Showing posts with label caregivers. Show all posts
Showing posts with label caregivers. Show all posts

Thursday, June 12, 2014

Caregivers Learning To Let Go At The End="Being"/Angels?




Philadelphia Inquirer, Sunday, June 8, 2014, HEALTH section, Lead Article, Front Page, Page G1:



Caregivers learning to let go at the end

Beth Connolly gives her husband, Jack, a kiss in his room at Penn Wissahickon Hospice. AKIRA SUWA / Staff Photographer
Beth Connolly gives her husband, Jack, a kiss in his room at Penn Wissahickon Hospice. AKIRA SUWA / Staff Photographer
POSTED: June 09, 2014
It is a pivotal point for a caregiver: the transition from doing to "being" as a loved one's life is ending.
Denise Brown, who runs the website www.caregiving.com, says this is when a caregiver's job shifts from making appointments, finding new treatments, and fighting decline to accepting that death is sometimes unstoppable.
The idea came to Brown after a reader wrote about caring for her mother, who was in her 90s. The woman had fought her mother's chronic urinary tract infections to the end, at the cost of considerable inconvenience and effort.
"I so wished I would have stopped all that doing . . . and just been with my mom," she wrote.
When I heard Brown speak recently about being at an Alzheimer's Association conference, I knew exactly what she meant. I had cared for my husband as he died of cancer, in hospice at home. I had watched with wonder as an old family friend, a woman with much caregiving experience, simply sat with Jeff. His breathing had grown labored by then and he was pale and shrunken from cancer. She was calm, peaceful, and totally accepting. It was beautiful.
I did it too, of course, but I never quite mustered the same attitude. Two years of frenzied Type A activity and monstrous stress had preceded those last quiet days. It wasn't easy to switch gears. Plus, it was hard to just "be" with the loss of my husband, my children's father.
Like so many things experts say about death and caregiving, just being in the presence of mortality is a lot easier said than done, and deserves more discussion.
Brown gets that. She thinks it's worth it to make the effort to let go. "I really think it's one of the best lessons you can learn in caregiving," she said.
For starters, she and other experts said, caregivers can think differently about the value of being present.
"I think they need to see that that is also active caregiving," said Shari Baron, a Havertown psychotherapist who cared for her father at the end of his life.
Ideally, someone on your loved one's medical team would tell you when it's time to do this, but that doesn't always happen. Doctors worry that patients will feel abandoned, or they sense that patients still want to fight.
Families are left to figure this out. "Most people know in their gut when it's time to let go," Baron said.
Ron King, a chaplain at Holy Redeemer Hospice, encourages caregivers to listen to their own bodies. When they feel more exhausted and realize "the process is getting bigger than me," it is a sign the tide has turned.
Brown, who lives in suburban Chicago, said the turning point is when families realize that there's a difference between a preventable decline and one that is inevitable. "It happens at the moment when the family caregiver understands that death will come and it's not related to how much they do," she said.
There certainly are opportunities to stop and experience the moment all along the "journey" toward death. Holidays, vacations, a cup of coffee on the patio, take on extra poignancy when time is precious. But, as David Casarett, director of hospice and palliative care at Penn Medicine, pointed out, patients get weaker and have more medical problems as the end draws closer. They need more help.
"Dealing with a serious illness is a lot of work," he said. "Some of the most burdened caregivers I see are the caregivers of patients who are very near to the end of life."
Small families, or those that can't afford to hire extra help, are working hard. "The ability to do that sitting, that 'being present'," he said, "is for many people a luxury."
Still, he said, the work slows down dramatically in the last few days, when patients stop eating and drinking and their bodies begin to shut down. At that point, he sees a lot of "awkwardness." The caregiving role may have defined people for years and now they feel lost. "What's my job? What's my role? . . . How do I just be?" they wonder. Sometimes hospice workers have to find tasks for them to do.
Gloria Allon, a nurse who runs Crossroads Hospice in Plymouth Meeting, said even she found it difficult to slow down as she cared for her mother. She made sure that everyone else in the family had time alone with her mother, but didn't do it herself.
"No one said that to me. 'Wait a minute. You are her daughter. Slow down a little. Come off the treadmill,' " she said.
Brown said there is comfort in the "busyness" of caregiving. The quiet of being requires a different kind of strength. As Allon observed, we are confronting our own mortality every time we witness a death. Sitting still allows powerful, frightening emotions to surface.
"If you are comfortable with being uncomfortable . . . it makes it easier," added Karen Mechanic, a psychiatrist at Fox Chase Cancer Center.
Caregivers also want to protect the dying person.
"I would get overcome with emotion and I didn't want her to see that because that would upset her," Gerry Davis, of Plymouth Meeting said. His wife Cyndi was 64 when she died of ovarian cancer last year.
Donald Phimister recalled sitting with his wife, a social worker who had once worked at Wissahickon Hospice, as she was dying of Alzheimer's disease. "When you start to sit, you know, pleasant experiences come back," he said. "You start beginning to think of your life. You take it for granted and then, all of a sudden, for one of you, it stops."
Some people never accept that death is a possibility, even when the diagnosis is dire.
Nate Eustis, whose wife Maria died of lung cancer in 2012 after a "50-month battle," said the couple were seeking new clinical trials almost to the end. He was still conflicted after their doctor said there was nothing left to try.
"It's one of those things where you're thanking God for 39 years that you've been together and you're cursing him for the 20 you've lost and I was kind of in that transition," said Eustis of Norristown.
Jennifer Maroun of Kennett Square said her father, Jack Connolly, who had pancreatic cancer, deflected her attempts to say goodbye. "Get out of here, you brat," he'd say. When he went to Penn Hospice at Rittenhouse, he said he didn't want visitors. "I just want to be left with my own thoughts," he told her and her mother. They came to sit with him anyway - holding his hand and telling him about his grandchildren - but also respected his pride.
Experts recommend talking to the dying loved one, even if you're not sure they can hear. "There is really an opportunity here for everyone to say 'Goodbye, thank you, forgive me, I forgive you,' " said Allon, the Crossroads director. Silence is fine, too.
Here's how Allon does it with patients. "I would go in and I would just sit and I would place my hand under their hand. I'd say, 'I'm just going to sit with you.' Sometimes people would actually cry. We didn't have to say a word. The touching part - that is so powerful."
She admitted she had trouble doing that with her own mother. "Really looking into your loved one's eyes, knowing that they're leaving you, is hard to do," she said.
Gabriel Rocco, a contemplative counselor who uses meditation skills to help people cope with cancer, said his approach is rooted in Buddhism. His goal is to connect with his "essential nature" while sitting quietly. When he visits the dying, he is offering "spacious awareness and warmth to the person I'm sitting with."
He suggests sitting in a comfortable chair and finding a comfortable position to minimize fidgeting. "Give yourself permission to have no goal other than to be present for your loved one," he said. Breathe deeply and focus on your breaths. When emotions arise, acknowledge them, then let them dissolve. Keep breathing.
Set the bar low. "Do your best to be completely present for the other person for a minute, no more than five," Rocco said.
You will often feel tremendous support from the dying person, he said. "When the person gets closer and closer to death, they also become more spacious."
Death itself, though, is a solitary experience. The living have to let go.
It's OK if you can't pull all that off. Everyone grieves at their own pace in their own way. You can say goodbye later, in a different way. You can accept that you did what you needed to do.
But King, the Holy Redeemer chaplain, said that, if we're open, the end of a loved one's life is a time to receive wisdom and to give love in the same wordless, primal way we do when we hold a baby.
"If God ever sends angels to be with us," he said, "it's at times like this, and we might miss it if we're too busy."

