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Parkinson's Support Group Panama City Parkinson’s disease Support, Education and Resources -www.BridgesOfCare.org - www.DementiaSOS.com

If ever I’m living with dementia (brain failure), I’d like my family to hang this wish list up on the wall where I live ...
22/10/2025

If ever I’m living with dementia (brain failure), I’d like my family to hang this wish list up on the wall where I live and do the following:
1. Every time you enter the room announce yourself. “Hi Mom. It’s ___.”
NEVER ask, “Do you know who I am?”That will cause me anxiety. I want you to do everything you can to decrease my stress.
2. I want my friends and family to embrace my reality. Go with my flow.
3. If I think my spouse is still alive, or if I think we’re visiting my parents for dinner, let me believe those things. I’ll be much happier for it.
4. Don’t argue with me about what is true for me versus what is true for you.
5. If I am not sure who you are, do not take it personally. My timeline is confusing to me. I’m doing the best I can. Don’t embarrass me.
6. If I can no longer use utensils, do not start feeding me. Instead, switch me to a finger-food diet and see if I can still feed myself. If you want to help, use hand-under-hand so I feel as if Im feeding myself .
7. If I am sad or anxious, hold my hand and listen. Do not tell me that my feelings are unfounded.
8. I don’t want to be treated like a child. Talk to me like the adult that I am.
9. If I appear to still want to enjoy the things that I’ve always enjoyed, help me find a way to do those things. I might do things differently, but help me do those things anyway (such as exercising, reading and visiting with friends).
10. Ask me to tell you a story from my past and refer to that story when I seem anxious. Remember my stories for me and use photos to help me remember my stories, too.
11. If I become agitated, take the time to figure out what is bothering me. Perhaps I have unmet needs but can no longer explain what my needs are.
12. Treat me the way you would want to be treated if you were living with brain failure. It can happen to anyone.
13. Make sure that there are plenty of snacks for me in the house. If I get hungry I might get angry but be unable to explain why.
14. Don’t talk about me as if I’m not in the room. I’m living with brain failure but I’m still here.
15. Don’t feel guilty if you cannot care for me 24 hours a day, 7 days a week. It’s not your fault and you’ve done your best. Find someone who can help you, or choose a great new place for me to live.
16. If I live in a dementia care community, please visit me often.
17. Don’t act frustrated if I mix up names, events or places. Take a deep breath. It’s not my fault. I’m living with brain failure. Imagine how frustrated I am that I can no remember things clearly.
18. Make sure I always have my favorite music playing within earshot. If I start to sing, encourage me - even if my voice is off key.
19. If I pick up items and carry them around, allow me to do so (if safe). Then return those items to their original place later.
20. Include me in parties and family gatherings, especially the holidays.
21. Know that I still like receiving hugs or handshakes.
22. Remember that I am still the person you know and love. I am living with brain failure and that changes everything.

ᴄᴏᴘʏ ᴀɴᴅ ᴘᴀsᴛᴇ in Honor of someone you know or knew who has/had dementia.

In Honor of all those I know, love and lost to Dementia. Alzheimer’s is the best known form of dementia but there are 80 different types of dementia.

For a free dementia training go to:
www.DementiaSOS.com

If you have questions about dementia, go to my website for a free dementia training.  Free handouts sent to your email. ...
24/08/2025

If you have questions about dementia, go to my website for a free dementia training. Free handouts sent to your email. Bee 🐝 Dementia Friendly. Learn strategies to use and strategies to avoid from Teepa Snow, dementia expert and educator.
TeepaSnow.com

If you have questions about what to do if you see a senior who appears lost, check out the app that helped one person reunite a woman living with dementia and her family.

https://www.dementiasos.com/post/create-a-safety-plan-for-people-living-with-dementia-who-wander

Create a Safety Plan for people at risk for getting lost - including people living with dementia.

