Careblazers: dementia care heroes all of the above!! Today is 1/13/18 and I did watch your other video. These are such great tips. My mother began passing out due to A-Fib about three hrs ago. Perhaps the first fall she had resulted in an undetected concussion and shortly thereafter we were faced with the dementia diagnosis. It has progressed rapidly and almost from the onset she began falling. I have Fibromyalgia and cannot pick her up due to pain. I cannot count how many of the falls resulted in a head injury needing stitches. Finally I was questioned on the possibility of placing my mom in nursing home care. The culture I come from sees that as a horrible thing! My mother fell yesterday and was rushed to the ER for stitches. Today I came home from Sunday School(my husband and I trade places going to church, it’s been a year since we’ve gone together) 😢 and I watched this video... thank you, now I know that what my culture thinks of me is non of my business! Your videos are a blessing, my best to you.
As a neurologist and son of a Alzheimers patient, I want to say how amazingly in tune you are with the issues surrounding Alzheimer’s patients and their caregivers and how well you communicate that knowledge to others. You are a fantastic resource. Great work!
We're just getting started with this journey. My husband is probably about 2 years into it, but I've only been noticing it for sure these past 4 to 6 months. Other friends have told me they've been seeing it for the past 2 years. I happened to cross Dr Natali's online helpful videos, and I am so thankful the Lord led me to her. She is such a kind and considerate person, and speaks with such a caring attitude. I plan to keep listening as my dear husband continues his journey with me at his side.
5 years after you posted this, finding myself asking these same questions about my mom. Struggling with guilt, self-blame, feeling like I should be doing more for her, exhaustion, depression, lack of focus, lack of motivation all combined. My mom and I were so close and it's really hard to be going through this without her to be there for me. I miss her so much even though she's still here in body.
I am in exactly the same situation as I have a beautiful mother who has been my best friend but who I no longer can talk to. This is the saddest thing ever to go through. Wishing you all good wishes with your mum.
Forget them. I have the same stuff happening. Forget them. I couldn't care less because they're not in the situation. It's easy to say something without knowing
The hardest thing for me when it was time for the nursing care facility was, he would no longer have the one on one care. At the nursing facility he would be one of many. He would have to wait his turn. At home I was able to take care of his needs immediately and sometimes even foresee what was coming and be ready with the clean shirt or warm washcloth, etc. I knew where to set his glass so he wouldn't spill his drink and what spoon he needed and when to step in and help or let him do it on his own. His daughters taking care of him every once in a while, without me there did three things. It gave them one on one alone time with their dad, gave me a break and let them know close up and first hand the progression of the disease. I had their full support when the time came to enter the nursing facility. I am a Lewy Body Careblazer. Thank you for these videos. I wish I had them before I became a caregiver.
Thought I was the only Lewy Body dementia careblazer... actually that is how I feel. My husband diagnosed with Parkinsonism with Lewy bodies. Thank you for sharing... also a great thank you for all the videos. It will be helpful to hear more about caring for a Lewy body dementia patient. Be blessed
Thank you for giving so much of your time to advise us. I am struggling with putting my husband in a nursing home right now. Your advice is so true. I lay at night beside my husband and grieve for him already. If I put him in a nursing home he will not be beside me when I wake up. Who will comfort him when he is confused? Who will.cover his feet at night when he kicks the blankets off? I could go on and on but all u out there that love your dementia relatives understand. Will they care for him and give him the love that I give him? No but I know I am eventually going to have to let him go. My heart is breaking. Right now I am content laying here beside him as I write this. I can't let him go yet. Soon but not yet.
This is the BEST dementia support channel ever! I loved the advise on this because it has been 3 years I had to place my mother in dementia care and still struggle with guilt. I placed her for all the right reasons but the guilt has been overwhelming leading to depression. The statements on this video are very comforting and I thank you very much. Please keep doing what you are doing.
