How prepared were you when you first became a caregiver?
Did you know what to do, where to go, what the medical terms being used even meant?
Did you know how and when to switch between the role of spouse/child/sibling/friend/parent/partner and caregiver?
If you are like most caregivers, you probably didn’t. Most of us didn’t plan on becoming caregivers. We acquired the role because “something” happened to someone we cared about or had the responsibility to protect. We did not apply for the job. It did not matter if we had prior training, had any competency or skill in knowing what to do. In some cases, it didn’t even matter if we wanted to do the job since we were obligated under a court-appointed mandate. We had the responsibility to be the caregiver, training or not, to care for and protect, this person placed under our responsibility. How could someone help but feel overwhelmed and uncertain in that situation?
Do you know the moment your life changed, and you became a caregiver? Perhaps the “moment” occurred suddenly through an accident or following a major complication of an illness? Rather than a “moment,” was the transition to caregiver a process that evolved over time as you assumed more and more responsibility for someone else’s life on a daily basis until one day you managed it all? Or, was joy turned into fear when your world turned upside down as a new baby arrived three months early along with an endless list of medical conditions you couldn’t even pronounce? Over 43 million people in the United States experienced one of those “moments” in their life leading them to accept the call to be an unpaid caregiver a family member in 2015. I would guess that number would be much higher now.
Forty-three million caregivers providing care to someone who cannot take care of themselves. Think about it…Think of how much those people save the government in providing care to their family members. Think of how many more hospitals and healthcare providers would be needed to provide care if these angels were not there. Knowing how much help they provide and how much they save the country in resources, they should be able to get help to do what they do but sadly, that is not the case. Most of you have not been so fortunate.
Figure 1: Estimates of Individual Caregiving Prevalence by Age of Recipient
| Type of Recipient | Prevalence | Estimated Number of Caregivers |
| Overall | 18.2% | 43.5 million |
| Only child recipients | 1.6% | 3.7 million |
| Only adult recipients | 13.9% | 33.3 million |
| Both adult and child recipients | 2.7% | 6.5 million |
Most new caregivers learn their jobs by trial and error. If a family member was recently hospitalized, the caregiver may have been shown how to do wound care or other procedure at least once before discharge and given a copy of printed instructions. Assuming that home health nursing gets approved, a nurse checks in with the family after discharge to go over those instructions and to ask if the family needs help with anything. Other than those resources, doctors and nurses tell the family at medical appointments what they need to know or provide brochures during appointments with information about the medical condition and how to get more information. In today’s environment, most information is gathered from the internet. Family members search the net for what they can find, hoping to locate reliable information that meets their needs and can answer questions they may not know to ask. Often the search leaves them frustrated and confused, still uncertain what they need to do.
One of the greatest failures in our healthcare industry is the failure to provide support to the family caregiver. A tragedy occurs. A significant other is grateful for the miracle survival of their loved one. Financial resources are limited. The patient improved and discharge approaches. Nurses show the family how to do dressing changes. They talk about cleanliness and if what if this happens or that. Instructions are written down. Plans are made and the patient discharged to home. Orders are written for home health which essential means maybe a one hour visit daily in rare cases or an hour visit 2-3 times per week to check on the status of the patient. The rest is up to the family.
The reality of what just hit them sets in about the time the family opens the front door of their home and they have to figure out how to get this very weak individual into their home and to their bedroom because often steps are the first obstacle to be breached and getting up them is a problem. After that, it’s a question of leaky body parts in the bed, helping to change positions, and how far away is the bathroom? Followed immediately by the question of, “which pills did she take today at the hospital and which ones still need to be taken today? This discharge paper doesn’t say. Oh, and the pharmacy was closed by the time we came by this afternoon. Now I don’t have anyone to stay with Mom in the morning while I go pick up her medication.”
When it’s time for the first dressing change, another reality hits home—they are not in a hospital setting where all the wound supplies are located at hand’s reach. They need to set up a workstation for their supplies. Plus, they have forgotten how to do sterile technique and there was a new looking spot on his butt that wasn’t there before. What do they do with that?
New caregivers feel overwhelmed. Many feel sure they might cause more harm than good and fear careless mistakes might cause them to hurt their Dad based on incorrect assumptions. They have no role models, no one to mimic or call for a quick “how did you handle this?” type of question. They feel isolated and alone. What’s worse is that they feel if they complain, they may be criticized for not wanting to provide care for a parent or spouse and may appear to be seemingly ungrateful for years of prior care themselves. Thus, the new caregiver begins to feel not only insecure but isolated as well.
Over time, holding in these feelings leads to resentment, anger, frustration, depression, and if care is needed for a long time, eventual compassion fatigue or caregiver burnout. In both situations, the caregiver’s own health suffers, as well as, their emotional well-being. In many cases, the person receiving care often survives longer than the one providing the care because caregivers tend to neglect their own well-being to provide for the one under their responsibility instead.
The picture of isolation and despair is one I hope to change and why I started this website. I have felt and still feel all those emotions at times. I know how you feel because I do what you do every day, and I want to help stop the hurt.
I am retired now and have someone who helps me during the day shift. I want to use that time when I have help to provide some support to those starting out and to encourage those who are already in the role to continue their walk through working together to strengthen one another. I think what I have to offer can make a difference in our lives if we all pull together and share what we know, and I’m will to coordinate that process to help make that difference. I hope you will join me in making that difference.
