have severe episodes of mania. She disrupted the entire town to the
point where the police were called repeatedly.
After several police calls, she was taken to a state hospital where she
usually spent a few months until she was stabilized and came home. That usually happened around Christmas
time. I was the oldest of 5 children so
I tried to keep things together. One-time
things got so bad my brother and I had to call the police ourselves and they
came down and told us that we wanted her ‘locked up like a chicken in a chicken
coop’. When I was a kid, I was not ashamed about the situation – I was pissed
off.”
Time was up. I was
not anxious or angry about what I had just said – but realized it was a very
sanitized version. I did not describe the symptoms – extreme
paranoia, irritability, impaired judgment, and anger. The disruption usually involved telephone
calls to public officials or the local radio station when she would announce
her name and begin swearing at whoever was on the other end of the phone. At
times she would get very angry and carry a knife around suggesting that we
should stab her with it. She would throw
us out in the middle of winter. We would
come home from school and find that she had thrown all of our clothing out of
an upstairs window and we had to pick it up off the ground. We would find strangers at dinner or once in
the bathtub. At night when we were
trying to sleep, she would play the stereo loudly all night long – usually Danny
Davis and the Nashville Brass Christmas album – punctuated by screaming up
the stairway at us. Hard to get up and
go to school the next day after one of those nights.
On a road trip – my wife and I stopped in to see her. The floor in the house was covered in about 6
inches of debris (from emptied drawers and closets). She would throw a dash of Galliano onto the
plies. She was making bizarre statements while circling the mouth of a jar of
peanut butter with a piece of celery and then throwing the molten peanut butter
over her shoulder. My wife was upset and
had to leave. She sobbed for the next half hour as we travelled down the road telling
me she was sorry for what I had to endure as a teenager.
Even if I had time to describe this additional information,
that only scratches the surface of my mother’s experience with severe mental
illness and the impact on the family. I
could write a book about what happened. I
am including it here just to illustrate the severity of the problem. These
symptoms typically lasted for many months and some eventually became
chronic. As a psychiatrist – I have no
illusions that her symptoms were anything but the product of a severe mental
illness that was not treated well.
Her primary care physicians at the time were using a
combination of amitriptyline and chlordiazepoxide – medication that
psychiatrists would not use – even back then. She eventually had access to a
psychiatrist and was given lithium but it was not very effective.
Stigma was not the main problem. The main problem is that when a person has a
severe mental illness like my mother it disrupts the relationship you have with
them, That disruption is more severe when you are a kid and can’t make sense of
it. It can affect your development and self-image. The broken relationship can be
permanent. It is more like grief and
loss rather than stigma and shame. After
a while my mother was not the same person any more. I no longer recognized
her. I could not remember what she was
like before the onset of severe bipolar disorder. I don’t think anybody did. It has a more severe impact on my mother than
anybody – but the emotional and interpersonal impact on everybody else was
undeniable.
All of the discussions of psychiatric diagnosis and
treatment do not touch on that. The
bizarre discussions of antipsychiatrists and philosophers don’t even come
close. If you are saying that my mother
was not mentally ill or did not have a “natural kind” of illness – you do not
know what you are talking about. If you
are suggesting that she needed “trauma informed care” – not much better. The unexpected death of her 43-year-old
husband was certainly stressful, but the expected reaction is not decades or
severe bipolar disorder. It is
bereavement, a universal experience, and all that involves. The lack of
psychiatric care early in the course of illness could certainly have been a
factor. Her care rarely involved any of
the family. I don’t think any of her
physicians knew how severe that impact was.
Despite the fact that she lived in the state where Assertive Community Treatment
was invented in the 1970s – it was a rural county and active outreach by cases
managers was decades away.
My mother’s siblings and parents were very supportive. It
would have been very difficult to have made it through many of these episodes
without them. It took an emotional toll
on all of them as they tried to reason with her and convince her to do the
right thing – like curbing excessive spending and trying to get some sleep. The female members of the family – my grandmother
and aunt were much more effective than the men. They were able to react at a level that was
not strictly emotional. The siblings who
remained in town or returned also had a stabilizing effect. She also had two supportive female neighbors
who spent hours talking with her despite the obvious problems. But despite all of those efforts my mother was
never restored to her baseline – a goal I eventually adopted with every person I
saw as a psychiatrist.
What seems like a good interactive exercise to make a point about
stigma is a very blunt instrument. There
is no doubt that some of the local officials discriminated against her (and us)
because of the stigma of severe mental illness.
That was not close to universal by any means. At a recent reunion I greeted a retired police
officer who was very helpful to our family with his advice and reassurance. He did everything possible to avoid conformations
with my mother when she was confrontational.
