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dementia

Alzheimer’s at the Movies

August 20, 2021

Over the past twenty years, several interesting feature films have been produced which explore the significance of Alzheimer’s Disease and its impact on patients and their families and caregivers.

For her performance as Alice Howland in 2014’s “Still Alice”, Julianne Moore received the Academy Award for Best Actress.  The film is based on a novel of the same title by Lisa Genova, herself a neuroscientist.  The film is the story of Alice Howland, an esteemed professor of linguistics at New York City’s Columbia University.  The story takes us from Alice’s first suspicions that something is amiss, through her diagnosis with Early Onset Alzheimer’s Disease, her various losses, and concluding with a touching scene featuring Alice’s free-spirited actress daughter Lydia who has assumed responsibility for her care.

As the story unfolds, we witness Alice and her family confront and come to terms with many of the challenges posed by Alzheimer’s Disease.  Alice’s particular form of the disease is called “familial”, meaning that in her family line, there have already been two or more relatives with the malady.  Since Alice is only fifty, her diagnosis is termed “early onset”.  The question is raised as to whether Alice’s three grown children want to be tested to determine if they are susceptible to the illness.  Daughter Lydia chooses not to.  Son Tom and the elder daughter Anna do want to be tested.  Anna is pregnant.  Though she is positive for the test, she follows through in giving birth to her twins.  This complex of factors are among several story lines in this captivating film.  Others include:  Alice’s secret preparations to end her own life when her memory loss and functioning progress to a certain point, her lingering desire to make a contribution to others living with the same disease, and family decisions around Alice’s care in conflict with the reality that “Life goes on”. Through all this, we see Alice’s progressive deterioration through the loss of her teaching career, her advancing inability to recognize those closest to her, disorientation within her own home, an interrupted suicide attempt, her husband’s decision to relocate in favor of his professional betterment, and the loving self-sacrifice of Lydia to care for her.  Despite the wasting away of the many qualities that made her the person she had been, she remains “still Alice” in a brief moment of recall when she is able to identify the importance of love.

In preparation for her role as Alice, Julianne Moore did extensive research about Alzheimer’s Disease.  Sadly, it also fell to her to dedicate her reception of the Academy Award to the memory of Richard Glatzer, one of the two writers and directors of the movie.  He died of ALS (“Lou Gehrig’s Disease) shortly before the awards ceremony.  “Still Alice” can be accessed on You Tube, Hulu, and Amazon Prime.

Closer to our time, the winner of the 2020 Academy Award for Best Actor was Sir Anthony Hopkins for his performance as Anthony in “The Father”.  Some years ago, Hopkins also won the Oscar in that same category as the infamous Hannibal Lechter in “The Silence of the Lambs”.  “The Father” is based on a French stage play by Florian Zeller who assisted in the adaptation and direction of the work for the screen.  “The Father” features Olivia Colman (currently seen as Queen Elizabeth II in Seasons Three and Four of the series “The Crown”). For her portrayal as Anne, Anthony’s daughter, Colman was nominated for the Academy Award for Best Supporting Actress.

Spoiler alert!  “The Father” immerses us within the thoughts, perceptions, and reactions of a man whose mind is unraveling because of dementia.  There are repeated events with some changes in character and setting that can be quite confusing and disconcerting until we perceive that this is purposefully done to draw us into Anthony’s experience.  It ushers us into the insecurity, denial, resistance, fear, anxiety, anger, and fragility of a man with dementia.

“The Father” begins with a confrontational conversation between Anne and Anthony who has become oppositional toward his paid caregiver.  We are immediately plunged into what becomes a slow-moving but steadily mounting storm system of suspicion, stubbornness, refusal, lapses of memory, disorientation, and eventual breakdown.  The persistent pace of the story’s development raises the sadly familiar challenges of living with and caring for someone with this illness. What to do about emerging potentially aggressive behaviors?  How to live with the strain imposed on other intimate relationships?  When does one arrive at the point of surrendering caregiving to a corps of providers in a setting that may better manage the patient’s needs?  Hopkins’ masterful performance in this intense drama can be seen on You Tube, Amazon Prime, and Vudu.