Life is full of "new normals" ,this is one of many. Thank you so much for your videos. No one understands unless they're in it. We can't do it all. At some point we are all in the same boat. God bless all
My biggest struggle with this was that nursing home care was NOT superior to what I could do even though I was almost completely alone as my Grandma's caregiver. She had so many other health issues besides dementia and there were several times I had no choice other than nursing home care. It was usually nightmarish and I was actually greatly relieved when she was well enough to come home. They would put her at the far end of the hall and neglect to watch her even though she needed constant supervision to keep her from hurting herself. It would be a wonderful world if a "skilled nursing" facility truly involved skilled and caring people taking excellent care of your loved one. But depending upon where you live, nursing home care can be truly horrible and neglectful.
I agree with you totally. My mother had alzheimers and was in several nursing homes. First thing they do is put them on anti pyscotics. That makes them dizzy and they fall and hurt themselves. Now I am taking care of my husband who has alzheimers for 10 years. I'm so depressed , crying and feel guilt because I can't handle him anymore.,but don't want to put him in a nursing home. I know he receives better care with me. But I don't think I can do it anymore.
Thank you. My mother was in nursing care for two and a half years. I've never been able to get rid of my guilt. To top it off, she died of covid-19 without her family being allowed to enter the facility.
Even if it's not permanent care.... Relizing you have to put your loved one in a nursing home at all is scary. To make it worse, no one talks about it with you, until you have no choice but to put them in one... I'm about to put my mom back in nursing home for rehab... I can't take care of her, work and school at the same time. She had back surgery, went to the nursing home I worked at, came home after two months.... Looking back, that wasn't enough time for her to heal. Got home, refused home health care. Finally when she accepted, it was 8 my later... By then I quit my job working at the nursing home as a CNA. Now after 4 months at home .. I'm at my breaking point. No one tells you it's time, until you have no other choice ....
Currently my Wife is in a skill nursing facility after a fall( day 22) , broken femur resulting in partial hip replacement that repaired the break. She a youthful 70 years old , hemorrhagic stroke , left brain in 2016 and as of a year and a half ago diagnosed with dementia after some alarming paranoia episodes we continue to experience related to me stealing things, having girls friends and just sadly her not liking me much from time to time. Throughout the time caregiving I completely remained dedicated to her recovery from the Stroke , did experience progress yet the dementia I believed was insult to injury that I won't be able to gain a sense of recovery for her. So currently , my family is encouraging me to let Mom ( my Wife ) transition to longer term care so I can begin to resume a life without ( and I can barley write it) the Caregiving lifestyle. Still struggling with the choice tearfully and everything you said fits my dilemma .
This is happening in my life right now. It is the most heart-wrenching, horrible thing I have ever had to do. This was very helpful. I just can’t get over the feeling that he is going to feel like I abandoned him. I wouldn’t want to be abandoned, just because I need care. Thank you for such wisdom.
I sincerely wish that you would create a video about the relationship between a sincere care provider & the children of the senior that care givers provide for. This is a very real issue . It's not always easy for a care provider to not only provide good care for the parent but to as well deal with the dynamics of his or her family members.
Thank you, please keep it up! It’s been 4 years since you made this video and my fiancé and I have your survival guide and took your course this last fall, including the VIP extension. At times, you are the only resource we can find that offers not only knowledgeable, but compassionate, and feasible medical guidance on how cope with this disease and care for not only our dementia loved one but ourselves too. We need you Dr. Natalia!!🙏🥰
Thank you for your wonderful advice. My husband is having his MRI on his brain my Husband of 54 years has Dementia. I think he is in the middle stages. He has been showing signs for the last ten years.
Thank you so much. My father is struggling with this situation now. We are all encouraging him to "pull the trigger" as you put it. And he keeps saying he is thinking. In the mean time, it allows time for bad things to happen. I will be sending him this link.
