My story over the last 43 years

I haven’t posted my story in awhile. So here goes.

There is always someone who has it worse than you.

Some people claim they have “mild” schizophrenia, I seriously doubt that that is possible. I’ve met and lived with and been hospitalized with a number of other schizophrenics over the course of my 43 years with this disease. I’ve heard some of their stories and I’ve observed them and I have not seen one of them who had it easy with this disease. I have not run into anyone who can say their disease was mild. I guess there’s the odd exception

But anyways, I can give you a brief part of my history and hopefully you can get something out of it. And by the way, I was diagnosed with paranoid schizophrenia in 1980 when I was 19 so I have been dealing with schizophrenia for almost 43 years. That’s a big chunk of change.

Anyway, I went into my first psyche ward when I was 19. I was in bad shape. After two weeks my parents found me a place to live which was a group home for schizophrenics. I went through hell there, I suffered a lot. Every minute of every day for about a year. I was 19 and I had no money, no girlfriend, no friends, no car, no school, no sanity. And that was true for the entire year. I had weird symptoms. It could take me an hour just to get dressed in the morning in a pair of jeans, a shirt, and socks and shoes.

I spent months sitting alone in an old dirty chair out in the backyard fighting to keep my sanity. Every day I felt like I was going to go stark raving mad. I felt hopeless, suicidal, lonely, crazy. I did not improve at all for that year. I saw no hope, no light at the end of the tunnel. I saw no end to my misery, no sign that I would ever get better. But I survived.

After spending a year there I moved back into my parents apartment. I lasted two weeks before they had to put me in a psyche ward again. From the psyche ward I was put in a locked psychiatric hospital for 8 months, where I stayed with a 100 other patients who were in crisis too. I got up at 8:00 a.m. for breakfast every morning and after breakfast the screaming started. After breakfast all my fellow patients for the next 8 hours would be screaming, arguing, cussing, threatening each other. And this is how it went until dinner time, every day of my stay there. They put me on medication there. It didn’t help me get better but I think it stopped me from getting much worse. I don’t know how many medications you’ve tried but as many of you know it is not unheard of to try many medications before you find one that works. And so I’ve been on medication for over 42 years.

And my symptoms were horrible for 8 months. It was like torture. But then I got out. I moved into a really nice, clean, safe, group home in a nice neighborhood. Things started looking up. My symptoms became more manageable. I started going to a day program 4 days a week. After 9 months in that home after a series of small steps, I got a job. I was 22 years old. I still had nothing but at least I was in a nice environment. I stayed at that job for four years and I was actively psychotic for a lot of that time. Well, eventually I got a car, a house to live in with two or three other people. I got a little money, a little power and control. I got pretty stable. I was doing good.

Then I got addicted to crack cocaine. I was addicted for four years and I went through the typical drug lifestyle. I was the victim of violence, I got robbed a couple of times, people conned me and I conned them. I often risked my life and my freedom to get my drugs for four years. Take my word for it, my addiction was not pretty. But I got clean in 1990 through AA and in the last 33 years I have not touched alcohol or drugs.

Well, I’m 62 now. A lot has happened since my disease started. I’m looking back on being employed almost steadily, albeit mostly part time, for the last 40 years. I got my license in 1997 and I have owned and driven a car since then. I went to college and graduated this year and even attended graduation ceremonies. I lived on my own for 20 years, usually renting rooms in peoples houses. I lived by myself in a studio for 6 years while working and taking online classes. In those 6 years I lived like anybody else. I shopped for food, I cooked, I kept my studio clean, I went shopping for shoes and clothes when I needed them, I made and went to all my appointments with doctors or Social Security. I even had my own cat, lol…

But my recent story is a little bad. in 2015 I was renting a room in someone’s house. I was working, taking classes. But then my mom died. I was under a lot of stress and my mom’s death tipped me over the edge. I lost my housing, I couldn’t drive, I had to drop out of school and I had to take two months away from work. and I had to go into the hospital for two days.

I’m just telling you this to illustrate that even when you’re doing OK life is going to throw you an ugly curve ball now and then. Life does not always go smoothly and it doesn’t always have a happy, fairy tale ending. I don’t want to paint an unrealistic, rosy picture of life.

Bad stuff happens to everybody, no one goes through life unscathed. No one. But life isn’t all bad. I’m back at my job, I got a 2012 Volkswagen car that runs well, my living situation isn’t all I would like it to be but it is not that bad. I slowly got back on my feet, I’m getting ready for another round of life’s ups and downs.