Obviously, films of this genre do not lend themselves to a family movie night of coziness while sitting in front of the flat screen with popcorn at hand.  They are, perhaps, most useful as a learning experience for mature adults who may be starting to consider addressing some of the serious “What if…” questions emerging in their lives as they age.  The value of these movies as “family drama” will have served a good purpose if they broaden out into thoughtful and serious discussions and actual planning and preparation that might avert being overwhelmed in a later future time of critical need.

Pemi-Baker Community Health offers community support groups for Caregivers and families living with dementia as well as one on one meetings for help filling out those all-important forms for end of life wishes and care. We encourage you to contact us with questions. PBCH is located at 101 Boulder Point Drive, Plymouth, NH. To contact us please call: 603-536-2232 or email: info@pbhha.org   Visit our website: www.pbhha.org  and like our Facebook Page: @PBCH4

With over 50 years of experience, serving clients from 28 towns in central and northern New Hampshire, Pemi-Baker Community Health is committed to creating healthier communities. Services include at-home healthcare (VNA), hospice and palliative care, on-site physical and occupational therapy and aquatic therapy in their 90-degree therapy pool. Providing compassionate care with experienced staff who are trained, certified professionals in the business because of their hearts. In your time of need, we’re right where you need us.

~written by Guy Tillson, MDiv, MA, Hospice Chaplain

Filed Under: Advance Care Planning, Bereavement, Caregivers, Press Release Tagged With: Caregivers, dementia, Support Groups

If You Live With a Serious Illness, Learn How to Improve Your Quality of Life

June 14, 2021

If you have cancer, lung, heart or kidney disease, Alzheimer’s, or another serious illness, you should know about a medical team that can address your symptoms and stress.

The medical team is called palliative care and they’re available in a variety of medical settings. Pemi-Baker Community Health (PBCH) offers palliative care in your home, making it easy for you and your family members to ask questions and relay concerns. Their focus is on relieving the symptoms and stress of your illness. The goal is to improve quality of life for both the patient and the family. This is done by coordinating the patient’s care as well as providing support for the caregivers if they are experiencing caregiver burnout.

Pemi-Baker Community Health’s palliative care is provided by a specially trained team of doctors, nurses and other specialists who work together with your other doctors to provide an extra layer of support. Palliative care is appropriate at any age and at any stage in your illness, and it can be provided along with curative treatment.

Is Palliative Care right for you?

Answer the following questions to determine whether palliative care might be right for you or someone close to you. Remember, you can receive palliative care at any point in your illness.

  1. Do you have one or more serious illnesses such as:
  • Cancer
  • Congestive heart failure (CHF)
  • Chronic obstructive pulmonary disease (COPD), emphysema, lung disease
  • Kidney failure
  • Liver failure
  • Neurological diseases (e.g., ALS, Parkinson’s)
  • Dementia
  1. Do you have symptoms that make it difficult to be as active as you would like to be, or impact your quality of life? These symptoms might include:
  • Pain or discomfort
  • Shortness of breath
  • Fatigue
  • Anxiety
  • Depression
  • Lack of appetite
  • Nausea
  • Constipation
  1. Have you, or someone close to you, experienced the following:
  • Difficult side effects from treatment
  • Eating problems due to a serious illness
  • Frequent emergency room visits
  • Three or more admissions to the hospital within 12 months, and with the same symptoms
  1. Do you, or someone close to you, need help with:
  • Knowing what to expect
  • Knowing what programs and resources are available
  • Making medical decisions about treatment choices/options
  • Matching your goals and values to your medical care
  • Understanding the pros and cons (benefits/burdens) of treatments (e.g., dialysis, additional cancer treatments, surgery, etc.)
  1. Do you, or someone close to you, need help with:
  • Coping with the stress of a serious illness
  • Emotional support
  • Spiritual or religious support
  • Talking with your family about your illness and what is important to you

If you answered yes to any of the questions above, you can benefit from palliative care. Ask your doctor for a palliative care referral with Pemi-Baker Community Health. Once PBCH receives the referral from your doctor they will contact you via phone to answer and ask questions and set up a meeting with you at your home.

