PeerGalaxy Original Calendar
Welcome to PeerGalaxy Calendar featuring over 336,800+ monthly offerings of FREE telephone- and online-accessible peer support, recovery support, and wellness activities! Plus 50+ warmlines, helplines, chatlines, and hotlines. Plus workshops, webinars, job postings, resources, observances, special events, consumer input opportunities and more.
WE ARE PEER FOR YOU!
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If you have an event to add, email us: [email protected]
Training Opportunities in July 2020
List Provided Courtesy of State of Oregon, Oregon Health Authority
Click here to download PDF Format, 16 pages
Calendar Event Sorting
At the top, the 24/7/365 SAMHSA Disaster Helpline and similar links.
Next, Bundled “All Day” Events
Some organizations (like 12 step recovery programs, AA, NA, AlAnon, etc.) have so many events happening throughout the day that they need to be in a bundled listing to spare endless scrolling. Often there is a link to look up events by zip code and other criteria.
Lastly, Time-Specific Events
So you can see what’s happening in the next hours, time specific events are tagged and listed by start time from 12:01am early morning to 11:59pm late night. There can be events and warmlines operating in different time zones, though we try to list all in Oregon’s Pacific Time Zone.
Page Advancement
The calendar displays ~50 listings per page. To advance to next page with ~50 more listings, click the right arrow in the lower left corner of the calendar
Alzheimer’s Association 24/7 Helpline
The Alzheimer’s Association operates a free, nationwide Helpline at 800.272.3900, connecting people living with dementia, caregivers, and families with live support, local resources, and crisis assistance in more than 200 languages. Trained Helpline Agents and master’s-level Care Consultants are available around the clock, 365 days a year, to help with everything from a new diagnosis to caregiver stress and care planning.
Alzheimer’s Association 24/7 Helpline — https://www.alz.org/help-support/resources/helpline · 800.272.3900 — available day or night, every day of the year
Support Services & Contact Information
Live Chat — https://www.alz.org/help-support/resources/helpline · Typically available Monday–Saturday, 5:00 AM–5:00 PM PST
Online Contact Form — https://www.alz.org/help-support/resources/helpline · For non-urgent questions — response within 24 hours
E-News Sign-Up — https://www.alz.org/e-news · Weekly updates on Alzheimer’s care, support, and research
Website
Alzheimer’s Association — https://www.alz.org
About Alzheimer’s Association
The Alzheimer’s Association was founded in 1980 by Jerome H. Stone and a group of family caregivers who saw the need for an organization to unite caregivers, provide support, and advance research into the disease. It is headquartered in Chicago with chapters in communities nationwide.
The Association’s mission is to lead the way to end Alzheimer’s and all other dementia by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support.
As the largest nonprofit funder of Alzheimer’s research, the Association serves people living with dementia, caregivers, and families across the country through its 24/7 Helpline, local chapters, education programs, and support groups.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Lewy Body Dementia Association
Lewy Line: (800) 539-9767
Monday–Friday, 5:00 AM–2:00 PM PST
The Lewy Body Dementia Association’s Support Services team and network of trained volunteers offer compassionate, confidential phone support to individuals and families navigating Lewy body dementia. Callers can reach trained support volunteers for emotional support, program referrals, and help identifying local education and community resources.
The Lewy Line
Individuals who are symptomatic or diagnosed with Lewy body dementia (LBD), and current or former care partners and family members in the United States, can call the Lewy Line for trusted and confidential support. Support Services team members and trained “Lewy Buddy” volunteers offer compassionate listening and emotional support, customized referrals to additional LBDA programs and support groups, and help identifying available education and community resources. Callers are asked to leave a message, and the Support Services team returns calls within 3 business days. LBDA is unable to return calls placed from outside the United States.
Time: Monday–Friday, 5:00 AM–2:00 PM PST
Date(s): Ongoing — no scheduled end date
Format: Virtual (phone, email, and online contact form)
Platform: Phone, email, and online form — Call (800) 539-9767 · Email [email protected] · Contact LBDA Online
Primary Resources
LBDA Website · Home base for LBD information, research updates, and ways to get involved
Understanding LBD · Overview of Lewy body dementia symptoms, diagnosis, and disease progression
Educational & Resource Programs
Education & Support · Latest information and research to build awareness and understanding of LBD
2026 Community Webinar Series · Free monthly webinars covering LBD science, care strategies, and everyday living
Lewy Publications · Printed and digital guides for patients, families, and healthcare professionals
LBDA Research · Current research initiatives and Research Centers of Excellence advancing LBD science
Social Media Connections
Facebook · Instagram · LinkedIn · X · YouTube
Crisis Support
988 Suicide & Crisis Lifeline · Call or text 988 for confidential 24/7 crisis support if you or a loved one is in crisis
About Lewy Body Dementia Association
The Lewy Body Dementia Association (LBDA) was founded in 2003 by a group of caregivers who connected through an online LBD support group and recognized the need for greater awareness and support. LBDA is a 501(c)(3) nonprofit and the leading national organization dedicated to Lewy body dementia.
Through outreach, education, and research, LBDA works to optimize the quality of life for those affected by LBD, accelerating awareness, advancing research for earlier diagnosis and improved care, and providing comprehensive education and compassionate support.
LBDA serves the estimated 1.4 million people in the United States living with Lewy body dementia, along with their care partners, family members, and the healthcare professionals who support them.
LBDA’s programs include the Lewy Line support services helpline, a network of local support groups, community and professional education, and a collaboration of Research Centers of Excellence advancing the science of LBD.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Alzheimer’s Association 24/7 Helpline
The Alzheimer’s Association operates a free, nationwide Helpline at 800.272.3900, connecting people living with dementia, caregivers, and families with live support, local resources, and crisis assistance in more than 200 languages. Trained Helpline Agents and master’s-level Care Consultants are available around the clock, 365 days a year, to help with everything from a new diagnosis to caregiver stress and care planning.
Alzheimer’s Association 24/7 Helpline — https://www.alz.org/help-support/resources/helpline · 800.272.3900 — available day or night, every day of the year
Support Services & Contact Information
Live Chat — https://www.alz.org/help-support/resources/helpline · Typically available Monday–Saturday, 5:00 AM–5:00 PM PST
Online Contact Form — https://www.alz.org/help-support/resources/helpline · For non-urgent questions — response within 24 hours
E-News Sign-Up — https://www.alz.org/e-news · Weekly updates on Alzheimer’s care, support, and research
Website
Alzheimer’s Association — https://www.alz.org
About Alzheimer’s Association
The Alzheimer’s Association was founded in 1980 by Jerome H. Stone and a group of family caregivers who saw the need for an organization to unite caregivers, provide support, and advance research into the disease. It is headquartered in Chicago with chapters in communities nationwide.
