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What is Frontotemporal Dementia? 

Dementia Careblazers
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Bruce Willis was recently diagnosed with Frontotemporal dementia. In this video I share how FTD differs from Alzheimer's disease and common symptoms of frontotemporal dementia.
Here at Dementia Careblazers It’s our mission to make dementia caregiving easier for families caring for a loved one with Alzheimer's disease, frontotemporal dementia, lewy body dementia, vascular dementia, or any other type of dementia. We do so by making free educational training videos like this so that anyone with an internet connection can access this information.
FREE Resource:
📺 Get Access to A FREE Dementia Caregiver Training on How to Care For a Loved One With Dementia- WITHOUT The Overwhelm, Dread, and Confusion: ➡︎ www.dementiacareclass.com/yt
RU-vid Playlists To Learn More:
Managing Stress and Burnout: • DEMENTIA SELF-CARE AND...
Dealing with Challenging Behaviors:
• DIFFICULT DEMENTIA BEH...
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In case you haven’t met me, my name is Natali Edmonds and I am a board certified geropsychologist. That means that I am a clinical psychologist who specializes in working with older adults. One day, while hiking a trail, I came up with the idea for Careblazers and I decided to see if posting videos online could provide help to the many other Careblazers in the world who don’t get to have help come directly to them in their homes. I hope that this work helps you in some way on your caregiving journey.
#alzheimer #dementia #caregiver

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26 июн 2024

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Комментарии : 166   
@mermaid2997
@mermaid2997 Год назад
My dad has FTD and his speech has almost become completely unrecognizable... It's been hard watching a man who once loved talking with everyone, become withdrawn and depressed because he now feels that he can not converse with people. I take extra time and let him just talk away - I see the joy it brings him in his eyes... every minute spent is precious, and i treasure it all ❤❤❤
@sherylcurry2000
@sherylcurry2000 4 месяца назад
I'm so sorry. I'm hustling now having symptoms or slurring and lazy tongue. Praying for all who are victims of this horrific ignored disease
@mermaid2997
@mermaid2997 4 месяца назад
@@sherylcurry2000 my heart goes out to you 🙏 praying they find a cure for these awful diseases.
@patriciacole8773
@patriciacole8773 4 месяца назад
God bless you!
@madeleinefraley8916
@madeleinefraley8916 Год назад
My husband was diagnosed with behavior variant FTD. During his illness I kept a journal documenting our challenges and joys over five years. That has been turned into a book, a memoir of our journey during that time. Our story is unique just as your story is one-of-a-kind. Share your story so others can learn and understand.
@DementiaCareblazers
@DementiaCareblazers Год назад
Thank you for sharing. 💖
@thomism1016
@thomism1016 Год назад
@sreneethomas
@sreneethomas Год назад
My mother passed away in 2021, she was diagnosed with bvFTD only one year before. Although she had symptoms for 5 years and was being treated for anxiety and doctors assumed it was an onset of Alzheimer’s. She was physically fit when symptoms started and 5 years later was wheelchair bound, unable speak and then passed away. I had never heard of bvFTD before this, and after researching it saw that many of her symptoms were clear for FTD almost immediately after she started showing symptoms. Unbelievable that doctors didn’t diagnose it for four years.
@sherylcurry2000
@sherylcurry2000 4 месяца назад
I used to excel creative writing in writing, but I find since my diagnosis it's hard to pick up a pen and actually write. I still think I'm going through the process of acceptance. What is the title of your book and can it be ordered on Amazon?
@sherylcurry2000
@sherylcurry2000 4 месяца назад
@@sreneethomas unfortunately, that's still the case. My primary doctor here since I moved out of my circumstances and couldn't work anymore had to move from Alaska Oregon. I've been seeing my primary for over a year and they are still in denial even though I've been diagnosed with three pet scans and an MRI from 2012 I'm so sorry that you went through this I'm trying to get the word out Bruce Willis has helped a little but we still have a long ways to go.
@rebeccaillingworth5015
@rebeccaillingworth5015 5 месяцев назад
Hi thanks for sharing this video. My brother is 58 and an alcoholic. He has recently been diagnosed with FLD due to having seizures, car accidents and falls. I live in MD and he in Maine, he and his wife have had a toxic relationship for several years as she also is an alcoholic. I don't know how to help him but worried about him all the time. He recently lost his job, he has worked for this company for 38 years. I feel so helpless!!
@sreneethomas
@sreneethomas Год назад
My mother passed away in 2021, she was diagnosed with bvFTD only one year before. Although she had symptoms for 5 years and was being treated for anxiety and doctors assumed it was an onset of Alzheimer’s. She was physically fit when symptoms started and 5 years later was wheelchair bound, unable speak and then passed away. I had never heard of bvFTD before this, and after researching it saw that many of her symptoms were clear for FTD almost immediately after she started showing symptoms. Unbelievable that doctors didn’t diagnose it for four years.
@carolbenson6524
@carolbenson6524 Год назад
I'm glad you are reviewing this. When I worked for a homecare company several years ago I had an 82 year old female patient that was diagnosed with this. She didn't speak much...did strange things when alone... however, when I involved her in a task or activity she listened and followed just as if she was normal. She did eventually go to a memory care facility and passed away two years ago. I miss her so much. She was a treasure!
