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Alzheimer's Association

The Alzheimer's Association is a major national dementia organization with a strong public support layer for caregivers and families. Its public help-and-support pages center a 24/7 Helpline at 800-272-3900 and route people toward local chapters, local programs, and other support resources3.

Dementia caregiving is among the most intensive forms of family caregiving, and national caregiver research treats it as a high-prevalence, high-intensity segment of family care1. Alzheimer's Association facts-and-figures reporting underscores the scale of that burden, with millions of Americans providing unpaid dementia care and caregiver strain increasing as disease progresses2. The organization's public support pages respond with local chapters, support groups, educational workshops, and a Community Resource Finder for navigating care and services3.

For caregivers reaching out for the first time, the 24/7 Helpline is the entry point. The public site presents it as a way to get information, local resources, and connection to chapter-based programs and support options at any hour3. That matters for dementia caregivers, whose needs often do not follow business hours.

The Alzheimer's Association addresses zone P1 (Social Support) through support groups, local chapters, and community-facing programs. It addresses zone P6 (Emotional Wellbeing) through its round-the-clock helpline and ongoing dementia-support resources3. For caregivers managing dementia specifically, it is one of the strongest national public resources available.

The Association's website at alz.org also points families toward local resources and a community resource finder, which makes it useful not only for education but for practical next steps3.


  1. AARP/NAC. "Caregiving in the United States 2025." Source → 

  2. Alzheimer's Association. "2025 Alzheimer's Disease Facts and Figures." Source → 

  3. Alzheimer's Association. "Help & Support." Source →