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Tuesday, September 25, 2012

After Cremation: Rituals, Storage, Disposal of Ashes (Cremains)--Research, Video 1:43


Although unique funerals continue to increase in popularity, cremation is definitely in the mainstream these days as a method of body disposal. People are finding interesting ways to dispose ashes or cremains of loved ones.

Traditionally, cremains are often stored by families who keep them in urns and other containers that vary in their uniqueness. These may include vases with pedestals or even personalized teddy bears with hidden pouches. Teddy bears can be sewn from the deceased person’s clothes. Among other uses, cremains are being used in jewelry, shotgun shells, and fireworks. In terms of destinations, cremains can be stored in cemetery plots, mausoleum, or scattered in a garden or body of water. For $5,300 cremains can be sent aloft into outer space, while $13,000 can send them into luna orbit.

One research study on cremation focused on how 87 people described their experiences with cremation, cremains disposal, and rituals regarding  their deceased loved ones. How did they view the experience? They felt the experiences were positive. Most research participants preferred to be cremated and honored through nontraditional rituals themselves.

With so many choices available, people should make plans in advance regarding disposal of their cremains if they choose to be cremated. In this video titled Scattering Parents’ Ashes, a daughter fulfills her deceased parents’ dream of world travel. View the unusual way she accomplishes this that includes many other people. If you choose to be cremated, what would you want to happen to your cremains after death?




Frances Shani Parker, Author
Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes is available in paperback at many booksellers in America and other countries and in e-book form at Amazon and Barnes and Noble booksellers.

Monday, September 17, 2012

Hospice-Palliative Care Volunteer Retention: Know How to Hold Them (Research)

                           Miss Ruby with Hospice Volunteer Frances Shani Parker

You’re a hospice-palliative care volunteer coordinator with a volunteer quota you’re always striving to maintain. Can secrets to keeping them be found in this research reported in the American Journal of Hospice and Palliative Care?

In this study, the 33-item Volunteer Retention Questionnaire was used to determine what really motivates volunteers to keep doing this work that baffled onlookers often tell us must be depressing. (If they only knew how much we enjoy it!) With responses from 119 hospice-palliative care volunteers from three community-based hospice programs, these were the results of how volunteers rated the importance of items in their decisions to keep on volunteering:

1)   First and foremost, they enjoyed the work itself. (Imagine that!)

2)   They felt adequately prepared/trained to perform their duties. (Coordinators, you’re doing a good job here!)

3)   They learned from their patients’ experiences and from listening to their stories. (Remember listen and learn?)

An interesting result is that being recognized (service pins, newsletters, etc.), volunteer coordinator phone calls and cards, and reimbursement for out-of-pocket expenses were among the lowest rated in retention importance. Personally, I think this speaks to the sincere and giving nature of volunteers, but these should still continue on some level. Praise is still a big motivator. 

Frances Shani Parker, Author
Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes is available in paperback at many booksellers in America and other countries and in e-book form at Amazon and Barnes and Noble booksellers.
Hospice and Nursing Homes Blog

Monday, September 10, 2012

Advice for Caregivers: Life, Death, Bereavement (Video 2:56)


Although many caregivers are actively involved in patient care for a considerable amount of time, they may not be confident or knowledgeable sometimes about the specifics of caring for someone else while maintaining their own quality of life. In addition, thoughts of preparing for a loved one’s death and their own future bereavement after the loved one dies often lurk in the background of their daily living. Healthcare providers can be a great source of support and information for caregivers in terms of confidence building and advisement.

The National Family Caregivers Association shares the following four-point message of advice for caregivers:

1)   Believe in yourself.

2)   Protect your health.

3)   Reach out for help.

4)   Speak up for your rights.

Frances Shani Parker, Author
Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes is available in paperback at many booksellers and in e-book form at Amazon and Barnes and Noble booksellers.

Monday, September 3, 2012

Older Adult, First-Time Grandparents: Interview with Frances Shani Parker (Baby Video)

New Grandparents Mitch and Lonnetta White with Amelia


Becoming grandparents for the first time can be quite spectacular, especially for older adults. My friends Lonnetta and Mitch White recently began this wonderful journey just in time for Grandparents Day on September 9th. Their contagious excitement over the birth of "Miss Amelia" prompted me to feature them on this blog. Not surprisingly, they were eager to share their pride, joys, concerns, and expectations in this interview.


1) What were your thoughts as you anticipated the arrival of your first grandchild?

Lonnetta

I have/had feelings of extreme happiness, joy, and excitement!
My thoughts were fantasies of how wonderful it is going to be to love and spoil a grandchild the way I was loved and spoiled by my paternal grandmother.

