Scars

The scars on my wrists tell a story. They tell many stories actually. They remind me of a life I once lived. If you could call it living at all. A life of anger. Of resentment. A mixture of mania and depression. A life of suicidal thoughts and tendencies. They remind me of how lost I once was. Of how I didn’t know what to do. The scars remind me of how hopeless I felt. I was defeated with a life out of control. The scars remind me of how I gave others power over my life. The scars remind me of what has been taken away from me and the many things I blatantly threw away out of selfishness. They remind me of how reckless I once was. How I didn’t care. My scars remind me of how important alcohol and addiction were and how unimportant the important things were. My scars remind me of how hard I had fight to stay alive. Just to breath. They remind me of how I almost lost. My scars remind me of all the things I could’ve lost. They remind me of how the emotional pain hurt so much more than the physical pain. They remind me of how shame can be so powerful.

My scars remind me that I am alive. My scars remind me I won, but that I still have a long way to go. My scars remind of how hard of a fighter I have become. They remind me I am a survivor. They remind me that not every success is a win. They remind me that I won because I failed. They remind that I am still here. They remind me what life is about. My scars remind me of what is actually important in life. The scars remind me to appreciate the things I would have never experienced….the people I would’ve never got to know and love. They remind me of the love I have received.

The scars on my wrists are not covered up. I will never hide them. On the left is a tattoo of a semi-colon. It reminds me my story isn’t over and that I am my own author. That I have so much more to write for my life. The cross tattoo on my right reminds me Who saved me. It reminds me of the hope I have come to live by.

The scars on my wrists remind me I am alive.

A New Journey

Tomorrow is my 47th birthday. Nothing special planned so far and that’s fine. I’ve had a pretty busy last two weeks anyway and I can use the down time. A lot has gone on in the past month and a half.

My wife and I moved from Oklahoma where we had lived our whole lives to Arkansas in the last week. She got transferred with job to here where her sister lives so we jumped at the opportunity to move so they can be closer together. I’m really looking forward to living out in the country again. We both grew up in the country and went to a very small school in the middle of nowhere before marrying and living in town. That was years ago.

I recently quit a job of 5yrs a couple of months ago. I loved my job as a General Manager at Papa John’s. In spite of my Parkinson’s I was still able to do the job. At least up until looking back about 4 months ago. My job performance declined drastically, and I didn’t realize it until way late. My ability to focus was almost non-existent while my attention was completely gone. I was easily aggravated and couldn’t remember anything for the life of me. I unintentionally let things fall through the cracks, and that’s not good when you’re running a business. My memory was shot. Something was going on. I hadn’t had problems with my cognition and memory in a long time, so I didn’t put two and two together. Looking back, I realized I would often find myself a bit more emotional than normal. Like I would get upset watching a commercial and tear up. My speech had become altered as if I was completely drunk all the time. I knew what I wanted to say but the slurring and jumbling of words made it almost impossible to make out what was actually coming out of my mouth. I used to be able to juggle at least two to three or four things at any given time. Eventually I found it difficult staying on one task at all.

I eventually found work to difficult to do so I stepped down and let my assistant run things. Even that proved to be too difficult for me. So, I quit. Luckily, I had a very understanding boss who worked with me through the whole process.

I got a hold of my Movement Disorder Specialist (MDS) and we agreed on starting Aricept which is for Alzheimer’s. It seems to be clearing the fogginess and helping. I was on Exelon a few years back for Parkinson’s dementia, but it didn’t seem to help much. I don’t see my MDS for another month, so I’ll have to wait till then to discuss our next step if any.

So currently just taking each day one at a time. I’ve only been here in Arkansas for four days so I’m just resting and taking time to get better.

I knew this day would come eventually. Later than sooner, I had hoped but it is what it is.

Childless Holidays…

I love the holidays. October to January is my favorite time of year. It’s not always easy to cope with but it is still my favorite. I love the change in weather as it goes from blazing hot to a frigid cold breeze that could cut you like a knife. I love to watch the colors of Oklahoma go from green to yellows and oranges and reds. I love the gatherings…the endless amounts of foods.

What I don’t love are the holidays without any of my kids or the reminders of their kidnapping. It was Christmas when they were taken 6 years go. It’s a balancing act. In one hand I want to break down and let the weight of their missing take over, while on the other hand I don’t think they would want to do that. To spend the remaining of the year overwhelmed and depressed. And I have to be honest last year was one of those years. I let the overwhelming weight of their missing take over and run ramped through my thoughts. It was all I could think of. But this year is different.