What happens at a first visit with a palliative care team?

The first step is for the palliative care team to get to know you as a person and find out who else is important in your care. They will want to hear your narrative – who you are, what you enjoy doing, and what is most important to you in your day-to-day life. They’ll review your medical information, ask what symptoms are of concern, and how much these affect your quality of life. They’ll ask questions to see if there are any care needs at home. They may also ask questions to learn what you know about your medical condition, and what concerns you about the future so they can plan how to help over time. The team will also ask questions about who you would want to help make decisions if you aren’t able to do so for yourself. This person is called a health care agent or proxy.

For more information on how Pemi-Baker Community Health can help please call 603-536-2232 or email us at info@pbhha.org.

With over 50 years of experience, serving clients from 22 towns in central and northern New Hampshire, Pemi-Baker Community Health is committed to creating healthier communities. Services include at-home healthcare (VNA), hospice and palliative care, on-site physical and occupational therapy and aquatic therapy in their 90-degree therapy pool. Providing compassionate care with experienced staff who are trained, certified professionals in the business because of their hearts. In your time of need, we’re right where you need us.

PBCH is located at 101 Boulder Point Drive, Plymouth, NH. Visit our website: www.pbhha.org  and like our Facebook Page: @PBCH4

~written by Anna Swanson

Filed Under: Advance Care Planning, Caregivers, Palliative Care Tagged With: Cancer, Caregiver support, CHF, COPD, dementia, Home Care, Kidney failure, Liver failure, Lung disease, Neurological diseases, palliative care, side effects

Learning About Caring For Dementia

April 16, 2021

When I first came on to Hospice work, my supervisor encouraged me to maintain ongoing self-study about various topics relevant to the work.  One day, I pulled a book from the shelf in our office.  An observant co-worker noticed and commented that I had grabbed “the Bible for caring for dementia.” The book is THE 36-HOUR DAY:  A Family Guide to Caring for People Who Have Alzheimer Disease, Other Dementias, and Memory Loss.  The title itself, as does the book, pulls no punches.  Providing ongoing care for a person with dementia is time-consuming, emotionally demanding, stressful, and exhausting, so that one’s days feel like they are longer than they are and packed with too much to do and remember.

The task can also be loving and rewarding, especially when the caregivers learn to take care of themselves as well.  The book is also what it says it is- a guide to caregiving.  The authors are Nancy L. Mace and Peter V. Rabins, both affiliated with the Department of Psychiatry and Behavioral Sciences at the John’s Hopkins University School of Medicine.  Don’t think, though, that it is written with sophisticated terminology or an excess of medical jargon, making it heavy and dense.  To its credit, the style is easily understandable and presented in a conversational, caring, and concerned tone directly to the reader who may already feel overwhelmed when first facing the challenge of caring for a spouse, a parent or grandparent, a sibling, or another acquaintance living with dementia.  Above all, it is a practical volume, with all sorts of advice when confronting the many challenges of this type of care.  Since its appearance in 1981, the book has been revised and edited six times to keep up with new information as it emerges.  Over three million copies have been sold worldwide as of the publication of the 2017 edition.

The reader/caregiver is immediately immersed into the experience as the first chapter opens with the case history of a woman who begins to notice her memory is slipping and moves along as her limitations compound.  The focus is first on her.  What is she experiencing?  What is she feeling?   What can she do?  Woven through this are brief accounts of her family members’ attempts to care for her and their experiences and feelings as their involvement becomes more complex.  It recounts a loss of skills around self-care and social interaction, moving us all the way through her journey which ultimately end with her admission to a long-term care facility when her family arrives at the point of no longer being able to care for her.

