
Caregiving has killed my personal life, and I find myself caring less and less about intimacy, yet I miss it deeply. I put so much energy into keeping everything together that some days I feel like I’ve disappeared in the process. I genuinely hope you all find that special someone who can share the load and still see you.
For me, that feels unlikely. The human interaction, the romance, the love, the physical closeness — they’ve become rare, almost like special treats I only get to remember instead of live. And I hate admitting it, but I long for it. I know I’m not alone here… has anyone else felt this way?
Said she-----------You are ALL those things.
And you are.
Did you see the movie Avatar?
Their highest compliment to each other was to say 'I see you'.
I really miss the person I was five years ago, I had a happy life and had joy in living my life back then. The experiences of dealing with my parents issues and all the other family baggage for the past five years have left me very depressed, angry and anxious. It continues to be soul sucking.
Caregivers with a positive attitude and creativity, do much better with their own quality of life, then the negative thinking caregivers who spend the whole day in the house complaining about life.
I did everything possible to help my loved one try to still enjoy life, even with a slow decline from dementia. We went out to restaurants, parks for picnics, walks with the wheelchair, played catch with a soft easy catch ball, enjoyed movies, tv shows, yummy meals together, music, arts and crafts, family time and reminiscing old stories, feeding birds, and watching wildlife, gardening, singing, exercising with bands or in a chair, etc…. If you truly love the person, you CAN make the most of the caregiving for everyone envolved. Ask for help when you need it.
No, you made the most of caregiving and it worked for you. This is not going to be everyone's situation.
There's a reason why homecare agencies, nursing homes, assisted living facilities, and memory care facilities are in business. They are for the people who could not take on the burden of caregiving, those who couldn't bear the burden anymore, or those people who don't have anyone who could take it on.
You made the choice to be a caregiver to someone with dementia. This does not make you a better person than someone who did not choose it and instead put their loved one into care.
Others can and will tell you how you "should" feel, and what a "joy" and "honor" it is to care give for someone you love. That you should sit around singing Kumbaya together every night. I'm here to tell you that's nonsense for a great many of us. We have LOs who drain us, who treat us like garbage, or, who treat us decently but STILL suck the life out of us. Please don't feel "less than" bc others tell you how you "should be" caregiving "properly". The only time I felt like I could start living my OWN life again, w/o stress and worry and endless phone calls, was after mom passed away. And then my husband had a liver transplant and shortly after he recovered, I was diagnosed with stage 4 cancer.
I've been in remission for over 2.5 yrs now, but treatment has left me disabled. What I can say to you is this. Try to take time for yourself thru the caregiving chaos. Hire help. Go on vacations and place your LO in respite care. You have lost a piece of yourself but it's still in there, not gone forever, just hibernating. Decide how long you'll do this and when you'll retire from caregiving permanently and what will be involved in doing so. Then Do It. Life is short and nobody knows what's lying ahead. Make the most of NOW.
My daughter is having a baby in Dec. I get to throw her a shower next month! I got to see her get married and look pretty myself! I get to feel joy now all the time, in spite of it all.
Best of luck to you. You're heard here, my friend.
So, my caregiving continued (though treated quite badly, mybempathy for what he was going through KINDA "eased" my caregiving of my heart.
1 year later and (we weren't asked) my Son and family moved to Mi for us to put them up in our tiny 1 bdrm farmhouse and finally when they got their own place...we had the little ones at our home helping to raise them. Still considered caregiving because it had now been 4 years of non stop caregiving. I was becoming resentful...abd guilty for feeling resentful that I rarely had time to dress each day. Caregiving now for all family at this point
Hhad reached 11 years...and no vacation or time even fir myself.
Then came my mother-in-law and a particularly hard time with a life as a narcissist, 3 years add'l caregiving...and for past 16 years my husband was showing signs of "forgetfulness" leaving stove burners on, and as time has gone on he became withdrawn, detached from himself, extremely aggressive towards me and quite dangerous. His whole personality changed as time went on.
Last 2 years i was having to seriously consider a shelter for me. FINALLY ...I kept noticing him constantly lightly rubbing his forehead and THAT clued me in. He had a horrific accudent years back and his forehead had been torn away and suffered of course damage to the brain! Not to mention he was a bullrider and with the jarring of brain while riding and falling...I began to put t all together...Frontaltemporal disease. He's in a quickly progressive stage of Dementia and I've journaled his behavior according to his timing each day together with a flow chart so we'll be ahead of the game when Neurologist initial appointment.
So all in all...been caregiving to all the family now including handling ALL financial responsibilities. I feel like I am yoyo'd and I m forgetting my own medications, skipping my own Dr appts/referrals showers, and not a vacation of any kind now since 2007. I'm exhausted and have nobody to help. Son now too lives in AZ as he wanted us to move back to AZ "because if anything happens to us...he just can't take of work. We're now living 3 hours away and hes "no time to drive to help me out...not even by phone call. So, dear person you certainly are NOT ALONE. But, I would like to give you some encouragement of love...His Heavenly love i find in Scripture and quotes i find along the way ive screenshot and they too have helped emotionally. I pull up my photos and file through until one of the quotes edifies me to get through an exhausted, discouraged moment. (Look up quotes on google.) This has been the best ways ive found for now on MY part. And, reading Psalms and the quotes made me feel not so alone.
Being told to rest yourself...etc...just makes things worth...because i haven't the time. God bless you for your loving sacrifuce and for sharing.