The Association’s mission is to lead the way to end Alzheimer’s and all other dementia by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support.
As the largest nonprofit funder of Alzheimer’s research, the Association serves people living with dementia, caregivers, and families across the country through its 24/7 Helpline, local chapters, education programs, and support groups.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Lewy Body Dementia Association
Lewy Line: (800) 539-9767
Monday–Friday, 5:00 AM–2:00 PM PST
The Lewy Body Dementia Association’s Support Services team and network of trained volunteers offer compassionate, confidential phone support to individuals and families navigating Lewy body dementia. Callers can reach trained support volunteers for emotional support, program referrals, and help identifying local education and community resources.
The Lewy Line
Individuals who are symptomatic or diagnosed with Lewy body dementia (LBD), and current or former care partners and family members in the United States, can call the Lewy Line for trusted and confidential support. Support Services team members and trained “Lewy Buddy” volunteers offer compassionate listening and emotional support, customized referrals to additional LBDA programs and support groups, and help identifying available education and community resources. Callers are asked to leave a message, and the Support Services team returns calls within 3 business days. LBDA is unable to return calls placed from outside the United States.
Time: Monday–Friday, 5:00 AM–2:00 PM PST
Date(s): Ongoing — no scheduled end date
Format: Virtual (phone, email, and online contact form)
Platform: Phone, email, and online form — Call (800) 539-9767 · Email [email protected] · Contact LBDA Online
Primary Resources
LBDA Website · Home base for LBD information, research updates, and ways to get involved
Understanding LBD · Overview of Lewy body dementia symptoms, diagnosis, and disease progression
Educational & Resource Programs
Education & Support · Latest information and research to build awareness and understanding of LBD
2026 Community Webinar Series · Free monthly webinars covering LBD science, care strategies, and everyday living
Lewy Publications · Printed and digital guides for patients, families, and healthcare professionals
LBDA Research · Current research initiatives and Research Centers of Excellence advancing LBD science
Social Media Connections
Facebook · Instagram · LinkedIn · X · YouTube
Crisis Support
988 Suicide & Crisis Lifeline · Call or text 988 for confidential 24/7 crisis support if you or a loved one is in crisis
About Lewy Body Dementia Association
The Lewy Body Dementia Association (LBDA) was founded in 2003 by a group of caregivers who connected through an online LBD support group and recognized the need for greater awareness and support. LBDA is a 501(c)(3) nonprofit and the leading national organization dedicated to Lewy body dementia.
Through outreach, education, and research, LBDA works to optimize the quality of life for those affected by LBD, accelerating awareness, advancing research for earlier diagnosis and improved care, and providing comprehensive education and compassionate support.
LBDA serves the estimated 1.4 million people in the United States living with Lewy body dementia, along with their care partners, family members, and the healthcare professionals who support them.
LBDA’s programs include the Lewy Line support services helpline, a network of local support groups, community and professional education, and a collaboration of Research Centers of Excellence advancing the science of LBD.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Alzheimer’s Association 24/7 Helpline
The Alzheimer’s Association operates a free, nationwide Helpline at 800.272.3900, connecting people living with dementia, caregivers, and families with live support, local resources, and crisis assistance in more than 200 languages. Trained Helpline Agents and master’s-level Care Consultants are available around the clock, 365 days a year, to help with everything from a new diagnosis to caregiver stress and care planning.
Alzheimer’s Association 24/7 Helpline — https://www.alz.org/help-support/resources/helpline · 800.272.3900 — available day or night, every day of the year
Support Services & Contact Information
Live Chat — https://www.alz.org/help-support/resources/helpline · Typically available Monday–Saturday, 5:00 AM–5:00 PM PST
Online Contact Form — https://www.alz.org/help-support/resources/helpline · For non-urgent questions — response within 24 hours
E-News Sign-Up — https://www.alz.org/e-news · Weekly updates on Alzheimer’s care, support, and research
Website
Alzheimer’s Association — https://www.alz.org
About Alzheimer’s Association
The Alzheimer’s Association was founded in 1980 by Jerome H. Stone and a group of family caregivers who saw the need for an organization to unite caregivers, provide support, and advance research into the disease. It is headquartered in Chicago with chapters in communities nationwide.
The Association’s mission is to lead the way to end Alzheimer’s and all other dementia by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support.
As the largest nonprofit funder of Alzheimer’s research, the Association serves people living with dementia, caregivers, and families across the country through its 24/7 Helpline, local chapters, education programs, and support groups.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Lewy Body Dementia Association
Lewy Line: (800) 539-9767
Monday–Friday, 5:00 AM–2:00 PM PST
The Lewy Body Dementia Association’s Support Services team and network of trained volunteers offer compassionate, confidential phone support to individuals and families navigating Lewy body dementia. Callers can reach trained support volunteers for emotional support, program referrals, and help identifying local education and community resources.
The Lewy Line
Individuals who are symptomatic or diagnosed with Lewy body dementia (LBD), and current or former care partners and family members in the United States, can call the Lewy Line for trusted and confidential support. Support Services team members and trained “Lewy Buddy” volunteers offer compassionate listening and emotional support, customized referrals to additional LBDA programs and support groups, and help identifying available education and community resources. Callers are asked to leave a message, and the Support Services team returns calls within 3 business days. LBDA is unable to return calls placed from outside the United States.
Time: Monday–Friday, 5:00 AM–2:00 PM PST
Date(s): Ongoing — no scheduled end date
Format: Virtual (phone, email, and online contact form)
Platform: Phone, email, and online form — Call (800) 539-9767 · Email [email protected] · Contact LBDA Online
Primary Resources
LBDA Website · Home base for LBD information, research updates, and ways to get involved
Understanding LBD · Overview of Lewy body dementia symptoms, diagnosis, and disease progression
Educational & Resource Programs
Education & Support · Latest information and research to build awareness and understanding of LBD
2026 Community Webinar Series · Free monthly webinars covering LBD science, care strategies, and everyday living
Lewy Publications · Printed and digital guides for patients, families, and healthcare professionals
LBDA Research · Current research initiatives and Research Centers of Excellence advancing LBD science
Social Media Connections
Facebook · Instagram · LinkedIn · X · YouTube
Crisis Support
988 Suicide & Crisis Lifeline · Call or text 988 for confidential 24/7 crisis support if you or a loved one is in crisis
About Lewy Body Dementia Association
The Lewy Body Dementia Association (LBDA) was founded in 2003 by a group of caregivers who connected through an online LBD support group and recognized the need for greater awareness and support. LBDA is a 501(c)(3) nonprofit and the leading national organization dedicated to Lewy body dementia.