No, I have not forgotten my kids. They are still there in my mind. But I have to focus on what and who is here. The one’s who have been here for me during the past six years. They are invaluable to me. I honestly don’t know if moving on without my children is getting easier or if my mind is beginning to repair itself. I know I’m not forgetting them. I’ve heard of some people buying and wrapping presents or hanging stockings for missing children. I just can’t do that. At the same time I can’t stop. I can’t place my life on hold. I will never stop hoping I will be reunited with them one day. Christmas is a time of hope and I will continue to do so.

Six Years….

Six years is a long time….yet it has went by fast. 2,190 days have passed since I’ve been able to see or speak to my kids. Let alone hug or kiss them. Not by choice though. And I would be lying if I said not a day goes by without me thinking of them on my mind. At the same time I have to admit it does get easier. And I don’t know if that’s awful or not. To say life without your own children is livable. I don’t know if my mind blocks them out or what. But the holidays are here and it was six years ago that they were taken. I love the holidays. It’s my favorite time of the year. Yet it’s also a bitter reminder of how evil people can be. To steal a child. To take them away. It’s just unfathomable to me. To be that cruel.

I wonder how they are doing….especially in the midst of this pandemic. In any case, I hope they are well and happy in my absence. Because in their absence I am not. I cannot begin to articulate the thought processes and emotions of the kidnapping of your own child. There are literally no words.

My story of parental alienation

Triggers. Some are mild while some are downright devastating. Almost life altering. Like the custody battle I went through with my ex-wife fighting for my children. She used my bipolar as a major part of her ammunition against me claiming I was unfit and a danger to our children in spite of the fact that we had had been married for over seven years and I had never displayed any dangerous behavior.

 

“I thought cowboys and Indians were extinct like the dinosaurs.”

This, my 7 seven year old says to me after I handed him a gold 50 cent piece. He asked me if it was one of the coins with the “Indians” on it.

“I think you’re right son. All the cowboys and Indians are extinct.” Figuratively that it is.

Continue reading “My story of parental alienation”

A childless Father’s Day

Father’s Day is here and for many it’s celebrated. For new dads it’s that long awaited finality as if it’s that stamp of completion…”you’ve arrived, welcome to the club.” Father’s Day is a bit more complicated for me so I don’t think much of it. You would think I would considering how big of a father’s heart I carry. Come Father’s day I grieve the loss of my six children. Three whom has already went home to heaven and three who are alienated from me. Father’s Day is not a day I like.

 

As much as I cherish all of my children, being with them and even crossing my mind when we are not together, shortly before Father’s Day my mind begins to remind me of the three who’s went on to heaven.

 

I think, and I may be wrong, that most people view miscarriages as something that only affects women. Contrary to that perception men in a devoted relationship are impacted by such an event; especially three of them.

 

Looking back I see that for the most I didn’t let myself grieve like I should have. Loss due to death has seemed to have shown up frequently throughout my life. The first experience, we were in our teens. We weren’t prepared or mature enough to handle something like this. Teenagers, young, scared and excited. You’re in love. Well, you think you are.

There are many things we all remember vividly within our lives. I remember that evening the phone rang. I remember the sound of her voice. I left to take care of my then high school girl friend. We moved on.

 

Fast forward about ten years. Married with already a one year old boy. It had already been a high risk pregnancy. The doctor advised any other would be just as well. Possibly higher. But soon we became pregnant and with the doctor’s orders we took every precaution. No work. No lifting, etc. Still there came a point where the baby stopped moving.  After rushing in to the doctor, the ultrasound confirmed no heartbeat.

 

With God’s help of modern science we were able to have a second son soon later. But then we experienced the same blow all over again.  At the time I was torn at the loss of each child. But looking back I realized I never processed the events. I had to take care of things. I was a stay-at-home-dad back then. I had a sick and depressed wife to take care. I was finishing up my bachelors during the first. During the second, I stayed home with the boys during the day and worked nights while sleeping an average of 4 hours a day while my marriage was failing and I was dealing with depression myself.

 

The last two impacted me emotionally. I just didn’t let it show. I didn’t have time. I was there for my wife. She was hit hard; especially the second time. I was neither here nor there. I was along for the ride and kept denying the fact that I was shaken up by all that had happened.

