He's wealthy, and can pay for experimental treatments, health care and since he's famous, he shouldn't have to worry about ending up in jail/ prison or the worst nursing home possible.
@@glennleslie6127 Ever heard of Therapeutic Ketosis? Keto is not a diet, it is a metabolic state. It has been proven effective in treating many different mental and overall health conditions. Don't trust your physician, dietitian or nutritionist to understand the therapy...their training curriculum was developed by corrupt pharmaceutical and food corporations 😮 I'm praying this message inspires YOU to keep believing there is hope, have faith not fear 🙏🙏🙏
My 64 year old husband was just diagnosed with this disease on his birthday 3 weeks ago. I’ve noticed changes with his speech, personality etc….I’m not sure what or how I will handle this or where to get help for him. We have insurance but the doctors aren’t really telling us much or helping at all. As far as our house well we lost our home 4 years ago and now we’re in a 3 story townhouse which I’m trying to get my credit score and finances together so I can get him into a ranch house so everything will be on one level. I’m still working full time and can’t afford to quit at this time but I know soon I will have to. Whoever reads this keep us in your prayers please! Thank You!
The sad answer is, nobody knows what to do. Research is ongoing, but very little is still known about brain functions. To be perfectly honest. However this form of dementia, usually, progressing is slowly. But we are all different so... Sorry.
My prayers go out to you and your husband and I know the feeling my husband whom is in his 30's is starting to have those changes due to early dementia symptoms
no GMO, High Animal Fat Diet (carnivore), selective dairy remove Glyphosate AMPA (roundup / COVID) sources Food, Water, Air, Soil as MUCH AS POSSIBLE it's the CAUSE 100% - we're lied to for 45 yrs
I would like to look into Etanercept we are being LIED TO, Miss Diagnosed, Passed around See a NaturalPath, Gut Panel, Vitamin Deficiencies, Bloodwork, Stool, Saliva (test for Glyphosate too)
My sister passed away at 57 years old from this horrible disease. It breaks my heart to think about what she went through. God bless anyone who has to go through this.
I actually worked at the facility that Mr. Johnson was a resident at and on his unit. I remember we had to put a lock on the staff refrigerator because he would go in there and eat all of our food. And I tell ya! He was one strong guy because he tore the entire lock off one day! Lol He was a handful but he was such a pleasure to be around and I love him just as much as I did my other memory care patients. He was definitely the most challenging patient I've had in my CNA career BY FAR. Seeing this brings tears to my eyes because I remember Amy and the children coming to see Mark and spend time with him. She would always leave with such a sad look on her face. Amy and Mark had such a big heart. When I had my son, Amy gifted my baby a beautiful blue blanket with planets on it. I still have it to this day and will never get rid of it. Rest In Peace, Mark. I am glad you are no longer suffering and are now able to watch over your family from heaven.
My Husband whom passed away on January 11 2016 Had Frontal Dementia, He had wore a 24 Hour Patch, he also battled Parkinson’s Disease. God was so GOOD, Al was such a KIND MAN, he was a JOY to care for never A JOB...My Al was A JOY, I would do it all over again.
Man, this was heavy. I know mark has since passed away and my heart breaks for the loss of his life far too soon, his children & his wife. I don’t think I will ever forget this story 😔
@@marvelcomiks8078 You know you're a troll trying to get on people's nerves. That's like something a narcissist pretending to be someone else would say. It makes no sense.
@@scottg4520 Karma does not make sense to people who likes to do vile stuff, otherwise they would stop their vile ways. Its meant to be that way. Remain blind.
@@marvelcomiks8078 Well Marvel Comics---that explains a lot about your thoughtless comment. Stay on the planet longer and that Karma theory will get busted by the facts. wish it were true, but its not. by the way it is NOT GOOD KARMA TO MAKE THOUGHTLESS COMMENTS ABOUT THE TROUBLES OF OTHERS. sorry you are sooo butthurt
This poor woman had to find an extra $7,000 every month on top of ALL this? Losing her husband, raising 4 young kids, having a full time job, paying all bills/mortgage, etc. Oh yeah plus $7,000. Absolutely obscene. She has some seriously impressive strength.
My wonderful neighbor back in NY was an eloquent, fun loving, witty, popular, much loved judge. When he was diagnosed, the sidewalk conversations we used to have...started to go...and I ached for that to return. John is no longer with us. I think of him so very often...
I have a friend who has this. Her whole personality changed. She divorced her husband of many years, exhibited bizarre behavior, and she's now aphasic. She gained about 200 pounds. Her kids are terrified because their grandmother also died from it. She was in a memory care facility and is now in a long-term care hospital. It's just awful.
One of the saddest things about this kind of illness is that after your loved one dies your strongest memories of them are about the last part of their lives. My father had always been a funny, creative, kind man who thought of others, but in his last years all that had gone. As his caretaker I witnessed the destruction of his personality and dealt with the negative behavior and now they are the main things I remember.
My great aunt, who was more of a grandmother to us, became aggressive and it was hard for me to accept that the most loving person in my life had become someone I couldn't recognize.
We are going through this now with my dad. That is some thing I worry about. Even now, it’s hard to remember what he sounded like and what his personality was like. So very hard
@@schrisdellopoulos9244 it’s ironic because I’m actually an atheist. It’s more of a sentiment of displaying hope and wishing good health despite the lack of a cure for such a terrible disease.
A family member of mine was diagnosed with FTD a couple years ago and it has been a really horrible decline since. Such a nightmarish diagnosis. It’s so hard caring for someone with it but I can’t imagine what it must be like for someone actually going through it- even if they aren’t aware of what’s going on it seems like there is so much suffering. Really heartbreaking. It’s so important to educate others about this.
Awww I love you comment and every word you said it so true. And yes it needs so much more attention on it. It seems anything to do with the brain they just say it's mental health. I think it's so much more complex. I was my mums full time carer. Until her mobility went, she was falling and I could not pull her up. It got so bad that I had no choice. The day we put her in a nursing facility my heart broke and I've never recovered. She really suffered. I would go visit every other day. I would watch all of the patients and it was such a sad place. My mum cried like a baby every time I left. My mum in the end could not swallow, move any part of her body, and got so many infections. The last was pneumonia and that was the one that she died from. Aug 8th 2016. Then in December 22nd 2016 I was diagnosed with cancer. So it was like oh well its my turn 😄 I got through it. But barely. I don't leave home as I have so much trauma grief. It's a hard life, I never imagined I would lose my mum at 55. It's like going down a rabbit hold and the door closes behind you. The world is forever changed and its darker and sharper In places. Some of it has light and you can pretend to go on. But deep inside what you went through never leaves. Ever.
@@jenniferrobinson1792 hey Jennifer I hope your doing ok? I know what your going through is so hard, frustrating and confusing. Stay close to love ones, take care of you. Sending you a big hug, best wishes 🤗
My mom got PPA at age 58 it's an absolutely horrific disease, the fact that she could not talk read or write was awful, she was proud that she won the spelling bees in school, plus she sang for a living..singing was her love.. The doctor said by looking at her scan, she probably had it already 8 years.. She died of aspiration at the age of 68.. I miss you so much, Mom.. My icon picture is her.