Mitch

I remembered the anticipated arrival of my son. Of course, in those days we didn’t know if we were having a girl or boy. The imaging technology simply hadn’t gotten that far. But I was there in the delivery room and had the privilege of seeing Amelia when she emerged from the delivery room. What a wonderful opportunity!

2) How did you feel during the first days after Amelia was born?

 Lonnetta

I felt proud and on top of the world. I was also pleased that she was FINALLY here healthy and absolutely gorgeous! I felt blessed to see, hold, kiss, cuddle, and in all ways experience my granddaughter.

Mitch

I was elated, in wonder of this child who came here with her eyes wide open.

3) What do you love most about this new chapter in you life?

Lonnetta

Life is good! Optimism is a constant companion and more easily accessible. My existence has given me a new lens through which I view the world. Every time I think of her I find myself smiling!

Mitch

She’s been here before!

4) Grandparents are an important influence in their grandchildren’s lives. How does Amelia influence your life?

Lonnetta

I brag incessantly. I now have a subscription to a magazine on parenting. In addition, I read all articles about babies and parenting. I want to do all that I can to help her to be the best at whatever it is she wants to be.

Mitch

I am the proud grandpa who never loses an occasion to show the latest picture or video of Amelia.  She’s the most observant child I have ever seen. I just want to be called Grampa, not Grandpa, but simply Grampa.


8)    What advice do you have for other grandparents in making their grandparent journey successful?

Lonnetta

LOVE, LOVE, LOVE your precious little ones! Enjoy, enjoy, enjoy! Encourage and support them in their endeavors to become happy, successful adults.

Mitch

I’m too early in this wonderful adventure to offer advice to others, but I do know that, whether you’re raising a child or supporting your grandchildren, it’s extremely important to show them love by attending to their needs, teaching them to share, and helping them to grow beyond themselves. Right now, Amelia is understandably egocentric. The world is her oyster. Getting her in another structured environment is the next step towards preparing her to interact with the world. She’ll be ready sooner than we think. She’s been here before.

Lonnetta and Mitch, thank you so much for your insightful responses to these questions on grandparenting. Happy Grandparents Day! Of course, our interview would not be complete without Amelia having her say. Welcome to the world, Amelia!





   Another Wonderful Grandchild! Welcome to the World, Emory!

Mitch

Emory's parents (Angie and Pops (Mitch, II) told us of the probable arrival of a new child in June 2015 while we were helping Miss Amelia celebrate her third birthday. We were all extremely excited. But I am Old School and did not want to know the sex of the new baby until Angie gave birth. I felt the same way when she was pregnant with Amelia. Someone let the secret out.

We wanted to be there at her birth just as we were when Amelia was born. But another set of grandparents who were not there when Amelia was born had their turn. Lonnetta and I were introduced to Emory when she was two weeks old by Amelia. It was very clear that Amelia was Emory's big sister. We witnessed the beginning of a bond that only gets stronger (in spite of the occasional sister tugs of war).

Lonnetta

I was surprised to learn that our daughter-in-law was pregnant and happy to know that another grandchild was on the way. Since becoming Nana (my first choice was Granny), I am consumed with a desire to nurture, please and satisfy. Becoming Emory's grandparent is a blessing. It is another opportunity to witness and contribute to the existence, development and maturation of a very special individual. 

Looking at Emory after she was born, I already knew I would do all I can to encourage her to be a proactive person who cares about improving society. I could already dream of her success in whatever field she chooses. I knew then that I wanted her to be a confident, independent and successful young woman. Emory's birth affirmed once again that children are God's gift to us. The miracle of meeting Emory was breathtaking. 





Amelia and Emory




You can read more about Lonnetta, Mitch, Amelia, and Emory at this blog post: "Grandparent Journey: Older Adult Seniors"


Frances Shani Parker, Author

Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes is available in paperback and e-book editions in America and other countries at online and offline booksellers.
Hospice and Nursing Homes Blog

Monday, August 27, 2012

Frances Shani Parker and Anne Marie Gattari Television Interview: Aging Well in America (Video 30:16)


Frances Shani Parker, an eldercare consultant, former school principal, hospice volunteer, and author of Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes, was featured guest on Aging Well in America, a television show hosted by Anne Marie Gattari. The interview covered these topics:

Hospice

Nursing Homes

Volunteering

Caregiving

Dementia

Death Preparations

Intergenerational Partnerships 

Older Adult Stereotypes





Frances Shani Parker, Author
Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes is available in paperback at many booksellers and in e-book form at Amazon and Barnes and Noble booksellers.

