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What It's Like to Experience Alzheimer's: A Virtual Dementia Tour

Shannon tends to ponder things a little more than in passing. Sometimes things are worth writing about in case others find interest as well.


Alzheimer's Disease is a particular form of dementia that steals more than just the memory of the person it takes over. It changes the way families interact with one another and it takes away a person's independence in the cruelest of manners. Unfortunately, there is nothing that can be done to stop it once it starts. It slowly destroys the brain cells until it eventually causes death. Though advancements have been made in treatment options and preventative measures, no cure has been found.

Most of us have dealt with the disease personally, either directly as a caregiver or indirectly watching someone else take care of an Alzheimer's patient. If neither of those scenarios fit, we know someone else who has had to deal with the awful reality of it somehow. But do we fully understand it? Many of us think we do, though our understanding of it is limited.

What if you could experience dementia firsthand? Would that make you more compassionate, more understanding, more patient, and less irritable when dealing with someone suffering from the disease? Most of us will never have much of an inkling of what it is like inside the mind of an Alzheimer's patient. Even after learning more about it, our understanding is limited. However, there is something everyone can do to grasp the reality an Alzheimer's patient is dealing with more effectively. Take a virtual dementia tour. It will change your perspective.


What Is a Virtual Dementia Tour

A virtual dementia tour simulates some of the things a person with dementia might be experiencing. Although it cannot accurately replicate the brain deterioration or other causes of dementia, it can provide a better understanding of why a person with dementia behaves a certain way. The experience sets the person taking the tour up for failure. Why? Because the goal is for people to understand that behavior is not always a choice, as we are conditioned to believe.

Individuals taking the tour have a device placed in their shoes to create some discomfort walking, which some elderly experience for various reasons. Next, gloves are put on the hand or tape is used to tape a couple of fingers together, which simulates arthritis or the loss of sensory and tactile function experienced as a normal part of aging. Goggles over the eyes simulate common eye conditions, such as glaucoma or macular degeneration. Last, a headset is placed over the ears constantly playing noises imitating all the cacophony that some patients have difficulty tuning out. Conversations, for instance, of several parties at once, a firetruck siren going by, or a telephone.

Then a person is given a list of five simple tasks to complete before being sent into a simulated living environment. Each person participating is given ten to fifteen minutes to perform these tasks to the best of their ability under those conditions. Many times, only one person at a time is sent in, but sometimes the guides stagger the starting time of the participants so that more than one person is in the living area at a time. No one is given the same list of tasks to complete as another participant, however. It sounds like a piece of cake. It is not.

Taking the Tour

This very eye-opening experience was something that I did with my best friend, Cheryl. In some ways, it was what I expected it to be after first learning about the tours. In other ways, it was not what I expected. There were many moments of clarity, especially afterward, and the discussion following the experience was perhaps the most enlightening for me. It was then that we were fully able to make connections between what we experienced for only ten minutes and what dementia patients experience on an ongoing basis. Reading and observing are very different from doing.

Before we started, we filled out a brief questionnaire relating to our current state of mind. Our answers were both the same.

  • Do you feel capable of carrying out simple tasks? Yes.
  • Are you relaxed? Yes.
  • Do you think people with dementia (always) get the care they need? No.
  • Do any of the following characteristics apply to you as of the last 10 minutes: pacing, negative thoughts, talking to self, following others, searching for items, difficulty understanding directions? No to all of the above.

Next, our guide explained how it works. In our case, we were sent in one at a time. The guide let us know that neither of us would have the same tasks. Also, there would be a list posted in the room of our particular tasks to complete. Neither of us remembered that fact, and we found out later that it would not have helped us much even if we had. Another tour guide went into the room with us, but only to observe our actions and behavior, or so we were told. At that point, our lesson began.

The Challenges and Tasks

Cheryl was the first to enter the room resembling a nursing home room. I sat patiently and watched as they equipped her for the simulation. I listened as the guide read her the list of tasks she was to complete:

  • find the white sweater,
  • write a three-sentence note to your family and put it in the envelope,
  • set the table for dinner,
  • fold all of the towels,
  • fill a cup 1/2 way with water and drink it.