Through outreach, education, and research, LBDA works to optimize the quality of life for those affected by LBD, accelerating awareness, advancing research for earlier diagnosis and improved care, and providing comprehensive education and compassionate support.
LBDA serves the estimated 1.4 million people in the United States living with Lewy body dementia, along with their care partners, family members, and the healthcare professionals who support them.
LBDA’s programs include the Lewy Line support services helpline, a network of local support groups, community and professional education, and a collaboration of Research Centers of Excellence advancing the science of LBD.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Alzheimer’s Association 24/7 Helpline
The Alzheimer’s Association operates a free, nationwide Helpline at 800.272.3900, connecting people living with dementia, caregivers, and families with live support, local resources, and crisis assistance in more than 200 languages. Trained Helpline Agents and master’s-level Care Consultants are available around the clock, 365 days a year, to help with everything from a new diagnosis to caregiver stress and care planning.
Alzheimer’s Association 24/7 Helpline — https://www.alz.org/help-support/resources/helpline · 800.272.3900 — available day or night, every day of the year
Support Services & Contact Information
Live Chat — https://www.alz.org/help-support/resources/helpline · Typically available Monday–Saturday, 5:00 AM–5:00 PM PST
Online Contact Form — https://www.alz.org/help-support/resources/helpline · For non-urgent questions — response within 24 hours
E-News Sign-Up — https://www.alz.org/e-news · Weekly updates on Alzheimer’s care, support, and research
Website
Alzheimer’s Association — https://www.alz.org
About Alzheimer’s Association
The Alzheimer’s Association was founded in 1980 by Jerome H. Stone and a group of family caregivers who saw the need for an organization to unite caregivers, provide support, and advance research into the disease. It is headquartered in Chicago with chapters in communities nationwide.
The Association’s mission is to lead the way to end Alzheimer’s and all other dementia by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support.
As the largest nonprofit funder of Alzheimer’s research, the Association serves people living with dementia, caregivers, and families across the country through its 24/7 Helpline, local chapters, education programs, and support groups.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Lewy Body Dementia Association
Lewy Line: (800) 539-9767
Monday–Friday, 5:00 AM–2:00 PM PST
The Lewy Body Dementia Association’s Support Services team and network of trained volunteers offer compassionate, confidential phone support to individuals and families navigating Lewy body dementia. Callers can reach trained support volunteers for emotional support, program referrals, and help identifying local education and community resources.
The Lewy Line
Individuals who are symptomatic or diagnosed with Lewy body dementia (LBD), and current or former care partners and family members in the United States, can call the Lewy Line for trusted and confidential support. Support Services team members and trained “Lewy Buddy” volunteers offer compassionate listening and emotional support, customized referrals to additional LBDA programs and support groups, and help identifying available education and community resources. Callers are asked to leave a message, and the Support Services team returns calls within 3 business days. LBDA is unable to return calls placed from outside the United States.
Time: Monday–Friday, 5:00 AM–2:00 PM PST
Date(s): Ongoing — no scheduled end date
Format: Virtual (phone, email, and online contact form)
Platform: Phone, email, and online form — Call (800) 539-9767 · Email [email protected] · Contact LBDA Online
Primary Resources
LBDA Website · Home base for LBD information, research updates, and ways to get involved
Understanding LBD · Overview of Lewy body dementia symptoms, diagnosis, and disease progression
Educational & Resource Programs
Education & Support · Latest information and research to build awareness and understanding of LBD
2026 Community Webinar Series · Free monthly webinars covering LBD science, care strategies, and everyday living
Lewy Publications · Printed and digital guides for patients, families, and healthcare professionals
LBDA Research · Current research initiatives and Research Centers of Excellence advancing LBD science
Social Media Connections
Facebook · Instagram · LinkedIn · X · YouTube
Crisis Support
988 Suicide & Crisis Lifeline · Call or text 988 for confidential 24/7 crisis support if you or a loved one is in crisis
About Lewy Body Dementia Association
The Lewy Body Dementia Association (LBDA) was founded in 2003 by a group of caregivers who connected through an online LBD support group and recognized the need for greater awareness and support. LBDA is a 501(c)(3) nonprofit and the leading national organization dedicated to Lewy body dementia.
Through outreach, education, and research, LBDA works to optimize the quality of life for those affected by LBD, accelerating awareness, advancing research for earlier diagnosis and improved care, and providing comprehensive education and compassionate support.
LBDA serves the estimated 1.4 million people in the United States living with Lewy body dementia, along with their care partners, family members, and the healthcare professionals who support them.
LBDA’s programs include the Lewy Line support services helpline, a network of local support groups, community and professional education, and a collaboration of Research Centers of Excellence advancing the science of LBD.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Alzheimer’s Association 24/7 Helpline
The Alzheimer’s Association operates a free, nationwide Helpline at 800.272.3900, connecting people living with dementia, caregivers, and families with live support, local resources, and crisis assistance in more than 200 languages. Trained Helpline Agents and master’s-level Care Consultants are available around the clock, 365 days a year, to help with everything from a new diagnosis to caregiver stress and care planning.
Alzheimer’s Association 24/7 Helpline — https://www.alz.org/help-support/resources/helpline · 800.272.3900 — available day or night, every day of the year
Support Services & Contact Information
Live Chat — https://www.alz.org/help-support/resources/helpline · Typically available Monday–Saturday, 5:00 AM–5:00 PM PST
Online Contact Form — https://www.alz.org/help-support/resources/helpline · For non-urgent questions — response within 24 hours
E-News Sign-Up — https://www.alz.org/e-news · Weekly updates on Alzheimer’s care, support, and research
Website
Alzheimer’s Association — https://www.alz.org
About Alzheimer’s Association
The Alzheimer’s Association was founded in 1980 by Jerome H. Stone and a group of family caregivers who saw the need for an organization to unite caregivers, provide support, and advance research into the disease. It is headquartered in Chicago with chapters in communities nationwide.
