Wednesday, April 2, 2014

How To Bring Out a Caregiver’s Inner Optimist

Bringing Out a Caregiver’s Inner Optimist


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.

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Dementia Caregiving: “It Could Be Worse”

My Mantra: “It Could Be Worse”


I have been a caregiver off and on for over forty years, first for my mother, then my father, followed by my sister, my first husband and now, Charlie – my second husband.


When I read posts from others on the AgingCare site I realize how lucky I have been. While they seemed daunting at the time I was gong through them, my experiences pale in comparison to what some of you are going through.

It really is frightening to read some of the horror stories from other caregivers.

Compared to them, Charlie is—so far—a piece of cake, and I realize I have a lot of nerve to complain and feel sorry for myself.

But it certainly makes me wonder what I am in for down the road. Charlie says he plans to live to be 94 (he just turned 80) and, given the changes in his dementia in the past four years, I can see it isn't going to be pretty fourteen years from now.

But then, like I keep telling him, I don't plan to stick around that long. My family genes, for the most part, don't lean toward that kind of longevity.

So the question becomes: What will happen to him if something happens to me?

This is a second marriage; we celebrate our tenth anniversary in July. My children have no obligation to care for him if I precede him in death. He has two adopted children who do not live near us and, for several reasons, are unlikely to be able to care for their father.

If Charlie out-lives me, then I am quite certain that assisted living will become his lifeline. That's why we've looked at some facilities in the area, to get an idea of what is available, and to get Charlie in the mind-set about the possibility of AL in his (our) future.

For now, he says he isn't going if he can't find a place that overlooks forestland or a wild life preserve. If and when the time comes, I'm not sure that option will be available. Transition is always difficult for the elderly, so I can only hope he will not have the presence of mind to care about such things when it's time to make a move.

As for me, for now at least, I am flexible in my thinking. I have always told my children that they should not hesitate to put me in a nursing home when I begin the downhill slide.
Well – it has already begun, but you know what I mean.

I wouldn't wish on them, or anyone, the things the elderly can put their caregivers through.
I pray I can outlive Charlie, if only to make his life easier, with little need for adjustment to various lifestyles over the few remaining years.

For now, life could be worse. This has become my daily mantra.


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A Dementia Looking Glass: Making Sense of Gibberish

I cdnuolt blveiee that I cluod aulaclty uesdnatnrd what I was rdanieg. The phaonmneal pweor of the hmuan mnid, aoccdrnig to a rscheearch at Cmabrigde Uinervtisy, it dseno’t mtaetr in what oerdr the ltteres in a word are, the olny iproamtnt tihng is that the frsit and last ltteer be in the rghit pclae. The rset can be a taotl mses and you can still raed it whotuit a pboerlm. This is bcuseae the huamn mnid deos not raed ervey lteter by istlef, but the word as a wlohe. Azanmig huh? Yaeh and I awlyas tghuhot slpeling was ipmorantt!

If you can raed this srhae teh lnik to tihs atrilce.

If you can read this, YAAAY. If you canNOT, you’ll feel what it’s like for someone with dementia.

Some days, the world makes sense for people living with dementia. Other days, it’s hard making sense of gibberish, like the paragraph above. Except for those recently diagnosed who can still function fairly well, despite the emotional weight of an incurable diagnosis; plain English even loses meaning for many living with dementia.

Did Cambridge University create this test?

I honestly don’t know. Still it is an interesting exercise in perception on this April Fool’s Day.

A couple thoughts to ponder:
  • If you can make sense out of this, what does this say about the power of our language?
  • Better yet, what does this say about your power to perceive?

If you made sense of it, you’re on a roll! Now, try the following:

7H15 M3554G3

53RV35 7O PR0V3

H0W 0UR M1ND5 C4N

D0 4M4Z1NG 7H1NG5!

1MPR3551V3 7H1NG5!

1N 7H3 B3G1NN1NG

17 WA5 H4RD BU7

N0W, 0N 7H15 LIN3

Y0UR M1ND 1S

R34D1NG 17

4U70M471C4LLY

W17H 0U7 3V3N

7H1NK1NG 4B0U7 17,

B3 PROUD! 0NLY

C3R741N P30PL3 C4N

R3AD 7H15.

PL3453 SA4RE 1F

U C4N R34D 7H15.

If you didn’t get it at first, close this page then come back to it at another time. Once you relax your eyes, your perceptual filters may open wider to invite in the meaning of the nonsense above.

I felt like a child riding a bicycle for the first time without any help! The meaning flowed from the passages above–EXCITING! Well, until I became aware my legs weren’t long enough to reach the pedal brakes! ARRRRGGGHH. Sometimes, it’s best to try again another time.

Thank you, Les Hurdle, for sharing this.


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