Funny Fridays: Because It’s Better to Laugh than to Cry!

December 19th, 2008

All I Needed to Know About Life I learned from Santa

1. Encourage people to believe in you.

2. Always remember who’s naughty and who’s nice.

3. Don’t pout.

4. It’s as much fun to give as it is to receive.

5. Some days it’s OK to feel a little chubby.

6. Make your presents known.

7. Always ask for a little bit more than what you really want.

8. Bright red can make anyone look good.

9. Wear a wide belt and no one will notice how many pounds you’ve gained.

10.If you only show up once a year, everyone will think you’re very important.

11.Whenever you’re at a loss for words, say:”HO, HO, HO!”

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Doctor: So what seems to be the problem?

Patient: I have an irrational fear of Santa …

Doctor: Sounds like you are Claus-trophobic.

(Rimshot!)

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A Jewish mother gave her son two neckties on Chanukah.

When she came over to visit, the boy hurried into his bedroom, ripped off the tie he was wearing, put on one of the ties his mother had brought him, and hurried back. “Look, Mama! Isn’t it gorgeous?”

“Mama asked, ‘What’s the matter? You don’t like the other one?’”

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To everyone in the TLeC community, have a wonderful holiday season! I’m off to enjoy time with my family — hope you do, too! And remember to always cherish the Golden Oldies in our lives.

See you in 2009! :-)

Inspiring Quotes for Caregivers: On Hope — 12/17/08

December 17th, 2008

Hope in the Thorns by orangeacid

The pessimist sees difficulty in every opportunity.

The optimist sees the opportunity in every difficulty.

~ Winston Churchill

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Once you choose hope, anything’s possible.

~ Christopher Reeve

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When the world says, “Give up,”
Hope whispers, “Try it one more time.”

~ Author Unknown

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Photo Credit: orangeacid’s photostream

Book Review: Designated Daughter — The Bonus Years With Mom

December 15th, 2008

I was afraid to read this book. Afraid it would hit too close to home.

And I was right . . . it did.

But I loved it so much, I read it cover-to-cover twice over!

What Is a Designated Daughter?

Here is the definition in the author’s words:

“When my mother became a widow, I became a Designated Daughter — the sibling who would try to take up the empty space that had always been filled by Dad. What I found in walking beside her was my own strong space. . . .

Designated Daughters are all over the country, all over the world. We are a secret society of women, instantly recognizable to one another. We sit in doctors’ waiting rooms holding our mothers’ hands. We hold the coats, we hold the purses, we hold our mothers’ arms like suitors. We become so close, so bonded, we form a two-person silhouette.”

This book recounts D. G. Fulford’s eight years as Designated Daughter for her mother, Phyllis Greene. Fulford writes honestly about the joy and sadness that result from living this role. Her words filled me with laughter, and yes, a few tears, as she recounts their time and travels together.

Phyllis Greene adds her unique perspective on their experiences at the end of each chapter. And this brings another important voice to the story, and the book is richer as a result.

A Part that Made Me Laugh

After a doctor referred to her mother’s breasts as “boobies,” Fulford writes:

“Boobies? Boobies? My mother did not have boobies, my mother had a bosom. A bosom is what ladies such as she have. (I have tits.) I called her on it in the car and she ‘fessed up. The booby bit had bothered her. We don’t even have to talk to communicate anymore.”

A Part that Is Just So Real

This one passage really hit me in the gut. I couldn’t have described being a Designated Daughter any better than this:

“It seems as if it happens in an instant, but it takes a lifetime. Our mothers go from aging to old. We Designated Daughters become familiar with crisis mode, as our mothers’ well-being differs from day to day. They put their trust in us though we do not always trust ourselves. The road ahead is not going to be easy, each step a different test.”

Greene writes humorously, yet with great insight, about her difficulty in accepting the aging process:

“Who ever would have thought a wheelchair would be a joyride?