As she was attempting to complete her tasks among all of the distractions and physical challenges, I chatted a little more with our tour guide. At one point, we heard a scream come from the room and our guide prepared herself for a rescue if need be, but all quieted right away, so she relaxed again. So I knew at the very least I was potentially in for quite a startling experience when it was my turn. It turns out that she managed to complete four of her tasks, a rare accomplishment and, in her case, completely by accident.

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With the room left just as it was when Cheryl completed her turn, I was sent in next. I had no idea what it was Cheryl had completed and did not remember her list. I did not pay much attention to her tasks because I knew mine would be different. I did have it in my mind, however, that I would try it like a memory game. You know the ones that have you naming a list and trying to recall the items in order? As it turns out, I could not hear what she was rattling off to me when she suddenly began telling me so that strategy was not going to work. I was still trying to tune out the noises in my ear enough to focus on her words and to hear them. My tasks:

  • put the belt through the belt loops on the pants,
  • match six pairs of socks,
  • clear the dinner table,
  • draw a picture of your family and name them,
  • find the necktie and put it on.

I completed only two of my five tasks. And actually, one of them was not fully completed.

After we both had our turns in the room, we discussed our experiences. The first question asked of me when I exited was how did I feel. Disoriented. We also answered the same questions we initially answered before going in. Do you feel capable of carrying out simple tasks? No. Are you relaxed? No. Do you think people with dementia get the care they need? No. Have any of the following characteristics applied to you in the last 10 minutes: pacing (both no), negative thoughts (both no), talking to self (Cheryl), following others (no, but might have happened had we been in the room together), searching for items (both of us), difficulty understanding directions (both of us).

Cheryl's Unique Experience

When the guide started reading the list to her, Cheryl was not prepared. It took her a few seconds to realize that it started. She thought she heard two of the tasks and focused on them as she went in. It was hard to see the items unless she was close to them. Vividly remembering she was supposed to write three sentences and that she needed to fold towels, she went straight to the bed and began folding them, first picking up a sheet that she thought was a towel. Tuning out the noises in her head was relatively easy until a firetruck siren sounded in her ear. It turns out that this noise was what startled her enough to scream. Coincidentally, an ambulance was also going by outside at about the same time. After the sound had startled her, it became harder to tune the others out. She sat on the bed and looked around the room a bit before resuming her task while remaining seated. A slamming door startled her somewhat, and a telephone ringing caused her to wonder if there was one in the room that she briefly looked around for in case she was supposed to answer it. Also, the pattern on the bed comforter was hard to see. Some of the towels blended in with it, too, making the task a little more difficult.

She folded the towels and left them neatly in the basket on the bed before going to the desk to write her three sentences, which she forgot to put in the envelope. A pitcher of water was sitting on the desk, so she poured a glass that she did not drink. Unsure of what to do next, she walked to the shelving unit at the foot of the bed, located in the corner. She noticed the shelf on top containing dishes but could not focus on the rack underneath where clothing hung on hangers. Her mind began to wander a little while looking at the shelves, thinking about what she could do next to pass the remaining time, and she ended up moving the ties and the socks to the basket on the bed before deciding to set the table. But it was hard to sort through the silverware. The bowls were easier to pick up, so she grabbed them first and set all four of them on the table, but her feet began hurting at this point. She found the knives first but did not want to walk anymore after they were set out. Still, she made it back over to the shelf. While trying to find matching fork sizes, she noticed an image of an elderly lady in the mirror and wondered if that was supposed to be herself.

At that point, she was planning just to sit down and wait, but her time was up. To her, ten minutes felt more like twenty while trying to complete tasks she couldn't remember and figure out what to do to pass the time. Relieved, she was sent to wait outside as I took my turn.

My Unique Experience

As I said earlier, I thought I was going to remember what most of my list was. I was wrong. Oh so wrong. Unlike Cheryl, I realized she was reading the list to me right away, but I wasn't ready to focus on what she was saying yet. Right before I entered the room, I said out loud, "I didn't catch most of that." Although, I did succeed in remembering I had to match six pairs of socks and clear the dinner table. The table was to my right as I walked in, so I thought I would start there. Pausing for a moment, I tried to familiarize myself with what was in the room and where. But for some reason, I didn't want to waste too much time, so I didn't linger long on fuzzy objects in the distance as I glanced around. I noticed a clothing rack in the corner with a distracting light flashing at the bottom of it, a bed straight ahead with a painting on the wall above it, a desk between the bed and the table, and a portable toilet across from the desk on the other wall. A window was on the wall that part of the desk blocked. It had blinds in it, but they were down. The room had no lighting. There was also the observer in the room, but I did not think I was allowed to interact with her. If anything, she made me a little self-conscience, but I did my best to ignore her presence altogether.

