Parkinson’s Disease Psychosis: A Caregiver’s Story

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Diane Sagen's husband, Jay, has Parkinson's disease and experiences hallucinations and delusions. In this video, Diane shares their experiences after Jay's diagnosis with what health care professionals call “Parkinson’s disease psychosis.”
For more information about hallucinations and delusions in Parkinson's disease, call our free Helpline at 1-800-473-4636 or visit parkinson.org/Understanding-Pa...

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2 ноя 2015

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Комментарии : 136

@pheebsphan1 6 лет назад

My father was diagnosed with Parkinsons's about three years ago, and the amount that his mind has changed since that time is unfathomable. My father has literally gone from being one of the most proactive hard-working people I know to someone who is always criticizing others, paranoid and borderline suicidal. On the worst days, I break down crying, wishing that I could have my dad back. I begged my father to seek therapy and treatment for his mental health, but he refuses and yells at me that I'm not his guardian. Watching this video brought me a small sense of comfort, because it reminded me that we are not alone. Thank you.

@FarnazIransoul 3 года назад

Same here..... you’re not alone🌹

@KoolT 11 месяцев назад

L DOPA itself can cause obsessive shopping, gambling and sex addiction. My husband went quiet delusional he was going to be a BIG music star.

@BravenBeautiful 8 месяцев назад

My father is also going through the same...worse symptoms,highly aggressive towards family and doubtful to doctor and family...if they wanna plot something against him. Not taking meds and food.sitting at one stance for hours

@donnaboulware580 2 месяца назад

Walking in those same shoes with my dad right now🥹

@seventhdayissabbath8747 2 месяца назад

@@donnaboulware580 me too..

@SchmeesCrotchFruit 4 года назад

Caring for my dad alone. 3 years and counting. PD, kidney disease, remission in A-HUS. I am exhausted.

@chrisfry436 3 года назад

Bless his heart, and Bless you two for taking care of him.

@michaelbiedassek7136 3 года назад

In this Situation one needs professional help but it’s just so expensive

@dyotiniroy3335 3 года назад

May God bless you abundantly. My prayers...I am also handling my mother in law past 5 years...except for the hallucinations she is perfectly fine...just praying better treatment comes soon for such patients.

@yevgeniadeguzman1986 2 года назад

Praying that God will sustain you with His strength. You are incredible and a beautiful person. God bless your heart, God knows what you’ve been through. Take heart!

@kavitadasify 2 года назад

bl ess u

@Zynbabwe902 9 месяцев назад

I’m 23 and My step dad was diagnosed 5 years ago. I have been the one looking after him as best as I can and man this is heartbreaking. He constantly thinks people are living in his home and says they’re eating his food and living there. Idk how to deal with this and feel hopeless yet I’m always there for him and never let him feel lonely. Man this disease

@ParkinsonDotOrg 9 месяцев назад

You and your family are not alone 🩵 Know that we have more information at Parkinson.org/Hallucinations You can also discuss these symptoms with our free Helpline at 1-800-4PD-INFO (473-4636) | Helpline@Parkinson.org

@rosered9029 5 месяцев назад

Stay in integrity and give yourself a cuddle that doesn't end. God's love is like that. Find the funny in life, all over the place. He lives in his world. You live in yours. Nurture yourself and you will have an overflow that he will benefit from. On bad days, just remember to breathe. Also remember that moments are a very alive thing: it won't remain the same over time. This is a HUG from...me.((❤)) Now share it😊😊

@4shys2 8 лет назад

My mom's had parkinsons' for over 20+yrs. Hallucinations have got more extreme,she's used a spray bottle to kill spiders she sees on the ceiling, fallen trying to get away from tigers. She is so afraid! I've slept with her in her twin sized bed.So I can be close.Even tho I have baby monitors in our rooms! She has made the decision not to attend church,because she needs constant help! Church was her main social circle of people to see and be with. She has recently started taking Quetiapine,and stopped her Mirapex.The side affects on the bottle are enough to frighten me. With her lack of sleep,and how bad her hallucinations are. I am so afraid of her pacemaker being changed out at the end of this month! She is a wonderful lady, it's difficult to watch her not being able to do crafts/draw anymore.Use her hands to simply put in a dvd. Bless the inventor of kindle fire. She uses one finger to play many games ,she really enjoys that! Our vacations are the local department store, and going out to eat! And any outing is considered on her strength to be able to stay out! It is a difficult and cruel disease! I pray for you and your husband' s continued strength!

