Top LBD Symptoms and How to Recognize Them
Lewy Body Dementia can be difficult to diagnose because its symptoms can easily be missed or attributed to…
WHAT IS THE LEWY BODY DEMENTIA RESOURCE CENTER (LBDRC)?
The Lewy Body Dementia Resource Center (LBDRC) is a charitable 501(c)(3) non-profit organization created to provide personalized essential resources and information to people with LBD, caregivers, and medical professionals. Founder and Executive Director, Norma Loeb, launched LBDRC in New York to provide LBD families with information on a local level and with a personalized approach. After her mother, Lillian, was misdiagnosed with several diseases—and eventually diagnosed with LBD—Norma realized there were very little resources available. What was even more disturbing to her was that few medical professionals understood how to diagnose or treat LBD. She soon discovered that patients were not only generally misdiagnosed but were also being mistreated with certain antipsychotic medications which could lead to severe side effects or potentially fatal results. In order to help bring awareness to LBD, Norma served on the board of the Lewy Body Dementia Association for three years and facilitated the only two LBD support groups in New York (in Manhattan and Nassau County) which have been taking place for over ten years. LBDRC now runs two additional support groups in Westchester and Suffolk Counties.

In 2016, together with four other former LBD caregivers, Norma launched the LBDRC website which is dedicated to providing resources to LBD families on a local level and with a personalized touch. Through its Helpline (516-218-2026), their team provides individualized guidance and information not limited to the following:
Lewy Body Dementia can be difficult to diagnose because its symptoms can easily be missed or attributed to…
It’s important to get the best medical care…
Art therapy and sensory stimulation are quickly gaining traction in the Lewy Body Dementia community for their ability…
LBDRC 由 Norma Loeb 创立,旨在为美国及全球应对路易体痴呆的个人和家庭提供免费支持、教育和社区关怀。
📞本网站及我们的帮助热线提供的信息仅作为LBD照护者的资源,并不意味着对任何产品、药物或医疗程序的认可,也不能替代专业的医疗建议。
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