There’s a an older lady I just sold my boat too, and living in a marina. She’s been a nightmare ever since I sold her the boat and the more I see/talk to her the more obvious her dementia is. She appears to be quite a well way into it. She’s quite an angry and depressed person, forgetful, struggles to complete sentences, gets confused and her walking gait is awkward, she struggles to walk and talk at the same time. She has already irritated other people at the marina as she’s very rude and confrontational over tiny things. And she will not stop texting me long texts complaining about anything and everything then apologising and asking me to come help her do things. I don’t know what to do, she has older sisters somewhere but no kids from what I can tell. She’s already damaged the beautiful boat I sold her, and it’s heartbreaking that she’s seemingly alone deteriorating on a boat she clearly can’t manage. The marina office lady is also concerned. I don’t want to offend people here, but I genuinely believe Dementia is demon possession. Even has Demon/demen in the name. It’s something dark and i think I will pray for this old ladies soul to be cleansed. Don’t know what else I can do.

This is mostly fairly accurate except the end stage sign is quite obvious.You begin to believe government statistics,you start imagining government is here to help,and politicians only have your best interest in mind and Kamala Harris is a genius.

I want to set a positive example by unaliving myself once I've lost my mind

My sister went through this process. Each time I visited her in the nursing home, she had slipped away a little more. When she finally passed away, I was unable to grieve. I realized I had been going through the stages of grief throughout her illness, and, by the time of her death, I had already reached acceptance.❤

Im amazed at how folk on the tube and net can delineate the characteristics of end stage dementia, yet not one - not one - doctor or nurse can help family by advising which stage the patient is in. Even a psychologist and psychiatrist were resistant on making any type of judgement. Sad. Especially with cracker jack certified medical staff in nursing homes. The patient and their caregiver family deserve more than a shoulder shrug.

My mom was offered hospice after a fall that left her unable to safely get up and do anything. She lost all interest in eating and 3 months later she died. I was just so glad to get the chance to say goodbye and do one last Christmas tradition we always did when I was younger. She didn't recognize me a lot but strangely always remembered my daughter, her granddaughter. After she died I learned that at least two generations past without the grandparents died without meeting granddaughters. I broke the trend. I was just so glad she remembered her every time we went to visit.

I’m also going through this with my father. My mom & dad were in home hospice from August 2023 through January 2024, but my mom fell again, she has been falling and being hospitalized since June 1st 2013, though she fell hard in May 2012, but she wasn’t hospitalized until 2013, she nearly died in 2013, her team of specialists told us on June 20, 2013, she had very little chance of living. In January, 3 of my sisters and my brother were visiting my parents and mom fell off her walker and cracked her femur, my parents both had to be put in a 24 hour Hospice Home, because none of me and my siblings live in Southern California, we live all over the USA, I went down with my husband 1st of February, my mom and I had such a special relationship, I was the first born, honeymoon baby, the eldest daughter, my mom begged me to stay with her and be with her till the end. My dad has had dementia since 2011 & he’s deaf, so it’s been so hard, my husband caught Covid mid February and we returned home and got well so we could go back asap, because I knew my mom was dying for real this time. It was just me and my husband,my siblings all went home. On March 16th, as soon as I walked in to their room I knew my mom had started her transition, I have watched so many Nurse Julie Hospice videos,including the trigger warning ones on active dying, so I knew what it looked like. My mom had managed to tell me over and over on March 15th “You are so beautiful, I love you, I love you, I love you. My dad became very lucid on March 17th, he knew she was dying and he cried on my shoulders for 45 minutes before the nurse came, to corroborate her transition, the night before, the head of their hospice came and he told me he had been trying to talk to my brother, I called my brother that Saturday night and let Rumel tell him that mom was dying right now and forget his flight on Wednesday, I also texted my sister, they drove from Utah and arrived on Sunday night. My mom passed away on Tuesday night at 7:03pm, March 19th, I was checking mom’s shallow breathing and comforting my dad, my siblings had gone to the airport to bring my brother in law, mom was waiting from 4 till they arrived, then she let go, I promised her over and over, that we would make sure dad was taken care of. Mom’s funeral was the most beautiful funeral I have ever been to. I had to leave to go home, but I am going back in a few weeks to visit dad and try to determine how he’s doing. He is having trouble swallowing food, that started on March 17th, my niece was feeding him stew, but the pieces were to big and he kept choking, I showed Kara to cut the pieces up, like for a baby. My dad is now refusing food and he doesn’t want to drink, he has asphsia, he lost the ability to stand and walk in early February, and now he has lost his talking, he did manage to say “I miss her” on Monday. My mom and I had plans to celebrate our birthdays together but we can’t, so I am going to take flowers to her grave and talk to her for my birthday, I just hope my dad is okay, I hope I make it back down there. My brother cleaned their hoarder house and 1/2 acre property, he’s been working on it since 2018, but we called in all the help we could get & the house funded yesterday, my brother needs that money to pay for my dad’s care. This is soooo hard. I miss my mama so much and I’m losing my beloved dad too, he deserves to be with my mom, they have been together since she was 18& he was 19, this year would have been their 70th Anniversary in August, my heart is broken 💔