DEMENTIA SENSORY ISOLATIONDementia progression commonly alters the five senses and affects their cognitive abilities and...
13/02/2025

DEMENTIA SENSORY ISOLATION

Dementia progression commonly alters the five senses and affects their cognitive abilities and behaviors. Sensory overload short-circuits the brain with a flood of information the person can't control. This commonly causes panic, confusion, or violent behavior.

Sensory deprivation, which is a lack of sensory information, often accelerates dementia progression, emotional withdrawal, and refusals to cooperate or participate in activities.

As humans, we depend on a functioning sensory system. Our visual, auditory, tactile, olfactory, and gustatory sensations are essential for us to “make sense” of our world. When even one of these senses isn’t functioning, our perception differs significantly from others.

SIGHT
Blindness is a disability for some people, and children with vision problems typically have difficulty learning. Most seniors experience visual loss with aging; many wear glasses and contacts or have laser treatments. Some develop cataracts and require surgery to prevent blindness.

Dementia progression commonly creates visual impairments, such as loss of depth perception, which causes misinterpreting distances, depth, and width and misjudgment of how fast something moves. Also, visual distortions create problems such as dark rugs resembling a hole in the floor, colorful patterns appearing to move, what’s in the distance seems right next to them, and stairs having no depth and resembling flat lines.

Peripheral vision is also lost, causing “Tunnel Vision,” where the outer edges of the visual field darken or blur. If you’re sitting next to the person and talking, they can’t see you, or if you stand in front of them while they are sitting, they only perceive your mid-section. This is why it is essential to always make eye contact when talking to them.

Another problem is visual focusing, where they can’t locate items surrounded by clutter,r like the inability to find their fork on a table full of items or with a patterned tablecloth.

AUDITORY
Aging commonly damages hearing, and some people need hearing aids. If we are totally deaf, we lose the everyday environmental sounds, people talking, or awareness of danger. Deafness is like being in a vacuum of silence.

Once, I lost my hearing completely when my ears didn’t adjust to the altitude pressure in an airplane. Although the deafness only lasted about an hour, I was terrified as I walked through the busy terminal,l seeing people’s mouths moving and not hearing a single sound. I couldn’t communicate in that nightmare of total silence, something I had never before experienced. I felt vulnerable and afraid.

Watching people’s lips move voicelessly, the television’s inaudible images, a pet’s soundless barking, cars whizzing silently, and worse yet, the feeling of dead silence can cause people with hearing loss to experience fear, frustration, and anger. Hence, they often begin to disengage from people and their environment.

Most people with advanced dementia possibly have hearing loss, but cognitive problems prevent them from following hearing test instructions or responding to the questions. This creates difficulty in knowing how much hearing is damaged. Worse yet, they’ll commonly remove their hearing aids or misplace them.

Dementia deterioration causes the brain to lose or misinterpret incoming sounds. Voices might seem garbled, or some words disappear. If they have tinnitus, a constant ringing in the ears, it's distracting, and what people say becomes confusing. They have trouble hearing high tones, so speaking to them using lower tones is essential.

Hearing loss increases dementia progression and symptoms, and the person often disengages from their surrounding,s refusing to interact with people. They may appear asleep or refuse to do anything asked of them.

TACTILE
Skin is our largest organ, encompassing our entire body. It has over five million nerve endings that sense touch, pressure, temperature, and pain. We are “in touch” with our environment through our skin, which signals the brain to activate the muscles. However, if our arm is numb, this feels like a “dead zone,” and muscles won’t respond.
Dementia typically causes disruption of tactile perception, thus sending the wrong signals to the brain. During progression into later stages, the mind/body connection becomes damaged, and the ability to interpret or locate pain is lost. The person might have numb areas or feel the pain but can’t tell you what is happening or localize where it hurts. Pain typically causes dementia symptoms to suddenly spike. The most common cause is a urinary infection (UTI) requiring medical attention.

Sometimes, there’s a hypersensitivity to tactile sensations, hot or cold, which is felt more intensely because the brain’s ability to regulate temperature is damaged.