Thank you, thank you, thank you for this video. I just put my husband who's 63 with Alzheimer's into Memory Care 2 weeks ago. It really wasn't as bad as the story you shared but I just couldn't do it anymore physically and mentally. We've been married almost 38 years. This great understanding really touches my heart almost to tears. SO right on for me. THANK YOU.
Thank you dear CAREBLAZER C.E.O! You are my Angel-friend here on RU-vid! You came to my rescue in the last month, and TODAY, this morning after 10 am I researched and reached out and Grace listened as I described yesterday afternoon , and into the night(my very favorite time -After all is calm and I get my time……
My husband has young onset PD. Diagnosed in 2005. He is in advanced stages. Although he is only 55 he is totally physically and mentally disabled, I’m looking into homes
Hello. I can relate to this story. I also have been married to my husband for 50 years. I was caring for him as his dementia increased without help or support from our children who live too far way to help out or even his brothers who lived nearby. It took me a long time to convince myself that I had to help myself to be able to help him. After months of crying and having panic attacks, I finally took the decision to find help for him. He is now in a "home" where he is doing very well as they have him on a daily routine. As for me, people tell me that I look very rested and even happy. I still feel guilty once in awhile but know that I have to be healthy to be able to care for him. Thanks for all your excellent help for we Careblazers.
My husband has been in care now for two weeks and I feel so sad to think that wonderful man I married 53 years ago had to sink to this level. I haven’t visited him yet as they won’t allow visiting for the first 2 weeks but I am going this week and I’m rather anxious about the reception I will receive and the reaction when I leave. Unless you have been in this situation you can never understand. Your videos are spot on and have been a tremendous help for me. Thank you so much.
Dementia nursing home? How much do they cost? My mom get 720 a month social security and that is it. I have no money to pay for one, I have kids of my own and can’t afford a descent nursing home for her. Nursing homes for the poor are horrible and a nightmare.
THAT'S the dilemma. People always assume you can just go out and find the best nursing home, but that's not always the case. You have to take what's available to you. And that makes the decision VERY tough.
M. Jones,I placed my Mom into a home a week ago. Check with her social worker. She should qualify for a program called CHOICES. Check it out. God bless
You are very wise my husband has mild cognitive problems I have been a carer all my life from working age mother .nursing now my husband .He is such a gentleman and at this moment I’ll take care of him but I know that his condition can get worse but he is mine I’ll do the job to the end for has long as it takes . But who knows what will happen thanks for your understanding.👌
It's the new year and I opened up to my mom how if this situation (my mom and I caring for my dad 24/7 with dementia) continues for another year I won't be able to handle it anymore to the point I feel like I might not even make it to the end of the year (that's how severely stressed I am) We've discussed and she agreed that putting him in a Nursing Home/ Assisted Living Facility, would be the best for him and our health. It's only the 2nd day of searching for good nursing homes and I'm here crying watching this 😭 overwhelmed with guilt when we've only just begun planning 🥺
i allowed my wife to move her mother in our home, the mother has dementia. i agreed to it becuase i love my wife and it was important to her.. but i am finding it harder and harder to be "ok" with it.. our relationship has suffered. not sure what to do, thank you.
Dr. Natali you just described my current situation. I have been married to my LOWD for 58 yrs and going thru all of those emotions you just said regarding putting him in a nursing home. I keep going back and forth for all the reasons you mentioned. You just get it! Thank you!
My husband got tested for dementia it was very helpful, but Very painful for me, my husband was a very smart man,but after The third testing, he know nothing, but its funny talking to him At home was a different story, so the testing was good in some Way, a terrible experience for me, Thank you for all your support. Olivette,
I clicked on the link to the survival guide and It went to click funnels and I didn’t see it there. Appreciate your videos. They are so helpful for my in-laws.
Our biggest problem is that the decision to put my mother in law in a care home sits with 4 siblings and a husband 3 of which won’t accept the safety concerns. It is causing a big problem, family breakdown and stress.