This broke my heart. My mum had FTD Dementia, she was diagnosed in 2013, she died in 2016. It was so fast and progressive. The rapid change in her completely stripped my mums character & personality. My mum was such a beautiful kind caring giving person. Loved by everyone and she was my best friend in the world. When my mum lost her mobility and her speech. That was the hardest. She couldn't lift her head up and her neck just hung forward and her head would bend over. I remember I would push her everywhere in her wheelchair. It was very difficult but I didn't care as long as she got outside and continued to shopping or have some food. The first time she choked we were in a cafe, and she forgot how to swallow. They wouldn't put a tube because they said she would pull it out. She then got infections all the time. Then she got pneumonia and we slowly watched her die. All I can say this is the cruelest disease I've ever known. It's so cruel and painful at the end. To watch my mum suffer in that way literally broke me. My mum passed and three months later I got breast cancer. The trauma from being my mums carer is still with me every day. I'm so grateful for videos like this. We need to get FTD dementia out there to the world. I pray no one has to go through this. I Hope they do find a cure and soon. God bless all the people with FTD, their family and friends 🙏 ❤️
I strongly suspect my father was in the early stages of FTD or something similar. He then got an aggressive cancer that took his life. In a way that might have been a blessing dementia is so incredibly cruel. A hug to everyone dealing with this.
@@greengorillah "I strongly suspect my father was in the early stages of FTD or something similar. He then got an aggressive cancer that took his life" Both are the same disease. It's the same diseases as Obesity, Diabetes, Heart diesease and so on. These are just all manifestation of hyperinsulinaemia / insulin-resistance. It is our western diet with a lot of sugar and plants and with a very little healthy meat which causes this.
@@ABlueState I think so, part of why I am saying this is that my mom developed dementia after my father passed away. She still realizes what is happening to her and that is awful. I am sorry for you and your mom and family.
My husband has FTD and was diagnosed three years after I took him to a Neurologist. He is now 80 and cannot walk without assistance, is nonverbal, incontinent and has no movement in his left arm. It is very sad to see a very active man in this condition.
This disease is heartbreaking. I lost my Mom to it. She was just 55 at diagnosis when we noticed symptoms. 6 years later, at age 61 she passed away. The decline was swift, aggravating, aggressive, and sobering.
I live in Australia and have recently been diagnosed with FTD. Thank you for this report. They don't seem as knowledgeable here and it's been wonderful to watch information on American tv.
My mother was diagnosed with this in March 2023. It is really very difficult to see her in this condition. She was loving, respectful, caring and compassionate. She has always been charitable and generous to others. Now, she’s the opposite of it all. I sometimes wonder where did the good karma go? She’s mean, she calls me names and uses degrading words and sometimes hits or scratches my arm. It is very difficult living with her like this. Just hoping and praying for strength at this point. 😢 💔
I lost my sister to FTD. It took only four years from normal to death for her. She died in February before she reached her 70th birthday. But at least she had most of her life. This poor woman with her 40 year old husband. . . omg.
@@rhondarobinson8443 Very sorry to hear that. And my heart goes out to you and your family. I am just curious whether she suffered a major trauma that triggered the condition? My friend's son and mother died in the years leading up to the onset. Her son was severely disabled from birth, so she had had 12 years of dealing with that, and then he died. It could also just be a coincidence. Did your sister suffer a trauma beforehand?
@@SedonaMethodPlus She had a traumatic divorce about 10 years ago which was preceded by an attempt to adopt 2 boys which ended with them returning the children after her husband became unexpectedly withdrawn. Also, a job loss 3 years ago. She’d never gotten enough therapy/counseling for these events in my opinion. She’s had rigid ideas about how the world should work. She had been periodically going to the ER for the last 4-5 years with stomach pains, but they never found much. She expressed to another sister that she’d be the 1st of us 4 sisters to pass away. She’s 57 y.o. I’m going to been leaning on prayer, EFT Tapping and other energy medicine.
My mom was an active athlete all her life - she developed a form of FTD called progressive supranuclear palsy which left her unable to move - not even her eyes. It’s heartbreaking. My childhood friend developed FTD
It's so sad when I see stories on FTD. I have FTD myself and as a 47 year old 5 years into it you really have no places to turn for help or support. Most places are for elderly or for alzheimers . Very few places ,help and support are for younger. Also getting diagnosed is years of test and stress. Now I am in decline. Its so sad and worrisome not knowing what's going to happen to me. Support groups I find really don't exist. I am not speaking of zoom. I can't even get on stuff like that. The physical groups aren't their for the younger people with this horrible existence. Bless everyone and their family who have or know someone who has this. It's pure evil.
God bless you, dear. My husband has FTD. If no-one is pestering him to shower or go to the doctor, it seems like his day-to-day experience is pretty zen-like and mellow. I hope you can find a comfortable place and have a cozy time of it.
It is really sad. Nothing can be done yet, however with more research there is hope. Maybe they can find preventative measures or a way to slow the progression of the disease to a point. 54 years ago saw the first human heart transplant. Science advances rapidly.
@@myce-liam they can’t do brain transplants though, and this disease is genetic so it’s highly unlikely to be cured. Maybe things to help it not be as terrible but that might be it
It can be completely reversed. Like all metabolic disorders, its root cause is insulin resistance. Consecutive dry fasts of 5-7 days duration will reverse the condition.
My mom developed FTD. Her behaviors became so bad that I could not take care of her. It broke my heart and hers. The ugly truth of FTD is that it does not effect intelligence so it’s hard for family to understand.
🙏🏿🙏🏿 sorry to hear that I took care of my grandmother for 4 years with dementia she passed the nursing home because you could no longer take care of her sending you healing and loving light and prayers to your family
My mother showed no sign of traditional dementia but living alone we noticed that there were reminder post it notes all over the house. Brain disease is the worst. Frustrating and painful to both patient and family. This country needs national health!
I feel you. My daughter is only 31 years old and has alzheimer's and seizures frontal lobe. It's a very hard road, but we all can do it. God doesn't give us things we can't handle. Bless you all 🙏
I had Brain Cancer, Surgery & Radiation & believe me, it has been a ruff road so in some ways I can relate. I am the only one that is still alive (BCancer) & I'm in an old people's home... I'm 57
Well I should of said I'm the only one who lived in the North West. I was in Alaska & had surgery in Seattle. I can't say for Dever. I'm ok but life gets harder every time the year starts to change: Spring ~ Summer ~ Fall ~ Winter. That's what GOD does for me, what would I do without HIM... Amen!
@@xiqueira I wanted to tell you personally, Thank ~ You. My surgery was in 2005 & I was in Alaska, I moved back to Wyoming in 2018 were most of my family is & that's all good cus I come from a huge family. God bless you!
Well she’s talking pretty well compared to my girlfriend who has it. Who has FTD. Now she can’t speak. She can’t walk. And she lost interest in everything, except food. Mostly sweets Coke, And french fries etc. so I really hope and pray she doesn’t end up like my girlfriend who was so independent and could dance great. It was very intelligent. That’s all gone. But I still go see her. And be with her. And tell her I love her and hold her hand.❤️
I am very glad that lady stayed with her husband she didn't break up with him my mom would have broke up with him just like after I got diagnosed with epilepsy/seizures she put me in foster care and my dad wouldn't allow that so she broke up with him and he raised me since I was 6years old and diagnosed with epilepsy/seizures
I can't believe that it is $7,000 a month. Coming from a speechless Australian. I just prayer that the pain has eased some. Much love and prayers to all of them.
