Dementia Support Group
Dementia is the progressive decline in cognitive function due to damage or disease in the brain beyond what might be expected from normal aging. Particularly affected areas may be memory, attention, language and problem solving, although particularly in the later stages of the condition, affected persons may be disoriented in time, place and person (not knowing who they...
We have taken plane trips and car trips.
He may not always remember where we are or where we have been but I make sure not to overtire him.
I point things out to him and make him think & speak.
At home we have picture signs on doorways so he knows what room is what. I carry an extra set of these signs with us and put them on doors so he knows where the bathroom is and what doors not to go through.
Activity can slow dementia.
I know this must be hard to swallow. So many of us are coping with a life we did not expect, deserve, nor prepare for.
I'm just plain scared: Binsheimer's patients usually live only about 5 years from onset, and he's been affected for a few years already.
Maybe you're actually more frightened than angry (?)
< HUG! >
I think what most of us experience is grief. Knowing that this is bringing a major change to our lives, effectively ending life as we know it and signaling the eventual death of a loved one. You should read about the stages of grieving, it can help you understand what you are feeling.
What has been hardest for my parents is the good days/bad days and never knowing what today will be. I call them several times a week. Some days I will hear how bad he is doing and my mom and I will talk about making changes like him not driving or not being able to attend my nieces wedding. But then there are days when mom will say something, I will suggest a change and she will vehemently refuse saying that he is OK. I think she is having a hard time accepting how this will change her life as well.
It may sound corny but AA has what they call the Serenity Prayer.
God give me the strength to change the things I can,
the courage to accept the things that I can't change,
and the wisdom to know the difference.
There are things that you can do, things you can't do. The trick is to understand where things fall and to accept that there are things that you can't control. Many times in the beginning (and still today) I found myself making complex plans for them. Then I would realize that I can't make this illness or my parents fit in the little boxes that I made.
If you can come to accept that this is your life for now you will be so much happier. Get some counciling and speak to your doctor. OFten the caregiver forgets to take care of themselves plus there are anxiety and anti-depressants that might help you. I also found that it has helped my mom to make some general plans..vacation, short trip, house project..but keep the details flexible. You don't need to sit at home waiting for him to get worse and die. Live life just on different terms.
I do extend my deepest sympathy for your losses in relationship to all the changes that have happened due to your husbands' dementia. First, the anger comes from not liking this new situation at all and also being angry at NOT being able to change it. You are experiencing several losses which one needs to process through as you adjust to this new reality. First, the interactional quality of your relationship with your husband has declined. He does not contribute his support to you like he used to by doing tasks or by encouraging you. Second, you have lost your dreams and expectations of what the future would look like. The hopes have died and now you need to come up with a new picture of the future. While you still have him, it will need to be a dual track picture, part of what your being with him looks like and the other part being how you relate to the rest of the world. I call it being "half a widow". Also, do develop some goals of what your life will have in it later, after he passes away. Be sure you make some dreams of a life you will enjoy. Most women outlive their husbands. Life will go on. Get counseling and support to help you develop goods things to come for you.
She just retired and thought they would do this and that and now his hallucinations are so bad she can not even leave him alone and he is up all night. He thinks she is out to get him so he can be mean to her and she is so sad, she had it all laid out and now everything is different and confusing. He is only 67 and we are trying to understand and find help in our area and coming against red tape and people not knowing what to do either and they are in the field.
Good Luck and take care
I will tell you being in an online support group is a big help, "Alzheimers group is amazing". It helps to just let it out to people who are/or have been where you are and say whatever with no judgement just caring. aLSO IF YOU CAN FIND A LIVE SUPPORT group that is good as well. (go to alheimers.org to find local groups) I waited longer than I should have on both counts but once I opened up my eyes and did so I was so glad I did.
Come her , or as I say the Alzheimer's support group also and get the friendship and sisterhood to help you through this journey. It's a tough one but we shall make it one day at a time...and TOGETHER!
God Bless..sherbear2
Your words rang so true for me and hit right at the core of my feelings. I think this gradual erosion is so very painful and learning to love differently is a challenge. Anger at the disease, not the person is what I'm trying to accomplish at this early stage, but I often find myself losing patience with my husband realizing my emotion is just plain fear...how much worse will it get? How much more can I withstand?
These are long and often dark days but I'm doing everything I know to find those bright spots.