 

Being a stay-at-home-dad, I was really looking forward to another kid each time. That’s not to say my wife was looking forward to another child any less than I, but I was already mentally prepared for the changes in my life. I was going to have to deal with poopy diapers and crying kids for that many years and my professional life was going to be on hold for that many more years was on my mind even months after the miscarriages.

 

We did have a third child. A little daughter. We called her our miracle baby because we needed medical assistance to get pregnant prior. We almost lost her too. She was an unplanned surprise without assistance or problems. Unfortunately, four months after her birth my wife left and took her from me. Maybe the fact that all six of my babies have been taken from me either by miscarriage or by my ex plays a large role in why I think about the three that are gone.

 

A miscarriage is losing all that could have been and that is very difficult thing to go through for both parents to be. Society tends to think it only affects women, but that truly is half the story. Dads experience feelings of intense grief, shock, helplessness and anger to name a few. I carried the weight of loss and caring for my wife while continuing to maintain my regular responsibilities. But that is what you do. Even the spouse tends to think the man isn’t caring or supportive when in reality we just do it differently.

 

The number one thing that dads have to deal with, in my opinion is denial and shock.  Our culture emphasizes the fact that women are the only one’s hurt by miscarriages. Sometimes I think even we men get caught up in that trend.  It’s ‘ok’ to get upset—you just lost a child to be.  I think I might even felt like nothing happened just after the miscarriage as a teenager.

 

I remember both nights of the miscarriage while married—I couldn’t do anything to help and it crushed me.  Helplessness; it’s the most scariest feeling in the world.  It is simply out of your control and although it sounds cliché—these things just happen.

 

As a guy, I remember thinking that maybe my swimmers were defective or even inadequate.  Maybe it was how I came to an abrupt stop in the minivan that one time or maybe it was that I didn’t pay attention as carefully as I should to my wife’s diet.  It took me a while to let go of that baggage, but it was for the best. Guilt. That’s what it boiled down to.

 

Anger!  Why does God let these things happen?  Why did God want my baby before he or she was born?  I have read that some dads might be angry with themselves or feel responsible for losing the baby and then project this anger onto their wives—this helps no one and is just another emotion that we feel as we go through the grieving process.

 

How could I not experience strong feelings of loss, not only for the child itself but for the life I imagined for me and my wife after the baby was born. I guess I superficially grieved.

 

Grief can make you think funny things like, “Maybe I am the cause of all this and not only did I screw up making the baby, but now I am not there for my wife like I should be because I feel so down.” Feelings of inadequacy, and they consume you.

 

We were pregnant, and then we’re not. I was there at the beginning and I was there at the end. Maybe men can know and understand many things about women, and maybe women can know what it is to be a man too, but if I don’t know what it means to carry life inside my body, I do know what it means to carry that life in my day dreams, and in my consciousness, and in my heart.

 

Fear confirmed is an odd thing. Emily Dickinson had it right when she wrote, “After great pain, a formal feeling comes…” A certain discreet propriety surrounds the open wound and scabs it so fast the whole organism can survive, and only that little bit that you invested dies. I guess I feel like that now. Then, what is left but a mass of cells to be removed in a quick painless procedure?

 

In a nutshell what does she mean? That little piece of us of that was hurt somehow becomes scarred and calloused in order to protect us from future hurts. After the loss of my child, never knowing whether it was boy or a girl, as a teenager I had put the experience in the back of my mind until the loss of my second child. Locked it away. It was the second that triggered the memory of the first.

 

It alone comes with its guilt for repressing. “Why would I push it back in my mind? Forget it? How could I not remember my child?” Since the second one occurred after my first son was born I began thinking of those two babies around Father’s Day. And then the third one after it occurred.

 

I love my children. I would never replace or trade any of them. I’ve never wondered why any of them are here while the others aren’t. I don’t consider them lost. Even though people say, “lost a baby.” I know where they are and Who has them. I find comfort that when they left, they left by the side an of angel who took them home. I know one day as long as I continue to follow the One keeps them I will meet them one day.