I never got the chance to thank the women in our neighborhood who helped
but did when I sought them out in a crisis.
Stigma can be an important factor – but the take home
message from this essay is that the overwhelming fact about severe mental
illness is the illness itself. It has a significant
emotional impact on everyone. It
disrupts interpersonal relationships – some of them permanently. Some of that can be grieving the loss of a
person who is never coming back. It
produces progressive isolation and alienation of the person with the illness.
It is used rhetorically at the political level - blaming people with mental
illness for violence and other ills of society. In the current context treatment resources are
being removed at the same time and that is probably the biggest societal ill.
At the rhetorical level stigma is also confused or conflated
with clinical psychiatry. The ultimate societal outcomes of stigma are
labelling and stereotyping to define the socially undesirable group. Much of the rhetoric aimed at psychiatry promotes
this fallacy. Psychiatry operates at the
level of disease reality. The same level
that affected my mother and my family.
The reality of mental illness is much more than stigma.
It was a simple enough exercise. Take about 90 seconds and say how mental
illness affected you or your family. Do
it in groups of six and when I say time is up - move on to the next
person. The exercise was suggested by a
conference speaker who said a similar disclosure during an interview had given
him cause for concern. The setting was a
psychiatry meeting focused on stigma and we had all spent the morning listening
to presentations on the topic.
I really don’t like any professional meeting that resembles
an encounter group and think it should be actively discouraged. I think most people are like me – they go to
professional meetings to hear experts and passively absorb information. Further - I had just commented on the
psychodynamics of shame a few weeks ago in the seminar that I coteach and defined
the emotion has origins in disclosing information that could be embarrassing or
that others would potentially criticize you for. Of the 5 other people at my table – I knew
one professionally and had just met two.
I was the oldest person (by 30 years) and the only man. When they asked for a volunteer to start – I
volunteered. I did not think there could
be a more severe story, was thoroughly habituated to telling it over the past
50 years, and knew that 90 seconds was not nearly enough time to describe how
bad it really was. I was right on all
three counts.
“When I was 15 – I went downstairs and found my father
dead. Sometime after that my mother
began to have severe episodes of mania. She disrupted the entire town to the
point where the police were called repeatedly.
After several police calls, she was taken to a state hospital where she
usually spent a few months until she was stabilized and came home. That usually happened around Christmas
time. I was the oldest of 5 children so
I tried to keep things together. One-time
things got so bad my brother and I had to call the police ourselves and they
came down and told us that we wanted her ‘locked up like a chicken in a chicken
coop’. When I was a kid, I was not ashamed about the situation – I was pissed
off.”
Time was up. I was
not anxious or angry about what I had just said – but realized it was a very
sanitized version. I did not describe the symptoms – extreme
paranoia, irritability, impaired judgment, and anger. The disruption usually involved telephone
calls to public officials or the local radio station when she would announce
her name and begin swearing at whoever was on the other end of the phone. At
times she would get very angry and carry a knife around suggesting that we
should stab her with it. She would throw
us out in the middle of winter. We would
come home from school and find that she had thrown all of our clothing out of
an upstairs window and we had to pick it up off the ground. We would find strangers at dinner or once in
the bathtub. At night when we were
trying to sleep, she would play the stereo loudly all night long – usually Danny
Davis and the Nashville Brass Christmas album – punctuated by screaming up
the stairway at us. That could happen for days or weeks at a time. Hard to get up and
go to school the next day after one of those nights.
On a road trip – my wife and I stopped in to see her. The floor in the house was covered in about 6
inches of debris (from emptied drawers and closets). She would throw a das of Galliano onto the
plies. She was making bizarre statements while circling the mouth of a jar of
peanut butter with a piece of celery and then throwing the molten peanut butter
over her shoulder. My wife was upset and
had to leave. She sobbed for the next half hour as we travelled down the road telling
me she was sorry for what I had to endure as a teenager.
Even if I had time to describe this additional information,
that only scratches the surface of my mother’s experience with severe mental
illness and the impact on the family. I
could write a book about what happened. I
am including it here just to illustrate the severity of the problem. These
symptoms typically lasted for many months and some eventually became
chronic. As a psychiatrist – I have no
illusions that her symptoms were anything but the product of a severe mental
illness that was typically not treated well.
Her primary care physicians at the time were typically using a
combination of amitriptyline and chlordiazepoxide – medication that
psychiatrists would typically not use – even back then. When she eventually had access to a
psychiatrist and was given lithium but it was not very effective.