The Association’s mission is to lead the way to end Alzheimer’s and all other dementia by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support.
As the largest nonprofit funder of Alzheimer’s research, the Association serves people living with dementia, caregivers, and families across the country through its 24/7 Helpline, local chapters, education programs, and support groups.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Alzheimer’s Association 24/7 Helpline
The Alzheimer’s Association operates a free, nationwide Helpline at 800.272.3900, connecting people living with dementia, caregivers, and families with live support, local resources, and crisis assistance in more than 200 languages. Trained Helpline Agents and master’s-level Care Consultants are available around the clock, 365 days a year, to help with everything from a new diagnosis to caregiver stress and care planning.
Alzheimer’s Association 24/7 Helpline — https://www.alz.org/help-support/resources/helpline · 800.272.3900 — available day or night, every day of the year
Support Services & Contact Information
Live Chat — https://www.alz.org/help-support/resources/helpline · Typically available Monday–Saturday, 5:00 AM–5:00 PM PST
Online Contact Form — https://www.alz.org/help-support/resources/helpline · For non-urgent questions — response within 24 hours
E-News Sign-Up — https://www.alz.org/e-news · Weekly updates on Alzheimer’s care, support, and research
Website
Alzheimer’s Association — https://www.alz.org
About Alzheimer’s Association
The Alzheimer’s Association was founded in 1980 by Jerome H. Stone and a group of family caregivers who saw the need for an organization to unite caregivers, provide support, and advance research into the disease. It is headquartered in Chicago with chapters in communities nationwide.
The Association’s mission is to lead the way to end Alzheimer’s and all other dementia by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support.
As the largest nonprofit funder of Alzheimer’s research, the Association serves people living with dementia, caregivers, and families across the country through its 24/7 Helpline, local chapters, education programs, and support groups.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Alzheimer’s Association 24/7 Helpline
The Alzheimer’s Association operates a free, nationwide Helpline at 800.272.3900, connecting people living with dementia, caregivers, and families with live support, local resources, and crisis assistance in more than 200 languages. Trained Helpline Agents and master’s-level Care Consultants are available around the clock, 365 days a year, to help with everything from a new diagnosis to caregiver stress and care planning.
Alzheimer’s Association 24/7 Helpline — https://www.alz.org/help-support/resources/helpline · 800.272.3900 — available day or night, every day of the year
Support Services & Contact Information
Live Chat — https://www.alz.org/help-support/resources/helpline · Typically available Monday–Saturday, 5:00 AM–5:00 PM PST
Online Contact Form — https://www.alz.org/help-support/resources/helpline · For non-urgent questions — response within 24 hours
E-News Sign-Up — https://www.alz.org/e-news · Weekly updates on Alzheimer’s care, support, and research
Website
Alzheimer’s Association — https://www.alz.org
About Alzheimer’s Association
The Alzheimer’s Association was founded in 1980 by Jerome H. Stone and a group of family caregivers who saw the need for an organization to unite caregivers, provide support, and advance research into the disease. It is headquartered in Chicago with chapters in communities nationwide.
The Association’s mission is to lead the way to end Alzheimer’s and all other dementia by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support.
As the largest nonprofit funder of Alzheimer’s research, the Association serves people living with dementia, caregivers, and families across the country through its 24/7 Helpline, local chapters, education programs, and support groups.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Lewy Body Dementia Association
Lewy Line: (800) 539-9767
Monday–Friday, 5:00 AM–2:00 PM PST
The Lewy Body Dementia Association’s Support Services team and network of trained volunteers offer compassionate, confidential phone support to individuals and families navigating Lewy body dementia. Callers can reach trained support volunteers for emotional support, program referrals, and help identifying local education and community resources.
The Lewy Line
Individuals who are symptomatic or diagnosed with Lewy body dementia (LBD), and current or former care partners and family members in the United States, can call the Lewy Line for trusted and confidential support. Support Services team members and trained “Lewy Buddy” volunteers offer compassionate listening and emotional support, customized referrals to additional LBDA programs and support groups, and help identifying available education and community resources. Callers are asked to leave a message, and the Support Services team returns calls within 3 business days. LBDA is unable to return calls placed from outside the United States.
Time: Monday–Friday, 5:00 AM–2:00 PM PST
Date(s): Ongoing — no scheduled end date
Format: Virtual (phone, email, and online contact form)
Platform: Phone, email, and online form — Call (800) 539-9767 · Email [email protected] · Contact LBDA Online
Primary Resources
LBDA Website · Home base for LBD information, research updates, and ways to get involved
Understanding LBD · Overview of Lewy body dementia symptoms, diagnosis, and disease progression
Educational & Resource Programs
Education & Support · Latest information and research to build awareness and understanding of LBD
2026 Community Webinar Series · Free monthly webinars covering LBD science, care strategies, and everyday living
Lewy Publications · Printed and digital guides for patients, families, and healthcare professionals
LBDA Research · Current research initiatives and Research Centers of Excellence advancing LBD science
Social Media Connections
Facebook · Instagram · LinkedIn · X · YouTube
Crisis Support
988 Suicide & Crisis Lifeline · Call or text 988 for confidential 24/7 crisis support if you or a loved one is in crisis
About Lewy Body Dementia Association
The Lewy Body Dementia Association (LBDA) was founded in 2003 by a group of caregivers who connected through an online LBD support group and recognized the need for greater awareness and support. LBDA is a 501(c)(3) nonprofit and the leading national organization dedicated to Lewy body dementia.
Through outreach, education, and research, LBDA works to optimize the quality of life for those affected by LBD, accelerating awareness, advancing research for earlier diagnosis and improved care, and providing comprehensive education and compassionate support.
LBDA serves the estimated 1.4 million people in the United States living with Lewy body dementia, along with their care partners, family members, and the healthcare professionals who support them.
LBDA’s programs include the Lewy Line support services helpline, a network of local support groups, community and professional education, and a collaboration of Research Centers of Excellence advancing the science of LBD.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
AFTD HelpLine
Monday–Friday, 6:00 AM–2:00 PM PST
Staffed by social workers at the Association for Frontotemporal Degeneration (AFTD), the AFTD HelpLine answers questions about frontotemporal degeneration (FTD) and connects callers to information, resources, and emotional support. The HelpLine serves people with FTD, their family members and care partners, and anyone navigating a new or existing diagnosis.
