On Acceptance: Morrie writes ~ “Acceptance is not passive-you have to work at it by continually trying to face reality rather than thinking reality is something other than what it is….People with great faith in God or strong spiritual ties may be more accepting of what goes on here and now because they know that this is just a temporary stopping place to the next world, so to speak…..Acceptance is not a talent you either have or don’t have. It’s a learned response……You may not be able to change your medical prognosis, but you can control the destructive emotions that can subvert your mental and physical health.”
Especially true of Bipolars who tend to isolate ~ Morrie on Maintaining an Active Involvement in Life: “Be occupied with or focused on things and issues that are of interest, importance, and concern to you. Remain passionately involved in them…… I tend to think that we do have core self. And that the more you know about who you are, the more actively you can be involved in the world around you……the self means nothing outside the context of community or meaningful contact with other people.” ~ Morrie Schwartz
For example, I have been a passionate and keen diarist since I was 12 years old. Writing is one of my greatest loves, and I have continued to do it for many, many years. It gives me pleasure, and is something I know I can do well. Starting this blog about a month ago is an example of this; it mixes two of my passions in life ~ writing and destigmatizing mental health issues. I write to live. It allows me to go back and take an objective view of my reaction or response to a situation, and then allows me to re-evaluate what I could have done or said differently, or if, in that particular situation, there really was no other option. In essence, writing takes the emotions, puts them into words on paper or a computer and “removes” them from you so you do not feel them as intensely. This allows you to be a more objective observer of yourself.
As person living with Bipolar Disorder, PTSD, and Panic disorder, I have a subjective view of mental illness since I obviously battle my moods everyday even though I am a “treated” Bipolar. Writing about my experiences with these illnesses makes that view objective, and I am able to look at them as part of me, but not the whole of me. I can see where my reaction to something minor may have been out of proportion, I can see when my moods have control of me, and when I have control of my moods.
The Diatribe Against this Countries Healthcare and Social Services Programs:
I am all for speaking out and talking about mental illness because, for some reason unbeknownst to me, it is “scarier” than a lot of physical ailments. I wonder if it is because the “common” view of mental illness is that homeless guy on the street ranting and raving to no one in particular? Or if it is scary because it involves the mind of which doctors and researchers know very little? Maybe, it is because one of people’s biggest fears is the unknown, and there is nothing about humans more unknown than the brain? Maybe, it’s that fear of ending up like Aunt So and So who went “nuts” and killed herself? I do not know, I am speculating. All I do know is there is this irrational fear of mental illness. They say that someone is “touched” (a nice way of saying crazy or nuts), they say he/she is different than everyone else. Maybe that’s it. Maybe it is people’s fear of the unknown and the different. However, you never really can tell (aside from the obvious cases) when a person suffers from mental illness, they could work next to you, and you wouldn’t know it. What is truly needed is open, objective, honest, and intelligent discussion about mental disorders of all kinds.
You cannot know anything about which you turn a blind eye the way most people do to the raving homeless man. You do not know his life story. He may have been a CEO who first lost his job, then his home, then his family, and now he’s out on the streets with paranoid schizophrenia. He may have been managing it since he was a teenager (the time when most serious mental ailments first present), but all of his losses combined to be one big trigger that sent him over the edge. He no longer has health insurance, so medication is beyond his reach. He is so lost in his own reality that it is unrealistic that unless someone intervenes on his behalf, his access to Medicare is limited, his access to treatment is non-existent because he doesn’t know where or who he is. How is he going to fill out the forms needed to get on Medicaid/Medicare in order to treat his illness? He cannot very well do it himself. So, he remains scattered on the street, homeless, alone, scared, and sick.
