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.
Hello all,
I am the primary caregiver for my 73 year old husband who has early stage Alzheimer’s and my 83 year old mom who lives with us. She has some form of dementia as well. I am 61. My dad died on 10/4/22 from stomach cancer so mom has come to live with us.
We’ve decided to move back to WA from AZ to be closer to our youngest daughter who is becoming a doctor. We just purchased a home about 20 minutes from her and are in the process of selling our AZ home. I will be diligent about not respecting her life and boundaries as I don’t want to burden her with our aging issues. Life is definitely a whirlwind and very stressful at times as any project or task that demands processes needs to be done by me. I am also the only one of the three of us who drives. Yikes! I try to make time each day for us to find joy and laugh together and to discuss the things we have to be grateful about. Some days I do a better job than others. I am praying we are making the right decision about making a move while my husband is excited about it and can hopefully learn where things are in our new home. It is a risk but I believe the right one. I look forward to learning from the group and supporting each other.
Wishing you all strength, peace and courage on the journey.
Kim Possible
Woman to woman, I’m grateful that God made you who you are. Thank you for being such a solid and purposeful helper to your family. You just gave health-related courage to another and I’m grateful.
@cburkett I see you have been a member for several years and have posted only a couple of times! Sp, welcome to Mayo Clinic Connect.
When you have the time, and would like to share, I'd love to hear the story behind your post?
Ginger
My husband of 51 years has Lewy Body Dementia. He’s 78 now, but the disease started out several years ago with what we thought were very vivid dreams. Not dreams, but full blown hallucinations. Taking care of his needs is the biggest challenge of my life. I will continue to love and care for him throughout his life or mine. As hard as it is for me, it’s an absolute hell for him. If it were reversed, I know he would do the same for me.
Hi, @john316ga I'm sorry to read of your husband's health journey. I'm Scott and I was my wife's caregiver during her journey with brain cancer, which gave her many dementia-like symptoms as well as for my MIL who had Frontotemporal Dementia.
I agree with you that caregiving is a tough job and your additional comment rang equally true to me in that I always felt I had the easy part of the deal since my wife was fighting for her life every day and I only had to be her caregiver.
I hope the sun is shining wherever you are today!
Strength, Courage, & Peace
It's heartbreaking @jeaniecdn, isn't it? Yet you somehow find the strength to manage. You're right. When I retired I noted changes in my husband's behavior, most of all in his ability to use the proper words. It was difficult for me to come to terms with the number of deficits he was experiencing. Now I've just learned to roll with them, but worry about what the future will bring. He has moderate Alzheimer's Disease now, still functions pretty well, although I am his memory and caregiver/guide. I can leave him for a few hours, but that's all. He likes to sleep, eat and watch what the neighbors are doing. We go for a 40 minute walks most mornings. He broke his hip in January, I was woriied the surgery and the stay in the rehab facility would worsen his condition, but it didn't. I wish you the best. Take care of yourself.
My husband is being tested for Lewy Body Dementia with a DAT test and skin biopsy due to REM sleep disturbance. He has already been diagnosed with Dis-executive Alzheimer’s. This journey is a challenging one to be sure!
i am currently caring for my 86 yo mom and my dad wanted her home for hospice yet is clueless about dementia and her care. so i am the main caregiver and it includes making sure my dad doens't get her up out of bed to fall again (she falls every week for past 6 or so months). he argues with her, calls her unreasonable, etc. he just doesn't understand.
@buggirl55, thank you for starting a new discussion about caring for both parents, especially when one doesn't understand dementia
- Dementia: When the other parent (spouse) isn't helpful https://connect.mayoclinic.org/discussion/when-the-other-parent-spouse-isnt-helpful/
My husband has multiple medical diagnoses; however, the one that is creating the most significant issues is dementia (previously dx as FTD and now unknown etiology). He’s changing quickly with marked executive function lapses in addition to diminished cognitive functioning. It’s as if we’re living in different worlds, yet I’m responsible for straddling both to maintain balance -which is eroding. Counseling seems to have lost its function due to seemingly weekly changes. I’m looking for a solid book as well as a open, understanding forum to share as my health is now being negatively
affected. It now feels as if I’m the “identified problem” as we try to walk through the various aspects of the disease.