Since I became a widow three years and five months ago (isn’t it amazing how widows always know how many days and months it has been, while at the same time suffering from the “Widow Brain.” How does that even work?) I’ve talked to many types of widows – suicide widows, cancer widows, accident widows, massive heart attack widows, don’t-know-what-happened widows, widows who lost their husbands to advanced age – many kinds of widows. I can sympathize with each kind because we have all lost our loves. All of our journeys are different, I know. I’d like to add one to the list-the caregiver widow. Caregiver widows can also be cancer widows, etc., but there is a piece of a caregiver’s grief that is difficult, at least it has been for me, to work through.
My husband was a disgustingly healthy and health-conscious man. Strong, athletic and for the most part, a very healthy eater. In fact, I always thought I’d be the one who left first because I was the less health conscious one between the two of us. Instead, my Tony was diagnosed with end-stage renal failure, with less than 5% kidney function remaining, due to lupus. He immediately stopped working and I immediately stepped up and began taking care of him. At first, this consisted of cooking healthier meals for him, monitoring his symptoms and making sure he took his meds on time and in the proper dosages.
As his symptoms progressed, he needed more and more attention and help from me, until ultimately he needed me to handle his every need. I bathed him, clothed him, fed him, made sure he received all of his meds on time every single day. I fought with his doctors to make sure they tried everything possible to at first cure him, then I fought them to keep him alive and comfortable.
Then he died. After all of that, he died.
That wasn’t fair, I thought. I stepped completely out of myself to take care of my love. I had to become a totally different person as he got sicker. I had to get stronger, more knowledgeable, more patient with him, more impatient with doctors. I had to learn how to do i.vs. I had to learn to dress and treat wounds. I had to learn to use a lift to put Tony in his wheelchair. I had to learn to administer dialysis at home. I had to learn how to hug my husband in his hospital bed and not hurt him. I had to learn to hide my fear and devastation at what was happening under a blanket of confidence and fearlessness.
What an act that was.
These are the tasks of a caregiver. Caregivers do not attend school. They do not get paid. They get very little support and they get all of the grief. They feel all of the pain and fear their loved one feels. That pain, on top of the caregiver’s pain, all has to be hidden and stuffed way down deep to allow her to carry on with her tasks.
Otherwise, she breaks and cannot be what her love needs her to be. Breaking is not allowed in this caregiving thing.
People who have never been caregivers don’t quite understand what it is to cope when her love passes away. There is a moment that goes through the caregiver’s head that goes something like this: “I worked so hard to keep him safe-alive-strong and nothing worked. He still died. What did I do wrong? What didn’t I do? What did I miss? Is it my fault?”
Guilt rules the caregiver’s mind and heart. Caregivers work extra hard to learn all they can about the disease the loved one has. So that they feel they should have cured their love. Should have saved him.
It does not help at all when well-meaning people tell the caregiver not to feel guilty and that it wasn’t her fault. We already know that. Knowing that does not help the pain. Having to hear it over and over doesn’t help either and forces the hurt back to the surface. Caregivers, after all, have learned to hide their pain from everyone and we certainly don’t want people to know how we really feel about everything that happened.
Caregiver grief is a strange grief: the caregiver grieves not only the losses associated with the death of the loved one, but also grieves the loss of feeling useful and needed. I found myself completely confused about my role in life after Tony died. I had not only been his wife and his Queen, the mother of his boys, but also the person he looked to for care, support and to help him fight his battles when that was necessary. I was absolutely the most important person in his life and after he died, I felt like nothing.
So you’ve got grief, feelings of guilt, anger, bitterness, and most of all, uselessness.
What in the world do I do now?
The question of the hour.
After my husband died, I had a lot to process. After years of getting up early, spending weekends in hospital and rehab room, I was at a loss. No more standing over nurses, supervising their work. No more hours of sitting at a bedside, hoping and praying. No more scaring doctors into doing their job. No more measuring out meds. No more anything to do with him.
It is difficult, letting all of that go. Being forced to try and move mountains for my husband built up muscles I didn’t know I had. I was constantly ready to spring into action. What happens to all of that when he dies? You use those muscles to beat yourself up, and that is precisely what I did. For months and months, I felt angry and guilty. I also felt bruised and broken.
I had to realize that I built those muscles for a reason and that they weren’t ever going to go away. I also had to realize I had to stop using them to beat myself up.
Ultimately, the realization that you, the caregiver did everything she could needs to come from within.
