My oldest son recently told me that his younger brother, 20, who has a summer break from college coming up, confided that he wants to come home to be with me, but can't live with his father, who has severe frontal lobe dementia due to CADASIL. For years our 3 boys have lived with their "quirky" father who seemed socially vacant and not available for any of us emotionally, unless it was by his unpredictable anger that caused such destruction to us as a family. Now he's disoriented & deconstructing, defiant, anxious and has logorrhea (never stops talking & is demanding of attention); he never sleeps & won't let us sleep, knocking on our doors all night. This abyss of dysfunction is shortening my life, I'm sure. And it's cumulative from decades of having to move state to state every few years due to my husband's job losses, and his bullying behavior, both probably due to the disease.
But, I didn't realize that my son, who's trying to find out who he is, yet is still a child & needs his family, is so torn. Now, without resources to place my husband in memory care I have to decide to let go of him to the care of others at great loss, ironically in particular, the sale of our home. If I don't do that, I feel that I'm going to be committing great harm to my son by shunning him from returning home; I have incredible guilt, but I choose my child over my husband. To make matters worse, CADASIL is inherited, and my boys have a 50% chance of having the same disease as their father: I had wanted to save as much money as I could for their long-term care should they inherit the autosomal dominant gene. I feel guilty...no matter what decision I make. Has anyone else been confronted with these choices?
My dad wanted to do most or all the caregiving for my mother as her Parkinson's progresses, and after 10+ years he's so exhausted and angry. I've recently realized I needed to take over their finances, do all the Medicaid planning, generally take the reins, and it's been much harder because my parents have been living in a fantasy about what my dad can and can't do. (Also, yes, Medicaid planning!)
There was a summer I spent at home as an adult (much older than your son) that was very helpful, but I'd say looking back I wish my parents had created some healthy boundaries and expectations for my dad's caregiving years ago. In other words, I wish my dad had taken better care of himself. Not only would it be less painful for the family, but it would even have been easier for me in the long run.
I faced a lot of pressure to be a martyr growing up, while practical, sustainable help I offered was often rejected (things like managing caregiver visits or setting up medicine reminders). I'm not at all saying that's what's happening here, just that your son needs to create healthy boundaries, and he needs to see examples of what they look like. Whatever help you can give him now may be important, but also in the long run taking care of yourself will benefit both you and your son.
Oh, to add one more thing, they did the best they could. He's doing the best he can. So is she. I do see that.
As for your son...I was afraid to leave my husband so I stayed the entire time we were raising our child. I'll never know if I had left if he would have turned out emotionally healthier or not. He is full of anger (and is now 45 and still full of anger), committed a felony when he was 22 and will never get a great job, and I don't know if he would have been the same way if I had left when he was still a child. (He is very much like his dad was.)
Your son sounds like he could use the emotional support of his mother. Oh how I wish I had been emotionally supportive of my son, but that's water under the bridge. I do not have a close relationship with my son. He says he doesn't blame me for staying with his dad (his dad was also abusive to him) and I'll never know if it would have made a difference.
We can't change the past, but we can do what we think is best for the present and future, for yourself, if not for your son too.
It's a hard decision to make, even harder to follow through, my thoughts and prayers are with you.
Absolutely. In many ways it can be worse, especially for children growing up. The big problem is no one sees the "bruises" and damage it causes. It is also sometimes insidious in that it starts slowly and builds, so at some point you begin to believe it is your fault.
First it is not just a matter of your husband or your child but also of you,.
There are statistics that show often a caregiver dies before the person they are caring for. If you have had years of this it is getting to me more than you can manage. And it will not get better.
In your case placing your husband is becoming a necessity not a want. And I do not say that easily. I always said I would keep my Husband home as long as it was SAFE, Safe for me to care for him and safe for him to have me care for him. It is sounding like this is becoming unsafe emotionally, mentally and possibly physically as well.
Are there medications that would help lessen the anxiety that your husband has?
One of the things you should do, if you haven't already is talk to an Elder Care Attorney to see what options there are for you. An Elder Care Attorney will also be well versed in other things you can do, Medicaid, if your husband is a Veteran...
I am sure one of the thing in your sons mind (maybe all of them) is what if I have inherited this gene? If there is as you say a 50/50 chance that is scary. Personally I don't know if I would want to be tested. And the thought of the prospect of this might also prevent me from making deep personal connections in my life. I don't think I would want to marry or have children. Every headache would scare me.
Do your other sons live with you or nearby? Can the 20 year old stay with them? Or a friend for a while during the summer?