 

My Own Identity

It’s been almost six months since my divorce. This is the first time I’m written about it. It took me a while to process it and come to terms with it. I’m sure I played a role in the downfall of my marriage but so far I still don’t understand what led to the demise of our relationship. Or what would make someone in a relationship reach the point of giving up. I wanted to save our marriage. I would’ve done anything to do so. I’ll admit I was in a pretty low slump for the first three months after the split. But by God’s grace He pulled me out of it.
But I’ve been doing a lot of soul searching if you will about me and my life. I’m not happy with my life and where I’m at. I always feel I could be doing more and be more productive. I lay the guilt trip on myself pretty heavy being on disability and not working. I have days where it’s almost impossible I have Parkinson’s and so I think to myself that I can get out there and work. Then on the other hand the rest of days I spend fighting against my own body that has a mind of its own. Not to the mention the pain and anxiety I feel. So I wrestle back and forth and beat myself up as to whether or not I can work.
I continue to be faithful in attending my local church. I’ve even strongly believed I can go on a missions trip overseas. So I’m in the works with that with my pastor.
I need something in my life. I don’t believe it’s another relationship. There is this void and I’m trying to find what can fill it. I have a heart for missions and think about it every day. But that in itself doesn’t mean that one is called onto the mission field. So I daily seek God’s direction and leading. Only He can fill the void in my life.
When my ex wife and I split a big part of my identity was lost. I played the role of a house husband. I took care of our home and many demands for my stepdaughter. But when we split I not only lost a wife I lost a daughter. My role as husband and father came to an abrupt halt. So I find myself seeking my own identity.
I know in time God will lead me on right path. In the mean time I continue to take care of myself regarding my bipolar and Parkinson’s. I’m currently stable and I have good days and bad days with my Parkinson’s.

Bipolar Anxiety

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I’ve been without my medication for my bipolar for a few weeks now. Currently I don’t have a doctor and I’m not scheduled to see one until the 14th of this month. I ran out of my medication. As far as depression or mania goes I’m still stable which is a surprise to me. The last time I went without my lithium I was depressed and back on my antidepressant within a week. Unfortunately I can’t say the same for my anxiety.
Anxiety is a common symptom of bipolar disorder itself, but about half of those with the condition have a co-existing anxiety disorder. Since my anxiety has been high I’m crossing my fingers I don’t slip into a depression or slide into a mania phase. Anxiety with depression greatly increases the risk of suicidal ideation. And mania with anxiety is marked with severe agitation. Psychosis for both phases is known to be increased. Treatment for both is severely diminished. Having both depression or mania with anxiety can be a living hell.
People with bipolar often experience anxiety as a symptom of their condition. Anxiety accompanies the deep depressions and the manic highs, prompting symptoms that include:
• Compulsive behavior
• Panic attacks
• Overwhelming fears and worries
• Feelings of terror
• Restlessness
• Avoiding people and places
• Physical distress such as shortness of breath, racing heart, nausea, sweating, shaking
• Having a hard time concentrating
However, many people with bipolar also have distinct anxiety disorder. Anxiety disorder occur when your worries or fears go on for months or even years. They continue whether or not there is any logical or sensible reason for them. You can become anxious just thinking about ordinary daily responsibilities and how you’re going to get through the day. This is what I tend to do. I ruminate on daily task and obsess of why am I wasting the day away as well as my life. My mind races with should I be doing this or that. I used to be severely obsessive compulsive with living with my wife and learning to give and take and compromise with her I have mellowed out fairly well in that area.
The combination of bipolar and anxiety can be difficult for patients. Bipolar patients with anxiety disorder are more likely to engage in substance abuse and suicidal behavior. Mood swings are much deeper and more pronounced, and intervals when a “normal” mood is present are briefer. Anxiety makes patients in manic phases more likely to engage in impulsive, self-destructive behavior. It’s also been shown that anxiety makes successful treatment of bipolar disorder much less likely.
Although research is continuing, doctors have found that anxiety disorder has some elements in common with bipolar disorder. Both have been linked to low levels of the neurotransmitter serotonin in the brain. Also, bipolar disorder treatments such as antipsychotic medications have been shown to relieve symptoms in patients with anxiety disorder. Triggers for different symptoms in each disorder also appear to cross over into the other. For example, insomnia is a common symptom of anxiety disorder and also has been shown to trigger manic episodes in bipolar patients. I for one have suffered from insomnia since childhood and frequently triggers psychosis after a prolong period of time without sleep.
Successful treatment must target both the anxiety and the bipolar disorders, but the co-existence of both makes the treatment plan much more complex. In general, doctors will begin addressing the bipolar disorder through a mood stabilizer like lithium which I take.
Once the bipolar symptoms have stabilized, then the doctor can prescribe medications for treating the anxiety disorder. Benzodiazepines are often used, as they appear to treat the anxiety without negatively affecting the bipolar disorder. If the person has a history of addiction then alternative medications tends to be used but then there are risks of complications to the bipolar disorder as well as being non-affective. Doctors usually don’t use antidepressants, a common class of anxiety medication, because they have been shown to destabilize and worsen bipolar symptoms.
Along with medication, doctors may also recommend therapy to address both bipolar disorder and anxiety; approaches include cognitive-behavioral therapy, family therapy, and relaxation therapy.

