I Can’t Stand Living With My Parents Anymore. I’m Ready to Go to a Handicap Accessible Home

I’m at my wits end. I can’t stand living with my elderly parents anymore. I’m tired of their complaining and irritability. My dad is almost deaf but he still tries to talk to people in different rooms even he’s almost deaf. Even hearing aids don’t help. He talks real loud and groans real loud when in pain, which is almost all the time anymore. I’m tired of his complaining. I’m tired of him not being able to hear me.

My mom isn’t much better. She can barely see yet refuses to wear glasses. She can’t even read a recipe card now. At least she doesn’t drive much. I don’t know why she won’t swallow her foolish pride and get glasses. She’s being really stubborn about this even though it’s obvious she needs glasses.

Physically I can stand up, transfer to the bed and wheelchair. But it’s pointless as all the doors in the house are too narrow for wheelchairs. I can’t even get into the bathroom. I’m maxed out on over the counter pain medications, force myself to do exercises even when sitting down, but I still have lots of pain when I try to stand up and walk.

I’ve given up on my family making the house wheelchair accessible. I just want to go to a home that is wheelchair accessible. I don’t care if it is assisted living or long term care. I keep getting turned down for homes. Some homes say I am too young. Others won’t take mentally ill people. Some say I’m too heavy. I mean, what nursing home doesn’t have lifts? And I don’t need any damn lifts. I just need a place that’s wheelchair accessible. Why is this so tough to understand.

At this point I don’t really care about losing most of my funding to go to a home. It’s gotten unbearable here in my parents’ house. My dad has lost patience with me and is making unrealistic demands. My mom isn’t as helpful and more irritated than she was even three months ago.

In short, I decided I want to go to a home. I want to have wheelchair accessible doors and hallways again. I want to have conversations with people who aren’t senile, stubborn, and bitchy even if it is just staff members and not residents. I’m tired of this shit. I never should have left Nebraska when I already had wheelchair accessible housing. Burns me that most houses and public places aren’t really wheelchair accessible.

And the worst part is my parents are starting to act like it’s all my doing that I ended up in a wheelchair, especially my dad. Can’t even rely on family anymore. And placement hasn’t come through even though we’ve been looking since last September.

Finding Strength: Managing Health and Family Doubts

Took a couple of days off this weekend. Back to the grind. The last several days I have been up most of the night and gotten my best sleep in the afternoons. I still sleep like ten hours a day, but most of it is during daylight hours.

I’m back on the Turmeric. I think it’s helping with the bad knees and ankles. I started taking Vitamin B and Vitamin D supplements a couple of weeks ago. I think I have more energy and optimism overall now.

I think I am losing weight. If the way my clothes fit is any indication I really am. Most of my shirts are quite baggy now. Might have to drop down a shirt size. It also looks like I’m carrying less fat on my abdomen. My calves are less swollen than six months ago as are my thighs. I don’t eat much anymore besides protein and vegetables. I try to avoid sugar and carbs.

Got turned down for a long term care facility. I’m not shedding any tears over it. In reality I don’t want to go to long term care. Ideally I would just stay in my current house and just widen all the doors to be wheelchair accessible. My parents aren’t on the same page as I am. They aren’t enthusiastic about making such modifications to the house.

I have come to the conclusion that I don’t want things to be easy. I want to struggle to get my walking ability back. I want people to doubt me. I want to be fought every inch of the way. I want even my own family to actively work against me. They originally doubted I could graduate college with schizophrenia. Proved them wrong. They originally thought I couldn’t live alone with schizophrenia and on disability pension. Proved them wrong for over seventeen years.

Most people thought I made a mistake when I went to long term care to get better. I was flat out told I would die in that facility. Well, eight months later I walked out the front door on my own two feet. I went in that facility on a hospital stretcher. I walked out on my own two feet after only eight months.

I’m facing doubts again. After this third stay in the hospital, I lost all of my mobility. Physical therapy hospital didn’t help at all. Neither did the home therapist. They all gave up on me too soon. Sure, it took a few months. But I am back to walking short distances within the same room. I can transfer into the wheelchair. It is a foldable wheelchair so I can get it through doors. I could already get everywhere in the house if the family would just break down and pay for the modifications.