For some reason I could barely hear this. I thought dementia had 7 stages

My mother is more than likely at this middle stage of having dementia, everything you’ve said in the video describes her situation perfectly. She was a very independent hard working RN, but now shes forgetting loved ones and can’t even hold a proper conversation. And she’s only 53. It breaks my heart every single day 💔

dementia can be heal , use vegetable oils in your food , coconut , avocado oil . eat only fruits , vegetables , nuts and seeds . do breathing exercizes . nuts look like a brain... so its good for your brain . learn meditating and focus on your brain , so u have blood circulation . Yoga is healty . U need lots of magnezium , favorit food of your brain . Cacaou , spinich , stinging nettle , alfalfa . Avoid burned oils , chemicals , acidic foods .

The final stage is joe 💀

Is there a point where one forgets what people even are? I notice the commonality of them forgetting WHO people are, but is there a deeper stage where they cant recognize WHAT a human is?

Lines are kind of blurred between Early and Late stages of Dementia. Gramps for the last 6? years has had early stages but also some late stage symptoms, he's 93 now. Still has speech, could not for the last 7 years pay bills correctly, delusions, hallucinations, memory loss, that grew or remained stagnant for years as well as many of the larger problems from dementia. He remained this way for a good 6~7 years I taken care of him. Almost overnight he dropped most of his vocabulary, complete personality change, aggressive, depressed, doesn't eat, and many other problems around personality. A wild experience, couldn't really spend more than 30 minutes without finding him trying to pack up and saying he has lost his home and everything (when he owns the deed and has nothing to worry about). No amount of trying to show him he's safe worked, it's just a constant battle with him to remain and it seems the only option is to lock him down despite him being able to walk and carry himself through the day. I'm 38 and my hair started to turn grey from constantly battling him over a year. We were doing fine then one day it all went away.

My wife has Lewy Bodies dementia and it is like the "step child" of dementia most people have not heard of it, even medical people. Care giving is tough and getting tougher.

My relative just passed away a few days ago. She was old, and our family first detected something that was suspect of dementia three years ago. I miss her and love her so much and blame myself I couldn't spend time with her because she lived in another country. She was so sweet and kind to me. 😢

A word salad? Might a holder of very high office produce such speech?

CAR don't C = correct A = argue R = reason with people with dementia.

no sound

😕Once you need people to do everything for you, and when you're also blind, life is pretty much over!! My dad's only pleasure in his final stages of life, was eating chocolate pudding!! But on his last day he had trouble swallowing and was even spitting the food out!! And couldn't use a straw to drink with anymore!! I would rather be dead than blind, even if I was healthy!!

DOES THAT APPLY TO LEWY BODIES DEMENTIA ALSO?

If I end up with shit, anyone I know has full permission to smother me with a pillow!

No! The final stage is you steal a presidential election and turn the greatest country ever into a flaming s@#thole.

My dad was forced to have the toxic experimental clot shots against his will. His early stage dementia went off the map very shortly afterwards. He died! I’m angry!

That’s not fair for the other person around them

Thank you for these videos... going through this now with my 87 year old aunt for whom I am the primary care provider and decision maker.

I need this. I’m very very close to my Aunt who now is in SNF advanced Lewy body. Trying to figure out when I visit what I should discuss that’s not about her illness

Stage 6 has no description

Excellent presentation

I wonder how long dementia has been around? Did people pre-WWI or WW2 experience this in the aged?

My Dad is currently suffering with end stage dementia. It's very hard to watch. 💕

This has to be the WORST DISEASE EVER!!!!

And their memories are all scrutched up like EATEOT stage 5.