@steviem5279
@steviem5279 Год назад
My dad passed away last summer after suffering from the behavioral variant FTD, he was older when he was diagnosed but he probably had it longer but we probably missed a lot of signs over the years. When the symptoms really started getting bad that's when my dad's doctor ordered an MRI and we learned that the frontal part of his brain was shrinking and in atrophy. For my dad, from diagnosis to death it took less than two years, a year and nine and a half months to be exact. As another poster mentioned I wrote a journal of everything he went through and it was challenging for sure as my mother and I were his caregivers the entire time. If there was one blessing it was that he never lost his memory of who my mom and I were so that was a good thing. I could write a book here on what we went through with this disease but almost seven months since his passing, I wish I could take care of him for just one more day.
@DementiaCareblazers
@DementiaCareblazers Год назад
Sending you so much love. 💖
@maureenbarton9606
@maureenbarton9606 Год назад
I love your last comment so very much. I will put in front and centre for my dearest sister. I've been documenting her journey too. Sorry for the loss of your dearest father
@carolbenson6524
@carolbenson6524 Год назад
I understand. I wish I could tell everyone that no matter how bad the patient gets .they are STILL HERE on the earth!
@steviem5279
@steviem5279 Год назад
@@maureenbarton9606 thank you for the kind words. The best thing to say is take things day by day, there will be some good days and some bad days but after they are gone, you will appreciate each day you had with them.
@DChase-ie4dd
@DChase-ie4dd 11 месяцев назад
I'm watching my mother endure this horrid condition and would not want her to suffer one more day more than her body, and God allows her to.
@jeanettestoffregen2874
@jeanettestoffregen2874 Год назад
My husband will be 80 this July. He began to act “different” 10 years ago. He has severe tinnitus and gets angry if I talk too loud or too soft. Three years ago we went to a neurologist and after brain MRI was diagnosed with age related dementia. Then last year doctor wanted to do another brain test (I don’t remember what it was called). My husband refused and has refused to go back to doctor. After listening to this I believe he definitively has FTD. It is impossible to have a conversation with him because he cannot say what he means. He doesn’t remember any friend that he does not see on a regular basis and names mean nothing to him. He moves slow and has no conception of time. He still insists on driving and thinks he has to take me everywhere. He drives OK, but i am concerned about his ability to make necessary decisions. He is very sweet, but also very dependent on me. I don’t trust him anymore and I am at a loss to know what to do.
@niwawang4394
@niwawang4394 10 месяцев назад
My husband was diagnosed 2 years ago. He hit the freeway wall while driving and sleeping, he refused to stop driving. My rib was broken, head injury...
@sherylcurry2000
@sherylcurry2000 Год назад
I was diagnosed with bvFTD in July 2022. Lost the ability to work and drive in one hour. I'm 62 and it took a long time to accept what happened to me. I've worked since I was eight years old. Once I got through the panic attacks, tremors, and dark depression, I'm finally adjusting;however, it's devastating to me that there is no cure or treatment for FTD. 😢
@kathyrickard9442
@kathyrickard9442 Год назад
I'm sorry that you are having to go through this. So challenging. I think my friend may have this...Can I ask are hand tremors a symptom?
@sherylcurry2000
@sherylcurry2000 Год назад
@@kathyrickard9442 yes, they can be. They have calmed down so I think it was exasperated by the stress of my diagnosis; however, my neurologist says that they can come back for sure. It's just so much to do it all at once in my whole identity, unfortunately was my career and losing that was hard to handle now I'm just learning to live in the moment and take it one day at a time one moment at a time, and hope for the best.
@laraeire
@laraeire 8 месяцев назад
@@sherylcurry2000hi! How are you doing nowadays? Do you have any help? How did you find out? My father-in-law has it too, he lives with us now… Best wishes, take care!
@lalail61
@lalail61 4 месяца назад
Check out Dr. Joe Dispenza's method. It may help.
@sherylcurry2000
@sherylcurry2000 4 месяца назад
@@kathyrickard9442 yes, they are
@Andrea-ue2uw
@Andrea-ue2uw Год назад
This sounds like a horrible form to have feel bad for Bruce Willis such a strong man and he gets this😢
@peggymonroe2728
@peggymonroe2728 Год назад
My husband was diagnosed with FTD 12 years ago. He is now 64 years old. It has been a long journey with different types of difficulty in each stage. It is a horrible disease.
@nathaliewalker7468
@nathaliewalker7468 6 месяцев назад
Glad to hear that he's still around after 12 yrs. Thx for the info to help patients out there. My hubby just diagnosed from FTD.
