senior-couple-caretaking
Caregiving
Environmental Health

How to Save Your Marriage After Becoming Your Husband's Caregiver

My husband and I were college sweethearts and had been together for 28 years when he suffered a cardiac arrest in 2003. He didn’t get enough oxygen to his brain and lapsed into a coma for 10 days. When he woke, he wasn’t the same person I had married. He had severe cognitive deficits; his thoughts were jumbled and at times incoherent. He suffered short-term memory loss and didn’t initiate speech. Although he regained the ability to walk, his balance was precarious. He was never able to resume his career as an attorney and needed full-time care at age 47.

Over the years, I learned to adapt to life with brain injury. He lived at home with me for 15 years, until he passed away six months ago. “Why do you stay?” I was often asked by acquaintances. I have to admit that I occasionally thought about placing him in an institution and walking away. But even though he couldn’t remember what had happened to him that day or the week before, his deep-seated, long-term memories remained. He never forgot his love for me and our two sons who were teenagers at the time of his brain injury. His face would light up at the sight of me or the boys and he would always smile and say, “I love you.”

His capacity for love is what sustained me through the years of disability. How could I possibly leave such a gentle, kind soul who wanted nothing more in life than to love and be loved by his wife and sons? I stayed with him because of who he was before his brain injury, for the devotion he had for his family and the respect he showed me and our sons. I wanted to keep him at home to make sure he was treated with the dignity and respect he deserved. I feared that he would become just another patient or another bedpan to change if he was put in a nursing home.

It was not easy during those 15 years. Caregiving for a brain injured husband while working full-time and raising two sons filled me with exasperation and hopelessness at times.

How did I keep faith in our marriage? Here are some ways that I learned to cope after becoming my husband’s caregiver.

  1. I reminded myself that it’s the brain injury and not him. There were times when I felt hurt that he didn’t remember the date of our anniversary or my birthday but I knew it was the brain injury, not that he didn’t care. Yet when I was in the throes of caregiving, it was hard to remember that his emotional responses were not intended to hurt me. The brain injury prevented him from remembering.
  2. I tried not to wallow in the past. I missed our old life filled with travel and hiking and camping. Rather than brood for the old days, I learned to travel and still enjoy the outdoors with accommodations for disability. I used wheelchairs and walkers and sought out paved paths in wilderness areas to get a glimpse of mountain peaks and the scent of pine trees.
  3. I let myself get frustrated with caregiving. I acknowledged that caregiving was stressful and that it was normal to feel angry at times. I was not a saint who could handle everything and I didn’t have to act like everything was under control. When I felt too overwhelmed, it was time to reach out to others for help.
  4. I took breaks from caregiving and carved out time for myself. I felt guilty each time I left my husband with the caregiver to spend an afternoon alone shopping or travel on my own. But I always felt rejuvenated afterwards and better prepared to meet the demands of caregiving. I had to remind myself that it was okay to experience life without disability once in a while.

Just as each recovery from brain injury is individualized, each caregiver has a unique story. My story affirmed for me that caregiving is the ultimate expression of love.

 

 

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