I started to pick up the silverware, before realizing it would be easier to carry if I stacked the bowls and then put the silverware in them. After I had all that in hand, I suddenly realized that I did not know where to take them once I cleared the table. Deciding the desk was the only logical location, I set them down there before trying to fold socks I could not find at first. I noticed the basket of neatly folded towels on the bed. In my mind, it made sense that the socks must be with the towels in the basket or near the basket. After all, I did not see any drawers to put them in through my distorted vision. Managing to find a couple of socks near the basket, I realized that this was not going to be such an easy task. For one thing, the gloves made it difficult to match socks quickly.

Five of the pairs were dark, and they blended in with the bedspread. I managed to match two pairs before realizing I did not have enough socks and had to find the rest. I decided to shake out a couple of towels, but no luck. Folding socks was the only other task that I remembered, and I was determined to complete it. I started moving the towels out of the basket, though I decided not to make a mess unfolding them all. How likely is it that a sock would get tangled in a folded towel? I did, however, find three socks at the bottom of the basket once I removed the towels. At some point, a slamming door in my ear made me jump even though I managed to tune out the rest of the cacophony enough think clearly. I matched a couple more socks before having to count them again to see how many pairs I had matched so far. Five. I needed one more pair, and I only had one white sock. Plus, I was not sure I matched the pairs exactly.

I decided to focus on finding that last sock first. No luck. I looked beneath the bedspread, put the towels back in the basket to see if I missed anymore under them, looked in the desk drawer, and felt around like an entirely blind woman to see if there were more drawers on the desk that I could not see before finally giving up. It was while looking in the desk drawer and around it that I first noticed the discomfort in my shoes. I chose to ignore it. I deal with that nearly every day anyway and have to ignore it when it happens, so that was almost second nature to me. Instead, I continued searching for the sock. In the process, I nearly knocked a glass of water on the desk over. I did not see it when I set the bowls there, so I had no idea it was even there in the first place, let alone filled. I saw the pitcher too and briefly contemplated whether or not I should take a sip of the water. Ultimately, I decided I might forget the socks if I kept getting distracted. I moved the bedding around a little more and briefly contemplated looking out the window when I caught a glimpse of light through the blinds. The pattern on the wall hanging was also distracting somewhat. Feeling like I was just making a mess, I ultimately gave up my search. It was frustrating to know that a little white sock was probably just blending in with its current surroundings.

I decided to look at the clothing rack, unsure of what to do next to pass the time. Up close, I discovered there was a shelf above the rack of clothes containing plates, some silverware, and what appeared to be cups. Aha! I grabbed the bowels off the desk to set on top of the plates. The silverware was a little more challenging because I noticed something did not feel quite right. It took me a second to figure out I had a couple of pens in my hand instead of knives. I managed to leave them at the desk, though.

After that, I had no idea what to do. I remembered that Cheryl was supposed to put on a white sweater, so I thought maybe I should put something on too. The only thing I knew for certain - do not put on the white sweater. While trying to figure out what the clothes on the rack were exactly, I noticed a face in the mirror. It was very disconcerting, enough to cause me to do a double-take. Imagine seeing a ghost-like image in the mirror. I realized it was the face of an elderly woman, but I looked closer just the same and almost touched it, wondering if it was supposed to be me. I did not dwell on that thought long, though, instead choosing a black sweater. Putting it on while wearing gloves was not so easy. Plus, my hair ended up caught underneath, and I had difficulty pulling it out. I am pretty sure I messed up my hair, which was down and is nearly to my waist. I felt as if I must have looked like I just woke up and threw on some clothes without brushing my hair, like throwing on a robe over pajamas when first waking up. At that point, I had no idea what to do next. Thankfully, my time was up before I could contemplate that thought further.