Monday, August 20, 2012

Caregiver–Patient Poem: Hospice, Dementia Aha! Moment with Music


Caregivers who embrace patient care with win-win expectations know that aha moments can come at any time. Meaningful conversations and feelings drift into a now/here place that helps us worm our way from the unknown to the known. Aha moments are not forced or always joyous and explosive occasions. Many times they are subtle, quiet with a settled satisfaction that brings whispered gifts of personal knowing about life lessons. One reason some people assume hospice work is depressing is that our aha moments with patients are not shared enough with people who are unaware of powerful scenarios we experience sometimes.

Recall a few of the aha moments you have known, especially those that made you better people. Many of you have had them. Share these enlightenments with others who wonder why you do this work or those who express a general interest in what your work entails. Aha moments can enhance lives of patients and caregivers.

This poem describes one of my favorite aha moments as a hospice volunteer. I had a very challenging patient whose name was Katherine. She usually lay in bed sleeping or looking up at the ceiling. I couldn’t tell if she was bored, unhappy, mellow, or all three. Rarely speaking, she never sat up on her own or walked. We mostly stared at each other while I talked.

Knowing that Katherine had been active in her Baptist church in the South at one time, I decided to use my CD player with headphones (this was before iPods, etc.) to help her enjoy music sung by Mahalia Jackson, whom many hail as the greatest gospel singer ever. After reading this poem, you’ll understand why it’s one of my favorite aha moments and why I still smile every time I read it. Share your aha moments with others, and you’ll be smiling, too.


Sounds of Ecstasy

Headphones frame your head.
You look at me, your volunteer,
wonder what they can be.
Mahalia Jackson’s song erupts,
“When the saints go marching in...”
Sleepy eyes widen like popped corn.
“It’s a CD player,” I say.
Your mental video rewinds
through time from the nursing home
to an Alabama church service
where bodies rock to music.
I join you clapping with the choir.
Your stiffened hands move
with a powerful energy that rises
like a resurrected hot flash.

“It’s wonderful,” you whisper.
Mahalia responds singing,
“Walk all over God’s heaven...”
I picture you joking with Death
when it’s your time to holy dance
to the Other Side of Through.
Mesmerized by the music,
you soak in every song.
A CD player exhilarates you
with sounds of ecstasy.
Such an easy thing for me
to bring, but before I leave,
you say you love me twice.

© Frances Shani Parker from Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes

Frances Shani Parker, Author
Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes is available in paperback at many booksellers in America and other countries and also in e-book form at Amazon and Barnes and Noble booksellers.

Monday, August 13, 2012

Service Robots: Long-Term Care Technology Helps Staff and Residents (Nursing Home Video 4:22)


Meet Care-O-Bot and CASERO, two German robot brothers that can provide needed services in long-term care facilities. Care-O-Bot is a robot assistant, while CASERO is an automated guided vehicle system. Previously, I shared information with you about Nursebot Pearl, a robot that services patients in private homes. She has a caregiving voice and an emotional face with interchangeable parts. 


Through robots, technology strives to meet the needs of our growing population of older adults who are living longer with healthcare concerns.  Of course, expensive robots will never replace compassionate and efficient healthcare workers. But they can provide services that allow healthcare workers to have more time with residents and enhance quality of their lives. Depending on the degree of dementia, robot trials indicate that people with dementia can accept robots and be amused by them.
What about our two robot brothers and some of the services they perform? Care-O-Bot, the younger of the two, can enter a room, introduce himself, pass out drinks, and even keep track of who drank and how much. With colored cameras used like eyes, this robot can recognize and respond to individual faces, play games, and lead residents in singing. CASERO, a more developed robot, uses its multiple cameras to monitor hallways and transports objects by guiding itself, sending for an elevator, and riding it to another floor. Change is slow, and, while everybody may not love service robots, many people do. You can read more about both robots in this article about service robots.
This video titled Service Robots in Nursing Homes: Care-O-Bot 3 and CASERO shows the robots in operation at Parkheim Berg, a nursing home in Germany:
         

Frances Shani Parker, Author
Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes is available in paperback at many booksellers and in e-book form at Amazon and Barnes and Noble booksellers.

Monday, August 6, 2012

Dementia Quiz: Four Questions (Research, Dementia Adult Daycare Video 2:46)


Can you answer these four questions about dementia? View answers below the dementia daycare video.

1)    Where do most people with dementia die (home or institution)?

2)    Name two illnesses people with dementia usually die from?

