Mom has beginning stages of dementia, step Dad is physically declining but his mind is sharp. I tried to get them to move to my town years ago, even purchasing a house up the street, but for various reasons won't move. My Mom would in a heart beat, but part of that is the dementia making the decision. I have been here over a week sorting & packing, the big move is tomorrow, into a nice facility in their hometown, but we are all stressed, and both of them are depressed. By the time I head home, I will have been here two weeks, and I feel very guilty about leaving during this transition time for them. My Mom will have a hard time, she's in denial about how much help she needs and my step Dad, chose this move trying to do the smart thing, is still depressed and on top of that, is still has to manage my Mom. I am concerned, worried, and of course have a full busy life full of responsibilities 1400 miles away...kids, hubby, small business, step kids, and grandchildren that I help care for. Any advice or encouragement would be greatly appreciated.
I, too, was worried about the move. I guess it feels like when a parent send a child off to college... you wonder if they will like the dorm... like the food... make new friends... and get to class on time :)
So far Dad is doing well, and is happy as a clam with his new place and not having to worry about keeping up with repairs in his previous house. But I did have to take over all the bill paying as Dad didn't want to bother with it... [sigh].
I have asked a slightly off topic question if anyone would care to advise
I've recently decide to no longer argue, beg or lecture my mom about getting help or moving. It will take some event to force the issue. It will have to be her decision unless she becomes incompetent.
Any input appreciated!
Also make sure there is a written Living Will and POA ( power of attorney Health and
financial)
A case worker ( not Medical Case Manager) can facilitate financial POA and Mefical!!!
Sky ping with your relatives at a distance can be arranged with most facilities.
Contact Case Management Society of America ( CMSA) for a CM in your area. There are over 2000 members and they would refer you to one in your area
I think we are all feeling better!
My parents hired a team of professionals who assist with this exact type of move, but kept putting off the sorting and packing until I got here. Now of course, I have spent the entire first week sorting and packing, and today my step Dad wants to know if I will stay longer to help with paperwork!!! My last day here is Friday, Mon and Tues will be mostly taken up with moving and unpacking, and I imagine we will all be wiped out the rest of the week.
My step Dad is very bright and has a sharp mind, but I wonder what version of reality he is living in at the moment....he kept procrastinating about the packing, despite my efforts and the professional estate manager. It got to the point that she was emailing me to see if I could get him to move along with packing because he kept cancelling and postponing. AND now the consequences of him putting that off has led us to not having more time to tackle anything else but the move. (although to be honest, I'm kind of surprised he thought we would have time for anything else)
I did offer to come back for a long weekend, 5 days in February to do paperwork, but I simply do not have it in me to stay any longer than I originally planned this trip, not to mention I still have a full month ahead of me with my own obligations to fulfill. AND OF COURSE, I feel guilty.
UGH.
Thanks again folks for your words of wisdom, and for listening to me vent a bit.
Your folks will find there are things to do at the Assisted Living, compared to sitting at home worrying about who will shovel the snow, or rake the leaves, and who would get their groceries or drive them to doctor appointments. Eventually there will be less stress for them once they settle in :)
And over time less stress for you, knowing they aren't home alone. You find yourself being able to finally sleep at night.
Assuming there are no other relatives nearby, I would contact their neighbors or any church members and ask if they can arrange to visit on a regular basis, and keep you updated as to any worsening of your parents' depression. I would also meet with the facility administration and ask the same thing. At least that way you'll have two different independent sources providing feedback.
I would also meet with the activities staff and ask if they'll make a special effort to get your parents involved in activities, and introduce them to other residents.
Call your parents regularly, and ask other family members to do the same. The goal is to make the transition and integration as smooth as possible, but also to be alert for worsening of their depression or other issues that may develop.
If it does appear that the situation isn't working out, and if you still have that house you bought, you can again raise the issue of their moving closer to you. If they did, you could at least have more up to date and intimate knowledge of their progress, and intervene if necessary to provide home care and assistance through vetted agencies. I do agree that eventually Mom's dementia may require a more supportive environment, but it's also possible that in AL the staff may be able to provide some aspect of that support.
Can you spend some time with them after they move in to also help in the transition process? Perhaps help them get acquainted, plan something special like a dinner out?
I also think Sunny's last 2 paragraphs on proactive planning are important to consider. Another thing for which to be thankful is that they're not remaining alone at home as Windy's parents are. There's so much uncertainty and anxiety in a situation like that. And NYDIL's suggestion on projects to help refocusing from the drastic change is good advice as well.
Do you have Durable Power of Attorney and Healthcare POA? I'd make sure you have that or someone in their state has it so they can act on their behalf if necessary.
I know that when my loved one went into AL, there were all kinds of paperwork to sign. If they become incompetent, the various medical facilities may need your signature.
Did your parents have an assessment by the AL facility to determine how they could meet their needs? I just hope that the services will meet their needs as they progress. If not, I'm sure they will let you know.
I would consider long range plans in case that happens. I would also encourage you to keep close watch on dad's health. It is extremely stressful to live with a person with dementia. As she progresses, it may cause him a lot of distress. That can't be good for his physical health. Eventually, she may need much more care and supervision that your dad can't provide.