Yes welcome to our crappy healthcare system here in the states. My mother was recently diagnosed with bvFTD and it will be expensive to find care for her.
I am a nurse assistant at a memory care facility in the states, average cost is around $30,000 a month. I make a little over minimum wage but I don't feel as sorry for myself as I do for the families that have to endure these costs.
I wish people would be honest with the reality of some medical conditions. It seems like most don't pay attention to the seriousness if the condition isn't visible.
He was not “just diagnosed” theses symptoms have n\been going on for decades, they just told the world, b/c he could no longer fake acting. He had been fed his lines thru n earpiece for years.
After coming to my mom's to relocate her husband to a care home I realized mom couldn't function alone. I moved to center Georgia several hours from home over 14 months ago. I know it's some form of dementia. We have spoken to our doctor about testing to define the type only to realize.....what for? She takes a "memory pill" but who knows if it's of benefit. The doctors and pharmacist agree that no matter the type, no real treatment plan. We got busy, walking two miles per morning. I took over cooking, paying bills, making appointments etc. Back in February covid pneumonia set her back. Well the lord spared her, we started our exercise regime but now 1 1/2 miles is a struggle. Mom's 78 and I commend her effort and exertion seems to help fight the dementia back. Even though I don't feel productive and am penniless, this has been such the blessing, caring for the sweet girl. Some days the blessing is hard to see thru my tears but they do exist. I may not be able to provide care once she slips further away and unable use the restroom alone? I worry that my never quit, marine corps ethos may keep me seeking better care later on. I guess I would be forced to sign over her home and car to the government in exchange for the care. It's a shame how the dollar keeps entering into the conversation. This disease that's killing her has laid waste to my personal future but I realize I would have had no chance at a future without her raising me. The Lord hasn't brought us this far to put us down and forget our needs. Please keep us in you're prayers. She loves and appreciates me greatly, but I feel like the old man son, interested on the SSI check arrival. My Ambition is gone.
Hi Steve, you need to seek legal advice on what to do so that your Mom's assets aren't taken for future care. There are ways around that, and so paying for a good estate attorney would be worth your while and money. Please do this ASAP
If you can get medical assistance to end your life if you have a terminal disease, why can't you get help to end your life if you have dementia? It's absolutely crazy! I guess they need as many people as possible so they can do their research?? I am 72, I would end my life as soon as I got diagnosed with it! I can't imagine living like that and putting my family through the expense of taking care of me. It would be a living nightmare for everyone concerned. My heart goes out to anyone who has to endure this.
FTD and dementia are diseases that diminish people's capacity to realise that they have changed. Assisted death might be a blessing to those unable to pull the plug themselves or unable to recognise the degree of their decline. Many people with dementia retain a distinct personality and are often present or shift in and out of being lucid and adrift or lost. The carers no doubt suffer more witnessing the decline and coping with the changes. Assisted living helps and sometimes a neutral person with training or experience dealing with dementia is better able to cope with defiant, puzzling, inappropriate, potentially dangerous, irrational and demanding behaviour. If only all people had ongoing contact with elderly and sick people instead of locking them away then the community would be more aware of differences and diverse needs and changes that often occur with age and illness. We sanitise and avoid illness, old age and death like Victorians sanitised sex in the nineteenth century yet accepted and laid dead bodies out for viewing in their homes and took photos of deceased children sitting with the living.
Thank you. I’d do the same. I just turned 76. Probably won’t get FTD but may someday get Alzheimer’s, especially if I live to 85 or so. Robin Williams killed himself after he was dx with Lewy Body Dementia. I wouldn’t want to become a shell of myself.
I'm going through the same thing. It's been difficult to get a diagnosis for my husband. His entire personality changed so much it's horrible. He lost so many jobs and has not worked for 3 yrs.
I hear you. My hubs has bvFTD too, and i suspect ALS. Hang in there. Mine is on the 4th (last?) month in assisted living on respite. It will be hard to keep him there because of the cost, and also, they rejected his application to stay long-term because of his diagnosis and my iffy financial position. I'm hoping to have a meeting with them soon and successfully beg them to keep him. It's so hard because socializing calls their brains to order, and they can function normally for an hour or two. Even close family, doctors and physical therapists often don't believe there's anything wrong. Then they sleep all day, can't function in a job, won't shower for weeks, are generally irrational, and exhibit a host of other weird behaviors, but don't recognize that anything is wrong with themselves.
@@pesterlig I did some research and feel that I may have found the correct diagnosis for my husband's issues. These doctors are NOT interested in helping anyone - everything has been CV19. I'm fed up with all of this insanity. If my husband's Neurologist doesn't help I may have to sue our Hospital System for Malpractice - that's how angry I am at this point.
My wife was diagnosed in 2014. Now ten years later her bowels don’t function, her speech is very rarely understandable. She aspirates foot particles and struggles to swallow. She craves chocolate and cakes and only eats decent food rarely. Now she sleeps for 16 to 18 hours per day. Her issues are multiplied by the fact that she has had MS since 1990 and has been chair or bed bound for the last 15 years. I hoisted her to bed at 18:00 yesterday and she is still asleep at 10:15 the day after. It’s an absolutely horrendous illness and I feel for everyone that has any involvement with this disease.
Young mother Amy Johnson of Windom Minnesota needs help as she shoulders a $7000.00 a month bill for her disabled by frontal lobe dementia 40 yr old husband's facility bill; this is financially impossible for her to sustain for 5 more years and also have to work constantly to provide for her life alone w her small children. Please help her and her four very young boys.
My Mom died 11 years ago from frontotemperal lobe dementia. She was 63 at death and 50 at diagnosis. She had aphasia and getting her to talk more than 2 words was hard.
Just lost someone to this. She was not herself in the end. She was completely out of it. She had to be under 24-7 care and it ran the entire family down with stressing about who was coming and sitting with Granny. We tried to keep her out of the nursing home until it wasn't possible. She was falling and gets injured. She was alsocdoqbetic and she would hit people who tried to help or check her insulin levels. She was an amazing person who loves Jesus and did what was right for anyone she came across. She didn't care about things or money. She loved her family and cooking for them. Once she had to go into a nursing home they placed her into a lockdown unit and medicated her so all she would do is sleep and wake up be mean to everyone. She would use the bathroom on herself then spread that all over her room herself and other patients rooms in the unit she couod get to. She constantly teied to escape and she alsp stole other patients belongings. It broke me having to watch this unfold and i would not wish it on my worst enemy.
My mother-in-law just passed at 82 from this. She lived with us for 5 years and we took care of her full time. She went from walking talking to completely bedridden non verbal and pretty much just there in body but her mind was gone. My heart goes out to other families who are going through this.
I took care of a patient that showed these symptoms and behavior. His daughter , her husband keep her at home but it was so difficult a lot of times. She died on 2015 .
As a 40 year childhood brain cancer survivor, I definitely feel like this regularly. Memory, mental and physical state have all continued to dateriate. I believe it does stem from 6 brain surgeries, 1 brain tumor relapse, 7 brain ablations and refractory epilepsy. The medication for the seizures make it worse too. All I can say is make each day count now for what it is. Ive been doing my bucket list with family and friends. I'm not going to let another diagnosis hold me back.
