Diagnosed schizophrenic, his erratic and unpredictable behavior over the years had taken a toll on the family and they cut him loose. No one knew where he was or what kind of mental health care, if any, he was getting.
She felt incredibly guilty. "If I had kept in touch maybe I could have helped him.
It is very easy for those not having experienced living with a mentally ill family member to say, " Put em away. Don't ruin YOUR life."
Little did I know at the time my coworker spoke with me that my teenager would be diagnosed as bipolar shortly after our conversation.
During the sixties, seventies and eighties, I worked as a social worker in short and long term psychiatric hospitals. My first job as a social worker was in a short term psychiatric facility. Treatments available? Electroshock therapy, haldol and lithium. Valium, opiates, seclusion and restraint. People would be locked in small rooms with padded walls and a mattress. The door had a small window. Aides would do clip board checks, peeking in the window to make sure the patient was safe.
Eventually, after massive doses of primative medications, patients came out, groggy, confused and subdued.
Over the three years I worked there many of the same people returned for treatment. Haldol created permanent damage , creating strange muscular mvements and spasms, permanent confusion and often hallucinations.
I suppose those were the only drugs available at the time and next to Electroconvulsive shock therapy those drugs were the babies.
I graduated from there to working with patients who had been sent to the state hospital for twenty or more years.
Up until the eighties it was common for family to lock up a family member for twenty or more years. Institutionalized, these individuals had no idea how to operate in the community. My job was to help them learn the skills to do that and help them move to special community homes in the cities and towns they came from.
It was a challenge. After so many years inside an institution learning how to communicate with the outside world created intense moments of wishing to return to institutional living. We did a lot of work but the joy and the pleasure in finding a place to fit and enjoying the freedoms were great incentives. I remember an older woman talking constantly about wanting catfish when she moved to her own place. One afternoon we went down to the river and fished for them. It was an activity she did as often as she could becuase it gave her great joy, brought up pleasurable memories and was cheap to do! Another woman spent her first monies buying lipstick at a department store. She had been the girlfriend of an mob member and used to spend time shopping-each week we went to the same store so she buy another lipstick.
Years pass and I live in the state of Nevada which has such poor services for the mentally ill you can find them frequently on the side of the road begging, in jail, the emergency rooms and frequently, dead in the hot summer of the desert. I don't want this to be my son's fate.
Whenever you see a homeless individual try thinking like a mother, I look at people and think, that individual was someone's baby-hopefully somewhere in this lifetime, that person was loved and cared for-and I feel sorrow. Don't give me that garbage about people choosing their fate. Yes, for many that is probably true, but for those with minds preceiving another reality, choosing can be a ittle off kilter.
My son is in his thirties now and he lives with me. Believe me there are challenges. When a person with bi-polar disorder goes off medicine the "I don't need medicine" manic phase kicks in. We can all see it but he refuses to believe his behavior is anything but truthful.
The problem with the new drugs is they don't give a person with Bi-polar disorder less emotion, they obliterate emotion. Literally my son feels very little emotion on medications. Off the medicine he feels immense joy and immense anger. But he feels.
He describes this flatness as looking at others and feeling deaf to emotion.
There is no village for the mentally ill anymore. What will happen to him when I am gone? I worry about that.
He is one of the fortunate. He is a part of and has a family who love him.
We used to care more about vulnerable citizens. The elderly, the chronically ill, the mentally challenged.
What happened to us?
What will happen to him and others like him?
Eventually, after massive doses of primative medications, patients came out, groggy, confused and subdued.
Over the three years I worked there many of the same people returned for treatment. Haldol created permanent damage , creating strange muscular mvements and spasms, permanent confusion and often hallucinations.
I suppose those were the only drugs available at the time and next to Electroconvulsive shock therapy those drugs were the babies.
I graduated from there to working with patients who had been sent to the state hospital for twenty or more years.
Up until the eighties it was common for family to lock up a family member for twenty or more years. Institutionalized, these individuals had no idea how to operate in the community. My job was to help them learn the skills to do that and help them move to special community homes in the cities and towns they came from.
It was a challenge. After so many years inside an institution learning how to communicate with the outside world created intense moments of wishing to return to institutional living. We did a lot of work but the joy and the pleasure in finding a place to fit and enjoying the freedoms were great incentives. I remember an older woman talking constantly about wanting catfish when she moved to her own place. One afternoon we went down to the river and fished for them. It was an activity she did as often as she could becuase it gave her great joy, brought up pleasurable memories and was cheap to do! Another woman spent her first monies buying lipstick at a department store. She had been the girlfriend of an mob member and used to spend time shopping-each week we went to the same store so she buy another lipstick.
Years pass and I live in the state of Nevada which has such poor services for the mentally ill you can find them frequently on the side of the road begging, in jail, the emergency rooms and frequently, dead in the hot summer of the desert. I don't want this to be my son's fate.
Whenever you see a homeless individual try thinking like a mother, I look at people and think, that individual was someone's baby-hopefully somewhere in this lifetime, that person was loved and cared for-and I feel sorrow. Don't give me that garbage about people choosing their fate. Yes, for many that is probably true, but for those with minds preceiving another reality, choosing can be a ittle off kilter.
My son is in his thirties now and he lives with me. Believe me there are challenges. When a person with bi-polar disorder goes off medicine the "I don't need medicine" manic phase kicks in. We can all see it but he refuses to believe his behavior is anything but truthful.
The problem with the new drugs is they don't give a person with Bi-polar disorder less emotion, they obliterate emotion. Literally my son feels very little emotion on medications. Off the medicine he feels immense joy and immense anger. But he feels.
He describes this flatness as looking at others and feeling deaf to emotion.
There is no village for the mentally ill anymore. What will happen to him when I am gone? I worry about that.
He is one of the fortunate. He is a part of and has a family who love him.
We used to care more about vulnerable citizens. The elderly, the chronically ill, the mentally challenged.
What happened to us?
What will happen to him and others like him?