@anithajacob7566 7 лет назад

God bless every care givers

@No.ThatPrettyGirl 5 лет назад

IN TEARS..... : ( I recently found out my mother has advanced Parkinson's disease. THANK YOU SO MUCH for sharing your story. Much love!

@Wisdom_Tale 11 месяцев назад

How's your mom bro.. Hope she is fine

@karami8844 3 года назад

My dad died last week from Parkinson’s disease with dementia. He was diagnosed with PD in 2015 and by 2018 with dementia. It was just so aggressive. His body wore down so fast, he had scary hallucinations. Once he broke all the windows in his room with a chair and yelled he wanted to burn the house down. He kicked us and wanted to run away. We knew it wasn’t him. It was the disease doing this to him. He would then fall asleep and wake up like if nothing ever happened. Towards the end stages, he was nonverbal, stared off into space. Sometimes he was mentally present but quickly faded away again. It’s very heartbreaking to see your dad, the family’s breadwinner and problem solver fade and get taken down so terribly by an incurable disease. It’s not fair 😢

@ParkinsonDotOrg 3 года назад

We're sorry to hear about your family's loss, Karami. We work every day toward better solutions with stories like your families in our hearts 💙

@Montanosluv 2 года назад

This is all so very scary for me because this sounds like my dad and the state he’s in at this very moment & I’m having a hard time excepting it because it happened very sudden It was one day to the next

@yisrahelgellman6971 6 месяцев назад

So true

@sandyd2527 8 месяцев назад

Diana, I'm there now. As a matter of fact I just came from the hospital because my husband's hallucinations and delusions are making him so agitated. My husband has said so many hurtful things to me. We've been together 35 years and I never taught that my marriage will go thru this.

@juvesteve 8 месяцев назад

Sorry to hear this. The personality and cognitive changes are something that I struggle to deal with. Stay strong, try to savour the good times.

@scottprendergast5262 6 месяцев назад

@juvesteve so sad, I am reading the comments and I see how people dont know just how good it is when health and sanity abound- Never any parkinsons here- But as a teenager (14) I was called upon to stay and take care of my mothers father, my grandfather, who suffered from post alcoholic leg paralysis and prostate cancer. Every weekend, Friday night to sunday, I slept over, fed, cleaned and kept him company- once there it suddenly seemed to me as if everyone else in the family figured it was not really necessary to go there anymore (not that they were frequent visitors) as I was now there. When he died a year later and had his wake everyone asked where I was, my mother told them : "His presence isn't really required here because he was there with poppy, taking care of him on hand and foot." 20 years later his son, my mother's brother, my uncle, (who said, when asked by my mother to help take care of poppy, "im not his f'king NURSEMAID!!!") Well, he was NOW ALSO bedridden with bladder/prostate cancer. Again, I was asked to please pitch in to help take care of him, which I did, until he died later that year in the hospital. At the wake, people, again, asked where I was My Mother once again stated : "His presence isnt required here because he lovingly took care of him for the last year... when no one ELSE came." I can relate in this way as sometimes familes do not want to deal with the horrible heartache AND pain of seeing a loved one slowly WASTING AND dying- in this case unbeknownst to me, caring is a calling as I could absorb these seemingly horrible situations I always reacted to them by trying to think of new ways to.comfort and make their moments better, helping every perceived need of the poor soul. I know this deeply because of that I commend you for your strenght, loyalty, loving and strong nature - as well as that ability to see the whole picture spiritually, which enables you to do what needs to be done..Bravo! I am now on my own and live in NYC. Life's gotten a lot better after all these years. Ironically now there's ansolutely no one left to care for.. except me, which I have never really been good at doing. That's a common malady suffered by caregivers. Try to do something nice for yourself now and then. Far from an expert I am not one who practices this. We will probably never meet but I somehow felt a strong need to reach out to you and let you know someone else cares and noticed you... the beautiful care you give. Happy new year God bless you. Scott Prendergast Brooklyn, NYC January 25th, 2024

@feedmechoc 8 лет назад

Only those who have been through what you had would understand. Take care and stay strong.

