My depressed and delusional husband (67) refuses to believe (or more kindly, "lacks insight") his diagnosis of Parkinson's dementia AND major depression with psychotic features. However, he is very smart, not suffering other cognitive problems, and most of the time can articulate his wishes. Since 2018 when he was first diagnosed with Parkinson's, he has refused treatment (from neurologists, psychiatrists, physical therapists). Why? His reasons, as I see it, are a complex combination of a lifelong resistance to medicine and newfound fears and delusions (for example, he insists he has no health insurance, owes thousands, and is being sued by medicare). I have a Med-POA. Since his new diagnosis of Parkinson's with dementia in March (which landed him a short stay in a geri-psych hospital) he's been on namenda, seroquil and anti-depressants. Thus far they seem to provide no relief of his depression and delusions. He's getting by--not well, but not in danger. (We don't live together, he's in independent living nearby with 3x meals and 2x per day aide drop-ins). I still hope we can find an effective medication for him. So here's the problem: We go to his psychiatrist, where my husband insists he doesn't want any increases or changes in medicine -- would prefer to be off them altogether. He doesn't like the way they make him feel, he says, and then argues that his problem is not in his head. (This is, again, delusional. He believes his body is failing systemically and doing things like "sweating excrement." Yes, we've ruled out physical ailments). So then the Dr. turns to me and says "Well, you're the MPOA, it's up to you to say yes to a change in his meds." What? But my husband's not in coma, he's sitting RIGHT THERE -- saying he doesn't want it. And his refusal is not completely illogical. He's battled depression his whole life and has never wanted to be on meds for it. Now he doesn't want anti-psychotics. Anyway, so I'm put in the terrible position of either (a) directing his meds against his wishes, (b) discussing, arguing, begging, and cajoling him to try news meds, or (c) letting him make his choices. On the one hand, I feel like I should just override his wishes and tell them to go ahead and change his meds. If my husband doesn't want to take them, that's his choice but at least I will have fulfilled the responsibility he conferred on me when we did our MPOAs years ago. On the other, he's capable of understanding why certain meds are advised and of articulating why he doesn't want them -- a test for competency that has led other Dr.'s to reject my attempts to override his wishes. Apparently competency is a fluid definition. Also, this is a gray area because, let's face it, different anti-psychotics may or may not help. It's not like I'm faced with a decision to give him surgery to save his life or keep him on a respirator. It's more like making a decision about giving chemotherapy to someone with advanced cancer. In the end, it comess down to a fundamental difference in the way my husband and I have always viewed life. I think it's worth saving at all costs and he doesn't. (When I went through a bout with cancer five years ago and was faced with an ambiguous choice about chemo, he suggested "don't do it". Good thing I DIDN'T listen to him). So what to do? We're seeing his psychiatrist this week. Change his meds in the hope of improving his state? Let him live with his delusions?
Ask for some anti anxiety meds for him, i bet you will see a huge difference with small doses 2-4 a times a day.
Research every medicine that any doctor suggest, talk with your husband about what you learned and give a recommendation, start with the least amount you can, don’t force anything and add one medicine at a time. Let him win, it is his life. If he goes on a medicine and tells you he doesn’t want to feel that way, listen intently. With dementia, at some point, you will have to make the med decisions but from what I think I understood from your comments, he seems capable. Hope you feel comfortable with whatever you decide, don’t feel rushed, do your research. Hugs to you.
I stand with the answer provided by Musicismymuse. I'm not in favor of too many meds....the side effects can ruin your life and affect those around you in a negative manner. The answer to life and its challenges, as well as a calm and beautiful passing lie with our Lord and Creator, Jesus Christ. In a case such as Bipolar, meds may be helpful....but, with dementia, Parkinson, and other age-related issues, a firm foundation of faith in God Almighty is essential, Plus, proper nutrition is key to healing of these maladies. Our bodies are fearfully and wonderfully made by God, and if properly nourished, can and will destroy cancer, diabetes, dementia and even Alzheimers. Amazing but true!!
You and your husband need to listen learn and change your dietary lifestyle. I'm 66, healthy, strong, and lost my belly fat, just by following some of his suggestions! Again, amazing but true!!