In this introductory section, there is a brief presentation raising the question “What Is Dementia?”  The book is careful to explore all sides of the challenges of caring for someone with dementia.  The authors really walk alongside the readers/caregivers in taking the first steps toward assuming the responsibility of caregiving. Having read the book, I am hard-pressed to discover any stone that has been left unturned.  Let me be quick to say that not all dementia patients end up in nursing homes.  Caregiving story endings vary from case to case, very much the result of the many factors both patients and caregivers bring to their own unique circumstances.

The practicality of the book is manifest in addressing particular experiences from both positive and negative perspectives. This is done throughout the book as it anticipates a wide variety of responses and reactions from patients and caregivers alike.  It progresses from dealing with initial manifestations of the disease through its more serious and complex concerns and on to end-of-life care.  The development of this style moves from what to do about things like home safety, nutritional needs, medical needs, and personal hygiene on to “sun downing” (worsening behavior as a day moves toward its end) and “shadowing” (a clinging trailing after the caregiver) and on to more serious behaviors as wandering, combativeness, and inappropriate sexual behavior.  These are only a smattering of the features presented throughout the book.  The work is chock-full of all sorts of valuable information.  A very simplified example of considering various sides of a problem might go something like this:  “If your father is doing X, try redirecting him toward trying Y.  If it works, and you can keep reinforcing it, all well and good.  If he is unsuccessful or refuses to try Y, try Z.  If the problem persists and remains unresolved, you may have to learn to tolerate X to avoid frustrating and angering the both of you.”  (Not a direct quote)

What comes through quite clearly is that the caregiver/s must make changes in themselves as their loved ones become less and less the persons we knew them to be.  Our intervention helps to support them and compensate for what they have lost.  This is not easy.  It is emotionally costly.  It becomes the nub for the necessity of self-care for the caregiver/s.  There is a whole chapter on “Getting Outside Help”.  The authors draw on a tremendous fund of knowledge and experience in their offerings of factual knowledge about dementia and practical suggestions pertinent to caregiving.  In many places, there are “Who to call or contact” directives regarding particular concerns.  Of course, readers/caregivers will need to locate those types of resources available in their own area.

The chapter entitled “Special Arrangements If You Become Ill” and its subsection “In the Event of Your Death” both contain practical information for anyone whether or not they are currently in a caregiving role.  The COVID pandemic has served to heighten our awareness for the need of preparedness in the possibility of emergency.  It is to be hoped that it also has brought home to us the preciousness of our loving connections so that we do not over-burden our loved ones through our lack of practical foresight.  There is another whole chapter “Caring for Yourself”. There is also a chapter regarding the needs of children and teenagers who may be living in a home setting where caregiving is being done.  There are also sections and chapters on end-of-life care, financial and legal issues, and considerations about relocating care outside the home.

It is not until Chapter 17 (“Preventing and Delaying Cognitive Decline”) that the book returns to a more specifically medical and scientific consideration of dementia and its causes (Chapter 18) and research about dementia (Chapter 19).

Click here and learn more about our PBCH support groups!

In drafting this review, it was challenging for me to try to choose items that might grab a reader’s/caregiver’s attention in order to reveal the book’s appeal.  I do hope I have done it enough justice so that you might consider borrowing a copy through the library you patronize or purchasing a copy for yourself.  I have seen copies of the book on the shelves of our independent bookstores (Innisfree Bookshop in Meredith, Bayswater Books in Center Harbor, and Gibson’s Bookstore in Concord).  Of course, it is readily available through Amazon and Books A Million.  Quite simply, it is a superb guide, and I recommend it most highly.

