Wednesday, October 30, 2019

November 1 is Social Media Action Day!


A Day of National “Hospice Awareness” Friday, November 1, 2019

#HospiceMonth   #HospiceAwareness #hpm

In recognition of National Hospice and Palliative Care Month, NHPCO encourages all member organizations, professionals and supporters to participate in our annual social media action day, traditionally the first Friday in November – this year, it’s Friday, November 1, 2019.

NHPCO wants the hospice and palliative care community to flood social media with images that promote awareness of hospice and palliative care. This guiding theme, My Hospice: A Program that works. A Benefit that Matters, will allow participants to share a wide range of photos, images or videos – all to help people better understand the value of hospice and palliative care.

Social media posts on November 1 should feature photos, graphics or short videos provided by hospice and palliative care organizations/professionals or individuals that capture hospice and/or palliative care at its best – the specific post we leave up to you!

Spread positive messaging on November 1 - and all month long in recognition of National Hospice and Palliative Care Month.

Download NHPCO's Social Media Action Day tip sheet (PDF).


Monday, October 21, 2019

Birdie's Heart for Hospice

As I walk into the Malone, New York office of Hospice of the North Country, I’m reminded of all the memories I have from working at the organization. I started my career in hospice and communications there twelve years ago.  Every day I was amazed at the work my clinical colleagues were doing. I wasn’t at the bedside, but occasionally, I got to go into patient’s homes and interview them and their families. It was the highlight of my job. I looked forward to lunches spent with the nurses, who would talk about the different events of the day. They never stopped thinking about their patients…even at a lunch break where they could easily use the time to talk about the latest episode The Bachelor (okay we did that sometimes!).

Now that I work at NHPCO, I am more aware of what is going on with hospice care on a national level. Regulatory changes, reimbursement cuts, and new payment models are just some of the things we are currently facing as a community. Healthcare in this country is constantly evolving and hospice is facing many challenges. The reality is that hospice will probably look different in five years. We are seeing a greater need for providers to be innovative when it comes to care delivery all while preserving the mission of hospice care.

Naturally, it’s easy to get wrapped up by these issues. They are so important to our community and at NHPCO, we must do everything we can to guide providers through these challenges. However, I wanted to get back to the basics, back on the ground meeting with those who are doing the work at the bedside. So, I went back to HONC and interviewed an amazing human being and hospice volunteer – Birdie Leavitt.

Birdie is a person I will remember for the rest of my life. She checks off all the hospice volunteer criteria – because her husband and family member received such quality hospice care, she felt she needed to give back and signed up to volunteer. She is willing to visit with anyone at any time, go into any living situation, and drive miles upon miles on country roads, sometimes in a snowstorm, to get to her patient’s home. She will come into the office and stuff envelopes, shred paper, and cuddle the office cats Alice and Tommy.

Birdie and one of the hospice cats.
I talked with Birdie about her experience as a hospice volunteer and I was so pleased to learn that she had the same passion, if not more, for hospice and volunteering now as she did when I worked with her seven years ago. Birdie has a binder that is full of memorabilia from her time at HONC. It’s a lot thicker today than it was the last time I looked through it. Since 2004, she has collected thank you notes, messages, obituaries, and mementos of the patients and families she cared for.

She reminisced about the range of activities she has performed as a hospice volunteer – making breakfast, doing dishes, picking up a few items at the grocery store for a family after their loved one died, singing along as a patient performed her daily comforting activity of playing the piano, and visiting with a patient and family on Thanksgiving Day.

Birdie told a story about a nursing home patient who didn’t have any family to provide support and companionship. This person had only the staff charged to care for them. The team at HONC made a commitment to staff five volunteers daily so the patient wouldn’t be alone in their final days. Birdie visited the patient and would wheel them out to the courtyard to look at the flowers and plants. It was one of the only times this patient left their room since being admitted weeks before. The patient’s disease had made it difficult for them to speak but, during one of Birdie’s visits, they communicated by grabbing Birdie’s hand and placing it against their cheek. Birdie had made an impact on this patient and they remembered her through the dementia and loneliness.

Many people don’t understand that hospice teams will go into any home and living condition to ensure that a patient is cared for. Birdie talked about two patients she was volunteering for. One of the patients lived in a beautiful home with a gorgeous chandelier. The other patient lived in a trailer with a hole in the floor. When Birdie sat down, a chipmunk peeked out its head. Her comment to this contrast in living situations, “With hospice, no matter how you live where you are, you get the same care as the next person.”

When I asked Birdie if she gets attached to her patients, she said without hesitation, “You do get attached to them. I can tell when the time is getting short, when it’s getting close.”