I know I was always there for him. I know I was everything – a good support, a good caregiver, a good wife should be. I know all of that. I have to tell myself every day these things to keep my mind from circling back onto itself and taking full blame for failing to keep him alive. That’s how I felt for months.
The muscles I developed have new tasks now – to care for and support myself. I work my mental muscles daily to keep from falling into that “I’m a failure” trap. I didn’t fail. He didn’t fail. His body is the only thing that failed and none of that is anyone’s fault. If love could have saved him, it would have.
I now focus on my boys and any friends who may need me. A good use of all of my skills. I feel that since I’ve been in the worst situations imaginable, I can beat anything…including the negative mindset I’ve carried since he died. Sure, the feelings of failure still arise, but I am more able to manage them and listen to the voice inside that says, “You did not fail him. Because you loved him you never failed him.”
With those thoughts, I flex my muscles and keep it moving.
I also lost my dear husband, Robert 4/24/18, at age 64, to end stage renal disease, plus a long list of other medical issues!
For the past 8 yrs that all of us struggled along side him with, surgeries, infections, cardiac arrest, after a knee replacement, wheelchairs, neck surgery, hosp & rehab stays.. just too much for one person in one lifetime. It was a difficult road for him & we did this together.
Trying to make this short as I can because I typed a novel a bit ago & I knew it was too
long. Working & being a caretaker was very difficult as you all very well know. We have 3adult children but my youngest, 24 yr old daughter helped me when she came home fr college 2 yrs ago. He was 64 yrs old, always a hardworking & funny man until he started having more heath issues, after 3 yrs on dialysis. He cried, because he didnt want to stop working, I talked him into it bc he was becoming weaker. But he had worked since age 13 bc his father left the family, he didn’t give much support or money for the last 4 ynger children, so Robert had to step in. Sad!
I was caretaker for my husband, especially the last 16mos of his life, he suffered so much, so sad to see, we cried with each other. Takes alot to care for a person day in & day out & I know he was grateful for the care we gave him.
He was a strong man, he tried to keep up his humerous side for us, up to the end of his journey. He passed away in the hospital after two cardiac arrests two days in a row. He looked very peaceful & that’s what got us through
So hard for us, we miss him alot. Yesterday wld have been our 37th wedding anniversary. Was difficult day, but Our children were there for me, as I know their Dad would have wanted them to be.
I Thank God for him & my God given strength he gave me during the difficult times!
And praying helped us through.
Now I find myself
lost at times, esp weeks after he passed.
May Love & Peace be with all of You Caretakers, knowing we did Our Best with our Love & Care!
Indeed we did and it was all for love of our dear ones. Blessings to you too!
Cheryl…you have described my life, the agony of being my husband’s caregiver..and being left behind, exhausted from the years of fighting for him, and devastated by the grief of his loss, only 6 Weeks ago. He was 47 years old. I fought..and fought…and feel like I failed my beautiful man, who also, was incredibly fit and healthy, a former soldier, never a sick day…until the cancer that came out of nowhere. Thank you for putting into words how we carers feel when we cannot save our beloved.
That sense of failure doesn’t really abate. But deep down, we know we didn’t fail. We did NOT fail. Love to you, dear one.
Oh my God! This is so similar to our story! Arlene was a type 2 diabetic, suffered kidney failure and became a dialysis patient for her last 30 months. At the time I was long term unemployed, so I added caring for her to looking for work. Compounding that, we were Superstorm Sandy Survivors. 6 weeks after the storm, she finally went to the hospital and in her last 30 months, had heart bypass and valve repair surgery, along with countless procedures to keep her access for dialysis working. In that time we became homeless and displaced because of issues from the storm, a bedbug infestation via donated blankets. So, along with trying to bring her home, I had to deal with insurance companies and try to put our house back together because we lost most of our furniture due to the infestation. Arlene didn’t sleep in our house for her last 23 months and because of calciphylaxis caused by dialysis (very rare) she developed gangrene in both legs, necesitating first one and then the other (while she was in her coma) being amputated below the knee. In her last 30 months she suffered 5 heart attacks, both legs amputated below the knee and a stroke, and oh yeah, a leukemia scare. I was there for all of it. When asked how I felt while I all this was going on, my answer was always that this was what you do when you love somebody.
This is what you do when you love someone. My Hub was also amazed at how much I did. I simply said,” It’s because I love you. ” We loved our people. That’s it.
I was a caregiver forseveral years.my husband, the love. Of my life we were married. 58 years.he taught me so much.then Parkinson’s took his life.I ‘m still lost.but have put Jesus. In mydaily prayers
Love and blessings to you.