Our movement

A growing, community-led movement

Dementia Friendly Nevada (DFNV) is both a network of grassroots community initiatives and a statewide movement. We believe people can live well with dementia with the right community support, and that an inclusive community is a stronger, brighter community for everyone.

What began in 2016 as four communities committed to becoming more dementia-friendly and inclusive has blossomed into a network of nine Community Groups and counting across rural, urban, and tribal regions. Each group is led by local volunteers and supported by the statewide DFNV Support Team, including DFNV Community Convener Casey Venturini.

Casey Venturini, DFNV Community Convener

DFNV Community Convener

Casey Venturini, MA

Casey supports the Community Groups and the statewide DFNV Support Team in building communities that are more dementia-friendly and inclusive. Reach out anytime to learn more or get involved.

Get in touch: casey.v@unr.edu

  • 2016 Movement launched
  • 9 Community Groups and counting
  • 1100+ Members

The Dementia Engagement, Education, and Research (DEER) Program in the School of Public Health at the University of Nevada, Reno proudly provides administrative support to Dementia Friendly Nevada.

Local Roots · Statewide Network

Find Your Local DFNV Community Group

Across Nevada, passionate community members are working toward communities that are more dementia-friendly and inclusive. Find the Community Group nearest you on the map, or contact us to launch a new Community Group in your area.

  • 9 communities and growing
  • Free & local, led by your neighbors
  • Urban, rural & tribal, all of Nevada

Explore the Dementia Friendly Nevada Values

Dementia Friendly Nevada is guided by a deep belief that each person living with dementia remains, and will always remain, a full human being and their rights as a citizen are, and shall always be, intact. To guide our dementia-friendly-and-inclusive efforts, we offer a set of values which can help serve as a type of ethical roadmap for restoring and ensuring fundamental rights and opportunities to people living with dementia who have been disenfranchised by a prevalent view that discounts and diminishes their value and contributions to our communities and state.

  • 1 People can live well with dementia.

    People living with dementia are not defined by their diagnosis. In order to support each person in living well with dementia, we must break the stigma of dementia and focus on strengths instead of just losses. Rather than using terms like “dementia sufferer” or “Alzheimer’s patient” that focus on the tragedy of dementia, we can honor the humanity of all people by using person-first language, like “people living with dementia.” People can live well with dementia when they are offered opportunities for meaning, purpose, and growth.

  • 2 Partnering with people living with dementia and honoring each individual’s lived experience opens a world of possibilities.

    People living with dementia are the genuine experts in the experience of living with dementia. Their perspectives, wishes, and preferences should always be respected in the decisions that affect their lives. Doing so requires understanding each person as a unique human being, as generalizations based on “age” or “stage” are limiting and often wrong. After all, if you know one person living with dementia, you only know one person living with dementia.

  • 3 Recognizing, validating, and responding to all forms of expression as meaningful communication supports well-being.

    People living with dementia can and do communicate and express themselves meaningfully throughout their dementia. What people talk about as “behavioral and psychosocial symptoms of dementia” (or “BPSDs”) are often forms of communication, where people living with dementia are expressing their identity, preferences, or unmet needs in the best way they can. Instead of seeing these so-called “behaviors” as problems, care partners and professionals should seek to understand, validate, and respond to what a person is trying to say through their actions.

  • 4 When supporting a person living with dementia, we should always strive to see the world from their perspective.

    “Redirection” is a code-word for distracting or charming someone living with dementia into doing what you want them to do. Instead of redirecting, care partners and community members should respond supportively and seek to understand the world from the other person’s perspective.

  • 5 People living with dementia have the right to freedom.

    Sometimes what makes care partners feel safe and secure makes people living with dementia feel trapped and anxious, including locked doors. People living with dementia have the right to access care and support in the least restrictive manner and should never be segregated. Residential care settings should not merely be “homelike;” they should be actual homes that uphold the right to self-determination. To support this right, safety and freedom should always be balanced, and connections to community should always be protected and promoted. We must always seek to foster security while upholding personal choice, and there are many ways to promote safety besides locked doors.

  • 6 People living with dementia can grow and thrive.

    Though most forms of dementia are degenerative, people living with dementia can continue to grow and thrive when care partners and organizations honor the right to autonomy and privacy and avoid protective measures that medicalize, monitor, and control all aspects of everyday life.

  • 7 Proactive supports and services reduce the need for reactive interventions.

    Communities and service agencies should offer affordable, easy-to-access help and support for everyone. With a focus on early detection and proactive community-based supports and services, we can avoid the need for expensive and reactive medical interventions and institutional care settings. When institutional care is necessary, people living with dementia should have access to affordable, high-quality residential care that nurtures each person’s well-being and upholds their personal decision-making to the greatest extent possible. This requires having enough staff on-hand to fully support each person.

  • 8 A dementia-inclusive community is a strong community; everyone needs community and communities need everyone!

    Just as the Americans with Disabilities Act ensures ramps for people living with physical disabilities, it should also ensure that communities provide adaptations and supports (in essence, “cognitive ramps”) for people living with dementia and other cognitive disabilities. When we support and include people living with dementia, it enhances their well-being. It also makes our communities stronger. Everyone needs community, and communities need everyone!

Voices from our community

I don’t feel sick. It’s such a weird kind of sickness, especially at the beginning of my dementia. But now it’s just kind of in the background. It’s like ‘hey, still here!’
RobertaLiving with dementia
Dementia takes, but it can also give. I got to experience my mother’s love in a way that made it real. It gave me her laughter, and the lightness that was within her but had been hidden. I am forever grateful.
A Family Care PartnerReflecting on her mother
I think the only way I’ve changed, and this probably comes with aging too, is to be more understanding of other people. There’s a love that comes through much more than it ever did before.
Mary LeeLiving with cognitive changes
One of the interesting things about my Dad’s dementia is how it has deepened our relationship. I feel like we know each other better, even though we’ve known each other my entire life, and for that I’m grateful.
JenniferFamily care partner
Free and Open to All

The series is a monthly conversation with leading voices in dementia-inclusive community work, dementia care and support, brain health promotion, and more, bringing world-class experts straight to your screen.

  • Second Monday of every month
  • 1:00–2:30 PM Pacific Time
  • Live on Zoom, join anywhere
  • Always free, all welcome

Upcoming Sessions

  1. Mon, Oct 122026

    Speaker to be announced

    Details coming soon.

  2. Mon, Nov 92026

    Speaker to be announced

    Details coming soon.

  3. Mon, Dec 142026

    Speaker to be announced

    Details coming soon.

Watch · Share · Change the Story

DFNV Public Service Announcements

These are short films with a big heart. Created by the Nevada Division of Public & Behavioral Health in partnership with Dementia Friendly Nevada and the DEER Program, they reshape how our state sees, speaks about, and stands beside people living with dementia and their care partners.

Watch the Campaign

Here are two messages of hope. Press play, then pass them on.

For people living with dementia

A Comma, Not A Period

A diagnosis is a turning point, not the end of the sentence. This PSA inspires people living with dementia to see their diagnosis as a beginning; a comma, not a period.

For family care partners

What If

This PSA is an honest tribute to the complexities of caregiving, and a gentle reminder to embrace “What If, What Is, Whatever Comes our Way.”