~Written by Guy Tillson, MDiv, MA, Hospice Chaplain

Filed Under: Advance Care Planning, Caregivers, Education, Free Community Service Tagged With: Advance Care Planning, Caregiver Shadowing, Caregiver support, dementia, Nancy L. Mace, Peter V. Rabies, Sun Downing, The 36-Hour Day

Self Care for Caregivers

January 16, 2020

When Alison’s Dad fell, she moved in with her parents to help out around the house and make sure they were taking their medications and getting proper meals.  With a full time job to manage, what started out as a good deed soon became overwhelming as her parents’ health declined.

The Cost of Compassion 

It is our nature to care for loved ones and, for many of us, it brings great satisfaction. Empathy and compassion are desirable character qualities, present in people to varying degrees. These enable us to identify, and in some cases, actually experience the feelings, thoughts, or attitudes of others we care about.

Compassion can come with an emotional cost when caring for someone with a long-term illness. The distress resulting from the constant demands of caring for another, consistently witnessing pain or cognitive decline, can have serious consequences.

In the book, “Overcoming Compassion Fatigue,” author Sharise M. Nance, LCW, CCTP, details how caregiver burnout can manifest itself in exhaustion, depression, apathy, and even physical or emotional disability. “People in ‘helping professions’ are regularly exposed to a range of emotions, from hope to dread, from gratitude to anger, from patience to frustration, and from grief to sorrow.”

One elderly woman had experienced several falls. She lives with her husband who is in advancing stage of dementia. He wakes up several times each night, turns the lights on and gets dressed. Each time, she has to wake up and guide him back to bed often unable to sleep herself. Before getting help, she found herself exhausted, discouraged, and at a greater risk for additional falls.

Some caregivers can internalize the issues of those under their watch, hoping by some herculean effort to fix everything. The sense of responsibility can become disproportionately burdensome and they may lose perspective about what they can and cannot do. This is particularly daunting when a patient has dementia and cannot communicate effectively, or acts out physically.

Making a Plan for Self Care

Prolonged stress is associated with distinct physiological responses that can have long term effects on both physical and emotional health. Often referred to as the fight, flight or freeze response, these chemical reactions are effective in urgent, life-threatening situations, but not sustainable over time.

Ms. Nance noted several emotional states that can accompany caregiver stress:

  • Guilt:  A sense of being responsible for the illness
  • Anger: Frustration with family members or health care workers
  • Sadness: Loss of the person as they once were
  • Fatigue: Exhaustion from extra work and irregular sleep
  • Apathy: Lack of energy to keep up with needed tasks

When these emotions arise, it can be a signal that the caregiver needs to take better care of themselves in order to do what is needed to care for their loved one. If you are in this situation, here are a few suggestions that might help:

  1. Pace yourself: Take advantage of family or friends who offer to help. Home Care agencies like Pemi-Baker Community Health can provide a volunteer companion or home health aide for a few hours a day to take on the more challenging tasks.
  2. Set boundaries: Make it clear to the patient and family members what you can and cannot do.
  3. Seek support: Pemi-Baker Community Health and many churches or senior centers offer support groups for caregivers. While it may not alleviate the challenges you are facing, it can be helpful to know how others are coping.
  4. Create a self-care plan: As impossible as it might seem, you need a plan for exercise, sleep and proper nutrition. If you are a spiritual person, spending time in prayer or meditation can be helpful.

“Self-care is not a selfish act, but a necessity and priority,” writes Ms. Nance.

Even health care professionals can become overwhelmed at times.  Pemi-Baker Community Health employs home health aides and homemaker companions serving clients in 18 central and northern NH towns. “As a licensed home care agency, we are vigilant about providing support to our caregivers,” said Chandra Engelbert, CEO. “We encourage them to practice their own self-care so they can provide the best possible care and attention to our clients.”

Caring for another person can be a gift but also a burden. Anyone in that role has to be mindful of the potential risks, and remember to monitor their own well-being at times, too.  All are welcome to our Drop-in Caregiver Support Groups on every 3rd Wednesday of the Month at the Plymouth Regional Senior Center.