My poor Father. He too had RTD. He was an executive for a petroleum company, huge in scope. He wasn’t fired. He was allowed a very tranquil retirement. Thank you Colonel Pipe Line.
it’s crazy how quickly this onsets. imagine… one day, you wake up and you’re suddenly gone. physically present but mentally poofed out of existence; a shell of your former self.
I lost my mother to Alzheimers decades ago. As I understand it, Alzheimers is also always fatal. Mom's progression took a bit over five years. Some of her symptoms resemble those of Mark Johnson (as covered here). For anyone who has had someone special progressively lose their memory and basic mental capacities over the course of years, they will know why the experience is sometimes called 'the long goodbye'. You continue to meet with, and speak to them for years. But in truth, they had 'checked out' long before the final 'GoodBye'.
You Cannot Challenge Them, You Just Have To Love Them Through...Remembering The Person The Whom They Really Are...LOVE MADE A COMPLETE CIRCLE FOR ME & MY AL, HE LOVED ME @ MY LOWEST & I SURE LOVED HIM @ HIS...HE NEVER WENT INTO A FACILITY...I LOVED HIM THOUGH IT ALL & I WOULD DO IT ALL AGAIN...AMEN❤️
We received the diagnosis that my mother had FTD after we took her to the emergency room for what we thought was a mental health crisis. The doctor told us it was the worst case he had ever seen. We thought she was suffering from severe anxiety and depression. She ended up dying a few days after we were given the news. Her health was failing and we had to make the decision to continue care or choose comfort care instead. Seeing this, I am glad we made the decision that we did. At least she was spared further suffering. The scary part is that there can be a genetic component to this. I don't worry about myself, but I would hate to think that my family might have to deal with this one day.
Yes, we finally have the diagnosis of FTD for my mother-in-law. We have relocated to England (2020) to care for her (she also has cancer) and my father-in-law who has been diagnosed with "Parkinson's disease with dementia". The psychiatrist told my husband that he may want to pursue genetic testing in the next few years.
In my mother's case, she was in the end stage of life and they removed all other care except pain management. She died within a couple of hours once they removed the oxygen and other medicines that were maintaining her blood pressure@@CraftingChristian
@@CraftingChristian My mother also had end stage COPD. Honestly she probably only had a few months to live (if we continued treatment) but she would have suffered the entire time with all the problems she had. She had fallen and broken her back, terrible anxiety from both the dementia and the difficulty breathing. She had been on oxygen for years. She wasn't allowed to go home with us, we were frantically looking for a nursing home that would take her because they would only release her to a facility. That was her worst nightmare. It was our choice whether or not to continue care or basically let her die. It seemed the kindest thing to do to let her go. But it was devastating.
Sending love to Bruce Willis and each and every other person affected by this disease. ❤😢
He's wealthy, and can pay for experimental treatments, health care and since he's famous, he shouldn't have to worry about ending up in jail/ prison or the worst nursing home possible.
There are many things worse than death, this (frontotemporal dementia) is one of them.
@@glennleslie6127 Ever heard of Therapeutic Ketosis? Keto is not a diet, it is a metabolic state. It has been proven effective in treating many different mental and overall health conditions. Don't trust your physician, dietitian or nutritionist to understand the therapy...their training curriculum was developed by corrupt pharmaceutical and food corporations 😮 I'm praying this message inspires YOU to keep believing there is hope, have faith not fear 🙏🙏🙏
@@glennleslie6127yeah
My 64 year old husband was just diagnosed with this disease on his birthday 3 weeks ago.
I’ve noticed changes with his speech, personality etc….I’m not sure what or how I will handle this or where to get help for him. We have insurance but the doctors aren’t really telling us much or helping at all. As far as our house well we lost our home 4 years ago and now we’re in a 3 story townhouse which I’m trying to get my credit score and finances together so I can get him into a ranch house so everything will be on one level.
I’m still working full time and can’t afford to quit at this time but I know soon I will have to.
Whoever reads this keep us in your prayers please! Thank You!
The sad answer is, nobody knows what to do. Research is ongoing, but very little is still known about brain functions. To be perfectly honest.
However this form of dementia, usually, progressing is slowly. But we are all different so... Sorry.
My prayers go out to you and your husband and I know the feeling my husband whom is in his 30's is starting to have those changes due to early dementia symptoms
no GMO, High Animal Fat Diet (carnivore), selective dairy
remove Glyphosate AMPA (roundup / COVID) sources Food, Water, Air, Soil as MUCH AS POSSIBLE
it's the CAUSE 100% - we're lied to for 45 yrs
I would like to look into Etanercept
we are being LIED TO, Miss Diagnosed, Passed around
See a NaturalPath, Gut Panel, Vitamin Deficiencies, Bloodwork, Stool, Saliva (test for Glyphosate too)
@@jeffmarkus5052 thank you I will be taking your advice and getting an appointment with a natural path right away
What a horrible way to lose a loved one. Unimaginable, really. Strength to all those who are going through this.
sending love
It really does suck, i miss how healthy my mom was before this =[ The woman in the video is in very early stages though.
My sister passed away at 57 years old from this horrible disease. It breaks my heart to think about what she went through. God bless anyone who has to go through this.
I’m very sorry❤️🌸🌼🌹🌷🌺🌻. How long ago was she dianosed with it before she passed?
I actually worked at the facility that Mr. Johnson was a resident at and on his unit. I remember we had to put a lock on the staff refrigerator because he would go in there and eat all of our food. And I tell ya! He was one strong guy because he tore the entire lock off one day! Lol He was a handful but he was such a pleasure to be around and I love him just as much as I did my other memory care patients. He was definitely the most challenging patient I've had in my CNA career BY FAR. Seeing this brings tears to my eyes because I remember Amy and the children coming to see Mark and spend time with him. She would always leave with such a sad look on her face. Amy and Mark had such a big heart. When I had my son, Amy gifted my baby a beautiful blue blanket with planets on it. I still have it to this day and will never get rid of it. Rest In Peace, Mark. I am glad you are no longer suffering and are now able to watch over your family from heaven.
Wow that’s really sad. Why would you work at a place like that it just seems so sad all around
It's a calling and we should be thankful for people like Chloie. They should also pay them more.
Not to intrude but many of the info you mentioned should’ve been kept confidential.
@@ranyataha7477 Nothing we didn't already know.
@@ranyataha7477 My first thoughts when I read it. I think it should be considered for deletion.
Here after Bruce Willis diagnosis. Man, this disease is heartbreaking.
My husband was diagnosed 3 yrs ago, they thought it was a stroke, to Ms, he has ppa w/ftd
@@Dhjcx Yeah I'm 38, they thought I had a stroke too. I hope you're doing well, since Dementia wears on the family and caregiver as well.
Mark's poor wife. What a beautiful woman to care for him for so long. I wish her all the best now and hope she can move on with her life ❤️
@Anonymous ...
@Anonymous wow, you're an awful person. You're probably really "fun" at parties, or maybe don't get invited for the very same reason.
@Anonymous you think that eating all the time is ok? You stupid? That's not normal. Did you see him at the end of the video?
Her kids too. They were so young…babies even.