And as I write this, it’s a nice night tonight, I’m relaxed and looking forward to tomorrow so I can get up tomorrow and go to my doctors appointment and maybe over to my sisters house for dinner. I really do hope someone gets something from all this. I can’t solve your problems, I can’t guarantee how your life will go but I hope I am instilling a ray of hope into your life and as you can see. It is possible to make great turnarounds in life.

I came from the bottom of life with nothing going for me, but look how things changed. Most people with schizophrenia show signs of improvement as they go through life. But sometimes there are no answers and you just have to endure the pain and agony and put one foot in front of the other and keep trudging along. There is no quick fix to our problems. You don’t get better overnight. Everybody has different problems and no two cases of schizophrenia are exactly alike.

Some of your symptoms may get better some may not. But you just have to keep trying like everybody else. I don’t want to give you false hope, I’m very lucky to do what I’ve been able to do. But other people besides me have suffered and then made dramatic comebacks. You can’t predict the future. Many people improve. Some don’t. Or you may improve a little or you may improve a lot. Who knows? But it’s worth sticking around and try to let people help you. Good luck.

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Thank you…. That was very inspiring and motivating. I am learning from you.

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How did you deal with boredom over the years?

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I didn’t start experiencing real boredom (except when I was in the hospital) until about 4 years ago. At first I welcomed it, after all the drama of my earlier years it was a relief for everything to slow down and I could just relax and have to consciously think of things to do. I guess I do what most people do. I’m busy at work or running errands or going to doctors appointments and when I’m at home I listen to music, get on the computer, cook, read, doodle around the house or go for a drive. In other words, I don’t do much but I’m working on changing that. I started physical therapy, that breaks up the monotony on my days off. Sometimes I go over my sisters house for dinner. I have a couple other plans of other things I can do.

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Oh so you don’t have enough to do. I have the same problem. At least you have a job that helps. I don’t have a job…… I am worse than you with having not enough to do. I think you are already doing everything you can do……as far having enough to do. I am trying to get a friend and that will help me. I am not sure if you want a friend…. but that would be my advice to you. :grinning:

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Boredom is my biggest problem. I used to rarely get bored as my brain was more energetic and interested in stuff. Now it is disinterested in things and angsty.

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Thanks for the novella, lol. I read the whole thing. I like to read. I feel guilty about not being a role model for newbies. I don’t want to be a presumptuous guru. But I could really help someone because I have gotten over a lot.

I don’t drive because of my slow moter responses. I think the medicine does that for some. I also am the kind of person to not take reality serious, like running over people.

I am also a recovering addict. I didn’t read the n.a. basic text until recently because I’m literary lol, choosing to read other more notable books. When I read it I realized I knew 99% of it because I had been to thousands of meetings and that was the language they spoke.

I got a compliment today from my dentist and I told him how it works. He asked how I kept a good attitude and I told him I don’t drink or smoke. He told me all his patients smoked weed. It is legal here. I am not extremely tempted to use it. Been there, done that.

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Thanks for sharing @77nick77 theres some great wisdom there.

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Now I don’t speak for everyone on the forum of course, but we love you @77nick77. The place would not be the same without you. You truly are an inspiration for those newly diagnosed and those seeking recovery.

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When people go into isolation chambers they experience voices as well.

Everyone has this, we just notice it more.

Personally i think its from environmental magnetic waves and frequencies acting on our brain.

Its inherently against us and we shape it as something so.

The drugs are used to reduce our brain activity so we dont get overexcited about it.

If you focus on it on the side of your head more you will hear it more cause its where the audio cortex is.

If you put it at the back of your head it will turn back into the sub, con, suss. Thats where most people usually put it.

I liked reading about your story. Did ever need disability checks? I’ve had a few jobs since diagnosed, but don’t consider getting one often. I have some other stuff I can do atm. If you get disability do they cut some of your check or how do you keep it?

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I get SSDI. You’re allowed to work and make a certain amount of money each month, if you go above that you would be in danger off losing your benefits. My check amount is based on how much I worked before I applied for SSDI, I get a raise the beginning of each year because of the annual Cost Of Living Adjustment (COLA) but my benefit stays the same throughout the year, it doesn’t go up or down except for the COLA.

When you get awarded SSDI they allow you to try working and give you “work trial periods” where you can test how much you are able to work and you can make any amount of money for a certain period go time; I think it’s 9 months and keep your benefits… There’s other rules but that’s basically it.

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Such an interesting life!
Thanks for sharing

Very inspiring!

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I hope you will have better life from now on.
Thanks for sharing … :v:

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That’s a good story @77nick77. It’s good to know we can still live a good life even with schizophrenia.

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Thanks for sharing. Very nice to hear.

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