← Return to Lewy Body Dementia - What are your questions?

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@jodimelius

These are excellent questions! First, I want to direct you to our upcoming LBD Summit on May 3rd. We will have expert presenters answering these very questions; as well as presenting a video series post event on these and other topics. Information and registration via this link: https://connect.mayoclinic.org/event/lewy-body-dementia-knowledge-support-summit/

It can be difficult for practitioners to diagnose LBD if they have not been exposed to diagnostic information about this type of dementia. LBD can start with sleep disorders years to decades before other symptoms appear. Mental health symptoms such as depression, apathy and anxiety can also appear first, and be a primary focus before memory and other cognitive changes appear. In short, it is a complex form of dementia with many symptoms to piece together in making an accurate diagnosis. Mayo Clinic and other research centers are working hard to provide this information to providers, allied health staff, families and community to help close this information gap.

There are medications that can help with symptom management; and there are medications that should NOT be given. Please join us for the Summit to hear more from expert presenters on this and the rest of your questions. Thank you for asking them!

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Replies to "These are excellent questions! First, I want to direct you to our upcoming LBD Summit on..."

Thanks for your reply, Jodi. I am registered for the May 3 event and I'm looking forward to it. I am the mentor for the Parkinson's discussion group on Mayo Clinic Connect and I've had some members report on an LBD diagnosis, mainly of their loved ones.
I also had a friend whose husband was misdiagnosed as Alzheimer's and then later saw another specialist who corrected the diagnosis to LBD. She felt a lot of time was wasted treating him with Alzheimer's meds and I was just wondering how doctors are now progressing with correcting this. Specifically, what tests provide a correct diagnosis. She now has a support group for LBD caregivers.