Our Observer's Observations

The observer was there to observe the behaviors we exhibited while completing our time in the room. She watched to see how many tasks we completed, noted if we needed reinforcement, had negative thoughts, subvocalized, asked for help, exhibited strange behavior, followed others around, did someone else's tasks, wandered, or hoarded objects. Though Cheryl said she did not recall doing it, she was observed using subvocalization, meaning she either spoke to herself or made some kind of verbal noise. Neither one of us asked for help or addressed the observer, but only because we assumed we would not receive any unless there were some safety issue involved. Both of us exhibited wandering characteristics. And I did one of her tasks because I could not remember what my own were. I did not hoard, but in retrospect, I easily could have. I had all of the bowls in my hand before realizing I did not know where to put them. I also thought about piling things in one corner of the bed to find the missing sock.

To better interpret the observations, it might help to understand what exactly the observer was looking for. Understanding also makes dealing with patient behavior a little easier.

Side note before proceeding: the list on the wall of our tasks was abnormal in appearance. The words were different sizes and not even in the correct order. There were even some missing words in the instructions. Had we remembered it was there, it would have been tough to read and then decipher through our already muddled vision and thoughts.

Why a List of Tasks?

The point of having participants complete a list of tasks is to provide a greater understanding of the pressure caregivers tend to place on dementia patients. Had we not had all the other challenges, we probably would have easily remembered most of the tasks and been able to complete them without a struggle. However, dementia patients are often expected to complete them as a person without challenges and caregivers become impatient when having to repeat themselves. They can also become upset when things are not done properly or at all. They need to understand it is not intentional.

Does Reinforcement Play a Factor?

Some participants do require help or assistance from the observer, even if it is just verbal reassurance that everything is okay. A little encouragement goes a long way when someone is discouraged. And positive statements reduce the anxiety levels, especially of patients suffering from depression as well.

How do Negative Statements Affect Individuals?

When people are particularly sad or vulnerable negative statements and thoughts are often a sign that dementia patients are depressed as a result of what is happening to them. Negative thoughts are also common when feeling overwhelmed.

What Is Subvocalization?

Subvocalization means that a person is talking to themselves, or verbalizing thoughts out loud. It can also include something like humming to oneself or making other vocal noises. The sound of one's voice can be comforting. It is best to allow dementia patients to soothe themselves in this manner if need be.

Asking for Help

Asking for assistance seems logical if someone is confused or otherwise needs assistance. But many people do not seek help out of fear or because they are uncomfortable asking. Many people with dementia need the extra help, but they do not receive it because people grow impatient with their neediness as if they simply are not paying attention to what was required.

Strange Behavior

It is hard to understand why people do certain things, but at the time, it makes perfect sense to the one doing it. Unless the patient or someone else is in danger, the behavior should be allowed. Also, do not laugh, ridicule, or berate a patient for their odd behaviors. Redirect it to other more appropriate ways without acting as if they are out of line.

Following Others

Following others around usually happens out of uncertainty. It is natural to look for someone else who appears to know what to do. Caregivers should not be offended if a patient is following them around. Mimicry is a compliment. They trust that you know what you are doing.


Wandering is a behavior most people are aware of doing. It happens because they are looking for familiarity, especially when already confused and lost. It also happens when looking for something the patient is urgently trying to locate. It can occur in a home, wandering around a room or from room to room. It does not always mean a patient is wandering in public. As long as it is safe, it is okay to allow it.


Hoarding is an attempt to control the environment around the patient. Some examples of things that patients might hoard are washcloths or paper towels. ( Or, in my case, I almost accumulated all of the clothing in one place an effort to find just one sock.) Taking away the hoarded items takes away the illusion of control, and it usually causes unnecessary outbursts. If an object must be removed for some reason, provide a replacement.