It would be great if he could put aside his feelings and help you out a bit, it sure would give you a break. But this might be a bit close if he is thinking this could be him in 20, 30 years.
However try Medicaid.
Get some help for you and your husband. Try not to loose your home. I’m truly sorry anyone has to go through dementia/Alzheimer’s. Whether it be the patient, spouse or children. God bless and keep you.
I have a son living with me. He was here before my second husband. My second husband has frontal lobe dementia. He’s getting worse. He wants to sleep all the time. His family has a lot of advice but they are no help. My son will watch him since my husband no longer wants to do anything. But my son says mom I’m not changing him that’s not my dad.
what I’m saying is your son could be a big help. I know you’re torn. I also know the sleep deprivation. It’s hard on one person.
May God be with you and help you
If my kid/adult, I would be pleased they wanted to come see me & doubly pleased they could draw their own boundaries regarding where they are prepared to live, who with & what they will/won't accept that may damage their own well being.
I applaud your son too for helping but also drawing his own boundaries.
If there is a genetic test for CADASIL that your kids can get, they might want to know if they have it. If they test negative it would alleviate any angst and if they test positive, they can plan accordingly and make there wishes known now of how they want to handle it. After watching their father, I am sure they have opinions on the matter. Just a suggestion.
All your advice would do me no good at all. We did a reverse mortgage just to stay in our house. I don't have the luxury of hiring someone to stay with dh (which is why having my 40yo boomerang son living here is a help, at least I can ask him to stick around when I go out, he carries in groceries, and handles the "man" work around the house). I don't have friends to go out to lunch with or any other activity because when your life has been totally dominated by a husband for years, there is no one else in your life. My big outing is the grocery store.
Good luck xx
I can only imagine, having grown up with this man and his "quirks" has done some emotional damage to you and your sons. It is a good thing that your son wishes to come home for the summer to be with you, but his reservations are valid.
As others have said, getting your husband the care he needs, should it require a facility, should NOT overburden you. There are protections in the Medicaid system that allow for splitting "liquid" assets and preserving the home for the "community" spouse, aka you. You would be wise to consult with an EC atty to make sure you are protected and then see if he might qualify for Medicaid. Any assets split between you (it isn't always a 50-50 split, they have formulas for ensuring YOUR income and assets are sufficient to preserve your lifestyle) would be used for his care initially. After those assets are used, Medicaid would take over - it is income based and varies by state, so you really need to speak with an EC atty to know where you stand.
Since summer is so close at hand, are there any options that might allow your son to return home, without having to deal with his dad? If your husband needs care, perhaps you could hire someone to care for him and find a summer rental for you and your son. If not, is it possible to at least find a place nearby for your son to stay over the summer, so he isn't exposed to your husband, but you can do things together while he is here?
Are there no medications that might address some of his symptoms? While there isn't a cure, toning down some of his behavioral issues could be helpful. In the end, you will most likely have to find a place for him, for your safety and his. It is important to consult with an EC atty, to get everything in place now while you can. If you don't have POAs, wills, etc set up, these need to be done asap, if your husband is still considered competent (The atty can talk with him privately, to determine if he feels competence is ok - my mother was in the early stages of dementia, and we needed to address some issues. We had POAs and will done previously, but needed to protect her assets from herself or unscrupulous people. He chatted with and queried mom apart from us and determined she could still make the decisions needed.) Many EC attys offer a limited free first consult, so have your questions and concerns, plus information about assets and income ready before you meet to get the most from your free time. Take notes to compare with others. Try several before you decide on one. The atty can also give recommendations about how to approach placement and assets, as well as Medicaid (from doing lookups to try to answer other questions, I have noted there are differences in income limits for "traditional" Medicaid, aka insurance, and LTC Medicaid (it is higher for the LTC.) Your best bet is seeing an EC atty.
As for your sons and their futures, would they object to being tested for the gene? Some people just don't want to know. It appears that they can have it, but that doesn't mean they will be impacted. Knowing more about it and how to lead a healthier lifestyle can help minimize the onset or impact. Keeping BP in check, not smoking, etc. If they were to develop symptoms, you'd all be aware and know how to "deal" with it, plus advances in medicine might have some kind of treatment in the future. None of us know what our futures hold, so we can't live in fear of what may be. Knowing there is potential for something like this might help them make better choices now, and focus on living the best they can.
Hoping you can at least find some respite for him, and allow you a break and allow your son to come home without concerns.
