For the past seven and a half years, my life has been largely defined by a series of responsibilities known as caregiving. For anyone who has ever been a caregiver, even for a short time, it is easy to understand what that entails, and what it means in the lives of those involved. Caregiving is not a job that usually becomes less demanding as time goes by, although that is not an impossibility. While caregiving is not an easy job, I can tell you from my personal experience that it is a very rewarding job. It is one that places you in a battle for life…or at least a battle to prolong life. While it is rarely a battle you can win in the end, you do win in that those final years are made more comfortable for the patient, and filled with the knowledge that you love that person so much that you are willing to make this sacrifice for them.
Now, after the passing of my dad, the recovery of my mom, the necessity of placing my mother-in-law in a nursing home, because Alzheimer’s Disease no longer allows her to stay at home, and the passing of my father-in-law, I find myself no longer in the position of being a full time caregiver. Yes, I still have minimal responsibilities with my mom and mother-in-law, like doctors appointments and visits with them, which are very important to their emotional well being, but the main responsibilities belong to others or are no longer necessary. So, I find myself wondering what do I do now that I am not a caregiver? What is life supposed to be like now? This has been who I was for so long. It was even all I talked about sometimes, as many of my family members can attest to.
A part of me is still very tired. At times during the day, I feel like I could sleep for a month, and yet, I have trouble getting to sleep at night. A part of me is ready to get back out on the trails…walking and breathing in the fresh air, and yet a part of me feels like I just want to sit and do nothing. Maybe it’s an emptiness because of no longer being needed as much as before. It seems like concentrating is very difficult…unless it’s about why we lost the battle for life, or what we might have done differently.
I know that I will get used to having more time again. And as with my dad’s passing, I will come to know that you don’t get over it…you just get on with it. I will get used to not being a caregiver, but I know too, that I will never be the same person I was before. I can’t be. I have seen too much…learned too much…felt too much…know too much, to ever be the same person I was before. I have experienced the adrenalin rush needed to hold myself together during life threatening illnesses reaching emergency levels, and making the decisions necessary to treat loved ones who can’t speak for themselves. I have held their very lives in my hands, and been responsible for trying to bring them back. And, I have lost that battle…twice. I will recover from caregiving and I will get on with it, but I will never be the same. I don’t think it is a bad thing, and I would not change any of it, except the loss of my dads, but while I would do it all again, I know that I have been forever changed by this experience.