AFTD HelpLine
HelpLine staff provide information on FTD subtypes, guidance on managing a new diagnosis, connections to resources and support, and emotional support for people affected by FTD. Contact can be made by phone, email, or by scheduling a call with HelpLine staff directly.
Time: Monday–Friday, 6:00 AM–2:00 PM PST
Date(s): Ongoing — no scheduled end date
Format: Virtual (phone and email)
Platform: Phone and email — Call 1-866-507-7222 (toll-free) · Email the HelpLine · Schedule a Call
Support Services & Resources
AFTD Support Groups · Find in-person and virtual support groups for people with FTD and their care partners
What Is FTD? · Overview of frontotemporal degeneration, its subtypes, and how it differs from other forms of dementia
Dear HelpLine Articles · Reader-submitted questions answered by HelpLine social workers on living with and caring for someone with FTD
Crisis Support
988 Suicide & Crisis Lifeline · Call or text 988, or chat online for confidential crisis support, available 24/7
About the Association for Frontotemporal Degeneration
AFTD was founded in 2002 by Helen-Ann Comstock, an FTD caregiver, working alongside other caregivers, physicians, and researchers. The AFTD HelpLine launched in 2005 to provide information and support to people living with FTD.
AFTD’s mission is to improve the quality of life of people affected by FTD and to drive research toward a cure, advancing research, public awareness, support, professional education, and advocacy.
AFTD serves people diagnosed with FTD, their family members and care partners, and the healthcare professionals who support them, offering information, referrals, and educational resources nationwide.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Alzheimer’s Association 24/7 Helpline
The Alzheimer’s Association operates a free, nationwide Helpline at 800.272.3900, connecting people living with dementia, caregivers, and families with live support, local resources, and crisis assistance in more than 200 languages. Trained Helpline Agents and master’s-level Care Consultants are available around the clock, 365 days a year, to help with everything from a new diagnosis to caregiver stress and care planning.
Alzheimer’s Association 24/7 Helpline — https://www.alz.org/help-support/resources/helpline · 800.272.3900 — available day or night, every day of the year
Support Services & Contact Information
Live Chat — https://www.alz.org/help-support/resources/helpline · Typically available Monday–Saturday, 5:00 AM–5:00 PM PST
Online Contact Form — https://www.alz.org/help-support/resources/helpline · For non-urgent questions — response within 24 hours
E-News Sign-Up — https://www.alz.org/e-news · Weekly updates on Alzheimer’s care, support, and research
Website
Alzheimer’s Association — https://www.alz.org
About Alzheimer’s Association
The Alzheimer’s Association was founded in 1980 by Jerome H. Stone and a group of family caregivers who saw the need for an organization to unite caregivers, provide support, and advance research into the disease. It is headquartered in Chicago with chapters in communities nationwide.
The Association’s mission is to lead the way to end Alzheimer’s and all other dementia by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support.
As the largest nonprofit funder of Alzheimer’s research, the Association serves people living with dementia, caregivers, and families across the country through its 24/7 Helpline, local chapters, education programs, and support groups.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Lewy Body Dementia Association
Lewy Line: (800) 539-9767
Monday–Friday, 5:00 AM–2:00 PM PST
The Lewy Body Dementia Association’s Support Services team and network of trained volunteers offer compassionate, confidential phone support to individuals and families navigating Lewy body dementia. Callers can reach trained support volunteers for emotional support, program referrals, and help identifying local education and community resources.
The Lewy Line
Individuals who are symptomatic or diagnosed with Lewy body dementia (LBD), and current or former care partners and family members in the United States, can call the Lewy Line for trusted and confidential support. Support Services team members and trained “Lewy Buddy” volunteers offer compassionate listening and emotional support, customized referrals to additional LBDA programs and support groups, and help identifying available education and community resources. Callers are asked to leave a message, and the Support Services team returns calls within 3 business days. LBDA is unable to return calls placed from outside the United States.
Time: Monday–Friday, 5:00 AM–2:00 PM PST
Date(s): Ongoing — no scheduled end date
Format: Virtual (phone, email, and online contact form)
Platform: Phone, email, and online form — Call (800) 539-9767 · Email [email protected] · Contact LBDA Online
Primary Resources
LBDA Website · Home base for LBD information, research updates, and ways to get involved
Understanding LBD · Overview of Lewy body dementia symptoms, diagnosis, and disease progression
Educational & Resource Programs
Education & Support · Latest information and research to build awareness and understanding of LBD
2026 Community Webinar Series · Free monthly webinars covering LBD science, care strategies, and everyday living
Lewy Publications · Printed and digital guides for patients, families, and healthcare professionals
LBDA Research · Current research initiatives and Research Centers of Excellence advancing LBD science
Social Media Connections
Facebook · Instagram · LinkedIn · X · YouTube
Crisis Support
988 Suicide & Crisis Lifeline · Call or text 988 for confidential 24/7 crisis support if you or a loved one is in crisis
About Lewy Body Dementia Association
The Lewy Body Dementia Association (LBDA) was founded in 2003 by a group of caregivers who connected through an online LBD support group and recognized the need for greater awareness and support. LBDA is a 501(c)(3) nonprofit and the leading national organization dedicated to Lewy body dementia.
Through outreach, education, and research, LBDA works to optimize the quality of life for those affected by LBD, accelerating awareness, advancing research for earlier diagnosis and improved care, and providing comprehensive education and compassionate support.
LBDA serves the estimated 1.4 million people in the United States living with Lewy body dementia, along with their care partners, family members, and the healthcare professionals who support them.
LBDA’s programs include the Lewy Line support services helpline, a network of local support groups, community and professional education, and a collaboration of Research Centers of Excellence advancing the science of LBD.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Alzheimer’s Association 24/7 Helpline
The Alzheimer’s Association operates a free, nationwide Helpline at 800.272.3900, connecting people living with dementia, caregivers, and families with live support, local resources, and crisis assistance in more than 200 languages. Trained Helpline Agents and master’s-level Care Consultants are available around the clock, 365 days a year, to help with everything from a new diagnosis to caregiver stress and care planning.