@lucilacarbone7718
@lucilacarbone7718 Год назад
Grandma developed dementia from korsakof syndrome Then it got to front temp and now it seems it woke alzheimer up as well. THANK YOU so much for being there for us caregivers, we really find help in listening to all you know and share
@rajkagolub8667
@rajkagolub8667 Год назад
Thanks for all the support and explanation regarding FTD. My husband is diagnosed a few years ago but now he doesn't want to go to the doctor to see the current situation. Everything started with maybe before our first visit to the neurologist , because he suffers from bipolar depression so changing of behaviour didn't alarmed me. When he started to have speech problems and consequently memory problems we started our journey to find out what is the diagnose. For the time being it's developing slowly and he can still go out alone, or drive a car in my presence, but he needs that someone is always present. I'm the only caregiver and it's tough but thanks to Dr. Natalie's advice I have less stress. Thanks once again
@DementiaCareblazers
@DementiaCareblazers Год назад
Sending you and your husband so much love.
@rajkagolub8667
@rajkagolub8667 Год назад
@@DementiaCareblazers ❤️
@manunited1132
@manunited1132 Год назад
Peace and love to everyone out there. Especially anyone going through this. Its very sad news about Bruce Willis such a talented man. Some of the best Action movies with Bruce in them
@francoforleo4971
@francoforleo4971 Год назад
After two years of caregiving, I’m finally getting to understand the type of dementia my partner has… this is something I find which doesn’t get explained by neurologists. Thank you for your guidance 🙏
@gailgreif4417
@gailgreif4417 11 месяцев назад
Thank you for this video. My mother has this terrible disease. It’s been difficult.
@wendycastagna8901
@wendycastagna8901 Год назад
My mom was diagnosed with this recently she is 77 she has been misdiagnosed for years with brain conversion disorder she has trouble with her legs and walking the last 3 months she had progressed to the full stage dementia. This has torn my family up and not much support here in Canada
@MarchBDRES
@MarchBDRES Год назад
Hello all; If I can offer any words of support to those caregivers it is this: DO NOT FORGET To TAKE CARE YOU! It is difficult to say I NEED TIME ALONE, but you must. I have had two aunts, one uncle, a friend, and two wife's that have succumbed to various form of dementias. I am 72 years old, and I Am tired all the time. There is no other family (on either side) or friends left. Yes, I DO take time away, (pay to have her watched) just not enough, a few of hours here, as much as six hours there. I know that one day (coming soon) Rosa (wife#4) will have to go to memory care, still very hard to let go BUT let go I must. Take care of yourself, because it you don't, there will be no one left who will. Time does not wait!
@DementiaCareblazers
@DementiaCareblazers Год назад
Wise words! 💖
@debby891
@debby891 Год назад
Easier said than done but so true
@olivetteheslop8798
@olivetteheslop8798 Год назад
Dementia is the most confusing and difficult thing to deal with Caring for love one, twenty four seven on your own.
@carolray9156
@carolray9156 Год назад
There are agencies that will help you. My friends husband has some kind of dementia he has home care 7 days a week also they come to her house pick him up and take him on outings for the entire day. It's a great help to her and he seems to love it and looks forward to it. She goes through a mental health hospital and they have a great reputation . I'm from RI so this hospital is called Butler hospital which is affiliated with Brown University. You should look into something like that in your state. And call Blue Cross Medicare and nag people and get the help you need Good luck
@maryrowe3981
@maryrowe3981 Год назад
thank you. I'm 69 and trying to recover from bacterial sepsis which crossed the blood-brain barrier; none of my other organs besides my skin were affected. With a maternal family history of dementia, I am wary of brain and behavioral issues and want to identify them as soon as possible.!
@DementiaCareblazers
@DementiaCareblazers Год назад
Sending you love and so wishing you an ongoing recovery! 💖
@raresmihaioglavie4704
@raresmihaioglavie4704 10 месяцев назад
My testimonity:i suffred from fronto temporal dementia at 15 yr old(idk how) and by the energy(grace) of the Heavenly Father i was HEALED❤❤❤❤❤❤❤❤❤❤❤❤
@corneswanepoel4890
@corneswanepoel4890 3 месяца назад
Good for you! Blessings. How did you heal?
@debludwig6302
@debludwig6302 Год назад
Thank you for all you do! Your advice and the information you provide on dementia is so helpful for those of is with a loved one suffering from dementia. God Bless You!!
@DementiaCareblazers
@DementiaCareblazers Год назад
Thank you for your kind words.
@jeannemccloskey9416
@jeannemccloskey9416 Год назад
Thank you Dr. Natalie!! So clear...
@zoeiiseda246
@zoeiiseda246 Год назад
Thanks for this timely info.
@airportnurse3380
@airportnurse3380 Год назад
Helpful overview. Thank you!
@patleo123
@patleo123 Год назад
Wow! You explained super clearly doctor ! 👍👍👍
@organicintelligence3137
@organicintelligence3137 Год назад
Thank You🙏🏻
@pandemicnova
@pandemicnova Год назад
Thank you for this
@denieseklinethatcher2715
@denieseklinethatcher2715 Год назад
Excellent Thank you hoping to see Teepa Snow & all who work in the dementia field including the Vascular dementia field so many doctors, nurses, rehab providers, mental health workers are clueless about these different types of dementia’s please pass the truth & tell & share!!!
@sandym4494
@sandym4494 Год назад
The symptoms with FTD also mimic Parkinsonism/Parkinson’s & Lewy Body Dementia. My spouse was diagnosed with bvFTD but dr. Changed the diagnosis. Now it’s Parkinson’s but I believe it’s Lewy Body Dementia. Hard to distinguish differences in the dementias. Thanks, Dr. Natali!
