top of page
top
TOP
Explore Resources:
National Organizations
National organizations play an important role in advancing dementia research, education, advocacy, and support services. This page features a collection of trusted national organizations that provide information, programs, caregiver resources, helplines, and opportunities to connect with broader dementia communities. Whether you are seeking guidance after a diagnosis, support for caregiving, or information about advocacy and research initiatives, these organizations can serve as valuable sources of assistance and expertise.
AfricanAmericansAgainstAlzheimer’s is the nation’s first organization dedicated to building a coordinated national response to eliminate and address Alzheimer’s disease (AD) among African Americans. The fourth leading cause of death for older African Americans, AD has a disparate impact on African Americans.
The AFA has activities happening almost every day in their online Teal Room.
Mission: To enhance the quality of life for those living with Dementia, caregivers, and the community!
Educate, Provide and Recognize
Dementia overview, symptoms, types
Care for Veterans with Alzheimer’s or dementia is provided throughout the full range of VA health care services. Depending on the Veterans needs, services may include Home Based Primary Care, Homemaker and Home Health Aide, Respite Care, Adult Day Health Care, outpatient clinic, inpatient hospital, Nursing Home, Palliative Care, or Hospice Care. Caregiver Support is also an essential part of these services.
Your destination for dementia information, resources, and research.
AFTD’s mission is to improve the quality of life of people affected by FTD and drive research to a cure. We work every day to advance:
Research, Awareness, Support,Education, Advocacy
FCA support and assists families and caregivers through education, advocacy and services. In addition to providing training to technical assistance to California’s Caregiver Resource Centers, FCA hosts the National Center on Caregiving (NCC).
CareNav is a simple, user-friendly tool designed to help families navigate the complexities of the caregiving journey. Register online or call us toll-free at 800.445.8106.
Through outreach, education and research, we support those affected by Lewy body dementias, their families and caregivers. We are dedicated to raising awareness and promoting scientific advances.
If you know someone with Alzheimer's disease or have been diagnosed yourself, this is your community. Alzheimers.net grew out of the need to have a social network that will be a respite, a resource and a way to connect with others who share a common bond. Get authoritative, up-to-date resources and advice from professionals with expertise about Alzheimer’s disease and related dementias.
US Centers for Disease Control and Prevention website dedicated to Alzheimer's
HealthAdvocateX is a national organization committed to helping you transform into an active participant in your care. We are committed to helping everyone understand what health advocacy is, how to boost health advocacy skills and knowledge regardless of who you are. We specialize in inspiring people to take action through community education, health advocacy events and by connecting you to trusted health advocacy resources.
The Rosalynn Carter Institute for Caregivers promotes the health, strength, and resilience of caregivers throughout the United States. Established in 1987 by former First Lady Rosalynn Carter, the Institute’s priority is the unpaid family caregiver: those individuals who care for a relative, friend, or loved one.
Formed in 1980, the Alzheimer's Association is the leading voluntary health organization in Alzheimer's care, support and research.
You are a Dementia Friend after you attend an in-person or virtual Dementia Friends Information Session. At the information session, you learn more about five key messages about dementia so that you can share with others.
Anyone of any age can be a Dementia Friend. We need everyone to be part of supporting people in our communities living with dementia.
501(c)3 nonprofit focused on improving the health and well-being of American Indians, Alaska Natives and other indigenous people as they move through the aging spectrum.
We’re a national advocacy and services organization that’s been looking out for LGBT elders since 1978. We build welcoming communities and keep our issues in the national conversation to ensure a fulfilling future for all LGBT people.
bottom of page