Things to Remember When Caring for a Dementia Patient

  • Allow plenty of time to complete tasks. It truly is difficult.
  • Distractions make it harder to concentrate and allow for even more forgetfulness. Cut down on them as much as possible. For instance, do not leave a television playing in the background. Even a crowded room can be distracting when several conversations are happening at once, among other things.
  • Socializing helps to prevent cognitive deterioration. Because of what is happening, it can be easier to retreat socially rather than risk feeling awkward or out of place. Doing so causes deeper depression and faster cognitive decline.
  • Allow a patient to do the same task over and over again. It is comforting and creates a feeling of safety, perhaps normalcy. It is similar to tour participants searching with steadfast determination for something she or is convinced must be located.
  • Strange behaviors are coping mechanisms, as are most others for that matter. Treat them as such. To fix the behavior, a caregiver must first figure out why the patient is doing it. Agitation may be a sign of needing something. That something could be anything from medication to a less noisy environment.
  • Focus on all of the things the patient can do instead of what they cannot. Always do your best to remain positive. Agitation and negativity will only increase unwanted outbursts and behaviors that are harder to deal with in the long run. It also helps the caregiver cope emotionally.
  • Three positive actions dementia patients need from others are reinforcements, encouragement, and reassurance. These things help prevent social withdraw and isolation that often leads to depression.
  • Taking care of a dementia patient is one of the most emotionally taxing jobs a caregiver can have. In many ways, it is harder than caring for other types of chronic diseases. A caregiver must always remember to take care of himself or herself, too, or the situation will become harder for everyone involved.

A News Segment About Virtual Dementia Tours

How Can You Participate in a Virtual Dementia Tour?

Created by Second Wind Dreams, The Virtual Dementia Tour is a non-profit organization dedicated to improving the care and quality of life of both dementia patients and their caregivers. To take the tour yourself, you can visit their website at, or you can contact local home care and nursing home facilities in your local area offering the service. They usually have scheduled public event days. And they provide it on demand as well. Simply call to schedule an appointment with a facility trained to give it. They might even come to your home or business to set up a tour.

After you take your tour, you can donate to the Second Wind Dreams program. It is a program similar to the Make a Wish Foundation's granting of wishes to children, except that it is for seniors. Many facilities will also donate something to the program for every person who takes the tour. It is a win-win situation for everybody. Learn how to be a better caregiver, spread more awareness about the disease, and help someone have a special once in a lifetime wish granted.

This content is accurate and true to the best of the author’s knowledge and is not meant to substitute for formal and individualized advice from a qualified professional.


Shannon Henry (author) from Texas on July 28, 2019:

Aw. Thank you, Lorna. I'm glad that it could bring back happy memories for you. I suppose the sad ones have their value as well.

Lorna Lamon on July 28, 2019:

This is an excellent article Shannon which brought back many memories both sad and happy for me. It touched my heart.

Shannon Henry (author) from Texas on March 01, 2019:

Oh, that's so sad, Dana. I am glad that you are able to offer some comfort to her. I know that many dementia patients are aware of what is happening to them by the time others start noticing, too. It must be scary. Perhaps you will be able to be of help to her in ways you don't realize now. I've no doubt your friendship is a blessing and a comfort.

Dana Tate from LOS ANGELES on March 01, 2019:

There's a beautiful woman who I see at my job often. We don't work together for she is retired and has received a nice inheritance when her parent's passed. She's a lady of leisure and I'm a working girl. She's much older than I am. She's Caucasian and I'm black. We have become dear friends or maybe dear acquaintances.

I call her my southern belle because she is such a refined lady. elegant and classy. We'll go to the café next to my work place and have lunch and coffee. Sadly, I see the beginning effects of dementia. She forgets where she puts things and is repeating herself. I worry about her because she has no children but the lady is full of pride and doesn't want much help or sympathy from anyone.

Shannon Henry (author) from Texas on February 27, 2019:

Hi Audrey. I'm sorry to hear that you have to watch a loved one go through this. I highly recommend taking this tour if you are able to find a place near by that offers them. I won't say it makes it any easier to witness, but I believe it does help control your own negative (although natural) frustrated responses.

I also recommend reading a book called 'Still Alice' if you can bring yourself to do so right now. It's very emotional, but it's written bfrom the perspective of a woman diagnosed with early onset Alzheimer's.

Don't forget to take care of yourself, too. Especially if you are the main caregiver.

Audrey Hunt from Pahrump NV on February 27, 2019:

Very helpful article and so glad you wrote about dementia. My sister is going through many changes with this terrible disease. Your list of things to remember when dealing with a person who has dementia is extremely helpful.