@whitneysawyer483
@whitneysawyer483 6 месяцев назад
Very helpful, thank-you for this information :)
@beverlyrosenthal7024
@beverlyrosenthal7024 Год назад
Thank you Dr. Natali. My husband was diagnosed with Alzheimer's. But he has the many of same symptoms as FTD...with the exception of behavior/personality (bvFTD). We have an upcoming call with a neurologist. I'll ask her about FTD.
@mrshypno1
@mrshypno1 11 месяцев назад
You can have both my mother in law has just been diagnosed with both they said the Fdt is the one that she will die from also has stage 4 cancer we think the last chemo round is what started it off,I just hope she doesn’t suffer for too long she’s having to have 24 hr care and this is so hard as was so independent and still tries to be and now a risk as neighbour s have caught her on camera at 4 am just wondering around.
@mickcarmody1490
@mickcarmody1490 Год назад
I was diagnosed with FTD in 2013 and I can still function pretty normally up to noww but that is another story for another time. I was wondering if it is possible to obtain a copy of your video in text as I have real trouble explaining to the naysayers exactly FTD is and most descriptions of FTD are very clinical and hard to follow. Yow explain every aspect of this insipid disease in very clear, concise and easy to understand English. Just as an instance this small paragraph took me over an hour to type.
@RonaldReagan7777
@RonaldReagan7777 Год назад
Thanks
@ednasheffield4606
@ednasheffield4606 Год назад
Thank you Dr. Natali for explaining FTD dementia. How does it differ from vascular dementia?
@louiselincoln
@louiselincoln Год назад
Thank you for this! Would you be happy to cover hepatic encepalothapy in relation to the similarities to dementia at some point? No worries either way - just sending a massive thank you for all you do.
@DementiaCareblazers
@DementiaCareblazers Год назад
Absolutely! Will add it to the future video list :)
@SandraGonzalez-ve9qt
@SandraGonzalez-ve9qt Год назад
I really have been enjoying your videos and they have been very educational. I would love to learn more about Lewy Body dementia. My father has been diagnosed with this along with Parkinson’s.
@DementiaCareblazers
@DementiaCareblazers Год назад
Here is an older video on LBD that you may find helpful. ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-jhgKhiWB8_8.html
@SandraGonzalez-ve9qt
@SandraGonzalez-ve9qt Год назад
@@DementiaCareblazers Thanks!
@denisemidkiff6448
@denisemidkiff6448 Год назад
My husband has this diagnosis also. LBD and Parkinson’s. We take one day at a time and it seems to be a slow progression but he’s now in an advance stage and in a dementia community. His caregivers are ‘angels on earth’ as well as my daily caregiving. Our faith, family and friend support and love give me the strength and courage needed for his/our journey! ❤
@hondafreedom9329
@hondafreedom9329 Год назад
Can you talk about the moca test and the mini mental? My person got 16/30 on the moca and 23/30 on the other. However, they are not putting her into memory care but with a more social aspect of assisted living. I have noticed decline the last 2 years but this person is also "there," able to function albeit with help in areas. I have been the sole caregiver for 3 years; it is A LOT. I do everything.
@giakamar
@giakamar 9 месяцев назад
My father passed away recently at the age of 73. He was diagnosed with FTD and Alzheimer. His father had Alzheimer as well, and iwas wondering if there is a DNA test that i can do to see if there is heredity in me and my sister. i wish we had tested my Father but everything escaletd really quickly the last 3 years that a DNA test never crossed my mind. It was an honour to care for him till the very end, i really miss him. He was so strong. Dementia is very cruel.
@maryamsalah4723
@maryamsalah4723 Год назад
My dad just diagnosed with FTD after years of uncertainty about what could his symptoms due to. I'm terrified
@avtarchand499
@avtarchand499 Год назад
I Hate FTD... I Lost my Dad to this bad disease. All started in 2015.
@susanoshaughnessy7019
@susanoshaughnessy7019 Год назад
Dr Natalie, Could you please create some videos on Lewy Body Dementia?
@DementiaCareblazers
@DementiaCareblazers Год назад
Here is an older video on LBD you may find helpful: ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-jhgKhiWB8_8.html
@anthonyqcolosimo5374
@anthonyqcolosimo5374 10 месяцев назад
My bf was just diagnosed with FTD last week. He is only 46 years old.😢 any help on what to do is greatly appreciated
@in_vino_veritas7938
@in_vino_veritas7938 10 месяцев назад
I'd like to know more about lethologica and lethonomia, please
@JennySimon206
@JennySimon206 8 месяцев назад
Mental disorders are early onset dementia. Even in the 1900's they noticed everyone in the asylum had "bumps on their necks". Hmm.. Not an acne zone. Funny, I have those weird bumps too on my scalp, neck and jawline. Not acne. Those are nerve pathways and nerve endings. Personality disorders are not treatable. My ex has Borderline personality disorder but it's turned into dementia. Why? I believe it is one and the same thing. It's a brain infection. New study out. 'Dense core plaques of Alzheimer's disease are granulomas'. It's an internal scar. A biofilm. Protection. Not the problem. The problem is more than likely a brain infection. Herpesviruses most common because herpes is so common. They find herpes DNA inside those plaques. They cover it up. Cash cow. Look into the Amyloid plaque research conspiracy. There's no way all those researchers using that research to build their own, didn't notice the fraud. It is too obvious. So obvious an 18 yr old college student noticed at a glance. People with BPD, put them in an MRI machine, watch their hippocampus turn off when recalling memory under stress, which is all the time. Bet every one of your dementia patients has a herpesvirus or Lyme or some neurotropic infection.
