Can Someone with Lewy Body Dementia Live Alone?
Living with Lewy body dementia (LBD) means facing hard questions, and whether your loved one can safely live…

Lewy Body Dementia currently affects 1.4 million Americans. Its symptoms are similar to Parkinson’s disease and Alzheimer’s disease, which leads to frequent misdiagnosis, delaying treatment and jeopardizing the patient’s health. Support for Lewy Body Dementia research helps doctors, scientists, caregivers, and researchers better understand the disease, allowing those suffering with LBD to receive an early and correct diagnosis. Here’s how you can support Lewy Body Dementia research.
Volunteers are essential in furthering Lewy Body Dementia research. Clinics, therapy centers, laboratories, and LBD non-profits utilize the help of volunteers. Regardless of your specific area of expertise, a variety of volunteer opportunities are available for those looking to get involved.
The Lewy Body Dementia Resource Center is the only organization in the country with a live helpline for caregivers who have questions about LBD. This helpline is volunteer-run and by utilizing the help of passionate, loving individuals who have experienced difficulty, we strengthen the Lewy Body Dementia support network and bring others into the fold.
Helping with a support group is another great way to volunteer your time. Support groups have a direct, positive impact on the LBD caregiver community but also generate personal conversation around the nuances of caring for an individual with Lewy Body Dementia. These communities indirectly support research because they facilitate the collection of information based on first hand experiences.
It’s no secret that medical research is extremely costly. While there is a variety of funding available, some grants and subsidies have restrictions or get funneled to the overarching diseases of Alzheimer’s, Parkinson’s, or general Dementia, instead of specific Lewy Body Dementia research.
Financial donations can also help fund outreach programs. Art classes, speech therapy, or dance lessons help improve the cognition and motor functions of those suffering from Lewy Body Dementia. Donations can help fund care centers and classrooms around the country.
Moreover, monetary gifts are a kind way to honor someone who has passed or who is currently suffering from Lewy Body Dementia. Memorial donations provide longer lasting benefits than flowers or gift baskets, and instead contribute to care, advancement, and education. For those grieving from the loss of a loved one to Lewy Body Dementia, a memorial donation can provide comfort in knowing their loved one is remembered.
Raising awareness within your local community for Lewy Body Dementia is important in furthering support and concern for the disease. The more awareness around the disease, the more accurate doctors can be when diagnosing patients with Lewy Body Dementia. If folks are unaware of symptoms, or even unaware of the disease’s existence, there may be a delay in getting their parent, friend, or loved one proper care.
Consider organizing a charity walk or hosting a booth at your local health fair to spread the word and raise money. Educate those around you on the early stages of Lewy Body Dementia, how to care for someone with LBD, or even highlight symptoms that people with LBD experience daily.
Raising awareness about LBD also provides an outlet for care partners of those living with Lewy Body Dementia. Caregivers need support, and by initiating conversations about Lewy Body Dementia, we connect families touched by the disease.
Donations to the Lewy Body Dementia Resource Center can help support all of the aspects mentioned, in addition to their support groups, helpline, comprehensive website, and personal attention.
Living with Lewy body dementia (LBD) means facing hard questions, and whether your loved one can safely live…
This June 24 – 26, the Cleveland Clinic will host its International Lewy Body Dementia Conference at Caesars…
Noting that tastes, likes and dislikes change and diminish appetites of many Lewy Body patients leaves the caregiver…
Lewy Body Dementia Resource Centerより、新しい記事、介護ガイド、ウェビナー、コミュニティイベントの情報をお届けします。
Norma Loebによって設立されたLBDRCは、レビー小体型認知症に向き合う個人やご家族に対し、米国全土および世界中で無料のサポート、教育、コミュニティを提供しています。
📞当ウェブサイトおよびヘルプラインで提供される情報は、LBDのケアを担当される方々へのリソースであり、特定の製品、薬、医療処置を推奨するものではありません。また、専門的な医療アドバイスに代わるものでもありません。
© 2026 Lewy Body Dementia Resource Center. All Rights Reserved.