As far as modifications go, all they would need is to widen all the doors, put a railing in the bathroom, and get some of the clutter out of the house. My parents have a hard time throwing anything away. I swear if I outlive them, I’m going to rent a dumpster and throw tons of Knick knacks and crap in. I refuse to deal with it after they are gone. I won’t live the life of a hoarder. Was forced to do it as a kid. Forced to do it again after being on my own for seventeen years. After my parents are gone or moved to a nursing home, never again.

Oddly I’m not feeling hurt or betrayed by my family not believing in me. In some ways they have never believed in me. I’m going to get mobile again, at least for short distances. I am going to keep losing weight. My goal is to eventually get back to the same weight I was as a freshman in college. I could easily walk three to five miles a day back then.

I might never be able to walk that far again. But, dammit, I refuse to give up. Between being severely bullied by my school mates as a kid, twenty five years of schizophrenia, three years of congestive heart failure, surviving eight months in a long term care facility, moving two states away to be closer to my brother (at least he believes in me), and seeing crazy ass tech advances in terms of AI, automation, biotech, fintech, etc.; I’ve come too far to cash out now. Give up? Not happening as long as I got breath in my lungs.

I don’t know why my parents refuse to make the modifications to the house to make it handicap accessible. Honestly, I don’t care. I’m going to get better and mobile in spite all the road blocks people keep throwing at me. I want to be doubted. I want to be told I am a liar and full of shit. It just makes me more determined to keep beating the odds. Beating the smart money has been the mode of operation for my entire life. Personally, I think the “smart money” ain’t as smart as it’s cracked up to be. I just keep proving them wrong because that’s what I’ve done my entire life.

Overcoming Mobility Challenges: My Journey to Independence

STILL haven’t heard anything from my possible new place. I’m giving up on that. I’ve pretty much come to the conclusion that I’m going to be living with my parents for the rest of my life. I’m tired of pretending that things are going to change in that regards.

There are worse things than living in the suburbs. It’s a safe neighborhood. I can get any restaurant within reason Door Dashed to my house. I get two day delivery on almost anything on Amazon. There isn’t much for homelessness near my house. And I live only a fifteen minute drive from my brother and his wife.

As I’m getting used to the fact that there won’t be a place coming open for me, I have decided to make the best of it. Mobility is slowly coming back. I can easily transfer from recliner to bed to wheelchair with only a little pain in my ankles. My knee pain has been completely solved. They don’t even pop and crack anymore. I’m so thankful for Turmeric.

Now that I can freely get back into a wheel chair, I’m on to my next project. That is moving about the house. The only real hang up in this house is the narrow doors. The hallways are wide enough for wheelchairs but not the doors. If anything happens to my parents where they have to move to a home and I get left behind, I’m so going to have to move my hospital bed and recliner into the living room. That’s been my plan all along. I just didn’t think that I would have to utilize it.

Finally got out under the overpayments I was paying back to social security. Looks like the timing was good. Sounds like the whole system has become a dumpster fire. While I’m all in favor of cutting government waste, I totally accept that the transition to a more efficient system is going to be tough and take years perhaps. I do have some money out of the system just in case of things like this. In social security’s case, it sounds like a modern day run on the bank.

My next goal as for my mobility is to stand up long enough to fold up my wheelchair and get it through a door. That will open up the entire house and the back yard to me. If I keep getting the run around from social services, I’m going to need to make myself as mobile as I can.

The only reason I was needing a place was because of the wheelchair, not because I am senile. I remember to take my pills daily. I can clean myself, at least with sponge baths and dry shampoo. Maybe that is why I can’t get a place. Because I’m still quite mentally sharp I’m not a high priority.

In some ways I’m glad I keep getting rejected for these places. Five months ago my ankles and knees were so bad I couldn’t even stand up on my own. I needed an ambulance crew to set me up in my own house. Spent from early October to early January learning to stand up again.