My Husband whom passed away on January 11 2016 Had Frontal Dementia, He had wore a 24 Hour Patch, he also battled Parkinson’s Disease. God was so GOOD, Al was such a KIND MAN, he was a JOY to care for never A JOB...My Al was A JOY, I would do it all over again.
🙏💐😭 I'm so sorry for your tremendous loss.
Man, this was heavy. I know mark has since passed away and my heart breaks for the loss of his life far too soon, his children & his wife. I don’t think I will ever forget this story 😔
@@marvelcomiks8078 You know you're a troll trying to get on people's nerves. That's like something a narcissist pretending to be someone else would say. It makes no sense.
@@scottg4520 Karma does not make sense to people who likes to do vile stuff, otherwise they would stop their vile ways. Its meant to be that way. Remain blind.
@@marvelcomiks8078 Well Marvel Comics---that explains a lot about your thoughtless comment. Stay on the planet longer and that Karma theory will get busted by the facts. wish it were true, but its not. by the way it is NOT GOOD KARMA TO MAKE THOUGHTLESS COMMENTS ABOUT THE TROUBLES OF OTHERS. sorry you are sooo butthurt
I'm here to support Bruce by learning more about this disease.
This poor woman had to find an extra $7,000 every month on top of ALL this? Losing her husband, raising 4 young kids, having a full time job, paying all bills/mortgage, etc. Oh yeah plus $7,000. Absolutely obscene. She has some seriously impressive strength.
Yep, they want their money….
Two very powerful episodes of 60 Minutes., which has compassionately educated the world for many years.
I feel so sorry for Amy and her little ones. I pray she finds peace of mind and strength when she needs it. She is a strong, good person.
My wonderful neighbor back in NY was an eloquent, fun loving, witty, popular, much loved judge. When he was diagnosed, the sidewalk conversations we used to have...started to go...and I ached for that to return. John is no longer with us. I think of him so very often...
My husband was diagnosed with the behavioral variant of Frontotemporal Degeneration in 2016. I advocate for him daily.
I feel so sorry for Amy and her children. May God be with you.
I have a friend who has this. Her whole personality changed. She divorced her husband of many years, exhibited bizarre behavior, and she's now aphasic. She gained about 200 pounds. Her kids are terrified because their grandmother also died from it. She was in a memory care facility and is now in a long-term care hospital. It's just awful.
One of the saddest things about this kind of illness is that after your loved one dies your strongest memories of them are about the last part of their lives. My father had always been a funny, creative, kind man who thought of others, but in his last years all that had gone. As his caretaker I witnessed the destruction of his personality and dealt with the negative behavior and now they are the main things I remember.
😔
Hugs. I’m so sorry.
😢
My great aunt, who was more of a grandmother to us, became aggressive and it was hard for me to accept that the most loving person in my life had become someone I couldn't recognize.
We are going through this now with my dad. That is some thing I worry about. Even now, it’s hard to remember what he sounded like and what his personality was like. So very hard
Prayers to any family that suffer from this.
Thoughts and prayers for Bruce Willis 😢
Yes, such an unforgiving disease. Aren’t they all. This one though is unforgiving in its own crappy way 😞🙏
Ts and Ps mean zero Ethan. Shame.
S. Chris,
Speak for yourself!
@@schrisdellopoulos9244 it’s ironic because I’m actually an atheist. It’s more of a sentiment of displaying hope and wishing good health despite the lack of a cure for such a terrible disease.
A family member of mine was diagnosed with FTD a couple years ago and it has been a really horrible decline since. Such a nightmarish diagnosis. It’s so hard caring for someone with it but I can’t imagine what it must be like for someone actually going through it- even if they aren’t aware of what’s going on it seems like there is so much suffering. Really heartbreaking. It’s so important to educate others about this.
Awww I love you comment and every word you said it so true. And yes it needs so much more attention on it. It seems anything to do with the brain they just say it's mental health. I think it's so much more complex. I was my mums full time carer. Until her mobility went, she was falling and I could not pull her up. It got so bad that I had no choice. The day we put her in a nursing facility my heart broke and I've never recovered. She really suffered. I would go visit every other day. I would watch all of the patients and it was such a sad place. My mum cried like a baby every time I left. My mum in the end could not swallow, move any part of her body, and got so many infections. The last was pneumonia and that was the one that she died from. Aug 8th 2016. Then in December 22nd 2016 I was diagnosed with cancer. So it was like oh well its my turn 😄 I got through it. But barely. I don't leave home as I have so much trauma grief. It's a hard life, I never imagined I would lose my mum at 55. It's like going down a rabbit hold and the door closes behind you. The world is forever changed and its darker and sharper In places. Some of it has light and you can pretend to go on. But deep inside what you went through never leaves. Ever.
@@jenniferrobinson1792 hey Jennifer I hope your doing ok? I know what your going through is so hard, frustrating and confusing. Stay close to love ones, take care of you. Sending you a big hug, best wishes 🤗
My mom got PPA at age 58 it's an absolutely horrific disease, the fact that she could not talk read or write was awful, she was proud that she won the spelling bees in school, plus she sang for a living..singing was her love.. The doctor said by looking at her scan, she probably had it already 8 years.. She died of aspiration at the age of 68.. I miss you so much, Mom.. My icon picture is her.
This broke my heart. My mum had FTD Dementia, she was diagnosed in 2013, she died in 2016. It was so fast and progressive. The rapid change in her completely stripped my mums character & personality. My mum was such a beautiful kind caring giving person. Loved by everyone and she was my best friend in the world. When my mum lost her mobility and her speech. That was the hardest. She couldn't lift her head up and her neck just hung forward and her head would bend over. I remember I would push her everywhere in her wheelchair. It was very difficult but I didn't care as long as she got outside and continued to shopping or have some food. The first time she choked we were in a cafe, and she forgot how to swallow. They wouldn't put a tube because they said she would pull it out. She then got infections all the time. Then she got pneumonia and we slowly watched her die.
All I can say this is the cruelest disease I've ever known. It's so cruel and painful at the end. To watch my mum suffer in that way literally broke me. My mum passed and three months later I got breast cancer. The trauma from being my mums carer is still with me every day.
I'm so grateful for videos like this. We need to get FTD dementia out there to the world. I pray no one has to go through this. I Hope they do find a cure and soon. God bless all the people with FTD, their family and friends 🙏 ❤️
I’m so sorry to hear this.
Sorry for your loss
Oh I'm so sorry.
Thank you Nikola for sharing your mothers story. It helps us understand what to expect.
Such a horrible disease.. so sorry about your Mum. ♡
That totally sucks and sorry for your ma but we don't need another one. It seems like every year there's a new disease.
I strongly suspect my father was in the early stages of FTD or something similar. He then got an aggressive cancer that took his life. In a way that might have been a blessing dementia is so incredibly cruel. A hug to everyone dealing with this.
Or maybe he had brain metastasis ?
@@lazarus8453 His behavioral changes preceded his cancer (by 5 years or so), so I think that chance is small.
@@greengorillah "I strongly suspect my father was in the early stages of FTD or something similar. He then got an aggressive cancer that took his life"
Both are the same disease. It's the same diseases as Obesity, Diabetes, Heart diesease and so on. These are just all manifestation of hyperinsulinaemia / insulin-resistance.