Even the perception of the feel of textures becomes different. One woman with dementia described the water of the shower as needles hitting her skin. Commonly, eating disorders are related to the texture of the food. At dinner in a nursing home, a man said his mashed potatoes felt like tasteless mud in his mouth, and I’ve heard complaints about how a wool sweater felt like a wire brush.

As we age, collagen breaks down, and the hypodermis, the fatty layer under the skin, becomes thinner. It leaves blood vessels closer to the surface, which quickly causes bruised or torn skin. Be careful when handling the person.

The manner of touching a person with dementia is also a way of communicating, and they should never be grabbed roughly or shoved. It’s essential to touch them in a way they feel secure and cared for.

OLFACTORY
Our sense of smell creates our strongest memories as the olfactory system directly influences the brain's hippocampus region, which is responsible for memory formation.

People with dementia often lose their olfactory sense early in their symptoms, especially those with Alzheimer’s, possibly because the hippocampus is one of the first areas damaged by the disease. Doctors consider olfactory loss as a possible early indicator of the disease.

Our senses of smell and taste are interconnected, and we even taste the air we breathe. When we lose our ability to smell, we lose our taste. I’m so hypersensitive to strong perfumes that sometimes I can taste the scent in my mouth for hours afterward.

Our sense of smell alerts us of dangerous situations like a gas leak or spoiled food. It also stimulates the appetite or repulses us. The smell of freshly baked cookies makes us salivate. However, the smell of Limburger cheese can cause gagging.

TASTE
We have an average of 10,000 taste buds on our tongue, which detect sweet, sour, bitter, salty, or savory. These are replaced about every two weeks. This is why when we burn our tongue, it heals so quickly.

Because our senses of smell and taste are interrelated, losing both can become a major contributor to the development of eating disorders in those with dementia. It’s also dangerous for those still living independently.

One of my friends had undiagnosed early Alzheimer’s and had lost both smell and taste. She would forget how long food had been in the fridge, and because of it, she couldn’t tell if the food was spoiled and was continually getting sick.

SENSORY STIMULATION
Sensory stimulation activities and exercises are a necessary part of slowing the progression of dementia and managing symptoms. Time should be set aside to make sure all five senses are activated, even if the sense of smell and taste seem absent. We never know how many of these senses still remain.

Help your loved one to “Make sense out of their world.”

Katya De Luisa resides in Costa Rica and is a dementia educator/consultant, writer, and author.
www.dementialearninginstitute.com

Many great tips from Teepa Snow.TeepaSnow.com
28/11/2024

Many great tips from Teepa Snow.
TeepaSnow.com

27/11/2024

🎙️ New Podcast Alert: The Evolution of Rock Steady Boxing and Its Role in Fighting Back Against Parkinson's 🎙️
In this inspiring episode, we recognize National Physical Therapy Month by exploring the impact of Rock Steady Boxing (RSB), a program designed to empower individuals with Parkinson's disease through a non-contact, boxing-based fitness curriculum. Join physical therapists Dr. Ryan Cotton, RSB’s President and CEO, and Dr. Connie Fiems, RSB’s Chief Scientific Officer, as they share the story behind RSB’s development and its evolution over the years. Watch it here: https://hubs.ly/Q02TRD8z0

Bee Dementia Friendly.🐝Free training: DementiaSOS.comTaught by Teepa Snow, dementia expert and educator.TeepaSnow.comFre...
27/11/2024

Bee Dementia Friendly.🐝
Free training: DementiaSOS.com
Taught by Teepa Snow, dementia expert and educator.
TeepaSnow.com
Free training handouts to your email.
“DEMENTIA: Keep Responses Positive” in the Fall 2023 issue of “Go Christian Magazine” which can be found online.

https://indd.adobe.com/view/9c4738a8-1809-4cb8-a82b-2479e4f2aafd
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DEMENTIA Awareness bumper stickers.

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