I can stand up again. Now I can walk real short distances. I’m working on cutting down the pain in my ankles. In the five plus months I have spent teaching myself how to stand and walk again, I haven’t fallen even once. And I have done it all without any help from anyone.

I had physical therapy come in back in October. But they gave up on me after 30 days because I wasn’t making “adequate progress.” As it is now, I don’t think I really need physical therapy. What I do need is wheelchair accessible doors and bathrooms. Not sure I can get that done in this house. I’m pretty sure my family could afford it if I really put the screws to my parents. Sometimes playing hardball and being a hard ass has to be done to get a point across. I swear some people are so oblivious.

In spite of my hurdles and set backs, I’m making decent progress in learning how to walk again. And I am doing it in spite of the roadblocks and hijinks and run around of social services. If anything, I enjoy the hardships.

I enjoy being told what I can and cannot do. That way I can rub it in people’s arrogant faces when I end up proving them wrong. People didn’t think I could graduate college with schizophrenia. I proved them wrong. People didn’t think I could hold a job with mental illness. I held a janitorial job for over four years. People didn’t think I could live on my own with schizophrenia. Proved them wrong for seventeen years without being even late on a rent payment. People didn’t think I could survive and recover from congestive heart failure. Definitely proved them wrong on that. People now think I’ll never walk again. That’s my next mission to prove people wrong.

Challenges in Securing Long-Term Care in Oklahoma

Rumor had it that a long term care facility an hour from the metroplex was already to accept me with open arms. That was over a week ago. Haven’t heard anything since. Getting into a care facility is proving to be impossible here in Oklahoma.

A few weeks ago Adult Protective Services were called on my behalf. My house isn’t handicap accessible and I need wheelchair accessible housing. I can transfer from a recliner or wheelchair to a hospital bed, but I still have pain in my ankles every time I walk. I can transfer but it is painful.

After APS was called on my behalf, I was sure I would get a placement within a couple of weeks. Normally they don’t get involved unless a situation is dire and beyond redemption. Well, both are the case in my situation.

I doubt my house can be made wheelchair accessible. Even if it could, I couldn’t afford even property taxes on this place after my parents are gone.

I’m just tired of the run around. I’ve had more problems with social security, Medicaid, healthcare, social services, hospitals, case workers, etc. in the two years I’ve lived in Oklahoma than my last seventeen years in Nebraska. Apparently, service quality varies greatly from state to state.

I’m to where I’m at my wit’s end. I’m tired of fighting and getting zero for results. I’ve grown hopeless and despondent. I sleep twelve hours a day to numb the pain. I’ve told off my parents a few times in the last several weeks because of frustration. I’m becoming something I don’t like. In short, I’m becoming the whining and bitter old man I promised myself I would never become.

I just want a permanent placing in a nursing home to where I can have wheelchair access and my day-to-day medical care provided. Apparently in the richest country in the history of the world that isn’t an option.

Navigating Accessibility Challenges This Spring

It’s officially the start of spring here in Oklahoma. Been feeling more spring like the last couple of weeks. Been really dry and windy too. Been having wildfires all over the state. Too early for this. Not a good sign.

Finally over a cold that has dogged me for weeks. Some days my nose was so runny and plugged I couldn’t breathe. It’s good that my sneezing fits are over.

Still haven’t received any word on a placement for a wheelchair accessible place. The main hangup is corporate has to make the decision. In short, if some suit in the office says no, than everything my doctors, caseworkers, and nurses have been saying for months is null and void. Burns me.

Personally I would love to stay in my current house in the suburbs and just make this house wheelchair accessible. Not sure it can be done. Even if it could, I couldn’t afford the property taxes and utilities.

The Impact of AI on Jobs and Relationships

The rapid rise of automation and artificial intelligence (AI) is reshaping the world in ways that were once relegated to science fiction. As machines become smarter and more capable of performing tasks traditionally done by humans, it’s crucial to explore the far-reaching implications of this technological revolution. This essay will examine the effect of automation and AI on the job market, personal relationships, government interventions, the possibilities of Universal Basic Income (UBI), finding meaning after employment, and what parents can teach their children to prepare them for a future dominated by AI and automation.