@sallymello1713 4 года назад

Thank you for your story, I am a nurse and take care of a man with Parkinson's disease. He has hallucinations , delusions, and paranoia, some days can be extrmely difficult. He has been on Nuplazid and after a year it stopped working, now he is on clozaril and seoquel but they are so sedating for him. So he takes them at bedtime only. May God bless you for sharing your story. People think I make up yhese stories. He accuses to of many things and I cry. I know he can not help it. Thanks again 💓

@CocoPuff689 8 лет назад

I remember taking my Mom to the neurologist and him asking if she was having any hallucinations...She said no...I said but what about the children and animals you see? Her response...I thought hallucinations were scary. In the later stages of my Mom's life I found the best way to deal with her hallucinations was to play along with whatever she said and reassure her. Worst part of my Mom's condition were the internal tremors she suffered with. She described them as feeling like snakes crawling inside her body. I spent many times crying because there was nothing I could do to relieve these symptoms.

@GK-mu5rn 3 года назад

I am so incredibly sorry for what you went through. May she Rest In Peace and I will pray for you.

@Nikita-nq6cw 3 года назад

God bless you... God bless all the parkinson's patients and family members!♡

@vickiwhitman2377 8 лет назад

Thank you for sharing Diane. My mother also suffers from Parkinsons and the psychosis as well. Please know that there are so many others who are dealing with the same situation and you and your husband. We too had no idea about this part of Parkinsons Disease. I pray for strength and guidance for you, your husband and everyone who suffers in any way from this horrible disease. Again, thank you for sharing your story.

@rick-ry3kj Год назад

I feel you, I took care of my dad during his final years with PD, I know what it feels like taking care of someone with this debilitating disease. It is mentally and emotionally exhausting. RIP Dad, I love you.

@margaretflanagan2146 8 лет назад

Diane, my husband is going through much the same thing as your husband, even the part about two of me. You are right, there is not enough information about this aspect of Parkinson's. Hopefully the new drugs that are being tested now will be approved and available in time for our husbands to use them.

@mrsjackieschannel 8 лет назад

Diane, thank you so much for sharing this. We are just starting to deal with the personality shifts and psychosis dimensions of Parkinson's. We had no idea (most books about Parkinson's don't cover the subject) that the night disturbances and the halucinations had anything to do with my husband's disease. We are just at the beginning (first 3 years) so knowing other's honest stories helps so much. By the way, we are happy too. We vow every day to walk in joy as well as we can.

@usertest5441 Год назад

No I'm no by ft r u u r6 r5 r6 5 fu hi

@whisperingeaglelanders2339 4 года назад

You have such a wonderful outlook despite your obstacles in your life now. The Lord is with y'all always!!☺❤❤❤

@lugandnut 8 лет назад

Thank you for sharing this - the lives of these two people BOTH ravaged by Parkinson's. My husband has it too, yet I doubt I have the strength to cope anywhere near as well as Diane seems to. We've lost everything but each other to this awful disease.

@deejaemma9021 2 года назад

Thank you for sharing, Diane. Recently my grandmother moved into our home. She is diagnosed with Parkinson. It is hard for our family to take care of her but I'm trying to understand the disease so that my grandmother can get the best treatment available.

@farofia2007 2 года назад

Thanks for sharing. Our lives are very difficult.

@user-fr2eq3hq9n 2 месяца назад

God bless and comfort you , there is always hope.

@Rebb88 3 года назад

Thanks Diane for sharing your story. It really helps people in the same situation. My 72 years old father also has Parkinson and it's like 1 or 2 years that he has psychosis, like hallucinations and paranoia. Most of the time he sees people in the house, sometimes are people he knows, like his little nephews, sometimes they are strangers without face or body parts. He doesn't talk much about his hallucinations and get angry if you talk about that. Sometime I see him drepressed and he doesn't talk much. I try to let him laugh or think about positive things, but it's very hard.

@CariCalifornia 6 лет назад

Thank you Diane...

@Loricampbellstudios 8 лет назад

Beautiful story, well portrayed. Thank you for your daily courage and sharing your experience.

