
Caring for a loved one with Alzheimer’s disease is emotionally and physically demanding. Research shows that participation in caregiver support groups can reduce caregiver stress, improve coping skills, and increase access to practical resources and local services. If you’re feeling overwhelmed, a support group can be an important first step toward better wellbeing for both you and the person you care for.
What are caregiver support groups?
Caregiver support groups are meetings, virtual or in-person, facilitated by trained professionals or experienced peers, where family members share experiences, practical tips, and emotional support. Groups range from general dementia caregiver groups to specialized options (spousal caregivers, early-onset dementia, Spanish-language groups, etc).
Benefits (practical & clinical)
- Emotional relief & reduced isolation: Hearing others’ experiences on Alzheimer’s disease, normalizes feelings and lowers stress.
- Practical problem-solving: Strategies for managing behaviors (validation, redirection, consistent routines), medication adherence, and daily care tasks.
- Connections to services: Groups often share local respite providers, home-care agencies, and community programs.
Improved caregiver health: Regular participation is associated with better caregiver wellbeing and coping.

How to find the right group
- Ask your neurologist, primary care provider, or clinic social worker many clinics host or can recommend groups.
- National organizations start with the Alzheimer’s Association and Family Caregiver Alliance for local listings and professionally moderated groups.
- Community & faith centers senior centers, libraries, and faith organizations frequently host caregiver meetups.
- Online options professionally moderated Zoom or telephone groups and vetted Facebook communities can be practical when in-person options are limited.
What to expect at your first meeting
Support group meetings typically last 60–90 minutes and include a check-in, short educational segment, problem-solving discussion, and resource sharing. Bring 1–2 specific questions, arrive a few minutes early, and ask about confidentiality policies.
Quick behavior-management tips (use right away)
- Validate feelings first: “I can see why that would upset you.” Focus on emotion rather than arguing about a memory.
- Redirect & simplify: Offer a one-step alternative activity (e.g., make tea) and use short instructions.
- Offer meaningful choices: Give two options to preserve autonomy (“Do you want water or juice?”). Keep routines predictable.
When a support group isn’t enough
Support groups are helpful, but they are not a substitute for clinical care. Contact your neurologist or primary care provider if you notice:
- New or worsening falls or mobility problems
- Sudden aggression or hallucinations
- Rapid cognitive decline over days–weeks
- Severe caregiver depression or thoughts of harming yourself
How to join Neurology One’s monthly support groups
Neurology One runs monthly caregiver support groups in partnership with the Alzheimer’s Association. Our team is trained and certified by the Alzheimer’s Association to facilitate these sessions, ensuring groups are professionally moderated, evidence-informed, and sensitive to caregivers’ needs. These sessions are professionally facilitated and available in English and Spanish when scheduled. To join or to learn upcoming dates, visit NeurologyOne.com or call (407) 706-3060. If you’d like, our team can help identify the session that best fits your schedule and caregiving role.
At Neurology One: We host monthly caregiver support groups, run in partnership with the Alzheimer’s Association.






