New Day News
The following was published in the Floyd Press on May 1, 2008.
Rosemary Wyman’s business, New Day, has been providing home health care and support to individuals and their families since 2005. The business is a natural extension of a life long interest of Wyman’s.
“Whenever I was asked what I wanted to be when I grew up, I would always say a nurse,” Wyman, a tomboy who grew up in New York, said. “The only reason I played with dolls was to use them as patients,” she added.
Wyman and her family moved to Floyd from Charlotte, North Carolina in 1999. She and her husband, Walter Charnley, have been parents to eight in a blended family that Wyman refers to as, “his, mine, and ours.”
Certified in hospice and as a palliative nurse assistant, Wyman has extensive experience with end of life care and has been educating others about this life passage. She’s worked for Good Samaritan Hospice in Roanoke and has done fill-in work at The Beulah Hospice House in Dublin. Although she’s provided care to a number of Alzheimer patients – including her own father – and has a special interest in the needs of the aging population, not all her clients are elderly. Last year Wyman provided care for two young women with terminal illnesses.
Tom Vangunten, who lost his wife, Laura, to cancer last fall thinks the contribution Wyman makes is “invaluable.” Like Wyman, he believes people would benefit from more education and preparation for end of life.
“We don’t prepare for death. I can’t believe I got to be forty-nine and didn’t know a thing about this. I think grief and loss should be taught in school along with Driver’s Ed and how to balance your check book,” he said.
Vangunten, who is now a single parent to his and his wife’s two young sons, explains how the support Wyman offered was for the whole family. “For people dealing with terminal illness, it affects everyone in your family. It’s helpful if you have someone who can guide you through it. What Rosemary did was invaluable. She coordinated with doctors and other care givers, and provided the personal. What ever needed to be done – if someone needed a hug – she stepped-up,” he said.
Many families dealing with the terminal illness of a loved one need more support than the one or two hours a day a hospice worker provides. New Day can offer what Wyman refers to as “hospice support.” While she gives direct care to clients – which might include bathing, wound dressing, and assisting with pain management – much of Wyman’s work is more subtle than that. Her presence often has a calming effect because she accepts people from where they are and can approach each new situation without family history, she says. “Sometimes things not being addressed can be addressed easier with someone outside the family. I like to go in like a breath of fresh air.”
Not all of Wyman’s clients are dealing with a terminal illness. Riner resident, Betty Bowman has a handicap that inhibits her balance and mobility.
Wyman visits her one day a week to clean, organize, assist with personal care and grooming, and whatever else Bowman needs.
“She takes me to the doctor and the grocery store,” Bowman said. When asked if Wyman helps with cooking, Bowman explained that since her mother died four years ago she’s been heating up frozen dinners in the microwave for herself; although she did remember a delicious bean salad that Wyman prepared from a recipe Bowman provided.
“Cleaning and cooking equal care. Whatever makes someone feel better is care,” Wyman said, recalling a day she spent washing one client’s entire knick knack collection. “Sometimes people feel better when their homes are clean and their lives are organized,” she added.
Since the inception of New Day, Wyman has worked with approximately twenty clients. Some have been referred to her by other agencies, but most come by word of mouth. Although she provides services considered typical in her field, sometimes her work involves the unusual and requires some on the spot problem solving.
On one such occasion, she was flown to NY to transport a local family’s elderly aunt, who had broken an ankle and was in rehab, back to Floyd. Upon arriving in New York and after locating the woman’s apartment, Wyman packed a month’s worth of whatever she thought the woman might need. She then negotiated the transport, first with rehab staff, and then with overzealous airport security, all the while reassuring the woman – who didn’t know Wyman – that everything was okay. Her short term memory was failing but “she had a great sense of humor,” Wyman remembered.
Support for care givers is an important component of Wyman’s work. In 2004, after being approached by Our Lady of the Valley, an assisted Living and Nursing Care facility in Roanoke, Wyman presented an “Intuitive Emotional Clearing” workshop for care givers that involved guiding them through the use of creative outlets, such as music, art, and movement. Wyman has also facilitated the formation of a “Share the Care” circle in Floyd, based on the book of the same name. She says when she first saw the book, which outlines a step-by-step model for organizing group care for someone ill, she knew it was “the wave of the future.”