Has anyone ever thought to talk to a person with an OBVIOUS mental illness; I am not talking about the ones that are easily hidden like treated Bipolar, Borderline Personality Disorder, situational and chronic depression, Narcissistic Personality Disorder, etc. I am talking about the ones that cannot be so easily hidden even when treated like the Schizophrenic spectrum, the Oppositional Defiance Personality disorder, the Anti-Social Personality disorders, the Schizoaffective disorders. The ones that make people seem strange and weird, and sometimes, frightening. A lot of these people want to talk because nobody WILL talk to them, ask them about their day, if there is something they can do for them, or even get them to a state agency where a social worker can serve as a liaison between the sick person and the System. I do mean to spell that with a capital “S.”
If someone or a group of people were willing to help these people get the care they need by getting them to a person who can help with the Medicaid/Medicare forms, can help them get into shelters rather than having the police round them up on very cold nights. A lot of homeless, mentally ill people will deliberately get arrested during the winter so they will get fed, and a warm place to sleep. That is not right or just. It only takes one person to make a difference in someone’s life. If a person or a group formed for the specific purpose of helping the mentally ill (many are homeless BECAUSE of their illness and lack of treatment) could get the homeless and mentally ill to an agency designed to help people in this condition do the paperwork they need to get treatment, get disability benefits, get food stamps, etc.
Cities with the help of State and Federal government funds could build housing strictly for the mentally ill, the residents would pay rent in accordance with the amount of their benefits (a sliding scale), there could be caretakers there whose job it is to make sure that people living in these subsidized apartments take their medication, that they use their food stamps (EBT/SNAP program card) for food, and not for illicit street drugs (drug and alcohol abuse are often co-morbid with mental illness), and that those who can function in a menial job (like being a janitor or a custodian at an office building) get jobs, and that they do not kill each other. Mentally ill people, especially schizophrenics and schizoaffectives can be violent even when treated. So can Bipolars if their illness is serious enough, especially during Manic phases when the person may or may not go psychotic from lack of sleep. Having something meaningful to do, like a job (or writing this blog), does wonders for a person’s outlook about themselves, and tends to make them want to stay on medication, want to maintain their functioning status. Although, with some of these illnesses, people are unaware of what they are like when un-medicated and not functional. People who consistently fail to meet these expectations would be asked to leave.
I am not creating a Utopia for the mentally ill, here. Residents would have to maintain themselves, and their apartments. There would be inspections. I realize this may be an invasion of privacy, but it happens all the time in the “real” world when a person rents a property. They would have to stay on medication, see their doctors regularly, pay their rent on time, feed themselves with their benefits, there would be a zero tolerance policy for drug and/or alcohol use unless medicinal marijuana is ordered by a legitimate physician (and if the person with the prescription was found sharing his medicinal marijuana, he/she would be warned that this is the only time they will be warned otherwise back out they go), maintain their work status, if applicable. In other words, do not take too many sick days unless you truly cannot function. I am not a Nazi. Sometimes, and I can attest to this, the meds just do not work for some reason, and your disease jumps up and bites you on the ass, and you have no control over it. So, employers would have to be carefully screened for compassion toward the mentally ill, and to allow for periods of time away from the job for the mentally ill just in case their illness becomes “active.” There could be a list of employers willing to take on the functioning mentally ill; kind of like employers that hire ex-cons so they can fulfill their parole conditions. There is/was a facility like this in Albuquerque, New Mexico about 7 or 8 years ago. I do not know if the program was stopped or not.
Okay, a quick Google search indicates there are programs out there, but once again, they are State run and require forms to be filled out, documentation to be brought in. Now, I am a high functioning Bipolar, and I have applied for housing assistance before. The packet of stuff to fill out is 10 pages long, and I did not understand half of it (and I have a college degree.) How do they expect that the average mentally ill person is going to be able to cope with that without some help? One of my biggest pet peeves is that the way our government (both State and Federal) appears to be designed to “let” people fall through the cracks, and then still be able to turn around and say, “Well, they could have taken advantage of X,Y, or Z program…” NO, they could not, because some group of not mentally ill people designed the programs to be difficult for even a non-mentally ill person to understand. I do not know how many times I went back to the Housing Authority in Albuquerque because they needed some other documentation of something. I personally think they make it up to annoy people, but imagine if you are mentally ill, and trying to deal with all of this red tape? You’d get lost, agitated, irritated, confused, and this is IF you are being treated. Anyone else who is not under a doctor’s care would be completely stymied by the way the system is set up. It is not “user-friendly” by any stretch of the imagination.
