PCPRV - Palliative Care Partnership of the Roanoke Valley

PCPRV - Palliative Care Partnership of the Roanoke Valley Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from PCPRV - Palliative Care Partnership of the Roanoke Valley, Nonprofit Organization, Roanoke, VA.

Our Mission
The Palliative Care Partnership of the Roanoke Valley exists to be a catalyst for community efforts that empower all people to plan and exercise their choices for quality palliative and end-of-life care. Our History
Established in 2001, the Palliative Care Partnership of the Roanoke Valley (PCPRV) is a non-profit with a long history of promoting Advance Care Planning in our community a

nd across Virginia. Members of the PCPRV include representatives from a range of health care agencies, to include hospitals, home health and hospice agencies, long-term care facilities, our Veterans Administration, local area agencies on aging and many other providers. The PCPRV meets monthly to share information and promote continuing education to healthcare providers and our community on Advance Care Planning and end-of-life care. Past Grant Funded Programs:

Since 2006, the PCPRV has received funding from the Geriatric Training and Education (GTE)Initiative Grant to promote Advance Care Planning initiatives. The GTE funds are from the General Assembly of Virginia and administered by the Virginia Center for Aging at Virginia Commonwealth University.

2006
POST Pilot Project for Virginia PCPRV planned, designed and implemented a POST Pilot Project for Virginia. The grant assisted 10 Pilot Project Stakeholder (PPS) groups in Virginia to design and implement POST pilot projects in their communities.

2009 - 2010
Training and Education in the Use and Implementation of the POST Form

2010 - 2011
Training and Education in the Implementation of the POST Pilot Projects and POST Advance Care Planning Facilitation in Designated Areas of Virginia

2011 - 2012
Training and Education in the Implementation of the POST Pilot Projects and POST Advance Care Planning Facilitation in Designated Areas of Virginia

2012 - 2013
Training and Education in the Implementation of POST Pilot Projects and POST Advance Care Planning Facilitation in Designated Areas of Virginia

2013-2014
Training and Education in the Implementation of POST Pilot Projects and POST Physician Education and Advance Care Planning Faculty Training in Designated Areas of Virginia

2014-2015
POST Training and Education of Attorneys, Physicians, Advance Care Planning Facilitators and Advance Care Planning Training Faculty in Virginia

2016-2017
The 3-R's of Advance Care Planning Navigation, A Training for Care Managers, Community Health Workers (CHW) and Clergy/Health Ministries

Trained 15 community care managers, health care workers and volunteers to serve as Advance Care Planning (ACP) Navigators. The Navigators were provided tools and information to promote outreach and access of ACP resources to low-income, chronically ill older adults residing in Northwest and Southeast Roanoke, two medically underserved communities.

07/21/2026

What makes a good day for you?

It’s a simple question, but the answer can help guide important healthcare decisions.

Advance care planning starts with understanding what matters most to you—your goals, values, and preferences for care. For individuals living with serious illness or frailty, these conversations can help ensure treatment aligns with what is most important to them. The POLST process supports these discussions by translating patient wishes into actionable medical orders.

Learn more about NPC and advance care planning: https://polst.org/

07/21/2026

A POLST form is not a one-time conversation.

As health conditions, goals, and treatment preferences change, it may be appropriate to review a POLST form with a healthcare professional. Review is also important during transitions between care settings to help ensure care continues to reflect a person's wishes.

Regular conversations about goals of care can help ensure treatment decisions remain aligned with what matters most.

Learn more: https://polst.org/

07/21/2026

Family gatherings often bring generations together, making them a natural opportunity to discuss what matters most.

Advance care planning is about sharing values, goals, and preferences — not just completing forms.

Starting the conversation today can help loved ones feel more prepared and confident in the future.

Learn more: https://polst.org

07/21/2026

Understanding POLST starts with having the right information.

Patients and families often ask:

- What is a POLST form?
- Who should have one?
- Can a POLST form be changed?
- Will my POLST form be honored if I move?

The National POLST Collaborative's Frequently Asked Questions page provides answers to common questions and helps support informed conversations about serious illness care.

Explore the FAQs: POLST.org/frequently-asked-questions-for-patients

07/21/2026

Please join us in welcoming the newest members of the National POLST Collaborative Board of Directors!

We are excited to welcome Wendy Davis (Virginia), Chelsey Patten (Colorado), Kandyce Powell (Maine), and Hilary Walker (Washington) to the Board. Their expertise and leadership will help advance our mission of improving person-centered care.

We also extend our heartfelt thanks to our retiring board members—Cindy Munn (Louisiana), Vicki Buchda (Arizona), and Judy Thomas—for their dedication, leadership, and service to the National POLST Collaborative.

We also recognize our continuing Board members for their ongoing leadership and commitment:
• Matt Kestenbaum (President, Virginia)
• Susan Nelson (Past President, Louisiana)
• Kim Callanan (Treasurer, Texas)
• Jennifer Ballentine (California)
• Jeannette Kojane (Hawaii)
• Christine McMichael (Massachusetts)
• Paula Sanders (Georgia)
• Karl Steinberg (California)

Together, we look forward to advancing high-quality, person-centered care.

07/21/2026
07/21/2026

You can have a say in your care. Treatments only work if they work for you.

If you like this messaging regarding advance care planning, check out a toolkit created in partnership during a three-year grant generously funded by The John A. Hartford Foundation and Cambia Health Foundation. Feel free to steal this messaging! All of the messaging, text, and images in this section is free. No copyright cost. No royalties. No restrictions.

Download the Serious Illness Messaging Toolkitfor more free messages, images and text: https://go.ihi.org/4gdGmyj

07/21/2026

Please join and New Jersey Advocates for Aging Well on July 22 at 3:00 PM for 𝐋𝐢𝐯𝐢𝐧𝐠 𝐖𝐞𝐥𝐥 𝐰𝐢𝐭𝐡 𝐒𝐞𝐫𝐢𝐨𝐮𝐬 𝐈𝐥𝐥𝐧𝐞𝐬𝐬: 𝐃𝐞𝐦𝐲𝐬𝐭𝐢𝐟𝐲𝐢𝐧𝐠 𝐏𝐚𝐥𝐥𝐢𝐚𝐭𝐢𝐯𝐞 𝐂𝐚𝐫𝐞, a free webinar designed for professionals, caregivers, and community members who support individuals living with serious illness.

This session will explore practical strategies for helping people live well with serious illness, resources available to support family caregivers, and new opportunities available through New Jersey's Medicaid Community-Based Palliative Care benefit. Learn how these services can improve quality of life, help people remain at home longer, and provide access to available support.

Register today: https://us02web.zoom.us/meeting/register/QTKmM3owS66X3Ln8hRgwZA #/registration

07/21/2026

"As I sat on the beach that day — sand between my toes, with my best friends from college at my side — I thought of how conversations about how we want to live at the end of our lives can and should happen whenever the opportunity arises. We should talk with those we care about where we feel comfortable and safe. We can have these discussions as often as we need them to make sure we are heard and listened to."

In her blog, our very own Patty Webster writes about the gift of starting conversations with your loved ones, how this can come up in any setting, with anyone it feels right to talk about with!

Click here to check out Patty's blog, "Beach Conversations": https://go.ihi.org/4eCBku3

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Roanoke, VA
24018

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