Shannon Henry (author) from Texas on September 16, 2018:

I'm sorry, Jackie. I can't imagine how hard that must have been to have to make that tough call not to take care of her anymore yourself.

The thought scares me too. Sometimes I have anxiety over nothing and sometimes random things trigger it. Then I have a train wreck of emotional, irrational thoughts. Because dementia has been in my family, when I forget things I feel I have no excuse for forgetting or use a random word that is far from the one I meant to use I worry about it.

Jackie Lynnley from the beautiful south on September 16, 2018:

Can't believe I somehow missed this.

I took care of my mother several years with this disease and with 24 hour care it is like living it yourself. You get so emotionally involved and feel distraught over the daily changes you see. I meant to take care of my mom until the very end but even with all the weight she lost I still could not handle her when she became weaker and more out of control.

She died in 2010 but if I start remembering it all comes back as if it were just yesterday.

Of course I fear having this disease and I do suggested things whether medically proven or not. I pray they will find a cure very soon. It is such a cruel disease.

ziyena from the Somewhere Out There on September 10, 2018:

yw ... any time

Shannon Henry (author) from Texas on September 09, 2018:

Thanks, Ziyena. I appreciate the encouragement.

ziyena from the Somewhere Out There on September 09, 2018:

Shannon, I completely understand and feel your frustrations about the editing process. I think we've all been there before. When I come across roadblocks like this ... especially with something new and revolutionary to the internet search then I will rework it until they cannot possibly deny its benefit to HubPages ... perhaps it's something simple. Don't give this piece up and keep trying! I feel that there are people out there searching for this valuable information ... Peace

Shannon Henry (author) from Texas on September 09, 2018:

Thank you, Ziyena. I'd hoped to make it a mainstay and felt like relaying the intensity of the personal experience would be of benefit, but HP must feel differently. They say it doesn't meet quality standards as it is. I've asked a few opinions and no one has an answer for me. So I assume it's the personal nature that's the problem. Just not sure how to change it and have the same impact. The point is to bring awareness to the tour, especially for caregivers. It truly changes perspective.

ziyena from the Somewhere Out There on September 06, 2018:

This is an incredibly personal experience and compilation on a tough subject matter ... this article is a mainstay and definitely information for those who are dealing with the onset of Alzheimer's or that of a loved one would highly appreciate. Great work and thank you!

Shannon Henry (author) from Texas on September 04, 2018:

Thanks, Joni. Despite doing the virtual tour, I really can't fully imagine what it must be like for those who suffer from the awful disease. The fear and frustration. Just the thought of not remembering my loved ones is sobering enough.

Joni Fletcher on September 04, 2018:

Very informative, I definitely know more after reading your article. Such a sad disease.

Shannon Henry (author) from Texas on July 16, 2018:

It really is a powerful experience and I would love to share this more widely. However, HP does not have it featured due to quality. I've tried a couple of times to edit and to find the issue. The only thing I can think of is that it is too much from a personal perspective. But that, to me, is part of what makes it so powerful. I felt like it was the only way that I can accurately share what the experience is like.

Linda Crampton from British Columbia, Canada on July 16, 2018:

Thank you for raising awareness about this horrible disease, Shannon. Your experience sounds interesting and powerful.

Shannon Henry (author) from Texas on October 03, 2017:

Hi Susan,

Thank you. I hope people can find something useful from this information and an experience like this. But HP doesn't like it enough to feature it so I may have to totally redo it. I was hoping that by rearing our personal experiences in such detail people could better connect to the lessons to learn from them. However, I also think that may be their issue. Perhaps when I get more time I will look more carefully.

It truly was an eye-opening experience. Something I expected, but only because I researched beforehand, and yet it was still almost surreal. I'm currently reading Still Alice and it reminds me of this experience with every page turn. The things she experiences as she deals with the disease are in tune with things we virtually experienced for only a few minutes and learned about afterward.

Susan Ream from Michigan on October 03, 2017:

My mother-in-law had Alzheimer's. It's a very sad disease. It was hard and painful to see life through her eyes and her reality.

I've never heard of this kind of a virtual experience. So interesting and helpful to those who need a better grasp and more compassion for those living in their own little confusing world.

Great job, Thanks!

William Stephens from Arkansas on July 31, 2016:

If you want to do something to fight dementia and Alzheimer's, visit this URL today:

Don't just sit on the sidelines!