~by Anna Swanson

Filed Under: Caregivers, Free Community Service Tagged With: Caregivers, dementia, Education, free community service, free support group, Stress

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The Rewards of Being a Hospice Volunteer

While I was familiar with Hospice for many years, I only have been a hospice volunteer with Pemi Baker Hospice and Home Health (PBHHH) since October 2021.  When I retired, I began searching for volunteer work that would allow me to give back to my community.  A newsletter from PBHHH arrived in my email announcing training for hospice volunteers.  My family had experienced the need for hospice twice, once in Ohio and again in Florida.  The relief my family and I felt when the hospice volunteers arrived was beyond measure.  I want to bring the same kind of assistance to others.  PBHHH given me that opportunity by providing professional training with knowledgeable nurses, doctors, social workers and other health care professionals.  Their guidance has enabled me to meet the challenges of being s hospice volunteer, and I am very glad that I did it.

Connie C.

Pemi-Baker Hospice & Home Health
2022-06-27T12:20:25-04:00

Connie C.

While I was familiar with Hospice for many years, I only have been a hospice volunteer with Pemi Baker Hospice and Home Health (PBHHH) since October 2021.  When I retired, I began searching for volunteer work that would allow me to give back to my community.  A newsletter from PBHHH arrived in my email announcing training for hospice volunteers.  My family had experienced the need for hospice twice, once in Ohio and again in Florida.  The relief my family and I felt when the hospice volunteers arrived was beyond measure.  I want to bring the same kind of assistance to others.  PBHHH given me that opportunity by providing professional training with knowledgeable nurses, doctors, social workers and other health care professionals.  Their guidance has enabled me to meet the challenges of being s hospice volunteer, and I am very glad that I did it.
https://www.pemibakerhospicehomehealth.org/testimonials/the-rewards-of-being-a-hospice-volunteer/

You give of yourselves day & night without end!

To the Pemi-Baker Hospice Team--Words really can't express my feelings-

Your help during one of the most difficult times of my life is SO appreciated.  I'm so grateful that because of you, Doug was able to get his wish not to spend the last of his days in a hospital, but at home with those of us who loved him.

And to be constantly reassured that if I needed anything you would be there-oh my gosh-ANYTIME!  Well, you people need to know how much you are appreciated.  You give of yourselves day & night without end!  God Bless you and thank you!

Pam O.

Pemi-Baker Hospice & Home Health
2020-06-11T07:31:14-04:00

Pam O.

To the Pemi-Baker Hospice Team--Words really can't express my feelings- Your help during one of the most difficult times of my life is SO appreciated.  I'm so grateful that because of you, Doug was able to get his wish not to spend the last of his days in a hospital, but at home with those of us who loved him. And to be constantly reassured that if I needed anything you would be there-oh my gosh-ANYTIME!  Well, you people need to know how much you are appreciated.  You give of yourselves day & night without end!  God Bless you and thank you!
https://www.pemibakerhospicehomehealth.org/testimonials/you-give-of-yourselves-day-night-without-end/

“My home physical therapy was fantastic.”

Pemi-Baker provided very good home therapy. All their therapists were pleasant, helpful in offering suggestions for better functioning after surgery, and practiced good health protocols. They were also very prompt in showing up for scheduled appointments.

Elizabeth B.

Pemi-Baker Hospice & Home Health
2019-11-07T12:26:12-05:00

Elizabeth B.

Pemi-Baker provided very good home therapy. All their therapists were pleasant, helpful in offering suggestions for better functioning after surgery, and practiced good health protocols. They were also very prompt in showing up for scheduled appointments.
https://www.pemibakerhospicehomehealth.org/testimonials/weve-loved-the-swim-lessons-at-pemi-baker/

“Your generosity with your time and your loving care is appreciated more than you know.”

Thank you to everyone who played a role in taking care of my mother and giving her the freedom of remaining home while suffering from dementia. Your generosity with your time and your loving care is appreciated more than you know. A special thanks goes to Macayla and Colleen, who visited her on a regular basis, and to Lauren who was helpful in connecting us with state services.