An open letter to my country America

What is wrong with you people of America? We used to be great. All we do now is gripe and moan and try to control each other under the guise of equality. When was the last time we looked around and saw the beauty and wonders of what used to make this nation great? We’ve become a nation of people so quick to point out what is wrong with its us that we have refused to even allow each other to shine.
We cry for equality but if we don’t believe or act same then we are no good for each other. Then you are the hypocrite and I’m not. There take that. And how dare you have your own opinion in this free country! After all it’s my country. We used to embrace our diversities. Now we can wait to slander each other for our differences as reach for torches and pick axes.
Why are we so quick to scream and lay the blame of racism on a symbol that’s become a national icon? What do they hope to accomplish by banning its existence? Racism will not cease to exist in this ugly world as long we grip so tight on to our ugly hearts. I said it before, racism is not a cafeteria line problem. We don’t the privilege of picking and choosing which parts get to go and which get to stay. We can’t knock out those nasty pieces of history just because some over zealot people refuse to think logically. Racism will not end after the last decal is removed from store shelf. Removing the flag will not accomplish anything. Why isn’t the Nazi memorabilia gone yet? Why are we Christians still allowed to display our crosses? There will always be someone offended by something. We can’t bow down to everyone’s whims. Besides America, that flag never did stand for racism. Get your history facts right. Do a little research before you go crying to someone.
We have become a nation of bullying. Ourselves! We scream and yell at other groups of people in our country in order to get what we want to make them do something for us. Instead of trying to force one race of people in submission why don’t they try to combat racism itself? They are only fueling hate with hate. They are bullying. And they are winning.
We need parents who are not afraid of their own children. Parents who will step up and start teaching their kids responsibility and how take a few insults without getting their little feelings hurt. I’m Hispanic and I got picked on when I was a kid. I got called names. Well boohoo. It happens. Parents who will invest in their kids and not replace themselves with activities and electronics. What happened to kids being accountable and learning responsibilities? We’ve become a nation of sheltering our kids in order to protect them too much.
We recently made marriage an equal opportunity. But apparently if someone doesn’t agree with it that makes them a hypocrite. I don’t understand this concept. Isn’t equality the freedom to have one’s own choice and opinion? Yet out of this decision is so much fighting. Because of this decision rainbow logos are popping up everywhere. But if I was to post a Straight Pride logo I would most certainly be targeted with hateful criticism being accused of being a bigoted hypocrite. More than likely from people who don’t even know me let alone not knowing the people I know and associate with. In this country if you are not for something then you are against them. There is no equality in this country. What is wrong with you people? It’s you judgmental hypocrites who are the judgmental hypocrites. Always pointing the finger shouting, “judgmental hypocrite!”
If we America want equality then let everyone speak. Wasn’t it us America who told Tim Tebow to shut up about his faith in Christ how it comes before his football career? Yet we can’t seem to get enough of Bruce Jenner turning into a woman making him brave and courageous while we have troops oversees in other countries away their families. Where is the equality in that? There is only a warped sense of equality that says it’s yours only if you believe and act the way I do. America has become blind and selfish.
We have become a nation of people who cry for higher wages while at the same time refusing to work harder for them. Why raise the minimum wage? We do minimum work. Don’t even start in how the Mexican’s are taking all the jobs. Maybe we handed them over. I’m a Mexican-American who grew up modestly and later earned a bachelor of science in psychology on grants and loans. And yes here in America! The means to get educated and trained for better work are out there. The problem is, is that we think some work is below us. We are too good for some jobs. We’ve become a nation of people who feel entitled. We want what America has to offer yet not give back. I’ve listened to people gripe about how little food stamps they were only allowed to receive while holding an iPhone in one hand and a cigarette in the other.
What is wrong with us America? God forbid if something like another Oklahoma City bombing occurred. Remember when one of our own attacked us and we were there for each other? Or what if another 9/11 happened? God forbid if another country attacked us. This nation would fall apart. How we be there for each other if all we can now see is our differences. Our president is incompetent and we hold some of the blame. We expect our leader to fail and our enemies know it. We are not a united country.
When are we going to stop looking for what is wrong with America and start looking for what is right? We are far too happy to point out what we need to remove in our country that we are blind to what we need to see. What is good with our country? What has happened to us?