The Job Market: Displacement and Transformation

One of the most immediate effects of automation and AI will be felt in the job market. According to various studies, millions of jobs across industries—ranging from manufacturing to service-oriented roles—are likely to be displaced by automation. Tasks that are repetitive, manual, or require basic decision-making are especially susceptible. In the automotive industry, for example, robots already perform much of the assembly work. Likewise, AI-driven technologies such as chatbots and algorithms are beginning to replace customer service representatives and data analysts.

However, it’s important to note that while some jobs will be lost, new ones will emerge. The creation of new industries and roles—such as AI specialists, data scientists, and automation engineers—will require a shift in the workforce. People may need to acquire new skills and adapt to a rapidly changing landscape. The future of work might be more focused on tasks requiring emotional intelligence, creativity, and complex problem-solving, which AI cannot easily replicate.

This transformation in the job market presents both challenges and opportunities. While some workers may face difficulties transitioning to new roles, others will benefit from the advancements in technology, particularly in the tech sector and industries that harness AI to drive innovation.

Personal Relationships in the Age of AI

The rise of AI and automation will inevitably influence personal relationships in complex ways. On one hand, automation could free people from the burden of repetitive and time-consuming tasks, allowing them more leisure time to spend with family and friends. The possibility of a more leisurely existence could foster deeper relationships, as individuals are able to focus on personal connections rather than the grind of work.

On the other hand, the increasing prevalence of AI in personal spaces, such as in the form of virtual assistants, autonomous vehicles, and AI-powered therapy bots, could alter the dynamics of human interaction. As AI systems become more adept at mimicking human behavior, there is a risk that people may start to rely on machines for emotional support and companionship. This could lead to feelings of isolation or a diminished sense of authentic human connection.

Furthermore, with a rapidly changing economy, some families may experience stress and disconnection as the roles of breadwinners and caregivers evolve. This change may also place additional pressure on individuals to maintain emotional resilience and adaptability in a world that is increasingly shaped by automation.

Government Intervention: Policy and Regulation

As the workforce changes and the effects of automation on society become more pronounced, governments will be faced with critical decisions on how to manage these transitions. Policymakers will need to enact policies that support workers displaced by automation, such as retraining programs and social safety nets. Governments may also be required to regulate AI technology to prevent monopolistic practices and ensure that its benefits are widely shared.

In particular, there is growing interest in the idea of Universal Basic Income (UBI), a policy proposal where the government provides all citizens with a regular, unconditional payment to cover basic living expenses. The argument for UBI is that as AI and automation reduce the need for human labor, UBI could provide a financial cushion for individuals who lose their jobs. By ensuring a stable income, UBI could also promote creativity, entrepreneurship, and personal growth, as people would no longer be beholden to traditional employment for survival.

Despite the potential benefits of UBI, implementing such a program presents challenges. Funding UBI could require significant taxation and a rethinking of current social welfare systems. Moreover, there are concerns about whether UBI would encourage or discourage work, and whether it would address the underlying issues of wealth inequality.

Finding Meaning After Employment

As automation takes over many of the tasks that once provided individuals with a sense of purpose, the question of what gives life meaning will become more pronounced. For centuries, employment has been central to people’s identity. A person’s job often dictates their social status, financial security, and sense of contribution to society. With AI and automation taking over many roles, people will be forced to grapple with the idea of meaning beyond work.

In this new world, individuals will need to find meaning through non-work-related pursuits. This could mean investing more time in family, hobbies, and community-building. People may seek personal fulfillment through creative expression, education, or spiritual growth. Philosophical questions surrounding the purpose of life and the role of human beings in an increasingly automated world will likely gain prominence.

The challenge will be to create a society where people are not defined solely by their economic productivity. To this end, fostering a culture that celebrates human creativity, emotional intelligence, and community engagement will be essential to finding fulfillment in a post-work society.

