Volunteers are the cornerstone of our organization and are vital to raising awareness in the communities in which they live and work. Our team is composed of volunteers throughout the country who give their time and expertise to help support those affected by Lewy body dementias.
For more information on how to become an LBDA volunteer, contact us by email at firstname.lastname@example.org.
Families need your help today.
LBD affects an estimated 1.4 million people living in the U.S. LBD is often misdiagnosed as a psychiatric disorder or another form of dementia. Most of these people have partners, family, friends and other loved ones whose lives are also impacted by this disease. You can help.
Ways you can help:
- Support: Provide one-on-one or group support to those affected by LBD (Lewy Buddy, Support Group Facilitator, or Facebook Moderator)
- Projects: Participate in project activities (participating in research studies, sharing your experience in a webinar, influencing legislation and policy)
- Fundraise: Organize a fundraiser to support LBDA’s mission
Questions on volunteering?
Contact LBDA at email@example.com.
What is the Lewy Body Dementia Association?
LBDA is a nonprofit 501(c)(3) charitable organization, dedicated to increasing awareness of Lewy body dementia, providing outreach to families worldwide, and encouraging research.
What are the volunteer requirements?
Volunteers must be a minimum of 18 years of age or have parental knowledge and consent. Some volunteer positions require at least a one-year commitment to LBDA to assure continuity and stability of our services. If the volunteer position requires a time commitment, this will be discussed during the application process.
How can I become a volunteer?
After you have completed the volunteer application, an LBDA representative will contact you to discuss the volunteer opportunity that is right for you.