I felt so much better after seeing this video. I felt she was talking to me. Because i feel like why can i be that person that took care of her husband at home. Now i know iam not that person and my husband own safety i could not keep him at home. Great program thank you.
I need to get my husband to watch your videos. His mother moved in with us 4 months ago after a massive stroke that left her paralyzed on one side. She also has dementia. My husband means well, but this situation is not working for anyone.
Medically, I couldn't take care of my dad. It wasn't dementia that took him away, but a G.I. bleeding internally, which was too far advanced for surgery. I am not qualified to care for him with this. I miss him tremendously.
My husband has dementia but functions okay if he can sleep. Every night is a battle and my own health has been impacted. He woke me up at 3am and I was still half asleep and screaming at him. I have been doing this for a year and I feel absolutely exhausted and miserable.I am 70 and feel perfectly awful most of the time.
I am struggling with this issue . I am losing myself in my husbands dementia. I have not been out for a fun day In almost five years. Just this week I have a sitter 5 hours per day. I can not get myself to leave him in her care. How do I let go. We have been married 58 years. Any advice for me?
Oh Barbara, my heart goes out to you. Consider joining the Careblazer Community for support and know that I am currently elbows deep into creating a course specifically for you. It's all about how to manage the stress of caring for someone. How to make sure you don't lose your health and sanity in the process. And how to work through feelings of guilt when you start to do nice things for yourself. I'm hoping it will be ready in about 4 weeks. Hang in there and in the meantime, consider joining the group here; facebook.com/groups/dementiacareblazers/
#1, their safety or your own sanity, when one is compromised both are at risk. everyone has a limit so setting future limits and reviewing them at regular intervals it important. either way we will feel guilt or regret. Its getting through it and over it when it rears its ugly head. I'm just glad I'm not aalone.thank you and God Bless you.
I am not against putting anyone in nursing homes but do please make sure its a good one. Make sure they'll really look after your loved one and they got enough trained staff to do the job and that they have lots of patients and compassion....very important....most nursing homes are a horror....but not all....God bless
My mom has FTD and I have decided to place my mom in a nursing home to get my life back. My children and husband need me and with a full time job it has become too much on me. I’ve only sacrificed 1 year if my life with my mom and yes I feel guilty but my teenage daughters need their mom. With my mother’s separation anxiety I am not able to leave the house with my daughters for a fun day for example as my mom tries to run away.when I return due to her separation anxiety issues. My question is: how do you bring someone to a nursing home when she doesn’t want to go to one. How do you tell a dementia patient that you can no longer care for them and they are moving to a home when that’s their biggest fear?
How did you go ? I am in the same situation with my MWD. She doesn’t want to go to a nursing home, but the caring is taking its toll on everyone. Most days now my MWD wants to go home as she is no longer familiar with her home with me ( 12yr) she also forgets she can’t driver and doesn’t like me being around so much and telling her what to do. when the opportunity arises I have been gently spoken about “ retirement village living “ or tri care where she can start in a live in your own type living.. hopefully when we go to a assisted living she will think she has done it herself. All the best for your journey
My MIL has Dementia and when it first started she got her husband to promise to never put her in a home. He has kept his word but its killing him. We know that if she could see what is happening right now, she wouldnt hold him to that promise. I don’t think there is a single friend or family member that doesn't think she should be placed. But we haven't been able to reason with him. Its one thing watching what's happening with loved ones going through this disease. Thats heartbreaking in itself. But its also uncontrollable. My husband finds it more difficult seeing the toll its taken on his Father because its self imposed. He's losing both his parents.
My grandmother raised me, because my birth mother abandoned me when I was 2 months old, my father (grandmother's son) has always been horrible to my grandmother, I'm only 21 years old and I have to make the decision whether to put her in a nursing home, she fell on December 26, 2018 and broke her arm and shoulder, she has depression and other medical problems I'm so terrified that she will hate me because of debating whether to put her in a nursing home or to quit my job to take care of her 24/7 I asked my father for help and he told me he wants nothing to do with her, I'm so stressed out.....any help?