Preparing Children for a World of AI and Automation

As the world shifts toward automation and AI, it’s essential for parents to prepare their children for this new reality. In many ways, the skills that will be most valuable in the future are those that cannot easily be replicated by machines. Critical thinking, emotional intelligence, creativity, and the ability to adapt to new challenges will be crucial.

Parents can emphasize the importance of learning how to learn, encouraging curiosity and a growth mindset. While traditional academic skills will still be important, fostering a love for problem-solving, collaboration, and innovation will ensure that children are well-equipped to navigate a rapidly changing world.

Moreover, exposure to technology from an early age will be critical. Children who grow up understanding the basics of programming, artificial intelligence, and data science will have a competitive edge in a future that revolves around these technologies. It is equally important for parents to teach children about the ethical implications of AI and automation, ensuring they develop a strong sense of responsibility and empathy in their interactions with machines and fellow humans.

Conclusion

The coming of automation and AI represents both an exciting and challenging shift in society. As machines increasingly perform tasks once reserved for humans, individuals, families, and governments will face new questions about work, meaning, and identity. While the changes in the job market and personal relationships will be significant, they also present opportunities for greater creativity, fulfillment, and innovation.

By preparing future generations to thrive in a world shaped by AI, teaching them to adapt, think critically, and work collaboratively, we can ensure that the coming era of automation is one in which humanity flourishes—not just survives. The future is uncertain, but with thoughtful planning and a focus on human-centered values, we can shape a world where technology empowers rather than diminishes the human experience.

Finding Wheelchair Accessible Housing: My Journey

I might be moving within the next few weeks or so. It’s tough to tell. My doctors and caseworkers agree with me that I need to be in a place that’s wheelchair accessible. My parents house sadly isn’t friendly to wheelchairs. The doors are too narrow, no sidewalk, and the driveway is too steep.

My doctors and caseworkers have already recommended me to a place about an hour drive from my parents’ house. I would still be in Oklahoma, but no longer in the Oklahoma City metro area. Right now, the only thing that hasn’t gone through is corporate approval at the facility.

Been fighting to get into a wheelchair accessible facility for months. It’s pretty obvious I can’t live on my own. My parents are elderly, slowing down a lot, and sometimes forgetful. It would be a burden off them if I did get into this new place.

Corporate is still the hangup. Previous places have denied me because of my age, my weight, my mental illness, etc. Even though I know I need to be in a care facility, if for no other reason than my lack of mobility, I dread losing my financial freedom.

Long term care facilities are expensive. They have already said they would take over 90 percent of my disability pension to cover expenses. That’s the way it was when I lived in a long term care back in Nebraska a few years ago.

My parents supposedly can’t afford a handicap acessible house. Even if they could, I couldn’t afford even the property taxes and ultilities on such a house. I make slightly less than 1000 a month from disability pension. Really pisses me off that so little help is available.

I’m not senile. I’m not forgetful. I take my meds on my own every day. I don’t need a nursing home because I am senile. I need it because I have no mobility. I can transfer from a wheelchair to a recliner and to a bed. But my current living arrangement isn’t set up for wheelchairs. And my parents supposedly can’t afford to widen all the doors in the house for me to do much of anything in my house. Hell, I haven’t even been outdoors in five months.

I’m frustrated by the lack of help and communication. I’m not damn senile. I’m wheelchair bound. Most places are not conducive to wheelchairs, certainly not wide ones like mine. And yet I will probably end up going to a long term care facility and treated like I’m brain dead because I am wheelchair bound. Burns my ass.

The Future of Home Care: Robots and Independence

My caseworker and my parents are trying to get me into a long-term care facility. I really don’t want to go back to one of those. I despise the idea of losing my freedom and finances. I just as well be sent to prison as far as I’m concerned.

I live in a house with no stairs. But the doors aren’t wide enough for a wheelchair. Any suggestions I make to widen the doors fall on deaf ears. It burns me that I still have all of my intelligence but might still have to go to a long-term care facility because of lack of handicap access.