Another aspect of the educational side of Wyman’s work played out when she participated in a day long event called “Successful Elder Care,” hosted by the Social Justice Committee of the Lutheran Churches of Floyd. She had planned to share a presentation about home assessment for people with limitations, something she and her husband do together, but ended up talking about Alzheimer care when another workshop leader who was scheduled to do that was unable to attend. Wyman remembers a fellow-presenter at the event who cited a Virginia Tech study on the growing needs of the aging population. “It was sobering,” she remarked.
Following her involvement in the Zion Lutheran Church day of resource sharing, Wyman embarked on a new venture, “End of Life Development,” with the intention of building on the educational outreach aspect of her work. Immediate plans include the formation of an advisory board made up of various professionals, social workers, doctors, clergy, and nurses – to determine what the greatest needs are for the aging population, she says. She also envisions workshops on how to manage progressive care, advance medical directives, and to set up proxy care for decision making. “Plans should be made before we are in crisis,” she said.
Last month Wyman received non-profit status as a subsidy of the Community Educational Resource Cooperative (CERC) for “End of Life Development,” along with a small seed grant. This support will be instrumental in assisting her educational initiatives in the community. It will also be helpful in allowing her do what she does best: easing the discomfort and grief of others and making it more viable for individuals at the end of life to remain home with their loved ones. “I consider every day spent at home a success. And sometimes you have to count these successes in days,” Wyman says. ~ Colleen Redman


Taking my bath at night with the lights dimmed low, I notice that the veins in my hands have started to become dark and raised like
I don’t go to the graveyard to feel the spirits of my loved ones. I dance. Through sustained dance I can forget my self. And if I dance long enough I sometimes come up against the veil between worlds. Sometimes I dance myself scared.
I was putting on mascara in the bathroom mirror when Joe called out from the kitchen to ask me where something was. “Ah nunno,” I mumbled back to him, trying not to break my concentration.
Last night while watching The News Hour, I couldn’t take my eyes off
It’s a yearly class on grief and loss for counseling students, taught by Radford University Professor
It ain't the heart, or the lungs, or the brain. The biggest, most important part of the body is the one that hurts. – poet,
The Irish look within and see behind – know the heart and read the mind ~ written on a plaque in my father’s bedroom
When my brothers, Jim and Dan, died in 2001, I was shattered awake to the reality of death. As I struggled to penetrate its mystery, I allowed myself to grieve long and deeply. One of the ways I immersed myself in actively mourning Jim and Dan was to write
With a blanket spread out on May’s green grass, my
Four days before this past Christmas, I went to my friend
After the church service, everyone adjoined to a room for refreshments. There, while nibbling on cheese and crackers, I counted a dozen other necklaces that Alex had made hanging from the necks of other women. I asked about the hoop of ribbons, and Paul explained that Alex, always the artist, had requested the last week of her life that an array of colorful scarves be draped around her bedside, the bed she was confined to in the study of her home where family, friends, and hospice volunteers gathered to visit and care for her. She died before her wish could be fulfilled, so friends made something beautiful they knew she would approve of to hang in the church. On the ribbons people wrote their last words to Alex, along with blessings and condolences for her family.
Dear Goddess of the spreading starry skies … whose shawl is the northern lights … and whose shoes are the polar ice floes …. Lead us ever in circles … Don’t stop dancing with us … Should disastrous death try to cut in … like an asteroid tapping on your shoulder … keep whirling … We don’t mind if our toes get stepped on … We’re having the time of our lives … ~ Excerpt from “A Line to the Goddess,” a poem by Alex Wind. 



The last few weeks of my brothers' lives played out like the conclusion of a dramatic Hollywood script, a plot with a twist. The road trip they took, two weeks before the first death, became the beginning of a larger journey, the one in which they would both leave this world. ~ excerpt from the back cover of
After completing “
Remember when you were a kid and you made an ugly face and someone told you that you better watch out because your face could get stuck that way?
When someone close to you dies, you begin to look at life through the eyes they no longer have, or you find yourself doing things they loved to do because they no longer can. When I hear music that I know my brother Danny would have liked, I close my eyes and let it sink in, listening for him. I write checks to the Red Cross or give money to the panhandling homeless, because I know Dan, 
My sisters and I have an unusual family trait. We remember events by what clothes we were wearing at the time. On the day my brother Dan’s doctor at St. Luke’s Hospital in Houston told me that Dan would not likely recover from the liver disease he was battling, I was wearing a short dungaree skirt, a white tee shirt and a matching dungaree jacket. My hair was pinned up, and I had my favorite leather sandals on.
“Look at me now