I think that at your age you HAVE to keep working, and that HAS to be your priority. IF you can find government programs that can provide caregivers to come to the home for enough time to do everything she needs (could be just preparing a meal, helping her to the bathroom, and turning on the tv) while you're at work, then you can keep her at home. But if you have to quit your job to do it, it's a NO GO for me. She had her life. Now it's time for you to live yours. That's just my opinion.
You can visit her frequently in the nursing home to brighten her day and remain close, but someone else will be taking care of her physically and mentally. You're too young to take on that responsibility, and your family is not helping, and you have to give up too much. When I say that you're too young, I don't mean that you can't do the job, I mean that this is an important time in YOUR LIFE, a time when you should be thinking of your future, building a career, meeting friends and having a place where you have privacy. Being a caregiver at first seems like something you can work into your life, but over time, it begins to completely take over YOUR life. Your life is at risk. If you could put her in the home just for rehabilitation that would be fine. BUT it sounds like she has too many other issues (depression and other medical problems) that it will be impossible for you to deal with AND STILL LIVE YOUR OWN LIFE. Here's an idea. Put her in for a few months until her shoulder is better. And then reassess at that point.whether the other problems are things you can handle, or whether she needs more care than you can give.
Hello @DementiaCareblazers, thank you for this informative video. I too am a dementia educator. May I share this in a workshop? If so, will it always play with the ads interspersed?
Hi I am currently helping my in laws (I refer to them as my parents) with their caregiving needs. My father has dementia at 90 yrs of age. My mom is 87 and healthy and strong, however she does a lot for her husband and does get worn out,. My father is extremely modest and will not aloud anyone to change of help in his personal hygiene which includes adult diaper change. How can I help him and her with this situation. My mom won't be able to do this with out feeling it's effects. She doesn't want him in a nursing home and I am available daily to care for my in-laws . I am 57.
Hello Sandra,I understand what you are saying. God bless your parents. Caregiving is very stressful and one can become overwhelmed. I know from experience. My Mother is 84 and I can no longer care for her at my home. I have to work and there's no one to assist me. God bless
My daughter's say no way will I put their dad in nursing home. I think they need to come here for 7 days 24 hours a day and see then tell me that. If I had someplace to go I would do just that
It IS so difficult. I am sorry you are going through this. Is there a social worker at your loved one's clinic? They may know of assistance available to help make nursing home more affordable, or even of medical foster homes or group homes that cost less but still provide the care your loved one needs.
What do you say to your husband in a care center when they beg and plead to come home, I’m at a loss as to what I can say to support his concerns. Please advise me,,,,🙏🏻🙏🏻🙏🏻😩
We are at 4' do I would love to know how long from there to nursing home would have been ideal. Thanks. ( I know it differs a lot, but I need to apply on time.).
What other people think about you is out of your control. You could be perfect in every way, yet many people would still find reasons to dislike you. It is out of your control.
My 93 year old mother has stage 4-5 Alzheimers and has lived on her own since dad died 31 years ago. Mother is registered with Adult Social Care Services. She still thinks she can look after herself and her bungalow without any help and therefore refuses or declines their offers of daily assistance. Mother has now reached the stage where intervention is required for her health and safety,but a Care Home option is very difficult to secure. Mother has been assessed for entry into a Care Home but her stubborn ,anti- social and deluded attitude have denied her access to such establishments. She is now on her 3rd set of daily home carers who come twice a day to assist her in medication,meals and small household tasks. Mother will be a problem for as long as she continues to exist in her bubble of ignorance and need.