I learned that HONC is taking steps to provide emotional care for their volunteers, to ensure that they understand and recognize the symptoms of grief that they might feel after losing their patients. Bereavement coordinators will be providing a seminar for all the volunteers in the organization this fall. Volunteers are encouraged to attend and have been told they can bring friends along because hospice cares for the whole community, not just those receiving hospice care.

Finally, I asked Birdie what hospice meant to her. She answered, “It means everything. It means doing something for somebody else. It means more for me than I could ever do for them.”

Birdie is the model hospice volunteer. But she’s so much more than that...just like hospice is more than just a piece of the United States healthcare system. There are thousands of hospice volunteers, like Birdie, across the country and they are one of the reasons hospice care is so unique. We often hear that volunteers are the “heart of hospice.” They are also the foundation of hospice, as this movement was started by volunteers. They are an integral component of the interdisciplinary model of care that makes hospice special. 

You will not find this type of care in any other part of healthcare in this country. I didn’t need to go back to HONC to understand why hospice is so important because I was already a believer and advocate for our community. But it’s always good to be reminded that people like Birdie are out there, willing to sit with your dying loved while you take a much-needed break, do the dishes that are piling up because you are more focused on caregiving, or sit by your side as you take your final breath.

Hospice might look very different five years from now. Let’s preserve and protect that pieces of  hospice care that make it so special. Let’s make sure the Birdies out there can continue to make house calls to patients and families who need a little extra help.

By Amanda Bow
Senior Director, Communications and Digital Strategy
NHPCO

Thursday, September 26, 2019

OIG Virtual Town Hall for NHPCO Members

NHPCO will host a free Virtual Town Hall for members on Thursday, October 24, 2019 from 1:00 – 2:00 p.m. ET with the Office of Inspector General for the Department of Health and Human Services.

As providers are likely to remember, in July 2019, two OIG reports were released (PDF) that identified concerns with the large number of hospices with survey deficiencies and examples of hospice patients in immediate jeopardy for harm. These two reports have received media and policymaker attention since their release.

This virtual town hall offers members a unique opportunity to learn more about the OIG's specific findings and the suggested reforms OIG is recommending for both CMS and Congress to undertake.

Participants will have the opportunity to learn and ask questions with the authors of the reports including Assistant Inspector General Erin Bliss, Assistant Inspector General for Evaluation and Inspections at HHS Office of Inspector General, Nancy Harrison, Deputy Regional Inspector General Office of Evaluation and Inspections in New York and Jodi Nudelman, Regional Inspector General for the Office of Evaluation and Inspections in New York.

Prior to registering for the Virtual Town Hall, members should review the OIG talking points (PDF) prepared by NHPCO.

Members will find a registration link in NewsBriefs issued September 26, 2019 and available online.



Wednesday, September 18, 2019

NHPCO Hospice Ambassadors on Capitol Hill


Hospice providers from NHPCO are on Capitol Hill, September 17 and 18, to advocate for reforms that would increase access to hospice and palliative care in America’s rural towns and improve hospice care quality.

“All Americans should be given access to quality hospice care, no matter their zip code,” said Sandy Kuhlman, Executive Director of Hospice Services of Northwest Kansas and one of NHPCO’s visiting My Hospice Ambassadors.  “For this reason, we are bringing our message to Washington and asking our representatives to improve and reform hospice and palliative care policies that will increase access, refine oversight, advance education and improve transparency for providers and consumers alike.” 

Hospice advocates are urging lawmakers to support the Rural Access to Hospice Act of 2019 (H.R. 2594), bipartisan legislation introduced by Representatives Ron Kind (D-WI) and Jackie Walorski (R-IN) that will allow Rural Health Centers (RHCs) and Federally Qualified Health Centers (FQHCs) to receive payment for serving as the hospice attending physician. If passed, the legislation would fix a technical glitch that currently prevents terminally ill beneficiaries in underserved and rural communities from utilizing the physician of their choice when entering hospice care.

NHPCO members will also talk to lawmakers about the organization’s Program Integrity Initiative, which overviews provider supported reforms and opportunities for proactive collaboration with Congress and federal regulators to increase oversight, education, and transparency.

“We look forward to working with the Administration and Congress to simplify and streamline the hospice benefit and compliance process to ensure taxpayer resources are spent wisely,” noted Kuhlman. “More oversight of new and poor-performing hospice providers would protect the most vulnerable, while easing unnecessary governmental red tape on honest and law-abiding hospice providers so they can continue to provide high-quality, person-centered care.  Accountability leads to credibility. Our goal is to ensure patients and their families have the utmost confidence in their hospice program.” 