3)    What is the second most common form of dementia affecting older adults after Alzheimer’s disease?

4)    Name two reasons dementia daycare is beneficial for caregivers and people with dementia.?


This video titled KRIV 26 - Sheltering Arms for Dementia Patients.flv supports not only people with dementia, but also those with several other impairments. It gives an overview of the kinds of activities that engage participants and improve their quality of life at daycare programs.




Answers (Good luck!):

1)    (Death Location) A widespread myth is that most patients with dementia live and die in nursing homes. Many people think that as the disease progresses, most patients go from home to hospital to a nursing home and stay there, but dementia patients make various transitions in care, following no definite path.

2)    (Death Illnesses) People with dementia, including advanced dementia, usually die from cancer, heart   disease or pneumonia.

3)    (Dementia 2nd) Dementia with Lewy bodies or Lewy body dementia is the second most common form of dementia to affect older adults after Azheimer’s disease.

4)    (Daycare Benefits) Dementia daycare programs allow people with dementia to continue living at home. They provide beneficial individual and group activities and additional support services. Caregivers enjoy having more time for themselves without worrying about loved ones’ safety and quality of life.

Frances Shani Parker, Author
Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes is available in paperback at many booksellers and in e-book form at Amazon and Barnes and Noble booksellers.

Monday, July 30, 2012

Compassionate Direct Care Workers with Patients: Healthcare Photos, Stories (Long-Term Care Research, Video 3:55)


Photography is such a fascinating process. Capturing that special something which means more than words can ever say by themselves connects people at a guttural level of humanity. What if you are a healthcare worker giving ongoing caregiving support to patients as part of your job? What would you want to capture in photos to show the world what you really want to convey about your relationships with patients? How would you envision a photograph of compassionate caregiving and an accompanying story about your interactions with patients?



Research on compassionate caregiving was done by the University of North Carolina, Charlotte. The study was designed to understand the views of direct care workers and included 15 nurse aides and medical technicians working in an assisted living and special care assisted living community for people with dementia. Participants were given digital cameras to create photographs showing what caregiving meant to them. Discussions, photographs, and written and oral stories revealed participants’ perceptions about their essential relationships with patients, not their required care relationships.

Like all direct care workers, doctors are also expected to demonstrate compassion in their care of patients. University of California San Diego Medical School is preparing aspiring doctors for practicing caring skills. In this video titled Putting The Care Back Into Health Care, KPBS Health Reporter Kenny Goldberg shares a compassionate care story of medical student Pritha Workman.




Frances Shani Parker, Author
Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes is available in paperback at many booksellers and in e-book form at Amazon and Barnes and Noble booksellers.

Monday, July 23, 2012

After Death To-Do List: Can You Add to This Checklist?


A sun has set. Someone has come face to face with the Other Side of Through.
This checklist includes tasks to do immediately after death:

  1. Some airlines have bereavement or compassion fares available for family members traveling for an imminent or actual death. These fares are discounted off the full price, but may not be the lowest fares available.
  1. If possible, the exact time of death should be recorded. Loved ones may want to spend time with the deceased. Institutions where deceased persons lived will have procedures to follow regarding death.
  1. Family  members, hospice staff, and possibly others such as a spiritual advisor and a mortuary for funeral arrangements, should be notified.
  1. Several certified copies of death certificates will be needed to collect insurance and other death benefits. These copies can be obtained from mortuaries, vital statistics offices, county health departments, and online at county and state Web sites. Wills, trusts, birth, marriage and divorce certificates should be available. Social security cards, veteran papers, an obituary, and other documentation will be needed.
  1. Family members may want to notify newspapers about publishing death notices and obituaries announcing the time and place of funeral or memorial services.
  1. Arrangements with an online memorial service, often affiliated with newspapers, can ensure that those who do not attend funeral or memorial services in person will have the opportunity to participate online.
  1. Contact should be made with insurance companies, unions, fraternal organizations, government offices, banks, credit unions, credit card companies, and real estate agencies to change titles if necessary.
  1. Employee benefits from all previous employers should be investigated.
  1. Arrangements for child care and out-of-town guests must be considered.
  1. In the midst of all this activity, family members and friends should also consider their own feelings about death and the person who has died. The occasion that they may have been expecting while the loved one was ill has finally come. A life has been lived.
Information above is from Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes.

Frances Shani Parker, Author
Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes is available in paperback at many booksellers and in e-book form at Amazon and Barnes and Noble booksellers.

Tuesday, July 17, 2012

Dementia Patients Eating (Alzheimer’s Research, Hospice Volunteer Story)

“Food? What food?”