People need to stop making these kind of videos They plant the idea that people should feel guilty about putting someone in a Home Not all of them are bad My mother actually likes it The have recreation and she gets physical therapy
I’m in NY. Spent 135K in less than a year. Put her in a medicare aided facility- Amber court in Smithtown NY. The aides have no business caring for anyone. The place gets paid to do what it does NOT do. She broke bones in her back 2 times. I finally had to bring her home because I’m afraid to put her anywhere. But this is getting to be too much for me. The guilt is what motivates me. She doesn’t even know who I am and hates the sight of me. I’m her daughter. Been here for her all her life- she’s always been a loaner. My brother and dad bailed.
This is an old video, but that's the great thing about RU-vid: you make a video once, and it keeps doing its job forever. This video covers an an important topic, and Dr. Natali, you nailed it. Your four points were right on, you're a genius! I loved how you said EVERYBODY is different. If her husband wants that moldy cheese or wine, he's probably bigger, stronger and more aggressive than her, she can't stop him. My mom also goes for moldy food she's hidden. But I'm a man, far stronger and bigger and younger than her, I can take the moldy food away. Also my house is mid century modern with shiny, stained concrete floors throughout - extrememly easy to clean, so when she has her "bathroom accidents" I just use a little blaach and a throw-away towel and its done! Someone with carpeting, or tiles with grooves would have a hell of a time. Also I have no other dependents, no kids, no wife - it's much easier. So I'm no hero, I just have an easier situation than others. I would like to add a #5 and hope it doesn't come off like I think I know everything. But all dementias cause patients to feel extremely fearful of the unfamiliar. The strange new environment of a nursing home would be terrifying. "Memory impairment" is a misnomer. It's more like, they just don't know anything anymore. They're afraid of microwave ovens, unfamiliar chairs and sofas, television sets, houseplants - each patient is scared of different things. Enter: Xanax. The fear buster. Who cares if its a dangerous, addictive controlled substance? Dementia is a one way ticket. On Xanax, their new scary bedroom at the strange nursing home ceases to be a bizarre place of terror in the night. The hanging coat ceases to be a murderer. The unfamiliar chair ceases to be a lion about to kill them. FEAR of the unfamiliar.That's the biggest problem in a nursing home for a dementia patient. Put 'em on Xanax, and the nursing home becomes 90% more pleasant. Thus the careblazer's guilt decreases by 90% too! Forget SSRIs, those should be for anxiety patients without dementia who can't take Xanax because of addiction. But for a dying Alzheimer's patient? What does addiction have to do with anything? They're near the end anyway. Let their final days, if in a nursing home, be free of fear.
There are a lot of Veterans not receiving the benefits they earned. If you are caring for a loved one that served our Country during a war. I strongly encourage you to collect their service records and take them to your local VA office. Along with their ID, insurance cards, a detailed medical history and the last four of their social security number. The development of a disability decades after their service, could be the result of a service connected disability. Your loved one that served during a war could be eligible to receive medical care through the VA along with additional tax free monthly compensation. My Dad retired from the Navy. He served as a Combat Medic during Vietnam. Other than his Military retirement and social security, I had no ideal that he qualifed for disability compensation through the VA. In January of 2018, at the age of 86 he was wearing his Vietnam hat while recovering from triple bypass surgery. When a nurse thanked him for his service. Then she told us that systemic heart disease and diabetes was linked to Agent Orange. Too good to be true. I went to my Dad's house and found his service records. Took them down to the VA office. I filed a claim along with applications to the four VA state nursing homes here in Alabama. The VA gave me forms to have filled out by his doctors. After returning the forms the VA sent my Dad to see a Endocrinologist. Within six months my Dad was awarded a 100% service connected impairment rating. Along with back pay back dated to March 1, 2018. Followed by additional tax free monthly compensation. Which has more than doubled his monthly income. Part of the which is Aid & Attendence. For which the VA provides my Dad with a home help aide five days per week until he goes into a VA state nursing home. Due to my Dad being 100% service connected the VA will pay for all of his care. My Dad will get to keep his social security, retirement and VA compensation benefits. VA benefits are not just for career Veterans like my Dad. If your loved one is a Veteran of war. I strongly encourage you to explore the possibilities by discussing your loved ones service with a VA representative.