I would like to get a home health aide that comes in once a day to help with things. I had to fire my cleaning lady a few months because she wanted me to sign off on her billing her company for time she didn’t work. Can you say disability fraud? Glad I got rid of her.

I watch a lot of videos and news programs talking about the possibility of humanoid robot assistants becoming available to the public within a few years. Yet about the only people who don’t think I’m totally full of crap when I talk about this are some friends online and my older brother.

My thinking is that I hold on for a few more years and get a home health robot to help around the house since none seem to be available for me. Hell, it took a miracle for me to get onto a service where a doctor comes to see me in my house every six weeks. We found out about this, not through my case workers, but from a friend in my mom’s church.

I’m afraid that I will get sent off to a nursing home due to lack of mobility, lose my freedom, lose my money, and lose the family house just right before EVERYTHING changes with home robots, automation, AI, improved personalized healthcare, and possibly even Medicare for All.

One thing I despise about being on disability is that my earnings are limited before I’m totally thrown out of the system. And since the USA refuses to act like a civilized nation and institute Universal Healthcare, I’m stuck in poverty just so I can get my treatments. And I’m damn sick of it.

I lived in a long-term care facility once for eight months. Hated damn near every second of it. Had no freedom. Had no privacy. I was chastised for not socializing with the other residents even though most were senile and or nearly deaf. The only thing worse would have being in prison.

I don’t really tell my parents how much I despise the idea of going to a home. In the first damn place, I don’t think I would need one if the house was more wheelchair accessible. But they won’t entertain the thoughts of making the house more wheelchair accessible. All they would have to do is widen the doors to my bedroom, the bathroom, the front door, and the back door.

As far as transportation goes, that is being solved already in spite of the run around I get from social services. My brother bought a Tesla with self-driving capabilities back in the spring. Just the other day he and my niece had to go to Kansas City (which is about six hours from our town). During the trip up and trip back, the car did over 98 percent of the driving on autopilot. I was calling this almost ten years ago. Now it’s pretty well mainstream.

I had a car accident in late 2015 that really screwed up my back and knees. I was talking about how nice self-driving cars would be when they become available. I remember one of my Facebook “friends” said, and I quote, “It will be a cold day in Hell before self-driving becomes a thing.” That was less than 10 years ago. Bust out the parka and long johns, because it’s getting awful damn chilly these days.

I’m seeing the same attitude towards robotics that I saw against driverless cars about 7 to 9 years ago. I have given up on trying to convince people that humanoid robot assistants will be a bigger game changer than even smart phones, military drones, or even the internet itself. Most people don’t want to listen, let alone people of my parents’ generation.

Once during the pandemic, I joked in one of my futurists’ groups on Facebook about having a goal of riding in a self-driving electric car with a robot friend, smoking a marijuana cigar, while driving past a police station before June 14, 2030 (my 50th birthday). If I can hold out for long enough to get a home help robot and I don’t get sent to a home before then, I’m going to make that dream come true, so help me God.

Even if my parents go get too impatient and send me to a nursing home before I can make my dream of robot assisted independence come true, I’m going to do everything within my power to get well enough that I can leave. If my parents don’t want to make our house wheelchair accessible, well that’s their hangups. Sucks to be elderly and not see the possibilities that probably will come by the end of the decade.

Hell, I want them to fight me on this. I want people to tell me what can and can’t be done/ I want people to throw up roadblocks. I want to be told I’m a liar and I’m full of shit. I have made an entire life of coming back from setbacks and proving people wrong. Their hatred and nay saying will just make my story telling even more interesting than it already is.

After surviving 25 years of schizophrenia, 16 years of Section 8 Housing, 3 years of congestive heart failure and being wheelchair bound, I’ve lost most of my fears. I don’t want things to be fair or easy for me. Life isn’t fair. I figured that out when that I was six years old. I figured out that life isn’t fair before I figured out Santa Claus was fake. I’ve been fighting my entire life. Why should the next few years before some major breakthroughs be any different? I have nowhere to go but up. And I’ll be damned to let even family stand in the way of my freedom and independence.

