I'm concerned with taking care of husband and doing a ton of the work he used to do outside etc. We went to our daughter's out west and it was over the top busy but great to be with them. But I'm finding myself since we got back thinking today is a different day. Forgetting what day it is. I'm scared half to death I might be in beginning stage of dementia that would be a nightmare being my husband's caregiver. I got done with my job last April and work out of the home once in a while with appointments, I told a woman I could tomorrow, but I would check when I get home (I was shopping, had respite) and realized I'm on the wrong day. Then last night set my alarm thinking today was Monday. It's Sunday...
I personally usually need to check the date. My solution is to keep a date book in my purse and immediately write down any appointments. The other annoying thing that happens is transposing letters and numbers.
As my physical health deteriorated these problems became worse and in the weeks since we moved till my husband died suddenly the stress became tangible and I felt as though I had PTSD. Of course I miss him terribly or at least the man he used to be but he gave me three beautiful caring children.
It has been verytressfull sorting out the estate because nothing was in order and just cancelling a credit card can cause requests for all kinds of paper work.
Now I just feel relieved that it is mostly over and like an onion that is having the outer layers of stress peeled away.
Don't worry about dementia.
Healing Hugs
My caregiver and DD were thinking I was depressed because i sometome just sit and do nothing. They wanted more meds but my Dr was reluctant which was good.
Now I try and make lists for everything and at least double check any numbers I enter.
L my caregiver thinks I am doing better this week but what everyone seems to fail to realize that at almost 80 it takes far longer to recover from stressful situations and there has to be time when you can just sit and think.
Not ready to resume hobbies I enjoy or go out nd socialize. never was one for that anyway and the idea of senior centers appalls me. I would much prefer to be hanging out with the horses in DD's barn
One time I was planning Saturday outing and so looking forward to tomorrow and my husband was like, its Tuesday. What? You mean I lost a whole weekend and Monday?
So, I think getting used to retirement and caregiver burnout can cause lapses in memory.
Hugs and God bless you.
God bless
SusyQ22, stress will do that to you. Today for a short second I questioned whether it was 2018 or 2019 … I picked up the phone, called my best friend and asked her what year it was … She didn't laugh at me, she paused for a second. Then she said, "Wait, is it, 2019? No, it's 2018." I told her she was no help, said goodbye, and hung up. I felt better about myself after that. (I'm not that old either.) I don't know if you are just worrying because of the stress you are undergoing. I understand your cause for concern, but I'm thinking you might just be overwhelmed. If it keeps happening get checked. Wishing you the best.
However, if you are concern please talk with your doctor.
Not a bad idea to get all you life paperwork none. Better to be safe than sorry.
SuzyQ22 it seems to me you just have a lot on your plate. The more you think about how you are forgetting things the more you will start forgetting. Try to relax.
The same goes for you cajohnston.
Heck, we all need to relax!
God bless
It is funny that you ask that because I have wondered that as well. I've wondered because I've seen it happen to so many people. My conclusion is the STRESS of looking after someone with dementia can cause it to happen to the caregiver. It truly is a different kind of stress and it is unrelenting. Sleep times are totally disrupted, every waking thought is about dealing with endless issues that pop up with the dementia patient.
I’ll just add add that I come from very healthy genetic stock and at the age of 35, I am also experiencing what you described! I got so confused about what day it was, I asked the PT and OT to text me their schedule for visiting the house because I just couldn’t keep it straight even with my datebook (it has Monday where Sunday usually goes, and that is enough to throw me off!). I regularly check my phone, which displays the date, day of the week, and time.
It is probably just being overwhelmed after your trip. But, you could make an appointment for the neurologist just to establish a relationship and get your baseline. Also, make a plan for the future. I heard elder attorneys are very good at presenting options.
The days of the week were artificially set by humans as are the hours of the day - this has become important only in the last century or so because the general population could not afford a clock - most people did the same work daily only switched up by Sunday churchgoing if they were close enough to go - humans haven't had these artificial markers long enough to be hard wired so whether you are aware of it or not humans make their own markers [mainly work & school] & this is 1 reason shift workers have sleep problems -
Taking someone with dementia on a trip would tire the spirit of anyone - best to get a bit more sleep [easier said than done] & realize that this may be a wake up sign for you to put a bit more time on/for YOU - time to be aware that Superwoman was not human & you are ... so start doing things that will help you - sometimes a small thing relieves much more like hiring a yard service to do the regular grass cutting or a cleaning service once a month to do some heavy cleaning so that your energy is kept for what is truly important ... caring for hubby
I see a neurologist and a neurosurgeon... and they have a baseline for what my “normal” is. I trust that when I start slipping, they will see the decline, and address the underlying cause.
maybe seeing a neurologist for some preliminary testing would put your mind at ease. Get a baseline so you have some information to measure a rate of decline.