@dessaarnold7540
@dessaarnold7540 7 месяцев назад
Yes I interesting
@robertar.5189
@robertar.5189 Год назад
Hi. What about dementia on a mixed base (vascular and degenerative)? Thank you 🤗
@robinroberts1616
@robinroberts1616 Год назад
I’m 53 diagnosed with FTD.
@rhondasingley7211
@rhondasingley7211 4 месяца назад
Thanks Dr. Natalie I was told I have Ftld Too and I'm just beginning to see some changes in myself 😕 and my family is taking good care of me and I pray this won't be Too hard on them.
@AndyInTheUK
@AndyInTheUK Год назад
Pretty sure my wife has non-fluent variant FTD. The official diagnosis is Alzheimer's but something isn't quite right about that. The striking symptoms are her real struggle to speak, and to understand even relatively simple sentences. Her memory is not great but her mother had pretty classic Alzheimer's so I know what that is like, and that is not what my wife has. Here is a strange thing - even when she is struggling to say something and I correctly guess what she is trying to say, after I prompt her with the correct word, she STILL can't put it into the sentence. "Have you got the ... the ... the ... the ...." (Front door key? Or back door key?) "Yes" (Front door key?) ... silence .... (Which key do you want?) "The the the ...." (front door key?) "Yes, the ... the .. key." (OK the front door key is in the top drawer in the kitchen.) .... blank stare .... "Where?" (In the kitchen drawer.) ... no response .... (Go to the kitchen, then I'll tell you then next bit.) ... confused. It is so tough on carers. We don't get a minute's rest. I don't want to just sit her down and do everything for her (and me!) but it takes three times as long to do anything if she helps and I end up exhausted, physically, mentally, and emotionally.
@Auggies1956
@Auggies1956 Год назад
I suspected I had brain function issues for a couple of years. Six months ago after many tests a neurologist said there was nothing wrong, but she thinks I was in pre dementia. Now today, my speech has been affected, making choices and planing things are getting harder. For a couple of years my walking gate has been affected. My fine motor skills with my hands is difficult. Reading an understanding what I read is harder. Plus I have ringing in my ears for over thirty years, which I understand is damaging to the brain.
@lindaanderson1016
@lindaanderson1016 Год назад
I am sorry. You wrote very clearly. Please read , or listen to the Gospel of John....We can know we have eternal Life.
@kg5521
@kg5521 5 месяцев назад
am@@lindaanderson1016 amen to that ! I think I may have this disease. I've had a lot of language issues. Mixing up words. My psychiatrist says it's my anxiety , but I think she's wrong. The language issues stated May 2020 . It's not getting worse but it's not getting any better either.
@vgomez509
@vgomez509 Год назад
What is the most important diagnostic tools to determine weather someone has FTD? Does it always show up on brain scans if it is early in the disease? Also, can cognitive testing fluctuate early on in the disease or will it just be progressively worse? Do you do consults?
@user-mk2eq6rv3o
@user-mk2eq6rv3o Год назад
My wife was diagnosed with FTD in 2016. She has had many neurologists over the last seven years, it seems she just keeps getting passed from one to another. I'm her husband and primary caregiver. I can never get a good answer to how far along she is with the disease. Is there a way of telling how far along your loved one is?
@janenebendrick1632
@janenebendrick1632 Год назад
My husband knows his family and friends and people on the news. He has trouble knowing how to put his clothing and diapers on the correct way. Fronts are in the back, coats are upside down, belts started in the wrong loops, shoes in the wrong feet. He gets easily distracted when performing any task, even making himself a sandwich, which could take him hours. Is this vascular dementia? The Doctor said it was not Alzheimer’s but didn’t tell us what type it was. Thank you for your time and expertise!
@susandiggs5733
@susandiggs5733 Год назад
My husband was dx with vascular dementia 3 yrs ago by neurophysiologist…he was spot on with the dx…at least I felt like he was. We saw a neurologist last week, and he is saying it isnt that because he has no vascular symptom such as high cholesterol, high bp, stroke etc. He says it is FTD semantic variant. We have another MRI of the brain and a Pet Scan of the brain March 8. After much research, it sounds like this is very hereditary. My son is very concerned. Any thoughts on the hereditary part?
@ossier2796
@ossier2796 Год назад
My companion was diagnosed with Alzheimer’s Dementia about 3yrs ago he’s 82. His symptoms are paranoia, hallucinations, I have to show him how to eat certain foods, he always wants to know what he’s eating and he has difficulty understanding me. I thought that maybe he has a different type of dementia.