Learn more about the My Hospice Campaign.

My Hospice Ambassadors with members of the board at NHPCO offices on September 17.


Friday, September 13, 2019

Final Day of Virtual Hill Week - Take Action!

Activity throughout Virtual Hill Week (September 9 – 13) has been amazing. Almost 400 advocates have taken over 2,500 Advocacy Actions! This morning, Hospice Action Network announced that there are 18 (!!) New Bill Cosponsors for legislation the hospice community supports.Click here for the list of new cosponsors.

HAN really want to get up to 500 Advocates and 3,000 Advocacy Actions, as well as ensure that every state has their voices heard! Today is the final day of Virtual Hill Day 2019. If you haven’t yet contacted your Members of Congress, please take five minutes to do so.

If you are very short on time, the most important action you can take is making a phone call on behalf of the Rural Access to Hospice Act. When you log in to the Take Action Module and put in your home address, look for the phone icon on the far left to get the phone numbers and short script. Phone calls have a higher likelihood of making an impact, so we encourage everyone to PLEASE, make your phone calls and send emails!


Hospice Action Networks thanks everyone who has participated so far: it is amazing to see the impact you can have in just a few days.


Tuesday, September 10, 2019

Hello and Goodbye: Perinatal Loss Doula Volunteers


The Suncoast Hospice Perinatal Loss Program started in 2004, has recently grown to include a new focus on early first trimester losses and expanded training of volunteer perinatal loss doulas. Our program offers specialized comfort, education, and support to patients and families who may experience, or have already experienced, a pregnancy loss, stillbirth, or death of a baby shortly after birth. Our compassionate team of expert nurses, social workers, chaplains, and trained doula volunteers help patients and their families find understanding and peace through every step of their journeys.

Perinatal loss is often disregarded, its impact negated, leaving the woman and her family struggling emotionally and spiritually. Our doulas (also known as birth companions) understand that birth is a key life experience. They listen thoughtfully to what is important to the woman and her family regarding the birth, providing insight on options for managing the labor and delivery. Doulas offer physical and emotional support to mothers and their partners during labor, delivery, and the immediate postpartum period. They provide a quiet, consistent presence throughout this experience.
After delivery, memory making is an important service that our doulas provide. This involves bathing and dressing the baby, creating hand and foot prints and molds, and obtaining hair locks. Empath Health sewing volunteers make special clothes and blankets used for the baby. These items are placed in a memory box for them to keep. Support pamphlets, brochures, and resources are given to the mother and family as applicable.

In addition, our counselors provide counseling prior to and after the loss. If the pregnancy results in a live birth, our team can work with the family and hospital staff to create a meaningful experience no matter the length of the child’s life. When appropriate, the family can be transferred home to receive care from our Suncoast Hospice pediatric team.

Our Perinatal Loss Program continues to grow and evolve which includes expansion to other hospitals. In turn, we have, and continue to expand the number of volunteer doulas in the program. This entails enhanced doula recruitment and training. To accomplish this, we continue to develop closer collaboration with our Empath Health volunteer department.

This session is intended to develop an increased recognition of the role of the doula during a perinatal loss. Provide a description of the special recruitment and training needs and requirements of Empath Health perinatal loss doula volunteers. Present and describe strategies to develop and implement a perinatal loss program using volunteer doulas.


By Vicki Haywood MSN,  RN, CPAN
Senior Staff Nurse/Care Team Manager
Children’s Program
Empath Health

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Vicki Haywood is among the faculty for NHPCO's 2019 Interdisciplinary Conference at the Gaylord Palms in Orlando, Florida. She will be presenting as part of the session, "Hello and Goodbye: Perinatal Loss Doula Volunteers," on Wednesday, November 6, 2019.


Monday, September 9, 2019

Virtual Hill Week Starts Today!

September 9-13, 2019, all hospice and palliative care advocates and supporters should join in Virtual Hill Week and contact their elected officials regarding the importance of hospice and palliative care and some of the legislation that will help improve access.

The Hospice Action Network makes participation easy. Visit the HAN online Take Action Module and you will find everything you need, from reviewing key messaging to finding your legislators and contacting them.

Should you want to take a couple extra minutes to familiarize yourself with this year's policy asks, so you can feel prepared, there is information on the HAN website.

All this week - Monday through Friday - join thousands of hospice and palliative care advocates to make your voice heard on Capitol Hill.  As a participant in Virtual Hill Week, you are standing up for patients and families!

Take action - and spread the word via social media with hashtag #MyHospice.