215-854-4944
@StaceyABurling

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Tuesday, April 22, 2014

Online Sites Help Caregivers Give Care - Reminders, Organization, and More

Philadelphia Inquirer, HEALTH section, Sunday, April 6, 2014, Page G4:



Online sites help caregivers give care

GALLERY: Online sites help caregivers give care

A few years back, Jonathan Schwartz found himself with two children and, along with his wife, five parents to worry about. All but one of the parents was over 80, and the couple was faced with "lots of stuff to worry about."
Schwartz, former head of Sun Microsystems, realized he was spending his time fixated on "medication lists, care routines, doctor's visits, garage codes to the parents' houses, passwords for online accounts - all the things you start to worry about when you care for someone else."
From that experience, CareZone.com and its app were born, one of several Web- and mobile-based companies that cater to the needs of caregivers. CareZone, which started in 2010, has about 1 million users of the free service and contains hundreds of CareZone groups.
Sometimes called the "anti-Facebook," the service allows people to keep and share information, such as a hospital report, updates from a doctor's visit, or a medication list - with others in a private, secure setting. By storing vital information in a single location, caregivers can avoid repetition of activities or missing an important appointment.
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  • "Facebook is good for social networking and LinkedIn is good for finding a job," says cofounder and CEO Schwartz. "We got together to think about what it would look like to care for someone online."
    Sites that organize caregiving are suddenly creating lots of buzz. The need is huge because the health system is so complex, and sites such as CaringBridge, CarePages, and LotsaHelpingHands have sprung up to meet the growing demand.
    One enthusiastic CareZone user is Sarah Davenport, 35, of Wilmington. A former marketing and public relations consultant, Davenport turned to CareZone while nursing her grandmother last year. At 85, her grandmother could no longer live by herself, so she moved in with Davenport and her husband until her health stabilized. CareZone helped to document her grandmother's activities and care and to share key facts with her brother in Elsmere, Del., and sister in Colorado.
    "By documenting daily what she ate and how much, it helped to track her progress," Davenport says.
    Interestingly, after her grandmother was moved to assisted living, Sarah Davenport, who skated on the Philly Roller Girls' roller derby team for eight years, was diagnosed with late-stage neurological Lyme disease. So she used CareZone to follow her own care and organize the tasks she needed to share with her husband, sister, and friends.
    She also uses a journal feature of CareZone to document "every single moment of her experience" to help her track the progress of her illness and communicate with people in her inner circle. Davenport, who is mostly bedridden by her disease, plans to use the journal as a foundation for a new nonprofit called Fearless Lyme Fighters, which was to have its debut fund-raiser April 4.
    "We were started to answer the question when there is a medical crisis or emergency, what can I do to help?" says Hal Chapel, cofounder of the Helping Hands site, based in the Boston suburb of Wellesley Hills. Using the website or a mobile app, people can create a small community, sign in with a private password, and view a calendar of tasks, such as "rides to chemotherapy, babysitting, housecleaning, bringing dinner - all things that can become a crisis in caregiving."
    So far, LotsaHelpingHands.com has more than 80,000 communities, with more than 1.5 million participants. Diseases represented "run the gamut from Alzheimer's to leukemia to strokes, but also when a loved teacher gets into an accident and a school community wants to give back," says Chapel.
    Unlike CareZone, which makes money off its premium services, LotsaHelpingHands uses a social entrepreneurial model, where the company licenses a branded version of the service to nonprofits. Subscribers include the American Lung Association, the Leukemia & Lymphoma Society, and AARP. Subscribers can co-brand and offer these caregiving services free to their audiences.
    "Part of what we offer is an easy way to coordinate care," says Chapel. "It's hard to ask for help, let alone again and again. This way you can go onto the site and sign up for what days or nights you want to help. People often discover, to their surprise, how many people want to support them."
    Recently, LotsaHelpingHands has branched into open community models, where people in a town, neighborhood, or congregation want to come together and help fellow citizens who need assistance.
    "We've tapped into a pent-up need for people to be back in community," says Chapel. "There's an intimacy when you share one another's lives and allow people to help you."