It is our western diet with a lot of sugar and plants and with a very little healthy meat which causes this.
It is a blessing. We are in the 11th year with my mom. She is basically a vegetable.
@@ABlueState I think so, part of why I am saying this is that my mom developed dementia after my father passed away. She still realizes what is happening to her and that is awful. I am sorry for you and your mom and family.
Sending blessings and best wishes to Bruce Willis and his family. May you be blessed with strength and surrounded by love throughout this journey.
My husband has FTD and was diagnosed three years after I took him to a Neurologist. He is now 80 and cannot walk without assistance, is nonverbal, incontinent and has no movement in his left arm. It is very sad to see a very active man in this condition.
Same
This disease is heartbreaking. I lost my Mom to it. She was just 55 at diagnosis when we noticed symptoms. 6 years later, at age 61 she passed away. The decline was swift, aggravating, aggressive, and sobering.
I’m so sorry to hear what you and your mum went through😔💔Can you explain the symptoms?🙏 Hope you’re okay
So sorry Heather, my mum is suffering with it now and it is so horrible. My life has been turned upside down. Hope you are okay xx
❤🌷🌻🌸❤️🌺🌹
I live in Australia and have recently been diagnosed with FTD. Thank you for this report. They don't seem as knowledgeable here and it's been wonderful to watch information on American tv.
I’m so sorry. Are you doing well nowadays?
@@jenniferrobinson1792times like these I wish I could send hugs over the internet ❤
Jennifer, I hope you received a diagnosis from a medical professional and it's something treatable or at least manageable.
My mother was diagnosed with this in March 2023. It is really very difficult to see her in this condition. She was loving, respectful, caring and compassionate. She has always been charitable and generous to others. Now, she’s the opposite of it all. I sometimes wonder where did the good karma go? She’s mean, she calls me names and uses degrading words and sometimes hits or scratches my arm. It is very difficult living with her like this. Just hoping and praying for strength at this point. 😢 💔
May the medicine to treat such a brutal disease come out soon and reach every nook and corner of the world! 🙏🏻
I'm praying for Bruce Willis and Wendy Williams as well as anyone else who's suffering. God Bless.
Bruce Willis FTD diagnosis brought me here. Such a terrible disease. Prayers to Bruce and his family.
I lost my sister to FTD. It took only four years from normal to death for her. She died in February before she reached her 70th birthday. But at least she had most of her life. This poor woman with her 40 year old husband. . . omg.
@@ssmith6963 Thank you for your thoughtful comment. I miss her so much.
My sister died of this disease at the age of 60.
@@ssmith6963 thanks Sonia was hands down one of the best people ever. I’d run to her for help instead of my parents . I was lucky to have known her.
@@marciabradley7660 .
How Amy says she misses Mark a lot, is heartbreaking…
I feel very sad for families that go thru this when someone is very young, I thank God that my husband’s dementia waited until he was 79
I had a friend who was diagnosed with this alongside ALS. Her behaviour was absolutely bizarre but she died after a few months. It was heartbreaking.
Im sorry for your loss. To have both of those is unbelievably cruel.
My sister has this combination. Keep us in your prayers.
@@rhondarobinson8443 Very sorry to hear that. And my heart goes out to you and your family. I am just curious whether she suffered a major trauma that triggered the condition? My friend's son and mother died in the years leading up to the onset. Her son was severely disabled from birth, so she had had 12 years of dealing with that, and then he died. It could also just be a coincidence. Did your sister suffer a trauma beforehand?
@@SedonaMethodPlus She had a traumatic divorce about 10 years ago which was preceded by an attempt to adopt 2 boys which ended with them returning the children after her husband became unexpectedly withdrawn. Also, a job loss 3 years ago. She’d never gotten enough therapy/counseling for these events in my opinion. She’s had rigid ideas about how the world should work. She had been periodically going to the ER for the last 4-5 years with stomach pains, but they never found much. She expressed to another sister that she’d be the 1st of us 4 sisters to pass away. She’s 57 y.o. I’m going to been leaning on prayer, EFT Tapping and other energy medicine.
My mother in law died of this. She was a smart psychologist at one time, reduced to nothing. Very sad.
I am so sorry for your family's loss. So heartbreaking.
God bless you and her soul.
I'm here because of Wendy Williams.
My mom was an active athlete all her life - she developed a form of FTD called progressive supranuclear palsy which left her unable to move - not even her eyes. It’s heartbreaking. My childhood friend developed FTD
It's so sad when I see stories on FTD. I have FTD myself and as a 47 year old 5 years into it you really have no places to turn for help or support. Most places are for elderly or for alzheimers . Very few places ,help and support are for younger. Also getting diagnosed is years of test and stress. Now I am in decline. Its so sad and worrisome not knowing what's going to happen to me. Support groups I find really don't exist. I am not speaking of zoom. I can't even get on stuff like that. The physical groups aren't their for the younger people with this horrible existence. Bless everyone and their family who have or know someone who has this. It's pure evil.
God bless you, dear. My husband has FTD. If no-one is pestering him to shower or go to the doctor, it seems like his day-to-day experience is pretty zen-like and mellow. I hope you can find a comfortable place and have a cozy time of it.
My heart goes out to you, Karen. I hope you have some sort of outlet, even if it's not in a group setting.
This is so very sad and there's nothing anybody can do!
It is really sad. Nothing can be done yet, however with more research there is hope. Maybe they can find preventative measures or a way to slow the progression of the disease to a point. 54 years ago saw the first human heart transplant. Science advances rapidly.
@@myce-liam they can’t do brain transplants though, and this disease is genetic so it’s highly unlikely to be cured. Maybe things to help it not be as terrible but that might be it
It can be completely reversed. Like all metabolic disorders, its root cause is insulin resistance. Consecutive dry fasts of 5-7 days duration will reverse the condition.
@@andyw6996really? Where can one find research about this cure?
My mom developed FTD. Her behaviors became so bad that I could not take care of her. It broke my heart and hers. The ugly truth of FTD is that it does not effect intelligence so it’s hard for family to understand.
No she didn’t. You just want attention
@@brettlinthicum9885 Shame on you
🙏🏿🙏🏿 sorry to hear that I took care of my grandmother for 4 years with dementia she passed the nursing home because you could no longer take care of her sending you healing and loving light and prayers to your family
None of the types of dementia affects intelligence i think
@@brettlinthicum9885 why would you assume that?
This is heartbreaking 💔 😢
So sorry to watch and listen to this testimonies, hope medicine will find a cure and my best wishes to the families keep fighting
It can be genetic and the main cause of it if not inherited is a mutation on a gene. So I think it’s highly u likely there will ever be a cure
Thoughts Love and Payers for Bruce and his family ❤
My mother showed no sign of traditional dementia but living alone we noticed that there were reminder post it notes all over the house. Brain disease is the worst. Frustrating and painful to both patient and family. This country needs national health!
Absolutely heartbreaking 💔
I feel you. My daughter is only 31 years old and has alzheimer's and seizures frontal lobe. It's a very hard road, but we all can do it. God doesn't give us things we can't handle. Bless you all 🙏
@Adam-qf8ps Yes. That is exactly what my daughter said. Hang in there. Don't let this bring your spirit down.