As a hospice volunteer in Detroit nursing homes, I had contact often with residents not assigned to me. My hospice patients were always my primary concern, but most of them shared rooms with up to three other people. At mealtimes, my patient and I shared a table with six other residents. In the excerpt below, I am the only one at the dinner table without dementia. Due to limited staff, I knew I would have to supervise, encourage, and generally keep an eye on everybody at the table. A public school principal, I was used to multi-task management and didn’t mind assisting them at all.


I continued talking to Naomi (my hospice patient) and assisting her while monitoring others at the table. I noticed that Petra had not touched anything. Petra was not a very independent eater, but I knew she was physically capable of feeding herself by any means necessary.

“Petra, your food is just sitting there getting cold. You have a whole tray of delicious things to eat. You should eat some and see how good it is. You’re a good eater. Eat your food.”
“Food? What food? I don’t have none.”
“The food on this tray is all for you, Petra. This is your food tray right in front of you. Watch me point to each item. You have coffee, juice, milk, mashed potatoes, fish, broccoli, bread, and fruit. That’s your name spelled P-e-t-r-a.”
“That’s not my name. My name is Petra. That’s somebody else’s name. That’s not my name. I know my name.”
“Well, that is still your food on the tray. You should eat before it gets cold. Go ahead and eat. Give it a try.”
“Eat? Eat what?”
“Your food, Petra, your fish, potatoes, and everything else.”
“Fish? What fish? I don’t have none. Do you see a fish here? I don’t see a fish. I don’t have none.” 
(Note: Nowadays, I would omit some of the above conversation to keep her calmer and more focused on eating.)

From previous experience, I knew that Petra and I could go on roaming forever around this same circle. Luckily, today she was sitting next to me. I gave her a taste of the fish because I knew she liked it. Then I placed her fork in her hand and started her off eating. I did this in steps by steering her hand and giving her directions on putting food into her mouth, chewing, and swallowing. Patients with dementia needed tasks broken into simple steps. Usually, she ate for a while by herself, even with her hands, once somebody started her off. But without any help getting started, she would sit and look at the food she said was not there. My other hand continued to assist Naomi.

“Don’t do that! Leave my food alone! Get your nasty hands off my plate! Help! Can somebody help me?” screamed a resident at our table as if she were under attack. All the nurse aides were occupied feeding residents at other tables and experiencing their own mealtime problems. I was resigned to be the unofficial table captain. I told Roscoe sternly to leave Charlena’s food alone. He gave me a confused look, pretended he didn’t know what I was talking about, but betrayed himself with a silly smirk he thought I didn’t see. I leaned across the table and directed his attention to his own plate by putting his spoon in his food. He picked up his spoon and started eating again. Then I reassured Charlena that everything was okay, and she could finish eating. Charlena smiled with an air of triumph. Roscoe was in trouble, and she relished knowing she helped to get him there.

Rita had been watching me help Naomi and Petra eat. Now, she was attempting to feed George, but with her own used utensils. George had his mouth open obligingly, anything to help the cause. I interceded before any damage was done. By this time, several residents had spilled food on the table or the floor and had food stains on their bibs. Petra had to be restarted twice to eat the food she insisted she’d never received. I had stood to lean across the table two more times to settle other table disputes involving food and different residents.

Naomi ate right along during all the interruptions. I had been giving her ongoing praise on how well she was doing. I also praised others at the table when they did well. They savored the attention, and Naomi wasn’t the least bit jealous. She had already told the others that I was her guest and even offered me food, which I declined. I hadn’t gone there to eat and couldn’t even think about eating if I had. When one resident was praised, another would often say, “Look at me. I’m eating, too.” This reminded me of students at my school who said the same thing when someone else was praised. I laughed, thinking the world was a universal classroom. Maybe the stars in the sky were created to be placed on billions of people’s foreheads when they did something praiseworthy.

© Frances Shani Parker, Author, Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes

My experience above is consistent with research findings on factors affecting independent eating among elderly patients with Alzheimer’s disease. Published in Geriatrics and Gerontology International, this Alzheimer's research study on independent eating is the first to generate objective data showing that difficulty in beginning a meal is a factor that hinders feeding independence by older adults with Alzheimer’s disease. The study also concludes that eliminating environmental interference factors and providing assistance promoting beginning a meal are necessary to assist older adults with Alzheimer’s disease.

Frances Shani Parker, Author
Becoming Dead Right: A Hospice Volunteer in Urban Nursing Homes is available in paperback and e-book editions in America and other countries at online and offline booksellers.