Alzheimer’s Association 24/7 Helpline — https://www.alz.org/help-support/resources/helpline · 800.272.3900 — available day or night, every day of the year
Support Services & Contact Information
Live Chat — https://www.alz.org/help-support/resources/helpline · Typically available Monday–Saturday, 5:00 AM–5:00 PM PST
Online Contact Form — https://www.alz.org/help-support/resources/helpline · For non-urgent questions — response within 24 hours
E-News Sign-Up — https://www.alz.org/e-news · Weekly updates on Alzheimer’s care, support, and research
Website
Alzheimer’s Association — https://www.alz.org
About Alzheimer’s Association
The Alzheimer’s Association was founded in 1980 by Jerome H. Stone and a group of family caregivers who saw the need for an organization to unite caregivers, provide support, and advance research into the disease. It is headquartered in Chicago with chapters in communities nationwide.
The Association’s mission is to lead the way to end Alzheimer’s and all other dementia by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support.
As the largest nonprofit funder of Alzheimer’s research, the Association serves people living with dementia, caregivers, and families across the country through its 24/7 Helpline, local chapters, education programs, and support groups.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Lewy Body Dementia Association
Lewy Line: (800) 539-9767
Monday–Friday, 5:00 AM–2:00 PM PST
The Lewy Body Dementia Association’s Support Services team and network of trained volunteers offer compassionate, confidential phone support to individuals and families navigating Lewy body dementia. Callers can reach trained support volunteers for emotional support, program referrals, and help identifying local education and community resources.
The Lewy Line
Individuals who are symptomatic or diagnosed with Lewy body dementia (LBD), and current or former care partners and family members in the United States, can call the Lewy Line for trusted and confidential support. Support Services team members and trained “Lewy Buddy” volunteers offer compassionate listening and emotional support, customized referrals to additional LBDA programs and support groups, and help identifying available education and community resources. Callers are asked to leave a message, and the Support Services team returns calls within 3 business days. LBDA is unable to return calls placed from outside the United States.
Time: Monday–Friday, 5:00 AM–2:00 PM PST
Date(s): Ongoing — no scheduled end date
Format: Virtual (phone, email, and online contact form)
Platform: Phone, email, and online form — Call (800) 539-9767 · Email [email protected] · Contact LBDA Online
Primary Resources
LBDA Website · Home base for LBD information, research updates, and ways to get involved
Understanding LBD · Overview of Lewy body dementia symptoms, diagnosis, and disease progression
Educational & Resource Programs
Education & Support · Latest information and research to build awareness and understanding of LBD
2026 Community Webinar Series · Free monthly webinars covering LBD science, care strategies, and everyday living
Lewy Publications · Printed and digital guides for patients, families, and healthcare professionals
LBDA Research · Current research initiatives and Research Centers of Excellence advancing LBD science
Social Media Connections
Facebook · Instagram · LinkedIn · X · YouTube
Crisis Support
988 Suicide & Crisis Lifeline · Call or text 988 for confidential 24/7 crisis support if you or a loved one is in crisis
About Lewy Body Dementia Association
The Lewy Body Dementia Association (LBDA) was founded in 2003 by a group of caregivers who connected through an online LBD support group and recognized the need for greater awareness and support. LBDA is a 501(c)(3) nonprofit and the leading national organization dedicated to Lewy body dementia.
Through outreach, education, and research, LBDA works to optimize the quality of life for those affected by LBD, accelerating awareness, advancing research for earlier diagnosis and improved care, and providing comprehensive education and compassionate support.
LBDA serves the estimated 1.4 million people in the United States living with Lewy body dementia, along with their care partners, family members, and the healthcare professionals who support them.
LBDA’s programs include the Lewy Line support services helpline, a network of local support groups, community and professional education, and a collaboration of Research Centers of Excellence advancing the science of LBD.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Alzheimer’s Association 24/7 Helpline
The Alzheimer’s Association operates a free, nationwide Helpline at 800.272.3900, connecting people living with dementia, caregivers, and families with live support, local resources, and crisis assistance in more than 200 languages. Trained Helpline Agents and master’s-level Care Consultants are available around the clock, 365 days a year, to help with everything from a new diagnosis to caregiver stress and care planning.
Alzheimer’s Association 24/7 Helpline — https://www.alz.org/help-support/resources/helpline · 800.272.3900 — available day or night, every day of the year
Support Services & Contact Information
Live Chat — https://www.alz.org/help-support/resources/helpline · Typically available Monday–Saturday, 5:00 AM–5:00 PM PST
Online Contact Form — https://www.alz.org/help-support/resources/helpline · For non-urgent questions — response within 24 hours
E-News Sign-Up — https://www.alz.org/e-news · Weekly updates on Alzheimer’s care, support, and research
Website
Alzheimer’s Association — https://www.alz.org
About Alzheimer’s Association
The Alzheimer’s Association was founded in 1980 by Jerome H. Stone and a group of family caregivers who saw the need for an organization to unite caregivers, provide support, and advance research into the disease. It is headquartered in Chicago with chapters in communities nationwide.
The Association’s mission is to lead the way to end Alzheimer’s and all other dementia by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support.
As the largest nonprofit funder of Alzheimer’s research, the Association serves people living with dementia, caregivers, and families across the country through its 24/7 Helpline, local chapters, education programs, and support groups.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Lewy Body Dementia Association
Lewy Line: (800) 539-9767
Monday–Friday, 5:00 AM–2:00 PM PST
The Lewy Body Dementia Association’s Support Services team and network of trained volunteers offer compassionate, confidential phone support to individuals and families navigating Lewy body dementia. Callers can reach trained support volunteers for emotional support, program referrals, and help identifying local education and community resources.
The Lewy Line
Individuals who are symptomatic or diagnosed with Lewy body dementia (LBD), and current or former care partners and family members in the United States, can call the Lewy Line for trusted and confidential support. Support Services team members and trained “Lewy Buddy” volunteers offer compassionate listening and emotional support, customized referrals to additional LBDA programs and support groups, and help identifying available education and community resources. Callers are asked to leave a message, and the Support Services team returns calls within 3 business days. LBDA is unable to return calls placed from outside the United States.