My dad never knows what day it is. He doesn’t know the year, month , or current President. He has a “moderate cognitive dysfunction”... the difference is- you KNOW that you don’t know the correct day of the week (but you could look on a calendar) He doesn’t know that he’s guessing- and he can’t figure out if he’s correct by using a calendar. He thinks he’s right! (Yep- Ronald Reagan is the President, it is 2017, and it’s November!) It was a pretty simple test, but painful to see him struggle.
I
Stay out of the middle aisles and get your nourishment around the walls of the grocery store. Veg, fruit, nuts, skip the bakery and hot dog/ham section, fish, beef, chicken, liver, dairy, eggs, juice.....
If you are blood type O avoid gluten and corn and emphasize blue, purple, red fruits and the lesser known grains, like quinoa. Rice is good if you tolerate it. But personally I don't eat it more than twice a week.
Make smoothies with real food and add hemp and chia seed for regularity and energy. Eat your smoothie, don't just swallow it down. Food requires saliva to get nutrition into your body. You can keep a smoothie in the fridge and consume as you feel the need. If you tolerate dairy, greek yogurt is indeed a good thing.
Type As do better as vegetarians. Processed meat products contain nitrites, which vegetarians should avoid. Bake broil or poach your fish.
Os and As don't tolerate dairy well, so see if you get gut problems and avoid dairy if you do. If you have gallbladder problems, nut butters are better than whole nuts. Mucus over production will tell you if a food is not healthy for you.
Eating right can make the difference between holding on and falling back.
I recommend, if you have time to read, "Eat Right for Your Type," by Dr. Peter J. D'Adamo. I only wish I had read his before my husband's long dying. I'd have been less exhausted. 24 hour care can wear you down, as you know. He offers a diet plan for each blood type, which gave me back my life, and I'll be forever grateful.
I have a calendar for birthdays and other occasions. Another, I check last thing at night and first thing in the morning for "must-do" appointments that day. A big desk calendar, if they still make them, helped me for a long time. My memory is still not back to where I'd like it to be, but we do what we can.... Good luck to you and yours.
As everyone else mentions, it could be stress, lack of regular work schedule, lack of sleep, exercise, good nutrition and enjoyment. It must be hard to arrange, but how about a meetup group or book club or regularly doing something fun?
Processed Foods have chemicals instead of nutritional values - I know it's not easy - my DH's last 6 months had me eating little besides Ice Cream and Fried Chicken. He wasn't eating so I wasn't eating well, at all.
Start with Vegetables & Fruits and find a way to get your proteins. I use a lot of Greek Yogurt on a daily basis.
You can do this!
The choice at that time was to put my newborn grandson, who was born with a disability, into daycare, or become half time daycare for him.
In addition, I have since become a care giver/errand runner/servicesarranger/whatever is needed for a cherished 90 yo relative with dementia who is in a local AL
I could testify in court-YES, STRESS DOES IMPACT ON MEMORY.
Don’t rule out getting paid help, speaking to a therapist, sharing your situation with close associates, getting pleasant, mindless exercise and fresh air, writing things down on paper or into a smart phone, using electronic gadgets if they help, getting a massage or an adjustment from a chiropractor.... and also, making your own PERSONAL list of good deeds to perform for YOU while you do the very good deed of putting your husband first.
None of these have “fixed” my struggles, but they ARE helping me to cherish my 2 1/2 yo AND my 90 yo charges and at the same time develop an improved perspective on managing my personal worries and forgetting, and figuring out where I fit into this daily circus that presently occupies so much of my life.
Good thoughts, prayers, and pats on the back to you!
You are on overload and need to find your, YOUR, own life preserver. I cared for my mom and stepdad for four years. When they went to a facility it took a full seven months to feel like I was getting my own mind back. Now it has been 3.5 years since and I still feel at times like I am losing it. You need to take care of you, find other solutions for mom and husband or you may be joining them.
Stress does effect brain function and health in general. So take care of you, it is past time!