Patrick Glithero

Patrick Glithero

Care Partner

Reflecting on more than 30 years of a loving marriage with his wife Nancy, Patrick Glithero describes her as both “my person” and “an anchor for everyone who met her.” She held a degree in special education and worked with people with disabilities.

In 2016, Nancy started having difficulties driving. Soon, she was forgetting the rules of Euchre, a card game she’d been playing since her youth. A neurologist recognized her ‘minor cognitive impairment,’ but her eventual diagnosis of Lewy body dementia was still years away.

As Nancy’s symptoms worsened, she experienced a fall that required reconstructive shoulder surgery. Hallucinations were next. Then, a chance meeting with a nurse led the couple to a specialist at Massachusetts General who diagnosed Nancy with Lewy body dementia.

Patrick recalls that Nancy accepted her diagnosis as “better than the unknown,” while he committed to becoming her care partner immediately. “I don’t remember ever thinking about another choice other than doing whatever I needed to do,” says Patrick.

Despite Nancy’s acceptance and Patrick’s commitment, he says they faced a wilderness of fear despite Nancy's acceptance and Patrick's commitment. He noted that, "I feared that I could not do it all, that I might die first. I feared trying to explain to family and friends what the Lewy journey meant.”

Fortunately, the couple found LBDA online, and with the encouragement of the staff at Massachusetts General, soon connected with the organization. LBDA Support Services helped the couple navigate the uncertainties of the disease and helped Patrick face the many challenges of being a care partner.

After 33 years together, Patrick lost Nancy to LBD. Since then, his involvement with LBDA and his gratitude for the organization has only grown. Today, he continues to give back as an LBDA support group leader, a Lewy Buddy, and a participant in LBD studies.

“LBDA, its staff, and those it serves, to Nancy and I was an island when we were adrift,” says Patrick. “We could not have coped without LBDA and the community that LBDA has developed around the world.”

Everything we do is thanks to people like you.

Lewy body dementia (LBD) is the second most common form of progressive dementia in the United States — yet it remains widely misunderstood and frequently misdiagnosed. The Lewy Body Dementia Association is working to change that. As the leading national organization dedicated to improving the lives of individuals and families affected by Lewy body dementia (LBD), we advance research for earlier and more accurate diagnosis, accelerate public awareness of this complex disease, and provide comprehensive education and compassionate support for individuals, care partners and healthcare providers. Through educational programming bringing together cutting-edge science, compassionate care and the power of the lived experience, a nationwide support network, and convening leaders from academia, industry and government to advance diagnostic innovation, we are strengthening both the clinical landscape and the day-to-day experience of families navigating LBD.

Together, we are improving the lives of those affected by Lewy body dementia (LBD) and ensure that no one has to face LBD alone. Please consider making a charitable, tax-deductible donation today.

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