Time: Monday–Friday, 5:00 AM–2:00 PM PST
Date(s): Ongoing — no scheduled end date
Format: Virtual (phone, email, and online contact form)
Platform: Phone, email, and online form — Call (800) 539-9767 · Email [email protected] · Contact LBDA Online
Primary Resources
LBDA Website · Home base for LBD information, research updates, and ways to get involved
Understanding LBD · Overview of Lewy body dementia symptoms, diagnosis, and disease progression
Educational & Resource Programs
Education & Support · Latest information and research to build awareness and understanding of LBD
2026 Community Webinar Series · Free monthly webinars covering LBD science, care strategies, and everyday living
Lewy Publications · Printed and digital guides for patients, families, and healthcare professionals
LBDA Research · Current research initiatives and Research Centers of Excellence advancing LBD science
Social Media Connections
Facebook · Instagram · LinkedIn · X · YouTube
Crisis Support
988 Suicide & Crisis Lifeline · Call or text 988 for confidential 24/7 crisis support if you or a loved one is in crisis
About Lewy Body Dementia Association
The Lewy Body Dementia Association (LBDA) was founded in 2003 by a group of caregivers who connected through an online LBD support group and recognized the need for greater awareness and support. LBDA is a 501(c)(3) nonprofit and the leading national organization dedicated to Lewy body dementia.
Through outreach, education, and research, LBDA works to optimize the quality of life for those affected by LBD, accelerating awareness, advancing research for earlier diagnosis and improved care, and providing comprehensive education and compassionate support.
LBDA serves the estimated 1.4 million people in the United States living with Lewy body dementia, along with their care partners, family members, and the healthcare professionals who support them.
LBDA’s programs include the Lewy Line support services helpline, a network of local support groups, community and professional education, and a collaboration of Research Centers of Excellence advancing the science of LBD.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Alzheimer’s Association 24/7 Helpline
The Alzheimer’s Association operates a free, nationwide Helpline at 800.272.3900, connecting people living with dementia, caregivers, and families with live support, local resources, and crisis assistance in more than 200 languages. Trained Helpline Agents and master’s-level Care Consultants are available around the clock, 365 days a year, to help with everything from a new diagnosis to caregiver stress and care planning.
Alzheimer’s Association 24/7 Helpline — https://www.alz.org/help-support/resources/helpline · 800.272.3900 — available day or night, every day of the year
Support Services & Contact Information
Live Chat — https://www.alz.org/help-support/resources/helpline · Typically available Monday–Saturday, 5:00 AM–5:00 PM PST
Online Contact Form — https://www.alz.org/help-support/resources/helpline · For non-urgent questions — response within 24 hours
E-News Sign-Up — https://www.alz.org/e-news · Weekly updates on Alzheimer’s care, support, and research
Website
Alzheimer’s Association — https://www.alz.org
About Alzheimer’s Association
The Alzheimer’s Association was founded in 1980 by Jerome H. Stone and a group of family caregivers who saw the need for an organization to unite caregivers, provide support, and advance research into the disease. It is headquartered in Chicago with chapters in communities nationwide.
The Association’s mission is to lead the way to end Alzheimer’s and all other dementia by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support.
As the largest nonprofit funder of Alzheimer’s research, the Association serves people living with dementia, caregivers, and families across the country through its 24/7 Helpline, local chapters, education programs, and support groups.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Lewy Body Dementia Association
Lewy Line: (800) 539-9767
Monday–Friday, 5:00 AM–2:00 PM PST
The Lewy Body Dementia Association’s Support Services team and network of trained volunteers offer compassionate, confidential phone support to individuals and families navigating Lewy body dementia. Callers can reach trained support volunteers for emotional support, program referrals, and help identifying local education and community resources.
The Lewy Line
Individuals who are symptomatic or diagnosed with Lewy body dementia (LBD), and current or former care partners and family members in the United States, can call the Lewy Line for trusted and confidential support. Support Services team members and trained “Lewy Buddy” volunteers offer compassionate listening and emotional support, customized referrals to additional LBDA programs and support groups, and help identifying available education and community resources. Callers are asked to leave a message, and the Support Services team returns calls within 3 business days. LBDA is unable to return calls placed from outside the United States.
Time: Monday–Friday, 5:00 AM–2:00 PM PST
Date(s): Ongoing — no scheduled end date
Format: Virtual (phone, email, and online contact form)
Platform: Phone, email, and online form — Call (800) 539-9767 · Email [email protected] · Contact LBDA Online
Primary Resources
LBDA Website · Home base for LBD information, research updates, and ways to get involved
Understanding LBD · Overview of Lewy body dementia symptoms, diagnosis, and disease progression
Educational & Resource Programs
Education & Support · Latest information and research to build awareness and understanding of LBD
2026 Community Webinar Series · Free monthly webinars covering LBD science, care strategies, and everyday living
Lewy Publications · Printed and digital guides for patients, families, and healthcare professionals
LBDA Research · Current research initiatives and Research Centers of Excellence advancing LBD science
Social Media Connections
Facebook · Instagram · LinkedIn · X · YouTube
Crisis Support
988 Suicide & Crisis Lifeline · Call or text 988 for confidential 24/7 crisis support if you or a loved one is in crisis
About Lewy Body Dementia Association
The Lewy Body Dementia Association (LBDA) was founded in 2003 by a group of caregivers who connected through an online LBD support group and recognized the need for greater awareness and support. LBDA is a 501(c)(3) nonprofit and the leading national organization dedicated to Lewy body dementia.
Through outreach, education, and research, LBDA works to optimize the quality of life for those affected by LBD, accelerating awareness, advancing research for earlier diagnosis and improved care, and providing comprehensive education and compassionate support.
LBDA serves the estimated 1.4 million people in the United States living with Lewy body dementia, along with their care partners, family members, and the healthcare professionals who support them.
LBDA’s programs include the Lewy Line support services helpline, a network of local support groups, community and professional education, and a collaboration of Research Centers of Excellence advancing the science of LBD.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Alzheimer’s Association 24/7 Helpline
The Alzheimer’s Association operates a free, nationwide Helpline at 800.272.3900, connecting people living with dementia, caregivers, and families with live support, local resources, and crisis assistance in more than 200 languages. Trained Helpline Agents and master’s-level Care Consultants are available around the clock, 365 days a year, to help with everything from a new diagnosis to caregiver stress and care planning.
Alzheimer’s Association 24/7 Helpline — https://www.alz.org/help-support/resources/helpline · 800.272.3900 — available day or night, every day of the year
Support Services & Contact Information
Live Chat — https://www.alz.org/help-support/resources/helpline · Typically available Monday–Saturday, 5:00 AM–5:00 PM PST
Online Contact Form — https://www.alz.org/help-support/resources/helpline · For non-urgent questions — response within 24 hours
E-News Sign-Up — https://www.alz.org/e-news · Weekly updates on Alzheimer’s care, support, and research
Website
Alzheimer’s Association — https://www.alz.org
About Alzheimer’s Association
The Alzheimer’s Association was founded in 1980 by Jerome H. Stone and a group of family caregivers who saw the need for an organization to unite caregivers, provide support, and advance research into the disease. It is headquartered in Chicago with chapters in communities nationwide.