Terry W.

Pemi-Baker Hospice & Home Health
2020-01-17T12:43:19-05:00

Terry W.

Thank you to everyone who played a role in taking care of my mother and giving her the freedom of remaining home while suffering from dementia. Your generosity with your time and your loving care is appreciated more than you know. A special thanks goes to Macayla and Colleen, who visited her on a regular basis, and to Lauren who was helpful in connecting us with state services.
https://www.pemibakerhospicehomehealth.org/testimonials/i-was-ready-to-give-up-before-i-met-the-pemi-baker-team/

“Pemi-Baker Hospice services provided kind, professional, competent services every step of the way-and even vaccinated us all for Covid/19!””

Our primary nurse, Fred, was outstanding, and others who filled in (Cathy, Penny, Colleen) were wonderful and a credit to your organization. Fred, you were amazing, not only for mom but for my husband and I as well. I will forever be grateful for your support, wisdom, humor and kindness, all along the end of life journey for mom. I am so deeply thankful that circumstances conspired such that mom was able to die at home, and your role made that time as seamless as it could be made.

Paula W.

Pemi-Baker Hospice & Home Health
2020-01-17T12:31:13-05:00

Paula W.

Our primary nurse, Fred, was outstanding, and others who filled in (Cathy, Penny, Colleen) were wonderful and a credit to your organization. Fred, you were amazing, not only for mom but for my husband and I as well. I will forever be grateful for your support, wisdom, humor and kindness, all along the end of life journey for mom. I am so deeply thankful that circumstances conspired such that mom was able to die at home, and your role made that time as seamless as it could be made.
https://www.pemibakerhospicehomehealth.org/testimonials/im-so-happy-that-i-found-pbch/

“Everyone is so understanding supportive and kind.”

From the director to the nurses to the health care workers.  So cheerful, helpful and accommodating.  This is our second time receiving assistance from Pemi-Baker and we are very lucky to have found this amazing group!  Thank you for your excellent care and compassion.

Leila L.

Pemi-Baker Hospice & Home Health
2020-01-17T13:19:24-05:00

Leila L.

From the director to the nurses to the health care workers.  So cheerful, helpful and accommodating.  This is our second time receiving assistance from Pemi-Baker and we are very lucky to have found this amazing group!  Thank you for your excellent care and compassion.
https://www.pemibakerhospicehomehealth.org/testimonials/everyone-is-so-understanding-supportive-and-kind/

Your courage during Covid-19 does not go unnoticed

Hello. We just wanted to take a moment and let you know how much we truly appreciate all that you do for us in these trying times. You're commitment to the health of our community is a special thing, and we know that you are working under stressful conditions due to the Covid 19 crisis. We realize that in order for you to treat those who may be ill, you are putting you're own lives and even you're own families lives in danger, and that is truly a courageous and honorable thing to do. We want you to know that it does not go unnoticed. Thank you all for all that you do!

Bryan and Renee C., and our mom Joan

Pemi-Baker Hospice & Home Health
2020-06-11T06:27:43-04:00

Bryan and Renee C., and our mom Joan

Hello. We just wanted to take a moment and let you know how much we truly appreciate all that you do for us in these trying times. You're commitment to the health of our community is a special thing, and we know that you are working under stressful conditions due to the Covid 19 crisis. We realize that in order for you to treat those who may be ill, you are putting you're own lives and even you're own families lives in danger, and that is truly a courageous and honorable thing to do. We want you to know that it does not go unnoticed. Thank you all for all that you do!
https://www.pemibakerhospicehomehealth.org/testimonials/your-courage-during-covid-19-does-not-go-unnoticed/
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Monday-Friday: 8:00 am to 4:30 pm

Tel: (603) 536-2232

Answering Service for Nurse nights/weekends:
Tel: (603) 536-2232

Pemi-Baker Hospice & Home Health
101 Boulder Point Drive, Suite 3
Plymouth, NH 03264

Fax: (877) 201-0469
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