Years ago, when we were on our way to Florida, I had caught a glimpse of a couple we knew crossing a concourse ahead of us. The wife was pushing her husband in a wheelchair, and I said to Bob, in my stupidity, ‘The day I need a wheelchair at the airport is the day I stop traveling.’ How cocksure I was, and how fast I changed. By 2002 air travel was a disaster, and I wasn’t so great myself in the walking category . . . . Never say never. I ordered a wheelchair as I made my reservations. It’s the only way to go!”

Who Is This Book For?

Even though the title says Designated Daughters, this book is for Designated Sons, too. While it is a fact more daughters than sons are family caregivers, sons will see themselves in many of the same situations Fulford faced with her mom and should also read this book.

In fact, all baby boomers should read this book! Because even if your Golden Oldies are healthy now and aging gracefully, as stated in Fulford’s quote above, it could take only an instant and you may find yourself as a Designated Son or Daughter before you know it.

Plus, it will deepen your appreciation for all the great (and even not-so-great) times you’re currently having with your aging parents. Even before you reach the Bonus Years.

What I Wish For

Reading this book made me feel like I had met these women. Even though the book was just published in 2008, I already want an update on how Phyllis Greene is doing health-wise and otherwise, and how D.G. Fulford is coping (and what color her hair is now). I hope there is a sequel planned by this special mother-daughter team.

Buy It Now

Click on this link to purchase the book (I will earn a few cents commission from Amazon.com):

Designated Daughter: The Bonus Years with Mom

Funny Fridays: Because It’s Better to Laugh than to Cry!

December 12th, 2008

This occurred during a blizzard in the late 1990’s when 54 inches of snow fell in 48 hours near Ward, Colorado. Meet Santa’s newest “reindeer,” Bailey.


I bet this video made you at least crack a smile, if not laugh out loud!

To everyone in the TLeC community, have a great weekend — and hope you get to frolic like Bailey! :-)

Inspiring Quotes for Caregivers: On Caregiver’s Rights — 12/10/08

December 10th, 2008

December 10th is Human Rights Day around the world. Sixty years ago today the Universal Declaration of Human Rights (UDHR) was published by the United Nations. The UDHR was the first international recognition that all human beings have fundamental rights and freedoms.

First, let’s take the concept of human rights from the global level to a personal one:

“Where, after all, do universal human rights begin? In small places, close to home – so close and so small that they cannot be seen on any maps of the world … Such are the places where every man, woman and child seeks equal justice, equal opportunity, equal dignity without discrimination. Unless these rights have meaning there, they have little meaning anywhere.”

~ Eleanor Roosevelt

And now let’s apply this concept to our caregiving world. Jo Horne, author of “Caregiving: Helping an Aging Loved One,” wrote this document:

Caregiver’s Bill of Rights

I have the right:

To take care of myself. This is not an act of selfishness. It will enable me to take better care of my loved one.

I have the right:

To seek help from others even though my loved one may object. I recognize the limits of my own endurance and strength.

I have the right:

To maintain facets of my own life that do not include the person I care for, just as I would if he or she were healthy. I know that I do everything that I reasonably can for this person, and I have the right to do some things for myself.

I have the right:

To get angry, be depressed and express other difficult emotions occasionally.

I have the right:

To reject any attempt by my loved one (either conscious or unconscious) to manipulate me through guilt, anger or depression.

I have the right:

To receive consideration, affection, forgiveness and acceptance from my loved one for as long as I offer these qualities in return.

I have the right:

To take pride in what I am accomplishing and to applaud the courage it sometimes takes to meet the needs of my loved one.

I have the right:

To protect my individuality and my right to make a life for myself that will sustain me when my loved one no longer needs my full-time help.

I have the right:

To expect and demand that as new strides are made in finding resources to aid physically and mentally impaired persons in our country, similar strides will be made toward aiding and supporting caregivers.

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My questions for you:

Is there anything you would like to add to the statements above?

Are you protecting and exercising your rights as a family caregiver?

A New Twist on Holiday Decorating for Your Aging Parents

December 9th, 2008

Hanukkah Menorahs

I just got back from decorating my mom’s room at the board and care cottage for Hanukkah. While she was being fed lunch in the kitchen, I played a CD of Hanukkah music as I cheerily put up the decorations. For about two-thirds of each day now, Mom, age 99, is in bed in her room, so I decided it was more important to put the decorations up in there rather than in the living room and kitchen which I have done in previous years.