I had Brain Cancer, Surgery & Radiation & believe me, it has been a ruff road so in some ways I can relate. I am the only one that is still alive (BCancer) & I'm in an old people's home... I'm 57
🙏 I lost two friends to brain cancer...😔
I am sorry you went through all this. I hope recovery is possible and you can find joy and peace again.
Well I should of said I'm the only one who lived in the North West. I was in Alaska & had surgery in Seattle. I can't say for Dever.
I'm ok but life gets harder every time the year starts to change: Spring ~ Summer ~ Fall ~ Winter. That's what GOD does for me, what would I do without HIM... Amen!
@@xiqueira
I wanted to tell you personally, Thank ~ You.
My surgery was in 2005 & I was in Alaska, I moved back to Wyoming in 2018 were most of my family is & that's all good cus I come from a huge family. God bless you!
Why are you in an old people home? :(
This is a sad story! I wish there was a way that this disease FTD could be detected.
Thank you for this great invaluable information!
It can be detected. Neuropsych eval then spinal tap and PET scan
Blessings and Prayers for Our Actor BRUCE WILLIS and his family! WE LOVE OUR ICONIC ACTOR BRUCE WILLIS!
FTD is so harrowing. I think probably most individuals would rate this as something they definitely do not want.
Well she’s talking pretty well compared to my girlfriend who has it. Who has FTD. Now she can’t speak. She can’t walk. And she lost interest in everything, except food. Mostly sweets Coke, And french fries etc. so I really hope and pray she doesn’t end up like my girlfriend who was so independent and could dance great. It was very intelligent. That’s all gone. But I still go see her. And be with her. And tell her I love her and hold her hand.❤️
I am very glad that lady stayed with her husband she didn't break up with him my mom would have broke up with him just like after I got diagnosed with epilepsy/seizures she put me in foster care and my dad wouldn't allow that so she broke up with him and he raised me since I was 6years old and diagnosed with epilepsy/seizures
Sorry to say this but your mom is a c*nt
I can't believe that it is $7,000 a month. Coming from a speechless Australian. I just prayer that the pain has eased some. Much love and prayers to all of them.
Yes welcome to our crappy healthcare system here in the states. My mother was recently diagnosed with bvFTD and it will be expensive to find care for her.
The USA is terrible
I am a nurse assistant at a memory care facility in the states, average cost is around $30,000 a month. I make a little over minimum wage but I don't feel as sorry for myself as I do for the families that have to endure these costs.
Really sad Bruce Willis will have to get through this, I hope somehow he gets well and healthy again.
Sorry man. This is a terminally illness. Once diagnosed there is no going back.
There is no coming back from this, their. Brain is mush…..dead before dying
He won’t sadly.
I wish people would be honest with the reality of some medical conditions.
It seems like most don't pay
attention to the seriousness if the condition isn't visible.
he won't
Unbelievably sad for the families and the people with FTD😢😢
Prayers to all who suffer.
Bruce Willis has just been diagnosed with this illness, his family said. How very sad😔 . This is a terrible affliction for everyone involved.
He was not “just diagnosed” theses symptoms have n\been going on for decades, they just told the world, b/c he could no longer fake acting. He had been fed his lines thru n earpiece for years.
@@Elena-rt9yu Tomatoes, tomaaatoes. It’s the first time the public heard about it. Thanks for your valuable contribution.
After coming to my mom's to relocate her husband to a care home I realized mom couldn't function alone. I moved to center Georgia several hours from home over 14 months ago.
I know it's some form of dementia. We have spoken to our doctor about testing to define the type only to realize.....what for? She takes a "memory pill" but who knows if it's of benefit. The doctors and pharmacist agree that no matter the type, no real treatment plan.
We got busy, walking two miles per morning. I took over cooking, paying bills, making appointments etc. Back in February covid pneumonia set her back. Well the lord spared her, we started our exercise regime but now 1 1/2 miles is a struggle. Mom's 78 and I commend her effort and exertion seems to help fight the dementia back.
Even though I don't feel productive and am penniless, this has been such the blessing, caring for the sweet girl. Some days the blessing is hard to see thru my tears but they do exist.
I may not be able to provide care once she slips further away and unable use the restroom alone? I worry that my never quit, marine corps ethos may keep me seeking better care later on. I guess I would be forced to sign over her home and car to the government in exchange for the care. It's a shame how the dollar keeps entering into the conversation. This disease that's killing her has laid waste to my personal future but I realize I would have had no chance at a future without her raising me. The Lord hasn't brought us this far to put us down and forget our needs.
Please keep us in you're prayers.
She loves and appreciates me greatly, but I feel like the old man son, interested on the SSI check arrival. My Ambition is gone.
Hi Steve, you need to seek legal advice on what to do so that your Mom's assets aren't taken for future care. There are ways around that, and so paying for a good estate attorney would be worth your while and money. Please do this ASAP
My wife’s had it since 2014 and is in the final stage. It devastates families.
I'm here after learning of Bruce Willis's diagnosis hoping to learn more
If you can get medical assistance to end your life if you have a terminal disease, why can't you get help to end your life if you have dementia? It's absolutely crazy! I guess they need as many people as possible so they can do their research?? I am 72, I would end my life as soon as I got diagnosed with it! I can't imagine living like that and putting my family through the expense of taking care of me. It would be a living nightmare for everyone concerned. My heart goes out to anyone who has to endure this.
FTD and dementia are diseases that diminish people's capacity to realise that they have changed. Assisted death might be a blessing to those unable to pull the plug themselves or unable to recognise the degree of their decline. Many people with dementia retain a distinct personality and are often present or shift in and out of being lucid and adrift or lost. The carers no doubt suffer more witnessing the decline and coping with the changes. Assisted living helps and sometimes a neutral person with training or experience dealing with dementia is better able to cope with defiant, puzzling, inappropriate, potentially dangerous, irrational and demanding behaviour. If only all people had ongoing contact with elderly and sick people instead of locking them away then the community would be more aware of differences and diverse needs and changes that often occur with age and illness. We sanitise and avoid illness, old age and death like Victorians sanitised sex in the nineteenth century yet accepted and laid dead bodies out for viewing in their homes and took photos of deceased children sitting with the living.
Do they know why all of a sudden we re seeing this??? The speech part is aphasia. It's out of the blue, to me? This new diagnosed disease.
Thank you. I’d do the same. I just turned 76. Probably won’t get FTD but may someday get Alzheimer’s, especially if I live to 85 or so. Robin Williams killed himself after he was dx with Lewy Body Dementia. I wouldn’t want to become a shell of myself.
My mother was diagnosed last year. It is sad that she is like a different person now, but she is still happy and knows Christ. I am thankful for that.
So sad about the father with the young family. And his wife.
With learning of this due to Bruce Willis, I wonder how many more will be diagnosed since we’re all getting educated, so sad for Bruce and family .
Wow, I felt so sad about her.
I'm going through the same thing. It's been difficult to get a diagnosis for my husband. His entire personality changed so much it's horrible. He lost so many jobs and has not worked for 3 yrs.
I hear you. My hubs has bvFTD too, and i suspect ALS. Hang in there. Mine is on the 4th (last?) month in assisted living on respite. It will be hard to keep him there because of the cost, and also, they rejected his application to stay long-term because of his diagnosis and my iffy financial position. I'm hoping to have a meeting with them soon and successfully beg them to keep him.
