New to Caregiving?
Prepare to become a caregiver. In 2015, research conducted by the American Association of Retired Persons (AARP) found that 43.5 million adults in the United States (approximately 29% of the adult population) had provided unpaid care to either a child or adult during that year. With the growing need for in-home medical interventions and the limited resources available, experts predict that most adults will, at some point during their adult lives, need to perform the role of caregiver to someone they know.
Becoming a Caregiver
Most of us become caregivers because we are no longer able to perform all our self-care independently. First, the transition to a caregiver from friend, spouse, sibling, or child may not be apparent. You merely lend a hand, offer encouragement, give a ride to a clinic appointment, or help with yard work. Gradually, however, the need for assistance increases, and you take on more responsibility. After a while, you realize you now provide greater support (i.e., it’s part of your daily life) because the one who needs your help cannot manage without you. You recognize that what was once voluntary support has become a basic need for care and your new normal.
Transitioning to Caregiving
When you transition over time into the caregiver role, you can ease into your new normal with the person receiving care. Transitioning to the new role is easier if you can talk about the changes as they occur.
- Establish personal boundaries for both of you.
- Identify lines of decision-making.
- Establish expectations for when you should step in to help and when you should let them struggle to do it themselves.
Personal Boundaries
I want to emphasize boundaries a bit because it’s one of the ongoing challenges of caregiving. They seem to change continuously. When my spouse cannot defend himself in a crisis, I become “him.” I am his voice. There have been several times when my husband has been in critical care where I monitored all activity surrounding him. At those times, I guarded his safety, protected his dignity, spoke up for his rights, comforted him, and offered him security. I placed a hedge of protection around him day and night until he could begin to reclaim some of his power. In other words, I had no boundaries at that time.
When he’s healthy, however, we share in decision-making based on who is performing the task at hand and what produces the greater good for his well-being. Most of the time, his needs come before mine, even when I’m sick because he can do nothing for himself. He crosses my boundaries if he becomes forgetful and, out of habit, asks for something when I’m sick, that is not essential. In that situation, I speak up, and we correct the situation. In caregiving, there must be a partnership of respect with clear communication of needs. Without it, resentment develops.
Emotions
Once you become a caregiver, you can expect to experience many positive and negative emotions. Emotions can be confusing, and sometimes conflicting emotions can come within minutes of each other. Learn to recognize your emotions as they surface and how to deal with them appropriately.
Caregiving can be a very rewarding experience for those who want to provide care. However, some caregivers provide care out of obligation to family members with strained histories such as past abuse or neglect. Therefore, providing care in and of itself is not always positive—it’s very individualized, but in most cases, it’s positive.
Positive Emotions
I would say in many family situations, many positive emotions flow forth from caregiving activities such as the ones I personally experienced below:
- I feel grateful that I can provide care for my husband.
- Our love for each other has grown stronger by the caregiving I provide.
- We celebrate each other’s progress and encourage each other regularly.
- My husband shows his appreciation often and abundantly, which brings me joy.
- I enjoy feeling helpful and having a sense of purpose and usefulness.
Negative Emotions
On the other hand, there are also many negative emotions that I also experience primarily due to exhaustion (lack of sleep mainly).
- Self-doubt: Will I ever be able to get it all done? Am I enough to meet all his needs?
- Fear: Over the years, fear has included so many topics. Concerning his health, the impact of caring for him affects the children, my job, my health, and my relationship with my extended family and friends.
- Anger: Though I feel ashamed of being angry, I am. I feel the loss of my freedom to be myself and to have a life because once I became a full-time caregiver, I no longer had a life apart from caregiving.
- Depression: See above. Anger turned inward and not allowed to be expressed results in depression. I’m overweight, out of shape, irritable, in a bad mood, and lonely.
- Frustration: Acting irritable, short-tempered, and impatient. Frustration comes from having too much to do and too little time to complete it.
- Guilt: For feeling all the above. I want to feel only positive emotions. My spouse has a medical condition he didn’t ask to have. He needs help, and when I married him, I agreed to “love him in sickness and health.” I want to make it all better all the time, but I can’t, and I feel guilty about that.
Best Advice
My best advice to all new caregivers has always been simple.
- Take each day as it comes. Do not look ahead.
It seems overwhelming if you look down the road to what might loom ahead. However, if you take each day as it comes and concentrate only on that day’s work, you’ll be fine. You will successfully complete the day and move forward. Then, when that day in the future becomes today, you’ll be ready.
- If something goes wrong today, cut yourself some slack.
You may have learned something new from a mistake you made that you won’t make tomorrow. If so, great job! It was a learning opportunity. Maybe even a great story to share later.
- Laugh when you can. It breaks the tension.
We have been in very tight situations where we didn’t think we could find a way out and would suddenly start laughing uncontrollably. After a while, we relaxed, a solution came, and we worked our way out.
- Gods got your back.
Remember that God’s always there if you’re a believer like I am. When I need help, I’ve asked, and He provided. He’s helped me out of many tough places and carried me through many more. Don’t be afraid to ask. You’re not alone.
This article originally appeared on Multiplesclerosis.Net by Health-Union, LLC, and has been reposted with permission.