The Association’s mission is to lead the way to end Alzheimer’s and all other dementia by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support.
As the largest nonprofit funder of Alzheimer’s research, the Association serves people living with dementia, caregivers, and families across the country through its 24/7 Helpline, local chapters, education programs, and support groups.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Alzheimer’s Association 24/7 Helpline
The Alzheimer’s Association operates a free, nationwide Helpline at 800.272.3900, connecting people living with dementia, caregivers, and families with live support, local resources, and crisis assistance in more than 200 languages. Trained Helpline Agents and master’s-level Care Consultants are available around the clock, 365 days a year, to help with everything from a new diagnosis to caregiver stress and care planning.
Alzheimer’s Association 24/7 Helpline — https://www.alz.org/help-support/resources/helpline · 800.272.3900 — available day or night, every day of the year
Support Services & Contact Information
Live Chat — https://www.alz.org/help-support/resources/helpline · Typically available Monday–Saturday, 5:00 AM–5:00 PM PST
Online Contact Form — https://www.alz.org/help-support/resources/helpline · For non-urgent questions — response within 24 hours
E-News Sign-Up — https://www.alz.org/e-news · Weekly updates on Alzheimer’s care, support, and research
Website
Alzheimer’s Association — https://www.alz.org
About Alzheimer’s Association
The Alzheimer’s Association was founded in 1980 by Jerome H. Stone and a group of family caregivers who saw the need for an organization to unite caregivers, provide support, and advance research into the disease. It is headquartered in Chicago with chapters in communities nationwide.
The Association’s mission is to lead the way to end Alzheimer’s and all other dementia by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support.
As the largest nonprofit funder of Alzheimer’s research, the Association serves people living with dementia, caregivers, and families across the country through its 24/7 Helpline, local chapters, education programs, and support groups.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Alzheimer’s Association 24/7 Helpline
The Alzheimer’s Association operates a free, nationwide Helpline at 800.272.3900, connecting people living with dementia, caregivers, and families with live support, local resources, and crisis assistance in more than 200 languages. Trained Helpline Agents and master’s-level Care Consultants are available around the clock, 365 days a year, to help with everything from a new diagnosis to caregiver stress and care planning.
Alzheimer’s Association 24/7 Helpline — https://www.alz.org/help-support/resources/helpline · 800.272.3900 — available day or night, every day of the year
Support Services & Contact Information
Live Chat — https://www.alz.org/help-support/resources/helpline · Typically available Monday–Saturday, 5:00 AM–5:00 PM PST
Online Contact Form — https://www.alz.org/help-support/resources/helpline · For non-urgent questions — response within 24 hours
E-News Sign-Up — https://www.alz.org/e-news · Weekly updates on Alzheimer’s care, support, and research
Website
Alzheimer’s Association — https://www.alz.org
About Alzheimer’s Association
The Alzheimer’s Association was founded in 1980 by Jerome H. Stone and a group of family caregivers who saw the need for an organization to unite caregivers, provide support, and advance research into the disease. It is headquartered in Chicago with chapters in communities nationwide.
The Association’s mission is to lead the way to end Alzheimer’s and all other dementia by accelerating global research, driving risk reduction and early detection, and maximizing quality care and support.
As the largest nonprofit funder of Alzheimer’s research, the Association serves people living with dementia, caregivers, and families across the country through its 24/7 Helpline, local chapters, education programs, and support groups.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.
Lewy Body Dementia Association
Lewy Line: (800) 539-9767
Monday–Friday, 5:00 AM–2:00 PM PST
The Lewy Body Dementia Association’s Support Services team and network of trained volunteers offer compassionate, confidential phone support to individuals and families navigating Lewy body dementia. Callers can reach trained support volunteers for emotional support, program referrals, and help identifying local education and community resources.
The Lewy Line
Individuals who are symptomatic or diagnosed with Lewy body dementia (LBD), and current or former care partners and family members in the United States, can call the Lewy Line for trusted and confidential support. Support Services team members and trained “Lewy Buddy” volunteers offer compassionate listening and emotional support, customized referrals to additional LBDA programs and support groups, and help identifying available education and community resources. Callers are asked to leave a message, and the Support Services team returns calls within 3 business days. LBDA is unable to return calls placed from outside the United States.
Time: Monday–Friday, 5:00 AM–2:00 PM PST
Date(s): Ongoing — no scheduled end date
Format: Virtual (phone, email, and online contact form)
Platform: Phone, email, and online form — Call (800) 539-9767 · Email [email protected] · Contact LBDA Online
Primary Resources
LBDA Website · Home base for LBD information, research updates, and ways to get involved
Understanding LBD · Overview of Lewy body dementia symptoms, diagnosis, and disease progression
Educational & Resource Programs
Education & Support · Latest information and research to build awareness and understanding of LBD
2026 Community Webinar Series · Free monthly webinars covering LBD science, care strategies, and everyday living
Lewy Publications · Printed and digital guides for patients, families, and healthcare professionals
LBDA Research · Current research initiatives and Research Centers of Excellence advancing LBD science
Social Media Connections
Facebook · Instagram · LinkedIn · X · YouTube
Crisis Support
988 Suicide & Crisis Lifeline · Call or text 988 for confidential 24/7 crisis support if you or a loved one is in crisis
About Lewy Body Dementia Association
The Lewy Body Dementia Association (LBDA) was founded in 2003 by a group of caregivers who connected through an online LBD support group and recognized the need for greater awareness and support. LBDA is a 501(c)(3) nonprofit and the leading national organization dedicated to Lewy body dementia.
Through outreach, education, and research, LBDA works to optimize the quality of life for those affected by LBD, accelerating awareness, advancing research for earlier diagnosis and improved care, and providing comprehensive education and compassionate support.
LBDA serves the estimated 1.4 million people in the United States living with Lewy body dementia, along with their care partners, family members, and the healthcare professionals who support them.
LBDA’s programs include the Lewy Line support services helpline, a network of local support groups, community and professional education, and a collaboration of Research Centers of Excellence advancing the science of LBD.
Disclaimer: This listing is shared for community information only. The event is organized and hosted by the listed organization, not by PeerGalaxy. Dates, times, and access links are subject to change — please confirm details with the organizer before attending.