So, 2 things: Come before Christ the Lord, ask Him for His forgiveness as all of us have broken His moral laws and are headed for Hell. He is just, perfect, and because of Christ's death on the cross, for us, He paid the Penalty for our transgressions, resurrected from the dead to ensure our Eternal destiny, and all you need to do is Repent of your sins, and ask Christ to save your souls from Hell! He will! It's wonderful! Read your Bible and pray to Him!
Your health will improve, and fear of death will be gone, because you know where you'll be spending eternity!! Forever in Heaven with Jesus, the Son of the Living God! Shalom! 💜🕊💜
Can you call his dr and share this with him ?
I have Mom living with me and she is end stage COPD & CHF. The stress is unreal, and every day I have to remind myself I am privileged to see her through the end of her life.
I wish you the best in a very difficult life situation. ❤️❤️❤️❤️
Whenever I hear of a doctor making a blunt statement such as this one, I think of the joke (well, it's sort of a joke) that doctors think MD stands for "minor deity".
Hope you don't mind the levity. I know you are going through a rough time.
THEY GAVE THOSE TO MY SISTER AND IT WAS TERRIBLE! YOU SHOULD NOT GIVE THESE TO SOMEONE WITH DEMENTIA! MY SISTER STARTED HAVING TERRIBLE FALLS AND COULD NO LONGER SPEAK AFTER THEY PUT HER ON IT!!! THESE DRUGS ARE DANGEROUS!
YOUR HUSBAND KNOWS WHAT HE IS FEELING! YOU ARE MAKING A MISTAKE GOING AGAINST HIS WILL AND IT WILL HURT YOUR HUSBAND ...I'VE BEEN THERE!
Although you did what was right for you (the chemo), why do you not understand that what HE wants to do what is right for him? My mother had dementia, but after I changed her diet and took away ALL grains, her mood and health greatly improved. People don't die of Alzheimer's, they die WITH it. They can die of broken hearts, loneliness, malnutrition, dehydration, etc., even with the best care and meds. When it is my turn, I hope that I can just 'pop off' in the arms of my loved ones, not in some sterile, unfriendly hospital hooked up to wires and zonked out of my mind.
This way of dying that people regard as 'normal' is not normal at all and has only been around for a short while in comparison with natural death. My father had cancer and a brain tumor, and he had NO pain and no medication. At all. Again, he was at home and had just seen the last member of his family that he wanted to say goodbye to. And with my mother, I told her she had been a good person, and the best mother to my sister and me and that whenever she thought it was time to go, we would be OK. She died the next evening, after a beautiful day of viewing photographs and listening to hymns.
There will be many who will disagree adamantly with me, but there are, I know, many who will understand that, "Life is not measured by the number of breaths we take, but by the moments that take our breath away."
When it comes to addressing the issues with your husband, you won't be able to convince him about the insurance or the sweating excrement, as you realise. So acknowledge his feelings but don't argue the case. State that this is your responsibility and you have decided to agree to a time-limited trial with the aim of relieving the symptoms he is experiencing.
I understand your concern about his different approach and I very much respect your respect for it. You are right on the money ethically. But you're not aiming for a cure, you're aiming to improve his quality of life and conserve the intelligence that is such an important part of him. If the meds help, great; if not, you and he have lost nothing.
The thing is, his thinking-through process at the moment has such major flaws in it. Yes he is taking in the information, yes he is processing it; but there are too many false beliefs at play for him to be actually rational. And as you rightly - again - remember, that's what he gave you MPOA for: to make the rational decisions on his behalf. This isn't life at all costs, this is a calculated (and reversible) decision aiming to restore function.
I believe way too many people are on way too many meds, especially the elderly.
You and your husband are different and think differently and meds can do more harm than good and you should let your husband make that choice himself, as it is his own body.
Im sure if the roles were reversed, you would want your husband to abide by your wishes.
You should also assure your husband that he dies in fact have Insurance to cover everything.
Believe me when I say that most Seniors are on a lot of meds they don't need to be on.
My 97 yr old Dad decided to stop all 12 of his meds 4 yrs ago and he always has good vital reports by his Nurse except she tells the Caregivers to get him to drink more fluids.
He does have an enlarged prostate that he was taking pills for so he did have to get catherized but at 97, you can't be getting up all day trying to make it to the bathroom to urinate and I was afraid his Caregivers wouldn't change him enough and wearing wet diapers he would end up with bad rashes.