Shannon Henry (author) from Texas on June 08, 2016:

Sounds interesting. Also seems it would increase migraine pain, but what I know? I've never had one.

Maybe later today. . .after I get off work. . No promises. LOL

Bill Holland from Olympia, WA on June 08, 2016:

I came back! There was a show on the television the other day about virtual reality for migraine was really fascinating. Anyway, just thought I'd toss that out there. When are you going to write something new? Inquiring minds want to know. :)

Shannon Henry (author) from Texas on May 26, 2016:

Hello, Say Yes. I'm so glad you found this information valuable enough to gain better understanding. Thanks for reading.

Yoleen Lucas from Big Island of Hawaii on May 25, 2016:

This is excellently written! It has given me new levels of understanding about dementia/ Alzheimer's. Thanks for writing this!

Shannon Henry (author) from Texas on May 23, 2016:

Thank you for reading. It is an uneasy feeling, for sure, but that uneasiness is precisely what promotes greater empathy and understanding. You have a good day as well.

DREAM ON on May 23, 2016:

I am moved by your total experience. All my thoughts and previous fears of what it might be like are kicking in. I am already overwhelmed with uneasy feelings and I haven't even done the tour. Thank you for sharing and helping us understand. Have a great day.

Shannon Henry (author) from Texas on May 22, 2016:

Oh, Ruby, I'm so sorry to hear that. It's especially hard to watch those we care about suffer that way. I've been told that it can happen to people even my age. But I am so glad to know people like you understand how important kindness and compassion is when caring for them.

Shannon Henry (author) from Texas on May 22, 2016:

Hello, Suzette. It's not as scary doing it, at least for me, as knowing it could be realty some day and already is for so many. The.difference us that I knew I was safe and I knew it was temporary. I'm glad you learned from reading this.

Shannon Henry (author) from Texas on May 22, 2016:

Hi, Paula! I agree that it can only be a positive thing in the long run. We truly do never know when we might need to draw from an experience like that. I am glad I set up the appointment.

I'm sorry you had to watch loved ones deal with it. It does tear families apart. It's horrible.

Ruby Jean Richert from Southern Illinois on May 22, 2016:

This is such an important article. Anyone taking this tour will understand the difficulties AD patients live with daily. I have worked with Alzheimer patients. They need to be loved and understood. I had a good friend, a 50 year old R.N. who developed this horrible disease. She went from teaching LPN training to being unable to cut her salad. This happened in a years time. She is now living in an Alzheimer's unit, unable to recognize her husband or son. Most people, when they think about this disease, think it only happens to older people, not true. Hopefully a cure is on the horizon, if not a cure, at least a drug to slow the process down. Thank you for sharing your journey. I can only imagine how terrifying it must have been...

Shannon Henry (author) from Texas on May 22, 2016:

I'm so sorry you have to watch someone you love go through that, Bill. It's never really easy. The emotional toll on the caregiver and the family is hard for sure. It's so easy to become.frustrated or to assume they are more capable than they are, that they remember more than they're on, etc. It becomes exhausting to constantly reinforce or to repeat the same things over and over. They get stuck in the same thought loops and fixated on certain thoughts, especially as the short term memory deteriorates more. It's a little like losing patience with.a child, except.that we expect more from adults so it even more irritating. Then it gets to the point the memory is clearly lost and only worsening. That's the saddest of all to me, to not remember loved ones and precious memories.

Music helps draw a lot of AD patients out of themselves a little more, I hear. They respond to it favorably. You might suggest it to your friend's family.

And if you or they want to put yourself almost in his shoes for ten minutes, I recommend you find a place.that offers the tours and take one.

Shannon Henry (author) from Texas on May 22, 2016:

I wish I could provide real hugs of comfort for you, Martie. It's a scary thought that any of us could potentially face this disease, especially if it runs in the family. And our guide said there are more cases of early onset. People my age are facing the early stages of it. It's a sobering thought that I will think of every time something feels off about my memory. We all have those moments sometimes, but AD patients are aware of it, too during the early stages and do not quite know what is happening. I am sure it's scary.