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I think hospice is one of the worst organizations there are for elderly patients especially with the dying process and dementia I had hospice which was a big mistake for my father the last 4 months of his life that he was in a nursing home because of a fall in the doctor suggested hospice me stupid as I was said yes without even knowing what hospital was really all about all it is is an early death sentence and they make you die in peace and quiet and dignity

What if the dementia patient refuses or won't except any help.

I just read your comment and I totally disagree with what you say working for hospice hospice to me is the biggest rip off I had it for my father and was taken in by the rules and regulations all hospice to me is a way to kill somebody faster if I had known that my father was going to be put on message to be put on morphine is eating not get him up out of bed to his dad and I found that very appalling and degrading I was told that they switched extensional patch to morphine because it's pain has gotten worse he's pain hadn't gotten worse he was living too long on methadone to on more hospice so he had to go they increased his benzodiazepine which is a wrong thing to do with someone is living with dementia because it makes him more confused more eligible for false infractions and more cases to be hospitalized equals sooner death I wish I was more a hearable to what hospice actually does to patients it actually allows them to die at a fast rate when my mother came time to have hospice I put my foot down I had many in arguments with a detox because they stressed methadone and I forbid any methadone to be injected into my mother till the day she died I forbid any house on I forbid and he mental drugs such as Adam and Xanax Clinton you name it I objected it I was not going to have my mother be a guinea pig or because I heard they had no still the doctor this patient has to go she's been living too long and taking up too much money she was over 6 months and getting stable on dementia and all of a sudden they won because somehow she was ended up in the hospital and she never regained consciousness and never came home because they put it on method don't behind my back and I wish that I know this I would have sued the hell out of vitas out of Middlebury Connecticut they are the worst hospice to ever ever send a patient too if you want to kill a loved one send them to hospital I have no sympathy for the nurses I don't care how much they have to work how much they overloaded they did this to themselves their object is to let the patient die and take the tea in the most fashionable fastest manner possible no matter what it takes at what cost with what prescriptions I had my mother switch to oxycontin no match mentally and she lives over 8 months on hospice care perfectly and died of natural causes why because I put my foot down it was on top of everything they did when they send my mother couldn't eat anymore I forced my mother to eat she had no exacerbation going too long she had no liver loving infections she had no food going down the wrong pipe because I took my time with her and I went the extra mile to make sure she has the longest life possible I don't just stop feeding my mother because she couldn't swallow that's not the way somebody who loves their mother treats their parents remember the saying a mother racist six children and never complains but when one child raises one mother they complain so my change everybody out there who was thinking of putting your parents in vitas

'Dad, what's my name?' 'Give us a clue'. 'My name begins with J'. 'Jim. Joseph ....give up'. 'Dad my name's Jon'. 'That's amazing, I've got a son called Jon'. 'Dad, that's me'. 'You're my son. Well what do you know. I didn't realise I was that old'.

Nursing homes doesn’t do much to help these patients . Too expensive. If you have someone to at home to help them it’s better . Why pay for someone to deteriorate faster

My neighbor is in late stage. He needs to be bathed, fed, and cannot walk unassisted becuase his knees do not straighten.He leans to one side and on a chair he will slide down to the floor becuase he cannot sit up straight.He has had this disease for over 10 years.He is now nonverbal.He is alert and babbles in his own language.His wife is in denial and won't leet him is a wheelchair and keeps taking him for phyhsical therapy thinking he will walk again. How long do peolple stay on like this?

my dads in the end stage, hasnt walked, said more than a word or recognized me in years, he had a 15 minute seizure this morning. Its sad but when you've seen the decline over years and years, the ending is almost welcomed, you dont want to see them suffer anymore with no hope. Im going to see him tomorrow. I hope he didnt suffer during the seizure. Has anyone else dealt with this at the end stage?

my left ear hears everything

My mom has dementia 😥, my heart breaks for her. She’s gotten to the point in which she doesn’t remember me and it broke me. We were so close always. I’m not sure how to handle this😢

I’m getting very forgetful! Is that normal?

You don't realize the value until it becomes a (burning memory)

I’m watching this to understand what’s happening to Brandon.

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That was great!!

dont listen to this with headphones

I am the caregiver (and grandson) of 2 dementia patients. They are 93 and 95, and are both in the final stages. I can state with certainty, this video is absolutely accurate. 🤧😔

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