In closing, let your husband do what he wants.
The doctor is turning to you to make the decision because your husband has dementia and is delusional.
anxiety. It’s progressive aggressive
illness. The best thing you can do
is try to make him comfortable !!!
seroquel antidepressants articept patch and Ativan (when needed) helped a lot ! ! ! It didn’t stop or reverse progression but helped moods and behaviours !
also I would find a really nice MC where he would get the attention and care he needs and deserves.
good luck with all of it … you’re on your own with this cruel disease
And I second the suggestion to read "Being Mortal."
If I had asked my dad if he wanted a certain medication he would have always said no but we added and discontinued meds as needed to help with his behavior and his depression and anxiety. At times he would refuse to take the meds…especially at the end years because he thought they were keeping him alive and he wanted to die. We couldn’t change his refusal but we knew we had done our best!
I am so very sorry that you are struggling with this situation. My mom recently died in a hospice house with end stage Parkinson’s disease and slight dementia. She was 95. She took Sinamet and was prescribed Seroquel towards the end of her life. While in hospice, she had Ativan when needed.
I cannot imagine how stressful this situation must be for you. I hope you don’t mind a brutally honest answer from me.
You know that your husband is delusional. You know that he has suffered with depression and has a neurological disorder. Parkinson’s disease in itself is brutal. It is a progressive disease without a cure. I wish that I could have taken this wretched disease away from my mom and I know that you wish the same thing for your husband, but no one can erase Parkinson’s disease from their loved one.
I seriously don’t feel like you have any other choice but to override your husband’s delusional thoughts and order the necessary meds for him. Yes, it’s trial and error. You know that what he is taking now isn’t working, so back to the drawing board. I hope the next drug cocktail will be applicable for his needs.
Best wishes to you and your husband. Keep us posted. We care.
Think of it this way...if he was driving a car. On some days he did great. On other days, he could kill someone. Wouldn't you take the car away? Thus, his delusional thoughts do not help him or keep him safe and therefore you must consider the medications.
If he is not incompetent then in theory he can make his own decisions. It should be that he gets to make decisions until he is declared incompetent THEN your MPOA becomes effective. It should not be that you make a decision for him in this matter but he can make a decision for himself in another matter.
The Parkinson's can not be cured.
The Dementia can not be cured.
All that you can expect is that death will be delayed.
With some dementia is delay a good thing?
He has valid points as do you.
By the way side note here. If you do not have a POLST completed for him (POLST has different names in different states but it is MUCH more detailed than a DNR) Please get one and discuss it with him while you can, while he can. It does go over different "life extending, saving(?) measures" Since you and he seem to be on different sides of the same coin this will get his wishes down and save you from agonizing decisions that you probably do not want to make.
Perhaps you're treating the wrong issue. He doesn't want the medications, so what can be done to promote quality of life over quantity, which you seem to know is his wish?
Talk to him and his doctor about what can be done to enable him to maintain his current level of independence as much as possible. Perhaps it means moving to assisted living to ensure he doesn't become more of a fall risk.
You don't live with him, so who is going to make sure he takes the meds. Not the aide unless she is a medtech or is an LPN. Aides are not allowed to administer medication. They are not medically trained. They can remind. They can't administer. Not even do a pill planner. Maybe thats why the Dr. said its your decision because he feels your husband is not competent to make his own.
"Parkinson's dementia AND major depression with psychotic features. However, he is very smart, not suffering other cognitive problems"
Is Parkinson's Dementia different from other Dementa's? To me what you describe here is a man who is not competent to make his own decisions. Being smart has nothing to do with Dementia. In my opinion, your husband needs more care than he is getting in independent living. He also needs meds.
I may not understand this properly, but when you have MPOA, doesn't that mean that the person is not competent if the doc is asking you to make the decisions?
Do you think he is really competent enough to make his own health care decisions? If so, then step aside and let him handle it. I wonder though since he's in AL because he needs some help and is not thinking at 100% anymore.
If he's always been anti-med, then I guess you do have to consider that. But was that anti-med mentality made with a clear mind? I am pretty anti-med and do not have any psych issues, etc.
Maybe a compromise would be to increase/change meds to for a pre-determined period of time to see if he improves? If not, back them down again?
Good luck.