    Caregiving Sites

    www.caringbridge.org
    The Minnesota nonprofit offers a calendar for people to help others. Its Amplifer Hub gives another way to share stories. Nearly all funding for the free site comes from donations of people who use the service.
    www.carepages.com
     This community claims more than 1 million unique visitors per month. Privately labeled CarePages websites are also offered by more than 625 U.S. and Canadian health-care facilities.
    www.lotsahelpinghands.com
     It claims more than 80,000 communities, with more than 1.5 million participants. It licenses a branded version of the service to nonprofits, such as the American Lung Association.
    https://carezone.com
     It claims to have about 1 million users of the free service, and contains hundreds of CareZone groups.

    mice30@comcast.net
    215-470-2998
    www.inquirer.com/health_science

    Read more at http://www.philly.com/philly/health/20140406_Online_sites_help_caregivers_give_care.html#rLuAW1HCqyCMLay6.99

    Tuesday, March 11, 2014

    "Ablution"-Lovely Poem Honoring Caregivers


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    American Life in Poetry: Column 468
    BY TED KOOSER, U.S. POET LAUREATE
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    Here’s another lovely poem to honor the caregivers among us. Amy Fleury lives and teaches in Louisiana.




    Ablution 

    Because one must be naked to get clean,
    my dad shrugs out of his pajama shirt,
    steps from his boxers and into the tub
    as I brace him, whose long illness
    has made him shed modesty too.
    Seated on the plastic bench, he holds
    the soap like a caught fish in his lap,
    waiting for me to test the water’s heat
    on my wrist before turning the nozzle
    toward his pale skin. He leans over
    to be doused, then hands me the soap
    so I might scrub his shoulders and neck,
    suds sluicing from spine to buttock cleft.
    Like a child he wants a washcloth
    to cover his eyes while I lather
    a palmful of pearlescent shampoo
    into his craniotomy-scarred scalp
    and then rinse clear whatever soft hair
    is left. Our voices echo in the spray
    and steam of this room where once,
    long ago, he knelt at the tub’s edge
    to pour cups of bathwater over my head.
    He reminds me to wash behind his ears,
    and when he judges himself to be clean,
    I turn off the tap. He grips the safety bar,
    steadies himself, and stands. Turning to me,
    his body is dripping and frail and pink.
    And although I am nearly forty,
    he has this one last thing to teach me.
    I hold open the towel to receive him.



    American Life in Poetry is made possible by The Poetry Foundation (www.poetryfoundation.org), publisher of Poetry magazine. It is also supported by the Department of English at the University of Nebraska-Lincoln. Poem copyright ©2013 by Amy Fleury from her most recent book of poems, Sympathetic Magic, Southern Illinois Univ. Press, 2013. Poem reprinted by permission of Amy Fleury and the publisher. Introduction copyright © 2014 by The Poetry Foundation. The introduction's author, Ted Kooser, served as United States Poet Laureate Consultant in Poetry to the Library of Congress from 2004-2006. We do not accept unsolicited manuscripts.
    ******************************
    American Life in Poetry provides newspapers and online publications with a free weekly column featuring contemporary American poems. The sole mission of this project is to promote poetry: American Life in Poetry seeks to create a vigorous presence for poetry in our culture. There are no costs for reprinting the columns; we do require that you register your publication here and that the text of the column be reproduced without alteration.