Holidays While Mentally Ill

Today is Christmas Eve. Probably won’t be doing much of anything for the holiday as both of my elderly parents have covid. I’m surprised that I haven’t caught it, at least yet. I’ve been avoiding them as much as possible. Covid while mentally ill and with heart issues could be a bad mix.

Holidays have been bittersweet for me in recent years. I miss the family gatherings from many years ago. But I am afraid of going to family functions anymore. Most of my family are deeply involved with politics and current events and don’t share my concerns about much of anything. Some of my family don’t even have sympathy for disabled people or believe that mental illness even exists. It’s why I haven’t voluntarily been to a family dinner since 2017.

I’ve found that as I age, my paranoia about people has gotten only worse. Naturally, my friends don’t understand. My best friend was hostile about it when I opened up to her about it just yesterday. But then, she has her own problems and is frequently pissed off anyway. That’s an entire series of stories by itself.

I do miss the family gatherings when things were more calm. I miss eating sugar cookies. I miss watching the kids play with their new gifts. I miss venturing out and looking at Christmas decorations. I miss people in general being more hopeful and helpful during the holiday seasons.

A lot has changed for me in 2023. I graduated from physical therapy for my heart issues. Moved out of rural Nebraska and into my parents’ guest wing in suburban Oklahoma City. Adjusted to new doctors and treatments. I still need the wheelchair whenever I leave the house.

I’ve also gotten to witness my parents as elderly people. It’s tough watching my parents sometimes be forgetful, have a hard time hearing, not having much of a social life outside of church. And now both of my parents have covid.

For myself, I’ve had to come to the acceptance that I might never regain my full mobility. This is easier for me to accept than it is for my friends. I’ve also come to accept that I have deep agoraphobia and almost never want to go anywhere. Complete change from my twenties and thirties.

My oldest friendship is all but dead at this point. She blames her dark moods, lack of energy, bad health, and general cynicism on menopause. But I think it’s deeper than that. When I suggested she seek professional help, she came unglued enough I thought the friendship was over. Another close friend of mine is going to spend the next few years in prison. I won’t talk about it so don’t ask.

In the last several years, I’ve lost contact with probably 80 percent of my extended family due to politics and current events. Two of my old college friends have died. My last grandparent died in 2015. Three of my best friends in my old apartment complex back in Kearney, Nebraska have died. I came close to getting evicted from my apartment due to my health issues. Don’t ask, I refuse to talk about that either.

As far as my own health issues go, I survived two near fatal bouts of heart failure. Also lost over 170 pounds. Been able to avoid going to a mental hospital for 10 years now. I can now walk without knee or back pain. Granted it took a daily healthy dose of supplements like Glucosamine, Turmeric, and Hemp Oil for those pains to finally clear up after four years. Still working on getting my heart back into healthy condition.

After surviving a near death experience, recovering from heart failure, being healthy enough mentally to not have to change my psych regiment for several years, I feel pretty decent physically and mentally. Not where I want to end up yet, but I think I am on the right track.

One of my happiest achievements of2023 is finding Medium.com. I treat it kind of like social media for writers. I love the fact that I can do what I love, writing essays and stories, and actually make a few bucks off it. Been on only since early September and have already turned a profit. And I don’t even deal with that many trolls. Heck of a lot better deal than most social media. Screw you Facebook and twitter (I refuse to call it ‘X’).

The Way a Different Mind Works

Different Ways of Learning

I confess I have different ways of learning and processing information than most people. And that has gotten me in much trouble over the years, especially while at a workplace. I never could read people’s body language well enough to be good at socializing. I can’t tell what they think just by watching them.

However, I can read through the lines of what they write. I have always been a much better reading learner than a hands-on learner. The reason I never became as good with my hands as I am with my mind is that I couldn’t see diagrams or what I was doing. And I never got enough repetition in to get good.