If you are planning to do some holiday decorating for your aging parents (and I hope you are), here are things I realized as I went along. The results look somewhat different than how we normally decorate at our house.

Decorating Changes I Made

Since Mom spends most of her time in bed, I put the majority of the decorations on the walls closest to her and lower down on the walls, so when she is lying on either of her sides they will be at eye level. I also put a few on the far side of the room, but I’m not really sure how well her eyes focus for distance, so the majority of the decorations are on the walls and closet doors closest to her or in her line of sight. I thought of the perspective as the “Bed Cam!”

I used the large-size decorations with bold colors on them because I think she will be able to see those more clearly than some of the smaller, daintier, pastel ones.

I bought a new stuffed animal to add to her stuffed animal collection — a cute Hanukkah bear that she can hold or cuddle any time.

Instead of real candles in the menorah (see photo above), I brought over an electric menorah that plugs into the wall and lights up. I don’t want to create any fire hazards in the board and care cottage!

I didn’t overdo the decorations; keeping it simple because Alzheimer’s disease patients could be agitated by too much stimulation (or changes in their rooms). Although at this late stage I’m not sure how aware my mom is of her surroundings, except for what is directly in front of her face.

I set the volume on the CD player a little louder than usual to insure she could hear the Hanukkah music from bed. (Years ago we had to take away her hearing aids because she would pop them out of her ears and start chewing on them, not knowing what they were.)

What Happened Next — Ta-Dah!

When she was finished eating, the caregiver brought my mom to her room to see what I had done. Unfortunately, she was already tired out and her eyes were closed as they wheeled her wheelchair into the room. Even though her eyes were shut, I told her I was there and had a surprise to show her . . . but she didn’t open her eyes. I stayed another 45 minutes, hoping she would wake up, but she didn’t.

Was I disappointed that I couldn’t share my splendid decorating job with her? I sure was!

Did I shed a few tears that we couldn’t share the fun of this together? I sure did!

Did I know I needed to change my expectations for the holidays as my mom aged? I sure did! And I thought I had this part down pat, but obviously I don’t.

So I’ll go back there tomorrow morning when she’s more likely to be awake and alert, and give her a “tour” of her decorated room then. One “plus” side of Alzheimer’s disease is that the decorations will be “new” to my mom every day during the holiday season! ;-)

Have you had to change your holiday traditions due to your parents aging? In what ways? How did you cope with it?

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Photo Credit: mamamusings’ photostream on Flickr

I’m an Official SOB and I Couldn’t Be Happier!

December 8th, 2008

I know what you’re thinking — has Linda lost her mind?

She’s been called an SOB and is telling the world about it? What’s up with that?

OK, OK, I’ll explain. It doesn’t stand for what you think!

Liz Strauss, a professional writer and blogger whom I respect greatly, has awarded me the coveted title of “SOB” or Successful and Outstanding Blogger.

Woo Hoo! I’m thrilled and honored to be included in the SOB Hall of Fame over at Liz’s blog.

Please check out her blog now. Who knows? Maybe you’ll get bitten by the blogging bug and she’ll be calling you an SOB some day, too. At the very least, you will find enough great reading at her blog and in the SOB blogs listed there to last a lifetime. Enjoy!

Thank you so much, Liz!

A Holiday Gathering for Family Caregivers

December 8th, 2008

I was planning to write a post about family caregivers, our aging parents and/or relatives, and the many issues we might face during the hectic holiday season. In organizing my own thoughts and researching this topic, I found there are many excellent resources already available on the internet about this very subject. Instead of reinventing the wheel, I’ll point you to the ones I believe are most helpful.

So grab a cup of hot chocolate (or a hot toddy), sit back and browse through this gathering of sites:

  • Valarie D’Acquisto’s Pleasant Days for Elders blog has an article entitled “Wishing You and Your Elder a Pleasant Christmas Season” that reminds us our Golden Oldies run colder than most people and gives practical advice on how to insure they are warm and toasty during these winter months. She also includes a list of possible gift ideas for seniors at the holidays that can be referred to all year long.
  • Caregiving.com founder, Denise Brown, offers an entire Holiday Survival Guide, which includes eight individual holiday articles on a wide-range of topics as well as an audio recording.

