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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.