CADASIL was new to me, too - I don't know where we'd all be without Wikipedia! - and it even sounds as if it's comparatively new in the world of neurology, as a distinct syndrome at least.
One rule I would stick to is not to try to understand others' points of view from second-hand reports. For example: thank your son for telling you what his younger brother said to him, then call your youngest son and encourage him to tell you what he's feeling. For this to work, he will have to understand first that - in the classic phrase - "it is okay not to be okay." It is okay for him not to be able to tolerate his father's disease when what he needs is to rest and unwind and prepare for next year.
But never mind that for the time being - communication is a big subject and you will develop your own ways as you go along. Meanwhile the here and now: what are your next steps?
Agree with SendHelp - doesn't have to be all or nothing thinking.
Can you look into short term respite care instead? Try all your local NHs. Try for 4 weeks.
You will get a break (I'm sure you need one). Son can stay in a more harmonious home, even if for a shorter visit than he planned. Your DH will have the experience of being cared for by others. (This may seem like a bad deal for him but he will need other non-you care at some stage I am guessing? Plus: who would care for DH if you were ill or injured? Having a respite backup is quite prudent.)
So it would be a compromise for all 3 of you. Anyway, that's my suggestion.
Your boy needs you. Let him come home.
Once DH is placed, then you make decisions about your son as you wish. You're not 'choosing' your son over your husband. You are making the only decision you can possibly make here, for everyone's benefit, and that is placing your husband. From there, all other choices and decisions can be made.
It is never a mistake to allow a child to move back home for a while. My own son was about 21 and going through a bad period of life when he asked if he could move back in with me for a while. Of course I said yes! How on earth would allowing him to move back in with me for 9 months 'retard his growing up'? In fact, what it did was it allowed him TO grow up by giving him a chance to pay off credit card debts he'd accumulated, unwisely, and stop drinking to excess, and to clear his head. A parent's door should always be open to her children. My daughter moved back in as well when she was about 20, for about 18 months while she went back to college to pursue a different degree. She's now a successful RN and her life is grand. Moving back in with mom and step dad surely didn't 'retard her growing up' at ALL!
Wishing you the best of luck with all you have on your plate right now. Please don't add guilt to the already heavy load you're juggling.
I don't know you, and this may sound harsh.
But choosing between your son and your husband is not an issue here.
You may be stuck in "All or nothing" thinking.
Or another cognitive error: Catastrophizing, over-thinking, or just panic.
You wait, you will find a much easier answer to all your important concerns soon. Just keep talking it out here, others can help you refocus on some viable solutions.
You haven't shunned your son. He can either grow up (which is what your 20s are for, or come home despite Dad. It is up to him. You are choosing the husband who you vowed to choose at the get go.
This isn't a fix-it situation. Everyone can't be 100% happy and you aren't responsible to make it so for them.
I am sorry and wish you the best.
I wonder if the sons should receive a test to determine if either or both carry the deleterious gene.
If you sell the home, it needs to be at Market Value if Medicaid is in DHs future. Most states the look back is 5 years. And if you sell, I would think 50% of the proceeds would be considered yours with the other half going towards his care. You need to talk to a caseworker at Medicaid to see what options u have. If it gets too confusing then consult with a lawyer well versed in Medicaid.
If your DH becomes violent, then call the police. He may be taken to a Psychic facility for monitoring. If this happens, tell them you are now afraid for your safety and he cannot come back to your home. If he lands in a hospital and/or rehab. Have him evaluated for 24/7 care. If found he needs it, tell the SW that you cannot care for him at home, have him placed in LTC and start the Medicaid application.
This is not the man you married. From what you describe he needs more care than you can give him. Seems to me he needs serious medications. You don't have to do this. At this point, yes your children and you are more important.
I had never HEARD of CADASIL before and after reading about it---my heart aches for you!
For what you have been through and for the knowledge of what is to come.
For WIW, MY choice would be my child, over my DH, no matter what. Esp when your son is still relatively young and needing you more than he thinks he does. He's had a 'different' upbringing due to his dad's condition---and I personally think he is owed some 'normalcy'.
Are you placing your DH in some kind of care facility? Or saying that it isn't possible?
You have no reason to feel guilt. It's a 'Sophie's Choice' situation, truly, but you are right, I think, to choose your son.
I hope you come back and lean on us for support--the little I read about this disease was just heart wrenching.
Perhaps others on the forum have had similar experiences and can help.
I certainly hear your pain and understand that you have a lot on your plate and important decisions to make.
I hope that you will find viable situations as you travel along this difficult journey.