@jrodt9 5 лет назад

parkinsons is a horrible disease. i miss my grandmother, this person we have with us today is not the grandmother she used to be. :(

@Sunny1414100 2 года назад

Thank you so much for sharing 💜

@SSK9s 6 лет назад

I am just about having to give up caring for my nearly 90 year old mum :( The paranoia that comes with her hallucinations are nothing less than terrible,,, terrible for her,, & terrible for me... I have had to hide the phone from her as she calls the police all the time about "Those strange men in the house, they scare me so much"!. To have your wonderful mother suddenly accuse you of "Leaving me with all those scary people, please don't make me have to do that again"!! This is just the tiniest bit of the tip of the iceberg. And this breaks my heart... We live 20 miles away from a large country town (Grafton NSW Australia) & the closest 'specialist' is at Coffs Harbor, well over an hours drive away, & it's not a drive I can do with my mother anymore in her paranoid & ill condition as she is almost completely crippled. No one can help, no one understands except for my mothers Doctor (a wonderful lady but her hands are bound regarding medications because she is not a 'specialist' & my mother cannot be taken to one so far away - and ffs, the specialist, of all bloody people, should understand this!). This really makes one feel like just giving up,, it's living moment by moment with her, with both of us sinking lower & lower, just struggling to get through each day. Parkinsons is one of the most insidiously disgusting diseases,, ever..!....

@sallymello1713 4 года назад

Have they tried cloziril. It helps some and seroquel. Prayers for you fot strength and peace. Again, I am so sorry. I get it.

@eshjane 2 года назад

Now that’s true love. Thank you for sharing

@rosered9029 5 месяцев назад

Thank you sooo much for this. ❤

@steveainsworth4656 7 лет назад

Thanks for posting this. My mother started hallucinating 3 weeks ago. It's mentally stressful for all concerned.

@nanno8483 Год назад

I was led to you through a RU-vid search on this topic. My father in law has displayed these symptoms for several years but he did not share his diagnosis (he does not believe it). Your video was so helpful to our family. Thank you so much for making it! Good luck on your journey

@xmasfolly 3 года назад

Thank you for sharing this. It is very helpful to know we are not alone.

@rodnichalet8429 6 лет назад

May God bless you. We are going through this with my father who is suffering from Parkinson disease psychosis. Thank you for sharing your story and making us feel that we are not alone with this debilitating aspect of Parkinson. Take good care and stay strong.

@SEllisASH Год назад

Thanks for sharing. I have Parkinson's and my husband is my caregiver. I know its a thankless hard job,

@ParkinsonDotOrg Год назад

You and your husband are not alone. We have resources for people living with Parkinson's and those who love them: 1-800-4PD-INFO (473-4636) | Helpline@Parkinson.org www.parkinson.org

@joannemosley3433 9 месяцев назад

Thank you for sharing, and may God be with you and your husband.

@ravenwings1131 7 лет назад

Thank you so much for sharing. My dad's had Parkinson's for a few years now and he's been seeing tigers in the corners of his eyes. Sometimes he wakes up dreaming that tigers are attacking him. He's asked me what that's all about and I told him I didn't know, but now I can tell him. It'll make him feel better, I hope.

@rnw2910 2 года назад

Thank you for sharing your life story. You make a loving example. Your work with your husband a true effort of love💗💕

@beatlejuice42 3 года назад

Thank you !!

@koagoodgirl1608 7 лет назад

Thank you so much for sharing. This is familiar to what I am going through. We are not alone !

@meduffer 7 лет назад

Thank you.

@normanrowe2831 5 лет назад

Thanks for sharing. I understand 100% I am a caregiver for my 100 year old mother. She is in late stage parkingson's and dementia. It's hard.

@jenniferlopez4510 6 лет назад

May God bless you!

@KoolT 11 месяцев назад

Thank you so much

@MyMikey65 2 года назад

My wife's psychosis is getting worse .She gets mad at me when I don't see all the people around her. She makes me go in another room to whisper things so the "other people" can't hear. She often considers me an enemy. It's so hard to deal with.

@987work 8 лет назад

My husband and I are going through the same problems that you are experiencing. When I spoke to our Neurologist about this, he looked at me for a minute or so and never said a word to me about the problem. It helps to hear from people who understand. Thanks for sharing.

@timbiglow9676 Год назад

Thank you

@terry3596 5 месяцев назад

Thank you for sharing this video. It's informative and a little scary to know what's ahead but I need to get myself prepared. My husband is in year 6 with PD and I'm seeing personality changes. I will strive to be as strong as you.