It's so hard because socializing calls their brains to order, and they can function normally for an hour or two. Even close family, doctors and physical therapists often don't believe there's anything wrong. Then they sleep all day, can't function in a job, won't shower for weeks, are generally irrational, and exhibit a host of other weird behaviors, but don't recognize that anything is wrong with themselves.
@@pesterlig I did some research and feel that I may have found the correct diagnosis for my husband's issues. These doctors are NOT interested in helping anyone - everything has been CV19. I'm fed up with all of this insanity. If my husband's Neurologist doesn't help I may have to sue our Hospital System for Malpractice - that's how angry I am at this point.
My husband is the exact same as Mark .. didn't think there was anything wrong with him abd didn't care.
My wife was diagnosed in 2014. Now ten years later her bowels don’t function, her speech is very rarely understandable. She aspirates foot particles and struggles to swallow. She craves chocolate and cakes and only eats decent food rarely. Now she sleeps for 16 to 18 hours per day. Her issues are multiplied by the fact that she has had MS since 1990 and has been chair or bed bound for the last 15 years. I hoisted her to bed at 18:00 yesterday and she is still asleep at 10:15 the day after. It’s an absolutely horrendous illness and I feel for everyone that has any involvement with this disease.
Young mother Amy Johnson of Windom Minnesota needs help as she shoulders a $7000.00 a month bill for her disabled by frontal lobe dementia 40 yr old husband's facility bill; this is financially impossible for her to sustain for 5 more years and also have to work constantly to provide for her life alone w her small children. Please help her and her four very young boys.
My Mom died 11 years ago from frontotemperal lobe dementia. She was 63 at death and 50 at diagnosis. She had aphasia and getting her to talk more than 2 words was hard.
Just lost someone to this. She was not herself in the end. She was completely out of it. She had to be under 24-7 care and it ran the entire family down with stressing about who was coming and sitting with Granny. We tried to keep her out of the nursing home until it wasn't possible. She was falling and gets injured. She was alsocdoqbetic and she would hit people who tried to help or check her insulin levels. She was an amazing person who loves Jesus and did what was right for anyone she came across. She didn't care about things or money. She loved her family and cooking for them. Once she had to go into a nursing home they placed her into a lockdown unit and medicated her so all she would do is sleep and wake up be mean to everyone. She would use the bathroom on herself then spread that all over her room herself and other patients rooms in the unit she couod get to. She constantly teied to escape and she alsp stole other patients belongings. It broke me having to watch this unfold and i would not wish it on my worst enemy.
My mother-in-law just passed at 82 from this. She lived with us for 5 years and we took care of her full time. She went from walking talking to completely bedridden non verbal and pretty much just there in body but her mind was gone. My heart goes out to other families who are going through this.
Who is here because of the Bruce ?
Poor Wendy 😢
Thank you for sharing your story.
$7,000 a month!! That poor woman...
Haha really a little selfish haha better check for ftd haha
It’s sad it’s like having amnesia all your memories are erased.you don’t even no what makes you happy anymore
You are not wrong
I took care of a patient that showed these symptoms and behavior. His daughter , her husband keep her at home but it was so difficult a lot of times. She died on 2015 .
This is devastating.
I would live to connect my sister in law with this young lady since she is going through this as well. It's so hard for our family.
I feel so bad for that lady it has to be devastating to have your best friend who u love not recognize u any more
As a 40 year childhood brain cancer survivor, I definitely feel like this regularly. Memory, mental and physical state have all continued to dateriate. I believe it does stem from 6 brain surgeries, 1 brain tumor relapse, 7 brain ablations and refractory epilepsy. The medication for the seizures make it worse too. All I can say is make each day count now for what it is. Ive been doing my bucket list with family and friends. I'm not going to let another diagnosis hold me back.
Heart breaking for Amy’s story 💔
I am here to support Carol and learn more of this horrible disease.
My poor Father. He too had RTD. He was an executive for a petroleum company, huge in scope. He wasn’t fired. He was allowed a very tranquil retirement. Thank you Colonel Pipe Line.
I'm shook. This is heartbreaking.
God bless and be with you sweetie.
I really hope people find a cure or a way to stop dementia
In Jesus Name Amen! ✝️🙏
it’s crazy how quickly this onsets. imagine… one day, you wake up and you’re suddenly gone. physically present but mentally poofed out of existence; a shell of your former self.
Prayers up to Bruce Willis and his family
this is so scary and sad
I lost my mother to Alzheimers decades ago. As I understand it, Alzheimers is also always fatal. Mom's progression took a bit over five years. Some of her symptoms resemble those of Mark Johnson (as covered here). For anyone who has had someone special progressively lose their memory and basic mental capacities over the course of years, they will know why the experience is sometimes called 'the long goodbye'. You continue to meet with, and speak to them for years. But in truth, they had 'checked out' long before the final 'GoodBye'.
I pray to god/Allah/Buddha..et that we find a cure for this and cancer soon. This was so heartbreaking to watch
As wonderful as life is we all have our crosses to carry...this is a tough one
extremely painful
You Cannot Challenge Them, You Just Have To Love Them Through...Remembering The Person The Whom They Really Are...LOVE MADE A COMPLETE CIRCLE FOR ME & MY AL, HE LOVED ME @ MY LOWEST & I SURE LOVED HIM @ HIS...HE NEVER WENT INTO A FACILITY...I LOVED HIM THOUGH IT ALL & I WOULD DO IT ALL AGAIN...AMEN❤️
@Anonymous What’s Thumbnail?
Tell me more about challenging them? What do you mean
We received the diagnosis that my mother had FTD after we took her to the emergency room for what we thought was a mental health crisis. The doctor told us it was the worst case he had ever seen. We thought she was suffering from severe anxiety and depression. She ended up dying a few days after we were given the news. Her health was failing and we had to make the decision to continue care or choose comfort care instead. Seeing this, I am glad we made the decision that we did. At least she was spared further suffering. The scary part is that there can be a genetic component to this. I don't worry about myself, but I would hate to think that my family might have to deal with this one day.
Yes, we finally have the diagnosis of FTD for my mother-in-law. We have relocated to England (2020) to care for her (she also has cancer) and my father-in-law who has been diagnosed with "Parkinson's disease with dementia". The psychiatrist told my husband that he may want to pursue genetic testing in the next few years.
What is the difference between comfort care and "continuing care"? Just wondering.
In my mother's case, she was in the end stage of life and they removed all other care except pain management. She died within a couple of hours once they removed the oxygen and other medicines that were maintaining her blood pressure@@CraftingChristian
@@hm5978 Im sorry to hear. That is so strange to me that they would remove care like that, but it's good to know.
@@CraftingChristian My mother also had end stage COPD. Honestly she probably only had a few months to live (if we continued treatment) but she would have suffered the entire time with all the problems she had. She had fallen and broken her back, terrible anxiety from both the dementia and the difficulty breathing. She had been on oxygen for years. She wasn't allowed to go home with us, we were frantically looking for a nursing home that would take her because they would only release her to a facility. That was her worst nightmare. It was our choice whether or not to continue care or basically let her die. It seemed the kindest thing to do to let her go. But it was devastating.
I do not ever want to experience the worst of dementia, it runs in my family and I. hate the idea of forgetting so much and being scared, terrifying