I remember my grandma yelling at me when I got annoyed at missing the same sharp turn so many times. I felt that by now, she should have anticipated it's sudden appearance when we rounded the curve and not missed it again. At the time, it was just annoyance and I don't remember what I said or did to express it, but I remember her response was, "I know, Shannon, it scares me too!" She said it in such an unexpectedly harsh tone that I was dumbfounded and didn't respond. But it was then that I realized she was experiencing other potentially more serious memory issues. Later, she was diagnosed with dementia, though I don't recall a formal diagnosis of it specifically being AD. Some of the behaviors I heard about and witnessed, though, tell me it might have been. Whatever it was, she knew something was wrong and it scares her. The patients are often aware something isn't right during the early stages but they rationalize it away. . .just tired. . .normal aging. . .etc. . .And it's often not until the moderate stages are reached that a diagnosis is made.

Shannon Henry (author) from Texas on May 22, 2016:

Hi, Theresa. Our guide said when she first took the tour she set down and cried because she knew her frustration was only temporary and the people she cared for faced it on an on going basis.

It is too bad you didn't know about this when your mother was suffering from it. It's not too late to set up a tour, though, and have a better understanding of why she possibly did some of the things she did and to know in case you have to care for someone else in the future. Yes, it is definitely frightening and heartbreaking, too, but well worth it.


Shannon Henry (author) from Texas on May 22, 2016:

Maria, it us good to know that other students take the tour, not just those working with dementia patients.

The things to remember section is just a small part of what can be done to make things easier. I think the best rule of thumb is not to react if it isn't hurting anyone, no matter how strange or unacceptable the behavior may seem. They can't help it and the more a caregiver reacts, the more the behavior turns to agitation and aggression.

suzettenaples on May 22, 2016:

What an amazing experience. Dementia of any kind is heart wrenching to see and experience. How brave you are to do the virtual tour. I had no idea you could do such a thing. Thank you for sharing this important experience with us. I know I learned a lot.

Suzie from Carson City on May 22, 2016:

Shan....This is positively wonderful information. It seems to me this tour could be only positive and beneficial for every person to experience. We just never know when we might be in a position to help and/or care for a patient/person with dementia. Just having the knowledge to pass on to others is a bonus.

I have had family members who suffered with dementia and am aware of the stress placed on them and their loved ones. To be armed with information of what we can do and what we should not do in order to benefit both the patient and others is invaluable.

Kudos to you Shan for taking this tour. I am grateful you have shared the experience with your readers. Your hub is a must read!

Bill Holland from Olympia, WA on May 22, 2016:

Fascinating read! My best friend has this disease and I've watched him diminish physically and mentally for the past five years....ugly, ugly way to die, but at a certain point it becomes much uglier for the family than for the victim. Anyway, I really enjoyed reading this.

Martie Coetser from South Africa on May 22, 2016:

Just reading this was a horrible traumatic experience. I'm so shocked, I can hardly type this comment. I'm crying like a baby.

May I never ever becomes a victim of this horrible decease!

I'm sharing this all over.

Thanks for the eye-opener, ..... I can't remember your name!!! Shannon!!

Faith Reaper from southern USA on May 22, 2016:

Dear Shan,

What an eye-opening experience for you and your friend to go through the virtual tour! Just reading of your experiences made me feel a bit anxious and so I cannot even imagine what one who is suffering with such a terrible disease is experiencing.

I wish I knew of this when my dear mother was alive to help me understand more of what she was experiencing. I think it would have been beneficial to all of my siblings too to take the virtual tour, although a bit frightening.

You’ve produced a well-written and insightful hub here. I am sharing everywhere to bring awareness on a most important topic. This I a must read for all caregivers!

Excellent article! I’m proud of you for taking the virtual tour.


Maria Jordan from Jeffersonville PA on May 22, 2016:

How wonderful that Second Wind Dreams makes this simulation experience available to the loved ones of those with AD and the general public as well.

I've participated in simulations of Alzheimer's and hallucinations - as do the nursing students in both universities I teach for. As you've so accurately detailed, there is no greater way to gain empathy and sensitivity than to 'literally' walk in their shoes - for even a little while.

"Things to Remember When Caring for a Dementia Patient" - what a comprehensive and meaningful compilation of strategies for all.

Your knowledge base will add much credibility to your future writings.

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