If you prefer to listen rather than read, you can load these five podcasts onto your iPod or mp3 player and listen while you’re on the go — recordings from the weekly “Ask Mr. Eldercare Show” at BlogTalkRadio.com. Martin Sabel, aka Mr. Eldercare, is the host who covers these holiday topics with his guests:

Home For The Holidays: Getting Ready To Visit Mom and Dad

What To Look For When Visiting Your Aging Parents Over The Holidays

Ask Mr. Eldercare About Aging Parents and The Holidays

Manage Holiday Caregiving Stress Before It Manages You

Before You Return Home for the Holidays, Do This

It is my hope that after reading or listening to these words of wisdom, you, your families and your aging loved ones will have a much less stressful and a far happier holiday season!

I like learning from you, too. What have you learned from your caregiving experience during the holidays?

Or please share other articles or resources about this topic in the comment section below. Thanks!

Funny Fridays: Because It’s Better to Laugh than to Cry!

December 5th, 2008

To everyone in the TLeC community, have a great weekend! :-)

Inspiring Quotes for Caregivers: On Community — 12/3/08

December 3rd, 2008

“We don’t accomplish anything in this world alone … and whatever happens is the result of the whole tapestry of one’s life and all the weavings of individual threads from one to another that creates something.”

~ Sandra Day O’Connor

As family caregivers we become so focused on the responsibilities we have for our care recipients, at times we can feel very alone. But no caregiver lives in a vacuum.

You may feel like you’re alone, but you’re not!

Even if you think your daily life consists solely of yourself and your aging parents (”Golden Oldies” is what I prefer to call them), your world must include, at the very least, a doctor, his or her staff, and probably a pharmacist, too. Keep reading to find out more reasons why you’re not alone . . .

Concentric Circles by SuperFantastic on flickr

I’ve recently been thinking about the caregiving world as a series of concentric circles, like a target. In the center of mine, in the smallest circle, are my mom and me. Right outside that tiny circle is the next circle of my immediate and extended family. The next larger circle surrounding that one consists of the board & care staff and health professionals who are part of our caregiving “village.” And the very next circle holds our friends and neighbors.

In October, I wrote about going back East on a short trip, and how it was going to “take a village” to care for my mom during that time. It struck me after my return that this village still exists, and that I had created it subconsciously, little by little, over time. It is very gratifying to realize how many people are supporting me and my mom in a “hands on” way on a day-to-day basis.

Perhaps you have done the same but, like me, haven’t taken the time to recognize your village?

It dawned on me that I’ve added a new, even bigger circle that you are all a part of because you are reading this post!

Now no family caregiver ever needs to feel alone — people all over the world can read the words written here 24/7 no matter what country or time zone they live in. In less than a year, I have readers from 12 countries around the world! TLeC has gone global and I couldn’t be happier!

The quote below expresses how I feel about the awesome community we are building here:

“A community isn’t built or befriended,
it’s connected by offering and accepting.
Community is affinity, identity, and kinship
that make room for ideas, thoughts, and solutions.
Wherever a community gathers, we aspire and inspire each other intentionally . . . And our words shine with authenticity.”

~ Liz Strauss, Successful-Blog.com

I have offered my ideas, and you have added to them in a myriad of ways through your comments and emails. My wish is that you will all gain something of value by participating in our growing community. One in which we share, learn together, and support each other through the roller coaster ride every family caregiver experiences. My vision is that TLeC will always be a place in which you can stop by for a visit, read a little or a lot, and then head back to your own world feeling better as a result of your time spent here.

Please know that in the increasing concentric circles of the TLeC caregiving community you are not alone!

What part of the world do you live in? Please tell us which city, state, county, country, continent or galaxy :-) in the comments below. OK, I’ll go first . . . I live in sunny California!

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Photo Credit: SuperFantastic’s Photostream on Flickr

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