Stigma was not the main problem. The main problem is that when a person has a
severe mental illness like my mother it disrupts the relationship you have with
them, That disruption is more severe when you are a kid and can’t make sense of
it. It can affect your development and self-image. The broken relationship can be
permanent. It is more like grief and
loss rather than stigma and shame. After
a while my mother was not the same person any more. I no longer recognized
her. I could not remember what she was
like before the onset of severe bipolar disorder. I don’t think anybody did. It has a more severe impact on my mother than
anybody – but the emotional and interpersonal impact on everybody else was
undeniable.
All of the discussions of psychiatric diagnosis and
treatment do not touch on that. The
bizarre discussions of antipsychiatrists and philosophers don’t even come
close. If you are saying that my mother
was not mentally ill or did not have a “natural kind” of illness – you do not
know what you are talking about. If you
are suggesting that she needed “trauma informed care” – not much better. The unexpected death of her 43-year-old
husband was certainly stressful, but the expected reaction is not decades of severe bipolar disorder. It is
bereavement, a universal experience, and all that involves. The lack of
psychiatric care early in the course of illness could certainly have been a
factor. Her care rarely involved any of
the family. I don’t think any of her
physicians knew how severe that impact was.
Despite the fact that she lived in the state where Assertive Community Treatment
was invented in the 1970s – it was a rural county and active outreach by cases
managers was decades away.
My mother’s siblings and parents were very supportive. It
would have been very difficult to have made it through many of these episodes
without them. It took an emotional toll
on all of them as they tried to reason with her and convince her to do the
right thing – like curbing excessive spending and trying to get some sleep. The female members of the family – my grandmother
and aunt were much more effective than the men. They were able to react at a level that was
not strictly emotional. The siblings who
remained in town or returned also had a stabilizing effect. She also had two supportive female neighbors
who spent hours talking with her despite the obvious problems. But despite all of those efforts my mother was
never restored to her baseline – a goal I eventually adopted with every person I
saw as a psychiatrist.
What seems like a good interactive exercise to make a point about
stigma is a very blunt instrument. There
is no doubt that some of the local officials discriminated against her (and us)
because of the stigma of severe mental illness.
That was not close to universal by any means. At a recent reunion I greeted a retired police
officer who was very helpful to our family with his advice and reassurance. He did everything possible to avoid conformations
with my mother when she was confrontational.
I never got the chance to thank the women in our neighborhood who helped
but did when I sought them out in a crisis.
Stigma can be an important factor – but the take home
message from this essay is that the overwhelming fact about severe mental
illness is the illness itself. It has a significant
emotional impact on everyone. It
disrupts interpersonal relationships – some of them permanently. Some of that can be grieving the loss of a
person who is never coming back. It
produces progressive isolation and alienation of the person with the illness.
It is used rhetorically at the political level - blaming people with mental
illness for violence and other ills of society. In the current context treatment resources are
being removed at the same time and that is probably the biggest societal ill.
At the rhetorical level stigma is also confused or conflated
with clinical psychiatry. The ultimate societal outcomes of stigma are
labelling and stereotyping to define the socially undesirable group. Much of the rhetoric aimed at psychiatry promotes
this fallacy. Psychiatry operates at the
level of disease reality. The same level
that affected my mother and my family.
The reality of mental illness is much more than stigma.
George Dawson, MD, DFAPA.
Supplementary 1:
I posted this about 10 years ago
on stigma. If you use the search box on
the front page of this blog there are 15 or additional posts where I mention
the term in one context or another.
Since then, the jargon has advanced to define separate types of
stigma. Per this CDC web page
there are now three types with their suggestions for combating it.
Mental health stigma can
take many forms (CDC)
- Structural stigma, involving laws, regulations, and policies that can limit the
rights of those with mental health conditions.3
- Public stigma, which include negative attitudes and beliefs from individuals or
from larger groups towards people with mental health conditions, or their
families or health care providers that care for them.3
- Self-stigma, which comes from within the person with a mental health condition.3 People
living with a mental health condition may believe they are flawed or blame
themselves for having the condition.4
These definitions leave out important dimensions. For example – where are the insurance
companies, managed care industry, pharmaceutical benefit managers, and
governments that limit mental health coverage and treatment resources. At the same conference I attended one of the
advocates talked about the state government no longer funding an important
clubhouse resource for people with mental illness.
The public stigma is devoid of the politics that
defines people with mental illnesses either as violent criminals or freeloaders
getting benefits that they are entitles to. If you really want to cancel that
stigma why not clearly identify where it comes from?
Self-stigma seems to be describing self-image, self,
and self-esteem concepts that most psychotherapy providers learn how to address
in that process.
For all of these reasons the stigma seems to be a rhetorical
stretch to me. If you want to address
these issues point to the source of the discrimination and don’t make it into a
general societal issue. It is a societal
issue only at the level that society never confronts the real source of
discrimination.

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