Introductions: Are you caring for someone with dementia?
My mother-in-law (MIL) had what was finally determined to be frontal temporal dementia. She had the disease from her 60s until she passed away at 86. My wife was especially involved in her mom's caregiving due to some serious denial in other family members and a GP who refused to diagnose, even when significant deficits were obvious (mistaking the UPS deliveryman for her husband and not knowing the difference between roads and sidewalks). The most unfortunate result of this, to me, was the lost time when my MIL and her family could have been having meaningful and important discussions about significant matters of importance to her and them.
In my wife's years of fighting her brain cancer, she, too, exhibited many of the aspects of mental degradation and physical losses one would affiliate with a dementia patient.
As an aside, for several years I worked for the national Alzheimer's Association raising money for their research programs nationwide.
I wish everyone struggling with this disease and their caregivers and families strength and peace.
Interested in more discussions like this? Go to the Caregivers: Dementia Support Group.
Hi - I am new to this forum and have very much appreciated all the information posted here. My situation is a little different in that my partner of 35 years does not live with me. He lives app. 1 mile away. When we first started dating we both had children and trying to live together at that point was not feasible, and it has just stayed that way. I have a good relationship with his daughters, but am the primary care giver. He has early to mid alz. He drives but only as far as my house or to the gas station etc . Everything is within a 5 mile radius. He spends most of the time with me. He can still use the phone, TV, heat meals in the microwave etc. He has no memory of recent events, but his long term memory is good.
My big concern now is that we are going on a cruise in January. I had planned on just having dinner each night without a reservation so that we didn't sit with the same people every night. Unfortunately, I have found out that they do not have anytime dining on this ship, only assigned dining. So it will be with the same people every night. As this is a 24 day cruise I am concerned about how to handle his dementia. He interrupts others conversation, talks about something that has no relationship to the conversation and says things that are absolutely impossible (ie he skated across the Atlantic ocean when it froze over). How should I handle this? I am concerned for the other people at our table.
Should I try to tell them he has alz, just not say anything? Thanks
That is a tough one. I'm fairly new here. I'm curious as to what others say?
My husband does the same sort of thing to me, (says things that don't make sense, doesn't listen or understand instructions), but in public he says nothing, except an agreeable "OK", or "whatever you want". He's always been like that, very shy...to the point of embarrassment, one guy asked "Do you talk?". How bad is your husband? I'd be inclined to tell them he has mild forgetfulness (to minimize it) and hopefully they will understand.
People pick up that my husband is "aging" now after talking with him for a few minutes. At first it wasn't so obvious.
Thanks for that, that is eye-opening. My husbands father (whom I never met) was like that to my husbands mother in the 1950's to an abusive point. He would lock the poor woman inside for fear she was having an affair. At first I did not realize my husbands father was a victim of Alzheimers. But now that hubby has it, it all makes sense.
Hi @traveler1717.
Earlier this month we had a similar question from @traveler17
https://connect.mayoclinic.org/discussion/meet-fellow-caregivers-introduce-yourself/?pg=1#post-243210
Could it be that you created a second account? If you like, please send me an email using this form and I can help merge the 2 accounts https://connect.mayoclinic.org/contact-a-community-moderator/
@pearlandpeacock
Thank you. I am very interested in hearing how it works out.
Macbeth
Yes, I did mistakenly sign up for two accounts. Could you please merge them for me. I appreciate the assistance.
No problem. We'll get it sorted.
Unfortunately he is very outgoing. I don't want other people to feel uncomfortable around him but that may not be possible. I like your suggestion of just saying he is dealing with aging and forgetfulness. Sure hope this works out.
My husband will be 69 in January, he was diagnosised with ALZ three years ago, but I'm sure he was suffering with it for at least two years prior to that. He has always been quiet, but the ALZ has made him more "bold" in his comments and actions. I am younger and have to work fulltime, he does well at home and still just suffers from the short term memory and processing. My biggest hurdle has been his driving. The doctors have all said for 2 years he should not drive. However, when I take that away it takes his independence and pride. I have really struggled with what to do. I did go to one vehicle so when he does drives I'm either in the car or he goes short distances. I know the risks and at this point so does he. He has a friend that takes him places sometimes, but not often and I don't want to impose. He also has other medical problems that require diffirent specialists so I miss a lot of work taking him to those appointments. Any words of wisdom or advice on how to determine when stop his driving altogether or possible safety suggestions?
I am so sorry for all your stress. I understand My Mom thankfully never drove but her uncle went through this step in his illness. His daughter took the approach that if the Doctors have said this is to be ,then it is so. The keys stay with her Its not an option anymore.
She had a fight at first until she told him that it is not for just worrying about his safety but for the safety of some small child that doesn't know any better & walks in front of his car or a young family with a car full of kiddies that don't survive or the children have to live their lives without their parents. His reaction times are not what they should be. The Doctors said so.
He didn't like it & protested at first but she spoke quietly & stood firm on it. In some cases thats all you can do. Stand firm, don't cave. Speak quietly & calmly but with firmness.
It is hard to accept , but you are the responsible adult now. You have to be there in that capacities for him from now on. That was one of the most difficult things , that affected me with my Mom & alz. Knowing that her sense of reasoning is now depleted lets say. More childlike & I am the resonsible adult now its up to you to take action Not wait Sorry. Hugs.