Boogeyman of dementia

boogeyman closet

I know hallucinations are common territory to different forms of dementia. It’s a common mistake to believe that hallucinations only inflict those with Lewey Body or Alzheimer’s. The truth is anyone who suffers from any form of dementia is at risk to feel their mind split from reality. What is consistent is that each form dementia tends to manifest hallucinations differently for each dementia.

This is my personal story of hallucinations. It is my desire to help loved ones and caregivers see the world of their LO from the inside out of what’s going on inside of their demented brain. I can only do this by writing about my own dementia.

I’m no stranger to hallucinations. If you’ve read any of my other reflections you know I’m bipolar. So I’ve been on anti-psychotics for years. But lately, about six months ago, when I could tell my dementia progressing I could also see an increase in the hallucinations.
If you have loved one who experience hallucinations try to imagine what they are feeling. The terror. The confusion. The lost feeling. Helplessness. What they need is security and redirection, comfort.

This is a story of one hallucination in particular that refuses leave me. One that is reoccurring.
This is one account of a repetitive hallucination I may encounter during the night as a complication of my insomnia. He is a man that hides in my closet whom I refer to as the boogeyman. Even though the man in the closet, the boogeyman is the scariest persona I encounter in my bedroom, or anywhere, at night in the dark it is the one I fear the most. I know the boogeyman isn’t real and has no real physical power over me. Others have come and gone, but not the boogeyman. It’s as if he is here to stay. The boogeyman is also the only hallucination to look at me directly in the face as if with intent. I’ve interacted with other persons of hallucinations but I couldn’t remember their faces or even know if I looked at their face. But the boogeyman will open the closet door just enough to be able to send an evil stare right at me. That’s how I know his eyes are yellowish. The boogeyman’s hallucinations are so powerful they are also auditory. Sometimes with the door closed noises will come from the closest. Bangs. Scratches on the door. I know they are not real. But combine all these together and it’s hard to control that fear. It’s hard to dismiss it all. The boogeyman makes it seem personal.

I don’t sleep very well. I never have. So being up late at night in my room in the dark or lying in bed is typical for me. Sometimes I put my headphones on but mostly I use the time for quiet time. It’s in those times that while laying in bed or sitting at my desk I would hear the turn of the closet doorknob followed by the creek of the door. Instantly I knew what it is. Instantly my heart would race while blood rush to my head. Terror engulfs me. This thing wasn’t real and I knew it every time but knowing it didn’t make it go away. The option was to look or ignore it. It had never come out of the closet before and I never wanted it to. If you could ever fathom a being released from the depths of hell this was it. This was pure evil that makes the howling sound of a dying animal. It is the epitome of ugly. And it’s noise pierces my ears like ice picks. My fear of not looking is that if I don’t maybe it will wander beyond the door and into the room. It’s always seemed to make its presence known, its power, and then leave. But not until it stabbed me with its own dark yellowish eyes. All I can do is freeze wherever I am and wait until it retreats back into the dark closet. I never know what it does just like I never know where it comes from in the closet once it gets back in but it bangs the walls as if its crawling back into a hiding place. The fear has not left. I know it’s not real but it has happened before and I know it will happen again. Maybe that is why the fear is so unconquerable. All I can do is wait.

Hallucinations requires medical attention. But the most powerful and affective treatment for hallucination is compassion and patience along with understanding. It’s often misunderstood that those with dementia will sometimes resist because of a hallucination. I will refuse to go to bed until my wife shuts the closet door. I will refuse to go into the closet in the middle of the night once the door is shut. This is only one example of how hallucinations can hinder progress for people with dementia. Hallucinations are terrifying, confusing, some are simple distractions that make any confusion worse, some are pure evil looking for a life to destroy. Hallucinations make big impacts on how someone with dementia functions.

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