Just an FYI: We like to say ‘place’ a loved one vs ‘put’. Love all your videos. My husband, with Parkinson’s & LBD, just passed away and always appreciate your education and comments. I’m trying to re-enter the world after years of caregiving. Hope your dad is settling in? 🙏🏻
I didn't care what others thought about my decision. I cared that my husband wanted me 24/7 and when I couldn't physically do that and he did go to memory care, that he was scared and more confused without me. He had a stroke on top of being in the end stages of dementia, but the stroke rapidly sped up the disease. I was able to care for him for about 6 weeks after the stroke, but he wandered, was physically strong, fell a lot, and was aggressive with the caregivers I hired to help me at home. Nothing worked. He is deceased. I still have guilt.
I really liked your video. You sound very caring and knowledgable on Dementia. I have been caring for my mother in and out of ALF's and nursing homes for 5 years now. I felt I needed to hear what you had to say, eventhough eveything you mentioned I have been through. The only thing that I did not hear is the after-affects of placing your loved one in a nursing home. What I mean to say is that I still feel so very quilty for placing my mother in a nursing home after 5 years and still feel I need to be there for her everyday. I know I need couseling and am working on getting the help. Please inform people that the feelings of guilt take time to go away. It is undetermined how long it takes as I am still working on letting go.
No no no ...I would now have no problem if my husband developed. Dementia he would be going in a nursing home pretty dam quick...... Why you may ask am I sure about this ..l will tell you...... my dad looked after my mother with dementia ....It wore him out...... he died .!!!!!!..my mother !!!!!is still with us now.... in a nursing home on last stage dementia ....a lot of the family fell out with me @ my sister because we did this ...@ the reason is self preservation I'm sorry but my life is important to me and my family...don't let anybody tell you what's best for you ....just don't be a marter... look after yourself 🙏oh yer we had the cousins who visited my parents once in a blue moon poking their noses in telling us we should not put mum in a home well they can go and do one ...We don't speak anymore after they reported us to social services can you believe what someone people are like .....just unbelievable behaviour untill you have walked the hell that is dementia it's in the title being demented. Then don't judge ...🙏
My situation is different I want to take my grandma out of the assisted living and taking her home. I feel that she should be home. I feel that most facility does not take care of her.
The only time he settles down is after I leave and the give him Ativan or halaperodol to get him to sleep. He has been in the hospital from having three ambulance calls in 24 hours. Dr. Thinks I need to have them activate the personal directive. My husband has heart, kidney and liver failure. He wouldn't allow me to have homecare come in. They are not sure what is causing the confusion,delusions and not wanting to lay down to sleep. He says he doesn't want to be alone so he is in a special chair tied in with alarms on him so he doesn't fall. So very sad
My 85 year old father has dementia. He is cared for tirelessly by my mother but it is a hard slog for her.I help out as does my brother. Luckily she does get occasional respite care here in Australia for him. I'm currently watching ALL these videos to help me deal with the huge resentment I have towards my father for the misery he has made my mother's life. He has always been needy and dependent even when he was well. This to me is the final straw - and the Christmas family gathering was pretty much unbearable. Of course I understand what dementia does to the brain but I am more interested in exploring the themes of frustration and angst that this disease causes for carers and family members. I am impressed with Dr Natalie and have made copious notes for a family meeting.
I just put my mom in a nursing home and I regret it I’m so sad. But then I think about if I didn’t I was cracking up I can’t see her for 2 weeks. I hope she doesn’t die on me yet
I know how you feel. My mother has been in the hospital for almost 1 month and I just saw her today, after they told me no, but I prayed. We have to wait till she's strong enough and then put her in a care home, or I don't know whats gonna happen. But, it breaks me to put her in a home, but we can't give 24 hour care.