@breverito138
@breverito138 7 месяцев назад
How is their memory affected? My mom has been diagnosed with FTD aphasia primary progressive. I don't know how much she remembers. Does she understand what's going on? Here in Mexico there's no a lot of information or specialists.
@terryvandyke5975
@terryvandyke5975 9 месяцев назад
Can I share this video with my husband who was diagnosed with FTD so he knows what he has? Would that be upsetting to him? Or should I not share this useful video-Terry
@theresagerhart3603
@theresagerhart3603 Год назад
Do you know : Does anomic aphasia get worse going into a more progressive aphasia? And can the person get on and off pressure or pain feeling in temples
@mychoicesvision8847
@mychoicesvision8847 8 месяцев назад
What is ftdp and why is it different? Thanks
@robstimson4234
@robstimson4234 5 месяцев назад
l call FTD 'Alzheimer's on steroids'. Both parents succumbed to Alzheimer's, and my brother succumbed to FTD last March. lf memory serves [no pun intended] David passed away roughly 2 1/2 years after his diagnosis.
@miumama2007
@miumama2007 Год назад
Is there a reason FTD has comparative shorter life span than other dementia?
@roxyp301
@roxyp301 Год назад
Hi do you know of a doctor like you on RU-vid that speaks in Spanish? My mom is 64 and diagnosed with dementia last year although I suspected it for the last three. It’s already at mid stage. She has an atrophied frontal lobe and the doctor doesn’t understand how it happened says maybe it was a previous brain infection. I am only 42 with no family of my own and I still wish it for myself but I feel that she will end up living with me I don’t have anyone to else to help me, and it’s incredibly difficult to take care of her already. I feel she is way too young for this and I worry I might have the same in the future. Please let me know. Thank you
@janicetiernan689
@janicetiernan689 9 месяцев назад
My hubby was diagnosed with AZ eight years a after a brain scan . However I was never told what kind . His personality didn’t change but his speech is almost non existent now .. and the lack of words and using the wrong words were very prevalent from about the beginning. His cognitive side is not good at all he can’t feed himself ,, only a sandwich or finger food… he can shower with my help but toileting is a problem and I feel when he’s tired he doesn’t understand what I’m asking him to do, like stand up , sit down ,when I’m trying to dress him . I’m his sole carer we manage ! My question is does the lack of speech only affect front lobal brain dementia ?
@mollyvollmer608
@mollyvollmer608 Год назад
It would be wonderful to have some insight about what is called “chemo brain.” Also, what the drug tamoxifen does to the brain especially to an elderly person who took it for 5 consecutive years from age 86 to 91 years of age. Thank you.
@amandabarnard2072
@amandabarnard2072 Год назад
My mother recently claimed she has "Chemo brain"...she won't say how or why or even when she had it. Her last radiation was in 2014. I'm not sure exactly what she have been diagnosed and she has been someone who I don't know anymore. I'm going thru a huge court custody case between her and myself too at the same time. She has mislead her Attorney therefore her Attorney withdrew after 2.5 in this on going suit. She is a retired CPs supervisor. I'm an only child. Since she filed this suit against me which I was never served or had the knowledge of she has slander me lied about me like I'm a villain to the court and the new community we just recently moved to which is her hometown. She moved me up to north texas under false pretentious from Houston. She filed an Emergency Order over me. Kick me out and Alligated her self from me and gave my daughter to someone I don't know and hid my child for 4months. Now it's all coming to light trying to start pre-trial in my favor. My mom was my best friend non judgemental all my life. Cool as a fan. Now I don't even know her and don't trust her. I have a clean record and she has nothing but hearsay. She ALWAYS goes back to 20years ago what I didn't di right like that's why now she is the way she is....Chemo brain...what is that and what does it fall into? Close family friends have told me she shows many signs of dementia but I will never get a straight answer out concern for her.
@mollyvollmer608
@mollyvollmer608 Год назад
@@amandabarnard2072 My mother had chemo therapy at the age of 85. Then she was prescribed tamoxifen by her oncologist which she took for 5 years to help prevent the return of her cancer. It is known that tamoxifen causes dementia. So, between the chemo & tamoxifen intake my mother became demented although she could sound as if she knew what she was talking about most of the time none of it was true! So, because myself another sister were closest to her and managed her care when she became ill again at the age of 93+ we were falsely accused by her of many things as were some of her nurses. At one point while she stood accusing me of all kinds of terrible things that would never even occur to me to do I looked at her and said, “I don’t even know who you are anymore.” Matters snowballed and everything became worse so much so that even after her death at age 95 our lives have become hell for the last 4 1/2 years due to some very malicious younger siblings who have done some really terrible things to us including suing us multiple times. The false accusations from our mother began the entire nightmare.
@amandabarnard2072
@amandabarnard2072 Год назад
"I do know you anymore" is the exact term I use all the time in my head towards her.
@DementiaCareblazers
@DementiaCareblazers Год назад
Will add "chemo brain" to the future video list!
@corneswanepoel4890
@corneswanepoel4890 3 месяца назад
Anxiety part of behaviour?
