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Bringing Out a Caregiver’s Inner Optimist

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Optimism; a word associated with sunny smiles and a Pollyanna-ish outlook on life.

But, what does it really mean to be optimistic? And—more important to the stressed-out caregiver—how can you be optimistic in the face of seemingly endless negativity?

Being optimistic does not mean that you have to constantly walk around with a smile plastered onto your face, burying your true feelings and pretending to be happy.

Rick Hanson, Ph. D., caregiver, and author of "Buddha's Brain: The Practical Neurosciences of Happiness, Love, and Wisdom," says that being optimistic means that you see the world accurately, taking in both the good and the bad. And yes, you can train yourself to be more optimistic.

Pessimism, on the other hand, is an unhealthy obsession with the negative, which can snowball until a person feels completely helpless and totally trapped.

Hanson says that it's unfortunately pretty easy to fall prey to pessimism because the human brain has a built-in survival mechanism—called the negativity bias—that makes us instinctually focus on the bad or threatening aspects of our environment while ignoring the good.

Caregivers can become so overwhelmed by the bad that it can be nearly impossible to see the good. Hanson offers three simple tips for caregivers who want to teach themselves to become more optimistic:

  1. Look for areas where you are the hammer, not the nail: The unfortunate reality is that many times, caregivers are like nails—constantly hammered down by selfish siblings, unhappy seniors, and difficult doctors. During these times it's especially important to remember that there are things about your life that you can control. Hanson says that the typical person has control over three main realms: the outside environment (fixing a leaky faucet, painting a wall, etc.), our bodies (exercise, taking the right medication), and our minds (our perspective, where we focus our attention). Caregivers often find themselves in a position where it becomes harder for them to affect change in the outside world and even in their own bodies. Hanson says that when caregivers find themselves experiencing this reduced sense of control, it's important to remember that you can always influence your thoughts. This doesn't mean that you have to ignore the bad things, sometimes you can't, no matter how hard you try. It means making the choice to change your perspective, in spite of those bad things.
  2. Be a sponge for positive experiences; savor the small things: Thanks to the negativity bias, Hanson says that negative experiences tend to get stuck in our psyche whereas positive experiences run right through it, like water in a sieve. Part of training yourself to become more optimistic is to practice noticing and holding on the positive things that exist in our everyday lives. Hanson suggests that each day, caregivers should try and find ten instances where they recognize something positive and focus on it for at least ten seconds. It doesn't have to be anything big—a flower blooming on the bedside table, or the sound of a child's laugh in the distance—things you normally wouldn't even notice. Pausing to reflect on a positive experience, even if it seems minor, will help you internalize and attach emotion to it, something that Hanson says the brain normally wouldn't do. This is why simply telling someone to think more positively is often unhelpful, because happy thoughts alone will still lack that emotional component. But Hanson feels that ten seconds, ten times a day, is enough to help you begin to train your brain to hang on to the simple happiness that surrounds even the most dire situations.
  3. Connect with others: Hanson also emphasizes the value of a solid social network, saying that caregivers need to try and seek out as many opportunities for social interaction as they can. He says that caregivers seeking to become more optimistic need a diverse support network that can offer them camaraderie and support along their journey, as well as an opportunity to vent. Being a caregiver for both his mother and father, Hanson knows that finding time to socialize can be challenging for time-strapped caregivers, and encourages them to just do what they can. It may also help to broaden your idea of what social interaction means. Animals and kids are two sources of socialization that most people may not think to utilize, but Hanson says that they can supply caregivers with much-needed comfort and perspective.

It's true that focusing on a beautiful sunset won't make you deaf to your loved one's resentful complaints, or make changing their diaper a pleasant task, but Hanson points out that research has consistently shown that people, no matter their circumstances, can learn to see the world in a more balanced way.

Will these tips work for you?

As with all things, you'll never know until you try. Challenge yourself to really take the time and employ these strategies; then let us know what you think by commenting below.

 
 

Comments

 
  •  Comments 1 to 3 of 3 
 
 

mslisadoll

Give a Hug

May 5, 2012

Thank you so much for this article as it is not easy for us to see the glass as half full instead of empty when we get in a rut and suffer from caregiver burnout. It does not help us or the ones we care for either. It made me more grateful to have a roof over our heads and a loving home with both of my parents here in their own house instead of a nursing home. Caregiving is so much easier for us if we are not stressed out, grumpy and tired all the time. It has taken me a long time to realize that to just go with the flow instead of being so resistant and bullheaded. It also brings down the people around you down and is hard on their health and well being. This article helped so much to see that their is a light at the end of the tunnel instead of that isolated, hopeless feeling. Also was feeling kind of down feeling abandoned that I never hear from or see my "so called friends" anymore, but that is their loss and there is not much I can do. It just makes it kind of more hesitant to trust other people or let them into my life. Friendship should be more about the person than money and a bunch of bs gossip. It should be more about being there to depend on each other when you need a shoulder to cry on or just somebody to talk to when you are having a hard time and that is not so easy to find sometimes. Anyway, hope this article helps us - caregivers as well as others that are involved in the care of our loved ones.

 
 

anonymous20452

Give a Hug

May 7, 2012

Wow..this woman displayed in the picture above is not at all what most caregivers look like...she looks very rested, relaxed, and even has time to go tanning, bleach her hair and sit in an overgrown grass field and smile at the butterflies and hummingbirds landing on her shoulders...this must have been right after her shower from changing her elder's depends? Or did the siblings finally bend under the guilt from not helping and took her elder for the month? Where is Mary Poppins when you need her?

 
 

lildeb

Give a Hug

Jun 9, 2012

I think the article had a few tips that can be tried to help make it a bit easier on both the care-giver n the person whom has AD. If the caregiver can at least take a few minutes to her or himself by looking at the bright clouds floating above to laying on the floor n babying talking to your pet or to taking a moment to listen to the birds chirping in the air would at least help a few minuets to get in that positive mode. Not that it will make the problem or what ever that was bothering you go away but maybe a better more relaxed for a few minuets to think before you say or do something later that u may regret.
I try everyday to outweigh the good with the bad when it comes to the mnl with AD and sometimes the bad can outweigh the good. That is where I try to find that little space of mine to rethink n redirect my mindset on how to handle things. Of course, they always don't work yet, some do work n some is better than none. I think that is what the article is trying to help us how to balance r life even though we will feel like we r riding a rollar coaster sometimes. To look at good of the outcome n not all the negative part for it will just multiply n then you r more miserable. I have to remind myself as well that, the mnl is not all their n that sometimes she don't fully understand what is going on for that time of day. That it is a shame n devastating disease such as AD that will slowly rob the person's independency. The least I can do is educate myself as I learn what works best for both of us in order to make our lives run as smooth as much as possible. Now, I have to check bathroom for poop on the toliet paper n toliet handle. Never a dull moment. ; )

 
  •  Comments 1 to 3 of 3 

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