23 Things Loved Ones Want Others to Know About Lewy Body Dementia

In November Robin Williams’ wife Susan Williams revealed that the beloved actor had been living with Lewy Body Dementia (LBD) before he took his own life in August 2014. This came as a shock to the public, but the news also helped raise awareness for the surprisingly common neurological condition.

LBD affects approximately 1.4 million people in the United States, and it may cause hallucinations, impairment of motor function and symptoms similar to Alzheimer’s and Parkinson’s disease, making it difficult to diagnose. In fact, it is only possible to conclusively diagnose through a postmortem autopsy.

In an effort to learn more about the disease, The Mighty teamed up with the Lewy Body Dementia Association and asked their community what loved ones want others to know about LBD, and how to prepare if a family member may have it.

Here’s what they had to say:

1. “It cannot be treated like Alzheimer’s or any other dementia.” —Melinda Fennell

drops of dew on a green grass bokeh

2. “There are very few doctors who can reach the diagnosis.” —Roland Boutin

3. “A diagnosis doesn’t mean the person isn’t the same as they were the day before diagnosis. Call, visit and don’t run away. As with any diagnosis, the person still needs love and care. Be the one to take the time.” —Dianne Bramer

Low angle view of wooden boardwalk with plant growing on it at Bald Head Island, North Carolina.

4. “Try to focus on what your loved one can do instead of what they can no longer do. My 72-year-old mother, who was diagnosed with Lewy Body Dementia, still loves to ride horses; it’s the highlight of her week!” —Carla Weinzetl-Christ

Sunflowers growing in garden

5. “Lewy Body is not just an ‘old people’ disease. My younger brother started exhibiting symptoms in his 50s and now, at 67, has been in a nursing home for over two years. My 92-year-old mother goes to visit her youngest child in a nursing facility every week.” —Karen Kornhauser

Beauty Romantic Girl Outdoors.

6. “Be patient with your loved one who suffers from this. My dad was fortunate enough to know everything as it developed. We kept nothing from him. His hallucinations became something he enjoyed sharing. That was all he had. We let him, and we listened. It’s a terrible disease. It took my dad from me less than a year ago. There needs be be more research.” —Deneice Spurgeon

Senior couple embracing on beach, rear view

7. “There can be highs and lows of alertness and mental issues from week to week, day to day, even hour to hour.” –Kathy Teyler Jarrett

8. “’Dementia’ isn’t the first word to focus on. Please educate yourself so you can help us.” —Cheryl Flippin

Flowers in antique pitcher vase on wooden decking

9. “All of the pain and suffering we experience in seeing our loved one progress with this disease is nothing compared to what they are feeling. Always remember to be loving, compassionate and selfless when dealing with them. They need your familiar words, melodies, cheerfulness to still be a part of their days. Even though your loved one can become unrecognizable from the person they used to be, I believe there are still glimpses of him or her if you are aware enough and are ‘listening’ to nonverbal signs.” —Michelle Moore

10. “Your loved one is not being cruel or angry on purpose.” —Stephanie White

water drop on boat window at sea for background

11. “No matter how confused the person is, he’s still in there. Look him in the eye when you talk to him. His heart can still hear you, even if he can’t express it.” —Traci Milan

Open diary with blank pages and pen

12. “You have to be prepared to fight and fight for a second, third, fourth opinion, brain scans, tests, memory assessments. If you think your loved one has this illness then don’t rest until every test has been done.” —Liz Carr

13. “Please don’t talk about them with them sitting in the room … they can still understand the words… If you are lucky they will let you know sometimes they are still in there. There were many occasions that my dad still let me know he remembered me.” —Tracy DesRoche

vintage armchair on white wall.

14. “It affects the whole family.” —Lynn Corpron

15. “Don’t try to correct them — comfort them during their hallucinations because to them, it’s really how they see or feel!” —Wendy Johnson Ledbetter

water drop on wire after rain

16. “More education is imperative, and the clock is ticking.” —Amy Sottosanti

17. “As a caregiver, keep a notebook. Be specific — not “recently” but “three days ago.” List anything unusual, date it, take the notebook to every doctor appointment and show it to the doctor.” —Peggy Smith

18. “Expect the unexpected… Some good and some bad.” —Casey Herzfeld Goldblat

Close-up of a dandelion (Taraxacum officinale)

19. “Staying active with a regular exercise routine helps improve quality of life. Try including a routine for the whole family.” —Missy Anne Olivia

20. “It’s the illness that’s the problem, not the person.” —Jacqui Valentine

Sunrise at countryside landscape

21. “It exists. So many people have never heard of LBD.” —Gina Mensone Reis

22. “Once the disease takes hold, there is a misconception that people with LBD are stupid. They are still very smart, but their words are just trapped inside. They should still be treated with the same respect as before.” —Sue Pierce

23. “Your loved one needs you. You will need to be an advocate for them and educate others working with them. If your loved one is being cared for by others (in home sitters, assisted care, nursing home), you need to educate the staff not only of what is LBD but who your loved one is.” —Daniel McIlwain

white mock up frame, hipster background,

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