@arnoldgibbs3089
@arnoldgibbs3089 Год назад
Are there ever wrong diagnoses with FTD? When I was in my 50’s I was diagnosed FTD by Dr Murray Grossman at Penn. He was the head of neurology at Penn and also involved with research there. I was in my 50’s when diagnosed. I am now 75 and I am here, not mort like Dr Grossman said to me. I have my own neurologist since I liked to scuba dive which is not the best thing for you neurologically. I am my personal neurologist if he thought it was true . He said one thing. How did I get to his office? I replied, I drove here in my car. He then said that would not be possible if I had FTD. What say you my dear?
@ronniedavis6524
@ronniedavis6524 2 месяца назад
Is Primary Progressive Aphasia (PPA) the same as Frontotemporal Dementia (FTD)? My sister, who is 64 years old, was diagnosed with PPA. She’s never been married or had children.
@michelleomalley698
@michelleomalley698 5 месяцев назад
I am struggling with my husband with Aphasia. He knows its worse. I dont know how to understand him. Advice please? He has VD.
@user-rz7cz2os6z
@user-rz7cz2os6z Год назад
I need help with visits to my loved one in memory care who talks about the same exact conversation at every visit💔
@corneswanepoel4890
@corneswanepoel4890 3 месяца назад
Yes, like the old vinyl records get stuck in one place. They say the same thing over and over and over.
@norapelamo5079
@norapelamo5079 9 месяцев назад
But how does it differ from alzheimers other than starting at a younger age? the symptoms can be so similar.
@tslilbearshoppe9870
@tslilbearshoppe9870 Год назад
my dad.
@corneswanepoel4890
@corneswanepoel4890 3 месяца назад
Is aggression part of Frontotemporal dementia? Part of behaviour?
@Lisa-xf5uf
@Lisa-xf5uf 10 месяцев назад
❤ty
@qpDemonqp
@qpDemonqp Год назад
Hello , i have a brain infection before 6 months ago and i have all dementia symptoms im 28 , is it possible to have dementia at this age ? i have all the symptoms , sometimes i got lost in fimilar places , my personality has changed , I can't concentrate and i cant focus
@krisbaksys6674
@krisbaksys6674 Год назад
Yea I have been living with dementia and with FTD for quite some time. You’re born with it and it’s in your genes. Just eat healthy and stay away from sugar, caffeine , smoking, drinking and stress. It all triggers flare ups and makes for bad days/weeks. You will be ok stay strong but yes it’s tough. I been living with the known symptoms of it for the last 20+ years but now it’s starting to hit me good with memory and muscle weakness. I’m 47 now and my dad is 75 and he’s got it as well but he has been bed ridding for the last 20 years. Praying for you but stay strong. There’ are some good days ahead for you.
@heidyacevedo3615
@heidyacevedo3615 Год назад
I would like to know how do I answer my husband when he’s hallucinating about a family member being in the house
@lesliedunn
@lesliedunn Год назад
I work with people affected by dementia. When one of them sees someone who’s not there, I don’t argue with their reality. Instead I ask how old the person they see is and try to start deflecting their attention with questions like, What’s the “visitor’s” favorite room in the house, or he/she (the “visitor”) likes springtime and is on their way to go outside. From there hopefully you can move to changing the topic to, for example, listing spring flowers, etc.
@veronicacarey7925
@veronicacarey7925 Год назад
This has happened to me with family members. I do not argue or say "you are seeing things". Instead, I say something like "I just asked them to wait outside for the person who is picking them up." I might ask "DID they have any important family news to share or were they just visiting?" Then we can talk about other family members or otherwise change the subject a bit.
@Cynthia534
@Cynthia534 Год назад
Doctors prescribing certain drugs, not knowing if the patient has FTD could it cause it to get worse
@AyeWitness
@AyeWitness Год назад
Make call is not difficult to figure out what they’re talking about 😅
@miumama2007
@miumama2007 Год назад
What will happen to a FTD patient down the road?
@DementiaCareblazers
@DementiaCareblazers Год назад
It progressively gets worse. There is no cure.
@gzmz1993
@gzmz1993 Год назад
I enjoy all your videos. But it’s becoming apparent to me that all these symptoms seem the same as all other dementias. Every dementia symptom I read about or listen to all appear to be the same and my mom goes through them all.
@DementiaCareblazers
@DementiaCareblazers Год назад
As all the different dementias progress, they tend to look the same. We see the most differences in the early stages.
@cindycarver2492
@cindycarver2492 Год назад
How is it diagnosed?
@laundrygoddess4
@laundrygoddess4 Год назад
My partner was diagnosed by CT, mri and a neuro cognitive testing
@DementiaCareblazers
@DementiaCareblazers Год назад
Neuropsychological testing is a must. brain imaging is also likely to happen to help with the diagnosis.
@susandiggs5121
@susandiggs5121 Год назад
My husband was dx with vascular dementia and after a recent visit to a neurologist, he says it is not vascular but FTD. Our son, the one snd only, has researched and FTD sounds very hereditary. I am scared. The statistics say 1 in 2 will get. Has anyone experienced that?
@cindycarver2492
@cindycarver2492 Год назад
How is it diagnosed?