The seriously mentally ill need advocates, people to stand up for them, people to help wad through the muck we have created to be the “Social Services” departments on both State and Federal levels. If a person is lucky, they will be a high functioning ill person like myself who can slog through all the crap on their own; although this is not to say I do it with a smile on my face because even my meds do not make me that happy. But, a seriously ill person is going to need a caretaker, some form of mediator between them and the System. Otherwise, they will become one of the millions who cannot get what this country has set up to help them.
The reason I say that it is time for open, objective, honest, and intelligent conversation in this country regarding mental illness is that first of all, many people suffer from some form of mental illness on a scale of severity, secondly, our programs designed to help the mentally ill or disabled are impossible to understand or access (unless you are an attorney or a politician), thirdly, there is such a stigma surrounding mental illness that nobody wants to talk about it like they are afraid its contagious (I assure you, it is not), fourth, the whole benefits system for the mentally ill and/or disabled needs to be completely dismantled and redone. I mean, people with debilitating illnesses unable to get social security benefits without an attorney, or being denied the first couple of times you apply. That is just, pardon my french, fucked up. Obviously, they need the benefits or they would not have applied (HELLO), they have provided adequate documentation for the benefits, and they are DENIED! Oh that just pisses me off! That’s what the Social Security Disability Insurance and Supplemental Income programs were set up for. People with disabilities that prevent them from working. Believe me, a lot of us are incredibly bored and sad because we can remember working, and feeling productive. We do not really want to be on disability.
The name really says it all: disability. Take a minute and think about what that word means to you….. to me it means incapable, unintelligent (many, many mentally ill people are highly intelligent), unable to do something, not productive, non functional. Do you see how even someone who is mentally ill herself can come up with labels to define the mentally ill? Now imagine that spread out to the people who are not mentally ill, and lack the compassion and empathy to even try to understand what it means to be mentally ill….. I can think of one person right now off the top of head who thinks they understand but they have such a poor understanding of what it is like and how tiring it is to try to be “normal.” I have loaned this person a book, one of the best called An Unquiet Mind: a Memoir of Moods and Madness written by a psychiatrist with Manic Depression who works at John’s Hopkins. I wanted him to see firsthand what it is like to be Bipolar, and able to function at a very high level. I do not know why I am disappointed. I never really expected them to read it anyway. When I came home from the hospital about a month ago, I brought him material on Manic Depression and Depression from the NIMH, and I do not know where that ended up. I didn’t really expect them to read that either. I do not know why I expect anything from this person. it’s like clapping with one hand; all it does is stir up the air a bit. I do not know why I expect them to read anything related to learning about my multiple diagnoses. It is like if they do, then it becomes more real, and they can no longer blame all of my behavior on my illnesses. They have to blame me sometimes. Because I have learned one thing about being mentally ill: IT DOES NOT DEFINE WHO YOU ARE!!!! You are you, your illness just makes you “mentally interesting.” Saw that on the web the other day, and really liked the description 🙂
The medication helps, but I have deliberately kept the doses right at therapeutic so I don’t feel over medicated like I was for a long time, and like many people still are because they have not learned how to stand up for themselves yet. It is vital that you advocate for yourself. If you can’t, find someone who can, a friend, parent, someone!
So, that’s my diatribe for the day. People, get over yourselves, the mentally ill are just like you and everyone you know. Their lives are just more challenging. You wouldn’t be afraid of an autistic child or a child with Down’s Syndrome, so it is time that you stop believing that ALL mentally ill people are violent, lazy, stupid, scary or any other adjective you can think of.