@annamariacantalupo9634 28 дней назад

Hello, Dianne...you are not alone.. my husband has the exact same symptoms and unfortunately, I had to put him in a nursing home in February.He took me for another person and said exactly what your husband said that someone was stealing money... I could no longer care for him on my own... it was impossible.. he became violent and I had not slept at night for 2 years... it really broke my heart to have to put him in a nursing home... I also miss the husband that he was years ago. 😥😥I pray that God gives you the strength to care for him... I could no longer lift him anymore....I feel so bad but unfortunately, this is the sad situation. My best to you., ❤

@michaelm3052 7 лет назад

Thank you for this video. I 'm my father's caregiver. The doctors said it was alzheimer's and dementia. This is so very similar to what my father is going through. I've suspected it all along, but those doctors didn't want to hear my opinion.

@melissasparber8443 7 лет назад

Michael M psychosis is a symptom of several different illnesses so it may be what they said

@anthonygulliver2880 Год назад

I have Parkinson’s I am 56. Thank you for this documentary . I have his delusion of seeing a cat this evening I thought I saw our ginger cat in my bedroom but it was in fact my dressing gown. This happens often. I am British and I’ve in England. Your documentary shows how m7ch you love your husband. Thanks for sharing ❤

@masoodkhalid21 2 года назад

God bless you all

@paddyolten4031 4 месяца назад

Thanks 🙏 ❤

@valelliott2106 Месяц назад

Right here with you.

@dbc2269 2 года назад

Keep your head up sweetheart ❤️

@iamraynash 7 лет назад

You are not alone Diane, even we here are suffering from the same.

@edesir 4 года назад

We need to start educating everyone on Parkinson’s and how it can affect the mind so once the onset of the disease begins they won’t be so much in denial of what they see. I find that people with a lot of previous drama in there life are the worst when PD kicks in.

@junemarcotte8863 Год назад

Thank you for sharing it sounds like my life. The phycosis has gone now and it is more the physical help he needs now but as my mother always said must is the master and we carry on.

@yvonneaucamp5348 7 лет назад

Thank you for sharing. Diane. We have been going through a tough time the last couple of months with severe hallucinations and delusions, which are now much less severe after discontinuing use of an antidepressant. But now at least after your video I know what to address with his neurologist on our next visit. But yes, it's a difficult journey for us caregivers as well.

@teresapuga9181 3 года назад

At 80 my father thought my 75 yeard old mom was cheating on him. She's been the most loving, caring, and loves my Dad more than herself. Parkinson's is a very sad disease.

@rkmugen 7 лет назад

I have no siblings, no other parent, I was fresh out of college and just started my career. I lost my job and have been 5 years unemployed because of the stress of caring for my parent with PD. Now the relative who is currently taking care of my parent is threatening to take my parent's home, the one I'm trying to hold together for him, so they can put him in a nursing home. I just got a new job and am still on probation. There is no way I can afford to take care of my parent with or without my new job. I am more than 30 years under retirement age. I live in a suburb of San Francisco. What am I supposed to do? The house is under my parent's name, and I don't know any legal stuff. I can't afford to pay for a lawyer. I don't even go to the doctor to take care of my immediate medical needs. What can I do?! I don't want to kill myself.

@amychoulat834 4 года назад

I hope things got better for you.

@morganmaguire5529 4 года назад

I'm from Ireland and going through a similar situation. I hope and pray that everything worked out for you and your father. It's far from easy, just the stress of watching someone you love suffer from PD is hard enough but to have all that in the periphery feels like the whole world is against you. All that gets me through is that both my parents done the best for me so I owe them to do the best I can. Take care and god bless.

@faridaomar2655 Год назад

Thank you so much for this video. For those who are caretakers , get more stronger everyday. Be closer to the patient to let them know that they have their people who care for them ❤.

@ParkinsonDotOrg Год назад

💙💙💪

@faridaomar2655 11 месяцев назад

This organisation does good work .❤❤ Always be blessed

@djbirdsong4868 2 года назад

Thank you for the video. Its somehow comforting to know that we’re not alone taking care of our loved ones

@nanayg1953 3 года назад

Very similar to our story. 😢

@yearofthedragonjane Год назад

I needed this. My dad experiences this

@ParkinsonDotOrg Год назад

Know that we are here for you and your family 💙

@carolbrett6231 2 года назад

God bless you. I know just how your life is. I am a caregiver to my husband too. In same circumstances. You are doing a great job, and the best you can.