@susandiggs5121
@susandiggs5121 Год назад
@@cindycarver2492 the doc looked at his MRI from 2020 and accessed him in the office. He ordered a new MRI and a FDG pet scan of the brain as well as the genetic swab. He said it wasn’t vascular because he has no symptoms such as high blood pressure, high cholesterol, heart disease etc.
@queenofdahouse1591
@queenofdahouse1591 Год назад
No one knows what the future holds. I have two fam members with two diff kinds… find a good neurologist, get your tests, stay healthy and enjoy quality of life… we each only have one day at a time. You can lose a lot of todays worrying about tomorrow. God bless. Oh God says Don’t fear six hundred times in scripture. He is a God of order. Tell Satan to get behind and live your best life. Find a support group for caregivers. You got this! And the men in your life are counting on you!
@queenofdahouse1591
@queenofdahouse1591 Год назад
@@cindycarver2492 MRI, physical and cognitive tests.
@cindycarver2492
@cindycarver2492 Год назад
@@susandiggs5121 thank you so much.
@CrankyGrandma
@CrankyGrandma Год назад
Would someone with verbal problems be able to communicate through signing?
@user-cf3oe8fi7y
@user-cf3oe8fi7y 4 месяца назад
What i was accused of would be adnormsl behavior Me too younger then it's should of happened never gambled ever saying I walked into a building my whole life walked by thouseds never did anything
@user-cf3oe8fi7y
@user-cf3oe8fi7y 4 месяца назад
If I attacked a person with dementia I would be trash but the ones who forced everything on dementia is not trash they knew I had it
@barryjensen-jc2rp
@barryjensen-jc2rp Год назад
What is the value of identifying the various types of FTD, etc.? Everyone i have met with a knowledge of FTD etc., says the same thing: There is no medical treatment for FTD.
@krisbaksys6674
@krisbaksys6674 Год назад
No medical treatments yet but having a healthy diet as a kid and maintaining it throughout life is very important. And keep your self from getting nervous and anxious cause it only leads to the progression. Stress kills and progresses it quicker
@stacieboucher1570
@stacieboucher1570 Год назад
When you know which type of dementia, you can kind of know what symptoms are going to happen. My husband started getting violent when he didn’t get his own way, and the Dr put him on Paxil. It’s an antidepressant that “ puts the brakes on” his compulsive behavior. We tell him it’s heart medicine. He was always a mellow person. Full of energy. Now he’s just like she said. Apathy, no motivation, ect. Shocking to see him change into a whole different person.I’m trying to not be resentful he doesn’t care if it kills me doing all the work! God Bless you. Keep asking questions!
@casualonemmo-player2167
@casualonemmo-player2167 Год назад
Eh... so basically... the same symptoms people can get when they get drunk.
@armyofmonks
@armyofmonks 9 месяцев назад
Firstly, the proper way to call this decease is Frontal Temporal DEGENERATION, not dementia. How would you like to be chastised as demented? Specially in the early stages. I’m not demented, yet. So it’s hurtful to be lumped with those that have already degenerated. Second, many of us don’t present behavioral aberrations. It’s disturbing how so many people love to emphasize the behavioral variant. The rest of us have to suffer the bigotry of people assuming we’ll misbehave when like me the problem is language expression and working memory. Another thing to consider is context. I once tested in my second language as exceptionally gifted which probably means I was a border line genius so my decease isn’t really noticeable. My wife says I’m only more normal these days. Anyways, I just wanted to ask you to not use the pejorative dementia word. It demoralizes those of us who are fighting to elude our eventual dementia. We’ll get there soon enough so there’s no need to project us all unto our demise. Thank you.
@SonnyGTA
@SonnyGTA Год назад
Biden, Fetterman. 🎯
@amandabarnard2072
@amandabarnard2072 Год назад
My mother recently claimed she has "Chemo brain"...she won't say how or why or even when she had it. Her last radiation was in 2014. I'm not sure exactly what she have been diagnosed and she has been someone who I don't know anymore. I'm going thru a huge court custody case between her and myself too at the same time. She has mislead her Attorney therefore her Attorney withdrew after 2.5 in this on going suit. She is a retired CPs supervisor. I'm an only child. Since she filed this suit against me which I was never served or had the knowledge of she has slander me lied about me like I'm a villain to the court and the new community we just recently moved to which is her hometown. She moved me up to north texas under false pretentious from Houston. She filed an Emergency Order over me. Kick me out and Alligated her self from me and gave my daughter to someone I don't know and hid my child for 4months. Now it's all coming to light trying to start pre-trial in my favor. My mom was my best friend non judgemental all my life. Cool as a fan. Now I don't even know her and don't trust her. I have a clean record and she has nothing but hearsay. She ALWAYS goes back to 20years ago what I didn't di right like that's why now she is the way she is....Chemo brain...what is that and what does it fall into? Close family friends have told me she shows many signs of dementia but I will never get a straight answer out concern for her.
@corneswanepoel4890
@corneswanepoel4890 3 месяца назад
It is a horrible disease.
@Lisa-xf5uf
@Lisa-xf5uf 10 месяцев назад
❤ty
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