Such a Troublesome Child

It always frustrated my teachers, bosses, and even family that it took more repetition for me to learn something than most people. But once I learned the skill, I remember it for life. I think I was given up on by teachers and employers too early in some cases because it takes me longer to learn through doing than most people. But once I learned something through doing, I have never forgotten it.

Even though I am pretty intelligent in some ways, I never did get the top grades in school or most of the accolades at work. Did well enough that I gave my teachers and bosses that false hope I could be a superstar student or employee.

Not Fitting the Normal

Yet, because of my mental make up being so much different than the norm, I couldn’t develop my skills fast enough for my employers and teachers to really see my potential. Never could read a teacher well enough to know what was on a test. Had to study the entire subject. It will make you well grounded in a subject, like biology or history, but it is not conducive to getting good scores on tests.

Likewise at work, I couldn’t read my bosses, coworkers, or customers very well. Certainly, couldn’t the first time I met them or even the first few. Like I said, it takes me more repetition to learn things than many people. Yet, once that knowledge is learned, it is learned for life.

Learning Comes Through Many Reptations of The Basics

Still remember many of the plays we used in football games and practice simply because our coaches believed heavily in repetition and details. I loved that kind of take on sport. Didn’t want to be fancy or eye catching, just wanted to win.

Yet because I couldn’t learn the way my bosses and clients preferred; I didn’t make a very good employee. For years I was convinced I was defective and was damaged goods. I believed it so much it’s why I went on disability insurance in spite having a college degree and good intelligence test scores.

Right Tools, Wrong Applications

I may have the natural brain power many employers are looking for. Yet, the way my mind works and learns is not what gets a person ahead at a job, most of which are service sector jobs. Attention to details and thoroughly learning your field was the way to go for a renaissance era craftsman or a high-end scholar.

Good luck finding those jobs today. I have ability, talent, and intelligence. Have a gift for learning new things. I remember those new things my entire life. In many ways I am far smarter now than I was when I graduated college in 2004.

Many Trials and Many Errors Lead to Knowledge

I became smarter because I found out through trial and much error how I effectively learned. I learn by reading and by doing many times, not by listening to a lecture or two and doing a few trial runs. It does take me longer to learn the basics than most people. But I remember the basics far longer. And I can build upon those basics to even incorporating some of my own takes on work tasks and ideas.

Sure, it is an odd way to learn. It is also one most teachers and employers especially don’t like. I lost more jobs than most people have had in a fifty-year career simply because my learning style didn’t fit modern corporate or service sector styles.

A Mind is a Terrible Thing to Waste

Have to wonder how many millions of people just in our day and age that live lives of quiet desperation and poverty yet would be model employees, crafts people, or business managers but never get the chance mainly because they learn things in different ways.

Met a handful of people in my life that were on the Autism spectrum. Some of them were extremely intelligent. Yet most of them struggled socially and especially at work. This was primarily because the learning styles and communication didn’t match up with the culture around them.

I think that things we classify as mental illness like schizophrenia, bipolar, autism, etc., have always been with our species. It just wasn’t as much of a disadvantage in a less structured Stone Age.

Tribute to the Square Pegs being forced into Round Holes

I imagine the first medicine men, shamans, astronomers, and priests were men and women who would be considered mentally ill by modern standards. But they had a different way of learning and looking at the world than most other people. And it helped to eventually launch civilizations.

It’s the eccentrics, the odd fellows, and odd ladies who took our species from only a few thousand wanderers to the billions who are making plans of colonizing other planets. Providing we don’t screw up this transition, who knows what the human species will be capable of given thousands of years.

Because of the oddballs who, while scorned and condemned among their contemporaries, led the way forward out of the Ice Age caves to now standing at the entry way to the cosmos.

My Personal Odd Fellow Journey

Been a long and strange journey. It’s one I hope is only entering a new phase rather than reaching its climax and decline. The choice is up to us who are currently alive and how much we chose to nurture those who don’t think like the norm.

I will never be one of these innovators who profoundly changes the world. I am content to be among those who appreciate the eccentrics and encourage them onward. The road to the stars is fraught with great difficulties. Because of the odd ones, I believe we are up to this task.