@maryamshariat6830 7 лет назад

thank you for sharing your story. stay strong

@JulieR73 2 года назад

My mom died 4 years ago after a 22 year battle with Parkinson’s disease

@Wisdom_Tale 11 месяцев назад

How old was your grandma? How long can one live with stage 5 ?

@radhekrishna3650 11 месяцев назад

Thankyou ohh dear divine mother universe❤❤❤

@chocmagic4846 2 года назад

Yep...very similar.but boy! I find it hard

@Deepika-tp1jd 5 месяцев назад

Same 😢

@KoolT 11 месяцев назад

My husband passed from this. He got it too. It happened after l dopa. And paranoia.

@ParkinsonDotOrg 11 месяцев назад

We're sending our condolences to you and your family 💙

@laj9832 3 месяца назад

My husband started having sundowning when he was switched to slow release madopar. And he became suicidal. It turned out they had built up too much in his blood and by the end of the day he was getting pysychotic. I reverse him off them and put him back on the previous dose of instant release madopar white tablets and he soon came right. Several years later he is doing well and the behaviours never came back. If the behaviour starts within weeks of starting a new or increased medication there is a good chance the symptom is caused by the new medication so try slowly reducing it and phasing it out. Tell the doctor what you re doing!

@Vbluevital Месяц назад

Good advise, Thank You My brother is suffering acting on unfounded paranoid thoughts. I read some studies which did state similar findings. Do you know if an increased dose of carpadopa levadopa can escalate paranoia and sleep problems?

@Vbluevital Месяц назад

Please pardon me, spell check .

@darlenegattus8190 Месяц назад

Im dealing with my Fad right now and my Mom has dementia. I am so overwhelmed.

@ParkinsonDotOrg Месяц назад

Know that we're here for you as a care partner. 🩵 We have resources that may be helpful to you here on our website: www.parkinson.org/resources-support/carepartners

@darlenegattus8190 Месяц назад

@@ParkinsonDotOrg ty!!

@gailcunningham182 Год назад

My MIL has Parkinson's Dementia. If you want to learn more about Parkinson's, check out any RU-vid videos with Teepa Snow. She is a wonderful professional and she discusses how to interact with someone suffering from this disease. It will open your eyes and help make this difficult situation more doable.

@ParkinsonDotOrg Год назад

To learn more about dementia as it relates to Parkinson's disease, we recommend visiting our website: www.parkinson.org/understanding-parkinsons/non-movement-symptoms/dementia

@Plainsman1300 Год назад

Have you looked into dket?

@watchensee 6 лет назад

Is this an actual part of the disease, or is it just caused by the medications? :(

@jayleehightower8322 6 лет назад

I believe it's the medication, but the doctors won't agree.

@ParkinsonDotOrg 5 лет назад

There are three main contributors to the development of Parkinson’s disease-associated psychosis: 1. MEDICATION The most common trigger of PD psychosis is medication. 2. DEMENTIA 3. DELIRIUM We recommend reading our free book on Psychosis: A Mind Guide to Parkinson's Disease for more information: www.parkinson.org/pd-library/books/Psychosis-A-Mind-Guide-to-Parkinsons-Disease

@CarmenGonzalez-xq9fu 5 лет назад

I'm going through so much my husband has Parkinson's over 10 years how he developed Dementia now that's a problem He see people in the house men having sex with my and we are the only one in the house ..he's very angry calls me names this is now day and nite 😥Any advice for me ??

@ParkinsonDotOrg 5 лет назад

Hi Carmen - We are here for you. One of our Foundation’s greatest resources is our toll-free Helpline. Our PD Specialists are here to support you with current disease information, emotional support, referrals to health professionals, local resources and more. Please call 1-800-4PD-INFO (1-800-473-4636) or email helpline@parkinson.org. parkinson.org/Living-with-Parkinsons/Resources-and-Support/Helpline

@priyapaul7490 2 года назад

@@ParkinsonDotOrg m

@ushasaseendran1892 3 года назад

My Father😢

@juvesteve 8 месяцев назад

Such a horrible disease

@kokewolfxo9710 2 года назад

You know it’s just going to get worse. Stop being selfish and pull a million dollar baby and put him out of his misery. I hope someone would end me if I became a mush brain burden.